Panjaitan Novaria Sari Dewi, Horng Yu-Tze, Chien Chih-Ching, Yang Hung-Chi, You Ren-In, Soo Po-Chi
Department of Laboratory Medicine and Biotechnology, College of Medicine, Tzu Chi University, No. 701, Sec. 3, Zhongyang Rd., Hualien 97004, Taiwan.
Graduate School of Biotechnology and Bioengineering, Yuan Ze University, Taoyuan 32003, Taiwan.
Microorganisms. 2021 Feb 8;9(2):335. doi: 10.3390/microorganisms9020335.
Capsular polysaccharide (CPS) is a crucial virulence factor for infection. We demonstrated an association of CPS production with two phosphoenolpyruvate:carbohydrate phosphotransferase systems (PTSs). Deficiency of , encoding enzyme IIA of PTS, in enhanced the transcriptional activities of , and , which are in the gene cluster, leading to high CPS production. A mutant exhibited a higher survival rate in 1% hydrogen peroxide than the wild-type. The mutant showed less sensitivity to engulfment by macrophage (RAW 264.7) than the wild-type by observing the intracellular bacteria using confocal laser scanning microscopy (CLSM) and by calculating the colony-forming units (CFU) of intracellular bacteria. After long-term incubation, the survival rate of the intracellular mutant was higher than that of the wild-type. Deficiency of enhanced the transcriptional activities of which encodes another putative enzyme II complex of a PTS. Deletion of in the mutant reduced CPS production and the transcriptional activities of compared to those of the mutant. These results indicated that one PTS component, Crr, represses CPS production by repressing another PTS component, EtcABC, in . In addition, PTS plays a role in bacterial resistance to macrophage phagocytosis.
荚膜多糖(CPS)是感染的关键毒力因子。我们证明了CPS的产生与两种磷酸烯醇丙酮酸:碳水化合物磷酸转移酶系统(PTSs)相关。在[具体菌株名称]中,编码PTS的酶IIA的[基因名称]缺失增强了位于[基因簇名称]基因簇中的[相关基因名称1]、[相关基因名称2]和[相关基因名称3]的转录活性,导致CPS的高产量。一个[突变体名称]突变体在1%过氧化氢中的存活率高于野生型。通过共聚焦激光扫描显微镜(CLSM)观察细胞内细菌并计算细胞内细菌的菌落形成单位(CFU),发现[突变体名称]突变体对巨噬细胞(RAW 264.7)吞噬的敏感性低于野生型。长期培养后,细胞内[突变体名称]突变体的存活率高于野生型。[基因名称]的缺失增强了编码PTS另一种假定酶II复合物的[相关基因名称4]的转录活性。与[突变体名称]突变体相比,在[突变体名称]突变体中缺失[基因名称]降低了CPS产量和[相关基因名称1]的转录活性。这些结果表明,一种PTS成分Crr通过抑制[具体菌株名称]中的另一种PTS成分EtcABC来抑制CPS的产生。此外,PTS在细菌对巨噬细胞吞噬的抗性中起作用。