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Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum

BACKGROUND: The cell invasiveness of Mycoplasma gallisepticum, the causative agent of respiratory disease in chickens and infectious sinusitis in turkeys, may be a substantial factor in the well-known chronicity of these diseases and in the systemic spread of infection. To date, not much is known ab...

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Autores principales: Fürnkranz, Ursula, Siebert-Gulle, Karin, Rosengarten, Renate, Szostak, Michael P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847126/
https://www.ncbi.nlm.nih.gov/pubmed/24011130
http://dx.doi.org/10.1186/1751-0147-55-63
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author Fürnkranz, Ursula
Siebert-Gulle, Karin
Rosengarten, Renate
Szostak, Michael P
author_facet Fürnkranz, Ursula
Siebert-Gulle, Karin
Rosengarten, Renate
Szostak, Michael P
author_sort Fürnkranz, Ursula
collection PubMed
description BACKGROUND: The cell invasiveness of Mycoplasma gallisepticum, the causative agent of respiratory disease in chickens and infectious sinusitis in turkeys, may be a substantial factor in the well-known chronicity of these diseases and in the systemic spread of infection. To date, not much is known about the host factors and mechanisms involved in promotion or obstruction of M. gallisepticum adherence and/or cell invasion. In the current study, the influence of extracellular matrix (ECM) proteins such as fibronectin, collagen type IV and heparin, as well as plasminogen/plasmin, on the adhesion and cell invasion levels of M. gallisepticum to chicken erythrocytes and HeLa cells was investigated in vitro. Two strains, R(high) and R(low,) which differ in their adhesion and invasion capacity, were analyzed by applying a modified gentamicin invasion assay. Binding of selected ECM molecules to M. gallisepticum was proven by Western blot analysis. RESULTS: Collagen type IV, fibronectin, and plasminogen exerted positive effects on adhesion and cell invasion of M. gallisepticum, with varying degrees, depending on the strain used. Especially strain R(high), with its highly reduced cell adhesion and invasion capabilities seemed to profit from the addition of plasminogen. Western and dot blot analyses showed that R(high) as well as R(low) are able to adsorb horse fibronectin and plasminogen present in the growth medium. Depletion of HeLa cell membranes from cholesterol resulted in increased adhesion, but decreased cell invasion. CONCLUSION: ECM molecules seem to play a supportive role in the adhesion/cell invasion process of M. gallisepticum. Cholesterol depletion known to affect lipid rafts on the host cell surface had contrary effects on cell adherence and cell invasion of M. gallisepticum.
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spelling pubmed-38471262013-12-04 Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum Fürnkranz, Ursula Siebert-Gulle, Karin Rosengarten, Renate Szostak, Michael P Acta Vet Scand Research BACKGROUND: The cell invasiveness of Mycoplasma gallisepticum, the causative agent of respiratory disease in chickens and infectious sinusitis in turkeys, may be a substantial factor in the well-known chronicity of these diseases and in the systemic spread of infection. To date, not much is known about the host factors and mechanisms involved in promotion or obstruction of M. gallisepticum adherence and/or cell invasion. In the current study, the influence of extracellular matrix (ECM) proteins such as fibronectin, collagen type IV and heparin, as well as plasminogen/plasmin, on the adhesion and cell invasion levels of M. gallisepticum to chicken erythrocytes and HeLa cells was investigated in vitro. Two strains, R(high) and R(low,) which differ in their adhesion and invasion capacity, were analyzed by applying a modified gentamicin invasion assay. Binding of selected ECM molecules to M. gallisepticum was proven by Western blot analysis. RESULTS: Collagen type IV, fibronectin, and plasminogen exerted positive effects on adhesion and cell invasion of M. gallisepticum, with varying degrees, depending on the strain used. Especially strain R(high), with its highly reduced cell adhesion and invasion capabilities seemed to profit from the addition of plasminogen. Western and dot blot analyses showed that R(high) as well as R(low) are able to adsorb horse fibronectin and plasminogen present in the growth medium. Depletion of HeLa cell membranes from cholesterol resulted in increased adhesion, but decreased cell invasion. CONCLUSION: ECM molecules seem to play a supportive role in the adhesion/cell invasion process of M. gallisepticum. Cholesterol depletion known to affect lipid rafts on the host cell surface had contrary effects on cell adherence and cell invasion of M. gallisepticum. BioMed Central 2013-09-05 /pmc/articles/PMC3847126/ /pubmed/24011130 http://dx.doi.org/10.1186/1751-0147-55-63 Text en Copyright © 2013 Fürnkranz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fürnkranz, Ursula
Siebert-Gulle, Karin
Rosengarten, Renate
Szostak, Michael P
Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title_full Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title_fullStr Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title_full_unstemmed Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title_short Factors influencing the cell adhesion and invasion capacity of Mycoplasma gallisepticum
title_sort factors influencing the cell adhesion and invasion capacity of mycoplasma gallisepticum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847126/
https://www.ncbi.nlm.nih.gov/pubmed/24011130
http://dx.doi.org/10.1186/1751-0147-55-63
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