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Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions
Molecules contributing to microbial cytoadhesion are important virulence factors. In Mycoplasma bovis, a minimal bacterium but an important cattle pathogen, binding to host cells is emerging as a complex process involving a broad range of surface-exposed structures. Here, a new cytoadhesin of M. bov...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074692/ https://www.ncbi.nlm.nih.gov/pubmed/31979335 http://dx.doi.org/10.3390/microorganisms8020164 |
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author | Zhu, Xifang Dong, Yaqi Baranowski, Eric Li, Xixi Zhao, Gang Hao, Zhiyu Zhang, Hui Chen, Yingyu Hu, Changmin Chen, Huanchun Citti, Christine Guo, Aizhen |
author_facet | Zhu, Xifang Dong, Yaqi Baranowski, Eric Li, Xixi Zhao, Gang Hao, Zhiyu Zhang, Hui Chen, Yingyu Hu, Changmin Chen, Huanchun Citti, Christine Guo, Aizhen |
author_sort | Zhu, Xifang |
collection | PubMed |
description | Molecules contributing to microbial cytoadhesion are important virulence factors. In Mycoplasma bovis, a minimal bacterium but an important cattle pathogen, binding to host cells is emerging as a complex process involving a broad range of surface-exposed structures. Here, a new cytoadhesin of M. bovis was identified by producing a collection of individual knock-out mutants and evaluating their binding to embryonic bovine lung cells. The cytoadhesive-properties of this surface-exposed protein, which is encoded by Mbov_0503 in strain HB0801, were demonstrated at both the mycoplasma cell and protein levels using confocal microscopy and ELISA. Although Mbov_0503 disruption was only associated in M. bovis with a partial reduction of its binding capacity, this moderate effect was sufficient to affect M. bovis interaction with the host-cell tight junctions, and to reduce the translocation of this mycoplasma across epithelial cell monolayers. Besides demonstrating the capacity of M. bovis to disrupt tight junctions, these results identified novel properties associated with cytoadhesin that might contribute to virulence and host colonization. These findings provide new insights into the complex interplay taking place between wall-less mycoplasmas and the host-cell surface. |
format | Online Article Text |
id | pubmed-7074692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70746922020-03-20 Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions Zhu, Xifang Dong, Yaqi Baranowski, Eric Li, Xixi Zhao, Gang Hao, Zhiyu Zhang, Hui Chen, Yingyu Hu, Changmin Chen, Huanchun Citti, Christine Guo, Aizhen Microorganisms Article Molecules contributing to microbial cytoadhesion are important virulence factors. In Mycoplasma bovis, a minimal bacterium but an important cattle pathogen, binding to host cells is emerging as a complex process involving a broad range of surface-exposed structures. Here, a new cytoadhesin of M. bovis was identified by producing a collection of individual knock-out mutants and evaluating their binding to embryonic bovine lung cells. The cytoadhesive-properties of this surface-exposed protein, which is encoded by Mbov_0503 in strain HB0801, were demonstrated at both the mycoplasma cell and protein levels using confocal microscopy and ELISA. Although Mbov_0503 disruption was only associated in M. bovis with a partial reduction of its binding capacity, this moderate effect was sufficient to affect M. bovis interaction with the host-cell tight junctions, and to reduce the translocation of this mycoplasma across epithelial cell monolayers. Besides demonstrating the capacity of M. bovis to disrupt tight junctions, these results identified novel properties associated with cytoadhesin that might contribute to virulence and host colonization. These findings provide new insights into the complex interplay taking place between wall-less mycoplasmas and the host-cell surface. MDPI 2020-01-23 /pmc/articles/PMC7074692/ /pubmed/31979335 http://dx.doi.org/10.3390/microorganisms8020164 Text en © 2020 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 Zhu, Xifang Dong, Yaqi Baranowski, Eric Li, Xixi Zhao, Gang Hao, Zhiyu Zhang, Hui Chen, Yingyu Hu, Changmin Chen, Huanchun Citti, Christine Guo, Aizhen Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title | Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title_full | Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title_fullStr | Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title_full_unstemmed | Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title_short | Mbov_0503 Encodes a Novel Cytoadhesin that Facilitates Mycoplasma bovis Interaction with Tight Junctions |
title_sort | mbov_0503 encodes a novel cytoadhesin that facilitates mycoplasma bovis interaction with tight junctions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074692/ https://www.ncbi.nlm.nih.gov/pubmed/31979335 http://dx.doi.org/10.3390/microorganisms8020164 |
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