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中国防痨杂志 ›› 2014, Vol. 36 ›› Issue (6): 447-452.doi: 10.3969/j.issn.1000-6621.2014.06.008

• 论著 • 上一篇    下一篇

快速检测技术在奶牛结核病检测中的应用研究

江渊 王曲直 张阳奕 沈素芳 李静 唐文红 桂晓虹 梅建 潘启超 沈鑫   

  1. 200336 上海市疾病预防控制中心结核病防治科(江渊、张阳奕、李静、桂晓虹、梅建、沈鑫),中心办公室(潘启超);上海市动物疫病预防控制中心郊区动物防疫科(王曲直、沈素芳、唐文红)
  • 收稿日期:2014-04-11 出版日期:2014-06-10 发布日期:2014-06-28
  • 通信作者: 潘启超;沈鑫 E-mail:qcpan@scdc.sh.cn;xshen@scdc.sh.cn
  • 基金资助:

    上海市科技兴农推广项目[沪农科推字(2010)第1-2号];上海市卫生局科研课题(20114073);上海市卫生系统优秀青年人才培养计划(XYQ2011051)

Rapid detection of Mycobacterium bovis for the diagnosis of tuberculosis in dairy cattle

JIANG Yuan, WANG Qu-zhi, ZHANG Yang-yi, SHEN Su-fang, LI Jing, TANG Wen-hong, GUI Xiao-hong, MEI Jian, PAN Qi-chao, SHEN Xin   

  1. Department of Tuberculosis Prevention and Control, Shanghai Municipal Center for Disease Control and Prevention, Shanghai 200336, China
  • Received:2014-04-11 Online:2014-06-10 Published:2014-06-28
  • Contact: PAN Qi-chao;SHEN Xin E-mail:qcpan@scdc.sh.cn;xshen@scdc.sh.cn

摘要: 目的 评价快速检测技术在奶牛结核病检测中的应用,为改进奶牛结核病检疫工作提供实验室数据支持。 方法  2010—2012年对上海市5家奶牛场9355头奶牛采用牛分枝杆菌提纯结核菌素皮内超敏反应方法(PPD试验)进行牛结核病筛查,筛查出223头阳性牛,5家奶牛场分别采用随机数字表法抽取PPD阳性牛,共抽取PPD 阳性牛49头;无菌采集肺部淋巴结组织样本,采用MGIT 960液体培养法对奶牛组织中分枝杆菌进行快速分离培养,采用免疫色谱法和基因测序进行快速基因分型及菌种鉴定。 结果  49头PPD试验阳性牛的组织样本,经MGIT 960液体培养、免疫色谱法初筛、基因分型和基因序列分析,最终病原学检测证实受分枝杆菌感染的奶牛有8头,其中受牛分枝杆菌感染的奶牛1头,受非结核分枝杆菌感染的奶牛7头,分别为鸟分枝杆菌感染6头,不产色分枝杆菌感染1头。 结论  建议将分枝杆菌快速分离培养及菌种鉴定检测技术引入到对PPD阳性牛的实验室诊断中,进一步提高牛结核病检测的特异度。

关键词: 分枝杆菌, 牛, 结核, 牛/诊断, 结核菌素试验

Abstract: Objective To evaluate a rapid diagnosis of tuberculosis among dairy cattles using a MGIT 960 system, and to provide a laboratory data for improving dairy cattle tuberculosis quarantine. Methods  Nine thousand three hundred and fifty-five dairy cattles were detected by tuberculin-test (PPD) from 5 different dairy farms in Shanghai during 2010 to 2012, and 223 dairy cattles were detected as PPD (+). Among those 223 PPD (+) cattles, 49 cattles were selected randomly using the random number table. A total of 98 lung lymph node tissue specimens were collected from these 49 PPD (+) cattles. Culture and identification of Mycobacterium for the 98 lymph node tissue specimens were performed by MGIT 960 methods, chromatographic immunoassay, PCR-based genomic deletion analysis and DNA sequencing.  Results A total of 8 dairy cattles were diagnosed as Mycobacterium among which 1 cattle was identified as M.bovis, 6 cattles were identified as M.avium and 1 cattle was identified as M.nonchromogenicum.  Conclusion In order to improve the specificity of detection for bovine tuberculosis, we recommend that culture and species identification by using rapid detection techniques should be introduced into the laboratory diagnosis as a supplement for tuberculin-test.

Key words: Mycobacterium bovis, Tuberculosis, bovine/diagnosis, Tuberculin test