Patterns and characteristics of hepatitis C transmission clusters among HIV-positive and HIV-negative individuals in the Australian trial in acute hepatitis C

G V Matthews, S T Pham, M Hellard, J Grebely, L Zhang, A Oon, P Marks, I van Beek, W Rawlinson, J M Kaldor, A Lloyd, G J Dore, P A White, ATAHC Study Group, John Kaldor, Gregory Dore, Gail Matthews, Pip Marks, Andrew Lloyd, Margaret Hellard, Paul Haber, Rose Ffrench, Peter White, William Rawlinson, Carolyn Day, Ingrid van Beek, Geoff McCaughan, Annie Madden, Kate Dolan, Geoff Farrell, Nick Crofts, William Sievert, David Baker, John Kaldor, Gregory Dore, Gail Matthews, Pip Marks, Barbara Yeung, Brian Acraman, Kathy Petoumenos, Janaki Amin, Carolyn Day, Anna Doab, Jason Grebely, Therese Carroll, Margaret Hellard, Oanh Nguyen, Sally von Bibra, Andrew Lloyd, Suzy Teutsch, Hui Li, Alieen Oon, Barbara Cameron, William Rawlinson, Brendan acka, Yong Pan, Rose french, Jacqueline Flynn, Kylie Goy, Gregory Dore, Margaret Hellard, David Shaw, Paul Haber, Joe Sasadeusz, Darrell Crawford, Ingrid van Beek, Nghi Phung, Jacob George, Mark Bloch, David Baker, Brian Hughes, Lindsay Mollison, Stuart Roberts, William Sievert, Paul Desmond, G V Matthews, S T Pham, M Hellard, J Grebely, L Zhang, A Oon, P Marks, I van Beek, W Rawlinson, J M Kaldor, A Lloyd, G J Dore, P A White, ATAHC Study Group, John Kaldor, Gregory Dore, Gail Matthews, Pip Marks, Andrew Lloyd, Margaret Hellard, Paul Haber, Rose Ffrench, Peter White, William Rawlinson, Carolyn Day, Ingrid van Beek, Geoff McCaughan, Annie Madden, Kate Dolan, Geoff Farrell, Nick Crofts, William Sievert, David Baker, John Kaldor, Gregory Dore, Gail Matthews, Pip Marks, Barbara Yeung, Brian Acraman, Kathy Petoumenos, Janaki Amin, Carolyn Day, Anna Doab, Jason Grebely, Therese Carroll, Margaret Hellard, Oanh Nguyen, Sally von Bibra, Andrew Lloyd, Suzy Teutsch, Hui Li, Alieen Oon, Barbara Cameron, William Rawlinson, Brendan acka, Yong Pan, Rose french, Jacqueline Flynn, Kylie Goy, Gregory Dore, Margaret Hellard, David Shaw, Paul Haber, Joe Sasadeusz, Darrell Crawford, Ingrid van Beek, Nghi Phung, Jacob George, Mark Bloch, David Baker, Brian Hughes, Lindsay Mollison, Stuart Roberts, William Sievert, Paul Desmond

Abstract

Background: Injecting drug users remain the population at greatest risk of acquiring hepatitis C virus (HCV) infection, although a recent increase in cases of sexually transmitted HCV infection has been observed among human immunodeficiency virus (HIV)-infected individuals. The extent to which these separate epidemics overlap is unknown.

Methods: The Australian Trial in Acute Hepatitis C (ATAHC) enrolled 163 individuals (29% of whom were HIV infected) with recent HCV infection. E1/HVR1 sequences were used to construct phylogenetic trees demonstrating monophyletic clusters or pairs, and viral epidemic history and phylogeography were assessed using molecular clock analysis. Individual clusters were characterized by clinical and demographic characteristics.

Results: Transmission through injection drug use occurred for 73% of subjects, with sexual transmission occurring for 18% (92% of whom were HIV infected). Among 112 individuals with available E1/HVR1 sequences, 23 (20%) were infected with a strain of HCV identical to that of another subject, comprising 4 homologous clusters and 3 monophyletic pairs, the majority of which (78%) were HIV infected. Clusters contained individuals with both injection drug use-related and sex-related acquisition, and in all clusters (except for 1 female HIV-uninfected pair), individuals identified as men who have sex with men, irrespective of HIV status.

Conclusions: This large unique study of HIV-infected and HIV-uninfected individuals with recently acquired HCV infection demonstrates that clustering is common in the HIV-infected population and that it occurred almost invariably among men who have sex with men, irrespective of the actual mode of acquisition. These findings suggest the coexistence of both injection drug use and sexual risk behaviors for individuals in the same social networks and have implications for the development of public health messages. Clinical trial registration. NCT00192569.

Figures

Figure 1.
Figure 1.
A, Phylogenetic analysis of 116 E1/HVR-1 sequences (657 bp) from 112 hepatitis C virus (HCV) RNA–positive patients demonstrating clustering of subjects enrolled in the Australian Trial in Acute Hepatitis C. Clusters are numbered 1–7. Spheres represent HCV sexual transmission, squares represent injection drug use–related transmission, and diamonds represent other modes of transmission. Filled symbols represent human immunodeficiency virus (HIV)–infected patients, and unfilled symbols represent HIV-uninfected patients. Patients (n = 23) in clusters are labeled from A to W. Cases with HCV reinfection did not cluster. HCV genotypes (G1, G2, and G3) are indicated along the major branches; reference HCV subtype sequences are also indicated. The percentage bootstrap values in which the major groupings were observed among 1000 replicates are indicated; only values > 70% are shown. The branch lengths are proportional to the evolutionary distance between sequences, and the distance scale, in nucleotide substitutions per position, is shown. B, Phylogeographic tree of all E1/HVR-1 sequences on a real time scale of 1 year spanning 1988–2004. Geographic status is indicated by color (green, New South Wales; red, Victoria; blue, South Australia, SA; orange, Queensland, QLD and pink, WA, Western Australia). Black dots represent migration events for each monophyletic cluster or pair. All 7 clusters or pairs are shaded and labeled 1–7.

Source: PubMed

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