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Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro

Mycoplasma agalactiae is the etiological agent of the contagious agalactia syndrome in sheep and goats and causes significant economic losses worldwide. Yet the mechanism of pathogenesis is largely unknown. Even whole-genome sequence analysis of its pathogenic type strain did not lead to any conclus...

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Autores principales: Hegde, Shrilakshmi, Hegde, Shivanand Manjunath, Rosengarten, Renate, Chopra-Dewasthaly, Rohini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035028/
https://www.ncbi.nlm.nih.gov/pubmed/27662492
http://dx.doi.org/10.1371/journal.pone.0163603
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author Hegde, Shrilakshmi
Hegde, Shivanand Manjunath
Rosengarten, Renate
Chopra-Dewasthaly, Rohini
author_facet Hegde, Shrilakshmi
Hegde, Shivanand Manjunath
Rosengarten, Renate
Chopra-Dewasthaly, Rohini
author_sort Hegde, Shrilakshmi
collection PubMed
description Mycoplasma agalactiae is the etiological agent of the contagious agalactia syndrome in sheep and goats and causes significant economic losses worldwide. Yet the mechanism of pathogenesis is largely unknown. Even whole-genome sequence analysis of its pathogenic type strain did not lead to any conclusions regarding its virulence or pathogenicity factors. Although inflammation and tissue destruction at the local site of M. agalactiae infection are largely considered as effects of the host immune response, the direct effect of the agent on host cells is not completely understood. The aim of this study was to investigate the effect of M. agalactiae infection on the quality and viability of host cells in vitro. Changes in cell morphology including cell elongation, cytoplasm shrinkage and membrane blebbing were observed in infected HeLa cells. Chromatin condensation and increased caspase-3 cleavage in infected HeLa cells 48 h after infection suggests an apoptosis-like phenomenon in M. agalactiae-infected cells. In compliance with these results, decreased viability and cell lysis of M. agalactiae-infected HeLa cells was also observed. Measurement of the amount of LDH released after M. agalactiae infection revealed a time- and dose-dependent increase in HeLa cell lysis. A significant decrease in LDH released after gentamicin treatment of infected cells confirmed the major role of cytadherent M. agalactiae in inducing host cell lysis. This is the first study illustrating M. agalactiae’s induction of cytopathic effects in infected HeLa cells. Further detailed investigation of infected host tissue for apoptotic markers might demonstrate the association between M. agalactiae-induced host cell lysis and the tissue destruction observed during M. agalactiae natural infection.
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spelling pubmed-50350282016-10-10 Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro Hegde, Shrilakshmi Hegde, Shivanand Manjunath Rosengarten, Renate Chopra-Dewasthaly, Rohini PLoS One Research Article Mycoplasma agalactiae is the etiological agent of the contagious agalactia syndrome in sheep and goats and causes significant economic losses worldwide. Yet the mechanism of pathogenesis is largely unknown. Even whole-genome sequence analysis of its pathogenic type strain did not lead to any conclusions regarding its virulence or pathogenicity factors. Although inflammation and tissue destruction at the local site of M. agalactiae infection are largely considered as effects of the host immune response, the direct effect of the agent on host cells is not completely understood. The aim of this study was to investigate the effect of M. agalactiae infection on the quality and viability of host cells in vitro. Changes in cell morphology including cell elongation, cytoplasm shrinkage and membrane blebbing were observed in infected HeLa cells. Chromatin condensation and increased caspase-3 cleavage in infected HeLa cells 48 h after infection suggests an apoptosis-like phenomenon in M. agalactiae-infected cells. In compliance with these results, decreased viability and cell lysis of M. agalactiae-infected HeLa cells was also observed. Measurement of the amount of LDH released after M. agalactiae infection revealed a time- and dose-dependent increase in HeLa cell lysis. A significant decrease in LDH released after gentamicin treatment of infected cells confirmed the major role of cytadherent M. agalactiae in inducing host cell lysis. This is the first study illustrating M. agalactiae’s induction of cytopathic effects in infected HeLa cells. Further detailed investigation of infected host tissue for apoptotic markers might demonstrate the association between M. agalactiae-induced host cell lysis and the tissue destruction observed during M. agalactiae natural infection. Public Library of Science 2016-09-23 /pmc/articles/PMC5035028/ /pubmed/27662492 http://dx.doi.org/10.1371/journal.pone.0163603 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Hegde, Shrilakshmi
Hegde, Shivanand Manjunath
Rosengarten, Renate
Chopra-Dewasthaly, Rohini
Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title_full Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title_fullStr Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title_full_unstemmed Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title_short Mycoplasma agalactiae Induces Cytopathic Effects in Infected Cells Cultured In Vitro
title_sort mycoplasma agalactiae induces cytopathic effects in infected cells cultured in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5035028/
https://www.ncbi.nlm.nih.gov/pubmed/27662492
http://dx.doi.org/10.1371/journal.pone.0163603
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