Yerly S, Rakik A, De Loes S K, Hirschel B, Descamps D, Brun-Vézinet F, Perrin L
Division of Infectious Diseases, Geneva University Hospital, Switzerland.
J Virol. 1998 May;72(5):3520-3. doi: 10.1128/JVI.72.5.3520-3523.1998.
Sequences of the human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) domain were determined by direct sequencing of HIV-1 RNA in successive plasma samples from eight seroconverting patients infected with virus bearing the T215Y/F amino acid substitution associated with zidovudine (ZDV) resistance. At baseline, additional mutations associated with ZDV resistance were detected. Three patients had the M41L amino acid change, which persisted. Two patients had both the D67N and the K70R amino acid substitutions; reversion to the wild type was seen at both positions in one of these patients and at codon 70 in the other one. Reversion to the wild type at codon 215 was observed in only one of eight patients. Unusual amino acids, such as aspartic acid (D) and cysteine (C), appeared at position 215 in four patients during follow-up. These variants isolated by coculturing were sensitive to ZDV. Overgrowth of these variants suggests that they have better fitness than the original T215Y variant. Intraindividual nucleoside substitutions over time were 10 times more frequent in codons associated with ZDV resistance (41, 67, 70, 215, and 219) than in other codons of the RT domain. The predominance of nonsynonymous substitutions observed over time suggests that most changes reflect adaptation of the RT function. The variance in sequence evolution observed among patients, in particular at codon 215, supports a role for chance in the evolution of the RT domain.
对8名血清转化患者连续采集的血浆样本中的人类免疫缺陷病毒1型(HIV-1)逆转录酶(RT)结构域序列进行了直接测序,这些患者感染了携带与齐多夫定(ZDV)耐药相关的T215Y/F氨基酸替代的病毒。在基线时,检测到与ZDV耐药相关的其他突变。3名患者发生了持续存在的M41L氨基酸变化。2名患者同时存在D67N和K70R氨基酸替代;其中1名患者这两个位置均回复为野生型,另1名患者仅密码子70回复为野生型。仅1名患者在密码子215处回复为野生型。随访期间,4名患者在位置215出现了异常氨基酸,如天冬氨酸(D)和半胱氨酸(C)。通过共培养分离出的这些变异体对ZDV敏感。这些变异体的过度生长表明它们比原始的T215Y变异体具有更好的适应性。随着时间的推移,个体内与ZDV耐药相关的密码子(41、67、70、215和219)中的核苷替代频率比RT结构域的其他密码子高10倍。随着时间的推移观察到的非同义替代占优势表明,大多数变化反映了RT功能的适应性。患者之间观察到的序列进化差异,特别是在密码子215处,支持了偶然性在RT结构域进化中的作用。