HIV type 1 genetic diversity and genotypic drug susceptibility in the Republic of Moldova

HIV-1 genetic diversity and, for the first time, genotypic drug susceptibility was investigated for strains circulating in the Republic of Moldova (of the former Soviet Union). Eighty-three samples from adults recently infected by intravenous drug use (IDU) (n = 60), heterosexual contact (n = 8), an...

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Veröffentlicht in:AIDS research and human retroviruses 2001-09, Vol.17 (13), p.1297-1304
Hauptverfasser: PANDREA, Ivona, DESCAMPS, Diane, APETREI, Cristian, COLLIN, Gilles, ROBERTSON, David L, DAMOND, Florence, DIMITRIENCO, Valeria, GHEORGHITA, Stefan, PECEC, Mihai, SIMON, Francois, BRUN-VEZINET, Francoise
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Sprache:eng
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Zusammenfassung:HIV-1 genetic diversity and, for the first time, genotypic drug susceptibility was investigated for strains circulating in the Republic of Moldova (of the former Soviet Union). Eighty-three samples from adults recently infected by intravenous drug use (IDU) (n = 60), heterosexual contact (n = 8), and from blood donors (n = 15) that tested positive from 1997 to 1998, and originating from different regions of Moldova were serotyped. By group-specific and subtype-specific peptide ELISA, patients were infected by serotype A (n = 65), serotype B (n = 1), or were nontypable (n = 17). Heteroduplex mobility assay (HMA) confirmed 11 subtype A and the one subtype B infection. Analyses of pol and env sequences for six of the IDUs confirmed that they were infected with subtype A strain. These strains clustered tightly with subtype A strains isolated from the former Soviet Union in phylogenetic analysis. No mutations associated with drug resistance were detected. The Republic of Moldova is culturally more closely related to Romania (where subtype F dominates the epidemic), but depends economically on Russia (where subtype A is established among IDUs). Thus, our results suggest that the spread of HIV in this region is driven by drug networks rather than being due to cultural similarities.
ISSN:0889-2229
1931-8405
DOI:10.1089/088922201750461375