Zhao Qiaoyun, Yin Wenzhu, Zhao Rulin, Wang Youhua, Song Conghua, Wang Huan, Rong Jianfang, Wang Fangfei, Xie Yong
Department of Gastroenterology, First Affiliated Hospital of Nanchang University, No.17 Yongwaizheng Street, Donghu District, Nanchang, 330006, Jiangxi, China.
Microbiology Laboratory, Gastroenterology Institute of Jiangxi Province, Nanchang, 330006, Jiangxi, China.
Med Microbiol Immunol. 2020 Oct;209(5):621-630. doi: 10.1007/s00430-020-00688-w. Epub 2020 Jun 30.
Outer inflammatory protein (OipA) is an important virulence factor of Helicobacter pylori (H. pylori), but the correlation between oipA copy number and its virulence remains unknown. The study was designed to investigate whether the duplicate oipA gene loci showed more virulent than one oipA gene in vitro. H. pylori strain CCS9803 (China Chongqing Strain 9803) that carries duplicate oipA loci was used to construct one or two oipA knockout mutant strain, which was further verified by qPCR and western blot. Gastric epithelial cells AGS and GES-1 were infected with wild-type (WT) or oipA mutants for 6 or 24 h. The expression levels of IL-8, bacterial adhesion, cell apoptosis and cell cycle were performed to analyze the function of oipA. The WT and oipA mutant strains induce significantly higher mRNA and protein levels of IL-8 than the uninfected group (P < 0.05), but only oipA2 mutants induced significantly decreased expression levels than the WT-infected group (P < 0.05). Adherence to gastric cells was significantly decreased by inactivated two oipA loci (P < 0.05). The WT strain caused a significant rising proportion of early apoptosis cell, which had dropped after duplicate oipA genes were both knockout (P < 0.05). WT and oipA1 mutants failed to affect cell cycle; however, the oipA2 mutants increased M phase and reduced S phase when compared to the uninfected group. In conclusion, our study demonstrated that oipA impacts IL-8 expression, adherence, cell apoptosis and cell cycle of gastric cells independent of its gene copy number.
外炎症蛋白(OipA)是幽门螺杆菌(H. pylori)的一种重要毒力因子,但oipA拷贝数与其毒力之间的相关性尚不清楚。本研究旨在调查在体外,具有两个拷贝的oipA基因位点是否比一个oipA基因更具毒力。携带两个拷贝oipA位点的幽门螺杆菌菌株CCS9803(中国重庆菌株9803)被用于构建一个或两个oipA基因敲除突变株,通过定量聚合酶链反应(qPCR)和蛋白质免疫印迹法(western blot)进一步验证。胃上皮细胞AGS和GES-1分别用野生型(WT)或oipA突变株感染6或24小时。检测白细胞介素-8(IL-8)的表达水平、细菌黏附、细胞凋亡和细胞周期,以分析oipA的功能。WT和oipA突变株诱导的IL-8 mRNA和蛋白水平均显著高于未感染组(P<0.05),但只有oipA2突变株诱导的表达水平显著低于WT感染组(P<0.05)。两个oipA位点失活后,对胃细胞的黏附显著降低(P<0.05)。WT菌株导致早期凋亡细胞比例显著升高,两个oipA基因均敲除后该比例下降(P<0.05)。WT和oipA1突变株不影响细胞周期;然而,与未感染组相比,oipA2突变株增加了M期细胞比例并减少了S期细胞比例。总之,我们的研究表明,oipA对胃细胞IL-8表达、黏附、细胞凋亡和细胞周期的影响与其基因拷贝数无关。