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Genetic evaluation of ESBL-producing Escherichia coli urinary isolates in Otago, New Zealand
被引:5
作者:

Hapuarachchi, Isuri U.
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Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Hannaway, Rachel F.
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Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Roman, Tabatha
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Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Biswas, Ambarish
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机构:
Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
AgResearch, Palmerston North, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Dyet, Kristin
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机构:
ESR, Wellington, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Morgan, Xochitl
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机构:
Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand

Ussher, James E.
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机构:
Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
Southern Community Labs, Dunedin, New Zealand Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
机构:
[1] Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
[2] AgResearch, Palmerston North, New Zealand
[3] ESR, Wellington, New Zealand
[4] Southern Community Labs, Dunedin, New Zealand
来源:
JAC-ANTIMICROBIAL RESISTANCE
|
2021年
/
3卷
/
04期
关键词:
SPECTRUM-BETA-LACTAMASE;
SEQUENCE TYPE 131;
ANTIBIOTIC-RESISTANCE;
ANTIMICROBIAL RESISTANCE;
BLA(CTX-M) GENES;
TRACT-INFECTIONS;
PLASMIDS;
EPIDEMIOLOGY;
IDENTIFICATION;
DISSEMINATION;
D O I:
10.1093/jacamr/dlab147
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Objectives The incidence of infections with ESBL-producing Escherichia coli (ESBL-Ec) in New Zealand is increasing. ESBL-Ec most commonly cause urinary tract infections and are seen in both community and hospitalized patients. The reason for the increasing incidence of ESBL-Ec infections is unknown. Methods In this study, 65 urinary ESBL-Ec isolates from the Otago region in 2015 were fully genetically characterized to understand the mechanisms of transmission. The ESBL gene, E. coli STs, plasmid types and genetic context (e.g. insertion sequences) of ESBL genes were determined by a combination of whole genome and plasmid sequencing. The phylogenetic relationships of the isolates were compared with ESBL-Ec isolates sequenced as part of the 2016 nationwide survey. Results Significant diversity of E. coli strains, plasmids, and the genetic context of ESBL genes was seen. However, there was evidence of common mobile genetic elements in unrelated ESBL-Ec. Conclusions Multiple introductions of ESBL resistance genes or resistant bacterial strains with limited horizontal transmission of mobile genetic elements accounts for the increased incidence of ESBL-Ec in this low prevalence area. Future studies should investigate modes of transmission of ESBL-Ec in the Otago region.
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