Rosen B I, Saif L J, Jackwood D J, Gorziglia M
Food Animal Health Research Program, Agricultural Research and Development Center, Ohio State University, Wooster 44691.
J Clin Microbiol. 1990 Nov;28(11):2526-33. doi: 10.1128/jcm.28.11.2526-2533.1990.
The serotypic specificities of Gottfried and OSU porcine rotavirus gene 9 probes were investigated in a dot hybridization assay. The probes were reacted with homologous and heterologous serotypes of group A rotaviruses of human and animal origin. Hybridizations were conducted under relatively low-stringency (52 degrees C, no formamide, 5 x SSC) and high-stringency (52 degrees C, 50% formamide, formamide, 5 x SSC) conditions (1 x SSC is 0.15 M NaCl plus 0.015 M sodium citrate). Under conditions of relatively low stringency, the Gottfried and OSU gene 9 probes demonstrated broad cross-reactivity and were useful in the detection of homologous and heterologous serotypes of group A rotaviruses. Under conditions of relatively high stringency, the Gottfried and OSU gene 9 probes were serotype specific. The Gottfried gene 9 probe (serotype 4) hybridized with homologous Gottfried porcine rotavirus as well as the serotype 4 human rotaviruses ST3 and VA70. The OSU gene 9 probe (serotype 5) hybridized with homologous OSU porcine rotavirus and the serotype 5 equine rotavirus H1. Hybridization was not observed with the antigenically distinct group B and C porcine rotaviruses or with other porcine enteric viruses, including calicivirus and a coronavirus, transmissible gastroenteritis virus, regardless of stringency conditions. Analysis of 14 group A rotavirus-positive field samples resulted in the serotypic differentiation, collectively, of six serotype 4 or 5 porcine rotaviruses. No field samples reacted with both the Gottfried and OSU gene 9 probes.
在斑点杂交试验中研究了戈特弗里德(Gottfried)和俄亥俄州立大学(OSU)猪轮状病毒基因9探针的血清型特异性。这些探针与人源和动物源A组轮状病毒的同源和异源血清型进行反应。杂交在相对低严谨度(52℃,无甲酰胺,5×SSC)和高严谨度(52℃,50%甲酰胺,5×SSC)条件下进行(1×SSC为0.15M氯化钠加0.015M柠檬酸钠)。在相对低严谨度条件下,戈特弗里德和OSU基因9探针表现出广泛的交叉反应性,可用于检测A组轮状病毒的同源和异源血清型。在相对高严谨度条件下,戈特弗里德和OSU基因9探针具有血清型特异性。戈特弗里德基因9探针(血清型4)与同源的戈特弗里德猪轮状病毒以及血清型4人轮状病毒ST3和VA70杂交。OSU基因9探针(血清型5)与同源的OSU猪轮状病毒和血清型5马轮状病毒H1杂交。无论严谨度条件如何,均未观察到与抗原性不同的B组和C组猪轮状病毒或其他猪肠道病毒(包括杯状病毒和一种冠状病毒——传染性胃肠炎病毒)发生杂交。对14份A组轮状病毒阳性现场样本的分析共鉴定出6份血清型4或5的猪轮状病毒。没有现场样本与戈特弗里德和OSU基因9探针都发生反应。