FORM 2
THE PATENTS ACT, 1970 (39 of 1970)
COMPLETE SPECIFICATION
SECTION 10
"A METHOD FOR THE PREPARATION OF A KIT FOR AMPLIFYING HEPATITIS C VIRUS (HCV) NUCLEIC ACID IN BIOLOGICAL SAMPLES"
RELIANCE LIFE SCIENCES PVT.LTD. an Indian Company having its Registered office at Chitrakoot, 2nd Floor, Shree Ram Mills Compound, Ganpath Rao Kadam Marg, Worli, Mumbai^- 400 013, Maharashtra, India.
The following specification particularly describes and ascertains the nature of this invention and the manner in which it is performed:-

A METHOD FOR THE PREPARATION OF A KIT FOR AMPLIFYING HEPATITIS C VIRUS (HCV) NUCLEIC ACID IN BIOLOGICAL SAMPLES
Background of the Invention
1. Field of Invention
[0001] The present invention relates to a method for the preparation of a kit for amplifying Hepatitis C Virus Viremia (HCV) nucleic acid in Biological samples.
2. Description of the Prior Art
Hepatitis C Virus (HCV) is a blood borne pathogens that is present in infected human blood and can infect and cause disease in persons who are exposed to blood containing the pathogen. HCV constitute a highly variable genus within the Flaviviridae with closest homology to the hepatitis G and GB virus and Pestiviruses. The positive stranded RNA genome encodes a polyprotein, which is co and post translationally cleaved into at least 9 (nine) proteins : Core, E1, and E2 (the structural proteins) NS2, NS3, NS4A.NS4B, NS5A and NS5B ( the non-structural (NS) proteins ) HCV is a single-stranded, positive sense RNA virus with a genome of approximately 10,000 nucleotides coding for 3000 amino acids.
HCV has become the most significant cause of chronic liver disease of infectious etiology. Hepatitis C has infected over 200 million worldwide. The recognition that HCV can be

transmitted perinatally or through transfusions and transplantation warrants particular attention. Although HCV can progress to irreversible liver damage, acute infection is often asymptomatic. Complications from this disease are already the leading cause of liver transplants.
Accurate diagnosis is essential to identify the presence of the virus in apparently symptom free carriers. Nucleic acid detection strategies allow the identification of the virus at extremely low levels. The use of HCV identification has proven valuable because the presence of RNA is an indicator of replicating HCV, whereas the presence of antibodies is not.
Several recent studies have indicated that the level of HCV viremia correlates with the clinical stage of disease; patients with advanced stages of liver disease such as severe chronic active hepatitis, cirrhosis and end stage liver disease had higher serum levels of HCV RNA than patients with mild HCV infections. Moreover, the HCV viremia titer may predict a subsequent response to antiviral therapy.
[0002] Early and rapid diagnosis of HCV infection is of great importance. Yet, conventional methods for detection of HCV from blood are inaccurate and/or slow.The presence of anti-HCV antibodies in patients infected with HCV has led to the development of the immunoserological tests that are specific for these antibodies. Implementation of these tests already has reduced the incidence of post-transfusion hepatitis worldwide. Additional supplemental testing has been performed using the RIBA (recombinant

immunoblot assay) to further evaluate samples that are repeatedly reactive in the antibody screening assay.
Recent evaluations have shown that interpretation of these immunological tests is difficult since 25-90% of the samples that are repeatedly reactive in the screening assay are negative upon supplemental evaluation with the RIBA assay. Immunoserological testing is a measure of current and/or prior exposure to HCV infection, but cannot discriminate between the two. At present, an immunolological assay for direct detection of HCV antigen is unavailable. Furthermore, in cases of acute HCV infection, individuals may fail to produce antibody to HCV, making diagnosis of current HCV infection impossible using Immunoserological techniques. Alternatively, detection of HCV RNA by Polymerase Chain Reaction (PCR) provides evidence for ongoing infection. Using PCR, it is possible to detect HCV viremia prior to Immunoserological sero-conversion. This procedure is also valuable in detecting HCV RNA in immunocompromised patients.
[0003] The following requirements need to be fulfilled for an optimal assay for HCV diagnosis.
• High sensitivity and specificity;
• Rapid results; and
• High reproducibility.
[0004] Kits for detection of HCV are commercially available. One such kit is produced by Hoffmann-La Roche and sold under the tradename Amplicor. This kit makes use of

amplification by Polymerase Chain Reaction (PCR) to create amplicons specific to HCV followed by Enzyme Linked Immunosorbent Assay (ELISA) to detect the amplicons.
In light of the foregoing, there is a need for a more sensitive and specific detection protocol for clinical samples. The inventors of the present invention have been successful in developing a kit and a method for detecting HCV in a more sensitive, specific and rapid manner. The present invention obviates the problems associated with the conventional kits.
[0005] Several terms used in the invention are defined as follows.
[0006] The term "primer" refers to a synthetic oligonucleotide sequence synthesized for annealing to a specific nucleotide sequence of interest. The primer initiates DNA synthesis to occur using thermostable DNA dependent DNA polymerase. Selecting the proper primer is one of the most important steps in designing a PCR kit. The primer set must hybridize to the target sequence with little or no hybridization to other sequences that are also present in the sample.
[0007] The term "probe" refers to a synthetic oligonucleotide sequence which lies internal to the + strand of the amplified product resulting from a PCR reaction.
[0008] The term "hybridization" refers to annealing of nucleotide sequences to each other under optimal conditions. Typically, a nucleotide A binds to nucleotide T and nucleotide G binds to nucleotide C.

[0009] The term "biological samples" refers to the samples selected from serum, plasma, and combinations thereof. When selected plasma will preferably include an anticoagulant, such as EDTA / and or ACD.
Summary of the Invention
[0010] It is an object of the present invention to develop an improved method for the preparation of a kit for amplifying Hepatitis C Virus Viremia (HCV) nucleic acid in Biological samples.
[0011] It is still an object of the invention is to develop a method using specific primer sets and detection probe having higher sensitivity and specificity as compared to the conventional assays.
[0012] These and other objects of the present invention are substantially achieved by a method for rapid clinical diagnosis of HCV in which the amplimers are transcripts of a polyprotein gene of HCV. The amplicons are hybridized to a specific oligonucleotide probe, which allows the amplicons to be detected.
Description of the invention

[0014] Selecting the target DNA sequence polyprotein gene for HCV depends upon identification of regions within the HCV genome that show maximum sequence conservation among all the serotypes of HCV.
[0015] The present invention has primers complementary to sequences flanking a segment polyprotein gene to be amplified. The primers of the present invention are selected on their ability to specifically recognize the polyprotein gene with a low mutation frequency.
[0016] The primers of the present invention are so designed to avoid hairpin loop structure formation. In addition, the selected primers have been subjected to a gene bank search to identify homologies and percent similarities to the target of interest.. The Blast results are as follows:
For nucleic acid SEQ.ID. No.1, SEQ.ID. No.2, and SEQ.ID. No.3 the accession No AY-051292 yielded 100% homology .
f00171 A diagnostic kit for detection of HCV in biological samples according to the present invention includes four components. The first component is the extraction of nucleic acid (RNA) from the biological sample. The second component is the reverse transcription of the extracted nucleic acid (RNA) with the reverse strand primer. The third component is amplification component, which is used to amplify the target sequence. The fourth component is the detection component, which is used to detect the amplicons produced by the amplification component.

[0018] The amplification component amplifies the target sequence via PCR and, therefore, will include a pair of amplification oligonucleotide primers, a RNA-dependent DNA polymerase; a DNA-dependent RNA polymerase, and deoxyribonucleoside triphosphates. The primers are labeled at their 57 end. Labels are preferable selected from the group consisting of biotin, digoxigenin, radioactive labels (32 P). A more preferable label is fluorescein.
[0019] The first oligonucleotide primer for use in reverse transcription and amplification component has the following nucleic acid sequence (SEQ. ID. NO. 1):
51 -gcagaaagcgtctagccatggcgt-37
SEQ. ID. 1 contains twenty four (24) continuous bases selected from the polyprotein gene sense strand. The Nucleotide Sequence position of SEQ. ID.No. 1 is 56-79. SEQ. ID.No.1 is preferably present in the amplification component in an amount of about 1|xl_ to about 10^L in a concentration of 10 -100 pM.
[0020] The second oligonucleotide primer for use in the amplification component has the following nucleic acid sequence (SEQ. ID. NO. 2):
5; -ctcgcaagcaccctatcaggcagt-37
SEQ. ID. 2 contains twenty four (24) continuous bases selected from the polyprotein gene antisense strand. The Nucleotide Sequence position of SEQ. ID.No. 2 is 276-299. SEQ.ID.No.1 is preferably present in the amplification component in an amount of about 1 |xL to about 10u.L in a concentration of 10 - 100 pM.

[0021] The annealing temperature of primer pair is generally calculated as 5° C lower than the estimated melting temperature. The annealing temperature for primers that are less than 20 bases is calculated using the following formula: [4(G+C) + 2 (A+T)]- 5°C. Ideally the annealing temperature of each primer should match and be within the 55° C and 75° C range. If the annealing temperature difference between the two primers is high, the lower annealing temperature can be increased adding to the length of that primer at either the 37 end (this can also keep the size of the amplified locus constant) or the b1 end. The annealing temperature for the primers of the present invention is about 60° C.
The RNA-dependent DNA polymerase may be any suitable reverse transcriptase. Preferably, the reverse transcriptase is derived from Avian Myeloblastosis Virus (AMV). The said polymerase is preferably present in an amount of about 5 Units to about 10 Units.
The reverse transcription is set up using reverse transcriptase buffer comprising of 50 mM Tris.Hcl ( pH 8.3), 6.0mM MgCI2, 40 mM KCI, 4.0 mM dithiothreitol, 5-10 Units of AMV reverse transcriptase, dNTP's in a concentration of 100 - 200 \M and is incubated at about 37° C to about 42° C for 30 min.
[0022] The DNA-dependent DNA polymerase may be any suitable polymerase. Preferably, the polymerase is derived from Thermus aquaticus (Taq) bacteria. The polymerase is preferably present in the amplification component in an amount of about 1 Unit to about 2.5 Units.

The deoxyribonucleoside triphosphates (dNTPs) useful in the present invention include: dATP, dCTP, 5MedCTP, dGTP, dITP, TTP, and dUTP. Preferably, the dNTPs are selected from dATP, dCTP, dGTP, dTTP, and combinations thereof. Preferably, each dNTP is present in the amplification component in an amount of about 100JLI M to about 200 jxM.
[0023] The amplification component may contain any other suitable additional ingredient and/or component, such as an amplification buffer. For example, suitable 10x amplification buffers for use in the present invention include 100 mM Tris HCI (pH 8.3), 500 mM KCI, and MgCI2.
[0024] A preferred amplification component includes:
(1) an amplification buffer having 10 mM Tris HCI ( pH 8.3) and 500mM KCI;
(2) about-100 to about 200 μM each of dATP, dCTP, dTTP and dGTP;
(3) sterile distilled water(nuclease free);
(4) about 1 unit to about 2.5 units of thermostable DNA-dependent DNA polymerase;
(5) about 10 to about 100 pM of the first oligonucleotide primer (SEQ. ID NO.1);
(6) about 10 to about 100 pM of the second oligonucleotide primer (SEQ. ID NO.2);
(7) about 1.5 to about 2.5 mM MgCI2; and
(8) the template to be amplified.

[0025] Preferably, the volume of the amplification buffer is about 25 to about 50 μL and the volume of the extracted sample is about 25 to about 50 jiL The final volume of the amplification component is about 50 to about 100 μL.
The detection component detects the amplified target sequence via ELISA and, therefore, will include a oligonucleotide probe immobilized upon a solid medium, a conjugate that is adapted to bind to a label present on the amplicons, and a complex that changes color in the presence of the conjugate.
[0026] The oligonucleotide probe has the following a nucleic acid sequence (SEQ. ID. NO. 3):
5' -gtcgtgcagccctccaggaccc-37 The Nucleotide Sequence position of SEQ.ID.N0.3 is 90-110 and contains twenty one (21) continuous bases. SEQ.ID.NO.3 is a region internal to the amplimers created using the primers of SEQ.ID.NO.1 and SEQ.ID.NO.2.
SEQ. ID. NO. 3 is specifically designed for capturing the amplification product. The oligonucleotide probe is preferably immobilized on a solid medium, such as a microwell plate. For example, the oligonucleotide probe may be labeled with biotin, which is substantially irreversibly bound to streptavidin coating the microwell plate.
The oligonucleotide probe is preferably present in the detection component in an amount of about 1OμL to about 100μL in a concentration of 10 -100 pM.

[0027] The enzyme on the conjugate may be any enzyme, depending only upon the selected substrate. For example, the preferred enzyme for the present invention is horse raddish peroxidase. However, other enzymes such as alkaline phosphatase may be used.
[0028] The substrate changes color in the presence of the enzyme conjugate to visibly show the presence of the amplimer bound to the oligonucleotide probe. Thus, a change in the color detection solution positively indicates the presence of the amplimer and, by extension, the presence of HCV in the original biological sample. The selection of the substrate is dependent upon the selected enzyme on the conjugate. A preferred enzyme and substrate combination for use in the present invention is hydrogen peroxide (H202) and 3,3',5,5'-Tetra methyl benzidine Dihydrochloride(TMB), present in an amount of 100 microlitres, which is oxidized by H202 in the presence of peroxidase and, thus, the detection solution changes from colorless to blue. Other suitable enzyme and substrate combinations are as follows:
Alkaline Phosphatase and 5-Bromo-4Chloro-3lndolyl Phosphate (BCIP)
Alkaline Phosphatase and Fast Red RC
Alkaline Phosphatase and Naphthol AS-TR Phosphate
Alkaline Phosphatase and Nitro BlueTetrazolium (NBT)
Alkaline Phosphatase and p-Nitrophenyl Phosphate (pNPP)
Peroxidase and 3-Amino-9-Ethylcarbazole (AEC)
Peroxidase and 5-Aminosalicyclic acid (5AS)
Peroxidase and 2,2'-Azino-bis(3-Ethylbenzthiazoline-6-Sulfonic acid)
Peroxidase and 4-Chloro-1 -Naphthol (4CIN)

Peroxidase and 3-3'DiaminobenzidineTetrahydro-chloride (DAB)
Peroxidase and o-Dianisidine
Peroxidase and o-Phenylenediamine Freebase (OPD)
[0029] A method for rapid clinical diagnosis HCV according to the present invention uses the first primer (SEQ. ID. NO. 1) and the second primer (SEQ. ID. NO. 2) in an amplification step, and the oligonucleotide probe (SEQ. ID. NO. 3) in a detection step.
In accordance with a second aspect of this invention, a method according to the present invention includes the steps of sample extraction, reverse transcription, amplification (preferably by PCR), and detection by enzyme immunoassay (preferably ELISA).
[0030] HCV nucleic acid is extracted from a biological sample, preferably using chaotropic agents such as urea, diethylamine, guanidium hydrochloride, potassium iodide, sodium dodecyl sulphate (SDS), Formamide and combinations thereof. Any suitable and/or known technique for extraction of nucleic acid may be used.
The extracted specimen is subject to reverse transcription and is then added to a mixture. The mixture contains the reverse strand primer of the present invention (SEQ.ID.No.2), deoxyribonucleoside triphosphates, and AMV reverse transcriptase ( RNA dependent DNA polymerase). The appropriate reverse transcriptase buffer comprises of 50 mM Tris.Hcl ( pH 8.3), 6.0mM MgCI2, 40 mM KCI, 4.0mM dithiothreitol, 5-10 Units of

AMV reverse transcriptase, dNTP's in a concentration of 100 - 200 μM and is incubated at about 37° C to about 42° C for 30 min.
The resulting complimentary DNA strand is then added to an amplification component. As discussed above, the amplification component contains the primers of the present invention (SEQ. ID. Nos. 1 and 2), having a label at their 5; ends, deoxyribonucleoside triphosphates and Thermus acqauticus(Taq) derived DNA dependent DNA polymerase.
[0031] Amplification is accomplished by repeated cycles of DNA denaturation, primer annealing, and extension of the primed DNA sequence by the DNA polymerase in the presence of added purine and pyrimidine bases. In general, each cycle will double the amount of the target DNA sequence. The amplification cycle is repeated until a detectable amount of the DNA sequence has been created. Further details of the PCR method are provided in U.S. Patent Nos. 4,683,195; 4,683,202; 4,965,188; and 5,075,216, which are incorporated herein by reference in their entirety.
[0032] The amplimers are preferably detected using ELISA. Denatured and labeled amplimers are added to a microwell containing the immobilized oligonucleotide probe of the present invention (SEQ. ID. NO. 3) and a hybridization solution, thereby immobilizing the amplimers by hybridization with the oligonucleotide probe. An anti-fluorescein conjugate with a selected enzyme is added to the microwell after excess unbound amplimers are washed away. Finally, a substrate is added to the microwell, which changes color in the

presence of the enzyme anti-fluorescein conjugate. Thus, the detection solution changes color if any amplimers are present in the microwell, which denotes a positive result for the presence of HCV in the original biological sample.
[0033] This method is rapid, automatable (ELISA type solid phase formats do not require gel electrophoresis) and applicable to large scale screening programs.
[0034] The following example illustrates the process according to the invention without limitation.
Example 1
An experiment was conducted to demonstrate the method of present invention. The initial
sample taken was plasma EDTA that was pre-determined as positive for the presence of
HCV mediated antibodies (IgG, IgM). The sample (0.2 ml) was extracted using RNA
isolation system sold by Qiagen Inc., Venlo, The Netherlands, under the tradename
QIAamp®.
Reverse transcription was set up using the reverse strand primer in a reverse transcriptase buffer including 50 mM Tris.Hcl ( pH 8.3), 6.0mM MgCI2, 40 mM KCI, 4.0mM dithiothreitol, 5-10 Units of AMV reverse transcriptase, dNTP's in a concentration of 100 - 200 f.iM was added to make the final concentration of about 1.5 mM to about 2.5 mM. The solution /reaction mixture was incubated at 42° C for about 30 min. The DNA resulting from reverse transcription is thereafter amplified.

The amplification reaction was set up using 25 μL of the above extracted nucleic acid and 25 μL of 10x amplification buffer including 100 mM Tris HCI,(pH 8.3), 500mM KCI, and MgCI2 was added to make a final concentration of about 1.5 mM to about 2.5 mM. The primers (SEQ. ID NO. 1 and 2) were labeled with fluorescein and provided in a concentration of 10 - 100 pM.
[0035]. Each dNTP (dATP, dCTP, dGTP, and dTTP) was provided in a concentration of 100-200 \M. AMV polymerase was provided in an amount of about 5- 10 units and Taq polymerase was provided in an amount of 1 - 2.5 units.
[0036] This reaction mixture was heated to 94°C for 10 min followed by 30
amplification cycles. Each amplification cycle included heating the reaction mixture to 94°C for 30 sec, cooling to 62°C for 45 sec, and heating to 72°C for 30 sec. Following the 30 amplification cycles, the final incubation was performed for 10 min at 72°C. The resulting amplimers were denatured using a solution of 0.4M NaOH.
[0037] The detection of the fluorescein labeled amplimers was done in the following manner:
[0038] (1) 50-100 μL of dilution buffer was pipetted into a microwell plate coated with streptavidin, to which was added 1-10 μL of the biotinylated oligonucleotide probe (SEQ. ID. NO. 3) in a concentration of 10 - 100 pM. The solution was incubated at 37°C for 30-60

min. Thereafter, the microwell plate was washed with PBS-T wash buffer, and 100 μL of the hybridization buffer was added and incubated for 15-30 min at 37°C. The hybridization buffer included sodium phosphate, sodium thiocyanade and Denhardts solution, which includes Polyvinylpyrollidine (PVP), Ficoll, Bovine Serum Albumin (BSA)
25 μL of denatured amplification product was added to the microwell plate and incubated for 30-60 min at 42°C. Following incubation, the microwell plate was washed 5 times with PBS-T wash buffer. 100 μL of diluted anti-fluorescein-HRP conjugate was added to the washed plate and incubated for 30-45 min at 37°C. Following incubation, the microwell plate was washed 5 times with PBS. 100 μL of TMB was added to the microwell plate and incubated substantially without light at room temperature for 15-30 minutes.
[0039] A color change from colorless to blue is observed after incubating for 15 min. 50 H-L of a stop solution containing 0.1 N H2S04 was added and the change in color from blue to yellow was noticed and the plate was read at 403 nm in acolorimetric plate reader.
[0040] In view of the foregoing descriptions and example, it will become apparent to those of ordinary skill in the art that equivalent modifications thereof may be made without departing from the spirit and scope of this invention. Various features are set forth in the following claims.

We Claim :
1. A method for the preparation of a kit for amplifying HCV nucleic acid in Biological samples, comprising RNA dependent DNA Polymerase (reverse transcriptase), DNA dependent DNA polymerase and deoxyribonucleoside triphosphates.
2. The kit according to claim 1, comprising a first amplification primer and a second amplification primer.
3: The kit according to claim 2, wherein a first amplification primer has the following sequence:
5' -gcagaaagcgtctagccatggcgt-3'
4. The kit according to claim 2, wherein the first amplification primer comprises at least twenty four continuous bases selected from the polyprotein gene sense strand.
5. The kit according to claim 2, wherein the first amplification primer is present in an amount of about 10 pM to about 100 pM.
6. The kit according to claim 2, wherein a second amplification primer has the following sequence:
5' -ctcgcaagcaccctatcaggcagt-3'

7. The kit according to claim 2, wherein the second amplification primer comprises at least twenty four continuous bases selected from the polyprotein gene anti-sense strand.
8. The kit according to claim 2, wherein the second amplification primer is present in an amount of about 10pM to 100 pm.
9. The kit according to claim 1, wherein the RNA dependent DNA polymerase is Avian Myeloblastosis Virus (AMV) present in an amount of about 5 units to about 10 units.
10. The kit according to claim 1, wherein the DNA dependent DNA polymerase is Taq polymerase present in an amount of about 1 Unit to about 2.5 Units.
11. The kit according to claim 1, wherein said deoxyribonucleoside triphosphate is selected from the group consisting of: dATP, dCTP, 5MedCTP, dGTP, dITP, TTP, dUTP, and combinations thereof.
12. The kit according to claim 10, wherein said deoxyribonucleoside triphosphate is present in an amount of about 100 to 200 uM.
16.The kit according to claim 2, wherein the first and second amplification primers have a label at their respective 5' ends.

17. The kit according to claim 12, wherein the label is fluorescein

.

Dated this 25th day of January 2002

For Reliance Life Sciences Pvt. Ltd.
K.V.Subramaniam Sr Executive Vice President