KR20110090004A - Primemrs and methods for detecting plasmodium vivax and plasmodium falciparum causing malaria, and detection kit thereof - Google Patents

Abstract

PURPOSE: A primer for gene test to diagnosing Plasmodium vivax and Plasmodium falciparum causing malaria is provided to enable simultaneous detection. CONSTITUTION: A method for gene test of Plasmodium vivax and Plasmodium falciparum for diagnosing malaria comprises: a step of isolating DNA from blood or blood paper analyte; a step of amplifying real time PCR using a primer set; and a step of performing melting curve analysis of the gene amplified product. The primer is selected from the group consisting of sequence numbers 1-5. The primer pair contains primers selected from the group consisting of sequence numbers 6-9.

Description

PRIME MRS AND METHODS FOR DETECTING PLASMODIUM VIVAX AND PLASMODIUM FALCIPARUM CAUSING MALARIA, AND DETECTION KIT THEREOF}

The present invention relates to a set of primers for amplifying trigeminal fever or tropical fever protozoa genes that cause malaria, a test method and a test kit using the same.

Malaria is a contagious disease transmitted by female Anopheles mosquito, a disease that occurs mainly in the tropics, with 200 to 300 million human infections and millions of deaths each year.

Causing parasites include Plasmodium vivax (vivax falciparum), Plasmodium faciparum (P. falciparum), Plasmodium malariae (four days heat protozoa), Plasmodium ovale (oval column protozoa). Among these, tropical fever parasites are the most common cause of infection, with the most serious symptoms. Complications include anemia, jaundice, cerebral malaria, renal failure, and hydrocephalus (hemolytic anemia and hemochromatosis). Tropical fever protozoa is the leading cause of death worldwide.

Malaria is a disease with a high morbidity and mortality, causing the largest number of infectious diseases except tuberculosis to death. The main source of infection is female Anopheles mosquito, but some of them may be caused by blood transfusions or vertical infections. Recently, domestic malaria infections mostly occurred near the armistice line, but are still south of Seoul's Gangbuk area, which poses a threat to national health improvement.

Conventional malaria tests include peripheral blood smear, antigen test, antibody test and genetic test. Peripheral blood smear is commonly used for thin or thick layer smearing, and Kimsa (Giemsa) staining. Among them, the Kimsa method is known to have a thicker layer coating method than the thin layer method, rather than the thin layer method. However, when confirming protozoa, an optical microscope can be used to make a mistake in mistaken foreign bodies or platelets as malaria protozoa, which requires a skilled inspector.

Fluorescence staining method such as acridine orange using a fluorescence microscope is economical and has the advantage that can be tested in a faster time than other staining method. However, there is a problem that the subjective judgment of the examiner can be involved.

Fluorescent staining is not currently used for purposes of testing parasitemia. Protozoan antigen testing is used in part by the Antigen capture ELISA method using monoclonal antibodies, but has a low sensitivity. Immunocapture (Dipstick) method has been developed a number of products, but using different target antigens, it is known that the sensitivity is lower than the existing method and there is a false positive method.

Protozoa antibody tests are used for epidemiological investigations and screening tests for blood products, or for diagnostic purposes for some antibodies. The presence of antibodies does not mean that antigens do not exist in the blood. have.

Protozoa gene testing includes malaria infection by performing polymerase chain reaction on genes encoding the Circumsporozoite protein (CS), the Merozoite surface protein 1 (MSP-1), the Erythrocyte binding protein (EBP), or the 18S ribosomal RNA. There is a way to check.

Sensitivity is the highest among the test methods, and species can be classified using PCR dot blotting, SSCP, and sequencing after gene amplification.

Malaria protozoa testing method using real-time polymerase chain reaction, which is widely used recently, is more economical and has a relatively shorter test time, and quantifies the blood concentration of malaria protozoa. Inspection method. Thin smear and thick smear are currently used for the treatment or post-treatment monitoring of malaria, but highly sensitive methods such as fluorescence staining and gene amplification are recommended.

An object of the present invention is to provide a primer set for amplification of trichoid protozoa or tropic filamentous protozoa genes that cause malaria.

Another object of the present invention is to provide a quantitative test method and test kit capable of diagnosing the trilobite protozoa and the tropical pyramidal protozoa by one test, and at the same time testing the blood concentration of each malaria protozoa.

Still another object of the present invention is to provide a kit comprising a primer and a test reagent used in the above method.

In order to achieve the above object, the present invention is one primer selected from the group consisting of the nucleotide sequence of SEQ ID NO: 1 to 5; Provided is a primer set for amplification of trifiltoid or tropic filamentous gene genes, which cause malaria, including one or more primer pairs consisting of one primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 6 to 9.

The primers consisting of the nucleotide sequences of SEQ ID NOs: 1 to 5 are upstream primers, and the primers consisting of the nucleotide sequences of SEQ ID NOs: 6 to 9 are downstream primers. One primer selected from SEQ ID NOs: 1 to 5 and one primer selected from SEQ ID NOs: 6 to 9 are combined to form a primer pair to serve as a primer set for gene amplification.

Examples of specific primer sets include primer pairs having a nucleotide sequence of SEQ ID NOs: 1 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 1 and 8; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 6; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 3 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 4 and 6; And at least one selected from the group consisting of a primer pair having a nucleotide sequence of SEQ ID NOs: 5 and 6 and a primer pair having a nucleotide sequence of SEQ ID NOs: 5 and 9.

The 5 'end of SEQ ID NO: 1 to 5 is attached to the fluorescent material can be easily performed. The former may be used without limitation as long as it is a substance used in the art. Specifically, the fluorescent material is Sybergreen, Evagreen, Cy3, Cy5, biotin binding material, Alexa 647 (Alexa 647), Alexa 555, (5- (2-aminoethyl) amino-1-naphthalene sulfate) (EDANS ), Tetramethyltamine (TMR), tetramethyltamine isocyanate (TMRITC), x- rhodamine and Texas red, but is not necessarily limited thereto.

In another aspect, the present invention provides a method for the genetic test of trilobite or tropical fever protozoa for the diagnosis of malaria. Specific test methods are as follows:

 Extracting DNA from blood or paper samples;

One primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 1 to 5; Amplifying the gene by a real-time polymerase chain reaction using a primer set including at least one primer pair consisting of one primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 6 to 9; And

Confirming genotypes of tricuspid or tropical filamentous protozoa using a melting curve analysis method for the gene amplification product.

In the step of extracting DNA from blood or paper samples, the cells are lysed with a cell lysis solution to obtain DNA from whole blood or blood samples.

In the next step of amplifying the gene by real-time polymerase chain reaction, real-time polymerase chain reaction of the DNA into primer sets of 5 'PCR primers and 3' PCR primers, which are primers specific to trigonate and / or tropic genes Amplify the gene using reagents. The 5 'PCR primers are described in SEQ ID NOs: 1 to 5, and 3' PCR primers in SEQ ID NOs: 6 to 9.

The primer pair is a primer pair having a nucleotide sequence of SEQ ID NO: 1 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 1 and 8; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 6; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 3 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 4 and 6; It may be one or more selected from the group consisting of a primer pair having a nucleotide sequence of SEQ ID NO: 5 and 6 and a primer pair having a nucleotide sequence of SEQ ID NO: 5 and 9.

In the step of confirming genotypes of trifluid or tropical fever protozoa using a melting curve analysis method, the gene amplification product is prepared by forming a melting curve from 95 ° C. to 50 ° C. using a real-time gene amplifier. By determining the melting temperature of the gene amplification of the species can be distinguished. Specifically, the melting curve analysis may be performed by performing the melting curve analysis of the gene amplification product with a slope of 0.1 ° C. from 95 ° C. to 50 ° C.

In addition, the present invention, DNA extraction reagent; And it provides a genetic test kit of trilobite or tropic fever for diagnosis of malaria comprising the primer set.

The base sequence structure of the primer set used for the real-time gene amplification for the trigeminal and tropic filamentous protozoa genes is shown in Table 1 below.

To prepare the test kit of the present invention, the kit was composed of the following reagents, instruments, and devices (see FIG. 1).

 30 ml tube containing proteinase K and extraction solution (10 mM Tris-Cl, 7% chelex) for DNA extraction from cells;

For real-time amplification of the tritidal and tropic filamentous genes,

① Taq DNA polymerase 250 unit (Amplitaq, PE, USA);

② Premix 1 solution [2X PCR buffer (100 mM-KCl, 20 mM Tris-HCl, pH 8.0), 2.0 mM MgCl ₂ ), 2.5 mM dNTP, 20 pmol 5 'and 3' primers, 0.001% Sybergreen or Evagreen];

③ Positive control [100 ng / ul of 18S rRNA gene of the gentile No. U83877 or the genus No. 11010278 of Genebank No. AL010278 included in the pGEM-T vector]

④ negative control [human genomic DNA 100 ng / ul] and

⑤ distilled water,

  And Roche's LC480 (Roche Diagnostics, USA) for distinguishing species of trifid and tropic flies from real-time gene amplification.

And the like.

The reagents, instruments, and equipment can diagnose the infection of trichophytes and tropical fever protozoa from blood and blood lipid samples, and based on this, the test kit was kitted.

1) for DNA extraction from cells,

① 30 ml tube containing extraction solution (10mM Tris-HCl (pH8.4), 7% chelex, 20mg / ml proteinase K)

2) for real-time gene amplification of tritus and tropic filaments

① Taq polymerase 250 unit (Amplitaq, PE, USA)

② Premix 1 solution [2X PCR buffer (100 mM-KCl, 20 mM Tris-HCl, pH 8.0), 2.0 mM MgCl ₂ ), 2.5 mM dNTP, 20 pmol 5 'and 3' primers, 0.001% Sybergreen or Evagreen];

③ 1.5 ml tube of positive control 100 ng / ul concentration

④ 1.5 ml tube of negative control 100 ng / ul concentration

⑤ 1 ml 1.5 ml tube of distilled water

The present invention provides a primer for gene amplification specific to trigeminal flies and tropical flies. In another aspect, the present invention is to provide a quantitative test method and test kit that can test the genus Trineum and tropical fever protozoa genes in a single test using the primer, and at the same time can test the blood concentration of each malaria protozoa Has

In addition, the genetic test method and kit for diagnosing triple fever protozoa and tropical fever protozoa infection using the real-time polymerase chain reaction of the present invention provides a quantitative value for calculating the blood concentration of infected malaria protozoa, thus, whether or not malaria infection is present. And quickly and accurately for post-treatment monitoring.

In addition, the test method according to the present invention is a very useful test method industrially because the time to confirm the infection within a total of 2 hours.

1 is a photograph showing the components constituting the genetic test kit of trilobite or tropic fever for diagnosis of malaria.
Figures 2a to 2c is a graph showing the results of real-time gene amplification test of trifilworms.
3A to 3C are graphs showing the results of real-time gene amplification test of tropical flies.
Figures 4a to 4d is a graph showing the results of differentiation of each species in the three days and tropical fever protozoa infection samples.
5a to 5h show sequencing results for confirming whether the PCR product according to an embodiment of the present invention correctly amplified genes of trifid and protozoan genes.
Figure 6 shows the change of the Ct value according to the concentration during real-time polymerase chain reaction for the gene extracted from the sample infected with malaria.

Hereinafter, the structure of the present invention will be described in more detail with reference to examples, but the scope of the present invention is not limited to the following examples.

Example 1 Extraction of DNA from Blood or Blood Samples

50 ul of whole blood or 0.5 cm of blood sample was added to a 1.5 ml microtube, 1 ml of Tris-Cl (10 mM, pH 8.0), centrifuged at 1,000 G for 10 minutes, the supernatant was discarded, and the extraction solution (10 mM Tris). Resuspended with -HCl (pH8.0), 7% chelex, 20 mg / ml proteinase K). This was allowed to stand at 55 ° C. for 1 hour, incubated for 10 minutes at 100 ° C., and centrifuged at 1,4000 g for 5 minutes, and the supernatant was used for genetic testing. Compared with the existing extraction method, the organic solvent used in the conventional extraction method is not used, so the risk of environmental pollution can be eliminated.

Example 2 Test Methods for Trifid and Tropical Fever Protozoa Genes

Real time gene amplification method was used. Primers used for malaria diagnosis were used in each primer set in Table 2 below. For real-time gene amplification, 5.0 μl of the sample was added to a 0.2 ml PCR tube and pre-denaturated at 95 ° C. for 10 minutes before PCR. 20 μl of distilled water was included, including 10.0 μl of 2 × premix buffer, 0.3 μl of Taq polymerase, and 5 μl of template DNA. Real-time gene amplification was performed 40 times for 30 seconds at 95 ° C, 30 seconds at 55 ° C, and 1 minute at 72 ° C (LC480, Roche Diagnostics). After real-time gene amplification, the gene amplification product was subjected to a melting curve analysis with a gradient of 0.1 ° C. from 95 ° C. to 50 ° C. (LC480, Roche Diagnostics).

Genetic test results of each of the three-day-old protozoan and tropical filamentous protozoa were confirmed by gene amplification in each primer set in the melting curve analysis (FIGS. 1 and 2).

Primer sequence structure SEQ ID NO: name division Sequence One mG-F1 Upstream GAA CGA GAT CTT AAC CTG C 2 mG-F2 Upstream AAC GAG ATC TTA ACC TGC T 3 mG-F3 Upstream CGA GAT CTT AAC CTG CTA A 4 mG-F4 Upstream TCT TAA CCT GCT AAT TAG C 5 mG-F5 Upstream CTT AAC CTG CTA ATT AGC G 6 mG-R1 Downstream GTT CCT CTA AGA AGC TTT A 7 mG-R2 Downstream ACC TGT TGT TGC CTT AAA C 8 mG-R3 Downstream AGA CCT GTT GTT GCC TTA A 9 mG-R4 Downstream CAT CAC AGA CCT GTT GTT G

Primer set configuration Primer set 5 'primer 3 'primer  One mG-F1 mG-R2  2 mG-F1 mG-R3 3 mG-F2 mG-R1 4 mG-F2 mG-R3 5 mG-F3 mG-R3 6 mG-F4 mG-R1 7 mG-F5 mG-R1 8 mG-F5 mG-R4

Example  3: Three days  And Tropical heat  Examination of specimen of duplicate infection of protozoa

The same real time gene amplification method as in Example 2 was used. Primers used for malaria diagnosis were used in each primer set in Table 2 above. For real-time gene amplification, 5.0 μl of the sample was added to a 0.2 ml PCR tube and pre-denatured at 95 ° C. for 10 minutes before PCR. 10.0 μl of premix buffer, 2.0 μl of 20 pmol primer, and 5 μl of template DNA were added to 20 μl with distilled water. Real-time gene amplification was performed 40 times, 30 seconds at 95 ° C, 30 seconds at 55 ° C, and 30 seconds at 72 ° C (LC480, Roche Diagnostics). After the real-time gene amplification, the gene amplification was subjected to the melting curve analysis with a slope of 0.1 ℃ from 95 ℃ to 50 ℃ (LC480, Roche Diagnostics).

As a result of the duplicate infection test of the three-day-old protozoan and the tropical heath protozoa, the peaks at different temperatures are shown in the melting curve analysis, indicating that the genes can be distinguished from each other (Table 3 and FIG. 4).

[Table 3] Comparison of Tm values according to species in three-day and tropical fever protozoan infection samples according to each primer set

Example  4: Comparison between the test method and the sequencing method of the present invention

After real-time polymerase chain reaction, sequencing was performed to determine whether the PCR product amplified the genes of trichophytes and tropics. The PCR product of each sample was used as a template, and 5 μl of the PCR product was added to 8 μl of Bigdye and 1 μl of the 5 ′ primer of each gene to be 20 μl in distilled water. The sequencing reaction was denatured at 95 ° C. for 2 minutes and performed 25 times at 95 ° C. for 20 seconds, 50 ° C. for 5 seconds, and 60 ° C. for 2 minutes (ABI3100, Applied Biosystems). As a result of the sequencing analysis, it was confirmed that the test method and the results of the present invention for each sample were identical (FIG. 5).

Example 5 Test Methods and Test Kits for Trifid and Protozoan Genetic Testing

The test kit of the present invention is composed of a kit for kitting a device for extracting DNA from blood or blood samples and a reagent, and a kit for kitting reagents necessary for real-time polymerase chain reaction of genes of trichophytes and tropics (Fig. 1).

5-1: Kit the DNA Extraction Method

The instruments and reagents prepared as described in Example 1 were kitted. Consists of a 30 ml tube containing 20 mg / ml proteenase (protienase K, Sigma, USA) and 7% chelex, all stored at room temperature. The processing operation and the usage method are the same as in Example 1.

5-2: Kitting of Reagents Configured for Real-Time Polymerase Chain Reaction

As described in Example 2, reagents for real-time gene amplification of trifiltoid and tropic flies are kitted. The composition is ① Taq. 1.5 ml tube containing 250 units of DNA polymerase (Amplitaq, PE, USA); ② 1.5 ml tube [2X PCR buffer (100 mM-KCl, 20 mM Tris-HCl, pH8.0), 2.0 mM MgCl ₂ ), 2.5 mM dNTP, 20 pmol 5 'primer, 20 containing 1 ml of premix 1 solution. pmol 3 'primer], ③. 1.5 ml tube containing 100 ul of 100 ng / ul positive control gene; ④ 100 ng / ul negative control gene is 1.5 ml tube containing 100 ul and ⑤ 1.5 ml tube containing 1 ml of distilled water. All of these are stored in a -20 ° C. freezer and the method of use is the same as in Example 2.

Kits of reagents for genetic testing of trigeminal fever and tropical fever protozoa for the diagnosis of malaria of the present invention can be easily and time-consuming test for a large amount of samples.

Example  6: Three days  Protozoa Tropical heat  At the time of protozoa gene test Quantitative  Test

In the same manner as in Example 2, real-time gene amplification of trifid and protozoan parasites was performed. Five-fold serial dilution of 300 ng / ul of genes extracted from malaria-infected samples resulted in changes of Ct values according to the concentrations of 60 ng / ul, 12 ng / ul and 2.5 ng / ul samples in real-time polymerase chain reaction. Confirmed. The results are shown in FIG.

<110> JUNG, Woon Won          KIM, Hyun Sook          MAXBiotech Co. <120> PRIMEMRS AND METHODS FOR DETECTING PLASMODIUM VIVAX AND          PLASMODIUM FALCIPARUM CAUSING MALARIA, AND DETECTION KIT THEREOF <130> P10-0026 <160> 9 <170> KopatentIn 1.71 <210> 1 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-F1 Primer <400> 1 gaacgagatc ttaacctgc 19 <210> 2 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-F2 Primer <400> 2 aacgagatct taacctgct 19 <210> 3 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-F3 Primer <400> 3 cgagatctta acctgctaa 19 <210> 4 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-F4 Primer <400> 4 tcttaacctg ctaattagc 19 <210> 5 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-F5 Primer <400> 5 cttaacctgc taattagcg 19 <210> 6 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-R1 Primer <400> 6 gttcctctaa gaagcttta 19 <210> 7 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-R2 Primer <400> 7 acctgttgtt gccttaaac 19 <210> 8 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-R3 Primer <400> 8 agacctgttg ttgccttaa 19 <210> 9 <211> 19 <212> DNA <213> Artificial Sequence <220> <223> mG-R4 Primer <400> 9 catcacagac ctgttgttg 19

Claims (7)

One primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 1 to 5; A primer set for amplification of trichoid or tropical filamentous protozoa genes, which cause malaria, comprising at least one primer pair consisting of one primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 6-9.
The method of claim 1, wherein the primer pair is a primer pair having a nucleotide sequence of SEQ ID NO: 1 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 1 and 8; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 6; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 3 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 4 and 6; Amplification of trilobite or tropical filamentous protozoan genes as a cause of malaria, characterized in that at least one selected from the group consisting of a primer pair having a nucleotide sequence of SEQ ID NOs: 5 and 6 and a primer pair having a nucleotide sequence of SEQ ID NOs: 5 and 9 Primer set for.
According to claim 1, wherein the primer set for amplification of trichophyta or tropic filamentous gene gene which is a cause of malaria, characterized in that the fluorescent material is attached to the 5 'end of SEQ ID NO: 1 to 5.
Extracting DNA from blood or blood samples;
One primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 1 to 5; Amplifying the gene by a real-time polymerase chain reaction using a primer set including at least one primer pair consisting of one primer selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 6 to 9; And
Identifying genotypes of trituses or tropics protozoa using a melting curve analysis method of the gene amplification product;
Genetic test method of trilobite or tropical fever protozoa for the diagnosis of malaria comprising a.
The method of claim 4, wherein the primer pair is a primer pair having a nucleotide sequence of SEQ ID NO: 1 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 1 and 8; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 6; Primer pairs having the nucleotide sequences of SEQ ID NOs: 2 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 3 and 7; Primer pairs having the nucleotide sequences of SEQ ID NOs: 4 and 6; Genes of trilobite or tropical filamentous genesis for the diagnosis of malaria, characterized in that at least one selected from the group consisting of a primer pair having a nucleotide sequence of SEQ ID NO: 5 and 6 and a primer pair having a nucleotide sequence of SEQ ID NO: 5 and 9. method of inspection.
The method of claim 4, wherein the melting curve assay, the gene amplification of the genus Trilobites or tropical fever for diagnosis of malaria, characterized in that for performing the melting curve analysis of the gene amplification at a slope of 0.1 ℃ from 95 ℃ to 50 ℃ method of inspection.
DNA extraction reagents; And
A primer set according to any one of claims 1 to 3
Genetic test kit of three days protozoa or tropical fever protozoa for diagnosing malaria.

Images