Cargando…
A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota
Bacterial adhesion is the initial step in surface colonization and community formation. At the single-cell level, atomic force microscopy (AFM) techniques have enabled the quantification of adhesive forces between bacteria and substrata. However, conventional techniques depend on the irreversible im...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591122/ https://www.ncbi.nlm.nih.gov/pubmed/30894689 http://dx.doi.org/10.1038/s41396-019-0404-1 |
_version_ | 1783429664356696064 |
---|---|
author | Mittelviefhaus, Maximilian Müller, Daniel B. Zambelli, Tomaso Vorholt, Julia A. |
author_facet | Mittelviefhaus, Maximilian Müller, Daniel B. Zambelli, Tomaso Vorholt, Julia A. |
author_sort | Mittelviefhaus, Maximilian |
collection | PubMed |
description | Bacterial adhesion is the initial step in surface colonization and community formation. At the single-cell level, atomic force microscopy (AFM) techniques have enabled the quantification of adhesive forces between bacteria and substrata. However, conventional techniques depend on the irreversible immobilization of cells onto cantilevers, thus hampering throughput. Here, we developed a modular AFM method to reversibly immobilize functionalized beads as surface mimic and to probe adhesion of individual bacteria. We performed single-cell force spectroscopies with phylogenetically diverse leaf isolates of various size and morphology. Adhesion measurement of 28 bacterial strains revealed large differences in hydrophobic interactions of about three orders of magnitude. The highest adhesion forces of up to 50 nN were recorded for members of the Gammaproteobacteria. The hydrophobicity of the different isolates correlated positively with the retention of bacteria observed in planta and might provide a basis for successful leaf colonization and potentially disease outbreaks of pathogens. |
format | Online Article Text |
id | pubmed-6591122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65911222019-09-20 A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota Mittelviefhaus, Maximilian Müller, Daniel B. Zambelli, Tomaso Vorholt, Julia A. ISME J Brief Communication Bacterial adhesion is the initial step in surface colonization and community formation. At the single-cell level, atomic force microscopy (AFM) techniques have enabled the quantification of adhesive forces between bacteria and substrata. However, conventional techniques depend on the irreversible immobilization of cells onto cantilevers, thus hampering throughput. Here, we developed a modular AFM method to reversibly immobilize functionalized beads as surface mimic and to probe adhesion of individual bacteria. We performed single-cell force spectroscopies with phylogenetically diverse leaf isolates of various size and morphology. Adhesion measurement of 28 bacterial strains revealed large differences in hydrophobic interactions of about three orders of magnitude. The highest adhesion forces of up to 50 nN were recorded for members of the Gammaproteobacteria. The hydrophobicity of the different isolates correlated positively with the retention of bacteria observed in planta and might provide a basis for successful leaf colonization and potentially disease outbreaks of pathogens. Nature Publishing Group UK 2019-03-20 2019-07 /pmc/articles/PMC6591122/ /pubmed/30894689 http://dx.doi.org/10.1038/s41396-019-0404-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Brief Communication Mittelviefhaus, Maximilian Müller, Daniel B. Zambelli, Tomaso Vorholt, Julia A. A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title | A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title_full | A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title_fullStr | A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title_full_unstemmed | A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title_short | A modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
title_sort | modular atomic force microscopy approach reveals a large range of hydrophobic adhesion forces among bacterial members of the leaf microbiota |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591122/ https://www.ncbi.nlm.nih.gov/pubmed/30894689 http://dx.doi.org/10.1038/s41396-019-0404-1 |
work_keys_str_mv | AT mittelviefhausmaximilian amodularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT mullerdanielb amodularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT zambellitomaso amodularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT vorholtjuliaa amodularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT mittelviefhausmaximilian modularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT mullerdanielb modularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT zambellitomaso modularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota AT vorholtjuliaa modularatomicforcemicroscopyapproachrevealsalargerangeofhydrophobicadhesionforcesamongbacterialmembersoftheleafmicrobiota |