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Genomic characterization of antimicrobial resistance in mcr-carrying ESBL-producing Escherichia coli from pigs and humans
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Whole-genome sequencing (WGS) was conducted to characterize mcr-carrying extended-spectrum beta-lactamase (ESBL)-producing
Escherichia coli
(n=7). These
E. coli
isolates originated from two pigs (TH2 and TH3) and two humans (TH8 and TH9) from Thailand, and three pigs from Lao PDR (LA1, LA2 and LA3). Four
E. coli
sequence types/serotypes – ST6833/H20 (TH2 and TH3), ST48/O160:H40 (TH8 and TH9), ST5708/H45 (LA1) and ST10562/O148:H30 (LA2 and LA3) – were identified. The plasmid replicon type IncF was identified in all isolates. The point mutations Ser31Thr in PmrA and His2Arg in PmrB were found concurrently in all isolates (colistin MIC=4–8 µg ml−1). LA1 contained up to five point mutations in PmrB, and the colistin MIC was not significantly different from that for the other isolates. All mcr-1.1 was located in the ISApl1-mcr-1-pap2 element, while all mcr-3.1 was located in the TnAs2-mcr-3.1-dgkA-ISKpn40 element. The mcr-3.1 and bla
CTX-M-55 genes were co-localized on the same plasmid, which concurrently contained cml, qnrS1 and tmrB. The bla
CTX-M-55 and mcr-3.1 genes were located on conjugative plasmids and could be transferred horizontally under selective pressure from ampicillin or colistin. In conclusion, comprehensive insights into the genomic information of ESBL-producing
E. coli
harbouring mcr were obtained. As mcr-carrying ESBL-producing
E. coli
were detected in pigs and humans, a holistic and multisectoral One Health approach is required to contain antimicrobial resistance (AMR).
Title: Genomic characterization of antimicrobial resistance in mcr-carrying ESBL-producing Escherichia coli from pigs and humans
Description:
Whole-genome sequencing (WGS) was conducted to characterize mcr-carrying extended-spectrum beta-lactamase (ESBL)-producing
Escherichia coli
(n=7).
These
E.
coli
isolates originated from two pigs (TH2 and TH3) and two humans (TH8 and TH9) from Thailand, and three pigs from Lao PDR (LA1, LA2 and LA3).
Four
E.
coli
sequence types/serotypes – ST6833/H20 (TH2 and TH3), ST48/O160:H40 (TH8 and TH9), ST5708/H45 (LA1) and ST10562/O148:H30 (LA2 and LA3) – were identified.
The plasmid replicon type IncF was identified in all isolates.
The point mutations Ser31Thr in PmrA and His2Arg in PmrB were found concurrently in all isolates (colistin MIC=4–8 µg ml−1).
LA1 contained up to five point mutations in PmrB, and the colistin MIC was not significantly different from that for the other isolates.
All mcr-1.
1 was located in the ISApl1-mcr-1-pap2 element, while all mcr-3.
1 was located in the TnAs2-mcr-3.
1-dgkA-ISKpn40 element.
The mcr-3.
1 and bla
CTX-M-55 genes were co-localized on the same plasmid, which concurrently contained cml, qnrS1 and tmrB.
The bla
CTX-M-55 and mcr-3.
1 genes were located on conjugative plasmids and could be transferred horizontally under selective pressure from ampicillin or colistin.
In conclusion, comprehensive insights into the genomic information of ESBL-producing
E.
coli
harbouring mcr were obtained.
As mcr-carrying ESBL-producing
E.
coli
were detected in pigs and humans, a holistic and multisectoral One Health approach is required to contain antimicrobial resistance (AMR).
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