コレラ菌がウイルス防御機構を交換する仕組みを解明(How cholera bacteria swap defenses against viruses)

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2026-04-10 スイス連邦工科大学ローザンヌ校(EPFL)

EPFLの研究は、コレラ菌がウイルス(バクテリオファージ)に対抗する防御機構を交換・共有する仕組みを解明したもの。細菌は可動遺伝因子を介して防御遺伝子をやり取りし、異なる防御システムを迅速に獲得できることが示された。これにより、ファージ感染に対する耐性を柔軟に変化させることが可能となる。さらに、この遺伝子交換は細菌集団内での生存競争や進化に大きく寄与することも明らかになった。本成果は、細菌とウイルスの軍拡競争の理解を深めるとともに、感染症制御やファージ療法の設計にも重要な知見を提供する。

コレラ菌がウイルス防御機構を交換する仕組みを解明(How cholera bacteria swap defenses against viruses)
Vibrio cholerae on a chitinous surface. Photo taken with a Scanning Electron Microscope. Credit: Graham Knott and Melanie Blokesch © 2026 EPFL

<関連情報>

Competence-mediated DNA uptake diversifies Vibrio cholerae sedentary chromosomal integrons

Laurie Righi, Sandrine Stutzmann, Loriane Bader, Alexandre Lemopoulos, and Melanie Blokesch
Science  Published:9 Apr 2026
DOI:https://doi.org/10.1126/science.aed0645

Editor’s summary

Vibrio cholerae bacteria contain a huge genetic element composed of multiple gene cassettes called a sedentary chromosomal integron (SCI). About 10% of the gene cassettes are important for phage defense. It was supposed that, under stress, the cassettes are shuffled to generate diversity, but this has not been observed for more than 60 years in human-associated pandemic cholera bacteria. Instead, Righi et al. show that the SCI diversifies in natural aquatic environments by the horizontal acquisition of genes released from dying bacteria growing on chitinous debris found in such environments. In human-associated environments, chitin is largely absent. That factor, as well as a nutrient-rich environment, tend to suppress competence for DNA uptake among V. cholerae and reduce the diversity of SCI-encoded phage defenses. —Caroline Ash and Stella M. Hurtley

Abstract

Bacteria often survive viral attack and environmental stress by sharing genes that enhance their defenses. The cholera pathogen Vibrio cholerae carries a sedentary chromosomal integron (SCI), a genetic element containing hundreds of mostly promoterless gene cassettes, about 10% of which encode antiviral systems. Cassettes are thought to reshuffle under stress to the favorable first array position, yet the SCI in pandemic V. cholerae has remained static for more than 60 years. In this study, we show that SCI diversification efficiently occurs by horizontal transfer linked to the genus’s aquatic lifestyle: DNA released from lysed cells is taken up by naturally competent vibrios and integrated into the first position of the SCI array, the primary site of strong expression, where it confers resistance to phage and potentially other threats.

細胞遺伝子工学
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