Molecular Detection of Hepatitis C Virus (HCV) by Conventional One-step RT-PCR Coupled with Nested PCR

Aims: HCV causes both acute and chronic infections and can be easily transmitted through contaminated blood or other body fluids. The present study deals with the molecular detection of HCV with help of one-step RT-PCR assay followed by nested PCR and agarose gel electrophoresis. Study Design: RNA extracted from the confirmed positive samples of HCV was utilized for the standardization of the one-step RT-PCR assay and nested PCR assay for diagnosis of HCV. Place and Duration of Study: Centre for Biotechnology, Maharshi Dayanand University, Rohtak Haryana, India, during period of one year (January-December 2015). Methodology: HCV positive samples were obtained from Department of Medicine, Maulana Azad Medical College (MAMC), New Delhi, India. Published primers from most conserved regions of HCV were taken and these primers were able to amplify all the strains of HCV. One-step RT-PCR kits, Short Research Article Sharma et al.; IBRR, 7(2): 1-6, 2017; Article no.IBRR.34463 2 primers, extracted RNA from these positive samples were used for standardization of molecular diagnostic assays. The results were checked by 2% agarose gel electrophoresis. Results: Positive samples of HCV were detected by nested PCR. Positive samples showed sharp band of 405bp while there was no amplification in the negative control. Conclusion: Rapid tests have low sensitivity and specificity while molecular assays are rapid, sensitive and specific. Conventional one-step RT-PCR assay followed by nested PCR is rapid, specific, sensitive and it is also less costly than real-time RT-PCR. Cost of an assay is an important factor in controlling a disease in resource limited settings of developing countries.


INTRODUCTION
Hepatitis C Virus (HCV) is one of the important viruses among other hepatitis viruses (A, B, D, and E) which are responsible for serious chronic infection of liver. First case of HCV was reported in the serum of a patient with Non-A, Non-B hepatitis by Choo et al. in 1989 [1]. HCV is a small (50 nm), enveloped, single-stranded, positive-sense RNA virus of family Flaviviridae and genus Hepacivirus. Genome of HCV contains 9500 nucleotides with one open reading frame which encodes for about 3000 amino acid polypeptides [2]. HCV contains highly variable genome with more than six major genotypes of HCV which are circulating worldwide [3]. An estimate made by World Health Organization (WHO) showed that about 71 million people have chronic hepatitis and about 0.4 million people die each year due to cirrhosis and hepatocellular carcinoma [4]. Another study estimated the number of HCV infected people may be 150-200 million globally [4,5,6]. The distribution pattern of HCV is not equal, with higher occurrence in developing part than the developed part of the world due to less health infrastructure and poor blood screening facilities. In India, there is no specific viral surveillance system, resulting in lack of exact data about HCV infections. Although some recent study estimated that prevalence of HCV is about 1.5% in India [5]. HCV is mainly spread by direct contact with infected blood or body fluids. HCV can be transmitted through the blood transfusion and items like contaminated needles, syringes or other medical equipment and needle-sharing among intravenous drug abusers [7]. Other social, cultural and behavioral practices (e.g., piercing, circumcision, tattooing) may become the reason for spreading of HCV, if inadequately sterilized equipments are used. Sexual transmission may also occur between partners although less frequently. Like HIV, HCV does not spread by sneezing, hugging, coughing, food or water, sharing eating utensils and casual contact [2,7,8,9]. HCV infections are broadly divided into acute and chronic types. Acute HCV occurs after an incubation period of 15 -60 days with majority of acute HCV infections doesn't show any symptoms [10]. Chronic HCV infections are less prevalent but more risky than acute infections and can cause liver cirrhosis and cancer in some cases. The clinical symptoms may vary from mild to life threatening. HCV patients show symptoms like malaise, vomiting, fatigue, lethargy, anorexia, abdominal pain, myalgia, jaundice, mild hepatosplenomegaly, maculopapular rash and arthralgia [2,5,7].
Clinically, we cannot differentiate HCV from other hepatitis viruses and precise diagnosis is possible with laboratory methods only. Laboratory diagnosis of HCV is done by conventional biochemical markers and liver function test (LFT) [2]. The most practical screening test for HCV infection is the enzyme linked immunosorbent assay (ELISA) but it has low sensitivity and specificity. Moreover, false positive ELISA results may occur in patients with autoimmune antibodies, paraproteinemia, EBVinfection or other reasons [2,7,11,12]. Recently, few companies have introduced some rapid detection kits for HCV but these also struggle with poor sensitive and specificity issues. The reverse transcription polymerase chain reaction (RT-PCR) is the most used direct method to detect HCV RNA in blood [13,14]. Molecular assays are preferred for the confirmation of HCV infections because of their high sensitivity. But HCV is a very slow replicating virus, containing low copy number and some RNA may be degraded during isolation process making conventional RT-PCR less sensitive. Conventional RT-PCR coupled with nested PCR has been used successfully for effective detection of HCV infections [15,16,17]. Real-time RT-PCR is another choice with high sensitivity and specificity but sophisticated equipments and costly reagents make the assay less economic for use in developing countries. As HCV is a highly dangerous virus having the capability to infect large segment of world population, the present study has been conceptualized to develop one-step RT-PCR assay followed by nested PCR for sensitive, specific and cost effective detection of HCV.

Positive Samples of Hepatitis C Virus (HCV)
HCV positive samples were obtained from the Department of Medicine, Maulana Azad Medical College (MAMC), New Delhi. At MAMC, these samples were positive for HCV by conventional RT-PCR and further confirmed by sequencing.

RNA Extraction from Positive Samples
Viral RNA was extracted from 200 µl of an aliquot of HCV positive sample. RNA extraction was done with the help of GeneJET Viral DNA/RNA Purification Kit (Thermo Fisher Scientific, USA) according to the manufacturer′s protocol. RNA was eluted with 50 µl of elution buffer and stored at −70°C for further use.

Standardization of One-step RT-PCR and Nested PCR for HCV Using Reference Strains
First round of one-step RT-PCR was standardized using Verso 1-Step RT-PCR Kit (Thermo Fisher Scientific, USA) as per manufacturer's instructions. Twenty five microliters of reaction mixture was prepared by adding 5 µl of extracted viral RNA and 0.2 µM of both outer forward and outer reverse primers into the master mixture. 5 µl of double distilled water was added into negative control. In One-Step RT-PCR assay, initially RT (conversion of RNA into cDNA) step was performed after that heat inactivation of RT enzyme was done followed by simple PCR steps. Second round of nested PCR was performed using 5 µl of amplicons of onestep RT-PCR as template. The reaction mixture comprised of 2.5 µl of 10 × Taq buffer (Bangalore Genei) with 15 mM MgCl 2 , 0.2 mM of each dNTPs (Bangalore Genei), 0.2 µM of both internal forward and internal reverse primers and 0.75 U Taq DNA polymerase (Bangalore Genei). Negative controls were also included in the assay.

Primers for One-step RT-PCR and Nested PCR
Published primers were selected from the 5' UTR-core region of HCV which is conserved region for all serotypes and able to amplify all strains of HCV [18]. The specificity of these primers was also checked by BLAST (Bioinformatics tool/software) at NCBI site. Details of primers are given in Table 1.

Agarose Gel Electrophoresis
Nested PCR amplified products were visualized on 2.5% agarose gel. Agarose gel was prepared in 1X TAE (Tris acetate EDTA buffer, pH 8) buffer and the amplicons were loaded with the help of 2 µl of 1X gel loading dye (Bangalore Genei). Electrophoresis was performed for about 60 min at a constant voltage of 80 V in running buffer containing 1X TAE and ethidium bromide (1 µg/ml). After electrophoresis gel was visualized in a gel documentation system or gel transilluminator.

Optimization of One-step RT-PCR and Nested PCR
One-step RT-PCR assay was standardized with 0.2 µM of external forward & reverse primers. Optimum RNA template amount was found to be 5 µl and 35 cycles were optimized for the onestep RT-PCR assay. Optimal cyclic conditions for one-step RT-PCR assay are given in Table 2.
Similarly nested PCR was also standardized by using 0.2 µM of internal forward & reverse primers and 5 µl of one-step RT-PCR product (first round). Negative controls were also included which contain 5 µl of nuclease free water in place of template DNA. Optimal cycling conditions for nested-PCR assay are given in Table 3.
After nested PCR assay the amplified products were electrophoresed using 2.5% agarose gel and positive sample showed a sharp band of 405 bp while there was no band in the negative controls (Fig. 1).

Specificity of the Assay
One-step RT-PCR and nested PCR assay were highly specific for HCV detection as these assays failed to detect RNA/DNA of other related hepatitis viruses (A, B, D and E). Currently, there is no vaccine available for HCV but timely treatment with antiviral medicines can cure the disease. Thus a rapid, sensitive, specific and cost effective diagnosis of HCV plays a crucial role in the prophylaxis of the disease.   [2,7,11,12]. PCR based assays are the most direct approach to detect HCV RNA in blood [13][14][15]. Confirmed virus detection and typing could be possible by virus isolation but absence of virus isolation in cell culture hampers the research on HCV. Molecular detection methods are replacing traditional virus culture methods as these are more rapid, sensitive and specific [18][19][20][21][22]. Molecular diagnostic assays are more reliable than virus isolation and rapid kits. Conventional RT-PCR, real-time RT-PCR, transcription mediated amplification and branched DNA based assays are the most common molecular methods used for the detection and quantification of HCV [23,24].
In the present study HCV diagnosis was done by one-step RT-PCR assay followed by nested PCR. This method was based on two rounds of PCR amplification thereby increasing the detection time but the sensitivity and specificity of the assay was high. As HCV is a very slow growing virus and producing small number of virion particles per cell, hence we need nested types of PCR to produce the enough DNA to be detected. Amplified products can be seen in the agarose gel after staining with ethidium bromide. According to literature, nested RT-PCR assay demonstrated comparable sensitivity and specificity when compared to other methods like real-time RT-PCR. Real time RT-PCR approach although considered as more rapid, sensitive and specific but too expensive for large-scale diagnosis and has not been widely used in the majority of clinical laboratories in developing countries [13][14][15][21][22][23]. The primer sequences used as external and internal primers in the assay were highly conserved and specific for HCV only making the assay non-specific for other related viruses like hepatitis A,B,D and E. This assay can be used as diagnostic tool for clinicians and also can be used for epidemiological surveillance studies and screening blood donors and would be suitable for any resource limited setup.

CONCLUSION
In the present study, a specific, sensitive and cost effective diagnostic assay for HCV was developed. Presently, HCV is detected by simple biochemical assays, rapid tests and modern molecular assays. Rapid tests have low sensitivity and specificity while molecular assays like real-time PCR are more rapid, sensitive and specific but costly. Cost of a diagnostic assay is an important factor in the developing countries like India. Non-availability of effective vaccines and antivirals make HCV infections more dangerous and a major problem world-wide. The present diagnostic assay was standardized using confirmed positive reference samples of HCV virus. The RT-PCR coupled nested PCR assay can be applied directly on HCV suspected patients' samples providing sensitive, specific, rapid and cost effective result within the reasonable time and cost. There is still a need to develop some therapeutic agents and vaccines against HCV infections. The present assay can be modified in multiplex format according to the need of time.

CONSENT
It is not applicable.

ETHICAL APPROVAL
It is not applicable.