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Sulfa or sulfone prophylaxis and geographic region predict mutations in the Pneumocystis carinii dihydropteroate synthase gene.

TitleSulfa or sulfone prophylaxis and geographic region predict mutations in the Pneumocystis carinii dihydropteroate synthase gene.
Publication TypeJournal Article
Year of Publication2000
AuthorsHuang, L, Beard, CB, Creasman, J, Levy, D, Duchin, JS, Lee, S, Pieniazek, N, Carter, JL, del Rio, C, Rimland, D, Navin, TR
JournalJ Infect Dis
Volume182
Issue4
Pagination1192-8
Date Published2000 Oct
ISSN0022-1899
KeywordsAdult, AIDS-Related Opportunistic Infections, Analysis of Variance, Antibiotic Prophylaxis, Continental Population Groups, Dihydropteroate Synthase, Ethnic Groups, Female, Genotype, Geography, Georgia, HIV Infections, Humans, Male, Mutation, Pneumocystis, Pneumonia, Pneumocystis, San Francisco, Sulfonamides, Washington
Abstract

To determine factors associated with mutations in the Pneumocystis carinii dihydropteroate synthase (DHPS) gene, a prospective study of human immunodeficiency virus (HIV)-infected patients with confirmed P. carinii pneumonia was conducted in Atlanta, Seattle, and San Francisco. Clinical information was obtained from patient interview and chart abstraction. DHPS genotype was determined from DNA sequencing. Overall, 76 (68.5%) of 111 patients had a mutant DHPS genotype, including 22 (81.5%) of 27 patients from San Francisco. In multivariate analysis, sulfa or sulfone prophylaxis and study site were independent predictors of a mutant genotype. Fourteen (53.8%) of 26 patients who were newly diagnosed with HIV infection and had never taken prophylaxis had a mutant genotype. The significance of geographic location as a risk factor for mutant genotype and the high proportion of mutant genotypes among persons never prescribed prophylaxis, including those newly diagnosed with HIV infection, provide indirect evidence that these mutations are transmitted from person to person either directly or through a common environmental source.

DOI10.1086/315824
Alternate JournalJ. Infect. Dis.
PubMed ID10979917
Grant ListP30 MH59037 / MH / NIMH NIH HHS / United States