Identification of novel mobile colistin resistance gene mcr-10

Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical...

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Published inEmerging microbes & infections Vol. 9; no. 1; pp. 508 - 516
Main Authors Wang, Chengcheng, Feng, Yu, Liu, Lina, Wei, Li, Kang, Mei, Zong, Zhiyong
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 01.01.2020
Taylor & Francis Ltd
Taylor & Francis Group
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Abstract Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
AbstractList Mobile colistin resistance ( mcr ) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10 , on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS 903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
Mobile colistin resistance ( ) genes represent an emerging challenge. Here we describe a novel gene, , on an IncFIA plasmid of an clinical strain. has the highest nucleotide identity (79.69%) with and encodes MCR-10 with 82.93% amino acids identical to MCR-9. confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible strain. By screening GenBank, was found in various species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS and may be mobilized by site-specific recombination or composite transposon. Our results indicate that is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
Author Zong, Zhiyong
Feng, Yu
Kang, Mei
Liu, Lina
Wang, Chengcheng
Wei, Li
Author_xml – sequence: 1
  givenname: Chengcheng
  surname: Wang
  fullname: Wang, Chengcheng
  organization: Center for Pathogen Research, West China Hospital, Sichuan University
– sequence: 2
  givenname: Yu
  orcidid: 0000-0002-5654-4256
  surname: Feng
  fullname: Feng, Yu
  organization: Center for Pathogen Research, West China Hospital, Sichuan University
– sequence: 3
  givenname: Lina
  surname: Liu
  fullname: Liu, Lina
  organization: Center for Pathogen Research, West China Hospital, Sichuan University
– sequence: 4
  givenname: Li
  surname: Wei
  fullname: Wei, Li
  organization: Department of Infection Control, West China Hospital, Sichuan University
– sequence: 5
  givenname: Mei
  surname: Kang
  fullname: Kang, Mei
  organization: Laboratory of Clinical Microbiology, Department of Laboratory Medicine, West China Hospital, Sichuan University
– sequence: 6
  givenname: Zhiyong
  orcidid: 0000-0002-7675-260X
  surname: Zong
  fullname: Zong, Zhiyong
  email: zongzhiy@scu.edu.cn, zongzhiyong@gmail.com
  organization: Department of Infection Control, West China Hospital, Sichuan University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32116151$$D View this record in MEDLINE/PubMed
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Copyright 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd 2020
2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Issue 1
Keywords Enterobacter roggenkampii
plasmid
Colistin resistance
mcr
mcr-10
Language English
License open-access: http://creativecommons.org/licenses/by/4.0/: This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.: http://creativecommons.org/licenses/by/4.0
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Supplemental data for this article can be accessed at https://doi.org/10.1080/22221751.2020.1732231
The authors contributed equally.
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Snippet Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter...
Mobile colistin resistance ( ) genes represent an emerging challenge. Here we describe a novel gene, , on an IncFIA plasmid of an clinical strain. has the...
Mobile colistin resistance ( mcr ) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10 , on an IncFIA plasmid of an Enterobacter...
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StartPage 508
SubjectTerms Amino Acid Sequence
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Colistin - pharmacology
Colistin resistance
Databases, Genetic
Drug Resistance, Bacterial
Enterobacter roggenkampii
Enterobacteriaceae - chemistry
Enterobacteriaceae - drug effects
Enterobacteriaceae - genetics
mcr
mcr-10
Models, Molecular
plasmid
Plasmids
Protein Structure, Tertiary
Sequence Analysis, Protein
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Title Identification of novel mobile colistin resistance gene mcr-10
URI https://www.tandfonline.com/doi/abs/10.1080/22221751.2020.1732231
https://www.ncbi.nlm.nih.gov/pubmed/32116151
https://www.proquest.com/docview/2508722152
https://www.proquest.com/docview/2369877296
https://pubmed.ncbi.nlm.nih.gov/PMC7067168
https://doaj.org/article/c0c774b757ab4e24a350a77d94552fb4
Volume 9
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