| Literature DB >> 28947652 |
Yogitha N Srikhanta1,2, Ka Yee Fung3, Georgina L Pollock3, Vicki Bennett-Wood3, Benjamin P Howden4, Elizabeth L Hartland3.
Abstract
Kingella kingae is a common etiological agent of pediatric osteoarticular infections. While current research has expanded our understanding of K. kingae pathogenesis, there is a paucity of knowledge about host-pathogen interactions and virulence gene regulation. Many host-adapted bacterial pathogens contain phase variable DNA methyltransferases (mod genes), which can control expression of a regulon of genes (phasevarion) through differential methylation of the genome. Here, we identify a phase variable type III mod gene in K. kingae, suggesting that phasevarions operate in this pathogen. Phylogenetic studies revealed that there are two active modK alleles in K. kingae Proteomic analysis of secreted and surface-associated proteins, quantitative PCR, and a heat shock assay comparing the wild-type modK1 ON (i.e., in frame for expression) strain to a modK1 OFF (i.e., out of frame) strain revealed three virulence-associated genes under ModK1 control. These include the K. kingae toxin rtxA and the heat shock genes groEL and dnaK Cytokine expression analysis showed that the interleukin-8 (IL-8), IL-1β, and tumor necrosis factor responses of THP-1 macrophages were lower in the modK1 ON strain than in the modK1::kan mutant. This suggests that the ModK1 phasevarion influences the host inflammatory response and provides the first evidence of this phase variable epigenetic mechanism of gene regulation in K. kingae.Entities:
Keywords: Kingella kingae; gene regulation; phase variation; phasevarion; type III restriction-modification systems
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Year: 2017 PMID: 28947652 PMCID: PMC5695113 DOI: 10.1128/IAI.00319-17
Source DB: PubMed Journal: Infect Immun ISSN: 0019-9567 Impact factor: 3.441