Sandra Timme, S. Wendler, T. Klassert, J. Saraiva, U. N. da Rocha, Manuel Wittchen, Sareda T. J. Schramm, R. Ehricht, S. Monecke, B. Edel, Jürgen Rödel, Bettina Löffler, Maria Soledad Ramirez, Hortense Slevogt, M. Figge, L. Tuchscherr
{"title":"Competitive inhibition and mutualistic growth in Co-infections: deciphering Staphylococcus aureus – Acinetobacter baumannii interaction dynamics","authors":"Sandra Timme, S. Wendler, T. Klassert, J. Saraiva, U. N. da Rocha, Manuel Wittchen, Sareda T. J. Schramm, R. Ehricht, S. Monecke, B. Edel, Jürgen Rödel, Bettina Löffler, Maria Soledad Ramirez, Hortense Slevogt, M. Figge, L. Tuchscherr","doi":"10.1093/ismeco/ycae077","DOIUrl":null,"url":null,"abstract":"\n Staphylococcus aureus (Sa) and Acinetobacter baumannii (Ab) are frequently co-isolated from polymicrobial infections that are severe and refractory to therapy. Here, we apply a combination of wet-lab experiments and in silico modeling to unveil the intricate nature of the Ab/Sa interaction using both, representative laboratory strains and strains co-isolated from clinical samples.\n This comprehensive methodology allowed uncovering Sa’s capability to exert a partial interference on Ab by the expression of phenol-soluble modulins. In addition, we observed a cross-feeding mechanism by which Sa supports the growth of Ab by providing acetoin as an alternative carbon source.\n This study is the first to dissect the Ab/Sa interaction dynamics wherein competitive and cooperative strategies can intertwine. Through our findings, we illuminate the ecological mechanisms supporting their coexistence in the context of polymicrobial infections. Our research not only enriches our understanding but also opens doors to potential therapeutic avenues in managing these challenging infections.","PeriodicalId":73516,"journal":{"name":"ISME communications","volume":null,"pages":null},"PeriodicalIF":5.1000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISME communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/ismeco/ycae077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Staphylococcus aureus (Sa) and Acinetobacter baumannii (Ab) are frequently co-isolated from polymicrobial infections that are severe and refractory to therapy. Here, we apply a combination of wet-lab experiments and in silico modeling to unveil the intricate nature of the Ab/Sa interaction using both, representative laboratory strains and strains co-isolated from clinical samples.
This comprehensive methodology allowed uncovering Sa’s capability to exert a partial interference on Ab by the expression of phenol-soluble modulins. In addition, we observed a cross-feeding mechanism by which Sa supports the growth of Ab by providing acetoin as an alternative carbon source.
This study is the first to dissect the Ab/Sa interaction dynamics wherein competitive and cooperative strategies can intertwine. Through our findings, we illuminate the ecological mechanisms supporting their coexistence in the context of polymicrobial infections. Our research not only enriches our understanding but also opens doors to potential therapeutic avenues in managing these challenging infections.
金黄色葡萄球菌(Sa)和鲍曼不动杆菌(Ab)经常在严重且难治的多微生物感染中共同分离出来。在这里,我们将湿实验室实验和硅学建模相结合,利用具有代表性的实验室菌株和从临床样本中共同分离出的菌株,揭示了 Ab/Sa 相互作用的复杂本质。这种综合方法揭示了 Sa 通过表达酚溶性调节蛋白对 Ab 产生部分干扰的能力。此外,我们还观察到了一种交叉供养机制,即 Sa 通过提供乙炔作为替代碳源来支持 Ab 的生长。这项研究首次剖析了 Ab 与 Sa 的相互作用动态,其中竞争与合作策略相互交织。通过我们的发现,我们阐明了支持它们在多微生物感染背景下共存的生态机制。我们的研究不仅丰富了我们的认识,还为治疗这些具有挑战性的感染打开了潜在的治疗途径。