Quadram Institute Bioscience, Norwich, UK.
School of Biological Sciences, University of East Anglia, Norwich, UK.
BMC Genomics. 2024 Aug 28;25(1):812. doi: 10.1186/s12864-024-10719-y.
Staphylococci cause a wide range of infections, including implant-associated infections which are difficult to treat due to the presence of biofilms. Whilst some proteins involved in biofilm formation are known, the differences in biofilm production between staphylococcal species remains understudied. Currently biofilm formation by Staphylococcus aureus is better understood than other members of the genus as more research has focused on this species.
We assembled a panel of 385 non-aureus Staphylococcus isolates of 19 species from a combination of clinical sources and reference strains. We used a high-throughput crystal violet assay to assess the biofilm forming ability of all strains and assign distinct biofilm formation categories. We compared the prevalence of Pfam domains between the categories and used machine learning to identify amino acid 20-mers linked to biofilm formation. This identified some domains within proteins already linked to biofilm formation and important domains not previously linked to biofilm formation in staphylococci. RT-qPCR confirmed the expression of selected genes predicted to encode important domains within biofilms in Staphylococcus epidermidis. The prevalence and distribution of biofilm associated domains showed a link to phylogeny, suggesting different Staphylococcus species have independently evolved different mechanisms of biofilm production.
This work has identified different routes to biofilm formation in diverse species of Staphylococcus and suggests independent evolution of biofilm has occurred multiple times across the genus. Understanding the mechanisms of biofilm formation in any given species is likely to require detailed study of relevant strains and the ability to generalise across the genus may be limited.
葡萄球菌可引起多种感染,包括植入物相关感染,由于生物膜的存在,这些感染难以治疗。虽然已经知道一些参与生物膜形成的蛋白质,但葡萄球菌种间生物膜产生的差异仍研究不足。目前,由于更多的研究集中在该物种上,因此对金黄色葡萄球菌生物膜形成的了解要好于属内的其他成员。
我们从临床来源和参考菌株中组合了 19 个种的 385 株非金黄色葡萄球菌葡萄球菌分离株。我们使用高通量结晶紫测定法评估了所有菌株的生物膜形成能力,并分配了不同的生物膜形成类别。我们比较了类别之间 Pfam 结构域的流行率,并使用机器学习来识别与生物膜形成相关的氨基酸 20 -mer。这确定了一些已经与生物膜形成相关的蛋白质内的结构域以及以前与葡萄球菌生物膜形成无关的重要结构域。RT-qPCR 证实了在表皮葡萄球菌中预测为编码生物膜内重要结构域的选定基因的表达。生物膜相关结构域的流行率和分布与系统发育有关,这表明不同的葡萄球菌种已经独立进化出不同的生物膜产生机制。
这项工作已经确定了不同葡萄球菌种生物膜形成的不同途径,并表明生物膜的独立进化在该属中已经发生了多次。要了解任何给定物种的生物膜形成机制,可能需要详细研究相关菌株,并且跨属概括的能力可能受到限制。