Details

Autor(en) / Beteiligte

• Fujiwara, Masatoshi
• Kodama, Eiichi N
• Okamoto, Masayuki
• Tokuhisa, Kenji
• Ide, Teruhiko
• Hanasaki, Yasuaki
• Katsuura, Kimio
• Takayama, Hiromitsu
• Aimi, Norio
• Mitsuya, Hiroaki
• Shigeta, Shiro
• Konno, Kenji
• Yokota, Tomoyuki
• Baba, Masanori

Titel

Characterization of Human Immunodeficiency Virus Type 1 Strains Resistant to the Non-Nucleoside Reverse Transcriptase Inhibitor RD4–2217

Ist Teil von

• Antiviral chemistry & chemotherapy, 1999-11, Vol.10 (6), p.315-320

Ort / Verlag

London, England: SAGE Publications

Erscheinungsjahr

1999

Quelle

Electronic Journals Library

Beschreibungen/Notizen

• The non-nucleoside reverse transcriptase (RT) inhibitor RD4–2217 is a thiadiazole derivative that has proved to be a highly potent and selective inhibitor of human immunodeficiency virus type 1 (HIV-1) replication in vitro. In this study we examined genotypic and phenotypic characteristics of RD4–2217-resistant mutants that have been obtained by serial passage of HIV-1 in MT-4 cells in the presence of increasing concentrations (0.05, 0.25, 1 and 10 μM) of the compound. The strains obtained, IIIB/2217RE/0.05 and IIIB/2217RE/0.25, were two-and 15-fold resistant to RD4–2217, respectively, whereas IIIB/2217RE/1 and IIIB/2217RE/10 displayed 161-and >238-fold resistance, respectively. Both IIIB/2217RE/1 and IIIB/2217RE/10 had two amino acid substitutions, V189I and T240I, in the RT. Furthermore, RD4–2217 did not inhibit the replication of an HIV-1 molecular clone, which had the same mutation, at concentrations up to 10 μM, indicating that the V189I plus T240I mutation confers high-level resistance to RD4–2217. Interestingly, the replicability of IIIB/2217RE/1 and IIIB/2217RE/10 appeared to be lower than that of wild-type IIIB in MT-4 cells, suggesting that the V189I plus T240I mutation may impair the enzymatic activity of HIV-1 RT.