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Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function

In dairy herds, mastitis caused by Staphylococcus aureus is difficult to completely cure on the account that S. aureus can invade bovine mammary epithelial cells (BMECs) and result in persistent infection in the mammary gland. Recent studies have demonstrated that autophagy can participate in cell h...

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Autores principales: Geng, Na, Wang, Xiaozhou, Yu, Xiaohui, Wang, Run, Zhu, Yiran, Zhang, Meihua, Liu, Jianzhu, Liu, Yongxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214833/
https://www.ncbi.nlm.nih.gov/pubmed/32431700
http://dx.doi.org/10.3389/fimmu.2020.00746
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author Geng, Na
Wang, Xiaozhou
Yu, Xiaohui
Wang, Run
Zhu, Yiran
Zhang, Meihua
Liu, Jianzhu
Liu, Yongxia
author_facet Geng, Na
Wang, Xiaozhou
Yu, Xiaohui
Wang, Run
Zhu, Yiran
Zhang, Meihua
Liu, Jianzhu
Liu, Yongxia
author_sort Geng, Na
collection PubMed
description In dairy herds, mastitis caused by Staphylococcus aureus is difficult to completely cure on the account that S. aureus can invade bovine mammary epithelial cells (BMECs) and result in persistent infection in the mammary gland. Recent studies have demonstrated that autophagy can participate in cell homeostasis by eliminating intracellular microorganisms. The aim of the study was to investigate why S. aureus can evade autophagy clearance and survive in BMECs. The intracellular infection model was first constructed; then, the bacteria in autophagosome was detected by transmission electron microscopy. The autophagy flux induced by the S. aureus was also evaluated by immunoblot analysis and fluorescent labeling method for autophagy marker protein LC3. In addition, lysosomal alkalization and degradation ability were assessed using confocal microscopy. Results showed that, after infection, a double-layer membrane structure around the S. aureus was observed in BMECs, indicating that autophagy occurred. The change in autophagy marker protein and fluorescent labeling of autophagosome also confirmed autophagy. However, as time prolonged, the autophagy flux was markedly inhibited, leading to obvious autophagosome accumulation. At the same time, the lysosomal alkalization and degradation ability of BMECs were impaired. Collectively, these results indicated that S. aureus could escape autophagic degradation by inhibiting autophagy flux and damaging lysosomal function after invading BMECs.
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spelling pubmed-72148332020-05-19 Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function Geng, Na Wang, Xiaozhou Yu, Xiaohui Wang, Run Zhu, Yiran Zhang, Meihua Liu, Jianzhu Liu, Yongxia Front Immunol Immunology In dairy herds, mastitis caused by Staphylococcus aureus is difficult to completely cure on the account that S. aureus can invade bovine mammary epithelial cells (BMECs) and result in persistent infection in the mammary gland. Recent studies have demonstrated that autophagy can participate in cell homeostasis by eliminating intracellular microorganisms. The aim of the study was to investigate why S. aureus can evade autophagy clearance and survive in BMECs. The intracellular infection model was first constructed; then, the bacteria in autophagosome was detected by transmission electron microscopy. The autophagy flux induced by the S. aureus was also evaluated by immunoblot analysis and fluorescent labeling method for autophagy marker protein LC3. In addition, lysosomal alkalization and degradation ability were assessed using confocal microscopy. Results showed that, after infection, a double-layer membrane structure around the S. aureus was observed in BMECs, indicating that autophagy occurred. The change in autophagy marker protein and fluorescent labeling of autophagosome also confirmed autophagy. However, as time prolonged, the autophagy flux was markedly inhibited, leading to obvious autophagosome accumulation. At the same time, the lysosomal alkalization and degradation ability of BMECs were impaired. Collectively, these results indicated that S. aureus could escape autophagic degradation by inhibiting autophagy flux and damaging lysosomal function after invading BMECs. Frontiers Media S.A. 2020-05-05 /pmc/articles/PMC7214833/ /pubmed/32431700 http://dx.doi.org/10.3389/fimmu.2020.00746 Text en Copyright © 2020 Geng, Wang, Yu, Wang, Zhu, Zhang, Liu and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Geng, Na
Wang, Xiaozhou
Yu, Xiaohui
Wang, Run
Zhu, Yiran
Zhang, Meihua
Liu, Jianzhu
Liu, Yongxia
Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title_full Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title_fullStr Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title_full_unstemmed Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title_short Staphylococcus aureus Avoids Autophagy Clearance of Bovine Mammary Epithelial Cells by Impairing Lysosomal Function
title_sort staphylococcus aureus avoids autophagy clearance of bovine mammary epithelial cells by impairing lysosomal function
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214833/
https://www.ncbi.nlm.nih.gov/pubmed/32431700
http://dx.doi.org/10.3389/fimmu.2020.00746
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