The novel loop-mediated isothermal amplification based confirmation methodology on the bacteria in Viable but Non-Culturable (VBNC) state

被引:16
|
作者
Li, Yanmei [1 ]
Yang, Ling [2 ]
Fu, Jie [1 ]
Yan, Muxia [1 ]
Chen, Dingqiang [2 ]
Zhang, Li [1 ]
机构
[1] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Haematol, 9 Jinsui Rd, Guangzhou 510623, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Guangzhou Med Univ, Affiliated Hosp 1, Dept Lab Med, Guangzhou 510120, Guangdong, Peoples R China
关键词
LAMP; VBNC; Foodborne pathogens; RAPID DETECTION; VIBRIO-PARAHAEMOLYTICUS; ESCHERICHIA-COLI; BRETTANOMYCES-BRUXELLENSIS; NONCULTURABLE STATE; PROPIDIUM MONOAZIDE; PATHOGENIC FEATURES; SPOILAGE CAPABILITY; QUANTITATIVE PCR; SOUTHERN CHINA;
D O I
10.1016/j.micpath.2017.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As a self-protection mechanism, the viable but non-culturable (VBNC) state provides the ability against conventional detection methods among various foodborne pathogens. The ability of forming colonies is lost while metabolism is still maintaining in VBNC state cells. Recently, ethidium monoazide (EMA) and propidium monoazide (PMA) have been widely applied on the detection of foodborne pathogens in VBNC state. Combined with loop-mediated isothermal amplification (LAMP), the PMA/EMA-LAMP showed a significant priority in high sensitivity, specificity and rapidity over conventional PCR based assays. Particularly, PMA/EMA-LAMP has been proved as an effective method in the detection of Escherichia coli, Vibrio parahaemolyticus and Staphylococcus in VBNC state. Based on the current investigations, the VBNC mechanism and current detection method for VBNC-state foodborne pathogens were introduced and discussed in this review. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:280 / 284
页数:5
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