Yu Min, Xu Min, Shen Yixin, Liu Yun, Xu Chi, Feng Tongbao, Zhang Ping
Department of Clinical Laboratory, The Affiliated Changzhou Second People's Hospital of Nanjing Medical University, Changzhou, 213000, China.
Department of Medical Microbiology, School of Medicine, Jiangsu University, Zhenjiang, 212013, China.
Heliyon. 2023 Jul 1;9(7):e17881. doi: 10.1016/j.heliyon.2023.e17881. eCollection 2023 Jul.
is the number of cag pathogenicity island (cagPAI) family in (), which encoded Cag2 protein. The aim of this study was to investigate the role of on the strain. We constructed the recombinant prokaryotic expression plasmid pET-32a- and pET-32a-. Then, we co-cultured the wild strain 26,695 and strain with GES-1 cells to detect CagA protein transport and IL-8 secretion. We found that mutation increased the expression of and promoted the transportation of CagA protein in GES-1 cells. In addition, we also observed that mutation had no effect on other cagPAI protein stability and the expression of IL-8. Our findings suggested that may down-regulated the expression of cagA, rpoB and inhibited the transportation of CagA protein in GES-1 cells and had no effect on growth.
是()中cag致病岛(cagPAI)家族的数量,其编码Cag2蛋白。本研究的目的是探讨其对菌株的作用。我们构建了重组原核表达质粒pET-32a-和pET-32a-。然后,我们将野生菌株26,695和菌株与GES-1细胞共培养,以检测CagA蛋白转运和IL-8分泌。我们发现突变增加了的表达并促进了GES-1细胞中CagA蛋白的转运。此外,我们还观察到突变对其他cagPAI蛋白稳定性和IL-8表达没有影响。我们的研究结果表明,可能下调cagA、rpoB的表达并抑制GES-1细胞中CagA蛋白的转运,且对生长没有影响。