ANALYSIS OF THE THYMIDINE KINASE GENE FROM CLINICALLY ISOLATED ACYCLOVIR-RESISTANT HERPES-SIMPLEX VIRUSES

被引:54
作者
CHATIS, PA [1 ]
CRUMPACKER, CS [1 ]
机构
[1] HARVARD UNIV,BETH ISRAEL HOSP,SCH MED,DIV INFECT DIS,BOSTON,MA 02215
关键词
D O I
10.1016/0042-6822(91)90093-Q
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The isolation and description of acyclovir-resistant (ACVR) herpes simplex-2 viruses from patients with AIDS has recently been reported. These ACVR viruses were all markedly decreased in their thymidine kinase (TK) activity, and 6 of 10 of these TK viruses were able to establish latency. In addition, one of these isolates, ACVR-86012 was neuropathogenic in a murine encephalitis model. In this paper, the characteristics of these isolates with respect to TK polypeptide synthesis are examined. All but one isolate synthesized a detectable TK protein by immunoprecipitation, and 9 10 of the TK proteins had an altered electrophoretic mobility as compared to wild-type. The TK polypeptide from the neuropathogenic isolate ACVR-86012 was full-length and the gene was sequenced. An amino acid change from a glutamine to a proline at amino acid residue 105 was detected compared to the wild-type HSV-333 strain. These results indicate that an amino acid change in the NH2 portion of the TK protein is associated with a full-length peptide with decreased enzyme activity but the virus retains neuropathic virulence. © 1991.
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收藏
页码:793 / 797
页数:5
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