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Draft genome sequence of CTX-M-5 variant-carrying Kluyvera ascorbata isolated from river water in Kumamoto, Japan
Takatoshi Yamamoto1, Chie Shitada2,3, Tatsuya Kawaguchi1
1Department of Medical Technology, Faculty of Health Sciences, Kumamoto Health Science University, Kumamoto, Japan.
Abstract:
The genus Kluyvera is presumed to be the original source of blaCTX-M genes, which encode one of the most prevalent extended-spectrum β-lactamases. We report the draft genome sequence of Kluyvera ascorbata strain KHSU-R5-7, a CTX-M-5 variant producing isolate obtained from Shirakawa River in Kumamoto, Japan.
Insights
The genus Kluyvera likely originated extended-spectrum beta-lactamase (ESBL) genes. Researchers sequenced the Kluyvera ascorbata genome from a CTX-M-5 variant isolate found in Japan.
Area of Science:
- Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- The genus Kluyvera is considered the likely origin of blaCTX-M genes.
- These genes encode prevalent extended-spectrum beta-lactamases (ESBLs), crucial in antimicrobial resistance.
- ESBLs confer resistance to broad-spectrum beta-lactam antibiotics.
Purpose of the Study:
- To perform whole-genome sequencing of a Kluyvera ascorbata isolate.
- To analyze the genome of a strain producing a CTX-M-5 variant.
- To contribute genomic data for understanding the evolution of ESBL genes.
Main Methods:
- Draft genome sequencing of Kluyvera ascorbata strain KHSU-R5-7.
- Isolate sourced from Shirakawa River, Kumamoto, Japan.
- Bioinformatic analysis of the sequenced genome.
Main Results:
- The draft genome sequence of Kluyvera ascorbata strain KHSU-R5-7 was successfully obtained.
- The isolate was identified as a producer of a CTX-M-5 variant.
- Genomic data provides insights into the genetic makeup of the Kluyvera genus.
Conclusions:
- This study reports the genome sequence of a significant Kluyvera ascorbata isolate.
- The findings support the role of Kluyvera as a reservoir for blaCTX-M genes.
- Further genomic studies are needed to fully elucidate the dissemination of ESBLs.
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