Noori Maryam, Azimirad Masoumeh, Eslami Gita, Looha Mehdi Azizmohammad, Yadegar Abbas, Ghalavand Zohreh, Zali Mohammad Reza
Department of Microbiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Foodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
BMC Microbiol. 2022 Oct 27;22(1):259. doi: 10.1186/s12866-022-02665-0.
Surface layer protein A (SlpA), the primary outermost structure of Clostridioides difficile, plays an essential role in C. difficile pathogenesis, although its interaction with host intestinal cells are yet to be understood. The aim of this study was to investigate the effects of SlpA extracted from C. difficile on tight junction (TJ) proteins expression and induction of pro-inflammatory cytokines in human colon carcinoma cell line HT-29. SlpA was extracted from three toxigenic C. difficile clinical strains including RT126, RT001, RT084 as well as C. difficile ATCC 700057 as non-toxigenic strain. Cell viability was performed by MTT assay, and the mRNA expression of TJ proteins and inflammation-associated genes was determined using quantitative RT-PCR. Additionally, the secretion of IL-8, IL-1β and TNF-α cytokines was measured by ELISA.
C. difficile SlpA from selected RTs variably downregulated the expression level of TJs-assassinated genes and increased the expression level of TLR-4 and pro-inflammatory cytokines in HT-29 treated cells. SlpA from RT126 significantly (p<0.05) decreased the gene expression level of claudins family and JAM-A and increased the secretion of IL-8, TNF-α and IL1-β as compared to untreated cells. Moreover, only SlpA from RT001 could significantly induce the expression of IL-6 (p<0.05).
The results of the present study highlighted the importance of SlpA in the pathogenesis of CDI and C. difficile-induced inflammatory response in the gut. Further studies are required to unravel the significance of the observed results in promoting the intestinal inflammation and immune response induced by C. difficile SlpA from different RTs.
表面层蛋白A(SlpA)是艰难梭菌的主要最外层结构,在艰难梭菌致病过程中起着至关重要的作用,尽管其与宿主肠道细胞的相互作用尚不清楚。本研究的目的是调查从艰难梭菌中提取的SlpA对人结肠癌细胞系HT-29中紧密连接(TJ)蛋白表达和促炎细胞因子诱导的影响。SlpA是从包括RT126、RT001、RT084在内的三株产毒艰难梭菌临床菌株以及作为非产毒菌株的艰难梭菌ATCC 700057中提取的。通过MTT法检测细胞活力,使用定量RT-PCR测定TJ蛋白和炎症相关基因的mRNA表达。此外,通过ELISA检测IL-8、IL-1β和TNF-α细胞因子的分泌。
来自选定RTs的艰难梭菌SlpA在处理的HT-29细胞中不同程度地下调了TJ相关基因的表达水平,并增加了TLR-4和促炎细胞因子的表达水平。与未处理的细胞相比,来自RT126的SlpA显著(p<0.05)降低了claudins家族和JAM-A的基因表达水平,并增加了IL-8、TNF-α和IL1-β的分泌。此外,只有来自RT001的SlpA能显著诱导IL-6的表达(p<0.05)。
本研究结果突出了SlpA在CDI发病机制以及艰难梭菌诱导的肠道炎症反应中的重要性。需要进一步研究来阐明不同RTs的艰难梭菌SlpA在促进肠道炎症和免疫反应方面所观察到结果的意义。