Grankvist O, Juto P, Settergren B, Ahlm C, Bjermer L, Linderholm M, Tärnvik A, Wadell G
Department of Virology, University of Umeå, Sweden.
J Infect Dis. 1992 May;165(5):934-7. doi: 10.1093/infdis/165.5.934.
A nested primer-based polymerase chain reaction was constructed for the detection of Puumala virus RNA in patient samples. Puumala virus RNA was detected in cells from the urinary and the respiratory tracts and in peripheral blood mononuclear cells of patients with nephropathia epidemica. After inoculation with nephropathia epidemica patient material on Vero E6 cells and propagation for nine passages (4 months), Puumala virus RNA was detected at every passage. Hybridization under high-stringency conditions revealed that the overall nucleotide homology between the different patient isolates and the prototype strain (Puumala) is high. Using cDNA from Hällnäs B1 strain as a probe, hybridization occurred only under low-stringency conditions.
构建了一种基于巢式引物的聚合酶链反应,用于检测患者样本中的普马拉病毒RNA。在流行性肾病患者的泌尿生殖道和呼吸道细胞以及外周血单核细胞中检测到了普马拉病毒RNA。用流行性肾病患者材料接种Vero E6细胞并传代培养9代(4个月)后,每一代均检测到普马拉病毒RNA。高严格条件下的杂交显示,不同患者分离株与原型株(普马拉)之间的总体核苷酸同源性很高。以Hällnäs B1株的cDNA为探针,仅在低严格条件下发生杂交。