KR101152840B1 - A probe for identifying hpv genotype and a method for identifying hpv genotype - Google Patents

Abstract

The present invention relates to a HPV genotype diagnostic probe and an analysis method thereof.

Description

HPP genotyping probe and analysis method {A PROBE FOR IDENTIFYING HPV GENOTYPE AND A METHOD FOR IDENTIFYING HPV GENOTYPE}

The present invention relates to a HPV genotype diagnostic probe and an analysis method thereof.

High risk (HPV) -HPV DNA is present in 99.7% of cervical cancer patients worldwide, and the persistence of such HR-HPV infection is known to cause metastasis to invasive cervical cancer and cervical precancerous cancer. Cervical cancer causes 500,000 cases worldwide and 6,000 new cases in Korea each year, with 50% fatal outcomes. Human Papilloma Virus (HPV) is known to be an important cause of the progression of cervical tumors, and HPV DNA is used for early diagnosis of cervical cancer (Bernard, HU, IE Calleja-Macias, and ST Dunn. 2006. Int J Cancer 118: 1071-6). HPV is a double-stranded DNA virus of about 7.9 kb, belonging to papovavirus, which contains more than 100 subtypes, of which 40 are known to infect the genitals. The HPV virus also contains 10 viral proteins that are involved in the replication of the virus, which determines the activity and latency of L1 and L2, two early gene products involved in the synthesis of structural proteins that make up the capsid of the virus, and the viral infection. It expresses eight late gene products, E1, E2, E3, E4, E5, E6, E7, and E8, which regulate protein synthesis. In particular, E6 and E7 encode precancerous proteins and are known to be associated with cancer (Sedman, SA, et al. 1991. J Virol 65: 4860-6). And is closely associated with various malignancies (Godfroid, E., et al. 1998. J Virol Methods 75: 69-81).

Cervical cancer in women is the second highest incidence in the world after breast cancer, with more than 1,000 deaths annually in Korea, making efforts for early diagnosis of cervical cancer very important (Wui, JH, etc.). 2006. Journal of Gynecologic oncology and Coloscopy 17: 39-4711.

There are currently over 100 known genotypes of HPV (Likes, WM, and J. Itano. 2003. Clin J Oncol Nurs 7: 271-6), of which about 30 are known to cause disease in humans. . The genotypes were high risk (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73, 82) and low risk (6, 11, 40, 42, 43, 44). , 54, 61, 70, 72, 81), and potential risk groups (34, 57, 83) (Munoz, N., et al. 2003. N Engl J Med 348: 518-27). HPV was found to be genotype-specific depending on the location of the lesion and the progression of the lesion, thereby recognizing the biological diversity of HPV infection.

The most commonly used method for diagnosing HPV infection is Papnicolaou Smear (Pap) method. Currently, histological diagnosis of cervical cancer is diagnosed by this test. It has a lot of dependence and has the disadvantage of poor accuracy (Kurman, RJ, DE Henson, AL Herbst, KL Noller, and MH Schiffman. 1994. JAMA 271: 1866-9). In addition, the vaginal magnification test is more accurate than the Pap smear, but requires a skilled technician and expensive equipment, and the HPV genotype cannot be distinguished. The disadvantage is that the risk of malignancy cannot be classified between different HPV genotypes.

In order to make up for the above drawbacks, studies of methods for diagnosing cervical cancer precancerous stage and confirming genotype through HPV-specific DNA amplification using PCR, HC, DNA chip, etc. are being conducted.

The present invention solves the above problems, and the object of the present invention is to provide a probe having a specificity and sensitivity for HPV better than the conventional DNA chip.

Another object of the present invention to provide a method for analyzing HPV genotype using the probe.

In order to achieve the above object, the present invention provides at least one HPV diagnostic oligonucleotide probe selected from the group consisting of the nucleotide sequences of SEQ ID NO: 5 to SEQ ID NO: 28 to achieve the above object.

In another aspect, the present invention provides a kit for diagnosing HPV comprising the probe and primer of the present invention.

In the present invention, the primer is preferably a primer described in SEQ ID NOs: 1 to 4, but is not limited thereto.

In one embodiment of the invention, the kit preferably further comprises a label means for detecting the PCR product.

The present invention also comprises the steps of: a) attaching the probe of the present invention to a solid support;

b) hybridizing the amplified HPV PCR product to the probe; And

c) providing a method for identifying HPV genotype comprising detecting the hybridized product.

In the present invention, the solid support is preferably a membrane, a slide, or a well plate, but is not limited thereto.

In one embodiment of the present invention, the detecting step is preferably detected using a luminescence or color reaction.

In the present invention, nucleic acid was extracted from a sample and PCR amplification was performed. Methods of extracting nucleic acids from cells and PCR methods were performed through methods well known in the art, such as those described in Molecular cloning (1989) by Sambrook et al.

The nucleic acid amplification method of the present invention used a primer. Generally, the primer is preferably about 10 to 25 bp in length oligonucleotide, but may be longer. The primer is preferably single stranded but may be present in double or single stranded form. It described in the Example.

The primers of the present invention were prepared by conventional oligonucleotide synthesis methods, and such synthesis methods are disclosed in US Pat.

Sequences such as primers of the invention can be used to form a double helix optionally with complementary sequences, such as DNA derived from a sample. One skilled in the art can alter the hybridization conditions to change the selectivity of the primer for the target sequence.

In some embodiments, nucleic acids of defined sequences of the invention may be employed in combination with appropriate means such as labels to determine hybridization. Suitable labeling means are various labeling means including fluorescence, radioisotope enzymes or other ligands.

Various template dependent processes are possible to amplify specific gene products present in a given cell sample. One of the most known amplification methods is polymerase chain reaction (PCR), which is described in US Pat. Nos. 4,683,202 and 4,800,159 and the like.

It is generally desirable to separate the amplification product from the template or excess primer or other amplification product in one or another step. For example, the amplification products can be separated using agarose, agarose-acrylamide or PAGE using the standard method described in Molecular cloning (1989) by Sambrook et al.

Chromatography, such as adsorption, partitioning and ion exchange, can also be employed as an effective separation method. These separations can be adapted to function in clinical settings to process large volumes of samples, and new methods for separating or detecting thousands of samples at once, FMAT (fluorometric microvolume assay technique), chemiluminescence, and sequence detection systems (Applied) Biosystems) and mass spectroscopy.

Nucleic acids according to the invention will be detected and quantified. In one embodiment the detection can be performed by visual means. Typical visual means method is to dye the gel with ethidium bromide and visualize the bands under UV light. If the amplification product is a nucleotide that is labeled with radiation or fluorescence, the isolated amplification product performs radiosynthesis or fluorescence detection of the inserted radioisotope label.

The present invention includes a kit for carrying out the method. In a non-limiting example, the kit of the present invention may include primers, enzymes for amplification and additional reagents. Thus, the kits will include these one or more reagents in suitable container means. The kits may also include reagents for isolating nucleic acids and purifying amplification products. The components of the kits may be packaged in an aqueous medium or lyophilized form, and suitable container means of the kit include at least one vial, test tube, flask, bottle, etc. into which the components may be placed. If one or more components are present in the kit, they may include other additional containers, such as second, third, etc., where the additional components may be located separately. However, a combination of components may be included in one container.

The nested PCR method used in the present invention generally means a two-tube nested PCR. 'Two-tube nested PCR' usually has a very limited amount of DNA in a sample, so the second PCR cannot be detected by a single PCR. In order to perform the amplification using the inner primer, four primers should be attached in order to amplify the desired part well.The first polymerase chain reaction using the outer primers is performed and the second amplification is performed with the product. In this case, the reaction can occur smoothly because new reagents are added again, and a pair of primers have a relatively small number of reactions, which has an advantage of increasing sensitivity and specificity compared to conventional PCR. The problem of contamination often occurs during the amplification process. To solve this problem, two pairs of primers are used in one tube. The attempt to put a one-tube nested PCR, could simultaneously reduce the problem of pollution in the sensitive area is better than the existing Two-tube PCR check it appears (see Example 8 and Figure 8 and 9).

In the HPV genotyping method of the present invention, PCR amplification of HPV L1 gene, a probe capable of specifically binding to each HPV type in its region, and reverse hybridization hybridization using ECL-Southern hybridization of amplified DNA on a membrane attached thereto As a method using torch, the end purpose is to develop a probe with better specificity and sensitivity than a conventional DNA chip and to develop a more economic method.

In particular, the present invention is to provide a new method for detecting HPV by observing the detection rate of HPV using one-tube nested PCR amplification by putting two pairs of primers in the same tube and comparing the results of PCR with other diagnostic methods.

As can be seen from the configuration and drawings of the present invention, the HPV genotype identification method of the present invention by PCR amplification of the HPV L1 gene, and in advance to prepare a probe that can specifically bind to each HPV type specific to the site, the membrane By using reverse hybridization hybridization using ECL-Southern hybridization, the amplified DNA was more specific, more sensitive, and more economical than conventional DNA chips.

1 is an explanatory diagram for the basic principle of Reverse Blot Hybridization mentioned in the present invention. That is, ① the amine-labeled probe is bound to the membrane. ② the target gene is amplified with a biotin-labeled primer and then reacted with the probe bound to the membrane. ③ Reacts with Streptavidin-conjugated alkaline phosphatase. ④ Alkaline
Detects defects in probes and amplified target genes by treating phosphatase substrates.
Figure 2 shows the PCR and amplification of the HPV L1 gene from the high-risk HPV type 35, 43, 56, 16, 18 and the low-risk HPV type 6. 11, 44 clones of the ATCC clones obtained and reverse blot hybridization Photo showing the reaction detected by luminescence.
Figure 3 is a photograph showing the REBA results of Capture ^® 2 High-Risk HPV DNA Test ™ (HC2) positive sample. In other words, PCR positive results were obtained from 31 specimens out of 44 specimens from the Digene (HC2) positive specimens, and 31 specimens were subjected to REBA (Reverse Blot Hybridization Luminescence Experiment), resulting in 16, 18, 31, 33, 35, 39, 19 specimens of single type of 56, 58 and 4 specimens of double type of 16/18, 16/58, 52/58, 59/68, 16/51/58, 16/56/58, 16/51 / Three samples from the triple type of 58, showing the HPV type in a total of 26 samples.
Figure 4 is a photograph showing the REBA results (color development experiments) of clinical samples. That is, as a result of color development experiment with membrane strip using 18 clinical samples, 12 specimens of single type of 16, 18, 53, 56, 58, 59, 70, 81, 58/70, 31/53, Three samples from the 66/43 double type, one from the 16/53/56 triple type, and one sample from the HPV-positive sample, such as sample 113, were isolated from each of the 17 types of HPV. In case of sample 131, PCR was not performed and accordingly, the picture showed that nothing appeared in REBA color development test.
Figure 5 is a diagram showing the sequencing results for the REBA results (coloring experiment-88) of the clinical sample. 5A is a sequencing using GP6 primer with clinical sample No. 88 from the color development result of FIG. 4, and the sequencing results are shown by listing each base sequence using chromas program. FIGS. 5B and C are FIGS. It is a photograph showing the result of blast search from http://blast.ncbi.nlm.nih.gov/Blast.cgi site with the nucleotide sequence shown in Figure 5a.
Figure 6 is a photograph showing the REBA results (luminescence experiment) of Plasmid DNA clone. That is, cloning was performed to use positive control with clinical samples of each type, and REBA (luminescence experiment) was performed with plasmid DNA clone obtained by cloning.
Figure 7 is a photograph showing the REBA results (color development experiments) of Plasmid DNA clone. In other words, cloning was performed to use positive control with clinical samples of each type, and REBA (coloring experiment) was performed with plasmid DNA clone obtained by cloning .
8 and 9 are photographs showing the results of two-tube nested PCR and one-tube nested PCR, respectively.

The present invention will now be described in more detail by way of non-limiting examples. However, the following examples are set forth to illustrate the present invention and the scope of the present invention is not to be construed as being limited by the following examples.

Example  One: HPV  Positive clone

Eight plasmids corresponding to eight of the HPV genotypes were obtained from ATCC, and in particular, pHPV-16 (Cat. No. 45133) was used as a positive control for the entire experiment. Plasmids obtained from ATCC are HPV-6b (Cat.No.45150), HPV-11 (Cat.No.45151), HPV-18 (Cat.No.45152), HPV-35 clone 2A (Cat.No.40330 ), HPV-43 Clone 2A (Cat.No.40338), HPV-44 Clone 2 (Cat.No.40353), HPV-56 Clone 2C (Cat.No.40549), all of which are transformed into E. coli After culturing, plasmid DNA was extracted (GeneAll, Seoul, Korea) and used as a template for polymerase chain amplification (Polymerase Chain Reaction, PCR).

Example  2: HPV  Acquisition of clinical specimen

The clinical samples used in the present invention were positive high-risk group among 137 patients who had already been tested with Hybrid Capture 2 High-Risk HPV DNA Test ™ (HC2, Digene, Gaithersburg, USA) at Gangseo MizMedi Hospital for 6 months from November 2005. High Risk, HR) was used as a test group of the present invention for 44 patients. For these clinical samples, 0.45N HCl was added in an equal amount to neutralize the solution containing DNA to amplify PCR efficiency, and then used as a template. In order to verify the reliability of this study, HPV type high risk group 16, 31, 33, 39, 51, 56, 58 and low risk group 6, 11 which were genotyping by sequencing among clinical specimens isolated from patients at MizMedi Hospital in Korea were obtained. HPV types 42 and 45 were obtained through biometrics, while high-risk HPV types 52, 53, 59, 68 and low-risk HPV types 70, 72, 81, 84, and 87 were obtained from Chonnam National University and Wonju-German Hospital.

Example  3: PCR  reaction

The PCR reaction was performed after the beta-globin PCR was performed to confirm that there was no inhibitor in the DNA product. The reaction conditions were preliminarily denatured at a denaturation temperature of 94 ° C. for 5 minutes, followed by 30 seconds of denaturation at 94 ° C., 30 seconds of annealing at 55 ° C., and 30 seconds of extension at 72 ° C. for a total of 35 times. The final elongation reaction was repeated for 7 minutes at 72 ° C.

After the reaction, one-tube nested PCR was performed using DNA of amplified product (positive sample). 20 mM Tris-HCl (pH8.0), 100 mM KCl, 0.1 mM EDTA, 1 mM DTT, 0.5% Tween-20, 0.5% Nonidet P-40 and 10 mM dNTP, 25 mM MgCl ₂ , Each 10 pmole primer and 1 unit of Taq polymerase were used, and the total reaction amount was 20 μl.

The reaction conditions were premodified for 5 minutes at a denaturation temperature of 94 ° C., followed by 30 cycles of degeneration at 94 ° C. and 15 cycles of reaction at 55 ° C. for 30 seconds, followed by 30 seconds of denaturation at 94 ° C. , 45 cycles were reacted by annealing at 52 ° C for 30 seconds, and finally the final elongation reaction was carried out at 72 ° C for 10 minutes. In this case, the primer used is MY11 / 09-GP5-1 / 6 +, and thus amplification products of 150bp can be obtained. The base sequence of each primer is shown in Table 1.

Table 1 shows the primer sequences. In Table 1 the MY11, MY09, GP5-1 and GP6 + sequences are set forth in SEQ ID NOs: 1-4, respectively.

Table 2 shows the PCR conditions.

Example  4: Probe Available as oligonucleotide Wow probe Of Membrane with Oxide

The oligonucleotide sequences of the HPV type specific probes are shown in Table 3.

The oligonucleotide to be used as a probe was commissioned to Bioneer (Korea) to add an amine group at the 5 'end so as to have a positive potential to bind to the negative carboxyl group of the membrane, and to prepare a probe with 0.5 M NaHCO ₃ solution. The total probe concentration was diluted to 100 pmole (adjusting the concentration for each type), and the probe was placed in each slot using Miniblotter-MN45 (Immunetics, Cambridge, MA) reacted for 10 minutes with 1.6 g / 10 ml EDAC. After loading it was reacted for 1 hour at room temperature. Thereafter, the reaction was performed with 100 mM NaOH for 9 minutes, and finally, non-bound probes were removed by reacting with 100 ml of 2X SSPE / 0.1% (w / v) SDS solution at 60 ° C. for 5 minutes.

Example  5: Reverse Blot Hybridization  ( REBA ) With luminescence Color  Experiment

In order to perform the reverse hybridization reaction, MY11 / 09-GP5-1 / GP6 + primers were labeled with 5'-biotin (biotin) to obtain PCR products having nucleotide sequences complementary to the probe. 20 μl of the 150 bp PCR product obtained from this primer was hybridized to a membrane to which HPV-specific probes were attached using a miniblotter. That is, 15 μl of the amplified PCR product was mixed with DS (0.2N NaOH, 0.2 mM EDTA) in the same amount and left at room temperature for 5 minutes to make single strand, followed by 115 μl of 2X SSPE / 0.1% (w / v) SDS. Diluted. Prior to hybridization of the PCR product to the membrane, it was placed in 100 ml 2X SSPE / 0.1% (w / v) SDS solution to activate the membrane and allowed to react for 5 minutes at room temperature, and then the membrane was placed on a support cushion placed on a miniblotter. The excess product in the slot was removed through the suction device and the PCR product was deposited by being perpendicular to the direction in which the probes were attached. The orientation to which the oligonucleotide probe is attached was indicated on the membrane before hybridization using ink. Empty slots around the slots in which PCR products were deposited were filled with 2 × SSPE / 0.1% (w / v) SDS to prevent crossflow. This was followed by hybridization formation reaction at 50 ° C. for 30 minutes, and then using a suction device to remove all remaining samples from the miniblotter, and then repeating the membrane twice for 10 minutes at 50 ° C. with 100 ml 2X SSPE / 0.5% SDS solution. Washed.

Membrane was placed in a rolling bottle, and the streptavidine-alkaline phosphatase conjugate (AP conjugate, Roche Applied Science, Germany) was diluted 1: 2000 (v / v) in a suitable amount of 2X SSPE / 0.5% SDS, mixed well, and then reacted at room temperature for 30 minutes. I was. The membrane was then washed twice with 100 ml of 2X SSPE / 0.5% SDS solution at room temperature and then twice with 100 ml of 2X SSPE solution. For chemifluorescence detection, the membrane was placed in 10 ml of CDP-Star ^TM detection reagent (Amersham pharmacia biotech., Buckinghamshire, England) and reacted for 4 minutes, and then exposed to a hyper sensitivity film for 20 minutes to confirm the result (FIG. 1).

For the color reaction, the membranes with AP conjugate reaction were washed twice with TBS (50 mM Tis-HCl, 150 mM NaCl, pH 7.5) for 1 min and NBT / BCIP (Nitro Blue Tertrazolium Chloride and 5-Bromo- 4-Chloro-3-indolyl Phosphate, Toluidine salt in 67% DMSO (v / v), Roche Applied Science, Germany) was added to TBS (100 mM Tis-HCl, 100 mM NaCl, 50 mM MgCl ₂ , pH 9.5). After diluting to 1:50 (v / v) and reacting for 5 minutes at room temperature, the desired color development was completed and the color development solution was completely removed and tertiary distilled water was added to stop the reaction.

Example  6: clinical sample plasmid DNA Cloning

HPV genotypes not cloned and cloned with HPV genotypes 42, 45 obtained from biometrics and reverse hybridization method to be finally tested for PCR with MY11 / 09-GP5-1 / 6 primers and then TOPO TA Cloning Cloning was performed using the kit. Positive clones were analyzed by requesting sequencing to Cosmo, and then analyzed for genotype correctness and secured as final HPV type clones.

Example  7: DNA  Sensitivity Comparison with Chip

Clinical samples of HPV were provided by Chonnam National University Medical School (Gwangju, South Korea). All HPV testing was accompanied by DNA chips.

Meanwhile, the HPV gene HPV extraction, PCR and reverse blot hybridization analysis of the present invention for comparing the sensitivity with the DNA chip were performed by the method described in the embodiment of the present invention.

Example  8: of the present invention one - tube PCR And conventional two - tube PCR Comparison of

Two-tube nested PCR for HPV is described in detail in Example 3 of Korean Patent Publication No. 10-2009-0129639. In summary, PCR is first performed using 45 cycles using an outer primer (MY11 / 09 primer), and then PCR is performed again with 45 cycles using an inner primer (GP5 / 6 primer) with the resulting product (FIG. 8). It was confirmed that the sensitivity of the PCR came out at this time 100ag. When the first polymerase chain reaction is performed and the second amplification is performed with the product, the reaction can be smoothly performed because new reagents are added again, and a pair of primers react with a relatively small number of PCRs. In comparison, it has the advantage of increasing the sensitivity and specificity, but there is a risk that the problem of contamination often occurs during the two amplification process by changing the tube.

In order to solve this problem, in the present invention, as in Example 3, two pairs of primers (MY11 / 9-GP5-1 / 6) are put together in one tube and amplified by 15 cylce at 55 ° C. and then lowered in temperature. Attempted to nested PCR (52 ℃), to reduce the problem of contamination at the same time the sensitivity of the existing two-tube PCR results (Fig. 9) appeared to establish a one-tube nested PCR conditions

The results of the above embodiment will be described below.

One) ATCC  Clone HPV typing  (Figure 2)

PCR was performed on clones obtained from ATCC, except for HPV type 43, and PCR products were amplified, and the product could be re-generated by reverse hybridization hybridization to the HPV-specific probe of the present invention. However, HPV type 43 showed nonspecific binding. In this experiment, two plasmids were extracted and PCR products were used. However, in the case of type 44, only one plasmid was extracted due to experimental problems.

2) reverse hybridization Hybridization  Through the way Digene Positive sample and already sequencing to genotype Validation of this confirmed clinical sample

In the case of high-risk results from the Digene (by HC2) positive sample from MizMedi Hospital, the first PCR using MY11 / 09 primer was amplified by 450 bp PCR product and the other, but all the first PCR products were nested primer GP5- As a result of PCR by 1/6 +, 31 samples out of 44 samples were positive for PCR, and 31 samples were HPV type confirmed by Reverse Blot Hybridization (REBA, FIG. 3). At this time, HPV type 56 clone obtained from ATCC was used as a positive control.

In the distribution of these HPV types, HPV type 16 accounted for 31.5% and HPV type 58 accounted for 21% of the total 19 infections. The results of the genotypes of other clinical specimens are shown in Table 4. In particular, seven out of 26 specimens determined by reverse hybridization hybridization (REBA) were duplicated, and all of them were considered to have high-risk groups that were more likely to develop cervical cancer (Table 4). In addition, some of the clinical specimens were tested by the color development method (FIG. 4), and some of them were confirmed by sequencing, which showed that they came out the same (FIG. 5).

No . REBA  result Sequencing  result Similarity 72 59 59 86% 73 58 58 89% 74 16, 53, 59 16, 54 71% 75 56 56 94% 76 16 16 100% 78 16, 53, 56 56 87% 81 18 18 98% 82 31, 53 31 77% 84 53 53 91% 88 58 58 97% 92 58 58 95% 102 16, 53, 56 16 94% 104 16, 70 16 92% 113 HPV  (+) 62 94% 116 70, 58 70 97% 119 81 81 95% 132 58 58 97%

Table 5 shows a comparison of REBA and sequencing results in clinical specimens.

3) Plasmid DNA  Secure clones

In order to finally genotyping the above-described samples, the present invention was to obtain a plasmid DNA clone of the product amplified by the HPV L1 gene with MY11 / 09-GP5-1 / 6 primer. Clones of HPV type 31, 33, 35, 39, 45, 51, 52, 53, 56, 58, 66, 59, 68, 42, 43, 70, 72, 81, 84, 87 of DNA isolated from clinical specimens Secured. The REBA results of these plasmid DNA clones were shown to be the same as those performed in other populations using the probe and test method (REBA) used in the present invention as shown in FIG. 4 (FIG. 6). The same result was obtained by performing the color reaction through the obtained results (FIG. 7).

4) Sensitivity Comparison with DNA Chip

As can be seen in Table 6, when comparing the sensitivity of the DNA chip and the method of the present invention, the DNA chip had a sensitivity of about 94%, but the present invention showed a sensitivity of 100%. In addition, the results of the sequencing comparison showed that the REBA results were more accurate. That is, in Table 6 below, four samples of HPV (-) samples appeared in the DNA chip (in other words, four samples could not be read), but in the REBA results, HPV positive probes were attached to the HPV Universal probe. As a result of sequencing, it was found out that it came out of 25 types in REBA and other types. Therefore, all 70 were read by REBA method, but only 66 (94.29%) were read by DNA chip, so REBA method was better than DNA chip. The results were confirmed.

In addition, the use of DNA chip requires expensive equipment according to advanced technology, scanner and calibration, but the REBA of the present invention can perform experiments without the need for special equipment. have.

Attach an electronic file to a sequence list

Claims (8)

HPV diagnostic oligonucleotide probe composition consisting of the nucleotide sequence of SEQ ID NO: 5 to SEQ ID NO: 29. HPV diagnostic kit comprising the probe composition of claim 1 and a primer. The diagnostic kit for HPV according to claim 2, wherein the primers are primers set forth in SEQ ID NOs: 1-4. The kit for diagnosing HPV according to claim 2 or 3, wherein the kit further comprises labeling means for detecting a PCR product. a) attaching the probe of claim 1 to a solid support;
b) hybridizing the amplified HPV PCR product to the probe; And
c) HPV genotyping method comprising the step of detecting the hybridized product. 6. The method of claim 5, wherein said solid support is a membrane, slide, or well plate. The method of claim 5, wherein the PCR product is HPV genotype identification method characterized in that the amplification through the primers described in SEQ ID NOS: 1-4. The method of claim 5, wherein the detecting step is HPV genotyping method, characterized in that the detection using a luminescence or color reaction.

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