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Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli
mBio, Volume: 9, Issue: 4
Swansea University Author:
Jon Tyrrell
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© 2018 Shen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
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DOI (Published version): 10.1128/mbio.00943-18
Abstract
The recent emergence of a transferable colistin resistance mechanism, MCR-1, has gained global attention because of its threat to clinical treatment of infections caused by multidrug-resistant Gram-negative bacteria. However, the possible transmission route of mcr-1 among Enterobacteriaceae species...
| Published in: | mBio |
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| ISSN: | 2161-2129 2150-7511 |
| Published: |
American Society for Microbiology
2018
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa70426 |
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2025-10-17T09:30:55Z |
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<?xml version="1.0"?><rfc1807><datestamp>2025-10-16T15:29:00.6416389</datestamp><bib-version>v2</bib-version><id>70426</id><entry>2025-09-21</entry><title>Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli</title><swanseaauthors><author><sid>ad510c73555adf718387af219e235a6e</sid><ORCID>0000-0001-8565-2590</ORCID><firstname>Jon</firstname><surname>Tyrrell</surname><name>Jon Tyrrell</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2025-09-21</date><deptcode>MEDS</deptcode><abstract>The recent emergence of a transferable colistin resistance mechanism, MCR-1, has gained global attention because of its threat to clinical treatment of infections caused by multidrug-resistant Gram-negative bacteria. However, the possible transmission route of mcr-1 among Enterobacteriaceae species in clinical settings is largely unknown. Here, we present a comprehensive genomic analysis of Escherichia coli isolates collected in a hospital in Hangzhou, China. We found that mcr-1-carrying isolates from clinical infections and feces of inpatients and healthy volunteers were genetically diverse and were not closely related phylogenetically, suggesting that clonal expansion is not involved in the spread of mcr-1. The mcr-1 gene was found on either chromosomes or plasmids, but in most of the E. coli isolates, mcr-1 was carried on plasmids. The genetic context of the plasmids showed considerable diversity as evidenced by the different functional insertion sequence (IS) elements, toxin-antitoxin (TA) systems, heavy metal resistance determinants, and Rep proteins of broad-host-range plasmids. Additionally, the genomic analysis revealed nosocomial transmission of mcr-1 and the coexistence of mcr-1 with other genes encoding β-lactamases and fluoroquinolone resistance in the E. coli isolates. These findings indicate that mcr-1 is heterogeneously disseminated in both commensal and pathogenic strains of E. coli, suggest the high flexibility of this gene in its association with diverse genetic backgrounds of the hosts, and provide new insights into the genome epidemiology of mcr-1 among hospital-associated E. coli strains.</abstract><type>Journal Article</type><journal>mBio</journal><volume>9</volume><journalNumber>4</journalNumber><paginationStart/><paginationEnd/><publisher>American Society for Microbiology</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>2161-2129</issnPrint><issnElectronic>2150-7511</issnElectronic><keywords>E. coli, genetic diversity, mcr-1, population genomics, transmission</keywords><publishedDay>5</publishedDay><publishedMonth>9</publishedMonth><publishedYear>2018</publishedYear><publishedDate>2018-09-05</publishedDate><doi>10.1128/mbio.00943-18</doi><url/><notes/><college>COLLEGE NANME</college><department>Medical School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>MEDS</DepartmentCode><institution>Swansea University</institution><apcterm>Another institution paid the OA fee</apcterm><funders>This work was supported in part by the National Natural Science Foundation of China (grants 31672604 and 31422055) and the Natural Science Foundation of Zhejiang Province (2013C33G2010505), Higher Education Funding Council and European Commission, United Kingdom.</funders><projectreference/><lastEdited>2025-10-16T15:29:00.6416389</lastEdited><Created>2025-09-21T18:13:15.2418348</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Biomedical Science</level></path><authors><author><firstname>Yingbo</firstname><surname>Shen</surname><order>1</order></author><author><firstname>Zuowei</firstname><surname>Wu</surname><order>2</order></author><author><firstname>Yang</firstname><surname>Wang</surname><order>3</order></author><author><firstname>Rong</firstname><surname>Zhang</surname><order>4</order></author><author><firstname>Hong-Wei</firstname><surname>Zhou</surname><order>5</order></author><author><firstname>Shaolin</firstname><surname>Wang</surname><orcid>0000-0003-0866-4584</orcid><order>6</order></author><author><firstname>Lei</firstname><surname>Lei</surname><order>7</order></author><author><firstname>Mei</firstname><surname>Li</surname><order>8</order></author><author><firstname>Jiachang</firstname><surname>Cai</surname><order>9</order></author><author><firstname>Jon</firstname><surname>Tyrrell</surname><orcid>0000-0001-8565-2590</orcid><order>10</order></author><author><firstname>Guo-Bao</firstname><surname>Tian</surname><order>11</order></author><author><firstname>Congming</firstname><surname>Wu</surname><order>12</order></author><author><firstname>Qijing</firstname><surname>Zhang</surname><order>13</order></author><author><firstname>Jianzhong</firstname><surname>Shen</surname><order>14</order></author><author><firstname>Timothy R.</firstname><surname>Walsh</surname><order>15</order></author><author><firstname>Zhangqi</firstname><surname>Shen</surname><order>16</order></author></authors><documents><document><filename>70426__35371__18d76d42ae9043a5917afff812610e5b.pdf</filename><originalFilename>70426.VoR.pdf</originalFilename><uploaded>2025-10-16T15:26:50.9469917</uploaded><type>Output</type><contentLength>3551167</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>© 2018 Shen et al. 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2025-10-16T15:29:00.6416389 v2 70426 2025-09-21 Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli ad510c73555adf718387af219e235a6e 0000-0001-8565-2590 Jon Tyrrell Jon Tyrrell true false 2025-09-21 MEDS The recent emergence of a transferable colistin resistance mechanism, MCR-1, has gained global attention because of its threat to clinical treatment of infections caused by multidrug-resistant Gram-negative bacteria. However, the possible transmission route of mcr-1 among Enterobacteriaceae species in clinical settings is largely unknown. Here, we present a comprehensive genomic analysis of Escherichia coli isolates collected in a hospital in Hangzhou, China. We found that mcr-1-carrying isolates from clinical infections and feces of inpatients and healthy volunteers were genetically diverse and were not closely related phylogenetically, suggesting that clonal expansion is not involved in the spread of mcr-1. The mcr-1 gene was found on either chromosomes or plasmids, but in most of the E. coli isolates, mcr-1 was carried on plasmids. The genetic context of the plasmids showed considerable diversity as evidenced by the different functional insertion sequence (IS) elements, toxin-antitoxin (TA) systems, heavy metal resistance determinants, and Rep proteins of broad-host-range plasmids. Additionally, the genomic analysis revealed nosocomial transmission of mcr-1 and the coexistence of mcr-1 with other genes encoding β-lactamases and fluoroquinolone resistance in the E. coli isolates. These findings indicate that mcr-1 is heterogeneously disseminated in both commensal and pathogenic strains of E. coli, suggest the high flexibility of this gene in its association with diverse genetic backgrounds of the hosts, and provide new insights into the genome epidemiology of mcr-1 among hospital-associated E. coli strains. Journal Article mBio 9 4 American Society for Microbiology 2161-2129 2150-7511 E. coli, genetic diversity, mcr-1, population genomics, transmission 5 9 2018 2018-09-05 10.1128/mbio.00943-18 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University Another institution paid the OA fee This work was supported in part by the National Natural Science Foundation of China (grants 31672604 and 31422055) and the Natural Science Foundation of Zhejiang Province (2013C33G2010505), Higher Education Funding Council and European Commission, United Kingdom. 2025-10-16T15:29:00.6416389 2025-09-21T18:13:15.2418348 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Biomedical Science Yingbo Shen 1 Zuowei Wu 2 Yang Wang 3 Rong Zhang 4 Hong-Wei Zhou 5 Shaolin Wang 0000-0003-0866-4584 6 Lei Lei 7 Mei Li 8 Jiachang Cai 9 Jon Tyrrell 0000-0001-8565-2590 10 Guo-Bao Tian 11 Congming Wu 12 Qijing Zhang 13 Jianzhong Shen 14 Timothy R. Walsh 15 Zhangqi Shen 16 70426__35371__18d76d42ae9043a5917afff812610e5b.pdf 70426.VoR.pdf 2025-10-16T15:26:50.9469917 Output 3551167 application/pdf Version of Record true © 2018 Shen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. true eng https://creativecommons.org/licenses/by/4.0/ |
| title |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
| spellingShingle |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli Jon Tyrrell |
| title_short |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
| title_full |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
| title_fullStr |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
| title_full_unstemmed |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
| title_sort |
Heterogeneous and Flexible Transmission of mcr-1 in Hospital-Associated Escherichia coli |
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ad510c73555adf718387af219e235a6e |
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ad510c73555adf718387af219e235a6e_***_Jon Tyrrell |
| author |
Jon Tyrrell |
| author2 |
Yingbo Shen Zuowei Wu Yang Wang Rong Zhang Hong-Wei Zhou Shaolin Wang Lei Lei Mei Li Jiachang Cai Jon Tyrrell Guo-Bao Tian Congming Wu Qijing Zhang Jianzhong Shen Timothy R. Walsh Zhangqi Shen |
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mBio |
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10.1128/mbio.00943-18 |
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American Society for Microbiology |
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Faculty of Medicine, Health and Life Sciences |
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The recent emergence of a transferable colistin resistance mechanism, MCR-1, has gained global attention because of its threat to clinical treatment of infections caused by multidrug-resistant Gram-negative bacteria. However, the possible transmission route of mcr-1 among Enterobacteriaceae species in clinical settings is largely unknown. Here, we present a comprehensive genomic analysis of Escherichia coli isolates collected in a hospital in Hangzhou, China. We found that mcr-1-carrying isolates from clinical infections and feces of inpatients and healthy volunteers were genetically diverse and were not closely related phylogenetically, suggesting that clonal expansion is not involved in the spread of mcr-1. The mcr-1 gene was found on either chromosomes or plasmids, but in most of the E. coli isolates, mcr-1 was carried on plasmids. The genetic context of the plasmids showed considerable diversity as evidenced by the different functional insertion sequence (IS) elements, toxin-antitoxin (TA) systems, heavy metal resistance determinants, and Rep proteins of broad-host-range plasmids. Additionally, the genomic analysis revealed nosocomial transmission of mcr-1 and the coexistence of mcr-1 with other genes encoding β-lactamases and fluoroquinolone resistance in the E. coli isolates. These findings indicate that mcr-1 is heterogeneously disseminated in both commensal and pathogenic strains of E. coli, suggest the high flexibility of this gene in its association with diverse genetic backgrounds of the hosts, and provide new insights into the genome epidemiology of mcr-1 among hospital-associated E. coli strains. |
| published_date |
2018-09-05T05:26:06Z |
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11.089572 |

