| Jundishapur Journal of Microbiology | |
| Regulation of saeRS, agrA and sarA on sasX Expression in Staphylococcus aureus | |
| Yinjuan Guo1  Xiuqin Qi2  Shanshan Wang3  Yongpeng Shang4  | |
| [1] Department of Laboratory Medicine, Shanghai Pulmonary Hospital, Tongji University, School of Medicine. Shanghai, China;Department of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China;Department of Respiratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China;Key Laboratory of Medical Molecular Virology of Ministry of Education and Ministry of Public Health, Institute of Medical Microbiology and Institutes of Biomedical Sciences, Shanghai Medical School of Fudan University, Shanghai, China | |
| 关键词: Regulation of saeRS; agrA and sarA on sasX Expression in Staphylococcus aureus; Staphylococcus aureus; saeRS; agr; sarA; sasX; | |
| DOI : 10.5812/jjm.13821 | |
| 学科分类:微生物学和免疫学 | |
| 来源: Jundishapur Journal of Microbiology | |
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【 摘 要 】
The spread of Staphylococcus aureus and the types of infection caused by S. aureus are closely related to the secretion of a variety of adhesion proteins, which could be controlled by a variety of regulatory systems. However, for the newly discovered adhesion protein SasX, the regulatory mechanism is not completely clear.The current study aimed at investigating the regulation of Staphylococcal accessory gene regulator A (agrA), Staphylococcal accessory regulator A (sarA), and two-component signal transduction system (saeRS) on the adhesion protein SasX.In this research, a saeRS mutant strain, a sarA mutant strain, and a agrA mutant strain were constructed by allelic replacement. In this study mRNA and protein expression levels of sasX in wild-type HS770 and knockout strains were studied to investigate the effects of regulatory factor saeRS, agrA, and sarA on adhesion protein SasX.In contrast with the wild strain HS770, the transcriptional expression of sasX was highest at on the sixth hour time point in HS770ÎagrA and at nine and twelve hours in HS770ÎsarA. However, the sasX transcription level in HS770ÎsaeRS mutant strains had little change at different time points. Western-blot results suggested that the sasX expression level of wild strains was the highest at 6 hours; HS770ÎsaeRS mutation strains had no expression peak at 6 hours. The expression level of HS770ÎagrA mutant strains decreased at 6 hours of expression, however, increased at 9 hours and 12 hours; the expression level of HS770ÎsarA mutation knockout increased at three, six, nine, and twelve hours.All the results showed that agrA and sarA have negative regulation on sasX, but saeRS may not regulate sasX.
【 授权许可】
CC BY-NC
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201910251975722ZK.pdf | 804KB |
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