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Population-based Surveillance of Recent Infections in Quebec (1999-2005)
Bluma Brenner*1, M Roger2, D Moisi1, B Spira1, H Charest3, J P Routy4, M Wainberg1, and Quebec PHI Study Group
1McGill Univ AIDS Ctr, Montreal, Canada; 2Ctr Hosp Univ Montreal, Canada; 3Lab of Publ Hlth of Québec, Montreal, Canada; and 4McGill Univ Hlth Ctr, Montreal, Canada
Background: The
period following primary HIV-1 infection may account for a significant
proportion of new transmission events. This study characterized the
interrelationships of viral sequences from all genotyped, recent infections in
Quebec (1999-2005).
Methods: Sequence
data were complied from the 2 provincial testing laboratories (2001-2005) and
the Quebec Primary HIV-1 Infection cohort study (1998-2005). Phylogenetic tree
analysis determined sequence interrelationships of all recent infections, identifying
clustered transmission events and non-B subtype infections (n = 692).
Clinical information on age, sex, route of transmission, and time of infection
was obtained from questionnaires or validated genotypic test requisitions.
Results: Half
of subtype B infections in recently infected persons in Quebec are present in
transmission clusters having 2 to 14 persons/cluster. The median and mean
transmission interval for the 75 identified transmission clusters were 8±4.5
months and 10.8±1.1 months, respectively. Clustering was related with high-risk
sexual behavior, wherein 40% of male-sex-male clusters included persons having sex
with >5 persons in the 3-month interval prior to their diagnosis. The 35-55
age-groups were the at-risk population for subtype B infections. Non-B subtypes
represented 16% of new infections in Quebec, with subtype C (51%), A/CRF1
(18%), G/CRF2/CRF6 (18%), D (8%), F (1%), and K/J CRF (5%) distribution. Non-B
infections rarely represented clustered transmission events. Reported so far have
been 7 primary non-B transmissions, including 2 subtype C, 4 CRF2, and 1 CRF1 infection.
Conclusions: Routine
genotyping is important for screening HIV-1 transmission and the spread of non-B
infections, as well as for drug-resistance testing. Acute/early infection
accounted for at least half of all reported subtype B transmissions. Non-B
subtype infections are being rapidly introduced into Quebec, and public health
policies must address evolving trends in HIV-1 transmission.
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