High Rates of Forward Transmission Events after Acute/Early HIV‐1 Infection

Bluma Brenner(Jewish General Hospital), Michel Roger(Université de Montréal), Jean‐Pierre Routy(McGill University Health Centre), Daniela Moïsi(Jewish General Hospital), Michel Ntemgwa(Jewish General Hospital), Claudine Matte(Hôpital Notre-Dame), Jean‐Guy Baril, Réjean Thomas, Danielle Rouleau(Hôpital Notre-Dame), Julie Bruneau(Hôpital Saint-Luc), Roger LeBlanc, Mario Legault(Fonds de Recherche du Québec - Santé), Cécile Tremblay(Hôtel-Dieu de Montréal), Hugues Charest(Institut National de Santé Publique du Québec), Mark A. Wainberg(Jewish General Hospital), Quebec Primary HIV Infection Study Group
The Journal of Infectious Diseases
March 3, 2007
Cited by 651

Abstract

BACKGROUND: A population-based phylogenetic approach was used to characterize human immunodeficiency virus (HIV)-transmission dynamics in Quebec. METHODS: HIV-1 pol sequences included primary HIV infections (PHIs; <6 months after seroconversion) from the Quebec PHI cohort (1998-2005; n=215) and the provincial genotyping program (2001-2005; n=481). Phylogenetic analysis determined sequence interrelationships among unique PHIs (n=593) and infections from untreated (n=135) and treated (n=660) chronically infected (CI) potential transmitter populations (2001-2005). Clinical features, risk factors, and drug resistance for clustered and nonclustered transmission events were ascertained. RESULTS: Viruses from 49.4% (293/593) of PHIs cosegregated into 75 transmission chains with 2-17 transmissions/cluster. Half of the clusters included 2.7+/-0.8 (mean+/-SD) transmissions, whereas the remainder had 8.8+/-3.5 transmissions. Maximum periods for onward transmission in clusters were 15.2+/-9.5 months. Coclustering of untreated and treated CIs with PHIs were infrequent (6.2% and 4.8%, respectively). The ages, viremia, and risk factors were similar for clustered and nonclustered transmission events. Low prevalence of drug resistance in PHI supported amplified transmissions at early stages. CONCLUSIONS: Early infection accounts for approximately half of onward transmissions in this urban North American study. Therapy at early stages of disease may prevent onward HIV transmission.


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