Identification of two novel subtypes of hepatitis C virus genotype 8 and a potential new genotype successfully treated with direct acting antivirals
Hepatitis C virus (HCV) has a high genetic diversity and is classified into 8 genotypes and over 90 subtypes with some endemic to specific world regions. This could compromise direct-acting antiviral (DAA) efficacy and global HCV elimination. We characterised HCV subtypes 'rare' to the UK...
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creator | Mbisa, Jean L Lapp, Zena Bibby, David F Phillips, Laura T Manso, Carmen F Packer, Simon Simmons, Ruth Harris, Kathryn Mohan, Jaiganesh Chinnappan, Lalitha Leitner, Thomas Bradshaw, Daniel |
description | Hepatitis C virus (HCV) has a high genetic diversity and is classified into 8 genotypes and over 90 subtypes with some endemic to specific world regions. This could compromise direct-acting antiviral (DAA) efficacy and global HCV elimination.
We characterised HCV subtypes 'rare' to the UK (non-1a/1b/2b/3a/4d) by whole genome sequencing via a national surveillance programme. Genetic analyses to determine the genotype of samples with unresolved genotypes were undertaken by comparison with ICTV HCV reference sequences.
Two HCV variants were characterised as being closely related to the recently identified genotype 8 (GT8), with >85% pairwise genetic distance similarity to GT8 sequences and within the typical inter-subtype genetic distance range. The individuals infected by the variants were UK residents originally from Pakistan and India. In contrast, a third variant was only confidently identified to be more similar to GT6 compared to other genotypes across 6% of the genome and was isolated from a UK resident originally from Guyana. All three were cured with pangenotypic DAAs (Sofosbuvir + Velpatasvir or Glecaprevir + Pibrentasvir) despite the presence of resistance polymorphisms in NS3 (80 K/168E), NS5A (28 V/30S/62L/92S/93S) and NS5B (159F).
This study expands our knowledge of HCV diversity by identifying two new GT8 subtypes and potentially a new genotype. |
doi_str_mv | 10.1093/infdis/jiae253 |
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We characterised HCV subtypes 'rare' to the UK (non-1a/1b/2b/3a/4d) by whole genome sequencing via a national surveillance programme. Genetic analyses to determine the genotype of samples with unresolved genotypes were undertaken by comparison with ICTV HCV reference sequences.
Two HCV variants were characterised as being closely related to the recently identified genotype 8 (GT8), with >85% pairwise genetic distance similarity to GT8 sequences and within the typical inter-subtype genetic distance range. The individuals infected by the variants were UK residents originally from Pakistan and India. In contrast, a third variant was only confidently identified to be more similar to GT6 compared to other genotypes across 6% of the genome and was isolated from a UK resident originally from Guyana. All three were cured with pangenotypic DAAs (Sofosbuvir + Velpatasvir or Glecaprevir + Pibrentasvir) despite the presence of resistance polymorphisms in NS3 (80 K/168E), NS5A (28 V/30S/62L/92S/93S) and NS5B (159F).
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We characterised HCV subtypes 'rare' to the UK (non-1a/1b/2b/3a/4d) by whole genome sequencing via a national surveillance programme. Genetic analyses to determine the genotype of samples with unresolved genotypes were undertaken by comparison with ICTV HCV reference sequences.
Two HCV variants were characterised as being closely related to the recently identified genotype 8 (GT8), with >85% pairwise genetic distance similarity to GT8 sequences and within the typical inter-subtype genetic distance range. The individuals infected by the variants were UK residents originally from Pakistan and India. In contrast, a third variant was only confidently identified to be more similar to GT6 compared to other genotypes across 6% of the genome and was isolated from a UK resident originally from Guyana. All three were cured with pangenotypic DAAs (Sofosbuvir + Velpatasvir or Glecaprevir + Pibrentasvir) despite the presence of resistance polymorphisms in NS3 (80 K/168E), NS5A (28 V/30S/62L/92S/93S) and NS5B (159F).
This study expands our knowledge of HCV diversity by identifying two new GT8 subtypes and potentially a new genotype.</description><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Biological Science</subject><subject>DAA therapy</subject><subject>genetic diversity</subject><subject>genotype classification</subject><subject>HCV whole genome sequencing</subject><issn>0022-1899</issn><issn>1537-6613</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpFkU1P3DAQhi0Egi3tlSOyOPUS8EdiJ0e0ohQJqZdytrz2hDXK2iHjsNr_0R9cr3ZpTyPNPH5m5JeQK85uOevkXYi9D3j3FiyIRp6QBW-krpTi8pQsGBOi4m3XXZAviG-MsVoqfU4uZKu57qRekD9PHmIOfXA2hxRp6mneJhrTBwwU51XejYD77hrGQuSAdEk_wjQjfYWY9mPaUhs9tXRMee-yA42w_T_G2TlA7Odh2NE8gc3g6TbkNfVhApepdTnE1yLJoZjtgF_JWV8KfDvWS_Ly4-H38mf1_OvxaXn_XDkuhK4EB1aDkK3sQNqeCd9wzeq24TUrK532StRSMFWvPCgHyrdO6X6lwfGm9Z28JDcHb8IcDLqQwa1dirFcZUT5qobLAn0_QOOU3mfAbDYBHQyDjZBmNJI1ksu2blRBbw-omxLiBL0Zp7Cx085wZvZxmUNc5hhXeXB9dM-rDfh_-Gc-8i9_MpXh</recordid><startdate>20240508</startdate><enddate>20240508</enddate><creator>Mbisa, Jean L</creator><creator>Lapp, Zena</creator><creator>Bibby, David F</creator><creator>Phillips, Laura T</creator><creator>Manso, Carmen F</creator><creator>Packer, Simon</creator><creator>Simmons, Ruth</creator><creator>Harris, Kathryn</creator><creator>Mohan, Jaiganesh</creator><creator>Chinnappan, Lalitha</creator><creator>Leitner, Thomas</creator><creator>Bradshaw, Daniel</creator><general>Infectious Diseases Society of America</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OIOZB</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-0348-9679</orcidid><orcidid>https://orcid.org/0000000203489679</orcidid></search><sort><creationdate>20240508</creationdate><title>Identification of two novel subtypes of hepatitis C virus genotype 8 and a potential new genotype successfully treated with direct acting antivirals</title><author>Mbisa, Jean L ; Lapp, Zena ; Bibby, David F ; Phillips, Laura T ; Manso, Carmen F ; Packer, Simon ; Simmons, Ruth ; Harris, Kathryn ; Mohan, Jaiganesh ; Chinnappan, Lalitha ; Leitner, Thomas ; Bradshaw, Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1227-21e04e23839e3af02d5170485140ccec7d62432064bde6ce6d8c67fb7ec158d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biological Science</topic><topic>DAA therapy</topic><topic>genetic diversity</topic><topic>genotype classification</topic><topic>HCV whole genome sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mbisa, Jean L</creatorcontrib><creatorcontrib>Lapp, Zena</creatorcontrib><creatorcontrib>Bibby, David F</creatorcontrib><creatorcontrib>Phillips, Laura T</creatorcontrib><creatorcontrib>Manso, Carmen F</creatorcontrib><creatorcontrib>Packer, Simon</creatorcontrib><creatorcontrib>Simmons, Ruth</creatorcontrib><creatorcontrib>Harris, Kathryn</creatorcontrib><creatorcontrib>Mohan, Jaiganesh</creatorcontrib><creatorcontrib>Chinnappan, Lalitha</creatorcontrib><creatorcontrib>Leitner, Thomas</creatorcontrib><creatorcontrib>Bradshaw, Daniel</creatorcontrib><creatorcontrib>Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mbisa, Jean L</au><au>Lapp, Zena</au><au>Bibby, David F</au><au>Phillips, Laura T</au><au>Manso, Carmen F</au><au>Packer, Simon</au><au>Simmons, Ruth</au><au>Harris, Kathryn</au><au>Mohan, Jaiganesh</au><au>Chinnappan, Lalitha</au><au>Leitner, Thomas</au><au>Bradshaw, Daniel</au><aucorp>Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of two novel subtypes of hepatitis C virus genotype 8 and a potential new genotype successfully treated with direct acting antivirals</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2024-05-08</date><risdate>2024</risdate><volume>NA</volume><issn>0022-1899</issn><issn>1537-6613</issn><eissn>1537-6613</eissn><abstract>Hepatitis C virus (HCV) has a high genetic diversity and is classified into 8 genotypes and over 90 subtypes with some endemic to specific world regions. This could compromise direct-acting antiviral (DAA) efficacy and global HCV elimination.
We characterised HCV subtypes 'rare' to the UK (non-1a/1b/2b/3a/4d) by whole genome sequencing via a national surveillance programme. Genetic analyses to determine the genotype of samples with unresolved genotypes were undertaken by comparison with ICTV HCV reference sequences.
Two HCV variants were characterised as being closely related to the recently identified genotype 8 (GT8), with >85% pairwise genetic distance similarity to GT8 sequences and within the typical inter-subtype genetic distance range. The individuals infected by the variants were UK residents originally from Pakistan and India. In contrast, a third variant was only confidently identified to be more similar to GT6 compared to other genotypes across 6% of the genome and was isolated from a UK resident originally from Guyana. All three were cured with pangenotypic DAAs (Sofosbuvir + Velpatasvir or Glecaprevir + Pibrentasvir) despite the presence of resistance polymorphisms in NS3 (80 K/168E), NS5A (28 V/30S/62L/92S/93S) and NS5B (159F).
This study expands our knowledge of HCV diversity by identifying two new GT8 subtypes and potentially a new genotype.</abstract><cop>United States</cop><pub>Infectious Diseases Society of America</pub><pmid>38717937</pmid><doi>10.1093/infdis/jiae253</doi><orcidid>https://orcid.org/0000-0002-0348-9679</orcidid><orcidid>https://orcid.org/0000000203489679</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current) |
subjects | BASIC BIOLOGICAL SCIENCES Biological Science DAA therapy genetic diversity genotype classification HCV whole genome sequencing |
title | Identification of two novel subtypes of hepatitis C virus genotype 8 and a potential new genotype successfully treated with direct acting antivirals |
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