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Abstract
Salmonella is a prevalent zoonotic foodborne pathogen. Swine and pork are implicated as important sources of salmonellosis in humans. In Chiang Mai and Lamphun Provinces in northern Thailand, there has been a high prevalence of Salmonella persistence for over a decade. Infection is usually with dominant S. enterica serotypes, including serotypes Rissen and 1,4,[5],12:i:-. However, other serotypes also contribute to disease but are less well characterized. The whole genome sequencing data of 43 S. enterica serotypes isolated from pork production chain through 2011–2014, were used to evaluate genetic diversity and ascertain the possible source of Salmonella contamination based on Core Genome Multilocus Sequence Typing (cgMLST) approach. The Salmonella serotypes recovered from farms and slaughterhouses were re-circulating by swine environmental contamination. Conversely, the Salmonella contamination in the retail market represents cross-contamination from multiple sources, including contaminated foodstuffs. Salmonella contamination in the pork production chain has the competency for host cell adhesion, host cell invasion, and intracellular survival, which is enough for the pathogenicity of salmonellosis. In addition, all of these isolates were multi-drug resistant Salmonella, which contained at least 10 antimicrobial resistance genes. This result indicated that these S. enterica serotypes also pose a significant public health risk. Our findings support the need for appropriate surveillance of food-animal products going to market to reduce public exposure to highly pathogenic, multi-drug resistant Salmonella. Acquiring information would motivate all stakeholders to reinforce sanitation standards throughout the pork production chain in order to eradicate Salmonella contamination and reduce the risk of salmonellosis in humans.
Original language | English |
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Article number | 968695 |
Journal | Frontiers in Microbiology |
Early online date | 25 Aug 2022 |
DOIs | |
Publication status | Published - 25 Aug 2022 |
Funding
This research project was supported by National Research Council of Thailand (NRCT): NRCT5-RGJ63004-073. BP was funded by the Medical Research Council (MR/V001213/1) and National Institutes of Health (1R01AI158576-01). All high-performance computing was performed on MRC CLIMB (supported by MRC grants MR/L015080/1 and MR/T030062/1).
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- 1 Finished
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Genomic Epidemiology and Transmission of Campylobacter in Africa
Sheppard, S. (PI), Pascoe, B. (CoI) & Bayliss, S. (Researcher)
5/11/21 → 31/08/22
Project: Research council