Subgenotyping and genetic variability of hepatitis C virus in Palestine.

Hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. Genotyping of HCV is crucial for successful therapy. To determine the HCV subgenotypes circulating in Palestine and to study the genetic variability of their core, we collected 84 serum samples which had tested...

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Main Authors: Sahar Rayan Da'as, Maysa Azzeh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0222799
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spelling doaj-8d9d6cc360804209aad9f020f30045ba2021-03-03T21:11:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011410e022279910.1371/journal.pone.0222799Subgenotyping and genetic variability of hepatitis C virus in Palestine.Sahar Rayan Da'asMaysa AzzehHepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. Genotyping of HCV is crucial for successful therapy. To determine the HCV subgenotypes circulating in Palestine and to study the genetic variability of their core, we collected 84 serum samples which had tested positive for anti-HCV antibodies. Thirty-seven of these samples came from hemodialysis patients. Serum samples were subjected to viral RNA isolation and amplification of the HCV core gene. Thirty-three of the samples (39%) tested positive for HCV RNA. The HCV subgenotypes circulating in Palestine included 1a, 3a, and 4a, detected in 38%, 25%, and 22% of the samples, respectively. Furthermore, subgenotype 1b was present in three samples (9%), while the rare subgenotype 4v was present in two samples (6%). We identified a number of substitutions in the retrieved HCV core sequences, such as HCV 1b substitutions R70Q and M91L, which some studies have associated with hepatocellular carcinoma risk and poor virological response. In contrast to two previous studies reporting that HCV genotype 4 was predominant in the Gaza strip (present in just over 70% of samples), genotype 4 was detected in only 31% of the samples in our current study, whereas genotype 1 and 3 were present in 69% of samples. These differences may relate to the fact that many of our samples came from the West Bank and East Jerusalem. The co-circulation of different HCV genotypes and subgenotypes in Palestine suggests that subgenotyping prior to treatment is crucial in Palestinian patients.https://doi.org/10.1371/journal.pone.0222799
collection DOAJ
language English
format Article
sources DOAJ
author Sahar Rayan Da'as
Maysa Azzeh
spellingShingle Sahar Rayan Da'as
Maysa Azzeh
Subgenotyping and genetic variability of hepatitis C virus in Palestine.
PLoS ONE
author_facet Sahar Rayan Da'as
Maysa Azzeh
author_sort Sahar Rayan Da'as
title Subgenotyping and genetic variability of hepatitis C virus in Palestine.
title_short Subgenotyping and genetic variability of hepatitis C virus in Palestine.
title_full Subgenotyping and genetic variability of hepatitis C virus in Palestine.
title_fullStr Subgenotyping and genetic variability of hepatitis C virus in Palestine.
title_full_unstemmed Subgenotyping and genetic variability of hepatitis C virus in Palestine.
title_sort subgenotyping and genetic variability of hepatitis c virus in palestine.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Hepatitis C virus (HCV) is a major cause of liver cirrhosis and hepatocellular carcinoma. Genotyping of HCV is crucial for successful therapy. To determine the HCV subgenotypes circulating in Palestine and to study the genetic variability of their core, we collected 84 serum samples which had tested positive for anti-HCV antibodies. Thirty-seven of these samples came from hemodialysis patients. Serum samples were subjected to viral RNA isolation and amplification of the HCV core gene. Thirty-three of the samples (39%) tested positive for HCV RNA. The HCV subgenotypes circulating in Palestine included 1a, 3a, and 4a, detected in 38%, 25%, and 22% of the samples, respectively. Furthermore, subgenotype 1b was present in three samples (9%), while the rare subgenotype 4v was present in two samples (6%). We identified a number of substitutions in the retrieved HCV core sequences, such as HCV 1b substitutions R70Q and M91L, which some studies have associated with hepatocellular carcinoma risk and poor virological response. In contrast to two previous studies reporting that HCV genotype 4 was predominant in the Gaza strip (present in just over 70% of samples), genotype 4 was detected in only 31% of the samples in our current study, whereas genotype 1 and 3 were present in 69% of samples. These differences may relate to the fact that many of our samples came from the West Bank and East Jerusalem. The co-circulation of different HCV genotypes and subgenotypes in Palestine suggests that subgenotyping prior to treatment is crucial in Palestinian patients.
url https://doi.org/10.1371/journal.pone.0222799
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