Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells

Streptococcus pneumoniae is a leading cause of pneumonia and one of the most common causes of death globally. The impact of S. pneumoniae on host molecular processes that lead to detrimental pulmonary consequences is not fully understood. Here, we show that S. pneumoniae induces toxic DNA double-str...

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Main Authors: Rai, Prashant, Tay, Ian Jun Jie, Li, Na, Ackerman, Shelley, He, Fang, Kwang, Jimmy, Chow, Vincent T., Engelward, Bevin P., Parrish, Marcus Curtis, Tay, Jun Jie Ian
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: National Academy of Sciences (U.S.) 2016
Online Access:http://hdl.handle.net/1721.1/100789
https://orcid.org/0000-0002-5472-3621
https://orcid.org/0000-0002-7149-9369
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author Rai, Prashant
Tay, Ian Jun Jie
Li, Na
Ackerman, Shelley
He, Fang
Kwang, Jimmy
Chow, Vincent T.
Engelward, Bevin P.
Parrish, Marcus Curtis
Tay, Jun Jie Ian
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Rai, Prashant
Tay, Ian Jun Jie
Li, Na
Ackerman, Shelley
He, Fang
Kwang, Jimmy
Chow, Vincent T.
Engelward, Bevin P.
Parrish, Marcus Curtis
Tay, Jun Jie Ian
author_sort Rai, Prashant
collection MIT
description Streptococcus pneumoniae is a leading cause of pneumonia and one of the most common causes of death globally. The impact of S. pneumoniae on host molecular processes that lead to detrimental pulmonary consequences is not fully understood. Here, we show that S. pneumoniae induces toxic DNA double-strand breaks (DSBs) in human alveolar epithelial cells, as indicated by ataxia telangiectasia mutated kinase (ATM)-dependent phosphorylation of histone H2AX and colocalization with p53-binding protein (53BP1). Furthermore, results show that DNA damage occurs in a bacterial contact-independent fashion and that Streptococcus pyruvate oxidase (SpxB), which enables synthesis of H[subscript 2]O[subscript 2], plays a critical role in inducing DSBs. The extent of DNA damage correlates with the extent of apoptosis, and DNA damage precedes apoptosis, which is consistent with the time required for execution of apoptosis. Furthermore, addition of catalase, which neutralizes H[subscript 2]O[subscript 2], greatly suppresses S. pneumoniae-induced DNA damage and apoptosis. Importantly, S. pneumoniae induces DSBs in the lungs of animals with acute pneumonia, and H[subscript 2]O[subscript 2] production by S. pneumoniae in vivo contributes to its genotoxicity and virulence. One of the major DSBs repair pathways is nonhomologous end joining for which Ku70/80 is essential for repair. We find that deficiency of Ku80 causes an increase in the levels of DSBs and apoptosis, underscoring the importance of DNA repair in preventing S. pneumoniae-induced genotoxicity. Taken together, this study shows that S. pneumoniae-induced damage to the host cell genome exacerbates its toxicity and pathogenesis, making DNA repair a potentially important susceptibility factor in people who suffer from pneumonia.
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spelling mit-1721.1/1007892022-09-30T08:07:42Z Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells Rai, Prashant Tay, Ian Jun Jie Li, Na Ackerman, Shelley He, Fang Kwang, Jimmy Chow, Vincent T. Engelward, Bevin P. Parrish, Marcus Curtis Tay, Jun Jie Ian Massachusetts Institute of Technology. Department of Biological Engineering Parrish, Marcus Curtis Tay, Jun Jie Ian Ackerman, Shelley Engelward, Bevin P. Streptococcus pneumoniae is a leading cause of pneumonia and one of the most common causes of death globally. The impact of S. pneumoniae on host molecular processes that lead to detrimental pulmonary consequences is not fully understood. Here, we show that S. pneumoniae induces toxic DNA double-strand breaks (DSBs) in human alveolar epithelial cells, as indicated by ataxia telangiectasia mutated kinase (ATM)-dependent phosphorylation of histone H2AX and colocalization with p53-binding protein (53BP1). Furthermore, results show that DNA damage occurs in a bacterial contact-independent fashion and that Streptococcus pyruvate oxidase (SpxB), which enables synthesis of H[subscript 2]O[subscript 2], plays a critical role in inducing DSBs. The extent of DNA damage correlates with the extent of apoptosis, and DNA damage precedes apoptosis, which is consistent with the time required for execution of apoptosis. Furthermore, addition of catalase, which neutralizes H[subscript 2]O[subscript 2], greatly suppresses S. pneumoniae-induced DNA damage and apoptosis. Importantly, S. pneumoniae induces DSBs in the lungs of animals with acute pneumonia, and H[subscript 2]O[subscript 2] production by S. pneumoniae in vivo contributes to its genotoxicity and virulence. One of the major DSBs repair pathways is nonhomologous end joining for which Ku70/80 is essential for repair. We find that deficiency of Ku80 causes an increase in the levels of DSBs and apoptosis, underscoring the importance of DNA repair in preventing S. pneumoniae-induced genotoxicity. Taken together, this study shows that S. pneumoniae-induced damage to the host cell genome exacerbates its toxicity and pathogenesis, making DNA repair a potentially important susceptibility factor in people who suffer from pneumonia. 2016-01-11T00:47:43Z 2016-01-11T00:47:43Z 2015-06 2014-12 Article http://purl.org/eprint/type/JournalArticle 0027-8424 1091-6490 http://hdl.handle.net/1721.1/100789 Rai, Prashant, Marcus Parrish, Ian Jun Jie Tay, Na Li, Shelley Ackerman, Fang He, Jimmy Kwang, Vincent T. Chow, and Bevin P. Engelward. “ Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells .” Proc Natl Acad Sci USA 112, no. 26 (June 15, 2015): E3421–E3430. https://orcid.org/0000-0002-5472-3621 https://orcid.org/0000-0002-7149-9369 en_US http://dx.doi.org/10.1073/pnas.1424144112 Proceedings of the National Academy of Sciences Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf National Academy of Sciences (U.S.) National Academy of Sciences (U.S.)
spellingShingle Rai, Prashant
Tay, Ian Jun Jie
Li, Na
Ackerman, Shelley
He, Fang
Kwang, Jimmy
Chow, Vincent T.
Engelward, Bevin P.
Parrish, Marcus Curtis
Tay, Jun Jie Ian
Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title_full Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title_fullStr Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title_full_unstemmed Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title_short Streptococcus Pneumoniae Secretes Hydrogen Peroxide Leading to DNA Damage and Apoptosis in Lung Cells
title_sort streptococcus pneumoniae secretes hydrogen peroxide leading to dna damage and apoptosis in lung cells
url http://hdl.handle.net/1721.1/100789
https://orcid.org/0000-0002-5472-3621
https://orcid.org/0000-0002-7149-9369
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