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Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms
Salmonella Typhimurium and its monophasic variant S. 4,[5],12:i:- are the dominant serotypes associated with pigs in many countries. We investigated their population structure on nine farms using whole genome sequencing, and their genotypic and phenotypic variation. The population structure revealed...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586642/ https://www.ncbi.nlm.nih.gov/pubmed/31222015 http://dx.doi.org/10.1038/s41598-019-45216-w |
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author | Tassinari, Eleonora Duffy, Geraldine Bawn, Matt Burgess, Catherine M. McCabe, Evonne M. Lawlor, Peadar G. Gardiner, Gillian Kingsley, Robert A. |
author_facet | Tassinari, Eleonora Duffy, Geraldine Bawn, Matt Burgess, Catherine M. McCabe, Evonne M. Lawlor, Peadar G. Gardiner, Gillian Kingsley, Robert A. |
author_sort | Tassinari, Eleonora |
collection | PubMed |
description | Salmonella Typhimurium and its monophasic variant S. 4,[5],12:i:- are the dominant serotypes associated with pigs in many countries. We investigated their population structure on nine farms using whole genome sequencing, and their genotypic and phenotypic variation. The population structure revealed the presence of phylogenetically distinct clades consisting of closely related clones of S. Typhimurium or S. 4,[5],12:i:- on each pig farm, that persisted between production cycles. All the S. 4,[5],12:i:- strains carried the Salmonella genomic island-4 (SGI-4), which confers resistance to heavy metals, and half of the strains contained the mTmV prophage, harbouring the sopE virulence gene. Most clonal groups were highly drug resistant due to the presence of multiple antimicrobial resistance (AMR) genes, and two clades exhibited evidence of recent on-farm plasmid-mediated acquisition of additional AMR genes, including an IncHI2 plasmid. Biofilm formation was highly variable but had a strong phylogenetic signature. Strains capable of forming biofilm with the greatest biomass were from the S. 4,[5],12:i:- and S. Typhimurium DT104 clades, the two dominant pandemic clones found over the last 25 years. On-farm microevolution resulted in enhanced biofilm formation in subsequent production cycle. |
format | Online Article Text |
id | pubmed-6586642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65866422019-06-26 Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms Tassinari, Eleonora Duffy, Geraldine Bawn, Matt Burgess, Catherine M. McCabe, Evonne M. Lawlor, Peadar G. Gardiner, Gillian Kingsley, Robert A. Sci Rep Article Salmonella Typhimurium and its monophasic variant S. 4,[5],12:i:- are the dominant serotypes associated with pigs in many countries. We investigated their population structure on nine farms using whole genome sequencing, and their genotypic and phenotypic variation. The population structure revealed the presence of phylogenetically distinct clades consisting of closely related clones of S. Typhimurium or S. 4,[5],12:i:- on each pig farm, that persisted between production cycles. All the S. 4,[5],12:i:- strains carried the Salmonella genomic island-4 (SGI-4), which confers resistance to heavy metals, and half of the strains contained the mTmV prophage, harbouring the sopE virulence gene. Most clonal groups were highly drug resistant due to the presence of multiple antimicrobial resistance (AMR) genes, and two clades exhibited evidence of recent on-farm plasmid-mediated acquisition of additional AMR genes, including an IncHI2 plasmid. Biofilm formation was highly variable but had a strong phylogenetic signature. Strains capable of forming biofilm with the greatest biomass were from the S. 4,[5],12:i:- and S. Typhimurium DT104 clades, the two dominant pandemic clones found over the last 25 years. On-farm microevolution resulted in enhanced biofilm formation in subsequent production cycle. Nature Publishing Group UK 2019-06-20 /pmc/articles/PMC6586642/ /pubmed/31222015 http://dx.doi.org/10.1038/s41598-019-45216-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tassinari, Eleonora Duffy, Geraldine Bawn, Matt Burgess, Catherine M. McCabe, Evonne M. Lawlor, Peadar G. Gardiner, Gillian Kingsley, Robert A. Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title | Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title_full | Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title_fullStr | Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title_full_unstemmed | Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title_short | Microevolution of antimicrobial resistance and biofilm formation of Salmonella Typhimurium during persistence on pig farms |
title_sort | microevolution of antimicrobial resistance and biofilm formation of salmonella typhimurium during persistence on pig farms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586642/ https://www.ncbi.nlm.nih.gov/pubmed/31222015 http://dx.doi.org/10.1038/s41598-019-45216-w |
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