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机构地区:[1]解放军第306医院皮肤科,北京100101 [2]第四军医大学微生物学教研室,陕西西安710032
出 处:《中国皮肤性病学杂志》2010年第3期219-220,共2页The Chinese Journal of Dermatovenereology
基 金:首都医学发展科研基金资助项目(2005-3090)
摘 要:目的应用空斑抑制试验测定单纯疱疹病毒2型(HSV-2)药物敏感性,并建立体外耐药病毒株。方法将HSV-2接种于乳兔肾细胞中,加入不同浓度的阿昔洛韦(ACV),培养72h后固定、染色、清点空斑数并计算药物的半数抑制浓度(IC50),通过IC50来判断HSV-2的药物敏感性。将HSV-2在含ACV环境中连续培养9代,分别在第3,6和9代测定其IC50。结果ACV对HSV-2标准株Sav毒株的IC50为1.1μg/mL。HSV-2在含ACV的环境中连续培养3代后即产生了耐药性,第3,6和9代的IC50分别为8.4μg/mL,56.9μg/mL和121.3μg/mL。结论空斑抑制试验是测定病毒药物敏感性的有效、实用的方法,建立的体外耐药病毒株可用于HSV-2的耐药性研究。Objective To develop the method for measuring antiviral susceptibility and to establish an acyclovir(ACV) resistant herpes simplex virus type 2 (HSV-2). Methods Baby hamster kidney cells were inoculated with HSV-2, and ACV was added to the medium in various concentrations. After 72 hours incubation, plaques were counted and the 50% inhibiting concentration(IC50 )was calculated. HSV-2 was incubated in the presence of ACV for 9 passages. The IC50 of ACV was determined after the 3rd, 6th and 9th passage. Results The IC50 of ACV to HSV-2 Say was 1. 1μg/mL. In the presence of ACV, emergence of drug resistance was observed after passage 3 ; the IC50 of ACV after the 3rd, 6th and 9th passage was 8.41μg/mL,56. 9μg/mL and 121.3μg/mL respectively. Conclusion Plaque reduction assay is an efficient method for determination of antiviral drug sus- ceptibility of HSV and the establishment of ACV-resistant strain is essential for the study of resistance.
关 键 词:单纯疱疹病毒2型 耐药性 阿昔洛韦 空斑抑制试验
分 类 号:R373[医药卫生—病原生物学]
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