Distribution of heavy metal resistance elements in Canadian Salmonella 4,[5],12:i:- populations and association with the monophasic genotypes and phenotype
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...
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Published in | PloS one Vol. 15; no. 7; p. e0236436 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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27.07.2020
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Abstract | 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. |
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AbstractList | 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. 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. |
Audience | Academic |
Author | Landgraff, Chrystal Johnson, Roger Gannon, Victor P. J. Pollari, Frank Clark, Clifford G. Nadon, Celine Robertson, James Parker, Stephen Nash, John |
AuthorAffiliation | 4 PulseNet Canada, Public Health Agency of Canada, Winnipeg, Manitoba, Canada New York State Department of Health, UNITED STATES 3 FoodNet Canada, Public Health Agency of Canada, Guelph, Ontario, Canada 1 National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada 2 Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Guelph, Ontario, Canada 5 Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Lethbridge, Canada |
AuthorAffiliation_xml | – name: New York State Department of Health, UNITED STATES – name: 4 PulseNet Canada, Public Health Agency of Canada, Winnipeg, Manitoba, Canada – name: 5 Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Lethbridge, Canada – name: 3 FoodNet Canada, Public Health Agency of Canada, Guelph, Ontario, Canada – name: 2 Division of Enteric Diseases, National Microbiology Laboratory, Public Health Agency of Canada, Guelph, Ontario, Canada – name: 1 National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada |
Author_xml | – sequence: 1 givenname: Clifford G. orcidid: 0000-0003-0566-1468 surname: Clark fullname: Clark, Clifford G. – sequence: 2 givenname: Chrystal surname: Landgraff fullname: Landgraff, Chrystal – sequence: 3 givenname: James surname: Robertson fullname: Robertson, James – sequence: 4 givenname: Frank surname: Pollari fullname: Pollari, Frank – sequence: 5 givenname: Stephen surname: Parker fullname: Parker, Stephen – sequence: 6 givenname: Celine surname: Nadon fullname: Nadon, Celine – sequence: 7 givenname: Victor P. J. surname: Gannon fullname: Gannon, Victor P. J. – sequence: 8 givenname: Roger surname: Johnson fullname: Johnson, Roger – sequence: 9 givenname: John orcidid: 0000-0003-2925-8710 surname: Nash fullname: Nash, John |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32716946$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_celrep_2023_113227 crossref_primary_10_3390_antibiotics12030547 crossref_primary_10_1186_s12864_022_08458_z crossref_primary_10_3389_fmicb_2022_983083 crossref_primary_10_1080_1040841X_2021_1991271 crossref_primary_10_3390_antibiotics11060786 crossref_primary_10_3389_fmicb_2021_735364 crossref_primary_10_3389_fsufs_2021_725791 crossref_primary_10_3390_antibiotics10020185 crossref_primary_10_1371_journal_pone_0249079 crossref_primary_10_3389_fvets_2023_1186554 crossref_primary_10_1186_s13567_023_01143_3 crossref_primary_10_3390_antibiotics13040314 crossref_primary_10_1016_j_chemosphere_2021_132373 |
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Copyright | COPYRIGHT 2020 Public Library of Science 2020 Clark et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2020 Clark et al 2020 Clark et al |
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Snippet | 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... Salmonella 4,[5],12:i:- are monophasic S . Typhimurium variants incapable of producing the second-phase flagellar antigen. They have emerged since the... |
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SubjectTerms | Animals Antibiotic resistance Antibiotics Antigens Antigens, Bacterial - genetics Antimicrobial agents Antimicrobial resistance Base Sequence Biology and Life Sciences Canada Cloning Copper Data acquisition Deoxyribonucleic acid DNA Drug resistance Epidemics Flagella Genes Genetic aspects Genetic Variation Genome, Bacterial Genomes Genotype Genotype & phenotype Genotypes Health aspects Heavy metals Humans Insertion Interspersed Repetitive Sequences - genetics Laboratories Loci Medicine and Health Sciences Mercury Mercury (metal) Metals, Heavy - toxicity Mutation Outbreaks Phenotype Phenotypes Phylogeny Physiological aspects Plasmids Plasmids - genetics Public health Research and Analysis Methods Salmonella Salmonella typhimurium - drug effects Salmonella typhimurium - genetics Salmonella typhimurium - isolation & purification Serotypes Silver Swine Synteny - genetics |
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Title | Distribution of heavy metal resistance elements in Canadian Salmonella 4,[5],12:i:- populations and association with the monophasic genotypes and phenotype |
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