Journal article
High rates of human fecal carriage of mcr-1-positive multi-drug resistant Enterobacteriaceae isolates emerge in China in association with successful plasmid families
- Abstract:
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Objectives
mcr-1-mediated colistin resistance in Enterobacteriaceae is concerning, as colistin is used in treating multidrug-resistant Enterobacteriaceae infections. Rates of human mcr-1 gastrointestinal carriage have historically been low. We identified trends in human fecal mcr-1-positivity rates and colonization with mcr-1-positive+third-generation cephalosporin-resistant (3GC-R) Enterobacteriaceae in Guangzhou, China, and investigated the genetic contexts of mcr-1 in a subset of mcr-1-positive+3GC-R strains.
Methods
Fecal samples were collected from in-patients and out-patients submitting specimens to three hospitals (2011-2016). mcr-1 carriage trends were assessed using iterative sequential regression. A subset of mcr-1-positive isolates was sequenced (whole genome sequencing [WGS], Illumina), and genetic contexts (flanking regions, plasmids) of mcr-1 characterized.
Results
Of 8,022 fecal samples collected, 497 (6.2%) were mcr-1-positive, and 182 (2.3%) harbored mcr-1-positive+3GC-R Enterobacteriaceae. We observed marked increases in mcr-1 (0% [Apr/2011] to 31% [Mar/2016]) and more recent (since January 2014; 0% [Apr/2011] to 15% [Mar/2016]) increases in human colonization with mcr-1-positive+3GC-R Enterobacteriaceae (p<0.001). mcr-1-positive+3GC-R isolates were commonly multi-drug resistant.
WGS of mcr-1-positive+3GC-R isolates (70 Escherichia coli, 3 Klebsiella pneumoniae) demonstrated bacterial strain diversity (48 E. coli sequence types); mcr-1 in association with common plasmid backbones (IncI, IncHI2/HI2A, IncX4) and sometimes in multiple plasmids; frequent mcr-1 chromosomal integration; and high mobility of the mcr-1-associated insertion sequence ISApl1. Sequence similarity with published mcr-1 plasmid sequences was consistent with spread amongst animal/human reservoirs.
Conclusions
The high prevalence of mcr-1 in multidrug-resistant E. coli colonizing humans is a clinical threat; diverse genetic mechanisms (strains/plasmids/insertion sequences) have contributed to the dissemination of mcr-1, and will facilitate its persistence.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 542.8KB, Terms of use)
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- Publisher copy:
- 10.1093/cid/cix885
Authors
- Publisher:
- Oxford University Press
- Journal:
- Clinical Infectious Diseases More from this journal
- Volume:
- 66
- Issue:
- 5
- Pages:
- 676–685
- Publication date:
- 2017-10-10
- Acceptance date:
- 2017-10-10
- DOI:
- EISSN:
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1537-6591
- ISSN:
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1058-4838
- Keywords:
- Pubs id:
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pubs:734445
- UUID:
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uuid:c0a36b6b-6107-4caf-b3f6-9132b39abfc3
- Local pid:
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pubs:734445
- Source identifiers:
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734445
- Deposit date:
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2017-10-06
Terms of use
- Copyright holder:
- Zhong et al
- Copyright date:
- 2017
- Notes:
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© The Author(s) 2017. Published by Oxford University Press for the Infectious Diseases Society
of America. This is the accepted manuscript version of the article. The final version is available online from Oxford University Press at: https://doi.org/10.1093/cid/cix885
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