Literature DB >> 21333152

Comparison of reverse transcriptase PCR, reverse transcriptase loop-mediated isothermal amplification, and culture-based assays for Salmonella detection from pork processing environments.

Chayapa Techathuvanan1, Frances Ann Draughon, Doris Helen D'Souza.   

Abstract

Novel rapid Salmonella detection assays without the need for sophisticated equipment or labor remain in high demand. Real-time reverse transcriptase PCR (RT-PCR) assays, though rapid and sensitive, require expensive thermocyclers, while a novel RT loop-mediated isothermal amplification (RT-LAMP) method requires only a simple water bath. Our objective was to compare the detection sensitivity of Salmonella Typhimurium from the pork processing environment by RT-LAMP, RT-PCR, and culture-based assays. Carcass and surface swabs and carcass rinses were obtained from a local processing plant. Autoclaved carcass rinses (500 ml) were spiked with Salmonella Typhimurium and filtered. Filters were placed in stomacher bags containing tetrathionate broth (TTB) and analyzed with or without 10-h enrichment at 37 °C. Natural swabs were stomached with buffered peptone water, and natural carcass rinses were filtered, preenriched, and further enriched in TTB. Serially-diluted enriched samples were enumerated by spread plating on xylose lysine Tergitol 4 agar. RNA was extracted from 5 ml of enriched TTB with TRIzol. RT-LAMP assay using previously described invA primers was conducted at 62 °C for 90 min in a water bath with visual detection and by gel electrophoresis. SYBR Green I-based-real-time RT-PCR was carried out with invA primers followed by melt temperature analysis. The results of RT-LAMP detection for spiked carcass rinses were comparable to those of RT-PCR and cultural plating, with detection limits of 1 log CFU/ml, although they were obtained significantly faster, within 24 h including preenrichment and enrichment. RT-LAMP showed 4 of 12 rinse samples positive, while RT-PCR showed 1 of 12 rinse samples positive. For swabs, 6 of 27 samples positive by RT-LAMP and 5 of 27 by RT-PCR were obtained. This 1-day RT-LAMP assay shows promise for routine Salmonella screening by the pork industry.
Copyright ©, International Association for Food Protection

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Year:  2011        PMID: 21333152     DOI: 10.4315/0362-028X.JFP-10-306

Source DB:  PubMed          Journal:  J Food Prot        ISSN: 0362-028X            Impact factor:   2.077


  6 in total

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Authors:  Xinrui Lv; Weiwei Cao; Huang Zhang; Yilin Zhang; Lei Shi; Lei Ye
Journal:  Foods       Date:  2022-06-08

2.  Loop-mediated amplification accelerated by stem primers.

Authors:  Olga Gandelman; Rebecca Jackson; Guy Kiddle; Laurence Tisi
Journal:  Int J Mol Sci       Date:  2011-12-08       Impact factor: 5.923

3.  Evaluation of Two Loop-mediated Isothermal Amplification Methods for the Detection of Salmonella Enteritidis and Listeria Monocytogenes in Artificially Contaminated Ready-to-Eat Fresh Produce.

Authors:  Angeliki Birmpa; Konstantinos Kalogeropoulos; Petros Kokkinos; Apostolos Vantarakis
Journal:  Ital J Food Saf       Date:  2015-08-28

4.  Development of a Novel Quantum Dots and Graphene Oxide Based FRET Assay for Rapid Detection of invA Gene of Salmonella.

Authors:  Jiubiao Guo; Edward W C Chan; Sheng Chen; Zhenling Zeng
Journal:  Front Microbiol       Date:  2017-01-17       Impact factor: 5.640

5.  Development and Evaluation of the Rapid and Sensitive RPA Assays for Specific Detection of Salmonella spp. in Food Samples.

Authors:  Liwei Zhao; Jianchang Wang; Xiao Xia Sun; Jinfeng Wang; Zhimin Chen; Xiangdong Xu; Mengyuan Dong; Ya-Nan Guo; Yuanyuan Wang; Pingping Chen; Weijuan Gao; Yunyun Geng
Journal:  Front Cell Infect Microbiol       Date:  2021-02-25       Impact factor: 5.293

Review 6.  Loop-Mediated Isothermal Amplification for Salmonella Detection in Food and Feed: Current Applications and Future Directions.

Authors:  Qianru Yang; Kelly J Domesle; Beilei Ge
Journal:  Foodborne Pathog Dis       Date:  2018-06       Impact factor: 3.171

  6 in total

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