Cargando…
Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone
Epidemic and pandemic clones of bacterial pathogens with distinct characteristics continually emerge, replacing those previously dominant through mechanisms that remain poorly characterized. Here, whole-genome-sequencing-powered epidemiology linked horizontal transfer of a virulence gene, sopE, to t...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725340/ https://www.ncbi.nlm.nih.gov/pubmed/33112226 http://dx.doi.org/10.1099/mgen.0.000456 |
_version_ | 1783620686273576960 |
---|---|
author | Tassinari, Eleonora Bawn, Matt Thilliez, Gaetan Charity, Oliver Acton, Luke Kirkwood, Mark Petrovska, Liljana Dallman, Timothy Burgess, Catherine M. Hall, Neil Duffy, Geraldine Kingsley, Robert A. |
author_facet | Tassinari, Eleonora Bawn, Matt Thilliez, Gaetan Charity, Oliver Acton, Luke Kirkwood, Mark Petrovska, Liljana Dallman, Timothy Burgess, Catherine M. Hall, Neil Duffy, Geraldine Kingsley, Robert A. |
author_sort | Tassinari, Eleonora |
collection | PubMed |
description | Epidemic and pandemic clones of bacterial pathogens with distinct characteristics continually emerge, replacing those previously dominant through mechanisms that remain poorly characterized. Here, whole-genome-sequencing-powered epidemiology linked horizontal transfer of a virulence gene, sopE, to the emergence and clonal expansion of a new epidemic Salmonella enterica serovar Typhimurium (S. Typhimurium) clone. The sopE gene is sporadically distributed within the genus Salmonella and rare in S . enterica Typhimurium lineages, but was acquired multiple times during clonal expansion of the currently dominant pandemic monophasic S. Typhimurium sequence type (ST) 34 clone. Ancestral state reconstruction and time-scaled phylogenetic analysis indicated that sopE was not present in the common ancestor of the epidemic clade, but later acquisition resulted in increased clonal expansion of sopE-containing clones that was temporally associated with emergence of the epidemic, consistent with increased fitness. The sopE gene was mainly associated with a temperate bacteriophage mTmV, but recombination with other bacteriophage and apparent horizontal gene transfer of the sopE gene cassette resulted in distribution among at least four mobile genetic elements within the monophasic S . enterica Typhimurium ST34 epidemic clade. The mTmV prophage lysogenic transfer to other S. enterica serovars in vitro was limited, but included the common pig-associated S . enterica Derby (S. Derby). This may explain mTmV in S. Derby co-circulating on farms with monophasic S. Typhimurium ST34, highlighting the potential for further transfer of the sopE virulence gene in nature. We conclude that whole-genome epidemiology pinpoints potential drivers of evolutionary and epidemiological dynamics during pathogen emergence, and identifies targets for subsequent research in epidemiology and bacterial pathogenesis. |
format | Online Article Text |
id | pubmed-7725340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77253402020-12-14 Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone Tassinari, Eleonora Bawn, Matt Thilliez, Gaetan Charity, Oliver Acton, Luke Kirkwood, Mark Petrovska, Liljana Dallman, Timothy Burgess, Catherine M. Hall, Neil Duffy, Geraldine Kingsley, Robert A. Microb Genom Research Article Epidemic and pandemic clones of bacterial pathogens with distinct characteristics continually emerge, replacing those previously dominant through mechanisms that remain poorly characterized. Here, whole-genome-sequencing-powered epidemiology linked horizontal transfer of a virulence gene, sopE, to the emergence and clonal expansion of a new epidemic Salmonella enterica serovar Typhimurium (S. Typhimurium) clone. The sopE gene is sporadically distributed within the genus Salmonella and rare in S . enterica Typhimurium lineages, but was acquired multiple times during clonal expansion of the currently dominant pandemic monophasic S. Typhimurium sequence type (ST) 34 clone. Ancestral state reconstruction and time-scaled phylogenetic analysis indicated that sopE was not present in the common ancestor of the epidemic clade, but later acquisition resulted in increased clonal expansion of sopE-containing clones that was temporally associated with emergence of the epidemic, consistent with increased fitness. The sopE gene was mainly associated with a temperate bacteriophage mTmV, but recombination with other bacteriophage and apparent horizontal gene transfer of the sopE gene cassette resulted in distribution among at least four mobile genetic elements within the monophasic S . enterica Typhimurium ST34 epidemic clade. The mTmV prophage lysogenic transfer to other S. enterica serovars in vitro was limited, but included the common pig-associated S . enterica Derby (S. Derby). This may explain mTmV in S. Derby co-circulating on farms with monophasic S. Typhimurium ST34, highlighting the potential for further transfer of the sopE virulence gene in nature. We conclude that whole-genome epidemiology pinpoints potential drivers of evolutionary and epidemiological dynamics during pathogen emergence, and identifies targets for subsequent research in epidemiology and bacterial pathogenesis. Microbiology Society 2020-10-28 /pmc/articles/PMC7725340/ /pubmed/33112226 http://dx.doi.org/10.1099/mgen.0.000456 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. |
spellingShingle | Research Article Tassinari, Eleonora Bawn, Matt Thilliez, Gaetan Charity, Oliver Acton, Luke Kirkwood, Mark Petrovska, Liljana Dallman, Timothy Burgess, Catherine M. Hall, Neil Duffy, Geraldine Kingsley, Robert A. Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title | Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title_full | Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title_fullStr | Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title_full_unstemmed | Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title_short | Whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic Salmonella enterica serovar Typhimurium clone |
title_sort | whole-genome epidemiology links phage-mediated acquisition of a virulence gene to the clonal expansion of a pandemic salmonella enterica serovar typhimurium clone |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725340/ https://www.ncbi.nlm.nih.gov/pubmed/33112226 http://dx.doi.org/10.1099/mgen.0.000456 |
work_keys_str_mv | AT tassinarieleonora wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT bawnmatt wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT thilliezgaetan wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT charityoliver wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT actonluke wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT kirkwoodmark wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT petrovskaliljana wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT dallmantimothy wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT burgesscatherinem wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT hallneil wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT duffygeraldine wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone AT kingsleyroberta wholegenomeepidemiologylinksphagemediatedacquisitionofavirulencegenetotheclonalexpansionofapandemicsalmonellaentericaserovartyphimuriumclone |