Method to detect virulence gene rfbE of Escherichia coli O157:H7 in textiles

被引:0
作者
Li K. [1 ]
Zhang Z. [1 ]
Yu J. [1 ]
Lian S. [2 ]
Ding Y. [3 ]
Xie T. [4 ]
Fu K. [5 ]
Guo H. [1 ]
机构
[1] Zhengzhou Customs, Zhengzhou
[2] Shijiazhuang Customs, Shijiazhuang
[3] Nanjing Customs Industrial Products Testing Center, Nanjing
[4] Shenzhen Customs Industrial Products Testing Technology Center, Shenzhen
[5] Ningbo Institute of Inspection Science and Technology, Ningbo
来源
Fangzhi Xuebao/Journal of Textile Research | 2021年 / 42卷 / 10期
关键词
Escherichia coli O157:H7; Immunomagnetic bead; Real-time PCR; Textile; Virulence gene;
D O I
10.13475/j.fzxb.20201101207
中图分类号
学科分类号
摘要
In order to establish a sensitive, specific, rapid and efficient method to evaluate E. coli O157:H7 in textiles, the conservative rfb E sequence of E. coli O157:H7 was screened for the design of PCR specific primers and fluorescent double labeled probes. Combined with immunomagnetic beads technology, a new technology was developed for quick and efficient isolation of E. coli O157:H7 under the condition of low concentration and non-culturable target bacteria. A real-time fluorescent quantitative PCR method was developed, and the detection limit could reach 8 CFU/g. 30 positive samples were identified using this method, and the results were 100% consistent with the results from using the traditional methods. The results show that the new method is stable, rapid and sensitive in identifying E. coli O157:H7 in textiles. © 2021, Periodical Agency of Journal of Textile Research. All right reserved.
引用
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页码:92 / 98
页数:6
相关论文
共 19 条
[1]  
LEE Jae-Ik, KIM Sang-Soon, KANG Dong-Hyun, Susceptibility of Escherichia coli O157:H7 grown at low temperatures to the krypton-chlorine excilamp[J], Sci Rep, 9, 1, (2019)
[2]  
YANG G, WANG H, DONGY, Et al., High-throughput photoelectrochemical determination of E. coli O157:H7 by modulation of the anodic photoelectrochemistry of CdS quantum dots via reversible deposition of MnO<sub>2</sub> [J], Mikrochim Acta, 187, 1, pp. 20142-20147, (2019)
[3]  
LI B, LIU H, WANG W., Multiplex real-time PCR assay for detection of Escherichia coli O157:H7 and screening for non-O157 Shiga toxin-producing E.coli[J], BMC Microbial, 17, 1, (2017)
[4]  
PANG B, ZHAO C, LI L, Et al., Development of a low-cost paper-based ELSIA method for rapid Escherichia coli O157:H7 detection[J], Analytical Biochemistry, 542, 20, pp. 58-62, (2017)
[5]  
AL-NABULSI ANAS A, OLAIMAT AMIN N, OSAILI TAREQ M, Et al., Behavior of Escherichia coli O157:H7 and Listeria monocytogenes during fermentation and storage of camel yogurt[J], Journal of Dairy Science, 99, 3, pp. 1802-1811, (2016)
[6]  
LIU Qiyong, Epidemic profile of vector-borne diseases and vector controlstrategies in the new era, Chin J Vector Biol& Control, 30, 1, pp. 1-6, (2019)
[7]  
Global vector control response 2017-2030, (2017)
[8]  
YAN Jia, LI Gang, Research progress on medical textiles, Journal of Textile Research, 41, 9, pp. 191-200, (2020)
[9]  
O'TOOLE G, KAPLAN H B, KOLTER R., Biofilm formation as microbial development[J], Annual Review of Microbiology, 54, 1, pp. 49-79, (2000)
[10]  
GALIE S, GARCIA-GUTIERREZ C, MIGUELEZ E M, Et al., Biofilmsin the food industry: health aspects and control methods, Frontiersin Microbiology, 9, (2018)