Cargando…

Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States

Microbes frequently encounter heavy metals and other toxic compounds generated from natural biogeochemical processes and anthropogenic activities. Here, we analyzed the prevalence and association of genes conferring resistance to heavy metals, biocides, and antimicrobial compounds in 394 genome sequ...

Descripción completa

Detalles Bibliográficos
Autores principales: Souza, Stephanie S. R., Turcotte, Madison R., Li, Jinfeng, Zhang, Xinglu, Wolfe, Kristin L., Gao, Fengxiang, Benton, Christopher S., Andam, Cheryl P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626534/
https://www.ncbi.nlm.nih.gov/pubmed/36338064
http://dx.doi.org/10.3389/fmicb.2022.983083
_version_ 1784822755334553600
author Souza, Stephanie S. R.
Turcotte, Madison R.
Li, Jinfeng
Zhang, Xinglu
Wolfe, Kristin L.
Gao, Fengxiang
Benton, Christopher S.
Andam, Cheryl P.
author_facet Souza, Stephanie S. R.
Turcotte, Madison R.
Li, Jinfeng
Zhang, Xinglu
Wolfe, Kristin L.
Gao, Fengxiang
Benton, Christopher S.
Andam, Cheryl P.
author_sort Souza, Stephanie S. R.
collection PubMed
description Microbes frequently encounter heavy metals and other toxic compounds generated from natural biogeochemical processes and anthropogenic activities. Here, we analyzed the prevalence and association of genes conferring resistance to heavy metals, biocides, and antimicrobial compounds in 394 genome sequences of clinical human-derived S. enterica from New Hampshire, USA. The most prevalent was the gold operon (gesABC-golTSB), which was present in 99.2% of the genomes. In contrast, the other five heavy metal operons (arsenic, copper, mercury, silver, tellurite) were present in 0.76% (3/394)–5.58% (22/394) of the total population. The heavy metal operons and three biocide resistance genes were differentially distributed across 15 sequence types (STs) and 16 serotypes. The number of heavy metal operons and biocide resistance genes per genome was significantly associated with high number of antimicrobial resistance (AMR) genes per genome. Notable is the mercury operon which exhibited significant association with genes conferring resistance to aminoglycosides, cephalosporins, diaminopyrimidine, sulfonamide, and fosfomycin. The mercury operon was co-located with the AMR genes aac(3)-IV, ant(3”)-IIa, aph(3’)-Ia, and aph(4)-Ia, CTX-M-65, dfrA14, sul1, and fosA3 genes within the same plasmid types. Lastly, we found evidence for negative selection of individual genes of each heavy metal operon and the biocide resistance genes (dN/dS < 1). Our study highlights the need for continued surveillance of S. enterica serotypes that carry those genes that confer resistance to heavy metals and biocides that are often associated with mobile AMR genes. The selective pressures imposed by heavy metals and biocides on S. enterica may contribute to the co-selection and spread of AMR in human infections.
format Online
Article
Text
id pubmed-9626534
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-96265342022-11-03 Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States Souza, Stephanie S. R. Turcotte, Madison R. Li, Jinfeng Zhang, Xinglu Wolfe, Kristin L. Gao, Fengxiang Benton, Christopher S. Andam, Cheryl P. Front Microbiol Microbiology Microbes frequently encounter heavy metals and other toxic compounds generated from natural biogeochemical processes and anthropogenic activities. Here, we analyzed the prevalence and association of genes conferring resistance to heavy metals, biocides, and antimicrobial compounds in 394 genome sequences of clinical human-derived S. enterica from New Hampshire, USA. The most prevalent was the gold operon (gesABC-golTSB), which was present in 99.2% of the genomes. In contrast, the other five heavy metal operons (arsenic, copper, mercury, silver, tellurite) were present in 0.76% (3/394)–5.58% (22/394) of the total population. The heavy metal operons and three biocide resistance genes were differentially distributed across 15 sequence types (STs) and 16 serotypes. The number of heavy metal operons and biocide resistance genes per genome was significantly associated with high number of antimicrobial resistance (AMR) genes per genome. Notable is the mercury operon which exhibited significant association with genes conferring resistance to aminoglycosides, cephalosporins, diaminopyrimidine, sulfonamide, and fosfomycin. The mercury operon was co-located with the AMR genes aac(3)-IV, ant(3”)-IIa, aph(3’)-Ia, and aph(4)-Ia, CTX-M-65, dfrA14, sul1, and fosA3 genes within the same plasmid types. Lastly, we found evidence for negative selection of individual genes of each heavy metal operon and the biocide resistance genes (dN/dS < 1). Our study highlights the need for continued surveillance of S. enterica serotypes that carry those genes that confer resistance to heavy metals and biocides that are often associated with mobile AMR genes. The selective pressures imposed by heavy metals and biocides on S. enterica may contribute to the co-selection and spread of AMR in human infections. Frontiers Media S.A. 2022-10-19 /pmc/articles/PMC9626534/ /pubmed/36338064 http://dx.doi.org/10.3389/fmicb.2022.983083 Text en Copyright © 2022 Souza, Turcotte, Li, Zhang, Wolfe, Gao, Benton and Andam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Souza, Stephanie S. R.
Turcotte, Madison R.
Li, Jinfeng
Zhang, Xinglu
Wolfe, Kristin L.
Gao, Fengxiang
Benton, Christopher S.
Andam, Cheryl P.
Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title_full Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title_fullStr Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title_full_unstemmed Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title_short Population analysis of heavy metal and biocide resistance genes in Salmonella enterica from human clinical cases in New Hampshire, United States
title_sort population analysis of heavy metal and biocide resistance genes in salmonella enterica from human clinical cases in new hampshire, united states
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9626534/
https://www.ncbi.nlm.nih.gov/pubmed/36338064
http://dx.doi.org/10.3389/fmicb.2022.983083
work_keys_str_mv AT souzastephaniesr populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT turcottemadisonr populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT lijinfeng populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT zhangxinglu populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT wolfekristinl populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT gaofengxiang populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT bentonchristophers populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates
AT andamcherylp populationanalysisofheavymetalandbiocideresistancegenesinsalmonellaentericafromhumanclinicalcasesinnewhampshireunitedstates