TY - JOUR
T1 - Patterns and correlates of hepatitis C virus phylogenetic clustering among people living with HIV in Australia in the direct-acting antiviral era
T2 - A molecular epidemiology study among participants in the CEASE cohort
AU - Bartlett, Sofia R.
AU - Verich, Andrey
AU - Carson, Joanne
AU - Hosseini-Hooshyar, Samira
AU - Read, Phillip
AU - Baker, David
AU - Post, Jeffrey J.
AU - Finlayson, Robert
AU - Bloch, Mark
AU - Doyle, Joseph S.
AU - Shaw, David
AU - Hellard, Margaret
AU - Martinez, Maria
AU - Marks, Philippa
AU - Dore, Gregory J.
AU - Matthews, Gail V.
AU - Applegate, Tanya
AU - Martinello, Marianne
N1 - Funding Information:
The generous cooperation of participants in the CEASE study is gratefully acknowledged, as is the work of site staff involved in this study. This study was supported by Gilead Sciences, Inc (investigator‐initiated study). The Kirby Institute is funded by the Australian Government Department of Health and Ageing. The Burnet Institute has received untied educational grant funding from Gilead Sciences, Inc. M. Martinello., G.J.D., G.V.M., and M.H. are supported through National Health and Medical Research Council Fellowships (M. Martinello.: Early Career Fellowship; G.V.M. and J.S.D.: Career Development Fellowship; G.J.D.: Practitioner Fellowships; M.H.: Principal Research Fellowship).
Funding Information:
S.R.B. has received speakers' honoraria and participated in medical advisory board programs with Gilead Sciences and AbbVie (all personal payments given as unrestricted donation to BC Centre for Disease Control Foundation), and received research funding from Gilead Sciences through her institution. G.J.D. is a consultant/advisor and has received research grants from Abbvie, Bristol Myers Squibb, Gilead, Merck, Janssen and Roche. JSD has received consultancies to his institution from Gilead, Abbvie and Merck. J.S.D. and M.H. receives investigator‐initiated research funding from Gilead Sciences, Abbvie, Merck, and BMS. P.R. has received speaker's honoraria from Gilead Sciences and Abbvie, and research funding from Gilead Sciences. No commercial entities nor the supporting/funding source had any involvement in study design, data collection, data analysis, interpretation of data, writing of the report, or the decision to submit the report for publication.
Publisher Copyright:
© 2022 The Authors. Health Science Reports published by Wiley Periodicals LLC.
PY - 2022/9
Y1 - 2022/9
N2 - Background and Aims: In moving towards the elimination of hepatitis C virus (HCV) infection among people living with HIV, understanding HCV transmission patterns may provide insights to guide and evaluate interventions. In this study, we evaluated patterns of, and factors associated with HCV phylogenetic clustering among people living with HIV/HCV co-infection in Australia in the direct-acting antiviral era. Methods: HCV RNA was extracted from dried blood spot (DBS) samples collected between 2014 and 2018 in the CEASE cohort study. The HCV Core-E2 region was amplified by a polymerase chain reaction and Sanger sequenced. Maximum likelihood phylogenetic trees (1000 bootstrap replicates) were used to identify patterns of clustering (3% genetic distance threshold). Mixed-effects logistic regression was used to determine correlates of phylogenetic clustering. Factors assessed were sexual risk behavior, education, injecting drug use, housing, employment, HIV viral load, age, sex, and sexuality. Results: Phylogenetic trees were reconstructed for HCV subtype 1a (n = 139) and 3a (n = 63) sequences, with 29% (58/202) in a pair or cluster. Overall (n = 202), phylogenetic clustering was positively associated with younger age (under 40; adjusted odds ratio [aOR] 2.52, 95% confidence interval [CI] 1.20–5.29), and among gay and bisexual men (n = 168), was positively associated with younger age (aOR 2.61, 95% CI 1.10–6.19), higher education (aOR 2.58, 95% CI 1.09–6.13), and reporting high-risk sexual behavior (aOR 3.94, 95% CI 1.31–11.84). During follow-up, five reinfections were observed, but none were in phylogenetic clusters. Conclusion: This study found a high proportion of phylogenetic relatedness, predominantly among younger people and gay and bisexual men reporting high-risk sexual behavior. Despite this, few reinfections were observed, and reinfections demonstrated little relationship with known clusters. These findings highlight the importance of rapid HCV treatment initiation, together with monitoring of the phylogeny.
AB - Background and Aims: In moving towards the elimination of hepatitis C virus (HCV) infection among people living with HIV, understanding HCV transmission patterns may provide insights to guide and evaluate interventions. In this study, we evaluated patterns of, and factors associated with HCV phylogenetic clustering among people living with HIV/HCV co-infection in Australia in the direct-acting antiviral era. Methods: HCV RNA was extracted from dried blood spot (DBS) samples collected between 2014 and 2018 in the CEASE cohort study. The HCV Core-E2 region was amplified by a polymerase chain reaction and Sanger sequenced. Maximum likelihood phylogenetic trees (1000 bootstrap replicates) were used to identify patterns of clustering (3% genetic distance threshold). Mixed-effects logistic regression was used to determine correlates of phylogenetic clustering. Factors assessed were sexual risk behavior, education, injecting drug use, housing, employment, HIV viral load, age, sex, and sexuality. Results: Phylogenetic trees were reconstructed for HCV subtype 1a (n = 139) and 3a (n = 63) sequences, with 29% (58/202) in a pair or cluster. Overall (n = 202), phylogenetic clustering was positively associated with younger age (under 40; adjusted odds ratio [aOR] 2.52, 95% confidence interval [CI] 1.20–5.29), and among gay and bisexual men (n = 168), was positively associated with younger age (aOR 2.61, 95% CI 1.10–6.19), higher education (aOR 2.58, 95% CI 1.09–6.13), and reporting high-risk sexual behavior (aOR 3.94, 95% CI 1.31–11.84). During follow-up, five reinfections were observed, but none were in phylogenetic clusters. Conclusion: This study found a high proportion of phylogenetic relatedness, predominantly among younger people and gay and bisexual men reporting high-risk sexual behavior. Despite this, few reinfections were observed, and reinfections demonstrated little relationship with known clusters. These findings highlight the importance of rapid HCV treatment initiation, together with monitoring of the phylogeny.
KW - gay and bisexual men (GBM)
KW - hepatitis C
KW - HIV
KW - molecular sequencing
KW - phylogenetic analysis
UR - http://www.scopus.com/inward/record.url?scp=85138745761&partnerID=8YFLogxK
U2 - 10.1002/hsr2.719
DO - 10.1002/hsr2.719
M3 - Article
C2 - 36000082
AN - SCOPUS:85138745761
SN - 2398-8835
VL - 5
JO - Health Science Reports
JF - Health Science Reports
IS - 5
M1 - e719
ER -