Distribution of heavy metal resistance elements in Canadian Salmonella 4,[5],12:i:- populations and association with the monophasic genotypes and phenotype.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 05 03 2020
accepted: 06 07 2020
entrez: 28 7 2020
pubmed: 28 7 2020
medline: 23 9 2020
Statut: epublish

Résumé

Salmonella 4,[5],12:i:- are monophasic S. Typhimurium variants incapable of producing the second-phase flagellar antigen. They have emerged since the mid-1990s to become one of the most prevalent Salmonella serotypes causing human disease world-wide. Multiple genetic events associated with different genetic elements can result in the monophasic phenotype. Several jurisdictions have reported the emergence of a Salmonella 4,[5],12:i:- clone with SGI-4 and a genetic element (MREL) encoding a mercury resistance operon and antibiotic resistance loci that disrupts the second phase antigen region near the iroB locus in the Salmonella genome. We have sequenced 810 human and animal Canadian Salmonella 4,[5],12:i:- isolates and determined that isolates with SGI-4 and the mercury resistance element (MREL; also known as RR1&RR2) constitute several global clades containing various proportions of Canadian, US, and European isolates. Detailed analysis of the data provides a clearer picture of how these heavy metal elements interact with bacteria within the Salmonella population to produce the monophasic phenotype. Insertion of the MREL near iroB is associated with several deletions and rearrangements of the adjacent flaAB hin region, which may be useful for defining human case clusters that could represent outbreaks. Plasmids carrying genes encoding silver, copper, mercury, and antimicrobial resistance appear to be derived from IS26 mediated acquisition of these genes from genomes carrying SGI-4 and the MREL. Animal isolates with the mercury and As/Cu/Ag resistance elements are strongly associated with porcine sources in Canada as has been shown previously for other jurisdictions. The data acquired in these investigations, as well as from the extensive literature on the subject, may aid source attribution in outbreaks of the organism and interventions to decrease the prevalence of this clone and reduce its impact on human disease.

Identifiants

pubmed: 32716946
doi: 10.1371/journal.pone.0236436
pii: PONE-D-20-06506
pmc: PMC7384650
doi:

Substances chimiques

Antigens, Bacterial 0
Metals, Heavy 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0236436

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Clifford G Clark (CG)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.

Chrystal Landgraff (C)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.

James Robertson (J)

Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Guelph, Ontario, Canada.

Frank Pollari (F)

FoodNet Canada, Public Health Agency of Canada, Guelph, Ontario, Canada.

Stephen Parker (S)

FoodNet Canada, Public Health Agency of Canada, Guelph, Ontario, Canada.

Celine Nadon (C)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
PulseNet Canada, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.

Victor P J Gannon (VPJ)

Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Lethbridge, Canada.

Roger Johnson (R)

Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Guelph, Ontario, Canada.

John Nash (J)

Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Guelph, Ontario, Canada.

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Classifications MeSH