Genome-wide identification of Pseudomonas syringae genes required for fitness during colonization of the leaf surface and apoplast

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 116; no. 38; pp. 18900 - 18910
• Main Authors: Helmann, Tyler C., Deutschbauer, Adam M., Lindow, Steven E.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 17.09.2019
• Subjects: Alginates; Alginic acid; Amino acids; Apoplast; Biological Sciences; Biosynthesis; Colonization; Extracellular Space - microbiology; Fitness; Gene expression; Gene Expression Profiling; Genes; Genes, Bacterial; Genetic Fitness; Genome, Bacterial - genetics; Genomes; Host-Pathogen Interactions - genetics; Leaves; Mutation; Pathogens; Phaseolus vulgaris; Plant Diseases - microbiology; Plant Leaves - cytology; Plant Leaves - microbiology; Polysaccharides; Pseudomonas; Pseudomonas syringae; Pseudomonas syringae - genetics; Pseudomonas syringae - physiology; Secretion; Transcription; epiphytes; endophytes; gene expression
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1908858116

The foliar plant pathogen Pseudomonas syringae can establish large epiphytic populations on leaf surfaces before apoplastic colonization. However, the bacterial genes that contribute to these lifestyles have not been completely defined. The fitness contributions of 4,296 genes in P. syringae pv. syringae B728a were determined by genome-wide fitness profiling with a randomly barcoded transposon mutant library that was grown on the leaf surface and in the apoplast of the susceptible plant Phaseolus vulgaris. Genes within the functional categories of amino acid and polysaccharide (including alginate) biosynthesis contributed most to fitness both on the leaf surface (epiphytic) and in the leaf interior (apoplast), while genes involved in type III secretion system and syringomycin synthesis were primarily important in the apoplast. Numerous other genes that had not been previously associated with in planta growth were also required for maximum epiphytic or apoplastic fitness. Fourteen hypothetical proteins and uncategorized glycosyltransferases were also required for maximum competitive fitness in and on leaves. For most genes, no relationship was seen between fitness in planta and either the magnitude of their expression in planta or degree of induction in planta compared to in vitro conditions measured in other studies. A lack of association of gene expression and fitness has important implications for the interpretation of transcriptional information and our broad understanding of plant–microbe interactions.