Cargando…

The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation

Biofilms are commonly defined as accumulations of microbes, embedded in a self-secreted, polysaccharide-rich extra-cellular matrix. This study aimed to characterize specific morphological changes that occur in Bacillus subtilis biofilms under nutrient-limiting growth conditions. Under varying levels...

Descripción completa

Detalles Bibliográficos
Autores principales: Gingichashvili, Sarah, Duanis-Assaf, Danielle, Shemesh, Moshe, Featherstone, John D. B., Feuerstein, Osnat, Steinberg, Doron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023499/
https://www.ncbi.nlm.nih.gov/pubmed/31905847
http://dx.doi.org/10.3390/microorganisms8010062
_version_ 1783498263737925632
author Gingichashvili, Sarah
Duanis-Assaf, Danielle
Shemesh, Moshe
Featherstone, John D. B.
Feuerstein, Osnat
Steinberg, Doron
author_facet Gingichashvili, Sarah
Duanis-Assaf, Danielle
Shemesh, Moshe
Featherstone, John D. B.
Feuerstein, Osnat
Steinberg, Doron
author_sort Gingichashvili, Sarah
collection PubMed
description Biofilms are commonly defined as accumulations of microbes, embedded in a self-secreted, polysaccharide-rich extra-cellular matrix. This study aimed to characterize specific morphological changes that occur in Bacillus subtilis biofilms under nutrient-limiting growth conditions. Under varying levels of nutrient depletion, colony-type biofilms were found to exhibit different rates of spatial expansion and green fluorescent protein production. Specifically, colony-type biofilms grown on media with decreased lysogeny broth content exhibited increased spatial expansion and more stable GFP production over the entire growth period. By modeling the surface morphology of colony-type biofilms using confocal and multiphoton microscopy, we analyzed the appearance of distinctive folds or “wrinkles” that form as a result of lysogeny broth content reduction in the solid agar growth media. When subjected to varying nutritional conditions, the channel-like folds were shown to alter their morphology; growth on nutrient-depleted media was found to trigger the formation of large and straight wrinkles connecting the colony core to its periphery. To test a possible functional role of the formed channels, a fluorescent analogue of glucose was used to demonstrate preferential native uptake of the molecules into the channels’ interiors which supports their possible role in the transport of molecules throughout biofilm structures.
format Online
Article
Text
id pubmed-7023499
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70234992020-03-12 The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation Gingichashvili, Sarah Duanis-Assaf, Danielle Shemesh, Moshe Featherstone, John D. B. Feuerstein, Osnat Steinberg, Doron Microorganisms Article Biofilms are commonly defined as accumulations of microbes, embedded in a self-secreted, polysaccharide-rich extra-cellular matrix. This study aimed to characterize specific morphological changes that occur in Bacillus subtilis biofilms under nutrient-limiting growth conditions. Under varying levels of nutrient depletion, colony-type biofilms were found to exhibit different rates of spatial expansion and green fluorescent protein production. Specifically, colony-type biofilms grown on media with decreased lysogeny broth content exhibited increased spatial expansion and more stable GFP production over the entire growth period. By modeling the surface morphology of colony-type biofilms using confocal and multiphoton microscopy, we analyzed the appearance of distinctive folds or “wrinkles” that form as a result of lysogeny broth content reduction in the solid agar growth media. When subjected to varying nutritional conditions, the channel-like folds were shown to alter their morphology; growth on nutrient-depleted media was found to trigger the formation of large and straight wrinkles connecting the colony core to its periphery. To test a possible functional role of the formed channels, a fluorescent analogue of glucose was used to demonstrate preferential native uptake of the molecules into the channels’ interiors which supports their possible role in the transport of molecules throughout biofilm structures. MDPI 2019-12-30 /pmc/articles/PMC7023499/ /pubmed/31905847 http://dx.doi.org/10.3390/microorganisms8010062 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gingichashvili, Sarah
Duanis-Assaf, Danielle
Shemesh, Moshe
Featherstone, John D. B.
Feuerstein, Osnat
Steinberg, Doron
The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title_full The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title_fullStr The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title_full_unstemmed The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title_short The Adaptive Morphology of Bacillus subtilis Biofilms: A Defense Mechanism against Bacterial Starvation
title_sort adaptive morphology of bacillus subtilis biofilms: a defense mechanism against bacterial starvation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023499/
https://www.ncbi.nlm.nih.gov/pubmed/31905847
http://dx.doi.org/10.3390/microorganisms8010062
work_keys_str_mv AT gingichashvilisarah theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT duanisassafdanielle theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT shemeshmoshe theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT featherstonejohndb theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT feuersteinosnat theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT steinbergdoron theadaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT gingichashvilisarah adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT duanisassafdanielle adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT shemeshmoshe adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT featherstonejohndb adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT feuersteinosnat adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation
AT steinbergdoron adaptivemorphologyofbacillussubtilisbiofilmsadefensemechanismagainstbacterialstarvation