Transcriptome change of Staphylococcus aureus in infected mouse liver.
Hiroshi HamamotoSuresh PantheeAtmika PaudelSuguru OhgiYutaka SuzukiKoichi MakimuraKazuhisa SekimizuPublished in: Communications biology (2022)
We performed in vivo RNA-sequencing analysis of Staphylococcus aureus in infected mouse liver using the 2-step cell-crush method. We compared the transcriptome of S. aureus at 6, 24, and 48 h post-infection (h.p.i) in mice and in culture medium. Genes related to anaerobic respiration were highly upregulated at 24 and 48 h.p.i. The gene expression patterns of virulence factors differed depending on the type of toxin. For example, hemolysins, but not leukotoxins and serine proteases, were highly upregulated at 6 h.p.i. Gene expression of metal transporters, such as iron transporters, gradually increased at 24 and 48 h.p.i. We also analyzed the transcriptome of mouse liver infected with S. aureus. Hypoxia response genes were upregulated at 24 and 48 h.p.i., and immune response genes were upregulated from 6 h.p.i. These findings suggest that gene expression of S. aureus in the host changes in response to changes in the host environment, such as the oxygenation status or immune system attacks during infection.
Keyphrases
- gene expression
- staphylococcus aureus
- genome wide
- single cell
- dna methylation
- immune response
- rna seq
- escherichia coli
- biofilm formation
- bioinformatics analysis
- genome wide identification
- methicillin resistant staphylococcus aureus
- mesenchymal stem cells
- metabolic syndrome
- type diabetes
- bone marrow
- cystic fibrosis
- antimicrobial resistance
- candida albicans
- adipose tissue
- transcription factor
- skeletal muscle
- insulin resistance
- sewage sludge
- drug induced