Ali Sura, Stavropoulos Alexander, Jenkins Benjamin, Graves Sadie, Ahmadi Atiyeh, Marzbanrad Vania, Che Geoffrey, Cheng Jiujun, Tan Huagang, Wei Xin, Egan Suhelen, Ingalls Brian, Neufeld Josh D, Eckhard Ulrich, Charles Trevor C, Doxey Andrew C
Department of Biology and Waterloo Centre for Microbial Research, University of Waterloo, Waterloo, Ontario, Canada.
The University of New South Wales Sydney, Sydney, New South Wales, Australia.
mBio. 2025 Jun 11;16(6):e0106925. doi: 10.1128/mbio.01069-25. Epub 2025 May 21.
The marine bacterium, , is a useful model for studying biofilm development due to its ability to colonize and form biofilms on a variety of marine and eukaryotic host-associated surfaces. However, the pathways responsible for biofilm formation are not fully understood, in part due to a lack of functional information for a large proportion of its proteome. We used comparative shotgun proteomics to explore biofilm development from the planktonic phase throughout early, middle, and late biofilm stages. A total of 248 biofilm-associated proteins were identified, including many hypothetical proteins, as well as previously known biofilm-related proteins, such as the autocidal enzyme AlpP, violacein proteins, S-layer protein SLR4, and various pili proteins. We further investigated the top identified biofilm-associated protein, a previously uncharacterized 1,600-amino acid protein (EAR30327), which we designate as "BapP." Based on AlphaFold modeling and genomic context analysis, we predicted BapP as a distinct Ca-dependent biofilm adhesin. Consistent with this prediction, a Δ knockout mutant was defective in forming both pellicle- and surface-associated biofilms and rescued by re-insertion of into the genome. Similar to the mechanisms of RTX Bap-like adhesins, BapP-mediated biofilm formation was influenced by Ca levels, and BapP is potentially exported by a Type 1 secretion system. Ultimately, our work not only provides a useful proteomic data set for studying biofilm development in an ecologically relevant organism but also adds to our knowledge of bacterial adhesin diversity, emphasizing Bap-like proteins as widespread determinants of biofilm formation in bacteria.
Understanding how bacteria form biofilms is essential because biofilms play a crucial role in bacterial survival and interaction with their environments. The marine bacterium is a valuable model for studying biofilm formation, as it colonizes diverse marine surfaces and host organisms. By identifying proteins involved in biofilm development, our study sheds light on the specific proteins that help transition from a free-swimming state to a stable biofilm. This work highlights the role of a large, calcium-dependent protein, BapP, which we found to be essential for biofilm stability and structure. This protein and hundreds of others identified provide new insights into bacterial adhesion mechanisms, expanding our understanding of biofilm formation in marine environments and potentially informing broader studies on biofilm-related processes in other bacteria.
海洋细菌[细菌名称未给出]由于能够在各种海洋和与真核宿主相关的表面上定殖并形成生物膜,是研究生物膜形成的有用模型。然而,负责[细菌名称未给出]生物膜形成的途径尚未完全了解,部分原因是其蛋白质组的很大一部分缺乏功能信息。我们使用比较鸟枪法蛋白质组学来探索[细菌名称未给出]从浮游阶段到生物膜早期、中期和晚期的生物膜发育过程。总共鉴定出248种与生物膜相关的蛋白质,包括许多假设蛋白质,以及先前已知的与[细菌名称未给出]生物膜相关的蛋白质,如自溶酶AlpP、紫罗碱蛋白、S层蛋白SLR4和各种菌毛蛋白。我们进一步研究了鉴定出的与生物膜相关的首要蛋白质,一种先前未表征的1600个氨基酸的蛋白质(EAR30327),我们将其命名为“BapP”。基于AlphaFold建模和基因组背景分析,我们预测BapP是一种独特的钙依赖性生物膜粘附素。与这一预测一致,Δ敲除突变体在形成菌膜和表面相关生物膜方面存在缺陷,并通过将[基因名称未给出]重新插入基因组而得到挽救。与RTX Bap样粘附素的机制类似,BapP介导的生物膜形成受钙水平影响,并且BapP可能通过1型分泌系统输出。最终,我们的工作不仅为研究生态相关生物体中的生物膜发育提供了有用的蛋白质组数据集,还增加了我们对细菌粘附素多样性的了解,强调了Bap样蛋白是细菌生物膜形成的广泛决定因素。
了解细菌如何形成生物膜至关重要,因为生物膜在细菌生存及其与环境的相互作用中起着关键作用。海洋细菌[细菌名称未给出]是研究生物膜形成的有价值模型,因为它能在各种海洋表面和宿主生物体上定殖。通过鉴定参与生物膜发育的蛋白质,我们的研究揭示了有助于[细菌名称未给出]从自由游动状态转变为稳定生物膜的特定蛋白质。这项工作突出了一种大型钙依赖性蛋白质BapP的作用,我们发现它对生物膜的稳定性和结构至关重要。这种蛋白质以及鉴定出的其他数百种蛋白质为细菌粘附机制提供了新的见解,扩展了我们对海洋环境中生物膜形成的理解,并可能为其他细菌中与生物膜相关过程的更广泛研究提供信息。