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ID 70240
フルテキストURL
fulltext.pdf 2.85 MB
著者
Hongu, Kinuka Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Ishikawa, Kazuya Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kosaki, Tomoki Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Miyoshi, Shin‐Ichi Research Center for Intestinal Health Science, Okayama University
Furuta, Kazuyuki Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kaito, Chikara Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
抄録
The emergence of bacteria with both antimicrobial resistance and high virulence has become a global health concern, underscoring the urgent need to elucidate the molecular basis underlying these traits. Here, we employed the silkworm (Bombyx mori) infection model, which is suitable for high-throughput screening, together with an Escherichia coli library containing plasmid clones of all genes from strain W3110, to identify genes whose overexpression enhances virulence. We found that overexpression of the uncharacterized protein YaiX promoted bacterial proliferation in silkworms and increased host lethality. Compared with the empty-vector control, the YaiX-overexpressing strain exhibited resistance to multiple antimicrobial agents with diverse mechanisms of action, including β-lactams, tetracyclines, fluoroquinolones, aminoglycosides, cationic surfactants, and hydrogen peroxide. Sequence analysis revealed that amino acids 18–52 of YaiX contain a transferase hexapeptide domain predicted to form a left-handed parallel β-helix. Overexpression of YaiX mutants lacking regions outside this domain conferred ampicillin resistance, whereas deletion of the hexapeptide domain abolished this phenotype. RNA sequencing and GO enrichment analyses further indicated that YaiX overexpression altered the expression of genes encoding RNA-binding proteins and porins. These findings suggest that YaiX overexpression, through its hexapeptide domain, modulates gene expression and contributes to both multidrug resistance and enhanced virulence in E. coli.
キーワード
Escherichia coli
hexapeptide domain
multidrug resistance
pseudogene function
RNA‐seq
silkworm infection model
virulence
yaiX
発行日
2026-02-25
出版物タイトル
Microbiology and Immunology
出版者
Wiley
ISSN
0385-5600
NCID
AA00738350
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2026 The Author(s).
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1111/1348-0421.70049
ライセンス
http://creativecommons.org/licenses/by/4.0/
Citation
K.Hongu, K.Ishikawa, T.Kosaki, S.-I.Miyoshi, K.Furuta, and C.Kaito, “Overexpression of Escherichia coli yaiX Confers Multidrug Resistance and Enhances Virulence in the Silkworm Infection Model,” Microbiology and Immunology0 (2026): e70049. https://doi.org/10.1111/1348-0421.70049.
助成情報
23K24131: 細菌の潜在的病原性をつかさどる分子基盤の解明 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
23K06130: 樹状細胞の抗原提示プロセスに対する細菌の作用の解明 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
24K01760: 細菌と植物のヘムを巡る攻防の分子基盤 ( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
24wm0125004: ( 文部科学省 / Ministry of Education )
( 国立研究開発法人日本医療研究開発機構 / Japan Agency for Medical Research and Development )