Clonal spread of mcr-1 in PMQR-carrying ST34 Salmonella isolates from animals in China
Since initial identification in China, the widespread geographical occurrence of plasmid-mediated colistin resistance gene mcr-1 in Enterobacteriaceae has been of great concern. In this study, a total of 22 Salmonella enterica were resistant to colistin, while only five isolates which belonged to ST...
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Published in | Scientific reports Vol. 6; no. 1; p. 38511 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
05.12.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 2045-2322 2045-2322 |
DOI | 10.1038/srep38511 |
Cover
Summary: | Since initial identification in China, the widespread geographical occurrence of plasmid-mediated colistin resistance gene
mcr-1
in
Enterobacteriaceae
has been of great concern. In this study, a total of 22
Salmonella enterica
were resistant to colistin, while only five isolates which belonged to ST34
Salmonella enterica
serovar Typhimurium (
S.
Typhimurium) were
mcr-1
positive. Four of them shared nearly identical PFGE type, although they were from different host species and diverse geographical locations. All the
mcr-1
-positive
S.
Typhimurium exhibited multi-resistant phenotypes including ampicillin, streptomycin, gentamicin, florfenicol, nalidixic acid, tetracycline, trimethoprim-sulfamethox, in addition to colistin. The
oqxAB
and
aac
(
6
′)
-Ib-cr
genes were present alone or in combination in four (80.0%) and five (100%) isolates, respectively. The
mcr-1
gene was located on a transferable IncI2 plasmid in the four genetically related strains. In the other one strain,
mcr-1
was located on an approximately 190 kb IncHI2 plasmid. In conclusion, we report five
mcr-1-
positive
S.
Typhimurium/ST34 isolates. Both clonal expansion and horizontal transmission of IncI2-type plasmids were involved in the spread of the
mcr-1
gene in
Salmonella enterica
from food-producing animals in China. There is a great need to monitor the potential dissemination of the
mcr-1
gene. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep38511 |