Nanoscale Spatiotemporal Dynamics of Microbial Adhesion: Unveiling Stepwise Transitions with Plasmonic Imaging
Source abstract
Abstract
Understanding bacterial adhesion at the nanoscale is crucial for elucidating biofilm formation, enhancing biosensor performance, and designing advanced biomaterials. However, the dynamics of the critical transition from reversible to irreversible adhesion has remained elusive due to analytical constraints. Here, we probed this adhesion transition, unveiling nanoscale, step-like bacterial approaches to substrates using a plasmonic imaging technique. This method reveals the discontinuous nature of adhesion, emphasizing the complex interplay between bacterial extracellular polymeric substances (EPS) and substrates. Our findings not only deepen our understanding of bacterial adhesion but also have significant implications for the development of theoretical models for biofilm management. By elucidating these nanoscale step-like adhesion processes, our work provides avenues for the application of nanotechnology in biosensing, biofilm control, and the creation of biomimetic materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Bacterial biofilms and quorum sensing · Microfluidic and Bio-sensing Technologies · Biochemical and Structural Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Hefei National Laboratory for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Urban Pollutant Conversion, Department of Environmental Science and Engineering, University of Science and Technology of China, Hefei 230026, China
Department of Applied Chemistry, University of Science and Technology of China, Hefei 230026, China
Funding
National Natural Science Foundation of China · Chinese Academy of Sciences
References (40)
Show source-provided references
1. 10.1038/s41579-018-0019-y10.1038/s41579-018-0019-y ↗
2. 10.1016/j.watres.2017.12.04310.1016/j.watres.2017.12.043 ↗
3. 10.1038/s41579-022-00791-010.1038/s41579-022-00791-0 ↗
4. 10.1038/s41579-022-00767-010.1038/s41579-022-00767-0 ↗
5. 10.1021/la800552s10.1021/la800552s ↗
6. 10.1021/la404673q10.1021/la404673q ↗
7. 10.1016/j.cis.2018.10.00510.1016/j.cis.2018.10.005 ↗
8. 10.1038/s41579-018-0057-510.1038/s41579-018-0057-5 ↗
9. 10.1016/j.bpj.2011.10.03410.1016/j.bpj.2011.10.034 ↗
10. 10.1038/s41579-019-0314-210.1038/s41579-019-0314-2 ↗
11. 10.1021/es303394w10.1021/es303394w ↗
12. 10.1016/j.bpj.2013.03.04610.1016/j.bpj.2013.03.046 ↗
13. 10.1021/la801824c10.1021/la801824c ↗
14. 10.1021/nn503025310.1021/nn5030253 ↗
15. 10.1038/nchem.143410.1038/nchem.1434 ↗
16. 10.1038/nature1215510.1038/nature12155 ↗
17. 10.1039/C7NR09483C10.1039/C7NR09483C ↗
18. 10.1021/es503680s10.1021/es503680s ↗
19. 10.1016/j.bios.2014.06.06910.1016/j.bios.2014.06.069 ↗
20. 10.1038/s41598-017-04703-810.1038/s41598-017-04703-8 ↗
21. 10.1016/j.colsurfb.2008.08.02110.1016/j.colsurfb.2008.08.021 ↗
22. 10.1038/nature0492810.1038/nature04928 ↗
23. 10.1016/j.cocis.2010.05.01410.1016/j.cocis.2010.05.014 ↗
24. 10.1038/s41467-019-10115-110.1038/s41467-019-10115-1 ↗
25. 10.1016/0370-1573(90)90099-N10.1016/0370-1573(90)90099-N ↗
26. 10.1002/adbi.20170016110.1002/adbi.201700161 ↗
27. 10.1021/la991013x10.1021/la991013x ↗
28. 10.1126/sciadv.aao117010.1126/sciadv.aao1170 ↗
29. 10.1038/s41579-019-0313-310.1038/s41579-019-0313-3 ↗
30. 10.1016/j.watres.2007.10.01310.1016/j.watres.2007.10.013 ↗
31. 10.1186/s13068-016-0444-y10.1186/s13068-016-0444-y ↗
32. 10.1038/nmat284910.1038/nmat2849 ↗
33. 10.1128/aem.01626-2210.1128/aem.01626-22 ↗
34. 10.1002/anie.20181356710.1002/anie.201813567 ↗
35. 10.1002/smll.20140301610.1002/smll.201403016 ↗
36. 10.1021/acs.langmuir.5b0467510.1021/acs.langmuir.5b04675 ↗
37. 10.1021/ja00246a01110.1021/ja00246a011 ↗
38. 10.1073/pnas.201013611710.1073/pnas.2010136117 ↗
39. 10.1021/acs.est.0c0696210.1021/acs.est.0c06962 ↗
40. 10.1126/sciadv.170062310.1126/sciadv.1700623 ↗