Tebas P, Scholl D, Jollick J, McHarg K, Arens M, Olivo P D
Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110, USA.
J Infect Dis. 1998 Jan;177(1):217-20. doi: 10.1086/517357.
A rapid assay was developed to screen for herpes simplex virus (HSV) isolates that are resistant to acyclovir and other antiviral agents. The assay is a modified plaque reduction assay (PRA) in which the number of plaques seen in the absence of acyclovir was compared with that seen in the presence of a single cutoff concentration of acyclovir (2 microg/mL). This assay utilizes a cell line that expresses beta-galactosidase only after infection with HSV. Since histochemically stained plaques are easily visualized, small plaques can be easily enumerated. This allows the assay to be performed on dilutions of untitered specimens in the small wells of a 24-well plate and allows the results to be read only 2 days after inoculation of the virus. The assay performed well compared with a standard PRA and should be a valuable tool in identifying drug-resistant HSV in a timely manner.
已开发出一种快速检测方法,用于筛选对阿昔洛韦和其他抗病毒药物耐药的单纯疱疹病毒(HSV)分离株。该检测方法是一种改良的蚀斑减少试验(PRA),其中将在无阿昔洛韦情况下观察到的蚀斑数量与在单一临界浓度阿昔洛韦(2微克/毫升)存在时观察到的蚀斑数量进行比较。该检测方法利用一种仅在感染HSV后才表达β-半乳糖苷酶的细胞系。由于经组织化学染色的蚀斑易于观察,小蚀斑也能轻松计数。这使得该检测方法能够在24孔板的小孔中对未经滴定的标本稀释液进行检测,并能在接种病毒仅2天后读取结果。与标准PRA相比,该检测方法表现良好,应成为及时鉴定耐药HSV的有价值工具。