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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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. |
format | Online Article Text |
id | pubmed-4991386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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