AU780017B2 - Nucleotide sequences of HIV-1 type (or subtype) O retrovirus antigens - Google Patents

Description

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION

C

S

S

NAME OF APPLICANT: Institut Pasteur ADDRESS FOR SERVICE: DAVIES COLLISON

CAVE

Patent Attorneys Level 3 303 Coronation Drive Milton, QLD, 4064 INVENTION TITLE: "Nucleotide sequences of HIV-1 type (or subtype) O retrovirus antigens" The following statement is a full description of this invention, including the best method of performing it known to us:- Q:\OPER\V PA\2287896C. 131 -10/500 la NUCLEOTIDE SEQUENCES OF HIV-1 GROUP (OR SUBGROUP) 0 RETROVIRAL ANTIGENS 5 The invention relates to the antigens obtained by expression of nucleotide sequences or by chemical synthesis, for example using Applied Biosystems brand synthesizers, present in HIV-1 group (or subgroup) 0 variants and more particularly the antigens 10 corresponding to those which may be isolated from viral particles. By way of example of HIV-1 viruses of the subgroup O, reference is made to the HIV-1,vAU) isolate and to the HIV- 1 isolate.

The invention also relates to monoclonal or polyclonal antibodies induced by these antigens.

The invention also relates to cloned DNA sequences either having sequence analogy or complementarity with the genomic RNA of the abovementioned virus. The invention also relates to processes for the preparation of these cloned DNA sequences. The invention also relates to polypeptides containing amino acid sequences coded for by the cloned DNA sequences.

Furthermore, the invention relates to applications of the antigens mentioned above to the in 2 vitro detection in at-risk individuals of certain forms of AIDS and, as regards some of them, to the production of immunogenic compositions and vaccinating compositions against this retrovirus. Similarly, the invention relates to applications of the abovementioned antibodies for the same purposes and, for some of them, to their application to the production of active principles for medicinal products against this human

AIDS.

The invention also relates to the application of the cloned DNA sequences and of the polypeptides obtained from these sequences as probes or primers for gene amplification, in diagnostic kits.

The invention also relates to antigenic compositions which may be obtained by chemical synthesis or by expression in a recombinant cell host and which allow the diagnosis of an infection due to a human retrovirus of HIV type independently of the HIV-1 or HIV-2 subtype. Such compositions comprise at least 20 one peptide chosen from the antigenic peptides common to the HIV-1, HIV-2, HIV-1(,D) and HIV-l(VU) viruses or variants of the antigenic peptides possessing similar S" immunogenic characteristics.

The invention is also directed toward compositions which allow the specific diagnosis of an infection due to a human retrovirus of HIV-1 type, more particularly HIV-1, group M, HIV-2 or HIV-1 group (or subgroup) 0 and comprising at least one antigenic peptide specific for the HIV-1 virus, an antigenic peptide specific for the HIV-2 virus and an antigenic peptide specific for the HIV-1 group (or subgroup) 0 virus or variants of these antigenic peptides possessing similar immunogenic characteristics.

More particularly, the antigenic peptides are derived from the envelope protein of HIV-l group M and HIV-2 and HIV-1 group (or subgroup) 0 viruses.

3 The invention is moreover directed toward a peptide allowing detection of anti-HIV antibodies which the peptides of the prior art did not always make it possible to detect, based in particular on the discovery of a new HIV-1 strain: HIV-1 DUR. The antiserum directed against it does not always have reactivity with the peptides of the consensus HIV as it is used nowadays. The term "consensus HIV" refers to the regions which are conserved between isolates and whose demonstration is essential to the design of diagnostic reagents or vaccines, and whose mutations impart resistance to antiviral medicinal products. The term "peptide" used in the present text defines both oo oligopeptides and polypeptides.

State of the art Two types of human immunodeficiency virus (HIV) which have responsibility for the development of an LAS or AIDS have been isolated and characterized. A first 20 virus, known as LAV-1 or HIV-1, was isolated and described in GB patent application 8324,800 and patent application EP 84401,834 of 14/09/1984. This virus was also described by F. Barr6-Sinoussi et al. in Science (1983), 220, 868-871.

The type 2 HIV retrovirus belongs to a separate class and has only a limited immunological relationship with type 1 HIV retroviruses. HIV-2 retroviruses have been described in European patent application No.

87,400,151,4 published under the number 239,425.

The HIV-1 retrovirus is the most common and its presence is predominant in several regions worldwide.

As regards the HIV-2 retrovirus, it is most often found in West Africa, although its propagation outside this region has recently been documented by Grez et al., (1994) J. Virol. 68, 2161-2168.

The totality of primate immunodeficiency lentiviruses, comprising the type 1 and type 2 human immuno- 4 deficiency viruses as well as several types of nonhuman primate viruses, is increasing in size and complexity. The most common of these viruses, HIV-1, is currently spreading in the form of a worldwide epidemic and is responsible for a major public health problem.

Shortly after the identification and molecular characterization of this virus, it was recognized as being highly variable, and currently comprises several subtypes (Myers, 1994, Louwagie, et al. 1993, Louwagie et al. 1992, Myers, G. (1994) HIV-1 subtypes and phylogenetics trees. In: Human Retrovirus and AIDS 1994; Myers, Korber, Wain-Hobson, Smith, R.F. and Pavlakis, Eds. Los Alamos National Laboratory, Los Alamos, NM. III-2 111-9.). This 15 differentiation of subtypes is mainly based on the divergence of the gag and env genes. At least 6 subtypes have been identified, designated A to F, but several are still likely to emerge from the ongoing extensive worldwide survey on the isolates of HIV-1. It has been found that these various subtypes are equidistant from each other, in a phylogenetic profile termed star phylogeny, which suggests that the various

HIV-

1 subtypes might have evolved and diverged synchronously from a common ancestor.

Recently, two separate viruses of this group of

HIV-

1 viruses were isolated and characterized. These two viruses were obtained from patients living in Cameroon, in West Central Africa (Gurtler, et al. 1994, Vanden Heasevelde, et al. 1994). Their sequence, more particularly the sequence of their env (envelope) gene, shows clearly that these viruses belong to a separate category of HIV-l-related viruses, referred to as HIV-1 group 0 (Nkengasong et al., 1993).

However, the diversity of the isolates within this group of HIV-l-related viruses is not known, and its propagation outside Africa has not been documented.

5 A general constraint, in the development of HIV serological tests, is to avoid both falsely positive or falsely negative results while at the same time retaining or improving the sensitivity in terms of detection of seropositivity which the previous tests allow.

Tests based on the use of consensus peptide(s), essentially derived from the "env" gene, were considered as an almost ideal solution until the discovery of the HIV-1-O variant brought to light the possibility of falsely negative results (Genomic cloning and complete sequence analysis of a highly o divergent African human immunodeficiency virus isolate.

J. Virol. 1994; 68: 1586-96; a new subtype of human 15 immunodeficiency virus type 1 (MPV-5180) from Cameroon.

J. Virol. 1994; 68: 1581-85).

.The non-reactivity of certain tests with "env" peptide antigen, in patients nonetheless exhibiting certain clinical syndromes characteristic of AIDS or 20 lymphadenopathy syndromes which occasionally precede them, is, at the present time, occasionally attributed to an infection of the HIV-1-O group (HIV-1/HIV-2 seronegativity in HIV-1 subtype O infected patients, Lancet 1994; 343: 1393-94; New HIV-1 subtype in 25 Switzerland. Lancet 1994; 344: 270-71).

Description of the invention HIV-1 DUR retrovirus The aim of the present invention is to provide diagnostic 3 laboratories with means, in particular specific peptides, allowing a detection of anti-HIV antibodies which were hitherto liable to be undetected. The invention also relates to mixtures of peptides obtained from HIV-1 DUR and of corresponding peptides obtained from HIV-1 DUR and of corresponding peptides from other HIVs, so as to avoid potential "false negative" results.

In another aspect, the invention relates to a process of detection and of discrimination, in a biological 6 sample, between antibodies characteristic of an HIV-1-M type retrovirus and antibodies characteristic of an HIV-1 group (or subgroup) 0 retrovirus.

The invention stems from observations made on a seropositive woman who had stayed in the Cameroon and who had revealed an atypical serological reactivity, in the course of several tests of screening for HIV infection, these tests having been confirmed by "Western blot" techniques.

On account of this atypical serological reactivity, in particular the lack of reactivity to certain third-generation tests, even modified for the O ~type, the inventors considered it interesting to carry out sequencing of certain parts of the genome of this 15 HIV-1 DUR strain, more specifically of the GAG and ENV genes.

However, gene amplifications by PCR using primers obtained from the M group and known primers from the 0 group were unsuccessful for the parts coding 20 for the V3 loop of gpl20, and for the immunodominant region of gp41. Only the GAG region could be amplified using primers known in the prior art (Loussert-Ajaka I, Lancet 1994; 343: 1393). Another aim of the present invention is consequently to determine primers capable of overcoming this problem.

Partial sequences of the glycoproteins gp41 and gpl20 were determined, along with capsid proteins (GAG gene), from lymphocyte DNA and from viral cultures, indicating that this HIV-1 DUR strain belongs in part to the HIV-1-0 group, and that it differs considerably from the M group, more particularly as regards gp41 and Thus, it was possible to demonstrate, more particularly as regards the GAG sequence of HIV-l(D the existence of consensus sequences in the 0 group, in several regions, which are distinct from the consensus sequences of the M group in the same regions.

-7- Cloning of the sequences coding for the GAG, gp4l and gp12o fragments of llIV-l(,) was carried out in a BluescriptO plasmid containing a Pstl site. The amplification products were cloned either according to the standard techniques using T3 and T7 universal primers, or directly sequenced by using the primers of the preceding amplification. The sequences were than determined with the Applied Biosystems 373A automated sequencer

(ESGS

M.ontigny le Bretonneux, France).

Antigens.

In another aspect, the invention resides in an HIV-1. group (or subgroup) 0 retroviral protein, or natural or synthetic peptide or polypeptide comprising at least a part of said protein, which is capable of being recognized by antibodies which may be isolated from the serum obtained after an infection with an HIV-J. group 0 DUR strain.

In another aspect, the present invention relates to a peptide obtained from the HIV-1-0 DUR virus deposited on 23 20 February 1995 at the CNCM under reference number 1-1542, or a variant whose sequence is distinguished from the peptide by substitution,, deletion, or addition of amino acids, wherein the *****variant retains the antigenic characteristics of the peptide, wherein the peptide or the variant: binds to at least one antibody that specifically recognises the said virus; or binds to at least one antibody that recognises: a peptide sequence of the said virus, which is distinct from peptide sequences of known

H-IV

viruses described herein; or (ii) a peptide sequence of the said virus, which comprises a consensus sequence corresponding to 8 the HIV-l-o group of viruses, which consensus sequence is distinct from other consensus sequences corresponding to the HIV-1-M group of viruses; and wherein said peptide, with the exception of QGPKEPFRDYVDRF, does not consist of an amino acid sequence contained within the sequence

QGPKEPFRDYVDRFYKTLRAE.

Other peptides falling within the scope of the invention are defined below.

*goo 10 Thus, a preferred peptide of the invention is a peptide o* comprising at least 4 contiguous amino acids in the GAG sequence designated DUR as set forth in FIG. 8, or in an immunologically similar GAG sequence obtained from a variant of the HIV-l-O

DUR

virus, said contiguous amino acids defining a distinctive 15 sequence relative to sequences of known HIV-1 viruses described herein, said immunologically similar sequence being recognised by antibodies which also specifically recognise at least one of the sequences AHPQQA, LWTTRAGNP contained in the said

GAG

sequence.

20 Preferably, this peptide consists of a peptide whose amino S acid sequence is contained in a sequence selected from the group consisting of: SPRTLNAWVKAVEEKAFNPEIIPMFMALSEGA MLNAIGGHQGALQVLKEVIN GPLPPGQIREPTGSDIAGTTSTQQEQI IPVGDIYRKWIVLGLNKMVKMYSPVSILDI AHPQQA LWTTRAGNT and 9 an immunologically similar sequence corresponding to any one of the sequences set forth in to wherein said peptide comprises at least 4 contiguous amino acids of any one of the sequences set forth in to Preferably also, this peptide consists of a peptide whose amino acid sequence is contained in a sequence selected from the group consisting of: SPRTLNAWVK (6) 10 GSDIAGTTST and QGPKEPFRDYVDRF Peptides which are particularly preferred in the present invention are the peptides comprising: the amino acid sequence NPEI (9) 15 or the amino acid sequence AVEEKAFNPEIIPMFM and more particularly peptides whose amino acid sequence is contained, in any one of the following sequences: IGGHQGALQ (23) REPTGSDI (24) or in a corresponding immunologically similar sequence, this peptide containing at least 4 contiguous amino acids of one of said sequences, as well as the peptide whose amino acid sequence is contained, in the following amino acid sequence: INDEAADWD or in a corresponding immunologically similar sequence, this peptide contained at least 4 contiguous amino acids of said sequence.

A peptide derived from the HIV-1-O DUR virus defined above 10 also falls within the scope of the present invention, said peptide comprising at least 4 contiguous amino acids, whose entire sequence is contained in the sequence of the region of the V3 loop of gpl20 which sequence is designated DUR as set forth in FIG. 9A, or in the corresponding immunologically similar sequence obtained from a variant of the HIV-1 O DUR virus, said contiguous amino acids defining a distinctive sequence relative to sequences of known HIV-1 viruses described herein, said immunologically similar sequence being recognized 10 by antibodies which also specifically recognise at least one of the sequences selected from the group consisting of: KEIKI (12); EREGKGAN (13); CVRPGNNSVKEIKI and 15 QIERREGKGANSR This peptide preferably comprises a) the sequence: CVRPGNNSVKEIKIGPMAWYSMQIEREGKGANSRTAFC or a 2i portion of this sequence consisting of at least 4 contiguous amino acids; or b) a variant of the sequence or portion set forth in a), which variant is produced by replacement of at least one amino acid of the said sequence or portion with a different amino acid, with the proviso that the peptide comprising the variant is reactive with an antiserum against the said sequence or portion; or c) a variant of the sequence or portion set forth in a), which variant is produced by deletion of at least one amino acid of the said sequence or portion, or by 11 addition of at least one amino acid to the said sequence or portion, with the proviso that the peptide comprising the variant is reactive with an antiserum against the said sequence or portion; or d) an immunologically similar sequence corresponding to any one of the sequences set forth in a) to c).

Preferably also, this peptide comprises the sequence KEIKI (12) or 1 0 the sequence EREGKGAN (13) or the sequence GPMAWYSM (16).

In a particularly preferred manner, a peptide as defined above contains the amino acid sequence CVRPGNNSVKEIKI (14) or 15 the sequence QIEREGKGANSR A peptide derived from the HIV-1-O DUR virus as defined above also falls within the scope of the invention, said peptide comprising at least 4 contiguous amino acids, whose entire sequence is contained in the sequence of the immunodominant region of gp41 as set forth in FIG. 9B or in a corresponding immunologically similar sequence obtained from a variant of the DUR virus, said contiguous amino acids defining a distinctive sequence relative to sequences of known HIV-1 viruses described herein, said immunologically similar sequence being recognized by antibodies which also specifically recognise at least one of the sequences selected from the group consisting of: RLLALETLMQNQQL (17); LNLWGCRGKAICYTSVQWNETWG (18); 12 CRGKAI (19); SVQWN RLLALETLMQNQQLLNLWGCRGKAICYTS and QBQQKKBKWGCRGKAICYTSVQWN (22).

This peptide is preferably a peptide comprising the sequence RLLALETLMQNQQL (17) or the sequence LNLWGCRGKAICYTSVQWNETWG or a portion of these sequences comprising: a) i) the sequence CRGKAI or ii) the sequence SVQWN (20) in which Q is replaced ~by a different amino acid, wherein the different amino acid is not K; iii) the sequence set forth in a) i) and the sequence set forth a) ii); or b) a variant of a sequence set forth in which variant ~is produced by replacement of at least one amino acid of the said sequence with a different amino acid, with the proviso that the peptide comprising the variant is reactive with an antiserum against the said sequence; or c) a variant of a sequence set forth in a),which variant is produced by deletion of at least one amino acid of the said sequence, or by addition of at least one amino acid to the said sequence, with the proviso that the peptide comprising the variant is reactive with an antiserum against the said sequence; or d) an immunologically similar sequence corresponding to 13 any one of the sequences set forth in a) to c).

Preferably also, this peptide possesses one or the other of the following characteristics: its N-terminal sequence which contains at least 8 amino acids is not immunologically recognized by antibodies formed against the sequence RILAVERY contained in the immunodominant region of gp41 of the HIV-1-LAI strain; it is not recognized by antibodies formed against the peptide SGKLIC of the HIV-1-LAI strain; 1 0 it contains either of the following two sequences: RLLALETMONQQLLNLWGCRGKAICYTS (21) QNQQLLNLWGCRGKAICYTSVQWN (22) Corresponding and consensus peptides Also falling within the scope of the invention are the 5 corresponding peptides obtained from corresponding structural proteins of other HIV-1 group (or subgroup) O or HIV-1 subgroup M viruses, in particular those derived from the GAG, gpl20 and gp41 structural proteins whose parts are indicated in the diagrams, wherein the homologous peptide is derived by aligning an HIV-M virus sequence shown in Figures 8 and 9 with the corresponding HIV-1-O DUR sequence shown in the same figures, and identifying the homologous peptide that is aligned with an amino acid sequence contained within the corresponding HIV-1-o DUR sequence.

Similarly, certain homologous peptides may be used in those tests which make it possible to carry out discriminations between HIV-O group viruses and HIV-M group virus, as described infra, it being understood in this case that they are then used in place of the corresponding peptides, derived from GAG, and gp41 structural proteins.

-14- Comparison of the GAG sequences On comparison of the GAG sequence obtained with the other two 0 strains published, ANT70 and MVP5180, as well as with the representative sequences of the M group (Figure it was possible to observe that an O consensus sequence exists in several regions, which is distinct from the M consensus sequence in the same regions. Two hypervariable regions, which are more variable for 0 than for M, and a few point differences for one or the other strain may also be found. Nevertheless, the 10 regions SPRT SEGA, MLNAI.... KEVIN, GPLPP.... QQEQI and VGD...SPV appear to discriminate between the O consensus sequence and the M consensus sequence.

The regions QQA and LWTTRAGNP are hypervariable regions.

The HIV-1 group (or subgroup) O DUR strain is conspicuously 15 different in three positions with respect to the M and O consensus sequence (L for I and twice for E) and takes a specific amino acid in three isolated hypervariable positions, V position L9; A position A77; L position 110.

In addition, it is possible to define in the GAG region segments common to the O group and to the M group, such as SPRTLNAWVK, GSDIAGTTST and

QGPKEPFRDYVDRF.

Comparison of the seauences of the V3 loop This comparative study revealed considerable differences of up to 56V for protein differences with the HIV-1 subgroup M consensus sequence, and 35 to 42t with the other HIV-1 group (or subgroup) 0 consensus sequences.

The alignments of peptide sequences in the regions of the V3 loop of gp120 and in the immunodominant region of gp4l is given in Figure 9. The sequence of the interior of the V3 loop of the DUR strain differs substantially from that of the HIV-1 subgroup M consensus sequence. It shares the motif GPMAWYSM with the VAU and ANT70 strains but not with the MVP strain, which has. two substitutions: R for A and R for Y.

The left and right parts of the rest of the V3 loop are markedly different from all the other HIVs known and do not leave it possible to imagine other cross-reactivities. Furthermore, the V3 loop of DUR is one amino acid longer than the other 0 sequences, which are themselves another one amino acid longer than the sequences of the HIV-1 M group.

Comparison of the aliQnments concerning the immunodominant region of =p41 The "mini loop" of the DUR strain, having the sequence tRGKAIC, proved to be very specific for this strain: it might constitute an epitope (see Figure 9).

In addition, this sequence might be likely to be involved in the modification of the conditions of unfolding of the gp4l glycoprotein, and consequently in the infectiousness of the strain.

A long sequence of 11 amino acids flanking this loop on the left is identical to the VAU sequence. A -16polymorphism of the DUR strain may be noted for an S or T position according to the clones analyzed.

Corresponding peptides obtained from other known retroviral strains are also represented in Figure 9.

The DUR strain also makes it possible to define an HIV subgroup 0 consensus sequence of the gp41 region, several sufficiently long homologous regions of which might be used. These homologous regions are, 10 inter alia: RL'ALET,QNQQ,LWGC and CYTV ('representing a variable amino acid).

S

Serological correlations: The anti-DUR antiserum does not react with the 15 peptides of the V3 loop of the HIV-1-M consensus sequence, of HIV-1 MAL, of HIV-1 CPZ or of HIV-1 group (or subgroup) 0 MVP5180 but does, however, react with the peptide of the V3 loop of HIV-1-0 ANT70. As regards the gp41 immunodominant region, this does not react with the "standard" HIV-1 subgroup M consensus sequence, but does, however, react, weakly but surprisingly, with the HIV-1 subgroup M right-extended consensus sequence.

-17- Nucleic Acids The invention, in another aspect, provides oligonucleotide primers having a sequence consisting of at least eight contiguous nucleotides of the following nucleotide sequences: 5'-ATT CCA ATA CAC TAT TGT GCT CCA -3' GAA TTC TCC ATG ACT GTT AAA-3' ATA GTG CAA CAG CAG GAC AAC-3' 5'-AGA GGC CCA TTC ATC TAA CTC-3' These primers may be used in a gene amplification process, 1 0 for example by PCR or an equivalent technique, of a nucleotide sequence coding for a peptide of the invention, as described hereinafter. Tests carried out with these primers gave conclusive results.

The present invention, in another aspect, relates to the nucleic acid sequences coding for peptides (24) and Sas well as the nucleic acid sequences coding for the immunologically similar sequences, as well as compositions comprising at least one of these nucleic acids.

The invention also relates to a plasmid chosen from those which were deposited at the CNCM on 24 February 1995 under the references 1-1548, 1-1549, and 1-1550.

The invention is also directed towards nucleic acids containing a sequence which codes for each of the peptides (1) to (20) defined in the present invention.

Among the preferred nucleic acid sequences, the nucleotide sequences represented in Figures 10, 11 or 12 will be chosen.

The invention also relates to vectors containing a nucleic acid as defined above.

The invention is also directed towards cells liable to contain any one of said nucleic acids or of said vectors.

18- Methods of detection Protein-based detection methods The invention, in another aspect, relates to a process of detection and discrimination, in a biological sample, between antibodies characteristic of an HIV-1 group (or subgroup) O retrovirus and antibodies characteristic of a retrovirus of the HIV-1-M type, characterized by contacting the biological sample with a peptide which does not react with the antibodies characteristic of a retrovirus of the HIV-1-M type, in 10 particular one chosen from the peptides and (10) described above.

Also, the invention relates to a process of detection and discrimination, in a biological sample, between antibodies characteristic of an HIV-1 group (or subgroup) O retrovirus and 15 antibodies characteristic of a retrovirus of the HIV-1-M type, characterized by contacting the biological sample with a peptide whose sequence is contained within any one of the HIV-1-M virus sequences shown in Figures 8 and 9, wherein the peptide is homologous with a reference peptide selected from the group consisting of peptides and (10) described above, and wherein the homologous peptide is derived by aligning an HIV-1-M virus sequence shown in Figures 8 and 9 with the corresponding HIV-1-0 DUR sequence shown in the same figures, and identifying the homologous peptide that is aligned with an amino acid sequence contained within the corresponding HIV-1-0 DUR sequence and defined by the reference peptide.

According to the present invention, the process of detection and discrimination between infection by an HIV-1 group (or subgroup) O retrovirus and an HIV-1 subgroup M retrovirus is characterized by placing serum, obtained from individuals subjected to an AIDS diagnostic test, in contact, in particular, with the peptide RILAVERY.

-19- In addition, the process for detection of infection due either to an HIV-1 subgroup 0 or HIV-1 subgroup M retrovirus is characterized by the use of mixtures of two categories of peptides, those of the first category corresponding to the peptides and Moreover, the process for discrimination between an infection due to an HIV-1-0 DUR retrovirus and an infection due to another type of HIV-1-0 retrovirus, is characterized by placing the biological test sample in contact with any of the peptides (11) to (15) or of the peptides (17) to In another aspect, the invention extends to a process for discrimination between infection by an HIV-1 group (or subgroup) O retrovirus and infection by an HIV-1 subgroup M type retrovirus, said process comprising detection of cleavage or 15 non-cleavage of the V3 loop of gpl20 of a retrovirus under test with a serine protease that cleaves an SR dipeptide, wherein cleavage is indicative of HIV-1-0 DUR retroviral infection and non-cleavage is indicative of HIV-1-M type retroviral infection.

In yet another aspect, the invention relates to a composition for detection and discrimination, in a biological sample, between an HIV-1 subgroup M retrovirus and an HIV-1 S" group (or subgroup) O retrovirus, comprising a mixture of two categories of peptides, the first being in particular those identified and Monoclonal antibodies specific for the sequences of each of the peptides to (20) also fall within the scope of the present invention.

Nucleic acid based detection methods Also falling within the scope of the present invention is a process for detection of the presence, in a biological sample, of nucleic acid(s)characteristic of an HIV-1 group (or subgroup) 0 DUR retrovirus, including a retrovirus according to the invention. This process comprises a placing in contact of a cDNA formed from RNA(s) contained in this biological sample, under conditions allowing the hybridization of this cDNA with at least one oligonucleotide encoding a peptide of the invention, and amplifying a target sequence of the said nucleic acid by gene amplification techniques.

The oligonucleotide primers described supra are particularly preferred for use in the above process.

In yet another aspect, the invention extends to the use of at least one nucleic acid coding for peptides (24) and (25) as well as the nucleic acid sequences coding for the immunologically similar sequences, as well as compositions comprising at least one of these nucleic acids, for detection and discrimination between HIV-1 group M and HIV-1 group O 15 strains.

Viruses The present invention also relates to a virus such as that deposited on 23 February 1995 at the CNCM under the reference I- 1542.

20 A virus also falling within the scope of the invention is a virus of the same group as the above, characterized in that consensus peptides of this virus are recognized by antibodies which specifically recognize a polypeptide or a peptide defined above.

The genomic RNA of this virus also falls within the scope of the invention.

Kits Also falling within the scope of the invention is a box or kit for detection of antibodies in the serum or any other biological sample from a patient liable to be infected with a human retroviruses of the HIV type, characterized in that it comprises: -21at least one polypeptide or at least one peptide having, in particular, as its sequence one of the sequences to described above.

means allowing the reaction for formation of an immunological complex between the polypeptide(s) or the peptide(s) and the antibodies which may be present in a biological sample to be tested, for example one or more incubation buffers, if needed, a negative control sample, 10 means for visualizing the antigen/antibody complex formed.

Also according to the invention, this kit may contain in addition, at least one consensus peptide derived from another HIV strain, or from a peptide comprising: 15 a variant of the consensus peptide, which variant is produced by replacement of at least one amino acid of the consensus peptide with a different amino acid, wherein the variant is reactive with an antiserum against the consensus peptide; or a variant of the consensus peptide, which variant is produced by deletion of at least one amino acid of the consensus peptide, or by addition of at least one amino acid to the consensus peptide, with the proviso that the variant is reactive with an antiserum against the consensus peptide.

Preferably, a kit according to the invention will contain, in addition, at least one peptide or polypeptide derived from another HIV strain, preferably the HIV-LAI strain.

Also, the invention relates to a kit allowing amplification by PCR or an equivalent technique described above.

-22- The invention also relates to a polypeptide composition for the in vitro diagnosis of an infection due to a retrovirus according to the invention, or to one of its variants, this diagnosis being made on a biological sample liable to contain antibodies formed after said infection. This composition is characterized in that it comprises at least one of the peptides (1) to The biological sample may consist in particular of blood, plasma, serum or any other biological extract. The above compositions may be used for the detection of antibodies in one of the abovementioned biological samples.

The invention is therefore also directed toward a method for the in vitro diagnosis of an infection due specifically to a retrovirus of the HIV type, characterized by the steps of: placing a biological sample, which is liable to contain antibodies produced after an infection by an 20 HIV-1 group (or subgroup) 0 retrovirus, in contact with a peptide as defined above, or with a peptide .composition as defined above, under suitable conditions which allow the formation of an immunological complex of the antigen/antibody type, detection of the possible presence of the complex.

The invention moreover relates to an immunogenic composition, characterized in that it comprises at least one peptide in combination with a pharmaceutical vehicle which is acceptable for making up vaccines.

The invention also relates to a process for the preparation of capsid proteins and gp41l and glycoproteins of a retroviral strain according to the invention, the process being characterized by the following steps: -23lysis of the cells infected with an HIV-1 retrovirus according to the invention and separation of the supernatant and of the infected cells or lysis of the viral pellets prepared by centrifugation, deposition of the cell extract and/or of the viral extract on an immunoadsorbant containing purified antibodies, which are obtained from the serum of an individual infected by a retrovirus according to the invention and advantageously attached to a suitable support, said serum of the infected individual having the capacity to react strongly with envelope proteins of the virus according to the invention, incubation in the presence of a buffer and :for a sufficiently long period to obtain the formation of an antigen/antibody immunological complex, washing of the immunoadsorbant with a buffer in order to remove the molecules not retained on the support, recovery of the desired antigenic proteins.

20 According to a first embodiment of this preparation process, the separation and the recovery of the capsid proteins and of the gp41 and glycoproteins of HIV-1 DUR are carried out by electrophoresis and by electroreduction of the proteins.

According to another embodiment of this preparation process, the proteins are recovered by: elution of the proteins attached to the above immunoadsorbant, purification of the products thus eluted on a chromatography column containing, attached to the separation support, antibodies which recognize the capsid proteins and the gp41 and gpl20 glycoproteins of HIV-1 group (or subgroup) 0 DUR.

-24- Production of peptides and nucleic acids Also falling within the scope of the invention is a process for the production of a peptide or polypeptide according to the invention, this peptide or polypeptide being obtained either by expression of a nucleic acid of the invention, or by chemical synthesis, by addition of amino acids until this peptide or this polypeptide is obtained.

The standard principles and processes of genetic engineering may be used here ("Molecular cloning", Sambrook, 10 Fritsch, Maniatis, CSH 1989).

Also falling within the scope of the invention is a process o for the production of a nucleic acid defined above, which may be produced either by isolation from a virus of the invention, or by chemical synthesis, or by using techniques of in vitro 15 amplification of nucleic acids from specific primers.

Viral lysates The invention also relates to a viral lysate as obtained by lysis of cells infected with a virus according to the invention.

A protein extract from an HIV-1I() (or HIV-,vA strain containing in particular a peptide or a polypeptide as defined above also falls within the scope of the invention.

The invention relates to specific peptides obtained from the structure of HIV-1 group (or subgroup O DUR or from variants of this retrovirus and which make it possible either to discriminate, depending on the case, globally between HIVs-1 belonging to the category O and HIVs-1 belonging to the category M, or, more specifically, between viruses belonging to the subgroup characteristic of the HIV-1 group (or subgroup) O DUR 0 and other viruses of the subgroup O, or, on the other hand, to recognize most, if not all, of the retroviruses both of the group (or subgroup) 0 and of the subgroup M.

HIV-1 VAU Retrovirus Within the context of the present invention, the inventors have isolated and sequenced the env gend from an 0 group isolate, HIV-lv,=, obtained from a French patient who had never traveled outside Europe and who died of AIDS in 1992. According to its envelope i. sequence, HIV-1V u) is related to two recently 6 characterized Cameroonian viruses HIV,n, and HIVs,$ 6 0 ::96 Phylogenetic analysis of the env sequences reveals that the three viruses appear to constitute a separate group, which will be referred to herein as HIV-1 group 0. The isolation of HIV-l(vAu) from this patient also indicates that a degree of propagation of HIV-1 group 0 has already occurred outside Africa.

Isolation of the HIV-l(v,,) virus HIV-1(VA.) was isolated in 1992 from a 41-year-old French patient suffering from AIDS. This patient exhibited, in 1986, a severe leuconeutropenia associated with a carcinoma of the uterine cervix. However, she gradually showed signs of opportunistic infections, with a reduction in the number of circulating CD4" T cells and she died of AIDS in 1992. Anti-HIV-I antibodies were first detected by ELISA (Elavia, Sanofi Diagnostics Pasteur and Abbott test) in 1990.

The patient had never traveled outside Europe, had not used intravenous medicinal products and had not received any known blood transfusion. No sexual partner of African origin has been identified. She gave birth to -26a healthy child in 1971, but a son, born in 1980, died at the age of one following a clinical episode highly suggestive of neonatal AIDS. Her third child, born in 1983, and her husband are currently in good health and not infected.

The isolation of the virus was carried out in the following manner: the CD8* cells present in the PBMCs (peripheral blood lymphocytes) of the patient were removed using beads coated with IOT8 antibodies 10 (Immunotech). These remaining PBMCs were stimulated with PHA, then cocultured with CD8-depleted PBMCs obtained from a healthy donor and stimulated with PHA. Viral growth in the coculture was monitored by assaying the reverse transcriptase (RT) activity of the supernatant and by ELISA test of the HIV-1 p24 (diagnostic kit marketed by DuPont de Nemours). The virus obtained from the initial coculture was subjected to several passages in CD8-depleted and PHA-stimulated PBMC cultures.

Several attempts were made to infect, with the HIV-l(VA), 20 various transformed cell lines, including MT4 cells (Harada, et al. 1985) and CEM cells (Rey, et al: 1989), as well as the Hela-CD4-LTRLacZ cell line P4-2 (Clavel and Charneau 1994).

Biological characterization of HIV-(1,,, Two weeks after coculturing the patient's CD8-depleted, PHA-stimulated PBMCs with similar cells from a healthy donor, the production of virus was detected in the form of an RT activity peak in the culture supernatant. This virus could then be subjected to serial passages on CD8-depleted, PHA-stimulated normal PBMCs. In Figure 1, plate A represents the production of HIV-l1 in infected PBMC culture supernatants, checked by RT assay (filled circles) and HIV-1 p24 antigen capture ELISA (empty circles). The concentration of HIV-1 p24 is expressed in ng/ml and the RT activity in cpm/pl. In plate B, the same experiment -27was carried out with a standard primary HIV-1 isolate from an AIDS patient.

Although the growth of HIV-1,,vA was easily detected by RT assay, the detection of virus in the culture supernatants by HIV-1 p24 ELISA (DuPont) was substantially less sensitive. Figure 1 shows the comparison between the profiles of productive infection of PBMCs either with HIV-I,(v) or with a primary HIV-1 isolate from an AIDS patient, assayed by RT or p24. For equivalent quantities of particles, determined by assay of RT activity in the supernatants assayed, approximately 25 times less p24 was detected in the case S.of HIV-1,, than in the case of the other HIV-1 isolate.

SThe difference may be due to the fact that the monoclonal antibody specific for HIV-1 p24, which is used to coat the ELISA plates, has only a weak affinity for the gag products of HIV-1,,,r Several negative attempts were made to propagate S: HIV-1vI on transformed human T cell lines sensitive to 20 HIV-1. In particular, cocultures between PBMCs infected with HIV-1(VAU) and either MT4 cells or CEM cells did not lead to propagation of the virus. It was also found that this virus was not capable of infecting CD4* HeLa Scells (P4-2) (Clavel and Charneau 1994) carrying a lacZ gene inducible by the tat gene. Likewise, no replication of HIV-l,(V) could be detected in activated peripheral blood lymphocytes from several chimpanzees.

Analysis of the HIV-lcvAu) envelope sequence, which will be described in detail later, and its comparison with that of the two recently described Cameroonian isolates indicate that all three viruses belong to the same group of HIV-1-related viruses.

Furthermore, this comparison indicates that these three variants of the virus are approximately phylogenetically equidistant from each other. Consequently, each of the three virus variants constitutes on its own a distinct subtype of their group, which is now called HIV-1 group -28- 0. This group is different from the group of other HIV-1 isolates, identified up until now, which the inventors call here HIV-1, group M.

The appearance of this new group poses the question of its origin: did group 0 evolve from group M viruses (or conversely) or does each group have a different history? The inventors think that, insofar as both group M and group 0 have a similar internal divergence profile, it is likely that they each correspond to the diversification of distinct viral ancestors in distinct human populations. It is not possible to assess from the phylogenetic and virological data currently available whether the ancestor of either of the two groups affected humans naturally or was introduced into humans from other species. The only virus similar to HIV-l present in a nonhuman primate is the SIVCPZGAB isolate (Huet, et al. 1990), isolated from a chimpanzee apparently infected naturally, which is clearly different both from group M and from group 0, and for which no human equivalent has been found. It is unlikely that the group 0 viruses evolved recently from a chimpanzee virus insofar as HIV-lcv,, has not succeeded in replicating in chimpanzee lymphocytes.

Why does the group 0 epidemic appear only now, some 15 to 20 years later than group M? There are three possible explanations: firstly, the introduction of the ancestor of the group 0 viruses into humans is thought to have occurred more recently than that of group M; secondly, it is possible that group M was allowed to spread earlier compared with group 0 because of different social conditions in their region of origin; and thirdly, the group 0 viruses could have a lower capacity for transmission compared with that of the group M viruses. It has been proposed that such a property explains the absence of significant worldwide propagation of HIV-2, for which a smaller viral load in infected subjects is linked to reduced transmissibility -29- (De Cock, et al. 1993). In this regard, although no data are available on the viral load in patients infected with an HIV-1 group 0, the pathogenicity of these viruses does not appear to be different from that of HIV-1. The patient from whom HIV-1,A,, was isolated died of AIDS, like the patient from whom the HIV, 1 pe group 0 isolate was obtained.

However, the natural history of infection of the HIV-1(,V, patient is still not clear, but there are several indications that this patient was infected before 1980, as suggested by the death on that date of her second child suffering from a syndrome resembling

AIDS.

The invention relates to any variant of the 15 nucleic acid sequences of the HIV-l,,, virus or of any group O equivalent virus, containing structural proteins which have the same immunological properties as the structural proteins coded for by the env gene comprising the sequence described in Figure 6 and called "vau", 20 also designated by SEQ ID No. The present invention also relates to compositions containing either antigens according to the invention, or a mixture of antigens according to the invention combined with extracts originating from one or more HIV-1 group O viruses or from other variant viruses, on the one hand, and from one or more HIV-2 and/or HIV-1 viruses, on the other hand, these compositions being optionally labeled. It is possible to use any type of appropriate label: enzymic, fluorescent, radioactive, etc.

Nucleic acids The invention, in another aspect, relates to the DNAs or DNA fragments, more particularly cloned DNAs and DNA fragments, obtained from RNA, cDNA or primers which can be used in PCR, or other gene amplification methods, derived from the HIV-1(vAU) retrovirus RNA or DNA. The P: OPERVPA\228789.DIV -10/5/00 invention relates more particularly to all the equivalent DNAs, especially to any DNA having sequence homologies with the HIV- 1 (Au) DNA, in particular with the sequence coding for the env region of the HIV-1(vAu) strain comprising the sequence corresponding to SEQ ID NO:5 represented in Figure 6 and called "vau". The homology with HIV-1 group M is at least equal to preferably to 70% and still more advantageously to about Generally, the invention relates to any equivalent DNA (or RNA) capable of hybridizing with the DNA or RNA of a group 0 HIV-1 retrovirus.

The invention also relates to the RNA sequences corresponding to the DNA sequences defined above.

The invention also relates to the HIV-1(vAU) virus integrase gene comprising the sequence identified by the name SEQ ID NO:7 represented in Figure 7 or hybridizing with SEQ ID NO:7. The invention also relates to the RNAs corresponding to the DNA described above.

The subject of the invention is also compositions containing the peptide or polypeptides encoded by the 20 abovementioned DNA or DNA fragments.

"1 Oligonucleotides derived from the VAU sequence oralternatively from the HIV-lcvAu virus integrase gene, particularly oligonucleotides comprising at least 9 nucleotides, may be used for the detection of group O HIV-1 virus DNA or RNA sequences in biological samples, cell cultures or cell extracts, by the PCR technique or any other gene amplification technique.

These sequences could be used either as gene amplification primers or as probes for the specific detection of the gene amplification products. Also capable of being used as hybridization probes are the amplification products, or theircorresponding synthetic sequence, obtained by chemical synthesis (Applied Biosystems).

The invention also covers any fragment of at least 100 nucleotides which may be used as a probe in hybridizationreactions and capable of permitting -31reaction with part of the genome of an HIV-1lc, variant under high stringency hybridization conditions.

Cloninq and sequencing of the HIV-lAU env gene For the initial PCR amplification of the HIV- 1 DNA, the total DNA was extracted from PBMCs infected with HIV-1(,, and a segment of the pol gene (integrase region) was amplified using degenerate primers: primer 4506: 5 'AGTGGAT(A/T) (T/C)ATAGAAGCAGAAGT3 Seq.

*ID No. 1; primer 5011: 5 ACTGC(C/T) CCTTC(A/C/T)CCTTTCCA3'; Seq.

ID No. 2; The reaction medium including 50 mM KC1, 10 mM 15 Tris-HCI (pH 1.5 mM MgCl,, 0.1 mg/ml gelatin, 0.2 mM dNTP, 1U of Taq polymerase (Amersham). The PCR was carried out in 43 thermal cycles at 92 0 C for seconds, 50 0 C for 1 minute and 72 0 C for 40 seconds.

**The resulting amplification product was cloned into a pBluescript vector, generating the clone ph4, deposited at the CNCM on 20 October 1994 under No.

1. -1486, which was subsequently used as a prone to screen a lambda library of low molecular weight DNA, which was digested with EcoRI and was obtained from cells infected with HIV-l1I(V,. Briefly, the PBMCs infected with HIV-l(v, were cocultured for 24 hours with new PBMCs stimulated with PHA and depleted of CD8' cells, after which a high cytopathic effect (CPE) was visible. The low molecular weight DNA was then extracted according to the Hirt method (Hirt 1967), and digested with the enzyme EcoRI.

A previous Southern-blot analysis of this DNA had indeed shown that the HIV-1(VU) genome contained only one EcoRI site, permitting the cloning of nonintegrated circular DNA species representing the entire viral genome. The resulting digestion product was subjected to agarose gel electrophoresis, and the population of DNA fragments of approximately 8-12 kb in size was purified and ligated -32to EcoRI-digested lambda Zap DNA (Stratagene). After encapsidation, plating and screening by hybridization with "P-labeled ph4 DNA, a clone, 1H34, was identified as being positive, and amplified. The EcoRI insert was purified, sonicated, and cloned by the "shotgun" technique into the phosphatase-treated vector M13mpl8 digested with the enzyme Smal. One hundred and fifty of the clones obtained were sequenced in a 373A

DNA

sequencer (Applied Biosystems), and the resulting 10 sequences were assembled into a single sequence using the Wisconsin GCG DNA analysis package.

Analysis of this sequence revealed numerous nonsense codons in all the reading frames, which is highly suggestive of a hypermutated genome (Vartanian, et al. 1991). This sequence being unusable, it was consequently decided to amplify, by PCR, the HIV-1,v, env gene using the total DNA from PBMCs infected with HIV-l), and the oligonucleotide primers derived from the sequence XH34: primer TH2 5'GCTCTAGATGGGGATCTCCCATGGCAGG 3 Seq.

ID

No. 3; primer UH2 5

'GCTCTAGATCAGGGAAGAATCCCTGAGTGT

3 Seq. ID No. 4.

The PCR amplification was carried out in 35 thermal cycles at 92 0 C for 15 seconds, 520C for 1 minute, 60°C for 2 minutes and 72 0 C for 2 minutes. The resulting amplification product, of 3.5 kb in size, was cloned into the M13mpl8 vector and sequenced by successive reactions, first using the M13 universal sequencing primer, and then the primers deduced from the upstream sequences. Analysis of the nucleotide and peptide sequences was carried out using the Wisconsin GCG DNA analysis package. The HIV-I(v.A env gene codes for 877 amino acids in total, including the signal peptide. The nucleotide sequence of the HIV-lvAu> env gene corresponds to Seq. ID No. 5 (see Figure 3).

-33- Use of nucleic acids as probes In ahtther aspect, the invention extends to the use of DNA, cDNA or fragments thereof, or of recombinant plasmids or other equivalent vectors containing these fragments, as probes, for detecting the presence or otherwise of the HIV-Iv,,,, virus in serum samples or other biological fluids or tissues obtained from patients suspected of being carriers of the HIV-Au virus. These probes are optionally labeled (radioactive, enzymic or fluorescent labels and the like). Probes which are particularly valuable for the implementation of the method for detecting the HIV-11VAu) virus or an HIV-lcVA, variant may be characterized in that they comprise all or a fraction of the DNA complementary to the HIV- 1 1 ,Au virus genome or alternatively especially the fragments contained in various clones. An HIV-v,,u cDNA fraction containing all or part of the env region will be mentioned more particularly.

The probes used in this method for detecting the [20 HIV-1, virus or in diagnostic kits are not in any way limited to the probes described previously. They comprise all the nucleotide sequences obtained from the genome of the HIV-lvAu) virus, an HIV-I(vAu) variant or a virus similar by its structure, provided that they allow the detection, using biological fluids from individuals likely to have AIDS, of an HIV-1 group 0 virus, in particular HIV-l(vAu) by hybridization with the HIV-lvw.A) virus DNA or RNA.

Particularly advantageous are the probes which, when hybridized with HIV-1, give a strong reaction with HIVs belonging to group 0 and a weak reaction with HIVs belonging to group M. By way of nonlimiting example, a probe constructed from the HIV-l1v1,) virus integrase gene sequence (SEQ ID No. 7) gives, when it is hybridized with HIV-1 under hybridization conditions such as those described in Patent EP 178 978, a strong reaction with group 0 HIVs and a weak reaction with group M HIVs.

-34- The detection may be performed in any manner known per se, especially: by bringing these probes into contact either with the nucleic acids obtained from cells contained in biological fluids (for example spinal fluid, saliva and the like), or with these fluids themselves, provided that their nucleic acids have been made accessible to hybridization with these probes, and this under conditions permitting hybridization between these probes and these nucleic acids, and by detecting the hybridization which may be produced.

The abovementioned diagnosis involving hybridization reactions may also be performed using 15 mixtures of probes derived from HIV- HIV-1 and HIV-2 respectively, provided that it is not necessary to make a distinction between the desired HIV virus types.

The subject of the invention is also expression vectors containing the sequence coding for the HIV-1 envelope proteins or containing the sequence coding for the integrase.

The invention comprises compositions for detecting the presence or otherwise of the HIV-1Au virus in serum samples or samples of other biological fluids or tissues, obtained from patients likely to be carriers of the HIV-lAu virus. These compositions are characterized in that they comprise at least one probe obtained from a nucleotide sequence obtained or derived from the HIV-lvu virus genome, particularly an HIV-lvu DNA fragment containing the region or part of the region coding for for the env protein of the HIV-lu, virus or of an HIV-1vAu variant.

Advantageously, the composition described above also comprises a probe obtained from a nucleotide sequence derived from HIV-1 or HIV-2.

Other diagnostic compositions comprise the primers of the invention which are capable of being used in gene amplification of subgroup 0 retroviruses or variants of these retroviruses.

Antigens, especially proteins and glycoDroteins The invention, in another aspect, relates to an HIV-1 group (or subgroup) O retroviral protein, or natural or synthetic peptide or polypeptide comprising at least a part of said protein, which is capable of being recognized by antibodies which may be isolated from serum obtained after an infection with an HIV-1 group O VAU strain.

10 Preferably, the retroviral protein is an external envelope protein of the HIV-lVA retrovirus encoded by the gene comprising the sequence corresponding to SEQ ID NO:5 (Fig. According to a preferred embodiment of the invention, this protein is in addition characterized in that it comprises the amino acid 15 sequence corresponding to SEQ ID NO:6 represented in Figure 3 and comprising amino acid residues 1 to 526. The subject of the invention is also any polypeptide or variant which is derived from said sequence having an epitope which may be recognized by antibodies induced by the HIV-la u virus.

20 The abovementioned protein may be obtained in a glycosylated or nonglycosylated form.

Suitably, the retroviral protein is an envelope transmembrane protein comprising the amino acid sequence SEQ ID NO:8 represented in Figure 3 between amino acid residues 527 and 877. This transmembrane protein is, within the scope of the invention, in glycosylated or nonglycosylated form.

The invention, also extends to all the antigens, especially proteins, glycoproteins, polypeptides or peptides, obtained by expressing coding sequences of the HIV-1(,A genome and having immunological properties equivalent to those of HIV-1(VAU. The antigens are said to be equivalent within the scope of the present -36invention provided that they are recognizable by the same antibodies, especially antibodies which can be isolated from serum obtained from a patient who has been infected with an HIV-l(VAU)- In particular, the subject invention contemplates peptides or polypeptides which are synthesized chemically and whose amino acid sequence is contained in that of the HIV-lvn, envelope proteins, which sequence is represented in Figure 3, or the equivalent peptides 10 or polypeptides.

There should also be included among the equivalent peptides, polypeptides, proteins or glycoproteins, the fragments of the above antigens and the peptides which are prepared by chemical synthesis or 15 by genetic engineering, so long as they give rise to immunological cross-reactions with the antigens from which they are derived. In other words, the invention relates to any peptide or polypeptide having epitopes which are identical or similar to the epitopes of the abovementioned antigens and which are capable of being recognized by the same antibodies. Forming part of this latter type of polypeptides are the products of expression of DNA sequences corresponding to DNA sequences coding for for the polypeptides or antigens mentioned above.

More particularly, the antigens which are obtained from the HIV-1,,) virus or produced by genetic engineering or conventional chemical synthesis, and which are of the greatest interest within the context of the present invention, are the antigens which make it possible to obtain a clear distinction between the HIV-l(v1 viruses of the invention and the viruses of the HIV-1 and HIV-2 groups. In this regard, considerable differences have been observed at the level of the HIVliVAU, virus envelope protein as well as at the level of the immunodominant epitope of the external portion of the PM protein. It appears that the gag and pol proteins -37exhibit greater similarity with the HIV-1 virus than the envelope protein.

In yet another aspect, the invention relates to peptides or polypeptides which are identical to the immunodominant region of the HIV-,I( envelope transmembrane glycoprotein. This region is represented in Figure 3.

Preferred polypeptides of this region are, for example, those which contain the sequence CKNRLIC or correspond to this sequence. They may also be peptides or polypeptides corresponding to the sequence RLLALETFIQNWWLLNLWGCKNRLICor comprising this sequence.

Another preferred peptide, identified below by the name "VAU peptide", corresponds to the following sequence or comprises this sequence or any part of this sequence capable of being recognized by antibodies directed against the HIV-lv,v retrovirus

RARLLALETFIQNQQLLNLWGCKNRLICYTSVKWNKT.

Variant polypeptides of this sequence are for example the polypeptides represented in Figure 4 for the HIV-(,v, 51 ,a and HIV-1,,an.,, isolates. These polypeptides may also be derived from the preceding ones by insertion Sand/or deletion and/or substitution, for example copservLtive substitution by amino acid residues.

-38- Synthesis of VAU peptides A VAU peptide was prepared by the conventional solid phase peptide synthesis technique using the "continuous flow" Fmoc method. The peptide was prepared using a Milligen 9050 PEP synthesizer and using the "Millipore" PEG PAL resin, substituted with the first C-terminal amino acid residue. The side chains of the amino acids are protected by the following groups: Pmc for arginine; Trt for asparagine, glutamine and 15 cysteine; Boc for lysine; tBu ester for glutamic acid; tBu ether for serine, threonine and tyrosine. The temporary Fmoc groups are removed with a 20% piperidine solution in DMF. The reactions for coupling each amino acid are performed with 6 equivalents of DIPCDI and HOBT. Some residues require a double coupling especially arginines 1 and 23, cysteines 19 and 26, asparagine 11, glutamines 10, 12 and 13, alanine 4, isoleucine 9 and leucines 2, 3, 14 and After coupling, the resin is dried under vacuum.

The peptide is cleaved from the support by the K reagent Sfor 4 hours at room temperature. The crude peptide is precipitated and washed with ethyl ether. The product is purified by high-pressure liquid chromatography (HPLC) in a WATERS LC PREP 4000 instrument with WATERS Delta Pak C18 40 x 100 mm cartridges, flow rate 30 ml/min, acetonitrile/0.1% TFA gradient. The fractions containing the peptide are combined, concentrated in a rotary evaporator and then lyophilized.

Cyclization The peptide (0.025 mM) is dissolved in a 10 mM ammonium acetate solution. The pH is adjusted to -39with 1M ammonium hydroxide solution. The pH is readjusted after 3 or 4 hours. The cyclization is monitored by HPLC at 214 nm and 280 nm, WATERS Delta Pak C18 5p column, acetonitrile/0.1% TFA gradient. The cyclization is complete after 15 hours. The pH is brought to 6 using 97-100% acetic acid, the solution is lyophilized and then purified under the same conditions as for the crude peptide.

The peptide is checked by HPLC and by mass 10 spectrometry according to the electrospray technique (FISON VG Trio 2000 spectrophotometer).

Fmoc: 9-Fluoroenylmethyloxycarbonyl :*Pmc: 8-Methylpentane-6-sulfonylchroman Trt: Tritryl 15 Boc: Tertbutyloxycarbonyl tBU: tert butyl DMF: Dimethylformamide DIPCDI: Diisopropylcarbodiimide HOBT: 1-Hydroxybenzotriazole TFA: Trifluoroacetic acid Reagent K: Phenol/water/thioanisole/ethanedithiol/TFA; 2.5 ml/2.5 ml/2.5 ml/1.5 ml/41 ml Comparison of the amino acid sequence of the HIV-l(cvu) envelope with the corresponding sequence of other HIV viruses.

Western-blot analysis of a series of serum samples obtained from a patient infected with HIV-1,v,,, is presented in Figure 2. Nitrocellulose strips, carrying proteins separated by electrophoresis and obtained from purified HIV particles (LAV BLOT, SANOFI DIAGNOSTICS PASTEUR), were incubated with serum samples and their reactivity was evaluated according to the procedures recommended by the manufacturer. The results obtained are the following: strip 1: proteins specific for HIV-2, which have been reacted with a serum sample obtained in February 1992 from the HIV-1(v) patient.

Strips 2-7: HIV-1 positive sera; sera from the HIV-1i(u) patient: 2: obtained in November 1990; 3: in December 1990; 4: in February 1991; 5: in February 1992; 6: negative control; 7: positive control (serum from an individual infected with HIV-1). The names and the size of the proteins (in kD) are indicated in the margin.

Figure 3 shows an alignment of the amino acid sequence of the HIV-1,i, envelope with the corresponding sequence of the HIV-1-LAI reference isolate (Wain- Hobson, et al. 1985). The signal peptides, the V3 loop 10 and the gp41 immunodominant epitope are highlighted by o shaded rectangles. The site of cleavage between the external envelope glycoprotein gpl20 and the transmembrane gp41 is indicated by arrows. The vertical lines between the amino acid letters indicate complete 15 identity, colons indicate high homology, and dots indicate limited homology between individual amino acids. The alignment was performed using the GAP program of the Wisconsin GCG package.

The original version of the GAP and BESTFIT programs was written by Paul Haeberli. from a detailed study of the publications of Needleman and Vunsch Mol. biol. 48, 443-453 (1970) and of Smith and Waterman (Adv. Appl. Math. 2; 482-489 (1981). The limited alignments were developed by Paul Haeberli and added to the package to constitute the 3.0 version. They were then fused into a single program by Philip Marquess to constitute the 4.0 version. The gap absence penalties in the alignment of the proteins were modified as suggested by Rechid, Vingron and Argos (CABIOS 5; 107- 113 (1989)).

The alignment of Figure 3 shows numerous regions of high divergence, with a few domains retained here and there. These retained regions correspond roughly to the domains also retained in the conventional HIV-1 isolates (Alizon et al. 1986, Benn et al. 1985) Among the divergent domains, the V3 loop, also called principal determinant of neutralization (Javaherian et al. 1990, -41- Javaherian et al. 1989, Matsushita et al. 1988) is clearly one of the most divergent, although the two cysteines defining the loop are retained. The sequence of the cap of the loop, GPGRAF for HIV-1-LAI is GPMAWY in HIV-1,,. This unit of the cap is identical to that of the Cameroonian group 0 isolate HIV,, 0 (Van den Heasevelde et al. 1994), but is different from that of the other group O isolate, HIVe,, 0 (Girtler et al.

1994), for which the motif is GPMRWR.

10 In the entire envelope, 29 potential N-glycosylation sites were identified in total, of which 13 are retained compared with other HIV-1 envelope proteins. 19 retained cysteines were also found in total, which indicates that the overall folding 15 architecture of the protein is retained, but nonretained cysteines were found.

Figure 4 shows the multiple alignment of the immunodominant peptides in the extracellular segment of the transmembrane envelope glycoprotein of various HIV-1 20 isolates. All the sequences are compared to the HIV-1- LAI reference sequence. Hyphens indicate identity with SHIV-1-LAI. The alignment was made with the aid of the PILEUP program of the Wisconsin GCG package.

In the PILEUP program, the assembling strategy represented by the dendrogram is called UPGMA, which means "unweighted pair-group method using arithmetic averages" (Smith, P.H.A. Sokal, R.R. (1973) in Numerical Taxonomy (pp. 230-234), W.H. Freeman and Company, San Francisco, California, USA). Each pair alignment in PILEUP uses the Needleman and Wunsch method (Journal of Molecular Biology 48; 443-453 (1970)).

As shown in Figure 4, the amino acid sequence of the immunodominant epitope of the external portion of the TM protein (Gnann et al., 1987) is substantially different from that of other HIV-1 and HIV-2 isolates.

However, it retained most of the amino acids which were -42found to be conserved between the HIV-1 and HIV-2 viruses.

It was found that some specific amino acids were conserved only between group 0 viruses: such is the case for lysine in position 21 in a peptide of 26 amino ~acids, for threonine in position 7 and asparagine in o^ position 11. These differences could explain the absence of detection of conventional HIV-1 envelope antigens by one of the sera from the HIV-I,) patient and also 10 probably by that of the patients infected by other group 0 viruses. Overall, the comparison between the HIV-1-LAI and HIV-I(v,) envelope sequences showed a 50% identity.

*The HIV-l1cvU envelope sequence was also compared to that of other HIV representatives including the two members 15 of HIV-1 group 0 described and sequenced: HIV-I.

70 and *Oe HIV-l, 5 ,o 0 and SIV representatives. The results of this analysis, which are presented in Table 1, establish that HIV-1v,^ belongs to group 0. The HIV-l1,VAU, envelope is 70% identical to the HIV-I,, 0 envelope and 71% identical to HIV-lM, 1 8 0 Among the most common HIV-1 subtypes, the identity at the level of the envelope is comparable, ranging from 74% to e H I V-1tu 77 HIV-1,AAt 176 1 80 1 H I V-l, 45 S IVCPZOAB 1 74 1 7 1 H I V-2oo 38 39 39 40 39

SIVAC

2 31 37 37 36 36 38 74 SIVAOMtYO 37 36 37 38 40 46'

HIVANTT

3: HIVmvpsioJ 51 52 14 51 52 3 3 6 47 32 33 34 SIVMAcIS }I 50 51 52 j 51 54 HIV-1m HIV.-lu HI I mk H I V-l Ue sivcpzgu 35 R I VL2noo 33 34 35 SIVAMr 0 T0 H IVAN r ?o 71 IIVavpug A a AI 43 The relationship between HIV-Ivx,, other members of the phylogeny of HIV-1 viruses and the two viruses of group 0 recently described was analyzed by constructing a phylogenetic tree of unweighted parsimony using the nucleotide sequence of the env transmembrane region. The result of this analysis is represented in Figure 5 in which the numbers indicate the number of nucleotide changes. Figure 5 shows that HIV-I(VAU) is roughly equidistant from the other two group 0 viruses and that, *10 overall, these three viruses appear to be approximately equidistant from each other. Indeed, the number of nucleotide changes between HIV-1HM28 0 and HIV-1vu) is 218 in the segment of the genome analyzed, whereas the distance is 183 between HIV-IWPsIO and HIV-,1,A"OI and 213 between HIV-lw7 0 and HIV-Iv.). This divetgence profile is very similar to that which exists in all the other HIV-1 subtypes, where the number of single nucleotide changes which exist between two different subtypes ranges from 157 (subtype E to subtype F) to 219 (subtype A to subtype D).

Table 1 shows the comparison of the envelope sequences of different viruses related to HIV-1. The numbers indicate the percentage of amino acid identity "between the envelope sequences, as calculated using the GAP program of the Wisconsin GCG package. o: in the case of HIVe, 0 only the external envelope protein was used in the comparison.

Compositions comprising HIV-(VAU) antigens Generally, the invention relates to any composition which can be used for the in vitro detection of the presence, in a biological fluid, especially from individuals who have been brought into contact with HIV-lcvu), or with antibodies against at least one of the HIV-l(vAu) antigens. This composition can be applied to the selective diagnosis of infection by an HIV-1 group 0 by using diagnostic techniques such an those described -44in Patent Applications EP 84401,834 and EP 87400,151,4.

Within the context of the present invention, any constituent comprising antigenic determinants capable of being recognized by antibodies produced against HIV-lcv,,, is used, for example recombinant antigens or peptides or chemically synthesized peptides defined from the sequence of the HIV-lvta, envelope. In this regard, the invention relates more particularly to compositions containing at least one of the HIV-lv,> virus envelope proteins. There may be mentioned, by way of examples of compositions, those which contain proteins, glycoproteins or peptides from the envelope protein corresponding to the entire 590-620 region of the HIV- 1,VAU) gp41 protein or to the parts of this region which 15 are specific for HIV-lvAu) such as the peptides TFIQN- or -WGCKNR-.

The invention also relates to compositions combining recombinant or synthetic proteins and/or glycoproteins and/or peptides with proteins and/or glycoproteins and/or peptides from HIV-1 and/or HIV-2 and/or from another HIV-1 group O which are :obtained by extraction or in lysates or by recombination or by chemical synthesis and/or peptides which are derived from these proteins or glycoproteins and which are capable of being recognized by antibodies induced by the HIV-1 and/or HIV-2 and/or HIV-1 group O virus.

The diagnostic compositions containing antigenic determinants capable of being recognized by antibodies directed against HIV-l(vAu, in particular the peptide compositions, may be included in or combined with compositions or kits already available for detecting infection by HIV-1 and/or HIV-2 retroviruses, so as to extend the detection range of the kits to the detection of HIV-1 group 0 retroviruses.

By way of nonlimiting examples: either core proteins, particularly the gag, pol, HIV-1 and HIV-2 proteins or peptides thereof, and HIV-1,,U) envelope proteins or peptides, or HIV-1 envelope glycoproteins, HIV-2 envelope glycoproteins and HIV-1,V, envelope glycoproteins, or mixtures of HIV-1 proteins and/or glycoproteins, HIV-2 proteins and/or glycoproteins and HIV-1(VAu, envelope proteins and/or glycoproteins.

It is important to note that, although the o antibodies from patients infected with HIV-1 group 0 viruses react strongly with gag and pol antigens from HIV-1 group M viruses, their reactivity is practically zero with group M virus envelope antigens. It is therefore important that the composition of the present invention comprise at least one protein or one peptide of the HIV-l(,A) envelope so that this virus can be detected with certainty.

Such compositions, when used in diagnosis, consequently help the diagnosis of AIDS or of the symptoms associated with it, which extend over a broader spectrum of causative etiological agents. It goes without saying that the use of diagnostic compositions which contain only HIV-I(v,, envelope proteins and/or glycoproteins is nonetheless useful for the more selective detection of the category of retrovirus which may be held responsible for the disease.

Methods and kits for the diagnosis of infections caused especially by the HIV-l(v, virus The present invention relates to a method for the in vitro diagnosis of infection caused by HIV viruses, etiological agents of AIDS and related syndromes, which comprises bringing a serum or another biological medium, obtained from a patient or subject being subjected to the diagnosis, into contact with a -46composition containing at least one protein, glycoprotein or peptide from and detecting a possible immunological reaction. Examples of such compositions were described above.

Preferred methods involve, for example, immunofluorescence or ELISA type immunoenzymic reactions. The detections may be effected by direct or indirect immunofluorescence measurements or direct or indirect immunoenzymic assays.

Such detections comprise for example: depositing defined quantities of the extract or of the desired antigenic compositions in accordance with the present invention into the wells of a microplate; introducing into each well a serum, diluted or undiluted, which is capable of containing the antibodies, the presence of which has to be detected in vitro; incubating the microplate; carefully washing the microplate with an appropriate buffer; introducing into the wells of the microplate specific labeled antibodies to human immunoglobulin, the labeling being performed with an enzyme chosen from those which are capable of hydrolyzing a substrate such that the latter then undergoes modification of its absorption of radiation, at least in a defined wavelength band, and detecting, preferably in a comparative manner relative to a control, the extent of the hydrolysis of the substrate as a measure of the potential risks or of the actual presence of the infection.

The present invention also relates to kits or boxes for the diagnosis of HIV-1(VAU) virus infection, which comprise in particular: -47an extract, a more purified fraction, or a synthetic antigen derived from the types of viruses indicated above, this extract fraction or antigen being labeled, for example, radioactively, enzymically, fluorescently or otherwise, antibodies to human immunoglobulins or a protein A (which is advantageously attached to a support which is insoluble in water) such as agarose beads for example) or microplate wells, and the like), optionally, a sample of biological fluid or S. cells obtained from a negative control subject; buffers and, where appropriate, substrates for visualizing the label.

The subject of the invention is also immunogenic compositions which are capable of inducing the formation of antibodies recognizing antigens which can be obtained by chemical synthesis or by recombination.

Serology S. 20 The capacity of the serum antibodies from the patient infected with HIV-1(v, to react with HIV-1 antigenic preparations was evaluated using various commercially available kits: Sanofi Diagnostics Pasteur, (Genelavia Mixt) Abbott, Wellcome, and Behring. The reactivity of these antibodies with various HIV-1 proteins was examined using the Sanofi Diagnostics Pasteur Western-blot kit, following the procedures recommended by the manufacturer.

More precisely, the patient's serum was examined several times using HIV-1 specific ELISA kits. It was first tested and proved to be positive in 1990, being noted 7.33 (this figure corresponds to the ratio of the measured OD to the background OD) with the Sanofi Diagnostics Pasteur kit, 3.50 with the Abbott kit and 2.70 with the Wellcome kit. During the use of reagents specific both for HIV-1 and HIV-2, the serum was noted -48- 1.42 with the Behring kit and 4.40 with the Wellcome kit.

The capacity of the patient's serum to react on different dates with different HIV-1 structural proteins was studied using the HIV-1 LAV BLOT immunoblot assay, a test marketed by Sanofi Diagnostics Pasteur. As shown in Figure 5 with all the serum samples tested, only a very weak reactivity of the serum with the HIV-1 env proteins and gpl20 was noted. However, the serum reacted strongly with the HIV-1 gag proteins p55 (gag precursor) and p24 and with the pol products p66 (RT) and p34 By HIV-2 immunoblotting, only a very weak reactivity was detected with the gag p26.

This illustrates that the detection of 15 antibodies specific for group 0 with commercially available serum diagnostic kits should be carefully controlled. Although serum antibodies from patients infected with group O viruses show strong crossreactions with the group M gag and pol antigens, they show few or no reactions with the group M envelope antigens. Consequently, it is possible to assume that a significant proportion of these patients might not be detected using some kits based on group M envelope antigenic reagents. Indeed, in a recent preliminary study of several sera from patients infected with group O, it was found that the capacity to detect antibodies specific for group O was very different depending on the detection kit used (Loussert-Ajaka, Ly, Chaix, Ingrand, Saragosti, Courrouc6, Brun- Vezinet, F. and Simon, F. (1994). HIV-1/HIV-2 seronegativity in HIV-1 subtype 0 infected patients.

Lancet. 343, 1393-1394.). This implies that a careful and extensive study of the reactivity of a large number of group 0 sera with all the diagnostic kits available on the market is necessary.

-49- Compositions comprising polyclonal or monoclonal antibodies prepared from recombinant or synthetic antigens from the HIV-livA, virus.

The invention relates to a serum capable of being produced in animals by inoculating them with HIV- l(vl,, particularly the antigenic epitopes of HIV-l(V,,A and more particularly the antigenic epitopes of the HIV-1,v virus envelope protein. The invention relates more particularly to the polyclonal antibodies more specifically oriented against each of the antigens, especially proteins or glycoproteins of the virus. It also relates to monoclonal antibodies produced by o* various techniques, these monoclonal antibodies being respectively oriented more specifically against the 15 various HIV-Iev,,, proteins, particularly the HIV-1(v, envelope proteins.

These polyclonal or monoclonal antibodies can be :used in various applications. There may be mentioned essentially their use for neutralizing the corresponding proteins, or even for inhibiting the infectivity of the whole virus. They may also be used for example to detect viral antigens in biological preparations or to carry out procedures for purifying the corresponding proteins and/or glycoproteins, for example during their use in affinity chromatography columns.

By way of example, anti-envelope antibodies or anti-gag antibodies are reagents which can be used in diagnosis, in particular for the detection of HIV-1 group O particles by antigen capture ELISA.

The invention relates to antibodies directed against one or more HIV-lcvAu viral antigens produced from amino acid sequences of HIV-l,(VA). Techniques for obtaining antibodies from antigenic epitopes similar to the antigenic epitopes of the HIV-l(,, virus. of the present invention have been described previously.

The technique for the preparation of antibodies which is described in the publication by Ulmer et al., 1993, may be used by persons skilled in the art to prepare the antibodies of the present invention, the modifications which make it possible to adapt this technique to the antigens of the present invention forming part of the knowledge of persons skilled in the art.

Study of the immunoreactivity of the vau peptide The immunoreactivity of the vau peptide was confirmed, after experimental ELISA plates had been prepared, according to a procedure established for a screening test for anti-HIV antibodies. This test is 15 based on the detection of a solid phase prepared with the peptide which mimics the immunodominant epitope of the envelope glycoprotein of the HIV-1 group (or subgroup) 0 virus, VAU isolate. The implementation of the test was modeled on the procedure proposed by the Genelavia® Mixt kit, using the reagents in that kit.

The experimental data collated in the two tables of Figures 21 and 22 show that: a) the four sera taken from patients contaminated with the HIV-1 group (or subgroup) O virus are very reactive with the vau peptide; b) the ten sera supposedly taken from patients contaminated with the HIV-1 (group or subgroup) 0 virus, among the 19 sera sent out by the Pasteur Institute of Yacound6, are also highly reactive with this same peptide; c) the sera (4 samples) taken from individuals contaminated with the HIV-1 subtype B virus (in the acute phase) are not reactive with the vau peptide; -51 d) the sera taken from asymptomatic blood donors (48 samples tested) are not reactive with the vau peptide; These experimental data, although limited (in view of the paupicity of HIV-1 group (or subgroup 0) antibody-positive samples), bear witness to the sensitivity and specificity of the peptide selected.

From the above text, it follows that the invention also relates to the detection of the HIV-1,,v, virus or of a variant by virtue of the use of the antibodies described above in a method involving various stages, these stages being specifically intended to reveal the characteristic properties of the HIV-1(vA~ virus.

SThe invention also relates to the detection of the virus by molecular hybridization.

Generally, this. method for detecting the HIV- **(VAi virus or a variant in serum samples or samples of other biological fluids or tissues, obtained from patients liable to be carriers of the HIV-1,vA, virus, 20 comprises the following stages: the manufacture of at least one optionally labeled probe; oo at least one hybridization stage performed under conditions permitting hybridization by bringing the nucleic acid of the suspect patient's sample into contact with said labeled probe and optionally immobilizing the complex formed on an appropriate solid support, where appropriate, washing said solid support with a suitable washing solution, the detection of said complex and therefore of the presence or otherwise of the HIV-1,mu virus by an appropriate detection method known to those skilled in the art.

-52- In another preferred embodiment of the method according to the invention, the abovementioned hybridization is performed under nonstringent conditions and the membrane is washed under conditions adapted to those for the hybridization.

By using serology or a gene amplification technique such as specific Polymerase Chain Reaction (PCR), the extent of the HIV-1 group 0 epidemic was precisely evaluated. It was found that 5 to 10% of patients infected with HIV-1 in Cameroon are in fact infected with group O viruses. However, apart from the virus isolate described here, the propagation of the group O virus outside West Central Africa has not been documented. The patient from whom HIV-l(V,, was isolated has always lived in France and has never traveled to Africa. Up until now, we have no precise proof relating to the origin of her infection, but this case indicates that a degree of propagation of the group O viruses in Europe has already occurred.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, 25 and should not be taken as, an acknowledgement or any form of suggestion that that prior art forms part of the common general knowledge in Australia.

53

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Claims (10)

1. An isolated nucleic acid for the specific detection of HIV-1VAU virus selected among: i) a sequence comprising SEQ ID NO: ii) a nucleic acid which hybridizes specifically with SEQ ID NO 5 under high stringency conditions, iii) a sequence comprising SEQ ID NO:7, or, iv) a nucleic acid which hybridizes specifically with SEQ ID NO: 7 under high stringency conditions.

2. The nucleic acid of claim 1, characterized in that it is an RNA sequence.

3. A composition for the detection of the HIV-lvAu retrovirus, in samples of serum or other biological liquids or tissue obtained from patients suspected of being carriers of an HIV-1vAu retrovirus, said composition being characterized in that it comprises at least one probe obtained from a nucleic acid of claim 1.

4. A composition for the detection of the HIV-lvAu retrovirus, in a biological sample, said composition being characterized in that it comprises at least two nucleic acids according to claim 1, which nucleic acids can be used as primers for amplification of the DNA and/or RNA of HIV-1vAu. An isolated envelope protein of the HIV-1VAu retrovirus, S.*i characterized in that it may be obtained by expression, P.MOpaAVpaWPA Prosactm 22796 mmde Ciu bstia p.Pau 141doC-24/V94 -58- in a host cell, of a nucleic acid according to claim 1, and in that said protein comprises either the amino acid sequence between residues 1 and 526 of figure 3, or, the amino acid sequence between residues 527 to 877 of figure 3.

6. An isolated polypeptide or peptide specific of the HIV- iVAU virus whose sequence is contained in the sequence of the envelope protein according to claim characterized in that it comprises an epitope which is capable of being recognized by antibodies induced by the HIV-1vAu virus.

7. An isolated polypeptide or peptide according to claim 6, characterized in that it comprises a sequence selected among the following: TFIQN, WGCKNR, CKNRLIC, the sequence RLLALETFIQNWWLLNLWGCKNRLIC, or a variant of that sequence such as RLQALETLIQNQQRLNLWGCKGKLIC, the sequence RLLALETLLQNQQLLSLWGCKGKLVC, the sequence RARLLALETFIQNQQLLNLWGCKNRLICYTSVKWNKT, or a variant of these sequences by conservative substitution of amino of claims 6 and 7 characterized in that it is a synthetic peptide.

9. A composition for the in vitro detection of the presence, in a human biological sample, of anti-HIV-1vAu antibodies, said composition comprising at least one antigen comprising a polypeptide or peptide of the antigen comprising a polypeptide or peptide of the P.IOpoWp\VA Po-tic227896 aod clims inrt po 14 1 Ad-24O/O4 -59- envelope protein of HIV-1vAu according to any of claims to 8. The composition according to claim 9, characterized in that it also comprises an antigen of an HIV-1 virus not belonging to the O group and/or of an HIV-2 virus and/or, an antigen derived from a HIV-1 virus not belonging to the O group and/or from an HIV-2 virus, having an epitope which may be recognized by the antibodies induced by the HIV-1 virus not belonging to the 0 group and/or the HIV-2 virus.

11. The composition according to claim 10, characterized in that the antigens of HIV-1 not belonging to the 0 group and/or of HIV-2 are gag or pol proteins or fragments of gag or pol proteins.

12. The composition according to claim 10, characterized in that the antigens of HIV-1 not belonging to the O group and/or of HIV-2 are envelope glycoproteins. 12, characterized in that said composition comprises a :peptide sequence corresponding to the entire region

590-620 of the gp41 protein of HIV-1VAU or a part of this •io" region which is specific for HIV-1VAu. 14. The composition according to claim 13, characterized in that said peptide sequence is the sequence TFIQN, CKNRLIC or WGCKNR \OpAVpa\VA Pmascvtiw\21796 amcdna claims iaWMt p9cm 141dc-24/O504 An isolated antibody which may recognize an envelope protein of HIV-1vAu according to claim 5 or (ii) a peptide or a polypeptide according to any of claims 6 to 8. 16. A process for the in vitro detection of an infection caused by the HIV-1VAU virus, said process comprising: i) the placing in contact of a serum or of another biological medium, obtained from a patient suspected of being carriers of the HIV-1VAU virus, with at least one of the envelope protein according to claim 5, or of a peptide or polypeptide according to any of claims 6 to 8 or a composition according to any one of claims 9 to 14, and ii) the detection of an immunological reaction. 17. A reagent required for the Western blot or ELISA reaction, containing an envelope protein of the HIV-1IvA virus according to claim 5, or a peptide or polypeptide according to any of claims 6 to 8, or a composition according to any one of claims 9 to 14. 18. Use of a nucleotide sequence according to claim 1 in order to induce in vivo the synthesis of antibodies directed against the antigen coded for by said sequence. *ee. *e 19. The composition according to any one of claims 9 to 14, which is capable of inducing antibodies in animals 6- 1-05;13:16 ;DAVIES COLLISON CAVE Pat. &Trad :61 7 3368 2262 5/ 8 61- A diagnostic kit for the in vitro detection, on a biological sample, of an infection with an HIV-lvAu retrovirus, characterized in that it comprises: -a composi.tion according to claim 4; -reagents' required for the gene amplification reaction. 21. A diagnostic kit for the in vitro detection, on a biological sample, of an HIV- 1VAU retrovi-us, characterized in that it comprises as optionally labelled probe, at least one nucleotide sequence according to claim 1 or a composition according to claim 3, and optionally another nucleotide probe according to said composition being optionally *immobilized on a solid support. The kit according to claim 21, characerized in that it also comprises the reagents required for carrying out hybridization. 23. Bacterial strain deposited at the CNCM on 20 October 1994 under the Access Number 1-1486. 24. Plasrnid contained in the bacterial strain off claim 23. Isolated protein extract of HIV-l group OvAU strain containing in particular an antigenic peptide according to any of Claims 6-8. 6- 1-05;13:16 ;DAVIES COLLISON CAVE Pat.&Trad ;61 7 3368 2262 6/ 8 -62- 26. A process of detection and discrimination between infection with a retrovirus of the HIV-1-O type and of the HIV-1-M type, characterized by contacting sera obtained from a patient suspected of being carriers of the HIV-IvA virus, with at least one of the envelope protein according to claim 5, or of a peptide or polypeptide according to any of claims 6 to 8 or a composition according to any one of claims 9 to 14, and detecting an immunological reaction. 0* 27. A nucleic acid according to any one of claims 1 and 2, or a composition according to any one of claims 3 and 4, or an isolated envelope protein according to claim 5, or an isolated polypeptide according to any one of claims 6-8, or a composition according to any one of claims 9-14, or an isolated antibody according to claim 15, or a process according to claim 16, or a reagent according to claim 17, or a use according to claim 18, or a composition according to claim 19, or a diagnostic kit according to any one of claims 20 and 21, or a kit according to claim 22, or a bacterial strain according to claim 23, or a plasmid according to claim 24, or an isolated protein according to claim 25, or a process according to claim 26, substantially as herein before described with reference to the figures and/or examples. DATED this 6th day of January 2005 Institut Pasteur DAVIES COLLISON CAVE Patent Attomeys for the applicant