The Vibrio cholerae var regulon encodes a metallo-β-lactamase and an antibiotic efflux pump, which are regulated by VarR, a LysR-type transcription factor
The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG...
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Published in | PloS one Vol. 12; no. 9; p. e0184255 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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01.09.2017
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Abstract | The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli (ΔacrAB) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG, varGA and varBC located upstream and adjacent to varG, varA and varC, respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/varRG-DNA complex, indicating that the de-repression of varR by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V. cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures. |
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AbstractList | The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli (ΔacrAB) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG, varGA and varBC located upstream and adjacent to varG, varA and varC, respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/varRG-DNA complex, indicating that the de-repression of varR by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V. cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures. The genome sequence of V . cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance ( var ) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli ( ΔacrAB ) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG , varGA and varBC located upstream and adjacent to varG , varA and varC , respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/ varRG -DNA complex, indicating that the de-repression of var R by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V . cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures. The genome sequence of V . cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance ( var ) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli ( ΔacrAB ) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG , varGA and varBC located upstream and adjacent to varG , varA and varC , respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/ varRG -DNA complex, indicating that the de-repression of var R by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V . cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures. The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli (ΔacrAB) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG, varGA and varBC located upstream and adjacent to varG, varA and varC, respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/varRG-DNA complex, indicating that the de-repression of varR by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V. cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures.The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a transcriptional activator (VarR), which is divergently transcribed relative to the putative resistance genes for both a metallo-β-lactamase (VarG) and an antibiotic efflux-pump (VarABCDEF). We sought to test whether these genes could confer antibiotic resistance and are organised as a regulon under the control of VarR. VarG was overexpressed and purified and shown to have β-lactamase activity against penicillins, cephalosporins and carbapenems, having the highest activity against meropenem. The expression of VarABCDEF in the Escherichia coli (ΔacrAB) strain KAM3 conferred resistance to a range of drugs, but most significant resistance was to the macrolide spiramycin. A gel-shift analysis was used to determine if VarR bound to the promoter regions of the resistance genes. Consistent with the regulation of these resistance genes, VarR binds to three distinct intergenic regions, varRG, varGA and varBC located upstream and adjacent to varG, varA and varC, respectively. VarR can act as a repressor at the varRG promoter region; whilst this repression was relieved upon addition of β-lactams, these did not dissociate the VarR/varRG-DNA complex, indicating that the de-repression of varR by β-lactams is indirect. Considering that the genomic arrangement of VarR-VarG is strikingly similar to that of AmpR-AmpC system, it is possible that V. cholerae has evolved a system for resistance to the newer β-lactams that would prove more beneficial to the bacterium in light of current selective pressures. |
Author | Lu, Wen-Jung Wang, Yen-Jen Anna Borges-Walmsley, Maria Ines Shen, Yu-Chi Hsu, Pang-Hung Chen, Yu-Hou Lin, Chen-Ping Lin, Hong-Ting Victor Massam-Wu, Teresa Walmsley, Adrian Robert |
AuthorAffiliation | 2 Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung, Taiwan 3 Department of Biosciences, Durham University, Durham, United Kingdom 4 Department of Bioscience and Biotechnology, National Taiwan Ocean University, Keelung, Taiwan 5 Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan University of Cambridge, UNITED KINGDOM 1 Department of Food Science, National Taiwan Ocean University, Keelung, Taiwan |
AuthorAffiliation_xml | – name: 5 Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan – name: University of Cambridge, UNITED KINGDOM – name: 2 Center of Excellence for the Oceans, National Taiwan Ocean University, Keelung, Taiwan – name: 4 Department of Bioscience and Biotechnology, National Taiwan Ocean University, Keelung, Taiwan – name: 3 Department of Biosciences, Durham University, Durham, United Kingdom – name: 1 Department of Food Science, National Taiwan Ocean University, Keelung, Taiwan |
Author_xml | – sequence: 1 givenname: Hong-Ting Victor surname: Lin fullname: Lin, Hong-Ting Victor – sequence: 2 givenname: Teresa surname: Massam-Wu fullname: Massam-Wu, Teresa – sequence: 3 givenname: Chen-Ping surname: Lin fullname: Lin, Chen-Ping – sequence: 4 givenname: Yen-Jen Anna surname: Wang fullname: Wang, Yen-Jen Anna – sequence: 5 givenname: Yu-Chi surname: Shen fullname: Shen, Yu-Chi – sequence: 6 givenname: Wen-Jung surname: Lu fullname: Lu, Wen-Jung – sequence: 7 givenname: Pang-Hung surname: Hsu fullname: Hsu, Pang-Hung – sequence: 8 givenname: Yu-Hou surname: Chen fullname: Chen, Yu-Hou – sequence: 9 givenname: Maria Ines surname: Borges-Walmsley fullname: Borges-Walmsley, Maria Ines – sequence: 10 givenname: Adrian Robert orcidid: 0000-0002-5136-0511 surname: Walmsley fullname: Walmsley, Adrian Robert |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28898293$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1128/jb.179.13.4123-4128.1997 10.1038/35020000 10.1042/bj2720627 |
ContentType | Journal Article |
Copyright | 2017 Lin 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. 2017 Lin et al 2017 Lin et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Current address: Departamento de Bioquímica, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, Brazil These authors are first authors on this work. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | The genome sequence of V. cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance (var) regulon that is predicted to encode a... The genome sequence of V . cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance ( var ) regulon that is predicted to encode a... The genome sequence of V . cholerae O1 Biovar Eltor strain N16961 has revealed a putative antibiotic resistance ( var ) regulon that is predicted to encode a... |
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SubjectTerms | Anti-Bacterial Agents - metabolism Anti-Bacterial Agents - pharmacology Antibiotic resistance Antibiotics Antimicrobial agents ATP-Binding Cassette Transporters - genetics ATP-Binding Cassette Transporters - metabolism Bacteria Base Sequence beta-Lactamases - genetics Biology and Life Sciences Carbapenems Cephalosporins Cholera Deoxyribonucleic acid DNA DNA, Intergenic Drug resistance Drug Resistance, Bacterial Drugs E coli Efflux Epidemics Food contamination & poisoning Food science Gene expression Gene Expression Regulation, Bacterial Gene regulation Genes Genes, Bacterial Genomes Hydrolysis Kinetics Medicine and Health Sciences Membrane Transport Proteins - genetics Meropenem Metallography Microbial Sensitivity Tests Nucleotide sequence Pathogens Penicillin Promoter Regions, Genetic Protein Binding Regulation Regulon Research and Analysis Methods Spiramycin Transcription Factors - metabolism Transcription, Genetic Vibrio cholerae - drug effects Vibrio cholerae - genetics Vibrio cholerae - metabolism Waterborne diseases |
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Title | The Vibrio cholerae var regulon encodes a metallo-β-lactamase and an antibiotic efflux pump, which are regulated by VarR, a LysR-type transcription factor |
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