Kidd A H, Harley E H, Erasmus M J
J Clin Microbiol. 1985 Dec;22(6):934-9. doi: 10.1128/jcm.22.6.934-939.1985.
A dot-blot hybridization test was developed which allowed the direct detection of fastidious enteric adenovirus DNA in stool specimens from children with diarrhea and simultaneous typing of the viruses as adenovirus type 40 (Ad40) or Ad41. Cloned PstI fragments of Ad40 and Ad41 were used as 32P-labeled probes in the test, which allowed detection of picogram quantities of viral DNA in 20 to 40 microliter of stool suspension. Results were obtained within 48 h. The type specificity of the test was evaluated with 76 specimens known to contain either Ad40 or Ad41 by restriction enzyme analysis. Sixty-one specimens had sufficient DNA to be detected without any removal of protein. Thirty-one adenoviruses were typed as Ad40, and 30 were typed as Ad41, giving 100% correlation with the results of restriction enzyme analysis. The other 15 specimens were detected and typed as Ad40 or Ad41 only after removal of protein by a phenol extraction method. The dot-blot hybridization method is particularly useful for identifying those Ad40 and Ad41 strains which defy all attempts at culture and will be a useful tool in the epidemiology of fastidious enteric adenovirus infections.
开发了一种斑点杂交试验,可直接检测腹泻患儿粪便标本中难培养的肠道腺病毒DNA,并同时将病毒鉴定为腺病毒40型(Ad40)或腺病毒41型(Ad41)。Ad40和Ad41的克隆PstI片段用作该试验中的32P标记探针,该试验可在20至40微升粪便悬液中检测到皮克量的病毒DNA。48小时内可获得结果。通过限制性酶切分析,用76份已知含有Ad40或Ad41的标本评估了该试验的型特异性。61份标本有足够的DNA,无需去除任何蛋白质即可被检测到。31株腺病毒被鉴定为Ad40型,30株被鉴定为Ad41型,与限制性酶切分析结果的相关性为100%。另外15份标本仅在通过酚抽提法去除蛋白质后才被检测并鉴定为Ad40或Ad41型。斑点杂交法对于鉴定那些无法培养的Ad40和Ad41毒株特别有用,将成为难培养肠道腺病毒感染流行病学研究的有用工具。