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Spatiotemporal distribution of different extracellular polymeric substances and filamentation mediate Xylella fastidiosa adhesion and biofilm formation

Identifieur interne : 000448 ( Main/Exploration ); précédent : 000447; suivant : 000449

Spatiotemporal distribution of different extracellular polymeric substances and filamentation mediate Xylella fastidiosa adhesion and biofilm formation

Auteurs : Richard Janissen [Brésil] ; Duber M. Murillo [Brésil] ; Barbara Niza [Brésil] ; Prasana K. Sahoo [Brésil] ; Marcelo M. Nobrega [Brésil] ; Carlos L. Cesar [Brésil] ; Marcia L. A. Temperini [Brésil] ; Hernandes F. Carvalho [Brésil] ; Alessandra A. De Souza [Brésil] ; Monica A. Cotta [Brésil]

Source :

RBID : PMC:4402645

Abstract

Microorganism pathogenicity strongly relies on the generation of multicellular assemblies, called biofilms. Understanding their organization can unveil vulnerabilities leading to potential treatments; spatially and temporally-resolved comprehensive experimental characterization can provide new details of biofilm formation, and possibly new targets for disease control. Here, biofilm formation of economically important phytopathogen Xylella fastidiosa was analyzed at single-cell resolution using nanometer-resolution spectro-microscopy techniques, addressing the role of different types of extracellular polymeric substances (EPS) at each stage of the entire bacterial life cycle. Single cell adhesion is caused by unspecific electrostatic interactions through proteins at the cell polar region, where EPS accumulation is required for more firmly-attached, irreversibly adhered cells. Subsequently, bacteria form clusters, which are embedded in secreted loosely-bound EPS, and bridged by up to ten-fold elongated cells that form the biofilm framework. During biofilm maturation, soluble EPS forms a filamentous matrix that facilitates cell adhesion and provides mechanical support, while the biofilm keeps anchored by few cells. This floating architecture maximizes nutrient distribution while allowing detachment upon larger shear stresses; it thus complies with biological requirements of the bacteria life cycle. Using new approaches, our findings provide insights regarding different aspects of the adhesion process of X. fastidiosa and biofilm formation.


Url:
DOI: 10.1038/srep09856
PubMed: 25891045
PubMed Central: 4402645


Affiliations:


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<p>Microorganism pathogenicity strongly relies on the generation of multicellular assemblies, called biofilms. Understanding their organization can unveil vulnerabilities leading to potential treatments; spatially and temporally-resolved comprehensive experimental characterization can provide new details of biofilm formation, and possibly new targets for disease control. Here, biofilm formation of economically important phytopathogen
<italic>Xylella fastidiosa</italic>
was analyzed at single-cell resolution using nanometer-resolution spectro-microscopy techniques, addressing the role of different types of extracellular polymeric substances (EPS) at each stage of the entire bacterial life cycle. Single cell adhesion is caused by unspecific electrostatic interactions through proteins at the cell polar region, where EPS accumulation is required for more firmly-attached, irreversibly adhered cells. Subsequently, bacteria form clusters, which are embedded in secreted loosely-bound EPS, and bridged by up to ten-fold elongated cells that form the biofilm framework. During biofilm maturation, soluble EPS forms a filamentous matrix that facilitates cell adhesion and provides mechanical support, while the biofilm keeps anchored by few cells. This floating architecture maximizes nutrient distribution while allowing detachment upon larger shear stresses; it thus complies with biological requirements of the bacteria life cycle. Using new approaches, our findings provide insights regarding different aspects of the adhesion process of
<italic>X. fastidiosa</italic>
and biofilm formation.</p>
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</back>
</TEI>
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<list>
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<li>Brésil</li>
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<li>État de São Paulo</li>
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<li>São Paulo</li>
</settlement>
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<name sortKey="Janissen, Richard" sort="Janissen, Richard" uniqKey="Janissen R" first="Richard" last="Janissen">Richard Janissen</name>
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<name sortKey="Cesar, Carlos L" sort="Cesar, Carlos L" uniqKey="Cesar C" first="Carlos L." last="Cesar">Carlos L. Cesar</name>
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<name sortKey="Niza, Barbara" sort="Niza, Barbara" uniqKey="Niza B" first="Barbara" last="Niza">Barbara Niza</name>
<name sortKey="Nobrega, Marcelo M" sort="Nobrega, Marcelo M" uniqKey="Nobrega M" first="Marcelo M." last="Nobrega">Marcelo M. Nobrega</name>
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