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使用种特异性寡核苷酸作为PCR引物检测结节拟杆菌。

Detection of Dichelobacter nodosus using species-specific oligonucleotides as PCR primers.

作者信息

La Fontaine S, Egerton J R, Rood J I

机构信息

Department of Microbiology, Monash University, Clayton, Vic., Australia.

出版信息

Vet Microbiol. 1993 May;35(1-2):101-17. doi: 10.1016/0378-1135(93)90119-r.

Abstract

Dichelobacter nodosus is an essential causative agent of ovine footrot, a disease of major economic significance. Four oligonucleotides complementary to variable regions of the 16S rRNA of D. nodosus were identified, synthesized and tested for their specificity and sensitivity as probes for the detection of D. nodosus. In hybridization reactions using total RNA as the target nucleic acid, three probes were found to be both sensitive and species-specific. When these probes were used as primers in PCR reactions, on both purified D. nodosus DNA and whole cells, the sensitivity of detection was increased by several orders of magnitude. Using PCR, it was possible to detect the presence of D. nodosus by direct examination of lesion material from footrot infected sheep.

摘要

结节拟杆菌是绵羊腐蹄病的重要病原体,该病具有重大经济意义。已鉴定、合成了与结节拟杆菌16S rRNA可变区互补的四条寡核苷酸,并测试了它们作为检测结节拟杆菌探针的特异性和敏感性。在以总RNA为靶核酸的杂交反应中,发现三条探针既敏感又具有种特异性。当这些探针用作PCR反应的引物时,无论是对纯化的结节拟杆菌DNA还是全细胞,检测灵敏度都提高了几个数量级。使用PCR,可以通过直接检测来自腐蹄病感染绵羊的病变材料来检测结节拟杆菌的存在。

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