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Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro

Mycoplasma hyopneumoniae, the agent of porcine enzootic pneumonia (EP), is able to persist in the lung tissue and evade destruction by the host for several weeks. To understand the mechanism of pathogen survival, phagocytic uptake of M. hyopneumoniae by primary porcine alveolar macrophages was inves...

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Autores principales: Deeney, Alannah S., Maglennon, Gareth A., Chapat, Ludivine, Crussard, Steve, Jolivet, Edmond, Rycroft, Andrew N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591956/
https://www.ncbi.nlm.nih.gov/pubmed/31234931
http://dx.doi.org/10.1186/s13567-019-0667-6
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author Deeney, Alannah S.
Maglennon, Gareth A.
Chapat, Ludivine
Crussard, Steve
Jolivet, Edmond
Rycroft, Andrew N.
author_facet Deeney, Alannah S.
Maglennon, Gareth A.
Chapat, Ludivine
Crussard, Steve
Jolivet, Edmond
Rycroft, Andrew N.
author_sort Deeney, Alannah S.
collection PubMed
description Mycoplasma hyopneumoniae, the agent of porcine enzootic pneumonia (EP), is able to persist in the lung tissue and evade destruction by the host for several weeks. To understand the mechanism of pathogen survival, phagocytic uptake of M. hyopneumoniae by primary porcine alveolar macrophages was investigated. Intracellular location and survival of the pathogen were explored using gentamicin survival assays, flow cytometry and confocal microscopy of M. hyopneumoniae 232 labelled with green fluorescent protein (GFP). Following 1 h and 16 h of co-incubation, few viable M. hyopneumoniae were recovered from inside macrophages. Flow cytometric analysis of macrophages incubated with M. hyopneumoniae expressing GFP indicated that the mycoplasmas became associated with macrophages, but were shown to be extracellular when actin-dependent phagocytosis was blocked with cytochalasin D. Confocal microscopy detected GFP-labelled M. hyopneumoniae inside macrophages and the numbers increased modestly with time of incubation. Neither the addition of porcine serum complement or convalescent serum from EP-recovered pigs was able to enhance engulfment of M. hyopneumoniae. This investigation suggests that M. hyopneumoniae evades significant uptake by porcine alveolar macrophages and this may be a mechanism of immune escape by M. hyopneumoniae in the porcine respiratory tract.
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spelling pubmed-65919562019-07-08 Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro Deeney, Alannah S. Maglennon, Gareth A. Chapat, Ludivine Crussard, Steve Jolivet, Edmond Rycroft, Andrew N. Vet Res Research Article Mycoplasma hyopneumoniae, the agent of porcine enzootic pneumonia (EP), is able to persist in the lung tissue and evade destruction by the host for several weeks. To understand the mechanism of pathogen survival, phagocytic uptake of M. hyopneumoniae by primary porcine alveolar macrophages was investigated. Intracellular location and survival of the pathogen were explored using gentamicin survival assays, flow cytometry and confocal microscopy of M. hyopneumoniae 232 labelled with green fluorescent protein (GFP). Following 1 h and 16 h of co-incubation, few viable M. hyopneumoniae were recovered from inside macrophages. Flow cytometric analysis of macrophages incubated with M. hyopneumoniae expressing GFP indicated that the mycoplasmas became associated with macrophages, but were shown to be extracellular when actin-dependent phagocytosis was blocked with cytochalasin D. Confocal microscopy detected GFP-labelled M. hyopneumoniae inside macrophages and the numbers increased modestly with time of incubation. Neither the addition of porcine serum complement or convalescent serum from EP-recovered pigs was able to enhance engulfment of M. hyopneumoniae. This investigation suggests that M. hyopneumoniae evades significant uptake by porcine alveolar macrophages and this may be a mechanism of immune escape by M. hyopneumoniae in the porcine respiratory tract. BioMed Central 2019-06-24 2019 /pmc/articles/PMC6591956/ /pubmed/31234931 http://dx.doi.org/10.1186/s13567-019-0667-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Deeney, Alannah S.
Maglennon, Gareth A.
Chapat, Ludivine
Crussard, Steve
Jolivet, Edmond
Rycroft, Andrew N.
Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title_full Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title_fullStr Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title_full_unstemmed Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title_short Mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
title_sort mycoplasma hyopneumoniae evades phagocytic uptake by porcine alveolar macrophages in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591956/
https://www.ncbi.nlm.nih.gov/pubmed/31234931
http://dx.doi.org/10.1186/s13567-019-0667-6
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