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[牛免疫缺陷病毒原病毒DNA在实验感染动物中的扩增]

[Amplification of proviral DNA of bovine immunodeficiency virus in experimentally infected animals].

作者信息

Lymans'ka O Iu, Rola M, Byka L, Kuzmak Ia, Volians'kyĭ Iu L, Puhach N B, Novikov S V, Lymans'kyĭ O P

出版信息

Mikrobiol Z. 2007 Jan-Feb;69(1):52-60.

Abstract

The primer set for detection of bovine immunodeficiency virus (BIV) proviral DNA, retrovirus of unknown pathology, by standard polymerase chain reaction was developed. Amplicon of the expected size was detected in DNA from peripheral blood mononuclear cells of seropositive experimentally BIV infected sheep and cattle. Primers targeted the short fragment of BIV pol gene. Sequences of BIV proviral DNA extracted from BIV infected cell culture as well as from experimentally infected cows were taken for targeted pol BI BPX gene locus. Problems of BIV detection from the clinical material of the experimentally and naturally infected animals are discussed.

摘要

开发了用于通过标准聚合酶链反应检测牛免疫缺陷病毒(BIV)前病毒DNA(一种病理不明的逆转录病毒)的引物组。在实验性感染BIV的血清阳性绵羊和牛的外周血单核细胞DNA中检测到预期大小的扩增子。引物靶向BIV pol基因的短片段。从BIV感染的细胞培养物以及实验感染的奶牛中提取的BIV前病毒DNA序列用于靶向pol BI BPX基因位点。讨论了从实验感染和自然感染动物的临床材料中检测BIV的问题。

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