Plant-exuded chemical signals induce surface attachment of the bacterial pathogen Pseudomonas syringae

PeerJ. 2023 Mar 27:11:e14862. doi: 10.7717/peerj.14862. eCollection 2023.

Abstract

Many plant pathogenic bacteria suppress host defenses by secreting small molecule toxins or immune-suppressing proteins into host cells, processes that likely require close physical contact between pathogen and host. Yet, in most cases, little is known about whether phytopathogenic bacteria physically attach to host surfaces during infection. Here we report that Pseudomonas syringae pv. tomato strain DC3000, a Gram-negative bacterial pathogen of tomato and Arabidopsis, attaches to polystyrene and glass surfaces in response to chemical signals exuded from Arabidopsis seedlings and tomato leaves. We characterized the molecular nature of these attachment-inducing signals and discovered that multiple hydrophilic metabolites found in plant exudates, including citric acid, glutamic acid, and aspartic acid, are potent inducers of surface attachment. These same compounds were previously identified as inducers of P. syringae genes encoding a type III secretion system (T3SS), indicating that both attachment and T3SS deployment are induced by the same plant signals. To test if surface attachment and T3SS are regulated by the same signaling pathways, we assessed the attachment phenotypes of several previously characterized DC3000 mutants, and found that the T3SS master regulator HrpL was partially required for maximal levels of surface attachment, whereas the response regulator GacA, a negative regulator of T3SS, negatively regulated DC3000 surface attachment. Together, our data indicate that T3SS deployment and surface attachment by P. syringae may be co-regulated by the same host signals during infection, possibly to ensure close contact necessary to facilitate delivery of T3SS effectors into host cells.

Keywords: Arabidopsis; Biofilm; Inter-Kingdom signaling; Pseudomonas syringae; Type III secretion.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Arabidopsis* / genetics
  • Bacterial Proteins / genetics
  • Pseudomonas syringae / genetics

Substances

  • Bacterial Proteins

Grants and funding

This work was supported by USDA National Institute of Food and Agriculture Predoctoral Fellowship 2020-67034-31746 awarded to Megan R. O’Malley, National Science Foundation grants IOS-1456256 and IOS-1953509 awarded to Scott C. Peck, and National Science Foundation grant IOS-1557694 awarded to Jeffrey C. Anderson. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.