Abstract
The survival of individual Pseudomonas syringae cells was determined on bean leaf surfaces maintained under humid conditions or periodically exposed to desiccation stress. Cells of P. syringae strain B728a harboring a GFP marker gene were visualized by epifluorescence microscopy, either directly in situ or after recovery from leaves, and dead cells were identified as those that were stained with propidium iodide in such populations. Under moist, conducive conditions on plants, the proportion of total live cells was always high, irrespective of their aggregated state. In contrast, the proportion of the total cells that remained alive on leaves that were periodically exposed to desiccation stress decreased through time and was only approximately 15% after 5 days. However, the fraction of cells in large aggregates that were alive on such plants in both condition was much higher than more solitary cells. Immediately after inoculation, cells were randomly distributed over the leaf surface and no aggregates were observed. However, a very aggregated pattern of colonization was apparent within 7 days, and >90% of the living cells were located in aggregates of 100 cells or more. Our results strongly suggest that, although conducive conditions favor aggregate formation, such cells are much more capable of tolerating environmental stresses, and the preferential survival of cells in aggregates promotes a highly clustered spatial distribution of bacteria on leaf surfaces.
MeSH Terms
Cell Division
Cell Survival
Cloning, Molecular
Escherichia coli/genetics
Fabaceae/microbiology
Genetic Markers
Green Fluorescent Proteins
Luminescent Proteins/analysis,genetics
Microscopy, Fluorescence
Plant Leaves/microbiology
Plasmids/isolation & purification
Pseudomonas syringae/cytology,genetics,growth & development
Salmonella typhimurium/genetics
Chemicals
Genetic Markers
Luminescent Proteins
Green Fluorescent Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Monier J-M
Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720, USA.
Lindow S E
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