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| Format: | Artículo científico |
| Sprache: | en |
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mBio
2025
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| Online-Zugang: | https://pubmed.ncbi.nlm.nih.gov/40396756/ |
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| author | 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 |
| author_facet | 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 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 |
| collection | PubMed - marine biology |
| contents | Comparative proteomics of biofilm development in discovers a distinct family of Ca-dependent adhesins. 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 Biofilms Pseudoalteromonas Proteomics Adhesins, Bacterial Calcium Proteome Bacterial Proteins 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. |
| format | Artículo científico |
| id | pubmed_40396756 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | mBio |
| record_format | pubmed |
| spellingShingle | Comparative proteomics of biofilm development in discovers a distinct family of Ca-dependent adhesins. 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 Biofilms Pseudoalteromonas Proteomics Adhesins, Bacterial Calcium Proteome Bacterial Proteins Comparative proteomics of biofilm development in discovers a distinct family of Ca-dependent adhesins. 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 Biofilms Pseudoalteromonas Proteomics Adhesins, Bacterial Calcium Proteome Bacterial Proteins 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. |
| title | Comparative proteomics of biofilm development in discovers a distinct family of Ca-dependent adhesins. |
| topic | Biofilms Pseudoalteromonas Proteomics Adhesins, Bacterial Calcium Proteome Bacterial Proteins |
| url | https://pubmed.ncbi.nlm.nih.gov/40396756/ |