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Evidence of Nef Truncation in Human Immunodeficiency Virus Type 2 Infection
Author(s) -
William M. Switzer,
Stefan Z. Wiktor,
Vincent Soriano,
Antonio SilvaGraça,
Kamal Mansinho,
IssaMalik Coulibaly,
Ehounou Ekpini,
Alan E. Greenberg,
Thomas M. Folks,
Walid Heneine
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/513819
Subject(s) - virology , biology , virus , asymptomatic , immunodeficiency , group specific antigen , gene , long terminal repeat , viral disease , simian immunodeficiency virus , human immunodeficiency virus (hiv) , immunology , medicine , genetics , immune system , genome
Human immunodeficiency virus (HIV)-2 differs from HIV-1 in its relative lower transmissibility and pathogenicity. To understand the virologic basis of these differences, the nef gene from HIV-2-seropositive persons was analyzed because of its importance for disease progression in the genetically related simian immunodeficiency virus (SIV[MAC]). Proviral nef sequences from 60 HIV-2-infected persons were amplified from peripheral blood lymphocytes, and nef open-reading frames were screened by a transcription and translation assay for the presence of full-length (32- to 36-kDa) or truncated (<32 kDa) Nef proteins. Overall, 6 (10%) of 60 persons had truncated Nef proteins; of these, 5 were among the 36 asymptomatic subjects (13.9%) and only 1 was among the 24 symptomatic subjects (4.2%) (P =.23). The results of this study document the presence of defective nef genes in HIV-2 infections with a prevalence higher than that previously seen in HIV-1-infected cohorts of long-term nonprogressors or patients with AIDS.

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