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 inPloS one Vol. 12; no. 9; p. e0184255
Main Authors Lin, Hong-Ting Victor, Massam-Wu, Teresa, Lin, Chen-Ping, Wang, Yen-Jen Anna, Shen, Yu-Chi, Lu, Wen-Jung, Hsu, Pang-Hung, Chen, Yu-Hou, Borges-Walmsley, Maria Ines, Walmsley, Adrian Robert
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Published United States Public Library of Science 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.
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
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  fullname: Lin, Hong-Ting Victor
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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
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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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content type line 14
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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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SSID ssj0053866
Score 2.3964882
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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doaj
pubmedcentral
proquest
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage e0184255
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
URI https://www.ncbi.nlm.nih.gov/pubmed/28898293
https://www.proquest.com/docview/1938124110
https://www.proquest.com/docview/1938600486
https://pubmed.ncbi.nlm.nih.gov/PMC5595328
https://doaj.org/article/03e7ed1823614df7b0bd7bc860e7d4bf
http://dx.doi.org/10.1371/journal.pone.0184255
Volume 12
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