Alginate gene expression by Pseudomonas syringae pv. tomato DC3000 in host and non-host plants

Microbiology (Reading). 2003 May;149(Pt 5):1127-1138. doi: 10.1099/mic.0.26109-0.

Abstract

Pseudomonas syringae produces the exopolysaccharide alginate, a copolymer of mannuronic and guluronic acid. Although alginate has been isolated from plants infected by P. syringae, the signals and timing of alginate gene expression in planta have not been described. In this study, an algD : : uidA transcriptional fusion, designated pDCalgDP, was constructed and used to monitor alginate gene expression in host and non-host plants inoculated with P. syringae pv. tomato DC3000. When leaves of susceptible collard plants were spray-inoculated with DC3000(pDCalgDP), algD was activated within 72 h post-inoculation (p.i.) and was associated with the development of water-soaked lesions. In leaves of the susceptible tomato cv. Rio Grande-PtoS, algD activity was lower than in collard and was not associated with water-soaking. The expression of algD was also monitored in leaves of tomato cv. Rio Grande-PtoR, which is resistant to P. syringae pv. tomato DC3000. Within 12 h p.i., a microscopic hypersensitive response (micro-HR) was observed in Rio Grande-PtoR leaves spray-inoculated with P. syringae pv. tomato DC3000(pDCalgDP). As the HR progressed, histochemical staining indicated that individual bacterial cells on the surface of resistant tomato leaves were expressing algD. These results indicate that algD is expressed in both susceptible (e.g. collard, tomato) and resistant (Rio Grande-PtoR) host plants. The expression of algD in an incompatible host-pathogen interaction was further explored by monitoring transcriptional activity in leaves of tobacco, which is not a host for P. syringae pv. tomato. In tobacco inoculated with DC3000(pDCalgDP), an HR was evident within 12 h p.i., and algD expression was evident within 8-12 h p.i. However, when tobacco was inoculated with an hrcC mutant of DC3000, the HR did not occur and algD expression was substantially lower. These results suggest that signals that precede the HR may stimulate alginate gene expression in P. syringae. Histochemical staining with nitro blue tetrazolium indicated that the superoxide anion () is a signal for algD activation in planta. This study indicates that algD is expressed when P. syringae attempts to colonize both susceptible and resistant plant hosts.

Publication types

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

MeSH terms

  • Alginates / metabolism*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Brassica / microbiology*
  • Carbohydrate Dehydrogenases / genetics
  • Carbohydrate Dehydrogenases / metabolism*
  • Gene Expression Regulation, Bacterial*
  • Nicotiana / microbiology
  • Plant Diseases / microbiology
  • Plant Leaves / microbiology
  • Pseudomonas / genetics*
  • Pseudomonas / metabolism
  • Pseudomonas / pathogenicity
  • Recombinant Fusion Proteins / metabolism
  • Solanum lycopersicum / microbiology*
  • Species Specificity
  • Superoxides / metabolism
  • Virulence

Substances

  • Alginates
  • Bacterial Proteins
  • Recombinant Fusion Proteins
  • Superoxides
  • Carbohydrate Dehydrogenases
  • GDPmannose dehydrogenase