首页> 外文期刊>Journal of food protection >Molecular Serogrouping of Listeria monocytogenes from Brazil Using PCR
【24h】

Molecular Serogrouping of Listeria monocytogenes from Brazil Using PCR

机译:巴西单核细胞增生李斯特菌的分子血清学研究

获取原文
获取原文并翻译 | 示例
           

摘要

We assessed the serotype distribution of Listeria monocytogenes isolates from clinical, beef, and environment samples using two PCR-based protocols for serogrouping. A panel of 134 isolates (22 clinical samples, 79 samples of beef cuts, and 33 samples from the beef processing environment) were subjected to conventional serology and identified as serotypes 1/2a (n= 12), 1/2b (n = 21), 1/2c (n = 71), and 4b (n = 30). Isolates from clinical samples were predominantly serotype 4b, and the most prevalent serotype among the beef cut and environment samples was 1/2c. The protocol described by M. Doumith, C. Buchrieser, P. Glaser, C. Jacquet, and P. Martin (J. Clin. Microbiol. 42:3819-3822,2004) produced contradictory results for seven 1/2a isolates, which were positive for imolllS and had the profile Ilc (serotypes 1/2c and 3c). Fifteen serotype 4b isolates amplified the target lmo0737, with the atypical profile IVb variant 1. The results obtained with the protocol described by M. K. Borucki and D. R. Call (J. Clin. Microbiol. 41:5537-5540, 2003) were in full agreement with those of the conventional serology. We recommend using this multiplex PCR approach by adding one pair of the reported primers to the panel to reduce total effort by one PCR while maintaining specificity. We present additional recommendations to improve the efficiency and reproducibility of this serogrouping assay.
机译:我们使用两种基于PCR的方案进行血清分组,评估了临床,牛肉和环境样品中李斯特菌李斯特菌分离株的血清型分布。对一组134个分离株(22个临床样品,79个牛肉切块样品和33个来自牛肉加工环​​境的样品)进行常规血清学分析,并将其鉴定为血清型1 / 2a(n = 12),1 / 2b(n = 21) ),1 / 2c(n = 71)和4b(n = 30)。从临床样品中分离出的血清型主要为4b,在牛肉切块和环境样品中最常见的血清型为1 / 2c。 M. Doumith,C.Buchrieser,P.Glaser,C.Jacquet和P.Martin(J.Clin.Microbiol.42:3819-3822,2004)所描述的方案对七个1 / 2a分离株产生了矛盾的结果,其中对imolllS呈阳性,特征谱为Ilc(血清型1 / 2c和3c)。 15个血清型4b分离物扩增了具有非典型谱IVb变体1的目标lmo0737。使用MK Borucki和DR Call(J. Clin。Microbiol。41:5537-5540,2003)描述的方案获得的结果与那些常规血清学检查。我们建议使用这种多重PCR方法,在面板上添加一对报告的引物,以减少一次PCR的总工作量,同时保持特异性。我们提出了额外的建议,以提高这种血清分组测定的效率和可重复性。

著录项

  • 来源
    《Journal of food protection》 |2016年第1期|144-147|共4页
  • 作者单位

    Universidade Federal de Vicosa, Departamento de Veterindria, Vigosa, MG, Brazil;

    Fundacao Oswaldo Cruz, Instituto Oswaldo Cruz, Laboratorio de Zoonoses Bacterianas, Rio de Janeiro, RJ, Brazil;

    Fundacao Oswaldo Cruz, Instituto Oswaldo Cruz, Laboratorio de Zoonoses Bacterianas, Rio de Janeiro, RJ, Brazil;

    Universidade Federal de Vicosa, Departamento de Veterindria, Vigosa, MG, Brazil;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号