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通过限制性内切酶分析和DNA杂交鉴定两组副结核分枝杆菌菌株

Identification of two groups of Mycobacterium paratuberculosis strains by restriction endonuclease analysis and DNA hybridization.

作者信息

Collins D M, Gabric D M, de Lisle G W

机构信息

Central Animal Health Laboratory, Wallaceville Animal Research Centre, Upper Hutt, New Zealand.

出版信息

J Clin Microbiol. 1990 Jul;28(7):1591-6. doi: 10.1128/jcm.28.7.1591-1596.1990.

Abstract

Genomic DNA was prepared from four reference strains of Mycobacterium paratuberculosis and 46 isolates of this organism from New Zealand, Australia, Canada, and Norway and also from two mycobactin-dependent "wood pigeon" strains. The DNA was characterized by restriction endonuclease analysis, both with and without DNA hybridization, with a probe specific to a repetitive DNA sequence in M. paratuberculosis. Both techniques differentiated M. paratuberculosis strains into two groups, but DNA hybridization revealed more differences between strains within the larger group. All the strains from cattle and many strains from other animals belonged to this group. The second group of nine strains included the Faroe Islands strain, all New Zealand sheep strains, and one New Zealand goat strain. Primary isolation of strains belonging to this group was difficult to achieve. DNA from acid-fast organisms harvested directly from intestinal tissues of sheep with Johne's disease was shown to have restriction and hybridization patterns identical to those of DNA obtained from M. paratuberculosis isolates cultured from the same tissues. Two Norwegian goat strains and the wood pigeon strains did not hybridize to the M. paratuberculosis probe and had restriction patterns very different from those of other M. paratuberculosis strains. The wood pigeon strains had restriction patterns very similar to those of strains of Mycobacterium avium, indicating that they should be classified as that species. The presence of two distinct groups of M. paratuberculosis strains and their predominant distribution in different host animals may be significant in management of mixed-animal farming operations.

摘要

从四株副结核分枝杆菌参考菌株以及从新西兰、澳大利亚、加拿大和挪威分离得到的46株该菌中提取基因组DNA,还从两株依赖分枝杆菌素的“林鸽”菌株中提取了DNA。通过限制性内切酶分析对DNA进行特征鉴定,包括有DNA杂交和无DNA杂交两种情况,使用的探针是针对副结核分枝杆菌中一个重复DNA序列的特异性探针。两种技术都将副结核分枝杆菌菌株分为两组,但DNA杂交揭示了较大组内菌株之间更多的差异。所有来自牛的菌株以及许多来自其他动物的菌株都属于这一组。第二组的九株菌株包括法罗群岛菌株、所有新西兰绵羊菌株和一株新西兰山羊菌株。属于这一组的菌株很难进行初次分离。从患有副结核的绵羊肠道组织中直接收获的抗酸菌的DNA,其限制性和杂交模式与从同一组织培养的副结核分枝杆菌分离株获得的DNA相同。两株挪威山羊菌株和林鸽菌株与副结核分枝杆菌探针不杂交,其限制性模式与其他副结核分枝杆菌菌株非常不同。林鸽菌株的限制性模式与鸟分枝杆菌菌株非常相似,表明它们应归为该物种。副结核分枝杆菌菌株存在两个不同的组及其在不同宿主动物中的主要分布情况,这在混合养殖经营管理中可能具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ad8/267994/09c546ab5379/jcm00055-0113-a.jpg

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