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Ecology and Function of the Transmissible Locus of Stress Tolerance in Escherichia coli and Plant-Associated Enterobacteriaceae
The transmissible locus of stress tolerance (tLST) is a genomic island which confers resistance to heat and chlorine. In this study, we determined that the tLST is frequent in genomes of those that occur in association with plants as well as the intestines of humans and animals and are relevant as n...
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Published in: | mSystems 2021-08, Vol.6 (4), p.e0037821-e0037821 |
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description | The transmissible locus of stress tolerance (tLST) is a genomic island which confers resistance to heat and chlorine. In this study, we determined that the tLST is frequent in genomes of those
that occur in association with plants as well as the intestines of humans and animals and are relevant as nosocomial pathogens, e.g., Klebsiella and
species. The tLST is more frequent in environmental and clinical isolates of Klebsiella pneumoniae than in animal isolates, and heat and chlorine resistance of tLST-positive strains of K. pneumoniae matched the resistance of tLST-positive strains of Escherichia coli. The function of 13 tLST genes was determined by assessing the heat and chlorine resistance of E. coli MG1655 mutants. The deletion of
,
,
,
,
, and
reduced both heat and chlorine resistance; deletion of
reduced only chlorine resistance. Genes coding for heat shock proteins
,
, and
decreased the oxidation of cytoplasmic proteins, while
decreased the oxidation of membrane lipids. The fitness cost of the tLST for E. coli MG1655 was assessed by pairwise competition experiments with isogenic tLST-positive or tLST-negative strains. The tLST imposes a fitness cost that is compensated for by frequent and lethal challenges with chlorine. All core genes need to be present to maintain the ecological advantage relative to the fitness cost. Taken together, core tLST genes are necessary to provide protection for E. coli against heat and chlorine stress, and the selective pressure for the tLST maintains core genes.
The transmissible locus of stress tolerance (tLST) is a genomic island comprising 10 core genes that occurs in diverse
and confers resistance to heat and chlorine. Experimentation described in the manuscript describes the physiological function of the core genes by characterization of the resistance of 13 single-knockout (KO) mutants and by characterization of protein and membrane oxidation in these strains after chlorine challenge. Results identify tLST resistance as a genomic island that is specific for those
that occur in plant-associated habitats as well in the intestines of vertebrates. In addition, the ecological function of the genomic island was characterized by large-scale genomic analysis and competition experiments of wild-type and mutant strains. Results suggest that tLST-mediated resistance to chlorine may contribute to the persistence of nosocomial pathogens in hospitals. |
doi_str_mv | 10.1128/mSystems.00378-21 |
format | article |
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that occur in association with plants as well as the intestines of humans and animals and are relevant as nosocomial pathogens, e.g., Klebsiella and
species. The tLST is more frequent in environmental and clinical isolates of Klebsiella pneumoniae than in animal isolates, and heat and chlorine resistance of tLST-positive strains of K. pneumoniae matched the resistance of tLST-positive strains of Escherichia coli. The function of 13 tLST genes was determined by assessing the heat and chlorine resistance of E. coli MG1655 mutants. The deletion of
,
,
,
,
, and
reduced both heat and chlorine resistance; deletion of
reduced only chlorine resistance. Genes coding for heat shock proteins
,
, and
decreased the oxidation of cytoplasmic proteins, while
decreased the oxidation of membrane lipids. The fitness cost of the tLST for E. coli MG1655 was assessed by pairwise competition experiments with isogenic tLST-positive or tLST-negative strains. The tLST imposes a fitness cost that is compensated for by frequent and lethal challenges with chlorine. All core genes need to be present to maintain the ecological advantage relative to the fitness cost. Taken together, core tLST genes are necessary to provide protection for E. coli against heat and chlorine stress, and the selective pressure for the tLST maintains core genes.
The transmissible locus of stress tolerance (tLST) is a genomic island comprising 10 core genes that occurs in diverse
and confers resistance to heat and chlorine. Experimentation described in the manuscript describes the physiological function of the core genes by characterization of the resistance of 13 single-knockout (KO) mutants and by characterization of protein and membrane oxidation in these strains after chlorine challenge. Results identify tLST resistance as a genomic island that is specific for those
that occur in plant-associated habitats as well in the intestines of vertebrates. In addition, the ecological function of the genomic island was characterized by large-scale genomic analysis and competition experiments of wild-type and mutant strains. Results suggest that tLST-mediated resistance to chlorine may contribute to the persistence of nosocomial pathogens in hospitals.</description><identifier>ISSN: 2379-5077</identifier><identifier>EISSN: 2379-5077</identifier><identifier>DOI: 10.1128/mSystems.00378-21</identifier><identifier>PMID: 34402641</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Antimicrobial Chemotherapy ; antimicrobial resistance ; Cronobacter sakazakii ; Enterobacteriaceae ; Klebsiella pneumoniae ; LHR ; Research Article ; transmissible locus of stress tolerance</subject><ispartof>mSystems, 2021-08, Vol.6 (4), p.e0037821-e0037821</ispartof><rights>Copyright © 2021 Wang et al.</rights><rights>Copyright © 2021 Wang et al. 2021 Wang et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a504t-c3e566c9886b3673b0a1792ab472eb9a03c93ed9ad1809e09ce18ea5f6a206cc3</citedby><cites>FETCH-LOGICAL-a504t-c3e566c9886b3673b0a1792ab472eb9a03c93ed9ad1809e09ce18ea5f6a206cc3</cites><orcidid>0000-0002-5757-641X ; 0000-0003-0972-928X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/mSystems.00378-21$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/mSystems.00378-21$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3174,27903,27904,36992,52730,52731,52732,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34402641$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Rodríguez-Verdugo, Alejandra</contributor><creatorcontrib>Wang, Zhiying</creatorcontrib><creatorcontrib>Hu, Huifeng</creatorcontrib><creatorcontrib>Zhu, Tongbo</creatorcontrib><creatorcontrib>Zheng, Jinshui</creatorcontrib><creatorcontrib>Gänzle, Michael G</creatorcontrib><creatorcontrib>Simpson, David J</creatorcontrib><title>Ecology and Function of the Transmissible Locus of Stress Tolerance in Escherichia coli and Plant-Associated Enterobacteriaceae</title><title>mSystems</title><addtitle>mSystems</addtitle><addtitle>mSystems</addtitle><description>The transmissible locus of stress tolerance (tLST) is a genomic island which confers resistance to heat and chlorine. In this study, we determined that the tLST is frequent in genomes of those
that occur in association with plants as well as the intestines of humans and animals and are relevant as nosocomial pathogens, e.g., Klebsiella and
species. The tLST is more frequent in environmental and clinical isolates of Klebsiella pneumoniae than in animal isolates, and heat and chlorine resistance of tLST-positive strains of K. pneumoniae matched the resistance of tLST-positive strains of Escherichia coli. The function of 13 tLST genes was determined by assessing the heat and chlorine resistance of E. coli MG1655 mutants. The deletion of
,
,
,
,
, and
reduced both heat and chlorine resistance; deletion of
reduced only chlorine resistance. Genes coding for heat shock proteins
,
, and
decreased the oxidation of cytoplasmic proteins, while
decreased the oxidation of membrane lipids. The fitness cost of the tLST for E. coli MG1655 was assessed by pairwise competition experiments with isogenic tLST-positive or tLST-negative strains. The tLST imposes a fitness cost that is compensated for by frequent and lethal challenges with chlorine. All core genes need to be present to maintain the ecological advantage relative to the fitness cost. Taken together, core tLST genes are necessary to provide protection for E. coli against heat and chlorine stress, and the selective pressure for the tLST maintains core genes.
The transmissible locus of stress tolerance (tLST) is a genomic island comprising 10 core genes that occurs in diverse
and confers resistance to heat and chlorine. Experimentation described in the manuscript describes the physiological function of the core genes by characterization of the resistance of 13 single-knockout (KO) mutants and by characterization of protein and membrane oxidation in these strains after chlorine challenge. Results identify tLST resistance as a genomic island that is specific for those
that occur in plant-associated habitats as well in the intestines of vertebrates. In addition, the ecological function of the genomic island was characterized by large-scale genomic analysis and competition experiments of wild-type and mutant strains. Results suggest that tLST-mediated resistance to chlorine may contribute to the persistence of nosocomial pathogens in hospitals.</description><subject>Antimicrobial Chemotherapy</subject><subject>antimicrobial resistance</subject><subject>Cronobacter sakazakii</subject><subject>Enterobacteriaceae</subject><subject>Klebsiella pneumoniae</subject><subject>LHR</subject><subject>Research Article</subject><subject>transmissible locus of stress tolerance</subject><issn>2379-5077</issn><issn>2379-5077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNplkk1rGzEQhpfS0gQ3P6CXomMv6-pjP6RLIQSnDRhasHsWI-3YltldpZK24FP_ehVvmiYUBCM08z4vGt6ieM_okjEuPw2bU0w4xCWlopUlZ6-KSy5aVda0bV8_u18UVzEeKaWsES3j6m1xIaqK8qZil8XvlfW9358IjB25nUabnB-J35F0QLINMMbBxehMj2Tt7RQfWpsUMEay9T3mAYvEjWQV7QGDswcHJBPdmfe9hzGV1zF66yBhR1ZjwuAN2FwcWAR8V7zZQR_x6rEuih-3q-3N13L97cvdzfW6hJpWqbQC66axSsrGiKYVhgJrFQdTtRyNAiqsEtgp6JikCqmyyCRCvWuA08ZasSjuZm7n4ajvgxsgnLQHp88PPuw1hORsj5pntgSVDVBVtZLQcmWEMTVrdsZamVmfZ9b9ZAbsLI4pQP8C-rIzuoPe-19aVrQVkmbAx0dA8D8njEnnJVvs87rQT1HzuuFcVCKfRcHmURt8jAF3TzaM6occ6CHOOdDnHGjOsmY5ayAOXB_9FMa82n-Czf-CD88_9GTxNybiD48Ewmo</recordid><startdate>20210831</startdate><enddate>20210831</enddate><creator>Wang, Zhiying</creator><creator>Hu, Huifeng</creator><creator>Zhu, Tongbo</creator><creator>Zheng, Jinshui</creator><creator>Gänzle, Michael G</creator><creator>Simpson, David J</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5757-641X</orcidid><orcidid>https://orcid.org/0000-0003-0972-928X</orcidid></search><sort><creationdate>20210831</creationdate><title>Ecology and Function of the Transmissible Locus of Stress Tolerance in Escherichia coli and Plant-Associated Enterobacteriaceae</title><author>Wang, Zhiying ; Hu, Huifeng ; Zhu, Tongbo ; Zheng, Jinshui ; Gänzle, Michael G ; Simpson, David J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a504t-c3e566c9886b3673b0a1792ab472eb9a03c93ed9ad1809e09ce18ea5f6a206cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antimicrobial Chemotherapy</topic><topic>antimicrobial resistance</topic><topic>Cronobacter sakazakii</topic><topic>Enterobacteriaceae</topic><topic>Klebsiella pneumoniae</topic><topic>LHR</topic><topic>Research Article</topic><topic>transmissible locus of stress tolerance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Zhiying</creatorcontrib><creatorcontrib>Hu, Huifeng</creatorcontrib><creatorcontrib>Zhu, Tongbo</creatorcontrib><creatorcontrib>Zheng, Jinshui</creatorcontrib><creatorcontrib>Gänzle, Michael G</creatorcontrib><creatorcontrib>Simpson, David J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>mSystems</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Zhiying</au><au>Hu, Huifeng</au><au>Zhu, Tongbo</au><au>Zheng, Jinshui</au><au>Gänzle, Michael G</au><au>Simpson, David J</au><au>Rodríguez-Verdugo, Alejandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ecology and Function of the Transmissible Locus of Stress Tolerance in Escherichia coli and Plant-Associated Enterobacteriaceae</atitle><jtitle>mSystems</jtitle><stitle>mSystems</stitle><addtitle>mSystems</addtitle><date>2021-08-31</date><risdate>2021</risdate><volume>6</volume><issue>4</issue><spage>e0037821</spage><epage>e0037821</epage><pages>e0037821-e0037821</pages><issn>2379-5077</issn><eissn>2379-5077</eissn><abstract>The transmissible locus of stress tolerance (tLST) is a genomic island which confers resistance to heat and chlorine. In this study, we determined that the tLST is frequent in genomes of those
that occur in association with plants as well as the intestines of humans and animals and are relevant as nosocomial pathogens, e.g., Klebsiella and
species. The tLST is more frequent in environmental and clinical isolates of Klebsiella pneumoniae than in animal isolates, and heat and chlorine resistance of tLST-positive strains of K. pneumoniae matched the resistance of tLST-positive strains of Escherichia coli. The function of 13 tLST genes was determined by assessing the heat and chlorine resistance of E. coli MG1655 mutants. The deletion of
,
,
,
,
, and
reduced both heat and chlorine resistance; deletion of
reduced only chlorine resistance. Genes coding for heat shock proteins
,
, and
decreased the oxidation of cytoplasmic proteins, while
decreased the oxidation of membrane lipids. The fitness cost of the tLST for E. coli MG1655 was assessed by pairwise competition experiments with isogenic tLST-positive or tLST-negative strains. The tLST imposes a fitness cost that is compensated for by frequent and lethal challenges with chlorine. All core genes need to be present to maintain the ecological advantage relative to the fitness cost. Taken together, core tLST genes are necessary to provide protection for E. coli against heat and chlorine stress, and the selective pressure for the tLST maintains core genes.
The transmissible locus of stress tolerance (tLST) is a genomic island comprising 10 core genes that occurs in diverse
and confers resistance to heat and chlorine. Experimentation described in the manuscript describes the physiological function of the core genes by characterization of the resistance of 13 single-knockout (KO) mutants and by characterization of protein and membrane oxidation in these strains after chlorine challenge. Results identify tLST resistance as a genomic island that is specific for those
that occur in plant-associated habitats as well in the intestines of vertebrates. In addition, the ecological function of the genomic island was characterized by large-scale genomic analysis and competition experiments of wild-type and mutant strains. Results suggest that tLST-mediated resistance to chlorine may contribute to the persistence of nosocomial pathogens in hospitals.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>34402641</pmid><doi>10.1128/mSystems.00378-21</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-5757-641X</orcidid><orcidid>https://orcid.org/0000-0003-0972-928X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antimicrobial Chemotherapy antimicrobial resistance Cronobacter sakazakii Enterobacteriaceae Klebsiella pneumoniae LHR Research Article transmissible locus of stress tolerance |
title | Ecology and Function of the Transmissible Locus of Stress Tolerance in Escherichia coli and Plant-Associated Enterobacteriaceae |
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