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The upper and lower respiratory tract microbiome in severe aspiration pneumonia
Uncertainty persists whether anaerobic bacteria represent important pathogens in aspiration pneumonia. In a nested case-control study of mechanically ventilated patients classified as macro-aspiration pneumonia (MAsP, n = 56), non-macro-aspiration pneumonia (NonMAsP, n = 91), and uninfected controls...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212968/ https://www.ncbi.nlm.nih.gov/pubmed/37250794 http://dx.doi.org/10.1016/j.isci.2023.106832 |
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author | Kitsios, Georgios D. Nguyen, Vi D. Sayed, Khaled Al-Yousif, Nameer Schaefer, Caitlin Shah, Faraaz A. Bain, William Yang, Haopu Fitch, Adam Li, Kelvin Wang, Xiaohong Qin, Shulin Gentry, Heather Zhang, Yingze Varon, Jack Arciniegas Rubio, Antonio Englert, Joshua A. Baron, Rebecca M. Lee, Janet S. Methé, Barbara Benos, Panayiotis V. Morris, Alison McVerry, Bryan J. |
author_facet | Kitsios, Georgios D. Nguyen, Vi D. Sayed, Khaled Al-Yousif, Nameer Schaefer, Caitlin Shah, Faraaz A. Bain, William Yang, Haopu Fitch, Adam Li, Kelvin Wang, Xiaohong Qin, Shulin Gentry, Heather Zhang, Yingze Varon, Jack Arciniegas Rubio, Antonio Englert, Joshua A. Baron, Rebecca M. Lee, Janet S. Methé, Barbara Benos, Panayiotis V. Morris, Alison McVerry, Bryan J. |
author_sort | Kitsios, Georgios D. |
collection | PubMed |
description | Uncertainty persists whether anaerobic bacteria represent important pathogens in aspiration pneumonia. In a nested case-control study of mechanically ventilated patients classified as macro-aspiration pneumonia (MAsP, n = 56), non-macro-aspiration pneumonia (NonMAsP, n = 91), and uninfected controls (n = 11), we profiled upper (URT) and lower respiratory tract (LRT) microbiota with bacterial 16S rRNA gene sequencing, measured plasma host-response biomarkers, analyzed bacterial communities by diversity and oxygen requirements, and performed unsupervised clustering with Dirichlet Multinomial Models (DMM). MAsP and NonMAsP patients had indistinguishable microbiota profiles by alpha diversity and oxygen requirements with similar host-response profiles and 60-day survival. Unsupervised DMM clusters revealed distinct bacterial clusters in the URT and LRT, with low-diversity clusters enriched for facultative anaerobes and typical pathogens, associated with higher plasma levels of SPD and sCD14 and worse 60-day survival. The predictive inter-patient variability in these bacterial profiles highlights the importance of microbiome study in patient sub-phenotyping and precision medicine approaches for severe pneumonia. |
format | Online Article Text |
id | pubmed-10212968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102129682023-05-27 The upper and lower respiratory tract microbiome in severe aspiration pneumonia Kitsios, Georgios D. Nguyen, Vi D. Sayed, Khaled Al-Yousif, Nameer Schaefer, Caitlin Shah, Faraaz A. Bain, William Yang, Haopu Fitch, Adam Li, Kelvin Wang, Xiaohong Qin, Shulin Gentry, Heather Zhang, Yingze Varon, Jack Arciniegas Rubio, Antonio Englert, Joshua A. Baron, Rebecca M. Lee, Janet S. Methé, Barbara Benos, Panayiotis V. Morris, Alison McVerry, Bryan J. iScience Article Uncertainty persists whether anaerobic bacteria represent important pathogens in aspiration pneumonia. In a nested case-control study of mechanically ventilated patients classified as macro-aspiration pneumonia (MAsP, n = 56), non-macro-aspiration pneumonia (NonMAsP, n = 91), and uninfected controls (n = 11), we profiled upper (URT) and lower respiratory tract (LRT) microbiota with bacterial 16S rRNA gene sequencing, measured plasma host-response biomarkers, analyzed bacterial communities by diversity and oxygen requirements, and performed unsupervised clustering with Dirichlet Multinomial Models (DMM). MAsP and NonMAsP patients had indistinguishable microbiota profiles by alpha diversity and oxygen requirements with similar host-response profiles and 60-day survival. Unsupervised DMM clusters revealed distinct bacterial clusters in the URT and LRT, with low-diversity clusters enriched for facultative anaerobes and typical pathogens, associated with higher plasma levels of SPD and sCD14 and worse 60-day survival. The predictive inter-patient variability in these bacterial profiles highlights the importance of microbiome study in patient sub-phenotyping and precision medicine approaches for severe pneumonia. Elsevier 2023-05-06 /pmc/articles/PMC10212968/ /pubmed/37250794 http://dx.doi.org/10.1016/j.isci.2023.106832 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kitsios, Georgios D. Nguyen, Vi D. Sayed, Khaled Al-Yousif, Nameer Schaefer, Caitlin Shah, Faraaz A. Bain, William Yang, Haopu Fitch, Adam Li, Kelvin Wang, Xiaohong Qin, Shulin Gentry, Heather Zhang, Yingze Varon, Jack Arciniegas Rubio, Antonio Englert, Joshua A. Baron, Rebecca M. Lee, Janet S. Methé, Barbara Benos, Panayiotis V. Morris, Alison McVerry, Bryan J. The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title | The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title_full | The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title_fullStr | The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title_full_unstemmed | The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title_short | The upper and lower respiratory tract microbiome in severe aspiration pneumonia |
title_sort | upper and lower respiratory tract microbiome in severe aspiration pneumonia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212968/ https://www.ncbi.nlm.nih.gov/pubmed/37250794 http://dx.doi.org/10.1016/j.isci.2023.106832 |
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