YjbH regulates virulence genes expression and oxidative stress resistance in Staphylococcus aureus.
Atmika PaudelSuresh PantheeHiroshi HamamotoTom GrunertKazuhisa SekimizuPublished in: Virulence (2021)
We previously reported that disruption of the yjbI gene reduced virulence of Staphylococcus aureus. In this study, we found virulence in both silkworms and mice was restored by introducing the yjbH gene but not the yjbI gene to both yjbI and yjbH genes-disrupted mutants, suggesting that yjbH, the gene downstream to the yjbI gene in a two-gene operon-yjbIH, is responsible for this phenomenon. We further observed a decrease in various surface-associated proteins and changes in cell envelope glycostructures in the mutants. RNA-seq analysis revealed that disruption of the yjbI and the yjbH genes resulted in differential expression of a broad range of genes, notably, significant downregulation of genes involved in virulence and oxidative stress. Administration of N-acetyl-L-cysteine, a free-radical scavenger, restored the virulence in both the mutants. Our findings suggested that YjbH plays a role in staphylococcal pathogenicity by regulating virulence gene expression, affecting the bacterial surface structure, and conferring resistance to oxidative stress in a host.
Keyphrases
- staphylococcus aureus
- genome wide identification
- genome wide
- biofilm formation
- oxidative stress
- escherichia coli
- pseudomonas aeruginosa
- copy number
- rna seq
- antimicrobial resistance
- gene expression
- single cell
- dna methylation
- genome wide analysis
- methicillin resistant staphylococcus aureus
- transcription factor
- dna damage
- type diabetes
- cell proliferation
- skeletal muscle
- metabolic syndrome
- poor prognosis
- cell therapy
- long non coding rna
- bone marrow
- heat shock
- resting state