AU4805301A - Method to detect dirofilaria immitis infection - Google Patents

Description

-1-

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT

ORIGINAL

Name of Applicant: Heska Corporation Actual Inventors: Robert B Grieve and Glenn Robert Frank and Roy R Mondesire and James P Porter and Nancy Wisnewski Address for Service: BALDWIN SHELSTON WATERS 60 MARGARET STREET SYDNEY NSW 2000 Invention Title: 'METHOD TO DETECT DIROFILARIA IMMITIS INFECTION' Details of Original Application No. 43537/97 dated 18 Sep 1997 The following statement is a full description of this invention, including the best method of performing it known to me/us:- File: 31869AUP00 IP Australia Documents received on: t 5 AY ju u1 Batch No: -la METHOD TO DETECT DIROFILARJA IMMITIS INFECTION Field of the Invention The present invention relates to a novel method to detect D. immitis infection in animals, particularly in cats. The present invention also includes novel kits to detect D.

immitis infection as well as methods to purify the detection reagent.

Background of the Invention The parasitic helminth D. immitis has been known for a long time to infect dogs, thereby leading to heartworm. Recently, it has become clear that D. immitis also infects other animals, such as cats and ferrets, even though such animals are essentially nonadpated hosts for the infection. That is, the parasitic relationship between D. immitis and adapted animals is well adapted, and there are very few clinical signs unless worm burden is very high. In contrast, non-adapted animals, such as cats and ferrets, have a parasitic relationship with D. immitis that is not well adapted, resulting in disease and sometimes death for the animal. Heartworm infection in non-adapted animals such as cats is hard to diagnose as there are a variety of clinical signs, some of which are also associated with other diseases. Heartworm disease may be acute or chronic, and can be associated with dyspnea, coughing and vomiting, lethargy, and/or anorexia. Thus, there 20 is a need for an unambiguous method to detect heartworm in animals.

The life cycle of D. immitis is complex in all animals it infects, and the organism is difficult to detect, particularly prior to adult worm maturation. Detection is particularly difficult in non-adapted hosts where the worm burden is very low. Cats, for example, harbor, on average, only two to three worms, making detection of D. immitisspecific antigens or antibodies difficult.

Sexually mature adults, after mating, produce microfilariae which traverse capillary beds and circulate in the vascular system of the host. One method of demonstrating infection in a dog, for example, is to detect the circulating microfilariae.

Another method is to detect D. immitis circulating parasite antigens in the blood; these antigens are associated with adult female worms and microfilariae (see, for example, U.S. Patent No. 4,839,275, issued June 13, 1989, by Weil). In a non-adapted host, however, D. immitis infection often results in the maturation of only a single worm, in which case there is no opportunity for reproduction, and eggs and microfilariae are not produced. In addition, the single worm is often a male worm.

If an infected animal is maintained in an insect-free environment, the life cycle of the parasite cannot progress. However, when microfilariae are ingested by the female mosquito during blood feeding on an infected animal, subsequent development of the microfilariae into larvae occurs in the mosquito. The microfilariae go through two larval stages (LI and L2) and finally become mature third stage larvae (L3) which can then be transmitted back to a host animal through the bite of the mosquito. It is this L3 stage, therefore, that accounts for the initial infection. As early as three days after infection, the L3 molt to the fourth larval (L4) stage, and subsequently to the fifth stage, or immature adults. The immature adults migrate to the heart and pulmonary arteries, where they mature and reproduce, thus producing the microfilariae in the blood.

"Occult" infection with heartworm in a host is defined as that wherein no microfilariae can be detected, but the existence of the adult heartworms can be determined by other methods.

Another method to detect heartworm is the use of crude preparations; see, for example, U.S. Patent No. 4,657,850, issued April 14, 1987, by Grieve. These assays, however, lack desired sensitivity and specificity, particularly to detect infection in a nonadapted host.

Hong et al, 1995, Proc. Heartworm Symposium, p. 33, reported the cloning of a gene encoding D. immitis antigen DiT33; also see Hong et al, 1994, Abstracts of Amer.

Soc. Trop. Med.Hyg. Meeting, p1 91-192. Hong et al., 1995, ibid., also reported that a .recombinant fusion protein consisting of DiT33 linked to maltose binding protein could detect D. immitis infection in dogs at 11 weeks but did not report any use of the protein 20 to detect D. immitis infection in a non-adapted host, such as in a cat or ferret.

Previously, several investigators had reported the use of the related protein Onchocerca volvulus Ov33 to detect 0. volvulus or D. immitis infection, as well as cloning of the gene encoding 0. volvulus Ov33; see, for example, Santiago Mejia et al, 1994, Parasite Immunol 16, 297-303; Ogunrinade et al, 1993, J Clin Microbiol 31, 1741-1745; Lucius 25 et al., 1992, Trop Med Parasitol 43, 1 3 9 -145; Lucius et al, 1988, J. Exp Med 168, 1199- 1204; Lucius et al, 1988, J. Exp Med 167, 1505-1510. -A related gene encoding Av33 has been isolated from Acanthocheilonema viteae; see, for example, Willenbucher et al, 1993, Mol. Biochem. Parasitol. 57, 349-351. Once again, there was no mention of the •ability of that protein to detect infection in an animal with a low worm burden prior to adult worm maturation.

There remains a need for an accurate and simple method to detect D. immitis infection. Particularly needed is a method that would detect D. immitis infection prior to maturation of larvae into adult heartworms, but would not detect early infections that never develop into full-term infections, infections that the host immune response is able to prevent from developing into mature worms.

-3- Summary of the Invention The present invention includes detection methods and kits that detect D. immitis infection prior to maturation of larvae into adult heartworms, but do not detect early infections that do not develop into full-term infections infections that do not lead to mature heartworm development).

The present invention includes a method to detect D. immitis in a non-adapted host that includes the steps of: contacting a bodily fluid collected from the host with a formulation comprising an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti-Di33 antibodies; and measuring immunocomplex formation between the Di33 protein and anti-Di33 antibodies, if any, in the fluid, wherein the presence of such an immunocomplex indicates that the host is or has recently been infected with D. immitis.

The present invention also includes a method to detect D. immitis in a host animal, which includes the steps of: contacting a bodily fluid collected from the animal with a formulation comprising an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti-Di33 S: IgE antibodies; and immunocomplex formation between the Di33 protein and anti- Di33 IgE antibodies, if any, in the fluid, wherein the presence of such an immunocomplex indicates that the animal is or has recently been infected with D.

20 immitis.

Also included in the present invention is a method to detect D. immitis infection in a non-adapted host within 10 weeks of infection, the method comprising detecting anti-Di33 antibodies in a bodily fluid collected from the host.

The present invention also includes a method to detect D. immitis in a non- 25 adapted host, that includes the steps of: contacting a bodily fluid collected from the host with a formulation comprising an isolated anti-Di33 antibody under conditions sufficient to form an immunocomplex between the anti-Di33 antibody and D. immitis Di33 protein; and measuring immunocomplex formation between the anti-Di33 e* antibody and D. immitis Di33 protein, if any, in the fluid, wherein the presence of such an immunocomplex indicates that the host is or recently has been infected with D.

immitis.

One embodiment of the present invention is a kit to detect D. immitis infection that includes an isolated D. immitis Di33 protein and a composition to detect antibodies capable of forming an immunocomplex with the Di33 protein. Another embodiment is a kit to detect D. immitis infection that includes an isolated anti-Di33 antibody and a composition to detect an immunocomplex between the anti-Di33 antibody and D.

immitis Di33 protein.

-4- The present invention also includes Di33 proteins, nucleic acid molecules encoding such proteins, as well as recombinant molecules and recumbinant cells comprising such nucleic acid molecules, and anti-Di33 antibodies. Examples of Di33 proteins include, but are not limited to, PHIS-PDi33 234 and PDi33 2 17 Examples of Di33 nucleic acid molecules include, but are not limited to, nDi33 3 46 nDi33 750 nDi33 702 nDi33 7 0s, and nDi33 651 Also included are methods to produce Di33 nucleic acid molecules, Di33 nucleic acid molecule-containing recombinant molecules, Di33 nucleic acid molecule-containing recombinant cells, Di33 proteins and anti-Di33 antibodies.

One embodiment of the present invention is a method to produce an isolated D. immitis Di33 protein that includes the steps of culturing a bacterium transformed with a D. immitis Di33 nucleic acid molecule to produce a D. immitis Di33 proteincontaining culture; recovering insoluble material comprising the Di33 protein from the culture; and purifying the Di33 protein from the insoluble material. Also included is a method for purifying a D. immitis Di33 protein comprising recovering Di33 protein from cation exchange chromatography of disrupted insoluble material obtained from a culture of D. immitis Di33 protein-producing recombinant cells.

Brief Description of the Figures Fig. 1 depicts ELISA results using a heartworm detection reagent of the present 20 invention to detect anti-Di33 IgG antibodies in D. immitis-infected cats.

Fig. 2 depicts ELISA results using a heartworm detection reagent of the present invention to detect anti-Di33 IgG antibodies in D. immitis-infected cats.

"Fig. 3 depicts ELISA results using a heartworm detection reagent of the present invention to detect anti-Di33 IgE antibodies in D. immitis-infected cats.

25 Fig. 4 depicts ELISA results using a heartworm detection reagent of the present invention to detect anti-Di33 IgE antibodies in D. immitis-infected cats.

Detailed Description of the Invention The present invention relates to the surprising discovery that D. immitis Di33 protein-based detection diagnostic, screening) methods and kits can detect D.

immitis infection in a non-adapted host an animal susceptible to heartworm infection in which D. immitis does not establish a parasitic relationship) at the time that the D. immitis larvae are maturing from L4 to L5, even though the worm burden in such a host is very low. As such, D. immitis detection methods and kits of the present invention are able to detect D. immitis in a non-adapted host prior to maturation of the D.

immitis into an adult heartworm. Thus, unlike assays based solely on detection of reagents linked to egg-laying, methods and kits of the present invention detect D.

immitis infection before adult heartworms are sexually active; heartworms usually become reproductively active at about 6.5 months post infection. D. immitis detection methods and kits of the present invention can detect D. immitis in a non-adapted host at least about ten weeks, and in some cases as early as about eight weeks post following) infection of the host with D. immitis. D. immitis infection can also be detected in non-adapted hosts harboring adult heartworms. As such, D. immitis infection can be detected at any time from about 8 to 10 weeks post infection through the adult life stage of the heartworm, which in cats, for example, is about 2 to 3 years. As such, D.

immitis can be detected at about 12 weeks, 16 weeks, 20 weeks, and 24 weeks about 6 months) following infection, as well as at any intermittant or later times. D.

immitis infections of less than about 4 to about 6 weeks, however, are not typically detected using Di33 protein. Detection methods and kits of the present invention are particularly useful in that they can detect infection in a non-adapted host harboring maintaining, having for a sustained time, infected with) only a single worm. Moreover, detection methods and kits of the present invention can detect an infection resulting in a S" single male worm or in a single female worm. It is to be noted, of course, that the D.

immitis Di33-based methods and kits of the present invention can also detect larger worm burden, including, but not limited to, 2, 3, 4 or 5 worms. Therefore, the methods and kits of the present invention can detect D. immitis infection in any infected non- 20 adapted host, except for very early-stage infections that are likely to resolve themselves or that may be treated by monthly anti-helminth drug applications, and thus do not develop into full-term infections infections that do not lead to mature heartworm development). Detection methods of the present invention are not only very sensitive, but also are specific for D. immitis infection.

25 Another discovery of the present invention is that D. immitis infection stimulates the production of anti-D. immitis Di33 immunoglobulin E antibodies (anti-Di33 IgE antibodies) as well as of other isotypes of anti-D. immitis Di33 antibodies, such as anti- D. immitis Di33 immunoglobulin G antibodies (anti-Di33 IgG antibodies). Thus, the present invention also includes D. immitis detection methods and kits based on detection of anti-Di33 IgE antibodies, as well as methods and kits based on detection of other isotypes of anti-Di33 antibodies, such as anti-Di33 IgG antibodies. While not being bound by theory, it is believed that anti-Di33 IgE-based methods and kits may have increased specificity compared to anti-Di33 IgG-based methods and kits, whereas anti- Di33 IgG-based methods and kits are more sensitive than anti-Di33 IgE-based methods and kits.

The present invention includes a method to detect D. immitis heartworm infection) in a non-adapted host using an isolated D. immitis Di33 protein to detect any -6anti-Di33 antibodies present in a bodily fluid collected from such a host. The present invention also includes a method to detect D. immitis in any animal susceptible to D.

immitis infection using an isolated D. immitis Di33 protein to detect anti-Di33 IgE antibodies. Another embodiment is the use of anti-Di33 antibodies to detect D. immitis infection. Also included in the present invention are kits to detect D. immitis infection based on such methods as well recombinant molecules and recombinant cells to produce D. immitis Di33 proteins and methods to purify such proteins.

It is to be noted that the term entity or "an" entity refers to one or more of that entity; for example, a protein refers to one or more proteins or at least one protein. As such, the terms (or "one or more" and "at least one" can be used interchangeably herein. It is also to be noted that the terms "comprising", "including", and "having" can be used interchangeably.

According to the present invention, an isolated, or biologically pure, D. immitis Di33 protein, is a protein that has been removed from its natural milieu. As such, "isolated" and "biologically pure" do not necessarily reflect the extent to which the protein has been purified. An isolated D. immitis Di33 protein of the present invention can be obtained from its natural source from D. immitis), can be produced using recombinant DNA technology or can be produced by chemical synthesis.

As used herein, an isolated D. immitis Di33 protein (also referred to herein as a 20 Di33 protein, or a D. immitis protein of about 33 kilodaltons can be a full-length protein or any homolog of such a protein. An isolated Di33 protein of the present invention, including a homolog, can be identified in a straight-forward manner by the Di33 protein's ability to form an immunocomplex with an anti-D. immitis Di33 antibody, also referred to herein as an anti-Di33 antibody; anti-Di33 antibodies are 25 described in more detail elsewhere herein. Examples of Di33 homologs include Di33 proteins in which amino acids have been deleted a truncated version of the protein, such as a peptide), inserted, inverted, substituted and/or derivatized by glycosylation, phosphorylation, acetylation, myristoylation, prenylation, palmitoylation, S. amidation and/or addition of glycerophosphatidyl inositol) such that the homolog includes at least one epitope capable of forming an immunocomplex with an anti-Di33 antibody.

Di33 protein homologs can be the result of natural allelic variation or natural mutation. Di33 homologs of the present invention can also be produced using techniques known in the art including, but not limited to, direct modifications to the protein or modifications to the gene encoding the protein using, for example, classic or recombinant DNA techniques to effect random or targeted mutagenesis. The nucleic acid sequence of the coding strand of a cDNA encoding an apparent full-length Di33 -7protein of the present invention is represented herein as SEQ ID NO:2. The doublestranded nucleic acid molecule including both the coding strand having SEQ ID NO:2 and the complementary non-coding strand the nucleic acid sequence of which can be readily determined by one skilled in the art) is referred to herein as Di33 nucleic acid molecule nDi33 750 Translation of SEQ ID NO:2 suggests that nucleic acid molecule nDi33750 encodes a full-length D. immitis Di33 protein of about 234 amino acids, referred to herein as PDi33 234 represented by SEQ ID NO:3, assuming an open reading frame having an initiation (start) codon spanning from about nucleotide 24 through about nucleotide 26 of SEQ ID NO:2 and a termination (stop) codon spanning from about nucleotide 726 through about nucleotide 728 of SEQ ID NO:2. The coding region encoding PDi33234, excluding the stop codon, is represented by nucleic acid molecule nDi33 702 having a coding strand with the nucleic acid sequence represented herein as SEQ ID NO:4. SEQ ID NO:4 appears to encode a signal peptide of about 17 amino acids as well as an apparent mature protein of about 217 amino acids, denoted herein as PDi33 21 7 the amino acid sequence of which is represented herein as SEQ ID S* NO:7. The nucleic acid molecule encoding the apparent mature protein is referred to as nDi33 651 the nucleic acid sequence of the coding strand of which is denoted herein as SEQ ID NO:6. Knowledge of these nucleic acid and amino acid sequences allows one skilled in the art to make modifications to the respective nucleic acid molecules and 20 proteins to, for example, develop a Di33 protein with increased solubility and/or a truncated protein a peptide) capable of detecting D. immitis Di33 infection. For example, modifications to PHIS-PDi33 234 (the production of which is described in the Examples) likely to yield a more soluble protein include, but are not limited to, deletion of the putative signal sequence and/or protein iodoacetimidation.

25 The present invention also includes the use of Di33 mimetopes to detect D.

immitis infection. In accordance with the present invention, a "mimetope" refers to any compound that is able to mimic the ability of a Di33 protein to bind to an anti-Di33 antibody. A mimetope can be a peptide that has been modified to decrease its susceptibility to degradation but that still retains antibody-binding activity. Other examples of mimetopes include, but are not limited to, carbohydrate-based compounds, lipid-based compounds, nucleic acid-based compounds, natural organic compounds, synthetically derived organic compounds, anti-idiotypic antibodies and/or catalytic antibodies, or fragments thereof. A mimetope can be obtained by, for example, screening libraries of synthetic compounds for compounds capable of binding to anti- Di33 antibodies. A mimetope can also be obtained by, for example, rational drug design. In a rational drug design procedure, the three-dimensional structure of a compound of the present invention can be analyzed by, for example, nuclear magnetic resonance (NMR) or x-ray crystallography. The three-dimensional structure can then be used to predict structures of potential mimetopes by, for example, computer modeling.

The predicted mimetope structures can then be produced by, for example, chemical synthesis, recombinant DNA technology, or by isolating a mimetope from a natural source.

Also included in the present invention are anti-D. immitis Di33 antibodies, also referred to as anti-Di33 antibodies. Such antibodies are able to selectively bind to a Di33 protein of the present invention. As used herein, the term "selectively binds to" refers to the ability of such an antibody to preferentially bind to a Di33 protein of the present invention, without being able to substantially bind to other proteins. Binding can be measured using a variety of methods known to those skilled in the art including immunoblot assays, immunoprecipitation assays, enzyme immunoassays

ELISA),

radioimmunoassays, immunofluorescent antibody assays and immunoelectron microscopy; see, for example, Sambrook et al., 1989, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Labs Press. Antibodies of the present invention can be either polyclonal or monoclonal antibodies. Antibodies of the present invention include functional equivalents such as antibody fragments, genetically-engineered antibodies, including single chain antibodies, and antibody mimetopes that are capable of selectively binding to at least one of the epitopes of a Di33 protein or Di33 mimetope used to 20 obtain the antibodies. Preferably, an antibody of the present invention has a single site binding affinity of from about 103 to about 101 2 for a Di33 protein of the present invention. A preferred method to produce antibodies of the present invention includes administering to an animal an effective amount of a Di33 protein or mimetope thereof to produce the antibody and recovering the antibodies. Antibodies raised against defined 25 products or mimetopes can be advantageous because such antibodies are not substantially contaminated with antibodies against other substances that might otherwise cause interference in a diagnostic assay or side effects if used in a therapeutic composition.

One embodiment of the present invention is a method to detect D. immitis infection in a non-adapted host which includes the steps of: contacting a bodily fluid collected from such a host with a formulation including an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti-Di33 antibodies; and measuring immunocomplex formation between the Di33 protein and anti-Di33 antibodies, if any, in the bodily fluid. Presence of such a Di33 protein:anti-Di33 antibody (Di33:anti-Di33) immunocomplex indicates that the host is infected or recently has been infected recently infected followed by chemotherapy treatment in a time frame that anti-Di33 antibodies are still present) with -9- D. immitis. As used herein, a non-adapted host refers to any animal susceptible to heartworm infection but in which D. immitis does not establish a xell- adapted parasitic relationship. Examples of non-adapted hosts include, but are not limited to cats, ferrets, and other members of the family Mustelidae. As used herein, a cat refers to any member of the cat family Felidae), including domestic cats, wild cats and zoo cats.

Examples of cats include, but are limited to, domestic cats, lions, tigers, leopards, panthers, cougars, bobcats, lynx, jaguars, cheetahs, and servals. A preferred cat to test for D. immitis infection is a domestic cat.

A bodily fluid refers to any fluid that can be collected obtained) from an animal, examples of which include, but are not limited to, blood, serum, plasma, urine, tears, saliva, lymph, nasal secretions, and feces.

A formulation comprising an isolated D. immitis Di33 protein refers to a composition that at least includes Di33 protein. Such a formulation can also, but need not, include, for example, a buffer in which the Di33 protein is solubilized, and/or a carrier. Suitable buffers and carriers are known to those skilled in the art. Examples of suitable buffers include any buffer in which a protein or antibody can function to selectively bind to its partner, such as, but not limited to, phosphate buffered saline, water, saline, phosphate buffer, bicarbonate buffer, HEPES buffer (N-2- 'hydroxyethylpiperazine-N'-2-ethanesulfonic acid buffered saline), TES buffer (Tris- 20 EDTA buffered saline), Tris buffer and TAE buffer (Tris-acetate-EDTA). Examples of carriers include, but are not limited to, polymeric matrices, toxoids, and serum albumins, such as bovine serum albumin. Carriers can be in admixture with the Di33 .protein or conjugated attached) to the Di33 protein in such a manner as to not substantially interfere with the ability of the Di33 protein to selectively bind to anti-Di33 25 antibodies. Formulations of the present invention can also include not only a Di33 protein or an anti-Di33 antibody but also one or more additional D. immitis antigens or antibodies useful in detecting D. immitis infection. Examples of such antigens and antibodies include, but are not limited to, D. immitis P22U (see PCT Publication No.

WO 94/15593, published July 21, 1994, by Grieve et D. immitis P39 (see WO 94/15593, ibid.), D. immitis Gp29 (see PCT Publication No. WO 95/24198, published September 14, 1995, by Tripp et al.) D. immitis cystatin, D. immitis ladder protein, D.

immitis circulating antigens (see, for example, U.S. Patent No. 4,839,275, ibid., and antibodies to any of those antigens.

As used herein, the term "contacting" refers to combining or mixing, in this case a bodily fluid with an isolated Di33 protein. Formation of an immunocomplex between a Di33 protein and an anti-Di33 antibody refers to the ability of the Di33 protein to selectively bind to the anti-Di33 antibody in order to form a stable complex that can be measured detected). As used herein, the term selectively binds to an anti- Di33 antibody refers to the ability of a Di33 protein of the present invention to preferentially bind to anti-Di33 antibodies, without being able to substantially bind to other antibodies.

Binding between a Di33 protein and an anti-Di33 antibody is effected under conditions sufficient to form an immunocomplex; such conditions appropriate concentrations, buffers, temperatures, reaction times) as well as methods to optimize such conditions are known to those skilled in the art, and examples are disclosed herein. Examples of immunocomplex formation conditions are also disclosed, for example, in Sambrook et al., ibid., the reference Sambrook et al., ibid, is incorporated by reference herein in its entirety.

As used herein, the term "measuring immunocomplex formation" refers to determining if any immunocomplex is formed, assaying for the presence of an immunocomplex. If immunocomplexes are formed, the amount of immunocomplexes formed can, but need not be, determined. The phrase "anti-Di33 antibodies, if any, in the bodily fluid" refers to the possibility that such antibodies may or may not be present depending on whether the animal is infected or whether infection is very early or has o: been resolved prior to anti-Di33 antibody formation. Immunocomplex formation, or selective binding, between Di33 and any anti-Di33 antibody in the bodily fluid can be measured detected, determined) using a variety of methods standard in the art (see, 20 for example, Sambrook et al. ibid.), examples of which are disclosed herein.

In accordance with the present invention, a Di33 protein can form an immunocomplex with any anti-Di33 antibody in a bodily fluid, including IgG, IgE, IgM and IgA antibodies. Preferred antibodies to detect include IgG, IgE and IgM antibodies, with IgG and IgE antibodies being even more preferred. In one embodiment in which 25 anti-Di33 IgE antibodies are being detected, the collected bodily fluid is pretreated to e*s remove at least some of the other isotypes of immunoglobulin and/or other proteins, such as albumin, present in the fluid. Such removal can include, but is not limited to, contacting the bodily fluid with a material, such a Protein G, to remove IgG antibodies and/or affinity purifying the IgE antibodies from other components of the body fluid by exposing the fluid to, for example, Concanavalin A.

An immunocomplex can be measured in a variety of ways including, but not limited to use of one or more of the following assays: an enzyme-linked immunoassay, a radioimmunoassay, a fluorescence immunoassay, a lateral flow assay, an agglutination assay, a particulate-based assay using particulates such as, but not limited to, magnetic particles or plastic polymers, such as latex or polystyrene beads), an immunoprecipitation assay, and an immunoblotting assay a Western blot). Such assays are well known to those skilled in the art. Assays can be used to give qualitative 11 or quantitative results depending on how they are used. Some assays, such as agglutination, particulate separation, and immunoprecipitation, can be observed visually either by eye or by a machines, such as a densitometer or spectrophotometer) without the need for a detectable marker. In other assays, conjugation of a detectable marker to the Di33 protein or to a composition that selectively binds to the antibody being detected (described in more detail below) aids in measuring immunocomplex formation. Detectable markers are conjugated to either the Di33 protein or the composition in such a manner as not to block the ability of the Di33 protein or composition to bind to the antibodies being detected. Examples of detectable markers include, but are not limited to, an enzyme label horse radish peroxidase, alkaline phosphatase), a radioactive label, a fluorescent label, a chemiluminescent label, a chromophoric label a colorimetric label), and a ligand biotin, avidin, streptavidin, and related compounds).

In one embodiment, an immunocomplex is measured by contacting the Di33 15 protein-contacted bodily fluid the result of contacting a bodily fluid with a Di33 protein) with a composition that selectively binds to one of the following antibody isotypes: an IgG antibody, an IgE antibody, an IgM antibody or an IgA antibody.

Examples of such a composition include, but are not limited to, a secondary antibody that is an anti-isotype antibody an antibody that selectively binds to the constant region of the host antibody that bound to Di33, such as an anti-feline immunoglobulin antibody), an antibody-binding bacterial surface protein Protein A or Protein an antibody-binding cell a B cell, T cell, or macrophage), an antibody-binding eukaryotic cell surface protein an Fc receptor), and an antibody-binding complement protein. Preferred compositions include an anti-IgG antibody, an anti-IgE 25 antibody, an anti-IgM antibody, an anti-IgA antibody, an Fcy receptor molecule, an Fcc receptor molecule, an Fc, receptor molecule, and an Fca receptor molecule. As used herein an Fc receptor molecule includes not only a complete Fc receptor but also any subunit or portion thereof that is capable of selectively binding to an antibody heavy chain constant region. For example, an FCe receptor molecule can be a complete Fc receptor (which can either be associated with a cell or isolated from a cell), an Fc, receptor a chain, or any portion of an Fcc receptor a chain that can selectively bind to an IgE antibody heavy chain constant region. It is within the scope of the present invention that the amount of antibody from the bodily fluid bound to a Di33 protein can be determined using one or more layers and/or types of secondary antibodies or other binding compounds. For example, an untagged secondary antibody can be bound to an anti-Di33 antibody from the bodily fluid and the untagged secondary antibody can then be bound by a tagged tertiary antibody.

12 In one embodiment an immunocomplex can be formed and measured in solution.

In another embodiment, either the Di33 protein or the composition being used to bind to the anti-Di33 antibody can be immobilized on coated onto) a substrate.

Immobilization techniques are known to those skilled in the art. Suitable substrate materials on which to immobilize a Di33 protein or a composition include, but are not limited to, plastic, glass, gel, celluloid, paper and particulate materials such as latex, polystyrene, nylon, nitrocellulose, agarose, PVDF (poly-vinylidene-fluoride), and magnetic resin. Suitable substrates include, but are not limited to, a well microtiter dish well), a plate, a dipstick, a bead, a lateral flow apparatus, a membrane, a filter, a tube, a dish, a celluloid-type matrix, a magnetic particle, and other particulates. In one embodiment, a substrate, such as a particulate, can include a detectable marker.

A preferred method to detect D. immitis infection is an immunosorbent assay. In one embodiment, a Di33 protein is immobilized on a substrate, such as a microtiter dish well or a dipstick. A bodily fluid collected from an animal is applied to the substrate and 15 incubated under conditions sufficient to allow for immunocomplex formation. Excess fluid, if any, is removed and a composition that can selectively bind to an anti-Di33 antibody bound to the Di33 protein, the composition being conjugated to a detectable marker (preferably to an enzyme label, to a colorimetric label, to a fluorescent label, to a radioisotope, or to a ligand such as of the biotin or avidin family), is added to the substrate and incubated to allow formation of a complex between the composition and the immunocomplex. Excess composition is removed, a developing agent is added if required, and the substrate is submitted to a detection device for analysis. Alternatively, an antibody-binding composition as described above is immobilized on a substrate, and bodily fluid is incubated with the substrate to form an immunocomplex.

25 Immunocomplex detection can then be accomplished by applying a marker-conjugated Di33 protein to the immunocomplex.

S. Another preferred method to detect D. immitis infection is a lateral flow assay, examples of which are disclosed in U.S. Patent No. 5,424,193, issued June 13, 1995, by Pronovost et al.; U.S. Patent No. 5,415,994, issued May 16, 1995, by Imrich et al; WO 94/29696, published December 22, 1994, by Miller et al.; and WO 94/01775, published January 20, 1994, by Pawlak et al.; each of these patent publications is incorporated by reference herein in its entirety. In one embodiment, a bodily fluid sample is placed in a lateral flow apparatus that includes the following components: a support structure defining a flow path; a labeling reagent comprising a bead conjugated to a Di33 protein, the labeling reagent being impregnated within the support structure in a labeling zone; and a capture reagent comprising an antibody-binding composition. The capture reagent is located downstream of the labeling reagent within a capture zone 13fluidly connected to the labeling zone in such a manner that the labeling reagent can flow from the labeling zone into the capture zone. The support structure comprises a material that does not impede the flow of the beads from the labeling zone to the capture zone. Examples of such a material include, but are not limited to, nitrocellulose and PVDF. The support structure defines a flow path that is lateral and is divided into zones, namely a labeling zone and a capture zone. The apparatus can further comprise a sample receiving zone located along the flow path, more preferably upstream of the labeling reagent. The flow path in the support structure is created by contacting a portion of the support structure downstream of the capture zone, preferably at the end of the flow path, to an absorbent capable of absorbing excess liquid from the labeling and capture zones.

In this embodiment, the bodily fluid is applied to the sample receiving zone which includes a portion of the support structure. The labeling zone receives the sample from the sample receiving zone which is directed downstream by the flow path. The labeling zone comprises the labeling reagent that binds to anti-Di33 antibodies. A 15 preferred labeling reagent is a Di33 protein conjugated, either directly or through a linker, to a plastic bead substrate, such as a to latex bead. The substrate also includes a .detectable marker, preferably a colorimetric marker. Typically, the labeling reagent is impregnated to the support structure by drying or lyophilization. The sample structure also comprises a capture zone downstream of the labeling zone. The capture zone receives labeling reagent from the labeling zone which is directed downstream by the flow path. The capture zone contains the capture reagent, in this case an antibodybinding composition, as disclosed above, that immobilizes the immunocomplexcontaining labeling reagent anti-Di33 complexed to the Di33 protein portion of the labeling reagent) in the capture zone. The capture reagent is preferably fixed to the 25 support structure by drying or lyophilizing. The labeling reagent accumulates in the capture zone and the accumulation is assessed visibly or by an optical detection device.

In another embodiment, a lateral flow apparatus used to detect D. immitis infection includes: a support structure defining a flow path; a labeling reagent comprising an antibody-binding composition as described above, the labeling reagent impregnated within the support structure in a labeling zone; and a capture reagent comprising a Di33 protein, the capture reagent being located downstream of the labeling reagent within a capture zone fluidly connected to the labeling zone in such a manner that the labeling reagent can flow from the labeling zone into the capture zone. The apparatus preferably also includes a sample receiving zone located along the flow path, preferably upstream of the labeling reagent. The apparatus preferably also includes an absorbent located at the end of the flow path.

14- Another embodiment of the present invention is a method to detect D. immitis in a host animal. The method includes the steps of: contacting a bodily fluid collected from the animal with a formulation that includes an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti- Di33 IgE antibodies; and measuring immunocomplex formation between the Di33 protein and anti-Di33 IgE antibodies, if any, in the fluid. Presence of such a Di33 protein:anti-Di33 IgE antibody immunocomplex indicates that the animal is or has recently been infected with D. immitis. As used herein a host animal refers to any animal that is susceptible to D. immitis infection and, as such, includes either adapted or non-adapted hosts animals with which D. immitis either does or does not, respectively, establish a parasitic relationship). Examples of host animals include any mammal susceptible to D. immitis infection, including, but are limited to, cats, dogs, ferrets as well as other members of the family Mustelidae, sea lions as well as other sea mammals of the order Pinnipedia, and humans as well as other primates. It is to be 15 noted that the term dog refers to any member of the family Canidae, including, but not limited to, domestic dogs, wild dogs, foxes, wolves, jackals, and coyotes. As noted above, a cat can be any member of the family Felidae. Preferred animals to test include domestic cats, domestic dogs, and ferrets. Immunocomplex formation and measurement methods are as disclosed above, except that antibody-binding compositions are limited to those compositions that bind to the heavy chain constant region of IgE, such as, but not limited to, anti-IgE antibodies and Fc, receptor molecules, such as a complete Fcr receptor, an Fc, receptor ca chain, or a portion of the Fc, receptor a chain that binds to the IgE heavy chain constant region. Not only can anti-Di33 IgE antibodies by detected using in vitro techniques such as those disclosed above, but anti-Di33 IgE antibodies can also be detected using in vivo techniques, such as skin testing. In vivo methods to detect IgE antibodies are known in the art; examples of such methods are disclosed in PCT Patent Publication No. WO 96/11271, published April 18, 1996, by Frank et al.; this publication is incorporated by reference herein in its entirety.

Yet another embodiment of the present invention is a method to detect D. immitis in a non-adapted host that includes the steps of: contacting a bodily fluid collected from the host with a formulation comprising an isolated anti-Di33 antibody under conditions sufficient to form an immunocomplex between said anti-Di33 antibody and D. immitis Di33 protein; and measuring immunocomplex formation between the anti- Di33 antibody and D. immitis Di33 protein, if any, in the fluid. Presence of such an immunocomplex indicates that the host is or recently has been infected with D. immitis.

Anti-Di33 antibodies of the present invention, as well as methods to produce same, are disclosed herein. Methods to form immunocomplexes and to measure immunocomplex 15 formation are similar to those disclosed elsewhere herein, except that in this case it is natural Di33 protein being detected using isolated antibodies. Those skilled in the art can make adjustments to the disclosed methods to practice this embodiment.

The present invention also includes kits to detect D. immitis infection based on each of the disclosed detection methods. One embodiment is a kit to detect D. immitis infection that includes an isolated D. immitis Di33 protein and a composition to detect antibodies capable of forming an immunocomplex with the Di33 protein. Another embodiment is a kit that includes an isolated anti-Di33 antibody and a composition to detect an immunocomplex between the anti-Di33 antibody and a D. immitis Di33 protein. For both embodiments, examples of such compositions are disclosed herein, such compositions being able to detect IgG, IgE, IgM or IgA antibodies. Preferred kits include those in which the Di33 protein or anti-Di33 antibody, respectively is immobilized to a substrate. A kit can also contain two or more diagnostic reagents for D. immitis infection, one being an isolated Di33 protein or an isolated anti-Di33 15 antibody, the other(s) being additional isolated D. immitis antigens and/or antibodies as disclosed herein. Also preferred are kits in which the antibody-binding composition is immobilized to a substrate. Particularly preferred are kits used in an immunosorbent assay or a lateral flow assay format.

The present invention also includes a method to produce Di33 proteins of the present invention. A Di33 protein of the present invention can be isolated from D.

immitis, can be produced recombinantly, or can be chemically synthesized. A preferred method to produce a Di33 protein is recombinant Di33 protein production.

One embodiment of the present invention is a method to produce a Di33 protein that includes the steps of: culturing a recombinant cell that expresses a Di33 protein 25 to produce the protein; and recovering the protein. As such, the present invention also includes isolated Di33 nucleic acid molecules that encode Di33 proteins of the present invention as well as recombinant molecules and recombinant cells that include such Di33 nucleic acid molecules. An isolated Di33 nucleic acid molecule refers to a nucleic acid molecule that has been removed from its natural milieu. As such, "isolated" and "biologically pure" do not necessarily reflect the extent to which the nucleic acid molecule has been purified. An isolated D. immitis Di33 nucleic acid molecule of the present invention can be obtained from its natural source from D. immitis), can be produced using recombinant DNA technology or can be produced by chemical synthesis.

An isolated D. immitis Di33 nucleic acid molecule is any molecule that encodes a Di33 protein of the present invention. Examples of Di33 nucleic acid molecules include, but are not limited to, nDi33 346 nDi33 750 nDi33 70 2 nDi33 708 and nDi33 651 the production of which is disclosed in the Examples.

-16 One embodiment of the present invention includes a recombinant vector, which includes at least one isolated nucleic acid.mrnolecule of the present invention, inserted into any vector capable of delivering the nucleic acid molecule into a host cell. Such a vector contains heterologous nucleic acid sequences, that is nucleic acid sequences that are not naturally found adjacent to nucleic acid molecules of the present invention and that preferably are derived from a species other than the species from which the nucleic acid molecule(s) are derived. The vector can be either RNA or DNA, either prokaryotic or eukaryotic, and typically is a virus or a plasmid. Recombinant vectors can be used in the cloning, sequencing, and/or otherwise manipulating of Di33 nucleic acid molecules of the present invention.

One type of recombinant vector, referred to herein as a recombinant molecule, comprises a nucleic acid molecule of the present invention operatively linked to an expression vector. The phrase operatively linked refers to insertion of a nucleic acid molecule into an expression vector in a manner such that the molecule is able to be 15 expressed when transformed into a host cell. As used herein, an expression vector is a 0* s DNA or RNA vector that is capable of transforming a host cell and of effecting 0 expression of a specified nucleic acid molecule. Preferably, the expression vector is also 0 ""capable of replicating within the host cell. Expression vectors can be either prokaryotic S""or eukaryotic, and are typically viruses or plasmnids. Expression vectors of the present invention include any vectors that function direct gene expression) in recombinant cells of the present invention, including in bacterial, fungal, parasite, insect, other S animal, and plant cells. Preferred expression vectors of the present invention can direct gene expression in bacterial, yeast, helminth or other parasite, insect and mammalian cells and more preferably in bacteria.

In particular, expression vectors of the present invention contain regulatory sequences such as transcription control sequences, translation control sequences, origins of replication, and other regulatory sequences that are compatible with the recombinant ;cell and that control the expression of nucleic acid molecules of the present invention.

Se" In particular, recombinant molecules of the present invention include transcription control sequences. Transcription control sequences are sequences which control the initiation, elongation, and termination of transcription. Particularly important transcription control sequences are those which control transcription initiation, such as promoter, enhancer, operator and repressor sequences. Suitable transcription control sequences include any transcription control sequence that can function in at least one of the recombinant cells of the present invention. A variety of such transcription control sequences are known to those skilled in the art. Preferred transcription control sequences include those which function in bacterial, yeast, helminth or other parasite, 17insect and mammalian cells. More preferred transcription control sequences include those that function in bacteria, such as, but not limited to, tac, lac, trp, trc, oxy-pro, omp/lpp, rrnB, bacteriophage lambda(such as lambda PL and lambda PR and fusions that include such promoters), bacteriophage T7, T71ac, bacteriophage T3, bacteriophage SP6, bacteriophage SP01, and antibiotic resistance gene transcription control sequences.

Suitable and preferred nucleic acid molecules to include in recombinant vectors of the present invention are as disclosed herein. Preferred nucleic acid molecules to include in recombinant vectors, and particularly in recombinant molecules, include nDi33346, nDi33 750 nDi33 702 nDi33 7 0s, and nDi33651. Particularly preferred recombinant molecules of the present invention include pXPR-nDi33 708 and pkPRnDi33 651 the production of which are described in the Examples section.

Recombinant molecules of the present invention may also contain secretory signals signal segment nucleic acid sequences) to enable an expressed parasitic •helminth protein of the present invention to be secreted from the cell that produces the protein and/or contain fusion sequences which lead to the expression of nucleic acid molecules of the present invention as fusion proteins. Examples of suitable signal segments include any signal segment capable of directing the secretion of a protein of the present invention. Suitable fusion segments for use with the present invention include, but are not limited to, segments that can: enhance a protein's stability and/or assist purification of a Di33 protein by affinity chromatography). A suitable fusion segment can be a domain of any size that has the desired function imparts increased stability and/or simplifies purification of a protein). Fusion segments can be joined to amino and/or carboxyl termini of the Di33 domain of the protein and can be susceptible to cleavage in order to enable straight-forward recovery of a Di33 protein.

Fusion proteins are preferably produced by culturing a recombinant cell transformed with a fusion nucleic acid molecule that encodes a protein including the fusion segment attached to either the carboxyl and/or amino terminal end of a domain. Preferred fusion segments include a metal binding domain a poly-histidine segment); an immunoglobulin binding domain Protein A; Protein G; T cell; B cell; Fc receptor or complement protein antibody-binding domains); a sugar binding domain a maltose binding domain); and/or a "tag" domain at least a portion of pgalactosidase, a strep tag peptide, other domains that can be purified using compounds that bind to the domain, such as monoclonal antibodies). A more preferred fusion segment is a metal binding domain. Examples of particularly preferred fusion proteins of the present invention include PHIS-PDi332 34 production of which is disclosed herein.

Another embodiment of the present invention includes a recombinant cell comprising a host cell transformed with one or more recombinant molecules of the 18present invention. Transformation of a nucleic acid molecule into a cell can be accomplished by any method by which a nucleic acid molecule can be inserted into the cell. Transformation techniques include, but are not limited to, transfection, electroporation, microinjection, lipofection, adsorption, and protoplast fusion.

Transformed nucleic acid molecules of the present invention can remain extrachromosomal or can integrate into one or more sites within a chromosome of the transformed recombinant) cell in such a manner that their ability to be expressed is retained. Preferred nucleic acid molecules with which to transform a cell include Di33 nucleic acid molecules disclosed herein. Particularly preferred nucleic acid molecules with which to transform a cell include nDi33 3 46 nDi33 750 nDi33 7 02 nDi33 7 0s, and nDi336s 5 1 Suitable host cells to transform include any cell that can be transformed with a nucleic acid molecule of the present invention. Host cells can be either untransformed cells or cells that are already transformed with at least one nucleic acid molecule. Host 15 cells of the present invention can be any cell capable of producing at least one protein of the present invention, and include bacterial, fungal (including yeast), parasite (including helminth, protozoa and ectoparasite), other insect, other animal and plant cells.

Preferred host cells include bacterial cells, with Salmonella, Escherichia, and Bacillus being more preferred and E. coli being particularly preferred. A recombinant cell is 20 preferably produced by transforming a host cell with a recombinant molecule comprising a Di33 nucleic acid molecule of the present invention operatively linked to an expression vector containing a transcription control sequence. The phrase operatively linked refers to insertion of a nucleic acid molecule into an expression vector in a manner such that the molecule is able to be expressed when transformed into a host cell. Particularly preferred recombinant molecules include pkPR-nDi3370s and pXPR-nDi33 6 s 1 Particularly preferred recombinant cells include coli:pkPR-nDi33 7 o 8 and E.

coli:pXPR-nDi33651. Details regarding the production of these recombinant cells are disclosed herein.

Recombinant DNA technologies can be used to improve expression of transformed nucleic acid molecules by manipulating, for example, the number of copies of the nucleic acid molecules within a host cell, the efficiency with which those nucleic acid molecules are transcribed, the efficiency with which the resultant transcripts are translated, and the efficiency of post-translational modifications. Recombinant techniques useful for increasing the expression of nucleic acid molecules of the present invention include, but are not limited to, operatively linking nucleic acid molecules to high-copy number plasmids, integration of the nucleic acid molecules into one or more host cell chromosomes, addition of vector stability sequences to plasmids, substitutions 19 or modifications of transcription control signals promoters, operators, enhancers), substitutions or modifications of translational control signals ribosome binding sites, Shine-Dalgarno sequences), modification of nucleic acid molecules of the present invention to correspond to the codon usage of the host cell, deletion of sequences that destabilize transcripts, and use of control signals that temporally separate recombinant cell growth from recombinant enzyme production during fermentation. The activity of an expressed recombinant protein of the present invention may be improved by fragmenting, modifying, or derivatizing nucleic acid molecules encoding such a protein.

Isolated Di33 proteins of the present invention, including, but not limited to PHIS-PDi33 234 and PDi33 21 7 can be produced in a variety of ways, including production and recovery of natural proteins, production and recovery of recombinant proteins, and chemical synthesis of the proteins. In one embodiment, an isolated protein of the present invention is produced by culturing a cell capable of expressing the protein under conditions effective to produce the protein, and recovering the protein. A preferred cell 15 to culture is a recombinant cell of the present invention. Effective culture conditions include, but are not limited to, effective media, bioreactor, temperature, pH and oxygen conditions that permit protein production. An effective, medium refers to any medium ."in which a cell is cultured to produce a Di33 protein of the present invention. Such medium typically comprises an aqueous medium having assimilable carbon, nitrogen and phosphate sources, and appropriate salts, minerals, metals and other nutrients, such as vitamins. Cells of the present invention can be cultured in conventional fermentation bioreactors, shake flasks, test tubes, microtiter dishes, and petri plates. Culturing can be carried out at a temperature, pH and oxygen content appropriate for a recombinant cell.

C Such culturing conditions are within the expertise of one of ordinary skill in the art.

Examples of suitable conditions are included in the Examples section.

Depending on the vector and host system used for production, resultant proteins of the present invention may either remain within the recombinant cell; be secreted into the fermentation medium; be secreted into a space between two cellular membranes, such as the periplasmic space in E. coli; or be retained on the outer surface of a cell or viral membrane.

The phrase "recovering the protein", as well as similar phrases, refers to collecting the whole fermentation medium containing the protein and need not imply additional steps of separation or purification. Proteins of the present invention can be purified using a variety of standard protein purification techniques, such as, but not limited to, affinity chromatography, ion exchange chromatography, filtration, electrophoresis, hydrophobic interaction chromatography, gel filtration chromatography, reverse phase chromatography, Concanavalin A chromatography, chromatofocusing and differential solubilization. Proteins of the present invention are preferably retrieved in "substantially pure" form. As used herein, "substantially pure" refers to a purity that allows for the effective use of the protein as a detection reagent.

One embodiment of the present invention is a method to purify a Di33 protein that includes the steps of: culturing a bacterium transformed with a D. immitis Di33 nucleic acid molecule to produce a D. immitis Di33 protein-containing culture; (b) recovering insoluble material (believed to be refractile bodies) that include Di33 protein from the culture; and purifying the Di33 protein from the insoluble material. The purifying step preferably includes the steps of disrupting the insoluble material to form a solution comprising Di33 protein; submitting the solution to cation exchange chromatography; and recovering the Di33 protein. Use of such a method results in a protein that is at least about 80% pure and preferably about 90% pure. If the recovered protein is then submitted to hydrophobic interaction chromatography and that protein recovered, the resultant protein is at least about 95% pure and preferably at least about 15 99% pure. The present invention also includes proteins purified according to these methods. Details of these methods are presented in the Examples. A preferred protein to purify according to these methods is PHIS-PDi33 234 PHIS-PDi33 2 34 has very low solubility in most solutions other than, for example, 8 M urea or 150 mM sorbitol. As such, developing a purification protocol was very difficult and the resultant protocol is 20 not obvious. The ability to accomplish hydrophobic interaction chromatography was particularly surprising since urea is not a component in a hydrophobic environment.

o* The following examples are provided for the purposes of illustration and are not intended to limit the scope of the present invention.

Examples Example 1 This Example describes the cloning and sequencing of a nDi33 nucleic acid molecule of the present invention. It is to be noted that the Examples include a number of molecular biology, microbiology, immunology, biochemistry and assay techniques considered to be known to those skilled in the art. Disclosure of such techniques can be found, for example, in Sambrook et al., ibid. and related references.

A D. immitis Di33 nucleic acid molecule was isolated by PCR amplification of adult male and female D. immitis cDNA libraries using primers designed by comparing the nucleic acid sequences of the coding regions of Onchocerca volvulus Ov33 (see, for example, Lucius et al, 1988, J. Exp. Med. 168, 1199-1204) and Acanthocheilonema viteae Av33 (see, for example, Willenbucher et al, 1993, Mol. Biochem. Parasitol. 57, 349-351). The designed primers were Di33-S having nucleic acid sequence -21 GCTGGATGTGTIGTIGTIGATAATAAACTGTTTGC 3' (denoted herein as SEQ ID NO:8) and Di33-A having nucleic acid sequence ATATTTCTGATAIGCTGTCATTTT 3' (denoted herein as SEQ ID NO:9). The PCR product of about 405 bp was submitted to nucleic acid sequence analysis. That analysis indicated the PCR product, denoted herein as nDi33 346 had a size of about 346 bp and a coding strand having a nucleic acid sequence denoted herein as SEQ ID NO:1.

Nucleic acid molecule nDi33 3 46 was 32p mixed-hexamer labeled and used to probe a D. immitis adult female cDNA library using stringent hybridization conditions as disclosed in Sambrook et al, ibid.). Fourteen positive plaques were PCR analyzed to identify those apparently including full-length coding regions. Nucleic acid sequencing of a nucleic acid molecule containing an apparent full-length coding region yielded SEQ ID NO:2. The nucleic acid molecule having a coding strand of SEQ ID NO:2 as well as the complementary strand (the sequence of which is easily determined by one skilled in the art) is denoted herein as nDi33 7 50 SEQ ID NO:2 has GenBank 15 Accession No. U31450.

Translation of SEQ ID NO:2 suggests that nucleic acid molecule nDi33 750 •encodes a full-length D. immitis Di33 protein of about 234 amino acids, referred to herein as PDi33 234 represented by SEQ ID NO:3, assuming an open reading frame having an initiation (start) codon spanning from about nucleotide 24 through about nucleotide 26 of SEQ ID NO:2 and a termination (stop) codon spanning from about nucleotide 726 through about nucleotide 728 of SEQ ID NO:2. The coding region encoding PDi3323 4 excluding the stop codon, is represented by nucleic acid molecule nDi33 702 having a coding strand with the nucleic acid sequence represented herein as SEQ ID NO:4. SEQ ID NO:4 appears to encode a signal peptide of about 17 amino 25 acids as well as an apparent mature protein of about 217 amino acids, denoted herein as PDi33 21 7 the amino acid sequence of which is represented herein as SEQ ID NO:7. The nucleic acid molecule encoding the apparent mature protein is referred to as nDi33 651 the nucleic acid sequence of the coding strand of which is denoted herein as SEQ ID NO:6.

The deduced amino acid sequence SEQ ID NO:3 suggests a protein having a molecular weight of about 26.4 kd and an estimated pl of about 8.55. SEQ ID NO:3 is about 82% identical to the amino acid sequence of 0. volvulus Ov33 and about identical to the amino acid sequence of A. viteae Av33. SEQ ID NO:4 is about 81% identical to the nucleic acid sequence of the coding region of 0. volvulus Ov33 and about 78% identical to the nucleic acid sequence of the coding region of A. viteae Av33.

22 Example 2 This Example discloses the production of a recombinant molecule and of a recombinant cell of the present invention.

Recombinant molecule pXPR-nDi3370g containing a D. immitis Di33 nucleic acid molecule operatively linked to lambda phage transcriptional control sequences and to a fusion sequence encoding a poly-histidine segment was produced in the following manner. An about 708-nucleotide DNA fragment containing nucleotides spanning from about 24 through about 731 of SEQ ID NO:1, denoted herein as nDi33 7 0s, (the coding strand of which has a nucleic acid sequence represented herein as SEQ ID NO:5) was PCR amplified from nucleic acid molecule nDi33 75 0 produced as described in Example 1, using the primers Di33-sen 5' GAAGGGATCCTATGAAAATTCTTTTCTGTTTCG 3' (denoted herein as SEQ ID NO: 10; BamHI site in bold) and Di33-ant GGACGAATTCTGTTTAATAAATTGCAATACAGAAATGTG 3' (denoted herein as SEQ ID NO: 11; EcoRI site in bold). Recombinant molecule pkPR-nDi33 7 0s was 15 produced by digesting the nDi33 7 0s-containing PCR product with BamHI and EcoRI restriction endonucleases, gel purifying the resulting fragment and directionally subcloning it into expression vector XPRcro/T2ori/RSET-B that had been cleaved with BamHI and EcoRI and gel purified. Expression vector XPRcro/T2ori/RSET-B contains the following nucleotide segments. An about 1990-bp Pvull to AatII fragment from pUC19 containing the ampicillin resistance gene and E. coli of replication; an about 1000-bp Pvull to BglII fragment from pRK248cIts (available from American Type Culture Collection, Rockville, MD) containing lambda transcriptional regulatory regions (including the gene encoding cI", the promoter PR, and a sequence encoding 22 amino acids of the cro protein); an about 60-bp BglII to Xbal fragment from pGEMEX- I1 (available from Promega, Madison WI) which contains the T7 promoter; an about 166bp Xbal to EcoRI fragment from pRSET-B (available from Invitrogen, San Diego CA) 0 which contains sequences encoding the T7-S 10 translational enhancer, the His 6 fusion, the 14-amino acid S 10 leader fusion, and an enterokinase cleavage site as well as the multiple cloning site; and an about 210-bp EcoRI to AatII fragment containing synthetic translational and transcription termination signals including the T translation terminators in all three reading frames, an RNA stabilization sequence from Bacillus thurengiensis crystal protein and the T 2 rho-independent transcription terminator from the trpA operon.

Recombinant molecule pkPR-nDi33 708 was transformed into E. coli to form recombinant cell E. coli.:pPR-nDi33 7 0 8 using standard techniques as disclosed in Sambrook et al., ibid.

23 Example 3 This Example discloses the production of a Di33 protein of the present invention in a prokaryotic cell as well as the production of anti-Di33 antibodies.

Recombinant cell E. coli:pXPR-nDi33 708 produced as described in Example 2, was cultured in shake flasks containing an enriched bacterial growth medium containing 0.1 mg/ml ampicillin and 1% glucose at about 32 0 C. When the cells reached an OD 600 of about 0.6, expression of D. immitis nDi33 7 08 was induced by quickly adjusting the temperature to 42 0 C and continuing cultivation of the cells for about 2 hours. Protein production was monitored by SDS PAGE of recombinant cell lysates, followed by immunoblot analysis using standard techniques. Recombinant cell E. coli:p)PRnDi33 708 produced a fusion protein, denoted herein as PHIS-PDi33 234 that migrated with an apparent molecular weight of about 35 kd.

Immunoblot analysis of recombinant cell E. coli:pkPR-nDi3370s lysates indicated that the about 35 kd protein was able to bind to a T7 tag monoclonal antibody (available from Novagen, Inc., Madison, WI) directed against the fusion portion of the recombinant PHIS-PDi33234 fusion protein.

The PHIS-PDi33234 histidine fusion protein was separated from E. coli proteins •by nickel chelation chromatography and a pH gradient. Protein purification was monitored by SDS PAGE followed by Coomassie Blue staining of the column eluate fractions. Immunoblot analysis of the E. coli:pkPR-nDi33708 lysate, column eluate and column void volume indicated that the PHIS-PDi33 2 34 35 kd protein isolated using nickel column chromatography was able to selectively bind to a T7 tag monoclonal antibody.

A rabbit was immunized four times with PHIS-PDi33 23 4 that had been purified 25 by chelation chromatography. Antisera collected from this rabbit was denoted anti- PHIS-PDi33234 antisera.

Example 4 This Example describes the production of a recombinant Di33 protein from a prokaryotic cell.

Recombinant cell E. coli:pkPR-nDi33 651 produced as descried in Example 2, was cultured in a manner similar to that described in Example 3. Insoluble material, apparently refractile bodies, containing PHIS-PDi33 234 protein were obtained as follows: A cell pellet was obtained from the culture using standard techniques centrifugation). The pellet was resuspended in Buffer A (50 millimolar (mM) phosphate, 150 mM NaCI, 10 mM EDTA, 1 mM PMSF, pH 5.75) to a final volume in milliliters (ml) of 10 times the original cell paste weight in grams until a -24 homogeneous suspension was obtained. Cells in the suspension were disrupted either by lysozyme treatment (final concentration of about 0.2 milligrams (mg) lysozyme per ml volume) followed by sonication or by microfluidization using a dynamic French press). The resulting lysate was clarified by centrifugation Sorval 3B centrifuge, GSA rotor, at 20Kxg for 30 minutes at 25 0 C. The resulting pellet included the insoluble material. The insoluble material-containing pellet was washed twice in a detergentcontaining solution as follows: The pellet was resuspended in Buffer B (50 mM phosphate, 150 mM NaCI, pH 5.75, plus 1% Triton X-100 and 1% deoxycholate) in a volume equivalent to that used of Buffer A. After mixing to obtain a homogeneous suspension, the suspension was centrifuged as described above and the pellet recovered.

The detergent was removed by differential extraction of the pellet with 5 M urea which solubilized contaminants but not PHIS-PDi33 234 The mixture was centrifuged and the pellet recovered.

The insoluble material was containing solution as follows: The recovered pellet 15 was resuspended in Buffer D (8 M urea, 50 mM phosphate, 150 mM NaCI, pH 5.75) in a volume equivalent to that used of Buffer A. Dithiothreitol was added to a final concentration of 10 mM. After mixing to a homogeneous suspension, the suspension was clarified by centrifugation. The Buffer D-extracted supernatant the PHIS- PDi33 234 protein-containing solution) was collected and the pH adjusted to pH 5.75 0.25, if necessary, using phosphoric acid or sodium hydroxide.

PHIS-PDi3323 4 protein was recovered, or purified, from the PHIS-PDi33 234 protein-containing solution by cation exchange chromatography. In one embodiment, the solution was applied to a SP Sepharose column pre-equilibrated with Buffer D. The column was sequentially washed with Buffer D, a gradient from Buffer D to 25 Buffer E (8 M urea, 50 mM phosphate, 1 M NaCI, pH 5.75), and 15% Buffer E/D 15% Buffer E/85% Buffer The PHIS-PDi33 234 protein was eluted from the column with 50% Buffer E/D. The PHIS-PDi33 234 -containing eluate was concentrated by ultrafiltration and adjusted to 100% Buffer D. Alternatively, the eluate was adjusted to 150 mM sorbitol, concentrated by ultrafiltration and buffer exchanged to Buffer G mM phosphate, 150 mM NaCI, 150 M sorbitol) slowly by multiple 50% dilution steps.

By either method, the recovered PHIS-PDi33 2 34 protein was at least about 80% pure; approximately 1 gram of Di33 protein was obtained from about 10 liters of culture medium. This preparation is at least pure enough to use as a diagnostic reagent.

In order to further purify PHIS-PDi33 234 PHIS-PDi33 234 recovered from the SP Sepharose column was submitted to hydrophobic interaction chromatography. The PHIS-PDi33 234 eluate from the SP Sepharose column was concentrated by ultrafiltration and buffer exchanged to Buffer F (8 M urea, 50 mM phosphate, 150 mM NaCI, 0.75 M

NH

4

SO

4 pH 5.75) or diluted slowly with Buffer Fx (8 M urea, 50 mM phosphate, 150 mM NaCI, 1.5 M NH 4

SO

4 pH 5.75 then applied to a butvl sepharose column, preequilibrated with Buffer F. After sample application, the column was washed sequentially with Buffer F, a reverse gradient to 15% Buffer D, and Buffer D/F. The PHIS-PDi33234 protein was eluted from the column with 50% Buffer D/F. The PHIS-PDi33 234 -containing eluate was concentrated by ultrafiltration and buffer exchanged to Buffer D. The recovered PHIS-PDi33 2 34 protein was at least about pure, appearing to be greater than 99% pure by gel analysis.

It is to be noted that PHIS-PDi332 34 has very low solubility in most solutions other than, for example, 8 M urea or 150 mM sorbitol. As such, developing a purification protocol was very difficult and the resultant protocol is not obvious. The ability to accomplish hydrophobic interaction chromatography was particularly surprising since urea is not a component in a hydrophobic environment.

15 Example This Example describes the production of another recombinant molecule, recombinant cell, and recombinant protein of the present invention.

Recombinant molecule pPR-nDi33 65 1 containing a D. immitis Di33 nucleic acid molecule operatively linked to lambda phage transcriptional control sequences is produced in the following manner. An about 651-nucleotide DNA fragment containing nucleotides spanning from about 75 through about 725 of SEQ ID NO: 1, denoted herein as nDi33 651 (the coding strand of which has a nucleic acid sequence represented herein as SEQ ID NO:6) is PCR amplified from nucleic acid molecule nDi3375o, produced as described in Example 1, using appropriate primers that include appropriate restriction 25 endonuclease sites. for cloning into an appropriate expression vector. Recombinant molecule pXPR-nDi33 65 1 is produced by digesting the nDi33 651 -containing PCR product with the appropriate restriction endonucleases, gel purifying the resulting fragment and directionally subcloning the fragment into an appropriately restricted expression vector containing lambda transcription control sequences similar to those in ?PRcro/T2ori/RSET-B such that nDi33 65 1 is operatively linked to the transcription control sequences.

Recombinant molecule p.PR-nDi33 651 is transformed into E. coli to form recombinant cell E. co1i.'pXPR-nDi33 651 using standard techniques as disclosed in Sambrook et al., ibid.

Recombinant cell E. colippXPR-nDi33651 can be expressed as described in Example 3 and purified using methods such as those described in Example 4 to produce an apparently mature D. immitis Di33 protein denoted herein as PDi33 2 17 -26 Example 6 This Example describes the ability of Di33 to detect heartworm infection in cats as early as 8 weeks post infection.

ELISAs were conducted as follows. Microtiter dish wells were coated with PHIS-PDi33 234 produced as described in Example 4, by incubating about 100 ul of 100 ng PHIS-PDi33 234 per ml of CBC buffer (50 mM carbonate/bicarbonate buffer, pH 9.6) in each well overnight at about 4 0 C. Solution remaining in the wells was discarded, and the wells were washed 4 times with 10 mM phosphate-buffered saline (PBS) with 0.05% pH 7.4 (PBST). About 100 ul of a 1:50 diluted feline serum sample (diluted in PBST) was added to each well. Each serum sample was applied in duplicate or triplicate wells. Positive and negative control samples were also applied to calibrate the assay.

The samples were incubated in the Di33-coated wells for 30 minutes at room temperature, at which time solution remaining in the wells was discarded. The wells were washed 4 times with PBST. To detect binding of feline anti-Di33 IgG antibodies to Di33, about 100 ul of a 1:5000 diluted goat anti-feline IgG (H+L):HRP goat antifeline IgG heavy and light chain conjugated to horse radish peroxidase; available from Kirkegaard Perry Labs Inc.(KPL), Gaithersburg, MD, Cat. No. 14-20-26) (diluted in PBST) was added to each well and allowed to incubate for 30 minutes at room *temperature. Solution remaining in the wells was discarded, and the wells were washed 4 times with PBST. About 200 ul of the TMB 3 ,3'5'5'-tetramethylbenzidine) Microwell Peroxidase Substrate System (available from KPL, Cat. No. 50-76-04) was added to each well and incubated for 5 minutes at room temperature. About 50 ul of 2.5 N sulfuric acid was the added to each well. Absorbances were determined at 450 nm (A S: [450 nm]) in an automated ELISA reader.

In a first study, each of eleven cats were infected with 40 D. immitis third stage larvae (L3) on day 0. Serum was collected from each of the cats on days 27, 55, 83, 111, 139 and 167 post infection. The ability to detect anti-Di33 antibodies in the collected sera using a recombinant D. immitis Di33 protein produced as described in Examples 3 and 4 was measured by ELISA. Cats were necropsied and the number of adult worms in the heart of each cat was determined. Results from the ELISAs evaluating the sera collected from the 11 cats over time are presented in Table I and Fig. 1. Table 1 also indicates the number of worms found in the heart of each cat upon necropsy.

27- Table 1. Cats infected with D. immitis L3 0* *e I 0 S

S*

06 9 OSe 0 *000 0 6* S S *0

S

9* 9955

S

*5

S

*96S Cat ID and ELISA Absorbance Values Days PI LAEI XFF2 XF2 HM2 LAE3 XEG1 LAE7 GFI ODS3 GP2 167 1.41 1.06 1.81 1.62 1.64 1.54 0.37 0.58 0.84 0.69 0.47 139 1.22 0.91 1.58 1.32 1.19 1.09 0.68 0.80 1.08 0.90 0.54 III 1 .31 0.74 1.39 1.30 0.97 0.99 0.60 0.93 0.72 1. 1 0.58 83 0.53 0.12 1.30 0.56 0.54 0.91 0.34 0.67 0.29 0.89 0.04 0.08 0.01 0.00 -0.03 0.05 0.04 0.01 0.05 -0.02 0.08 0.03 27 0.02 0.02 0.00 -0.02 0.03 0.03 0.02 -0.01 0.04 -0.05 0.03 0 0.01 0.01 0.02 -0.03 0.03 0.04 0.01 0.02 -0.02 0.05 0.08

HW

burden 7 9 3 7 4 8 3 0 2 3 4 In a second study, each of twelve cats were infected with 100 D. immitis third 5 stage larvae (L3) on day 0. Serum was collected from each of the cats 6 days prior to infection and on days 1, 29, 57, 93, 102, 117 and 145 post-infection. The ability to detect anti-Di33 antibodies in the collected sera using a recombinant D. immitis Di33 protein produced as described in Examples 3 and 4 was measured by ELISA. Cats were necropsied and the number of adult worms in the heart of each cat was determined.

Results from the ELISAs evaluating the sera collected from the 12 cats over time are presented in Table 2 and Fig. 2. Table 2 also indicates the number of worms found in the heart of each cat upon necropsy.

S

S.*

So 28 Table 2. Cats infected with D. immitis L3 0 Cat ID and ELISA Absorbance values Days PI 1145 1149 1344 1346 954 952 1304 1340 1163 950 948 988 145 0.76 0.80 1.26 0.84 1.32 0.42 1.30 0.93 1.11 1.24 1.29 0.86 117 0.73 1.12 0.72 0.62 1.24 0.42 1.24 0.94 1.11 0.91 1.25 0.02 102 1.16 1.03 0.82 0.70 1.37 0.24 1.07 1.06 1.27 0.74 1.32 0.05 93 0.80 0.35 1.00 0.07 1.21 0.81 1.08 1.02 1.04 0.37 1.24 0.02 57 0.19 0.00 0.15 -0.06 0.03 0.01 -0.01 0.01 0.00 -0.07 0.07 0.00 29 0.01 -0.01 0.04 -0.04 -0.02 -0.02 -0.04 -0.01 0.00 0.07 -0.02 -0.03 1 0.03 0.06 0.01 -0.05 -0.02 0.00 -0.04 -0.01 0.00 0.03 -0.02 -0.03 -16 0.03 0.03 0.00 -0.04 0.00 0.01 -0.02 -0.01 -0.02 0.00 -0.03 -0.03

HW

burden 1 4 1 2 11 1 11 13 1 3 12 0 The results of these studies indicate that anti-Di33 IgG antibodies are detectable in D. immitis cats as early as 8 weeks, and at high concentrations by 10 to 12 weeks post infection. The results also demonstrate that anti-Di33 antibodies can also be detected in animals as the D. immitis further develops into adults as well as in animals harboring adult heartworms.

Example 7 This Example demonstrates the ability of PDi33 to detect heartworm infection in cats infected with a single male or female worm.

In a first study, each often cats was infected with D. immitis by mosquito bites.

Serum was collected from each of the cats on day 0 prior to infection and at about 2, 4 and 6 months post-infection. The ability to detect anti-Di33 antibodies in the collected sera using a recombinant D. immitis Di33 protein produced as described in Examples 3 and 4 was measured by ELISA as described in Example 6. In this study, absorbances were reported as absorbance units per ml (AbU/ml); AbU/ml are derived from A[450 nm] by second order polynomic regression analysis of data points plotted against a 29standard curve. In this case, the cut-off value is between about 4 and 6 AbU/ml. Cats were necropsied and the number of adult worms in the heart of each cat was determined.

Results from the ELISAs evaluating the sera collected from the 10 cats over time are presented in Table 3, which also indicates the number of worms found in the heart of each cat upon necropsy.

Table 3. Cats infected with Heartworm by Mosquito Bite Number of Worms M F Cat I.D. Day P.1. AbU/ml GR3 0 MO 0 GR3 2 MO GR3 4 MO GR3 6 MO 100 1 0 BO1 0 MO 0 BOI 2 MO I BOI 4 MO 54 BOI 6 MO 83 2 0 CF3 0MO 0 CF3 2 MO 32 CF3 4 MO 100 CF3 6MO 100 0 2 NY4 2 MO 3 NY4 4 MO 34 NY4 6 MO 100 0 2 AEB3 0 MO 4 EB3 2 MO 2 EB3 4 MO 100 EB3 6 MO 100 0 3 GA2 0 MO 0 GA2 2 MO 0 GA2 4 MO 100 GA2 6 MO 100 0 1 VI2 0 MO 0 VI2 2 MO 2 VI2 4 MO 16 VI2 6MO 100 0 2 GJ2 0 MO 0 GJ2 2 MO 1 GJ2 4 MO 8 GJ2 6 MO 31 0 1 WV2 0 MO I WV2 2 MO 2 WV2 6 MO 43 1 1 K3 0 MO I K3 6 MO 100 1 2 In a second study, serum was collected from each of 8 cats that had been naturally infected with D. immitis at some stage during its life. The ability to detect anti- Di33 antibodies in the collected sera using a recombinant D. immitis Di33 protein produced as described in Examples 3 and 4 was measured by ELISA as described in Example 6, with absorbances being reported as absorbance units per ml (AbU/ml). The cats were necropsied and the number of adult worms in the heart of each cat was determined. Results from the ELISAs evaluating sera collected from the 8 cats are presented in Table 4, which also indicates the number of worms found in the heart of each cat.

Table 4. Naturally infected cats Cat I.D. AbU/ml M F immature C4 2 0 1 1 C6 17 0 1 0 S17 48 1 0 0 S19 12 1 0 0 S41 8 1 0 0 S42 22 0 0 1 B9 100 0 2 0 B32 5 1 0 0 These results indicate not only that a Di33 protein can be used to detect D.

immitis infection in a naturally-infected or mosquito-bite infected cat, but also that it is possible to detect infection in a cat in which D. immitis infection results in the maturation of only a single worm. Furthermore, it is possible to detect a single male 15 worm by the Di33-based assay, unlike the circulating antigen test (see, for example, U.S.

Patent No. 4,839,275, ibid.) which can only detect female worm infection.

Example 8 This Example demonstrates the specificity of Di33 to recognize heartworm infections. Specifically, Di33 does not cross-react with Taenia taeniaeformis, Toxocara cati, and Ancylostoma tubaeforme, each of which is a parasite that infects the gastrointestinal tract of cats.

Serum was collected from each of five cats infected with T taeniaeformis, T.

cati, and A. tubaeforme on day 0 prior to infection and at about 3, 4, 7 and 10 weeks post-infection. The ability of a recombinant D. immitis Di33 protein produced as described in Examples 3 and 4 to detect infection by T taeniaeformis, T. cati, and/or A.

tubaeforme was determined by ELISA as described in Example 6, with absorbances being reported as AbU/ml. Results from the ELISAs evaluating the sera collected from 31 the 5 cats over time are presented in Table 5. The results demonstrate that recombinant Di33 protein does not cross-react with antibodies produced upon infection of cats with T taeniaeformis, T cati, or A. tuba eforme.

Table 5. Cats infected with other G.I. parasites Cat I.D. Day P.1. AbU/rnl NELl 0OWK 0 NEL 1 3 WK 0 NELl1 4 WK 0 NEL 1 7 WK 0 NEL I IOWK 0 NCO 10WK 0 NCO 1 3 WK 0 NCO0I 4OWK 0 NCY 0 K NCOI 37WK 0 NC0I 7 WK 0 NCYI 10WK 0 NOYI 3 WK 0 NCYI 4 WK 2 NCYI 7 WK 2 BFJ2 IOWK 0 .::BFJ2 0WK 0 BF2 34WK0 .BFJ2 4WK 0 BFJ2 7OWK 0 BFL3 10WK 0 Example 9 This Example demonstrates that D. imrnilis infection stimulates the production of anti-Di33 IgE antibodies in cats and dogs. This Example also shows the ability of PDi33 to detect heartworm infection in cats and dogs by detection of anti-Di33 IgE antibodies.

-32 ELISAs were conducted as follows. Microtiter dish wells of Immulon II plates (available from Dynatech, Inc., Chantilly, VA) were coated overnight at 4 0 C with either about 1 ug per well of PHIS-PDi33 234 produced as described in Example 4, or with about 1 ug per well of HW Ag, which refers to a heartworm antigen preparation that is the clarified supernatant of adult heartworms homogenized in PBS by adding to the wells either about 100 ul of 10 ug PHIS-PDi332 34 per ml CBC buffer (50 mM carbonate/bicarbonate buffer, pH 9.6) or about 100 ul of 10 ug HW Ag per ml CBC buffer. Solution remaining in the wells was discarded, and the wells were washed 4 times with PBST. About 100 ul of 1:10 diluted feline or canine serum (diluted in PBST with 0.25% BSA was added to each well. Each serum sample was applied in duplicate wells. Positive and negative control samples were also applied to calibrate the assay.

The samples were incubated in the Di33- or HW Ag-coated wells for 1 hour at room temperature, at which time solution remaining in the wells was discarded and the wells washed 4 times with PBST. To detect binding of feline or canine IgE antibodies to Di33 15 or to HW Ag, about 100 ul of a 1:4000 diluted biotinylated Fc, receptor alpha chain (see, for example, U.S. Patent No. 4,962,035, issued October 9, 1990, by Leder et al), diluted in PBST with 0.25% BSA, was added to each well (about 1 ng protein per well) and allowed to incubate for 1 hour at room temperature. Solution remaining in the wells was discarded, and the wells washed 4 times with PBST. About 100 ul of a streptavidin-peroxidase complex solution diluted 1:4000 in PBST with 0.25% BSA (available from KPL, Cat. No. 14-30-00) was added to each well (about 0.125 ug per well) and incubated for 1 hour at room temperature. Solution remaining in the wells was discarded, and the wells washed 4 times with PBST. TMB substrate (available from KPL, Cat. No. 0-76-04) was added for 10 minutes, followed by stop solution (available from KPL). Optical densities (OD) were determined at 450 nm in an automated ELISA reader.

The following sera were tested by ELISA for the presence of anti-Di33 or anti HW Ag IgE antibodies: sera collected from cat AXH3 90 days prior to heartworm infection (Pre-Bleed cat AXH3 sera) and 168 days post heartworm infection (HW Cat AXH3 sera); sera collected from cat MGC2 90 days prior to heartworm infection (Pre- Bleed cat MGC2 sera) and 168 days post heartworm infection (HW Cat MGC2 sera); and pooled sera from 6 dogs infected with heartworm for at least 200 days (HW Dog Pool). Fig. 3 shows that only sera collected post D. immitis infection had detectable levels of anti-Di33 or anti-HW Ag IgE antibodies. Such antibodies were found in cats as well as dogs infected with D. immitis. Furthermore, the Di33 preparation appears to be more sensitive than the HW Ag preparation in detecting IgE antibodies.

-33 In order to further demonstrate that the antibodies being detected were IgE antibodies (as opposed to, for example IgG or IgA antibodies), equivalent sera samples of pooled sera from cats infected with heartworm, pooled sera from dogs infected with heartworm, or.(c) sera from cat MGC2 infected with heartworm, were either heated at 56 0 C for 4 hours prior to the ELISA or not heated prior to the ELISA, the ELISA plates in the experiment having been pre-coated with PHIS-PDi3323 4 as described above.

(Note that the binding between IgE and its receptor is heat labile; Fc, receptor does not bind heat-treated IgE.) Fig. 4 shows the heat lability of the binding reaction, once again demonstrating that Di33 can be used to detect D. immitis infection in animals by detecting anti-Di33 IgE antibodies.

Sequence Listing The following Sequence Listing is submitted pursuant to 37 CFR 1.821. A copy in computer readable form is also submitted herewith.

15 Applicants assert pursuant to 37 CFR §1.821(f) that the content of the paper and computer readable copies of SEQ ID NO:I through SEQ ID NO: 11 submitted herewith are the same.

Page(s) 4o -s2are claims pages they appear after the sequence listing -34- SEQUENCE LISTING GENERAL INFORMATION:

APPLICANT:

NAME: HESKA CORPORATION STREET: 1825 SHARP POINT DRIVE CITY: FORT COLLINS STATE: COLORADO COUNTRY: USA POSTAL CODE: 80525

TELEPHONE:

TELEFAX:

(ii) TITLE OF INVENTION: METHOD TO DETECT DIROFILARIA IMMITIS INFECTION (iii) NUMBER OF SEQUENCES: 11 (iv) CORRESPONDENCE ADDRESS: ADDRESSEE: LAHIVE COCKFIELD STREET: 28 STATE STREET CITY: BOSTON STATE: MASSACHUSETTS 25 COUNTRY: USA ZIP: 02109 COMPUTER READABLE FORM: MEDIUM TYPE: Floppy disk COMPUTER: IBM PC compatible OPERATING SYSTEM: PC-DOS/MS-DOS (CD) SOFTWARE: Microsoft Word for Windows, Version S(vi) CURRENT APPLICATION DATA: APPLICATION NUMBER: PCT/US 97/ FILING DATE: 18 SEPTEMBER 1996

CLASSIFICATION:

(vii) PRIOR APPLICATION DATA: APPLICATION NUMBER: US 08/715,628 FILING DATE: 18 SEPTEMBER 1996 (viii) ATTORNEY/AGENT INFORMATION: NAME: ROTHENBERGER, SCOTT D.

REGISTRATION NUMBER: 41,277 REFERENCE/DOCKET NUMBER: HKV-008PC (HW-1PC) (ix) TELECOMMUNICATION INFORMATION: TELEPHONE: 617/227-7400 TELEFAX: 617/742-4214 INFORMATION FOR SEQ ID NO.:1: SEQUENCE CHARACTERISTICS: LENGTH: 346 base pairs 35 TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:

GAACAGCTTC

CACAATATGT

TTGGAAGAAA

TGCTAAAGTT

A.AAAACCATC

GGTTGTATGG

TGATTTAACA

TATCTTCGTG

TGAAGATTCA

GACGTAAAGG

TTATCATCAT

ATTCTGCTCA

TTCAGAATAA

TCCGATGAAA

ATCTAACAAC

AATCAATACA

ATGGCAATTA

TAGCAGAAAA

GCTGGTGATA

TAAAATATAT

TAAATCAACT

CGAAGAGCAA

AAGAAGAAGT

GCACGACATG

GAAATTCCCA

CGACACAATA

GTGGGACGAA

GAAAACATTT

AGAGAACTTG

AAAGACATCA

GTGAGAAGGA

AAACCACCAA

CTATTTTGAT

TGTATGTACG

GATGCT

100 150 200 250 300 346 a a a a

.'J

*aa.

a a a a.

a a.

INFORMATION FOR SEQ ID NO:2: SEQUENCE CHARACTERISTICS: LENGTH: 750 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: CDS LOCATION: 24. .728 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: GAATATTTCA ACAAAATAAA ACT ATG AAA ATT CTT TrC TGT TTC Met Lys Ile Leu Phe Cys Phe GTA TTG CTT GCG ATA GCA GCA Val Leu. Leu Ala Ile Ala Ala 10 TTG CGA Leu Arg is GGA TTC Gly Phe GCA AGC GTC Ala Ser Val ATA AAT Ile Asn CGA CAC AAC Arg His Asn

AAA

Lys 25 CGT TTT GCC Arg Phe Ala AGT GTT GCT GGA Ser Val Ala Gly GGT GGA ACT GCC Gly Gly Thr Ala

GGA

Gly TGT GTT GTT GTT GAT AAT AAA CTT TTT Cys Val Val Val Asp Asn Lys Leu Phe CTT CGT GAT CTA ACA ACC GAA GAG CAA Leu Arg Asp Leu Thr Thr Giu Glu Gin 55

GCG

Ala s0 AAC AGC TTC TAT Asn Ser Phe Tyr AGA GAA Arg Giu CTT GCA CAA TAT Leu Ala Gin Tyr

GTT

Val 70 GAA GAT TCA AAT Glu Asp Ser Asn CAA TAC AAA Gin Tyr Lys 36 GAA GAA GTA AAG ACA TCA TTG GAA GAA AGA CGT AAA GGA TGG Giu Giu Val Lys Thr Ser Leu Glu Glu Arg Arg Lys Gly Trp 296 CAA TTA GCA CGA CAT GGT GAG AAG, Gin Leu Ala Arg His TCA TTA GCA GAA AAG Ser Leu Ala Giu Lys 110 Gly Giu Lys

GAT

Asp 100 GCT AAA GTT TTA Ala Lys Val. Leu

TCA

Ser 105 338 380 AAA TTC CCA AAA Lys Phe Pro Lys

CCA

Pro 115 CCA AAA AAA CCA Pro Lys Lys Pro

TCA

Se r 120 TTC TGC TCA GCT GGT GAT ACG ACA CAA TAC TAT TTT GAT Phe Cys Ser Ala Gly Asp Thr Thr Gin Tyr Tyr Phe Asp 125 1'1( 422 GGT TGT Gly Cys 135 ATG GTT CAG AAT Met Val Gin Asn

AAT

Asn 140 AAA ATA TAT GTG Lys Ile Tyr Val GGA CGA ATG Gly Arg Met 145 TAT GTA CGT Tyr Val Arg 150 ACA TTT GAT Thr Phe Asp GAT TTA ACA TCC Asp Leu Thr Ser GAA ATA AAT CAA Glu Ile Asn Gin CTG AAA Leu Lys 160 009 0 69* 9 094

GCT

Ala 165 AAA ATG ACA GCA Lys Met Thr Ala

TAT

Tyr 170 CAG AAA TAT TTG Gin Lys Tyr Leu 506 548 590 632 TCG TCC ATT CAA Ser Ser Ile Gin CAA GTT GAT AGC TTA TTT GGT GAT AAA Gin Val. Asp Ser Leu Phe Gly Asp Lys

TCA

Ser 35 190 AAT CTA TTC AAT Asn Leu Phe Asn

TTA

Leu 195 TTC ACT GAT ACA Phe Thr Asp Thr CAT GAA ACA His Giu Thr TCA TCA Ser Ser 205 CAA CCA TCC GAT Gin Pro Ser Asp

GCT

Al a 210 ACA ACA ATC TCG ACA ACA ACT Thr Thr Ile Ser Thr Thr Thr 674 CAA GCT CCA Gin Ala Pro 220 GTT GAA CCA CCC Val Giu Pro Pro

GAA

Giu 225 ACA CCA CAT TTC Thr Pro His Phe TGT ATT Cys Ile 230 716 GCA ATT TAT Ala Ile Tyr TAA ACAAAAAAAA AAAAAAA AA 750 INFORMATION FOR SEQ ID NO:3: SEQUENCE CHARACTERISTICS: LENGTH: 234 amino acids TYPE: amino acid TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE Met Lys Ile Leu Phe 1 -37- DESCRIPTION: SEQ ID NO:3: Cys Phe Val Leu Leu Ala Ile Ala A-la Leu Arg Ala Ser Val Ile Asn Arg His Asn Lys Arg Phe Ala 20 Gly Phe Ser Val Ala Val1 Asp Giu Giu 85 25 Lys Pro Thr Lys Asp 155 40 Ala Asp Thr Thr Val Lau Asp Glu Asp 100 Lys Thr Ile Glu Tyr 170 Ser Asp Thr Asp Thr Ser Arg Al a Pro 115 Gin Tyr Ile Gin Leu.

185 Thr Ile Asn Thr Asn Arg Lys Pro Tyr 130 Val Asn Lys Phe Arg 200 Ser Lys Glu Gin 75 Lys Vai Lys Tyr Gly 145 Gin T'yr Gly Hi s rhr 215 Gly Leu Giu Tyr Gly 90 Leu Lys Phe Arg Leu 160 Leu Asp Glu Thr Ile 35 Phe Gln Lys Trp Ser 105 Pro Asp Met Lys Ser 1.75 Lays rhr rhr Gl Al a 50 Arg Glu Gin Ser Ser 120 Gly T'yr rhr Ser Ser 1.90 Ser Gla rGI) Asn Glu 65 Glu Leu Leu Phe Cys 135 Val Phe Ser Asn Ser 205 Al a Thr Ser Leu Val1 Al a Al a Cys Met Arg 150 Asp Ile Leu Gin Pro 220 Al a Phe Al a Lys Arg Giu Ser Val Asp Ala 1.65 Glm Phe Pro Ial *Gly Tyr Gin Thr His Lys 110 Al a Gin Leu Lys Gin 180 Asn Ser Giu Tyr S er Gly Lys Gly 125 Asn I'hr Me t .In Leu 195 ksp Pro Val1 Leu Giu Phe Asp Asn 140 Ser Thr Val Phe Ala 210 Pro Cys Val Leu ArS Glu Thr Pro His Phe Cys Ile Ala Ile Tyr 38 INFORMATION FOR SEQ ID NO:4: SEQUENCE CHARACTERISTICS: LENGTH: 702 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: ATGAAAATTC TTT TCTGTTT AAGCGTCATA AATCGACACA GAATTGGTGG AACTGCCGGA AACAGCTTCT ATCTTCGTGA ACAATATGTT GAAGATTCAA TGGAAGAAAG ACGTAAAGGA GCTAAAGTTT TATCATCATT AAAACCATCA TTCTGCTCAG GTTGTATGGT TCAGAATAAT GATTTAACAT CCGATGAAAT GACAGCATAT CAGAAATATT GCTTATTTGG TGATAAATCA CATGAAAC.AT CAT CACAACC TCAAGCTCCA GTTGAACCAC

ACAAACGTTT

TGTGTTGTTG

TCTAACAACC

ATCAATACAA

TGGCAATTAG

AGCAGAAAAG

CTGGTGATAC

AAAATATATG

AAATCAACTG

TGTCATCGTC

AATCTATTCA

ATCCGATGCT

CCGAAACACC

TGCCGGATTC

TTGATAATAA

GAAGAGCAAA

AGAAGAAGTA

CACGACATGG

AAATTCCCAA

GACACAATAC

TGGGACGAAT

AAAACATTTG

CATTCAACAG

ATTTATTCAC

ACAACAATCT

ACATTTCTGT

AGTGTTGCTG

ACTTTTTGCG

GAGAACTTGC

AAGACATCAT

TGAGAAGGAT

AACCACCAAA

TATTTTGATG

GTATGTACGT

ATGCTAAAAT

CAAGTTGATA

TGATACACGT

CGACAACAAC

ATTGCAATTT

CGTATTG CTT GCGATAGCAG CATTGCGAGC 100 150 200 250 300 350 400 450 500 550 600 650 700 702 .0 INFORMATION FOR SEQ ID SEQUENCE CHARACTERISTICS: LENGTH: 708 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (xi) SEQUENCE DESCRIPTION: SEQ ID ATGAAAATTC TTTTCTGTTT CGTATTGCTT GCGATAGCAG CATTGCGAGC 39 AAGCGTCATA AATCGACACA ACAAACGTTT TGCCGGATTC AGTGTTGCTG GAATTGGTGG AACTGCCGGA TGTGTTGTTG TTGATAATAA AACAGCTTCT ATCTTCGTGA ACAATATGTT GAAGATTCAA TGGAAGAAAG ACGTAAAGGA GCTAAAGTTT TAT CAT CATT AAAACCATCA TTCTGCTCAG GTTGTATGGT TCAGAATAAT GATTTAACAT CCGATGAAAT GACAGCATAT CAGAAATATT GCTTATTTGG TGATAAATCA

TCTAACAACC

ATCAATACAA

TGGCAATTAG

AGCAGAAAAG

CTGGTGATAC

AAAATATATG

AAATCAACTG

TGT CAT CGTC

GAAGAGCAAA

ACTTTTTGCG

GAGAACTTGC

AGAAGAAGTA AAGACATCAT

CACGACATGG

AAATTCCCAA

GACACAATAC

TGGGACGAAT

AAAACATTTG

CATTCAACAG

TGAGAAGGAT

AACCACCAAA

TATTTTGATG

GTATGTACGT

ATGCTAAAAT

CAAGTTGATA

TGATACACGT

AATCTATTCA AT TTATTCAC CATGAAACAT CATCACAACC ATCCGATGCT ACAACAATCT CGACAACAAC TCAAGCTCCA GTTGAACCAC CCGAAACACC ACATTTCTGT ATTGCAATTT

ATTAAACA

INFORMATION FOR SEQ ID NO:6: SEQUENCE CHARACTERISTICS: LENGTH: 651 base pairs TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: CDS LOCATION: 1. .651 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: AGC GTC ATA AAT CGA CAC AAC AAA CGT TTT GCC GGA TITC AGT Ser Val Ile Asfl Arg His Asn Lys Arg Phe Ala Gly Phe Ser 150 200 250 300 350 400 450 500 550 600 650 700 708 42 84 1

GTT

Val GCT GGA ATT GGT GGA ACT GCC GGA TGT GTT GTT GTT GAT Ala Gly Ile Gly Gly Thr Ala Gly Cys Val Val Val Asp 20 AAT AAA CTT TTT GCG AAC AGC TTC TAT CTT CGT GAT CTA ACA 2.26 Asn Lys Leu Phe Ala Asn Ser Phe Tyr Leu Arg Asp Leu Thr 35 ACC GAA GAG CAA AGA GAA CTT GCA CAA TAT GTT GAA GAT TCA 168 Thr Glu Glu Gin Arg Giu Leu Ala Gin Tyr Val GiU Asp Ser AAT CAA TAC Asn Gin Tyr AAA GAA GAA GTA AAG

ACA

Lys Giu Glu Val. Lys Thr 65 TITA GCA CGA CAT Leu Ala Arg His TCA TTG GAA GAA AGA Ser Leu Glu Glu Arg CGT AAA GGA TGG Arg Lys Gly Trp

CAA

Gin

GGT

Gly GAG AAG, GAT GCT Giu Lys Asp Ala 210 252 294 336 GTT TTA TCA TCA Val .Leu Ser Ser

TTA

Leu GCA GAA AAG AAA Ala Giu Lys Lys CCA AAA CCA Pro Lys Pro ACG ACA CAA Thr Thr Gin 110 CCA AAA Pro Lys 100 AAA CCA TCA TTC Lys Pro Ser Phe

TGC

Cys 105 TCA GCT GGT GAT Ser Ala Gly Asp Z~TAC TAT TTT Tyr Tyr Phe 115 GTG GGA CGA Val Gly Arg GAT GGT TGT ATG Asp Gly Cys Met CAG AAT AAT AAA Gin Asn Asn Lys ATA TAT Ile Tyr 125

ATG

Met 130 TAT GTA CGT GAT Tyr Val Arg Asp

TTA

Leu 135 ACA TCC GAT GAA Thr Ser Asp Glu

ATA

Ile 140 AAT CAA CTG AAA Asn Gin Leu Lys

ACA

Thr 145 TTT GAT GCT AAA Phe Asp Ala Lys

ATG

Met 150 ACA GCA TAT CAG Thr Ala Tyr Gin 378 420 462 504 546

AAA

Lys 155 TAT TTG TCA TCG Tyr Leu Ser Ser

TCC

Ser 160 ATT CAA CAG CA.A Ile Gin Gin Gin

GTT

Val1 165 TTT GGT Phe Gly 170 GAT AAA TCA AAT Asp Lys Ser Asn

CTA

Leu 175 TTC AAT TTA TTC Phe Asn Leu Phe GAT AGC TTA Asp Ser Leu ACT GAT ACA Thr Asp Thr 1.80 ACA ACA ATC Thr Thr Ile 195 CGT CAT GAA Arg His Glu 185 ACA TCA TCA CAA Thr Ser Ser Gin TCC GAT GCT Ser Asp Ala TCG ACA ACA Ser Thr Thr

ACT

Thr 200 CAA GCT CCA GTT Gin Ala Pro Val

GAA

Giu 205 CCA CCC GAA ACA Pro Pro Giu Thr CAT TTC TGT ATT His Phe Cys Ile GCA ATT TAT Ala Ile Tyr 21.5 -41 INFORMATION FOR SEQ ID NO:7: SEQUENCE CHARACTERISTICS: LENGTH: 217 amino acids TYPE: amino acid TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: Ser 1 Val Asn Thr Asn 25 Arg Lys Pro Tyr Val Asn Lys 155 Phe Arg Val Al a Lys Glu Gln Lys Val Lys 100 Tyr Gly Gln Tyr Gly 170 His Ile Gly Leu Glu 45 Tyr Gly Leu Lys Phe 115 Arg Leu Leu Asp Glu 185 Ile Phe Gin Lys 60 Trp Ser Pro Asp Met 130 Lys Ser Lys Thr Gly Al a Arg Glu Gin Ser Ser Gly Tyr Thr 145 Ser Ser Ser Gly 20 Asn Giu Glu Leu Leu 90 Phe Cys Val Phe Ser 160 Asn Ser Thr Ser 35 Leu Val Al a Al a Cys 105 Met Axg Asp Ile Leu 175 Gln Al a Phe Ala 50 Lys Arg Giu Ser Val 120 Asp Al a Gin Phe Pro 190 Gly Tyr Gin Thr 65 His Lys Al a Gin Leu 135 Lys Gin Asn Ser Cys Leu Tyr Ser Gly Lys Gly Asn Thr Met 150 Gin Leu Asp Val Arg Val Leu Glu Phe Asp Asn S er Thr Val1 165 Phe Ala Val Asp Glu Glu Lys Pro Thr 110 Lys Asp Ala Asp Thr 180 Thr Val1 Leu Asp Giu Asp Lys Thr Ile 125 Glu Tyr Ser Asp Thr 195 Asp Thr Ser Arg Al a Pro Gin Tyr Ile 140 Gin Leu Thr Ile Pro 210 Asn Arg His Asn Lys Arg Phe Ala Gly Phe Ser S I n Ser Thr Thr Thr Gln Ala Pro Val Glu Pro Pro Glu Thr 200 205 -42- His Phe Cys Ile Ala Ile Tyr 215 INFORMATION FOR SEQ ID NO:8: SEQUENCE CHARACTERISTICS: LENGTH: 35 bases TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: primer (ix) FEATURE: NAME/KEY: N=INOSINE LOCATION: 12 (ix) FEATURE: NAME/KEY: N=INOSINE LOCATION: (ix) FEATURE: NAME/KEY:

N=INOSINE

**25 LOCATION: 18 o* (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: GCTGGATGTG TNGTNGTNGA TAATAAACTG TTTGC INFORMATION FOR SEQ ID NO:9: SEQUENCE CHARACTERISTICS: LENGTH: 24 bases TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: primer (ix) FEATURE: NAME/KEY: N=INOSINE LOCATION: 13 (xi) SEQUENCE DESCRIPTION: SEQ ID NO:9: ATATTTCTGA TANGCTGTCA TTTT 24 INFORMATION FOR SEQ ID SEQUENCE CHARACTERISTICS: LENGTH: 33 bases TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear 43 (ii) MOLECULE TYPE: primer (xi) SEQUENCE DESCRIPTION: SEQ ID NO: GAAGGGATCC TATGAAAATT CTTTTCTGTT TCG 33 INFORMATION FOR SEQ ID NO:11: SEQUENCE CHARACTERISTICS: LENGTH: 39 bases TYPE: nucleic acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: primer (xi) SEQUENCE DESCRIPTION: SEQ ID NO:11: GGACGAATTC TGTTTAATA.A ATTGCAATAC AGAAATGTG 39 44 While various embodiments of the present invention have been described in detail, it is apparent that modifications and adaptations of those embodiments will occur to those skilled in the art. It is to be expressly understood, however, that such modifications and adaptations are within the scope of the present invention, as set forth in the following claims.

a a e

Claims (65)

1. A method to detect D. immitis in a non-adapted host comprising: contacting a bodily fluid collected from said host with a formulation comprising an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti-Di33 antibodies; and measuring immunocomplex formation between said Di33 protein and anti-Di33 antibodies, if any, in said fluid, wherein the presence of said immunocomplex indicates that said host is or has recently been infected with D. immitis.

2. The method of Claim 1, wherein said method detects D. immitis in said host prior to maturation of said D. immitis into an adult heartworm.

3. The method of Claim 1, wherein said method detects D. immitis in said 15 host within at least about ten weeks post infection of said host with D. immitis.

4. The method of Claim 1, wherein said method detects D. immitis infection in a non-adapted host harboring adult heartworms.

5. The method of Claim 1, wherein said method detects D. immitis infection resulting in the maturation of a single adult heartworm.

6. The method of Claim 1, wherein said method detects D. immitis infection resulting in the maturation of a single adult male heartworm.

7. The method of Claim 1, wherein said method detects D. immitis infection resulting in the maturation of a single adult female heartworm.

8. The method of Claim 1, wherein said antibody in said immunocomplex is selected from the group consisting of IgG, IgM and IgA antibodies.

9. The method of Claim 1, wherein said antibody in said immunocomplex is an IgE antibody.

10. The method of Claim 1, wherein said host is selected from the group consisting of a cat and a ferret. 46

11. The method of Claim 10, wherein said cat is a domestic cat.

12. The method of Claim 1, wherein said immunocomplex is measured by contacting said Di33 protein-contacted bodily fluid with a composition that selectively binds to an antibody selected from the group consisting of an IgG antibody, an IgE antibody, an IgM antibody, and an IgA antibody.

13. The method of Claim 12, wherein said composition is selected from the group consisting of an anti-IgG antibody, an anti-IgE antibody, an anti-IgM antibody, an anti-IgA antibody, an Fcy receptor molecule, an Fc, receptor molecule, an Fc. receptor molecule, and an Fca receptor molecule.

14. The method of Claim 12, wherein said composition is conjugated to a detectable marker. The method of Claim 14, wherein said detectable marker is selected from the group consisting of an enzyme label, a radioactive label, a fluorescent label, a chemiluminescent label, a chromophoric label, and a ligand. 0**g

16. The method of Claim 12, wherein said composition is immobilized on a substrate.

17. The method of Claim 16, wherein said substrate comprises a material selected from the group consisting of plastic, glass, gel, celluloid, paper, and particulate 25 materials.

18. The method of Claim 16, wherein said substrate is selected from the group consisting of a well, a plate, a dipstick, a bead, a lateral flow apparatus, a membrane, a filter, a tube, a dish, a celluloid-type matrix, and a magnetic particle.

19. The method of Claim 1, wherein said Di33 protein is immobilized on a substrate. The method of Claim 19, wherein said substrate comprises a material selected from the group consisting of plastic, glass, gel, celluloid, paper, and particulate materials. -47-

21. The method of Claim 19, wherein said substrate is selected from the group consisting of a well, a plate, a dipstick, a bead, a lateral flow apparatus, a membrane, a filter, a tube, a dish, a celluloid-type matrix, and a magnetic particle.

22. The method of Claim 19, wherein said substrate further comprises a detectable marker.

23. The method of Claim 19, wherein said substrate is conjugated to a detectable marker.

24. The method of Claim 1, wherein said immunocomplex forms in solution. The method of Claim 1, wherein said step of measuring comprises an assay selected from the group consisting of an enzyme-linked immunoassay, a radioimmunoassay, a fluorescence immunoassay, a lateral flow assay, an agglutination assay, a particulate-based assay, an immunoprecipitation assay, and an immunoblotting assay.

26. The method of Claim 1, wherein said Di33 protein is conjugated to a detectable marker.

27. The method of Claim 1, wherein said bodily fluid is selected from the group consisting of blood, serum, plasma, urine, tears, saliva, lymph, nasal secretions and feces. see*

28. The method of Claim 1, wherein said formulation further comprises a carrier.

29. The method of Claim 1, wherein said formulation further comprises a D. immitis antigen other than said Di33 protein. The method of Claim 1, wherein said formulation further comprises an antibody raised against a D. immitis antigen.

31. The method of Claim 1, wherein said D. immitis antigen comprises a circulating parasite antigen. -48

32. A method to detect D. immitis in a host animal, said method comprising: contacting a bodily fluid collected from said animal with a formulation comprising an isolated D. immitis Di33 protein under conditions sufficient to form an immunocomplex between Di33 protein and anti-Di33 IgE antibodies; and measuring immunocomplex formation between said Di33 protein and anti-Di33 IgE antibodies, if any, in said fluid, wherein the presence of said immunocomplex indicates that said animal is or has recently been infected with D. immitis.

33. The method of Claim 32, wherein said animal is selected from the group consisting of cats, dogs and ferrets.

34. The method of Claim 32, wherein said method detects D. immitis in said animal within at least about ten weeks post infection of said animal with D. immitis.

35. The method of Claim 32, wherein said method detects D. immitis infection resulting in the maturation of a single adult heartworm.

36. The method of Claim 35, wherein said adult heartworm is male.

37. The method of Claim 35, wherein said adult heartworm is female.

38. A method to detect D. immitis infection in a non-adapted host within weeks of infection, said method comprising detecting anti-Di33 antibodies in a bodily fluid collected from said host.

39. The method of Claim 38, wherein said method detects D. immitis infection resulting in the maturation of a single adult heartworm.

40. The method of Claim 39, wherein said adult heartworm is male. 40. The method of Claim 39, wherein said adult heartworm is male.

41. The method of Claim 39, wherein said adult heartworm is female.

42. A kit to detect D. immitis infection comprising an isolated D. immitis Di33 protein and a composition to detect antibodies capable of forming an immunocomplex with said Di33 protein. -49-

43. The kit of Claim 42, wherein said antibodies are selected from the group consisting of IgG, IgE, IgM, and IgA antibodies.

44. The kit of Claim 42 further comprising a substrate on which said Di33 protein can be immobilized. The kit of Claim 42, wherein said Di33 protein is immobilized on a substrate.

46. The kit of Claim 42 further comprising a substrate on which said composition can be immobilized.

47. The kit of Claim 42, wherein said composition is immobilized on a substrate.

48. The kit of Claim 42, wherein said composition is selected from the group consisting of an anti-IgG antibody, an anti-IgE antibody, an anti-IgM antibody, an anti- IgA antibody, an Fc receptor molecule, an Fc, receptor molecule, an Fc, receptor molecule, and an Fc receptor molecule.

49. The kit of Claim 42 further comprising an apparatus comprising: a support structure defining a flow path; a labeling reagent comprising a bead conjugated to said Di33 protein, wherein said labeling reagent is impregnated within the support structure in a 25 labeling zone; and a capture reagent comprising said composition, wherein said capture reagent is located downstream of said labeling reagent within a capture zone fluidly connected to said labeling zone in such a manner that said labeling reagent can flow from said labeling zone into said capture zone. The kit of Claim 49, wherein said apparatus further comprises a sample receiving zone located along said flow path.

51. The kit of Claim 50, wherein said sample receiving zone is located upstream of said labeling reagent.

52. The kit of Claim 49, wherein said apparatus further comprises an absorbent located at the end of said flow path.

53. The kit of Claim 49, wherein said support structure comprises a material that does not impede the flow of said bead from said labeling zone to said capture zone.

54. The kit of Claim 49, wherein said bead comprises a latex bead. The kit of Claim 49, wherein said bead comprises a detectable marker.

56. The kit of Claim 49, wherein said Di33 protein is conjugated to a detectable marker.

57. The kit of Claim 42 further comprising an apparatus comprising: 15 a support structure defining a flow path; a labeling reagent comprising said composition, wherein said labeling reagent is impregnated within the support structure in a labeling zone; and a capture reagent comprising said Di33 protein, wherein said capture reagent is located downstream of said labeling reagent within a capture zone fluidly connected to said labeling zone in such a manner that said labeling reagent can flow from said labeling zone into said capture zone.

58. The kit of Claim 57, wherein said apparatus further comprises a sample receiving zone located along said flow path.

59. The kit of Claim 58, wherein said sample receiving zone is located upstream of said labeling reagent. The kit of Claim 42, wherein said kit further comprises a D. immitis antigen other than said Di33 protein.

61. A method to produce an isolated D. immitis Di33 protein comprising: culturing a bacterium transformed with a D. immitis Di33 nucleic acid molecule to produce a D. immitis Di33 protein-containing culture; recovering insoluble material comprising said Di33 protein from said culture; and purifying said Di33 protein from said insoluble material. -51

62. The method of Claim 61, wherein said step of purifying comprises the steps of: disrupting the insoluble material of step to form a solution comprising Di33 protein; submitting said solution to cation exchange chromatography; and recovering said Di33 protein.

63. The method of Claim 61, wherein said step of purifying comprises the steps of: disrupting the unsoluble material of step to form a solution comprising Di33 protein; submitting said solution to cation exchange chromatography to obtain a Di33 protein-containing fraction; 15 submitting said fraction to hydrophobic interaction chromatography; and recovering said Di33 protein.

64. An isolated D. immitis Di33 protein produced by the method of Claim 61.

65. A method for purifying a D. immitis Di33 protein comprising recovering Di33 protein from cation exchange chromatography of disrupted insoluble material obtained from a culture of D. immilis Di33 protein-producing recombinant cells.

66. An isolated D. immitis Di33 protein produced by the method of Claim

67. A protein selected from the group consisting of PHIS-PDi33 23 4 and S* PDi33 2 17

68. A nucleic acid molecule selected from the group consisting of nDi33 346 nDi33 75 0 nDi33 702 nDi33 708 and nDi33 651

69. A recombinant molecule comprising a nucleic acid molecule of Claim 68. The recombinant molecule of Claim 69, wherein said recombinant molecule is selected from the group consisting of pXPR-nDi33 70 8 and pkPR-nDi33 651 52

71. A recombinant cell comprising a nucleic acid molecule of Claim 68.

72. A method to produce an isolated D. immitis Di33 protein comprising culturing a recombinant cell comprising a nucleic acid molecule of Claim 68 and recovering said protein.

73. A method to detect D. immitis in a non-adapted host comprising: contacting a bodily fluid collected from said host with a formulation comprising an isolated anti-Di33 antibody under conditions sufficient to form an immunocomplex between said anti-Di33 antibody and D. immitis Di33 protein; and measuring immunocomplex formation between said anti-Di33 antibody and D. immitis Di33 protein, if any, in said fluid, wherein the presence of said immunocomplex indicates said host is or recently has been infected with D. immitis.

74. A kit to detect D. immitis infection comprising an isolated anti-Di33 antibody and a composition to detect an immunocomplex between said anti-Di33 antibody and D. :immitis Di33 protein. DATED this 25 th Day of May 2001 HESKA CORPORATION Attorney: DAVID A. ADAMTHWAITE Fellow Institute of Patent and Trade Mark Attorneys of Australia of BALDWIN SHELSTON WATERS °o*