4.7 Article

Discovery of Pantoea stewartii ssp stewartii genes important for survival in corn xylem through a Tn-Seq analysis

Journal

MOLECULAR PLANT PATHOLOGY
Volume 19, Issue 8, Pages 1929-1941

Publisher

WILEY
DOI: 10.1111/mpp.12669

Keywords

maize; outer membrane proteins; Pantoea stewartii; phytopathogen; Tn-Seq; wilt disease; xylem dwelling

Categories

Funding

  1. Virginia Tech Biological Sciences Department and Life Sciences 1 Building Fund
  2. Fralin Institute Genomics Analysis Incubator
  3. Graduate Student Development Award (GSDA) Fellowship from the Graduate School
  4. Graduate Research Development Program (GRDP) Award from the Graduate School

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The bacterium Pantoea stewartii ssp. stewartii causes Stewart's wilt disease in corn. Pantoea stewartii is transmitted to plants via corn flea beetles, where it first colonizes the apoplast causing water-soaked lesions, and then migrates to the xylem and forms a biofilm that blocks water transport. Bacterial quorum sensing ensures that the exopolysaccharide production necessary for biofilm formation occurs only at high cell density. A genomic-level transposon sequencing (Tn-Seq) analysis was performed to identify additional bacterial genes essential for survival inplanta and to provide insights into the plant-microbe interactions occurring during wilt disease. A mariner transposon library of approximately 40 000 mutants was constructed and used to inoculate corn seedlings through a xylem infection model. Cultures of the library grown in Luria-Bertani (LB) broth served as the invitro pre-inoculation control. Tn-Seq analysis showed that the number of transposon mutations was reduced by more than 10-fold for 486 genes inplanta compared with the library that grew in LB, suggesting that they are important for xylem survival. Interestingly, a small set of genes had a higher abundance of mutants inplanta versus invitro conditions, indicating enhanced strain fitness with loss of these genes inside the host. Inplanta competition assays retested the trends of the Tn-Seq data for several genes, including two outer membrane proteins, Lon protease and two quorum sensing-associated transcription factors, RcsA and LrhA. Virulence assays were performed to check for correlation between growth/colonization and pathogenicity. This study demonstrates the capacity of a Tn-Seq approach to advance our understanding of P.stewartii-corn interactions.

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