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首页> 外文期刊>Journal of Medical Virology >Nucleotide sequence of thymidine kinase gene of sequential acyclovir-resistant herpes simplex virus type 1 isolates recovered from a child with Wiskott-Aldrich syndrome: evidence for reactivation of acyclovir-resistant herpes simplex virus.
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Nucleotide sequence of thymidine kinase gene of sequential acyclovir-resistant herpes simplex virus type 1 isolates recovered from a child with Wiskott-Aldrich syndrome: evidence for reactivation of acyclovir-resistant herpes simplex virus.

机译:从一名患有Wiskott-Aldrich综合征的儿童中回收的连续1代无阿昔洛韦耐药的单纯疱疹病毒1型胸腺嘧啶核苷激酶基因的核苷酸序列:重新激活无阿昔洛韦耐药的单纯疱疹病毒的证据。

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摘要

Recurrent acyclovir (ACV)-resistant (ACV-r) herpes simplex virus type 1 (HSV-1) infections occurred in a patient with Wiskott-Aldrich syndrome, an X-linked recessive immunodeficiency syndrome composed of three clinical characteristics of immunodeficiency, thrombocytopenia, and an eczematous dermatitis. The patient had severe and recurrent ACV-r herpes simplex and was treated with vidarabine in a satisfactory manner from 1993 to 1997. During the 4-year observation period, two ACV-sensitive (ACV-s) HSV-1 isolates and five ACV-r HSV-1 isolates were recovered. The nucleotide sequence of the thymidine kinase (TK) gene from these sequential ACV-r isolates was compared with the ACV-s isolates. A single nucleotide deletion of cytosine (C) from homopolymer stretch of four C residues between nucleotide 1061 and 1064 of the open reading frame was found in all ACV-r isolates. No other differences were observed in the TK nucleotide sequence between ACV-s and ACV-r isolates. The TK nucleotide sequences of the two ACV-s isolates were identical to each other and those of the five ACV-r isolates were identical to one another. These results suggest that the ACV-r HSV-1 might have derived from the ACV-s strain in the patient body and that TK-associated ACV-r HSV-1 can reactivate from latency.
机译:患有Wiskott-Aldrich综合征(一种X连锁隐性免疫缺陷综合征,由免疫缺陷,血小板减少症,血吸虫病的三种临床特征组成)的复发性无环阿昔洛韦(ACV)(ACV-r)型疱疹病毒1型(HSV-1)感染和湿疹性皮炎。该患者患有严重且反复发作的ACV-r单纯疱疹,并于1993年至1997年间接受了维达拉滨的满意治疗。在4年的观察期内,分离了2例ACV敏感(ACV-s)HSV-1分离株和5例ACV- r HSV-1分离株被回收。将来自这些顺序的ACV-r分离株的胸苷激酶(TK)基因的核苷酸序列与ACV-s分离株进行了比较。在所有ACV-r分离物中都发现了开放阅读框核苷酸1061和1064之间四个C残基的均聚物延伸中胞嘧啶(C)的单核苷酸缺失。在ACV-s和ACV-r分离株之间的TK核苷酸序列中未观察到其他差异。两个ACV-分离株的TK核苷酸序列彼此相同,并且五个ACV-r分离株的TK核苷酸序列彼此相同。这些结果表明,ACV-r HSV-1可能源自患者体内的ACV-s株,并且与TK相关的ACV-r HSV-1可以从潜伏期重新激活。

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