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In Utero Ultrafine Particulate Exposure Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial Virus Infection
[Image: see text] Exposure to particulate matter (PM) is associated with lower respiratory tract infections. The role of ultrafine particles (UFPs, ≤0.1 μm) in respiratory disease is not fully elucidated, especially in models of immunologically immature populations. To characterize the effects of ma...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386899/ https://www.ncbi.nlm.nih.gov/pubmed/35926851 http://dx.doi.org/10.1021/acs.est.2c02786 |
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author | Lau, Carmen Behlen, Jonathan C. Myers, Alexandra Li, Yixin Zhao, Jiayun Harvey, Navada Wright, Gus Hoffmann, Aline Rodrigues Zhang, Renyi Johnson, Natalie M. |
author_facet | Lau, Carmen Behlen, Jonathan C. Myers, Alexandra Li, Yixin Zhao, Jiayun Harvey, Navada Wright, Gus Hoffmann, Aline Rodrigues Zhang, Renyi Johnson, Natalie M. |
author_sort | Lau, Carmen |
collection | PubMed |
description | [Image: see text] Exposure to particulate matter (PM) is associated with lower respiratory tract infections. The role of ultrafine particles (UFPs, ≤0.1 μm) in respiratory disease is not fully elucidated, especially in models of immunologically immature populations. To characterize the effects of maternal UFP exposure on neonatal infection, we exposed time-mated C57Bl/6n mice to filtered air or UFPs at a low dose (LD, ∼55 μg/m(3)) and high dose (HD, ∼275 μg/m(3)) throughout gestation. At 5 days of age, offspring were infected with a respiratory syncytial virus (RSV) strain known to mimic infant infection or sham control. Offspring body weights were significantly reduced in response to infection in the LD RSV group, particularly females. Pulmonary gene expression analysis demonstrated significantly increased levels of oxidative stress- and inflammation-related genes in HD-exposed male offspring in sham and RSV-infected groups. In males, the highest grade of inflammation was observed in the HD RSV group, whereas in females, the LD RSV group showed the most marked inflammation. Overall, findings highlight neonatal responses are dependent on offspring sex and maternal UFP dose. Importantly, infant RSV pathology may be enhanced following even low dose UFP exposure signifying the importance of preventing maternal exposure. |
format | Online Article Text |
id | pubmed-9386899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93868992022-08-19 In Utero Ultrafine Particulate Exposure Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial Virus Infection Lau, Carmen Behlen, Jonathan C. Myers, Alexandra Li, Yixin Zhao, Jiayun Harvey, Navada Wright, Gus Hoffmann, Aline Rodrigues Zhang, Renyi Johnson, Natalie M. Environ Sci Technol [Image: see text] Exposure to particulate matter (PM) is associated with lower respiratory tract infections. The role of ultrafine particles (UFPs, ≤0.1 μm) in respiratory disease is not fully elucidated, especially in models of immunologically immature populations. To characterize the effects of maternal UFP exposure on neonatal infection, we exposed time-mated C57Bl/6n mice to filtered air or UFPs at a low dose (LD, ∼55 μg/m(3)) and high dose (HD, ∼275 μg/m(3)) throughout gestation. At 5 days of age, offspring were infected with a respiratory syncytial virus (RSV) strain known to mimic infant infection or sham control. Offspring body weights were significantly reduced in response to infection in the LD RSV group, particularly females. Pulmonary gene expression analysis demonstrated significantly increased levels of oxidative stress- and inflammation-related genes in HD-exposed male offspring in sham and RSV-infected groups. In males, the highest grade of inflammation was observed in the HD RSV group, whereas in females, the LD RSV group showed the most marked inflammation. Overall, findings highlight neonatal responses are dependent on offspring sex and maternal UFP dose. Importantly, infant RSV pathology may be enhanced following even low dose UFP exposure signifying the importance of preventing maternal exposure. American Chemical Society 2022-08-04 2022-08-16 /pmc/articles/PMC9386899/ /pubmed/35926851 http://dx.doi.org/10.1021/acs.est.2c02786 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Lau, Carmen Behlen, Jonathan C. Myers, Alexandra Li, Yixin Zhao, Jiayun Harvey, Navada Wright, Gus Hoffmann, Aline Rodrigues Zhang, Renyi Johnson, Natalie M. In Utero Ultrafine Particulate Exposure Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial Virus Infection |
title | In Utero Ultrafine Particulate Exposure
Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial
Virus Infection |
title_full | In Utero Ultrafine Particulate Exposure
Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial
Virus Infection |
title_fullStr | In Utero Ultrafine Particulate Exposure
Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial
Virus Infection |
title_full_unstemmed | In Utero Ultrafine Particulate Exposure
Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial
Virus Infection |
title_short | In Utero Ultrafine Particulate Exposure
Yields Sex- and Dose-Specific Responses to Neonatal Respiratory Syncytial
Virus Infection |
title_sort | in utero ultrafine particulate exposure
yields sex- and dose-specific responses to neonatal respiratory syncytial
virus infection |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386899/ https://www.ncbi.nlm.nih.gov/pubmed/35926851 http://dx.doi.org/10.1021/acs.est.2c02786 |
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