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Published on: February 19, 2019
Evolutionary blueprint for host- and niche-adaptation in Staphylococcus aureus clonal complex CC30
Martin J McGavin1, Benjamin Arsic, Nicholas N Nickerson
1Department of Microbiology, Schulich School of Medicine and Dentistry, Siebens Drake Research Institute and Centre for Human Immunology, University of Western Ontario, London ON, Canada. martin.mcgavin@ schulich.uwo.ca
Staphylococcus aureus CC30 Clade 3 strains have evolved reduced virulence and adapted to specific niches. These hospital-associated MRSA and MSSA strains show genetic changes favoring adaptation over hyper-virulence.
Area of Science:
- Microbiology
- Evolutionary Biology
- Genomics
Background:
- Staphylococcus aureus clonal complex CC30 has a long history of causing infectious epidemics.
- Phylogenetic analyses revealed three major branches (Clades 1-3) within CC30.
- Clades 1 and 2 are hyper-virulent, while Clade 3 exhibits attenuated virulence.
Purpose of the Study:
- To investigate the evolutionary adaptations of Staphylococcus aureus CC30 Clade 3 strains.
- To assess the hypothesis that Clade 3 has evolved for niche adaptation.
Main Methods:
- In silico genome comparisons of 15 public domain CC30 genomes.
- Analysis of single nucleotide polymorphisms (SNPs) and other genetic traits.
- Phylogenetic analysis and comparative genomics.
Main Results:
- Clade 3 strains possess SNPs affecting alpha-hemolysin (Hla) production and accessory gene regulator (agr) signaling.
- Common Clade 3 traits include tryptophan auxotrophy, truncated IsdH, loss of toxin-antitoxin modules, and acquisition of SaPI4/SaPI2.
- S. aureus MN8 (Clade 3) shows unique ISSau2 insertion and enhanced toxic shock syndrome toxin (tst) production.
Conclusions:
- Clade 3 strains demonstrate an evolutionary trajectory towards niche adaptation.
- Genetic modifications in Clade 3 contribute to reduced virulence and specialized functions.
- These findings provide insights into the evolution of bacterial pathogenicity and adaptation.
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