EspP2 Regulates the Adhesion of Glaesserella parasuis via Rap1 Signaling Pathway.
Xinwei TangShiyu XuZhen YangKang WangKe DaiYiwen ZhangBangdi HuYu WangSan-Jie CaoXiaobo HuangQigui YanRui WuQin ZhaoSenyan DuXintian WenYiping WenPublished in: International journal of molecular sciences (2024)
Different levels of EspP2 expression are seen in strains of Glaesserella parasuis with high and low pathogenicity. As a potential virulence factor for G. parasuis , the pathogenic mechanism of EspP2 in infection of host cells is not clear. To begin to elucidate the effect of EspP2 on virulence, we used G. parasuis SC1401 in its wild-type form and SC1401, which was made EspP2 -deficient. We demonstrated that EspP2 causes up-regulation of claudin-1 and occludin expression, thereby promoting the adhesion of G. parasuis to host cells; EspP2 -deficiency resulted in significantly reduced adhesion of G. parasuis to cells. Transcriptome sequencing analysis of EspP2-treated PK15 cells revealed that the Rap1 signaling pathway is stimulated by EspP2. Blocking this pathway diminished occludin expression and adhesion. These results indicated that EspP2 regulates the adhesion of Glaesserella parasuis via Rap1 signaling pathway.
Keyphrases
- induced apoptosis
- signaling pathway
- cell cycle arrest
- biofilm formation
- poor prognosis
- pi k akt
- endoplasmic reticulum stress
- escherichia coli
- pseudomonas aeruginosa
- oxidative stress
- staphylococcus aureus
- single cell
- cell death
- cell migration
- candida albicans
- binding protein
- risk assessment
- antimicrobial resistance
- genome wide
- rna seq
- dna methylation