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用病毒基因组片段的克隆cDNA拷贝诊断轮状病毒感染

Diagnosis of rotavirus infection with cloned cDNA copies of viral genome segments.

作者信息

Lin M, Imai M, Bellamy A R, Ikegami N, Furuichi Y, Summers D, Nuss D L, Deibel R

出版信息

J Virol. 1985 Aug;55(2):509-12. doi: 10.1128/JVI.55.2.509-512.1985.

Abstract

The diagnostic potential of cloned cDNA copies of human rotavirus (strain WA) genome segments for the detection of rotavirus in clinical specimens has been determined. A hybridization assay in which a mixture of 32P-labeled cDNAs representing the 11 rotavirus segments was used as a probe compared favorably with three frequently used diagnostic tests for rotavirus in terms of both specificity and sensitivity. Significantly, clinical isolates could be readily distinguished when cloned cDNA copies of individual genome segments were used independently as a probe. In assays in which genome RNA from rotaviruses of known subgroups and serotypes were tested, cloned probes that encode nonstructural viral proteins hybridized efficiently to genome RNAs of all strains, whereas cloned probes corresponding to genome segments 6 and 9 exhibited the potential for differentiating strains of different subgroups and serotypes. Cloned cDNA copies of rotavirus genome segments therefore offer considerable potential for improved general diagnosis of rotavirus in clinical specimens, as well as for epidemiological studies in which virus isolates can be distinguished on the basis of nucleotide sequence homology of individual genome segments.

摘要

已确定人轮状病毒(WA株)基因组片段的克隆cDNA拷贝在临床标本中检测轮状病毒的诊断潜力。一种杂交试验,其中使用代表11个轮状病毒片段的32P标记cDNA混合物作为探针,在特异性和敏感性方面与三种常用的轮状病毒诊断试验相比具有优势。值得注意的是,当单独使用各个基因组片段的克隆cDNA拷贝作为探针时,可以很容易地区分临床分离株。在对已知亚组和血清型的轮状病毒基因组RNA进行检测的试验中,编码病毒非结构蛋白的克隆探针能有效地与所有毒株的基因组RNA杂交,而与基因组片段6和9对应的克隆探针显示出区分不同亚组和血清型毒株的潜力。因此,轮状病毒基因组片段的克隆cDNA拷贝在改进临床标本中轮状病毒的一般诊断以及在病毒分离株可根据各个基因组片段的核苷酸序列同源性进行区分的流行病学研究方面具有相当大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68c2/254963/9a58139870fe/jvirol00119-0264-a.jpg

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