4.7 Article

Identification of Salmonella enterica Typhimurium and variants using a novel multiplex PCR assay

期刊

FOOD CONTROL
卷 65, 期 -, 页码 152-159

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.foodcont.2016.01.015

关键词

Salmonella Typhimurium; Variant; MLST; Antibiotic resistance; Multiplex PCR

资金

  1. National Natural Science Foundation of China [31471638]
  2. General Administration of Quality Supervision [2014IK123]
  3. Fundamental Research Funds for the Central Universities [Z109021426]

向作者/读者索取更多资源

Salmonella Typhimurium is one of the most common Salmonella serovars and possesses many variants. The detection of this pathogen and its variants is imperative to trace the source of infection, to explore the transmission, and to prevent the spread of disease. A PCR assay was used and primers were designed against the gene STM4495 specific for S. Typhimurium, and oafA, fliC, and fljB encoding the 05, H1 and H2 antigens of S. Typhimurium. A novel multiplex PCR method was developed to detect S. Typhimurium and its variants, including Copenhagen, 1,4,12:-:1,2, 1,4,[51],12:i:- and 1,4,5,12:-:-. The detection limit of this method was found to be as low as 1.1pg/PCR for S. Typhimurium DNA template. S. Typhimurium and its variants were detected rapidly and accurately. Of 2350 isolates, 294 strains of S. Typhimurium, 13 strains of 1,4,[5],12:i:- and 1 strain of Copenhagen variant, were identified, consistent with serological testing. Thus, this multiplex PCR assay complements the serological method and enhances detection accuracy. All 1,4,[5],12:i:-strains were identified as ST34 by MLST analysis, which carried multidrug resistances. The expansion of multidrug-resistant S. Typhimurium variant strains must be controlled to limit further transmission from animal food to humans. (C) 2016 Elsevier Ltd. All rights reserved.

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