農作物への病原性細菌の侵入メカニズムを解明(How harmful bacteria hijack crops)

2025-09-09 ワシントン大学セントルイス校

ワシントン大学セントルイス校の研究で、植物病原菌 Pseudomonas syringae がトマトなどの作物に感染する際、植物のホルモン「オーキシン(auxin)」を利用して自身の病原性を強める仕組みが明らかになりました。植物がオーキシンを作ると、それを手がかりに細菌が攻撃が効果を発揮していると判断し、増殖と病原性遺伝子の発現を促進します。研究者たちは、細菌がオーキシン関連の化合物を感知するタンパク質「PmeR」を発見し、これが細菌が攻撃態勢に入るスイッチとして機能することを突き止めました。将来的には、このPmeRの作用を阻害する物質を作物に噴霧するなどして、細菌を「オーキシンを聞こえない状態」にして病害の進行を遅らせる可能性があるとしています。しかし、植物自身にとってオーキシンは成長に必須のホルモンであり、単にその生成を止めることはできないため、細菌側の感知機構を標的とする戦略が中心になる見込みです。

農作物への病原性細菌の侵入メカニズムを解明(How harmful bacteria hijack crops)
Spots on a tomato indicate bacteria infestation. WashU researchers have identified the protein involved in these costly plant infestations. (Photo: Shutterstock)

<関連情報>

PmeR, a TetR-like transcriptional regulator, is involved in both auxin signaling and virulence in the plant pathogen Pseudomonas syringae strain PtoDC3000

Chia-Yun Lee, Maya Irvine, Barbara Kunkel
mBio  Published:20 August 2025
DOI:https://doi.org/10.1128/mbio.01152-25

ABSTRACT

Plant pathogenic bacteria, such as Pseudomonas syringae strain PtoDC3000, respond to host signals through complex signaling networks that regulate bacterial growth and virulence. The plant hormone indole-3-acetic acid (IAA), also known as auxin, promotes bacterial pathogenesis via multiple mechanisms, including through reprogramming of bacterial transcription. However, the mechanisms that PtoDC3000 uses to sense and respond to auxin are not well understood. Here, we identify a novel bacterial auxin-signaling mechanism mediated by pmeR, which encodes a TetR-like family transcriptional repressor that acts as an important regulator of IAA-responsive gene expression in PtoDC3000. Using qRT-PCR and transcriptional reporter assays, we show that pmeR is induced by IAA and regulates several auxin-responsive genes. pmeR plays two different roles in the regulation of auxin-responsive genes: as a repressor of its own expression and as an activator of other genes. Plant infection assays further show that the disruption of pmeR results in reduced bacterial growth in Arabidopsis thaliana. Notably, although PmeR de-represses the transcription of pmeR upon IAA treatment, it does not appear to directly bind IAA. Rather, our biochemical results indicate that the auxin conjugate IAA-lysine may serve as a ligand for PmeR. Our findings reveal a complex signaling network through which IAA modulates bacterial gene expression and emphasize the role of PmeR in acclimating PtoDC3000 for growth in plant tissue.

1202農芸化学
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