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Evaluating Virulence and Pathogenesis of Aeromonas Infection in a Caenorhabditis elegans Model
Published on: December 20, 2018
Genome-wide identification of Pseudomonas aeruginosa virulence-related genes using a Caenorhabditis elegans infection
Rhonda L Feinbaum1, Jonathan M Urbach, Nicole T Liberati
1Department of Genetics, Harvard Medical School, and Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America. feinbaum@molbio.mgh.harvard.edu
Abstract:
Pseudomonas aeruginosa strain PA14 is an opportunistic human pathogen capable of infecting a wide range of organisms including the nematode Caenorhabditis elegans. We used a non-redundant transposon mutant library consisting of 5,850 clones corresponding to 75% of the total and approximately 80% of the non-essential PA14 ORFs to carry out a genome-wide screen for attenuation of PA14 virulence in C. elegans. We defined a functionally diverse 180 mutant set (representing 170 unique genes) necessary for normal levels of virulence that included both known and novel virulence factors. Seven previously uncharacterized virulence genes (ABC transporters PchH and PchI, aminopeptidase PepP, ATPase/molecular chaperone ClpA, cold shock domain protein PA0456, putative enoyl-CoA hydratase/isomerase PA0745, and putative transcriptional regulator PA14_27700) were characterized with respect to pigment production and motility and all but one of these mutants exhibited pleiotropic defects in addition to their avirulent phenotype. We examined the collection of genes required for normal levels of PA14 virulence with respect to occurrence in P. aeruginosa strain-specific genomic regions, location on putative and known genomic islands, and phylogenetic distribution across prokaryotes. Genes predominantly contributing to virulence in C. elegans showed neither a bias for strain-specific regions of the P. aeruginosa genome nor for putatively horizontally transferred genomic islands. Instead, within the collection of virulence-related PA14 genes, there was an overrepresentation of genes with a broad phylogenetic distribution that also occur with high frequency in many prokaryotic clades, suggesting that in aggregate the genes required for PA14 virulence in C. elegans are biased towards evolutionarily conserved genes.
Insights
A genome-wide screen identified 170 genes essential for Pseudomonas aeruginosa PA14 virulence in Caenorhabditis elegans. Many virulence genes are evolutionarily conserved, not specific to genomic islands.
Area of Science:
- Microbiology
- Genetics
- Pathogenesis
Background:
- * Pseudomonas aeruginosa* strain PA14 is an opportunistic pathogen infecting diverse hosts, including *Caenorhabditis elegans*.
- *C. elegans* serves as a model organism for studying bacterial virulence.
- Understanding PA14 virulence factors is crucial for combating infections.
Purpose of the Study:
- To conduct a genome-wide screen to identify genes essential for PA14 virulence in *C. elegans*.
- To characterize novel virulence factors and their roles in pathogenesis.
- To investigate the evolutionary origins and distribution of virulence genes.
Main Methods:
- * A non-redundant transposon mutant library of *P. aeruginosa* PA14 (5,850 clones) was screened.
- * Genome-wide screen in *C. elegans* to identify attenuated virulence mutants.
- * Characterization of novel virulence genes for pigment production, motility, and pleiotropic defects.
Main Results:
- * A set of 170 unique genes (180 mutants) was identified as necessary for normal PA14 virulence.
- * Seven previously uncharacterized virulence genes were characterized, most showing pleiotropic defects.
- * Virulence genes were found to be broadly distributed phylogenetically and not biased towards genomic islands.
Conclusions:
- * The study identified a comprehensive set of PA14 virulence genes in *C. elegans*.
- * Novel virulence factors were characterized, revealing complex roles in pathogenesis.
- * PA14 virulence genes are predominantly evolutionarily conserved, suggesting a broad importance across prokaryotes.

