Adaptation genomics of a small-colony variant in a Pseudomonas chlororaphis 30-84 biofilm

• Published in: Applied and Environmental Microbiology 2015-02, Vol.81 (3), p.890-899
• Main Authors: Wang, Dongping, Dorosky, Robert J, Han, Cliff S, Lo, Chien-Chi, Dichosa, Armand E K, Chain, Patrick S, Yu, Jun Myoung, Pierson, 3rd, Leland S, Pierson, Elizabeth A
• Format: Article
• Language: English
• Subjects: Adaptation, Biological; Anti-Bacterial Agents - metabolism; Antibiotics; Bacteria; Biofilms; Biofilms - growth & development; Drug resistance; Drug Tolerance; Evolutionary and Genomic Microbiology; Gene Expression Profiling; Genome, Bacterial; Genomics; Genotype & phenotype; Locomotion; Molecular Sequence Data; Phenazines - metabolism; Plant Roots - microbiology; Pseudomonas - drug effects; Pseudomonas - growth & development; Pseudomonas - metabolism; Pseudomonas - physiology; Pseudomonas chlororaphis; Sequence Analysis, DNA; Soil Microbiology; Triticum - microbiology; Triticum aestivum
• ISSN: 0099-2240; 1098-5336; 1098-6596
• DOI: 10.1128/AEM.02617-14

The rhizosphere-colonizing bacterium Pseudomonas chlororaphis 30-84 is an effective biological control agent against take-all disease of wheat. In this study, we characterize a small-colony variant (SCV) isolated from a P. chlororaphis 30-84 biofilm. The SCV exhibited pleiotropic phenotypes, including small cell size, slow growth and motility, low levels of phenazine production, and increased biofilm formation and resistance to antimicrobials. To better understand the genetic alterations underlying these phenotypes, RNA and whole-genome sequencing analyses were conducted comparing an SCV to the wild-type strain. Of the genome's 5,971 genes, transcriptomic profiling indicated that 1,098 (18.4%) have undergone substantial reprograming of gene expression in the SCV. Whole-genome sequence analysis revealed multiple alterations in the SCV, including mutations in yfiR (cyclic-di-GMP production), fusA (elongation factor), and cyoE (heme synthesis) and a 70-kb deletion. Genetic analysis revealed that the yfiR locus plays a major role in controlling SCV phenotypes, including colony size, growth, motility, and biofilm formation. Moreover, a point mutation in the fusA gene contributed to kanamycin resistance. Interestingly, the SCV can partially switch back to wild-type morphologies under specific conditions. Our data also support the idea that phenotypic switching in P. chlororaphis is not due to simple genetic reversions but may involve multiple secondary mutations. The emergence of these highly adherent and antibiotic-resistant SCVs within the biofilm might play key roles in P. chlororaphis natural persistence.