Schuster Christopher F, Wiedemann David M, Kirsebom Freja C M, Santiago Marina, Walker Suzanne, Gründling Angelika
Section of Molecular Microbiology and MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK.
Department of Microbiology and Immunobiology, Harvard Medical School, Boston, MA, USA.
Mol Microbiol. 2020 Apr;113(4):699-717. doi: 10.1111/mmi.14433. Epub 2019 Dec 16.
Staphylococcus aureus is an opportunistic pathogen that can cause soft tissue infections but is also a frequent cause of foodborne illnesses. One contributing factor for this food association is its high salt tolerance allowing this organism to survive commonly used food preservation methods. How this resistance is mediated is poorly understood, particularly during long-term exposure. In this study, we used transposon sequencing (TN-seq) to understand how the responses to osmotic stressors differ. Our results revealed distinctly different long-term responses to NaCl, KCl and sucrose stresses. In addition, we identified the DUF2538 domain containing gene SAUSA300_0957 (gene 957) as essential under salt stress. Interestingly, a 957 mutant was less susceptible to oxacillin and showed increased peptidoglycan crosslinking. The salt sensitivity phenotype could be suppressed by amino acid substitutions in the transglycosylase domain of the penicillin-binding protein Pbp2, and these changes restored the peptidoglycan crosslinking to WT levels. These results indicate that increased crosslinking of the peptidoglycan polymer can be detrimental and highlight a critical role of the bacterial cell wall for osmotic stress resistance. This study will serve as a starting point for future research on osmotic stress response and help develop better strategies to tackle foodborne staphylococcal infections.
金黄色葡萄球菌是一种机会致病菌,可引起软组织感染,也是食源性疾病的常见病因。这种与食物的关联的一个促成因素是其高耐盐性,使这种微生物能够在常用的食品保存方法中存活。这种抗性是如何介导的尚不清楚,尤其是在长期暴露期间。在本研究中,我们使用转座子测序(TN-seq)来了解对渗透应激源的反应有何不同。我们的结果揭示了对NaCl、KCl和蔗糖应激的明显不同的长期反应。此外,我们确定了含有DUF2538结构域的基因SAUSA300_0957(基因957)在盐胁迫下是必需的。有趣的是,957突变体对苯唑西林的敏感性较低,并且肽聚糖交联增加。青霉素结合蛋白Pbp2的转糖基酶结构域中的氨基酸取代可以抑制盐敏感性表型,并且这些变化将肽聚糖交联恢复到野生型水平。这些结果表明,肽聚糖聚合物交联增加可能是有害的,并突出了细菌细胞壁在抗渗透应激中的关键作用。这项研究将作为未来渗透应激反应研究的起点,并有助于制定更好的策略来应对食源性葡萄球菌感染。