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应用半巢式 IS900 聚合酶链反应检测老年屠宰牛回盲肠淋巴结中的鸟分枝杆菌副结核亚种。

Detection of Mycobacterium avium ssp. paratuberculosis in ileocaecal lymph nodes collected from elderly slaughter cows using a semi-nested IS900 polymerase chain reaction.

机构信息

Department of Animal Sciences, Institute of Veterinary Medicine, Division of Microbiology and Animal Hygiene, Faculty of Agricultural Sciences, Georg-August-University, Burckhardtweg 2, D-37077 Göttingen, Germany.

出版信息

Vet Microbiol. 2011 Dec 29;154(1-2):197-201. doi: 10.1016/j.vetmic.2011.06.033. Epub 2011 Jul 2.

Abstract

The aim of this study was to investigate the occurrence of subclinical Mycobacterium avium spp. paratuberculosis (MAP) infections at slaughter by testing ileocaecal lymph nodes with a semi-nested IS900 PCR. Tissue samples were available within the framework of a parallel study investigating BSE-susceptibility factors in members of BSE-cohorts in the German Federal State of Lower Saxony. Ileocaecal lymph nodes were collected over a 2-year sampling period from 99 slaughter cattle of a mean age of 6.5 years (5.5-7.5 years). A recently developed IS900 semi-nested polymerase chain reaction (snPCR) assay offering a sensitivity of 1 genome equivalent was used for the detection of MAP-DNA. Based on this snPCR, 17 out of the 99 samples gave positive results, indicating a MAP occurrence of 17.17% in the random sample. All PCR products were sequenced for screening of polymorphisms. Nucleotide homologies of 98.5-100% were found with respect to the MAP K10 reference sequence IS900 (GenBank: AE16958). PCR analysis of ileocaecal lymph nodes collected from slaughter cattle proved to be a suitable technique to determine MAP occurrence in the local cattle population.

摘要

本研究旨在通过检测回肠结肠淋巴结的半巢式 IS900 PCR 来调查屠宰时潜伏性禽分枝杆菌副结核病(MAP)感染的发生情况。在德国下萨克森州 BSE 队列成员中调查 BSE 易感性因素的平行研究框架内,可以获得组织样本。在为期 2 年的采样期间,从 99 头平均年龄为 6.5 岁(5.5-7.5 岁)的屠宰牛中收集回肠结肠淋巴结。使用最近开发的具有 1 个基因组当量灵敏度的 IS900 半巢式聚合酶链反应(snPCR)检测方法用于检测 MAP-DNA。基于此 snPCR,99 个样本中有 17 个呈阳性结果,表明随机样本中的 MAP 发生率为 17.17%。所有 PCR 产物均进行测序以筛选多态性。与 MAP K10 参考序列 IS900(GenBank:AE16958)相比,发现核苷酸同源性为 98.5-100%。从屠宰牛收集的回肠结肠淋巴结的 PCR 分析被证明是一种确定当地牛群中 MAP 发生情况的合适技术。

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