Department of Clinical Laboratory, the First Affiliated Hospital of Nanchang University, Nanchang, China.
Department of medicine, Nanchang University, Graduate school, Nanchang, China.
Microbiol Immunol. 2021 Sep;65(9):383-391. doi: 10.1111/1348-0421.12922. Epub 2021 Jul 21.
Coagulation is a critical pathogenic process in Staphylococcus aureus. Although the agglutination of S. aureus has been studied for a long time, the genes involved in this process are not completely clear. We performed tube agglutination and dynamic turbidimetry tests to identify novel genes involved in reduced plasma coagulation. A total of 15 genes were identified, including coa, clfA, vwbp, saeS, agrA, trpC, spdC, mroQ, cydA, qoxC, sucC, pyrP, menH, threonine aldolase, and truncated transposase for IS1272. The functions of these genes include bicomponent regulation, membrane transport, energy metabolism and biosynthesis, respectively. cydA, spdC, and mroQ genes were further studied by gene knockout and complementation. Results of gene knockout and complementation and real-time-qPCR proved that cydA, spdC, and mroQ genes are necessary for plasma coagulation. Furthermore, the survival ability of 7 day mice decreased significantly when cydA, spdC, and mroQ genes had been knocked out.
凝固是金黄色葡萄球菌的一个关键致病过程。尽管人们对金黄色葡萄球菌的凝集作用进行了长期研究,但涉及该过程的基因尚不完全清楚。我们通过管凝集和动态浊度测定试验,鉴定了参与降低血浆凝固的新基因。共鉴定出 15 个基因,包括 coa、clfA、vwbp、saeS、agrA、trpC、spdC、mroQ、cydA、qoxC、sucC、pyrP、menH、苏氨酸醛缩酶和 IS1272 的截断转座酶。这些基因的功能分别包括双组分调节、膜转运、能量代谢和生物合成。cydA、spdC 和 mroQ 基因进一步通过基因敲除和互补进行研究。基因敲除和互补以及实时 qPCR 的结果表明,cydA、spdC 和 mroQ 基因对血浆凝固是必需的。此外,当 cydA、spdC 和 mroQ 基因被敲除时,7 天的小鼠的生存能力显著下降。