Rossier E, Scalia V, Phipps P H, Kennedy D A, Brodeur B
J Clin Microbiol. 1985 Mar;21(3):335-9. doi: 10.1128/jcm.21.3.335-339.1985.
A microcarrier culture system in combination with enzyme immunofiltration with a herpes simplex virus (HSV) group monoclonal antibody was found to be as sensitive as immunofluorescence for the detection of HSV type 1 (HSV-1) in cell cultures and to give specific identification at the same time as the appearance of the cytopathic effect with very high infectious inocula and within 10 to 24 h of the appearance of the cytopathic effect with very high infectious inocula and within 10 to 24 h of the appearance of the cytopathic effect with low to high inocula. Multiplicities of infection from 10(-5) to 10(1) were tested at 8 to 96 h postinfection. When applied to the identification of HSV-1 and HSV-2 in cultures of clinical samples, the system detected HSV antigens in 50% of the samples after 2 days and in 100% of the samples after 3 days. With 2 ml of microcarrier suspension and with 50 to 300 microliter per sample, several portions are available for replicate and sequential sampling without destroying the culture. The system requires only that 2 X 10(5) microcarriers be added to the culture tube at the time or before it is seeded with cells, at an extra cost of 6 cents (U.S.) per tube and little extra labor.
发现一种微载体培养系统与单纯疱疹病毒(HSV)群单克隆抗体的酶免疫过滤相结合,在细胞培养物中检测1型单纯疱疹病毒(HSV-1)时与免疫荧光一样灵敏,并且在接种高感染性接种物出现细胞病变效应时以及在接种低至高感染性接种物出现细胞病变效应后的10至24小时内可同时进行特异性鉴定。在感染后8至96小时测试了感染复数从10^(-5)到10^(1)的情况。当应用于临床样本培养物中HSV-1和HSV-2的鉴定时,该系统在2天后检测到50%的样本中的HSV抗原,在3天后检测到100%的样本中的HSV抗原。使用2毫升微载体悬浮液,每个样本50至300微升,无需破坏培养物即可获得多个部分用于重复和连续采样。该系统仅要求在接种细胞时或之前向培养管中加入2×10^(5)个微载体,每管额外成本为6美分(美国),且几乎不增加额外劳动力。