Baxter B D, Couch R B, Greenberg S B, Kasel J A
J Clin Microbiol. 1977 Jul;6(1):19-22. doi: 10.1128/jcm.6.1.19-22.1977.
A comparison of Hanks balanced salt solution, veal infusion broth (VIB), and charcoal viral transport medium for maintaining viability of type A influenza virus indicated approximately equal survival of virus on all three media at -70 and 4 degrees C, whereas at 25 degrees C virus survived best in VIB. VIB supplemented with bovine serum albumin was used as transport medium in a community-wide surveillance of febrile respiratory disease for influenza viruses. Unfrozen throat swab specimens were placed in VIB and stored at 4 degrees C for up to 5 days without effect on isolation frequencies of either type A or type B influenza virus or type 1 or type 3 parainfluenza virus. Comparison of indirect immunofluorescence with hemadsorption for detection of type A influenza virus in rhesus monkey kidney cultures revealed a requirement for at least five fluorescing cells to eliminate false positive indirect immunofluorescence tests and at least 3 days of incubation to eliminate false negative tests when compared with hemadsorption at later times. Detection frequencies for the two methods after 2 and 3 days of incubation were not significantly different.
对用于维持甲型流感病毒活力的汉克斯平衡盐溶液、犊牛浸出液肉汤(VIB)和活性炭病毒运输培养基进行比较,结果表明,在-70℃和4℃时,病毒在这三种培养基上的存活情况大致相同,而在25℃时,病毒在VIB中存活得最好。在一项针对流感病毒的社区范围发热呼吸道疾病监测中,添加了牛血清白蛋白的VIB被用作运输培养基。未冷冻的咽拭子标本置于VIB中,在4℃下保存长达5天,对甲型或乙型流感病毒以及1型或3型副流感病毒的分离频率均无影响。在恒河猴肾培养物中,比较间接免疫荧光法和血细胞吸附法检测甲型流感病毒的情况,结果显示,与后期的血细胞吸附法相比,间接免疫荧光检测至少需要5个荧光细胞才能消除假阳性检测结果,且至少需要3天的孵育时间才能消除假阴性检测结果。孵育2天和3天后,两种方法的检测频率无显著差异。