MLST Subtyping and Virulence Genes Detection of Food-borne Listeria monocytogenes Isolates in Shanghai

被引:0
|
作者
Cheng M. [1 ]
Wang W. [1 ]
Shi X. [1 ]
Shi C. [1 ]
机构
[1] School of Agriculture and Biology, Shanghai Jiao Tong University, MOST-USDA Joint Research Center for Food Safety and Bor Luh Food Safety Center, Shanghai
关键词
Listeria monocytogenes; Multilocus sequence typing (MLST); Virulence genes;
D O I
10.16429/j.1009-7848.2019.02.028
中图分类号
学科分类号
摘要
To study the subtype and virulent gene prevalence, a total of 86 Listeria monocytogens isolates from retailed foods during June, 2013 to June, 2014 were characterized. In total, 15 MLST sequence types(STs) were identified, among which 80.2% isolates belong to Lineage II (69/86), and the others belong to Lineage I. These isolates were also characterized for the carryings of 10 virulence genes (prfA, hly, plcA, plcB, actA, clpE, mpl, inlA, inlB, and iap) by PCR. It revealed that all the isolates carried the 10 virulence genes investigated in this study. These results indicate us that there is a big risk of Listeria monocytogens to food safety existed in retailed foods in Shanghai, which calls stronger efforts on its surveillance, prevention and control. © 2019, Editorial Office of Journal of CIFST. All right reserved.
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页码:223 / 229
页数:6
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共 18 条
  • [1] Farber J.F., Peterkin P.I., Listeria monocytogenes, a food-borne pathogen, Microbiol Rev, 55, 3, pp. 476-511, (1991)
  • [2] Swaminathan B., Gerner-Smidt P., The epidemiology of human listeriosis, Microbes & Infection, 9, 10, pp. 1236-1243, (2007)
  • [3] Orsi R.H., Den Bakker H.C., Wiedmann M., Listeria monocytogenes lineages: Genomics, evolution, ecology, and phenotypic characteristics, Int J Med Microbiol Rev, 301, 2, pp. 79-96, (2011)
  • [4] Ragon M., Wirth T., Hollandt F., Et al., A new perspective on Listeria monocytogenes evolution, PLoS Pathog, 4, 9, (2008)
  • [5] Cooray K.J., Nishibori T., Xiong H.B., Et al., Detection of multiple virulence-associated genes of Listeria monocytogenes by PCR in artificially contaminated milk sample, Appl Environ Microbiol, 60, 8, pp. 3023-3026, (1994)
  • [6] Volokhov D., Basooly A., Chumakov K., Et al., Identification of Listeria species by microarray-based assay, J Clin Microbiol, 40, 12, pp. 4720-4728, (2002)
  • [7] Zhou X.H., Jiao X.N., Wiedmann M., Listeria monocytogenes in the Chinese food system: strain characterization through partial actA sequencing and tissue-culture pathogenicity assays, J Med Microbiol, 54, pp. 217-224, (2005)
  • [8] Marquis H., Goldfine H., Portnoy D.A., Proteolytic pathways of activation and degradation of a bacterial phospholipase C during intracellular infection by Listeria monocytogenes, J Cell Biol, 137, 6, pp. 1381-1392, (1997)
  • [9] Handa-Miya S., Kimura B., Takahashi H., Et al., Nonsense-mutated inlA and prfA not widely distributed in Listeria monocytogenes isolates from ready-to-eat seafood products in Japan, Int J Food Microbiol, 117, 3, pp. 312-318, (2007)
  • [10] Ragon M., Wirth T., Hollandt F., Et al., A new perspective on Listeria monocytogenes evolution, PLoS Pathogens, 4, 9, (2008)