Laboratory of Infection Immunology, Department of Life Science, National Institute of Technology, Rourkela, 769008, Odisha, India.
Microb Pathog. 2023 Dec;185:106432. doi: 10.1016/j.micpath.2023.106432. Epub 2023 Nov 4.
Salmonella spp. are facultative anaerobic, Gram-negative, rod-shaped bacteria and belongs to the Enterobacteriaceae family. Although much has been known about Salmonella pathogenesis, the functional characterizations of certain genes are yet to be explored. The rspA (STM14_1818) is one such gene with putative dehydratase function, and its role in pathogenesis is unknown. The background information showed that rspA gene is upregulated in Salmonella when it resides inside macrophages, which led us to investigate its role in Salmonella pathogenesis. We generated the rspA knockout strain and complement strain in S. Typhimurium 14028. Ex-vivo and in-vivo infectivity was looked at macrophage and epithelial cell lines and Caenorhabditis elegans (C. elegans). The mutant strain differentially formed the biofilm at different temperatures by altering the expression of genes involved in the synthesis of cellulose and curli. Besides, the mutant strain is hyperproliferative intracellularly and showed increased bacterial burden in C. elegans. The mutant strain became more infectious and lethal, causing faster death of the worms than the wild type, and also modulates the worm's innate immunity. Thus, we found that the rspA deletion mutant was more pathogenic. In this study, we concluded that the rspA gene differentially regulates the biofilm formation in a temperature dependent manner by modulating the genes involved in the synthesis of cellulose and curli and negatively regulates the Salmonella virulence for longer persistence inside the host.
沙门氏菌属是兼性厌氧、革兰氏阴性、杆状细菌,属于肠杆菌科。尽管人们对沙门氏菌的发病机制有了很多了解,但某些基因的功能特征仍有待探索。rspA(STM14_1818)就是这样一个具有假定脱水酶功能的基因,其在发病机制中的作用尚不清楚。背景信息显示,rspA 基因在沙门氏菌寄居巨噬细胞时上调,这促使我们研究其在沙门氏菌发病机制中的作用。我们在鼠伤寒沙门氏菌 14028 中生成了 rspA 敲除株和互补株。在体外和体内感染实验中,我们观察了巨噬细胞和上皮细胞系以及秀丽隐杆线虫(C. elegans)中的感染性。突变株通过改变参与纤维素和卷曲合成的基因的表达,在不同温度下差异地形成生物膜。此外,该突变株在细胞内过度增殖,并在秀丽隐杆线虫中表现出增加的细菌负荷。突变株的感染性和致死性增加,导致线虫更快死亡,并且还调节了线虫的固有免疫。因此,我们发现 rspA 缺失突变株更具致病性。在这项研究中,我们得出结论,rspA 基因通过调节参与纤维素和卷曲合成的基因,以依赖于温度的方式差异调节生物膜的形成,并负调控沙门氏菌在宿主内的更长时间持续存在的毒力。