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Hepatitis C virus transmission between eight high-income countries among men who have sex with men: a whole-genome analysis.

cris.virtual.author-orcid0000-0001-5297-6062
cris.virtualsource.author-orcid91a3060c-0e74-4217-944d-3471766e2083
datacite.rightsopen.access
dc.contributor.authorKoopsen, Jelle
dc.contributor.authorMatthews, Gail
dc.contributor.authorRockstroh, Juergen
dc.contributor.authorApplegate, Tanya L
dc.contributor.authorBhagani, Sanjay
dc.contributor.authorRauch, Andri
dc.contributor.authorGrebely, Jason
dc.contributor.authorSacks-Davis, Rachel
dc.contributor.authorIngiliz, Patrick
dc.contributor.authorBoesecke, Christoph
dc.contributor.authorRebers, Sjoerd
dc.contributor.authorFeld, Jordan
dc.contributor.authorBruneau, Julie
dc.contributor.authorMartinello, Marianne
dc.contributor.authorHellard, Margaret
dc.contributor.authorDore, Gregory J
dc.contributor.authorSchinkel, Janke
dc.contributor.authorvan der Valk, Marc
dc.date.accessioned2024-10-25T16:44:01Z
dc.date.available2024-10-25T16:44:01Z
dc.date.issued2023-08
dc.description.abstractBACKGROUND Microelimination of the hepatitis C virus (HCV) among men who have sex with men (MSM) could be complicated by continuous external introductions and the emergence of phylogenetic clusters harbouring clinically significant resistance-associated substitutions (RAS). To investigate international clustering and the prevalence and transmission of RAS, we aimed to analyse whole-genome HCV sequences from MSM with a recently acquired infection who participated in a large, international HCV treatment trial. METHODS For this whole-genome analysis, we obtained HCV sequences from 128 MSM who had acquired HCV within the past 12 months and were participating in the REACT trial. The participants from whom sequences were obtained were recruited at 24 sites in eight countries. We inferred maximum-likelihood phylogenies and identified transmission clusters for HCV genotypes separately. We constructed time-scaled phylogenies to estimate cluster introduction dates and used a Bayesian Skygrid approach to estimate the effective population size over the past 50 years. We calculated the prevalence of RAS and the extent of RAS transmission in the study population. FINDINGS The majority of recent HCV infections were part of international networks that arose in the late 1990s and early 2000s. Sequences obtained in the same country clustered frequently, and in 36% of subclusters since 2015 we found evidence of international transmission. European MSM were more likely than non-European MSM to be in a cluster (odds ratio 11·9 [95% CI 3·6-43·4], p<0·0001). The effective population size decreased rapidly since around 2015 in Europe. RAS associated with substantially diminished cure rates were infrequently detected and transmission of highly resistant viruses was not observed. INTERPRETATION Despite antiviral treatment becoming widely available, international transmission of HCV among MSM has still occurred over the past 8 years, which could complicate microelimination of the virus in this population. RAS-enriched clusters and widespread RAS transmission are currently not a threat to elimination goals. These findings support an international approach for HCV microelimination among MSM. FUNDING National Institutes of Health and Dr. C.J. Vaillant Fonds.
dc.description.sponsorshipUniversitätsklinik für Infektiologie
dc.identifier.doi10.48350/183551
dc.identifier.pmid37336226
dc.identifier.publisherDOI10.1016/S2666-5247(23)00108-8
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/167955
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofThe Lancet Microbe
dc.relation.issn2666-5247
dc.relation.organizationClinic of Infectiology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleHepatitis C virus transmission between eight high-income countries among men who have sex with men: a whole-genome analysis.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPagee631
oaire.citation.issue8
oaire.citation.startPagee622
oaire.citation.volume4
oairecerif.author.affiliationUniversitätsklinik für Infektiologie
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unibe.date.licenseChanged2023-06-20 10:53:30
unibe.description.ispublishedpub
unibe.eprints.legacyId183551
unibe.journal.abbrevTitleLANCET MICROBE
unibe.refereedtrue
unibe.subtype.articlejournal

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