# The role of quorum sensing in rhizosphere community regulation during bacterial wilt pathogen invasion

## TL;DR

This study explores how quorum sensing influences the rhizosphere microbial community during bacterial wilt infection, showing that the pathogen disrupts beneficial microbial interactions.

## Contribution

The study reveals how quorum sensing by Ralstonia solanacearum reshapes the rhizosphere microbiome during infection.

## Key findings

- QS genes in beneficial bacteria are down-regulated in wilt-infected rhizosphere.
- Pathogenic R. solanacearum up-regulates eight QS signaling pathways during infection.
- The QS gene network in infected rhizosphere becomes simplified and less connected.

## Abstract

Bacterial wilt, caused by the soil-borne pathogen Ralstonia solanacearum is a major threat to solanaceous crops worldwide. The onset of this disease is frequently associated with disruptions in the rhizosphere microbial community. Quorum sensing (QS), a key mechanism for microbial communication, plays a critical role in regulating microbial interactions and maintaining community structure. However, whether and how QS is involved in reshaping the rhizosphere microbiome during R. Solanacearum infection remains poorly understood. In this study we compared QS-related genes, signaling pathways, and network structures in metagenomes of healthy and wilt-infected rhizospheres. The results show QS-related genes of the plant beneficial bacterial were significantly down-regulate, whereas QS-related genes of pathogenic R. Solanacearum were up-regulated in wilt-infected rhizosphere. The up-regulated QS genes of pathogens belong to eight QS signaling pathways (AI-1, GABA, PapR, NprX, Phr, cCF10, and DSF). Network analysis showed a simplified structure in the wilt-infected rhizosphere. It is also found the number of connectors in the QS gene co-occurrence network was reduced in wilt-infected rhizosphere network. This is due to the upregulation of QS system allows the pathogen to mediate the rhizosphere microbial ecology network, and leads to destabilization of rhizosphere community. These findings demonstrate that QS system contributes to bacterial wilt infection by suppressing the QS-based interactions among plant beneficial microbes, thereby triggering community function disruption.