Evidence for onward transmission of HIV-1 non-B subtype strains in the United Kingdom

被引:38
作者
Aggarwal, I
Smith, M
Tatt, ID
Murad, S
Osner, N
Geretti, AM
Easterbrook, PJ
机构
[1] Kings Coll London, Sch Med, Guys Kings Coll, Dept HIV GU Med, London SE5 9RT, England
[2] St Thomas Hosp, Weston Educ Ctr, London SE5 9RT, England
[3] London S Specialist Virol Ctr, Hlth Protect Agcy London, London, England
[4] Hlth Protect Agcy, Cent Publ Hlth Lab, Sexually Transmitted & Blood Borne Virus Lab, London, England
基金
英国医学研究理事会;
关键词
HIV-1; subtypes; molecular epidemiology; transmission;
D O I
10.1097/01.qai.0000179430.34660.11
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An increasing proportion of new HIV diagnoses in the United Kingdom and other European countries are attributable to non-B subtype infections, mainly among black Africans with infections heterosexually acquired in sub-Sabaran Africa. We examined whether there was evidence for onward transmission of non-B subtypes within an ethnically diverse HIV-1-infected cohort in South London. Three hundred eighty-four HIV-1-infected patients attending Kings College Hospital were subtyped using an in-house enzyme-linked immunoassay and env sequencing. Epidemiologic data were obtained from medical chart review and the patients' physician and were used to establish the most likely source and country of infection. Overall, 344 patients (154 black African, 148 white UK-born, and 42 black Caribbean) had an identifiable subtype. The prevalence of non-B subtypes among the black African, white, and black Caribbean patients was 96.8%, 14.2%, and 31%, respectively. Most non-B subtype infections were identified in black Africans (149 of 183 cases) and were mainly acquired in sub-Saharan Africa, but 22.9% (42 of 183 cases) of all non-B infections were probably acquired in the United Kingdom. Among the 21 white UK-bom patients infected with a non-B subtype, 15 probably acquired the infection in the United Kingdom and only 6 of these patients reported a source sexual partner from an HIV endemic area. All 13 black Caribbean patients with a non-B infection most likely acquired their infection in the United Kingdom, most of whom (8 of 13 patients) were probably infected by a partner from an HIV endemic area. Potential acquisition of HIV infection in the United Kingdom was lowest among black African patients with a non-B infection, and most of these infections were probably acquired from a partner originating from an HIV endemic area. This study provides the first evidence for onward transmission of non-B subtypes in the United Kingdom, particularly among the black Caribbean population.
引用
收藏
页码:201 / 209
页数:9
相关论文
共 39 条
[1]   Similar rate of disease progression among individuals infected with HIV-1 genetic subtypes A-D [J].
Alaeus, A ;
Lidman, K ;
Björkman, A ;
Giesecke, J ;
Albert, J .
AIDS, 1999, 13 (08) :901-907
[2]   Most HIV-1 genetic subtypes have entered Sweden [J].
Alaeus, A ;
Leitner, T ;
Lidman, K ;
Albert, J .
AIDS, 1997, 11 (02) :199-202
[3]  
Balotta C, 2001, J ACQ IMMUN DEF SYND, V27, P499, DOI 10.1097/00126334-200108150-00012
[4]  
BONI J, 1999, J ACQ IMMUN DEF SYND, V22, P149
[5]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[6]   Serologic and phylogenetic characterization of HIV-1 subtypes in Uganda [J].
Brennan, CA ;
Lund, JK ;
Golden, A ;
Yamaguchi, J ;
Vallari, AS ;
Phillips, JF ;
Kataaha, PK ;
Jackson, JB ;
Devare, SG .
AIDS, 1997, 11 (15) :1823-1832
[7]   Resistance-associated mutations in the human immunodeficiency virus type 1 subtype C protease gene from treated and untreated patients in the United Kingdom [J].
Cane, PA ;
de Ruiter, A ;
Rice, P ;
Wiselka, M ;
Fox, R ;
Pillay, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (07) :2652-2654
[8]   HIV-1 diversity in France, 1996-1998 [J].
Couturier, E ;
Damond, F ;
Roques, P ;
Fleury, H ;
Barin, F ;
Brunet, JB ;
Brun-Vézinet, F ;
Simon, F .
AIDS, 2000, 14 (03) :289-296
[9]  
DELWART EL, 1995, PCR METH APPL, V4, pS202
[10]  
Dietrich U, 1997, AIDS, V11, P1532