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Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia

Neutrophil extracellular traps (NETs) are released by activated neutrophils to ensnare and kill microorganisms. NETs have been implicated in tissue injury since they carry cytotoxic components of the activated neutrophils. We have previously demonstrated the generation of NETs in infected murine lun...

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Autores principales: Moorthy, Anandi Narayana, Rai, Prashant, Jiao, Huipeng, Wang, Shi, Tan, Kong Bing, Qin, Liang, Watanabe, Hiroshi, Zhang, Yongliang, Teluguakula, Narasaraju, Chow, Vincent Tak Kwong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991386/
https://www.ncbi.nlm.nih.gov/pubmed/27034012
http://dx.doi.org/10.18632/oncotarget.8451
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author Moorthy, Anandi Narayana
Rai, Prashant
Jiao, Huipeng
Wang, Shi
Tan, Kong Bing
Qin, Liang
Watanabe, Hiroshi
Zhang, Yongliang
Teluguakula, Narasaraju
Chow, Vincent Tak Kwong
author_facet Moorthy, Anandi Narayana
Rai, Prashant
Jiao, Huipeng
Wang, Shi
Tan, Kong Bing
Qin, Liang
Watanabe, Hiroshi
Zhang, Yongliang
Teluguakula, Narasaraju
Chow, Vincent Tak Kwong
author_sort Moorthy, Anandi Narayana
collection PubMed
description Neutrophil extracellular traps (NETs) are released by activated neutrophils to ensnare and kill microorganisms. NETs have been implicated in tissue injury since they carry cytotoxic components of the activated neutrophils. We have previously demonstrated the generation of NETs in infected murine lungs during both primary pneumococcal pneumonia and secondary pneumococcal pneumonia after primary influenza. In this study, we assessed the correlation of pneumococcal capsule size with pulmonary NETs formation and disease severity. We compared NETs formation in the lungs of mice infected with three pneumococcal strains of varying virulence namely serotypes 3, 4 and 19F, as well as a capsule-deficient mutant of serotype 4. In primary pneumonia, NETs generation was strongly associated with the pneumococcal capsule thickness, and was proportional to the disease severity. Interestingly, during secondary pneumonia after primary influenza infection, intense pulmonary NETs generation together with elevated myeloperoxidase activity and cytokine dysregulation determined the disease severity. These findings highlight the crucial role played by the size of pneumococcal capsule in determining the extent of innate immune responses such as NETs formation that may contribute to the severity of pneumonia.
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spelling pubmed-49913862016-09-01 Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia Moorthy, Anandi Narayana Rai, Prashant Jiao, Huipeng Wang, Shi Tan, Kong Bing Qin, Liang Watanabe, Hiroshi Zhang, Yongliang Teluguakula, Narasaraju Chow, Vincent Tak Kwong Oncotarget Research Paper: Immunology Neutrophil extracellular traps (NETs) are released by activated neutrophils to ensnare and kill microorganisms. NETs have been implicated in tissue injury since they carry cytotoxic components of the activated neutrophils. We have previously demonstrated the generation of NETs in infected murine lungs during both primary pneumococcal pneumonia and secondary pneumococcal pneumonia after primary influenza. In this study, we assessed the correlation of pneumococcal capsule size with pulmonary NETs formation and disease severity. We compared NETs formation in the lungs of mice infected with three pneumococcal strains of varying virulence namely serotypes 3, 4 and 19F, as well as a capsule-deficient mutant of serotype 4. In primary pneumonia, NETs generation was strongly associated with the pneumococcal capsule thickness, and was proportional to the disease severity. Interestingly, during secondary pneumonia after primary influenza infection, intense pulmonary NETs generation together with elevated myeloperoxidase activity and cytokine dysregulation determined the disease severity. These findings highlight the crucial role played by the size of pneumococcal capsule in determining the extent of innate immune responses such as NETs formation that may contribute to the severity of pneumonia. Impact Journals LLC 2016-03-28 /pmc/articles/PMC4991386/ /pubmed/27034012 http://dx.doi.org/10.18632/oncotarget.8451 Text en Copyright: © 2016 Moorthy et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Immunology
Moorthy, Anandi Narayana
Rai, Prashant
Jiao, Huipeng
Wang, Shi
Tan, Kong Bing
Qin, Liang
Watanabe, Hiroshi
Zhang, Yongliang
Teluguakula, Narasaraju
Chow, Vincent Tak Kwong
Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title_full Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title_fullStr Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title_full_unstemmed Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title_short Capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
title_sort capsules of virulent pneumococcal serotypes enhance formation of neutrophil extracellular traps during in vivo pathogenesis of pneumonia
topic Research Paper: Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991386/
https://www.ncbi.nlm.nih.gov/pubmed/27034012
http://dx.doi.org/10.18632/oncotarget.8451
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