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Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data
BACKGROUND: Co-circulating respiratory pathogens can interfere with or promote each other, leading to important effects on disease epidemiology. Estimating the magnitude of pathogen-pathogen interactions from clinical specimens is challenging because sampling from symptomatic individuals can create...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845514/ https://www.ncbi.nlm.nih.gov/pubmed/35169816 http://dx.doi.org/10.1101/2022.02.04.22270474 |
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author | Burstein, Roy Althouse, Benjamin M. Adler, Amanda Akullian, Adam Brandstetter, Elizabeth Cho, Shari Emanuels, Anne Fay, Kairsten Gamboa, Luis Han, Peter Huden, Kristen Ilcisin, Misja Izzo, Mandy Jackson, Michael L. Kim, Ashley E. Kimball, Louise Lacombe, Kirsten Lee, Jover Logue, Jennifer K. Rogers, Julia Chung, Erin Sibley, Thomas R. Van Raay, Katrina Wenger, Edward Wolf, Caitlin R. Boeckh, Michael Chu, Helen Duchin, Jeff Rieder, Mark Shendure, Jay Starita, Lea M. Viboud, Cecile Bedford, Trevor Englund, Janet A. Famulare, Michael |
author_facet | Burstein, Roy Althouse, Benjamin M. Adler, Amanda Akullian, Adam Brandstetter, Elizabeth Cho, Shari Emanuels, Anne Fay, Kairsten Gamboa, Luis Han, Peter Huden, Kristen Ilcisin, Misja Izzo, Mandy Jackson, Michael L. Kim, Ashley E. Kimball, Louise Lacombe, Kirsten Lee, Jover Logue, Jennifer K. Rogers, Julia Chung, Erin Sibley, Thomas R. Van Raay, Katrina Wenger, Edward Wolf, Caitlin R. Boeckh, Michael Chu, Helen Duchin, Jeff Rieder, Mark Shendure, Jay Starita, Lea M. Viboud, Cecile Bedford, Trevor Englund, Janet A. Famulare, Michael |
author_sort | Burstein, Roy |
collection | PubMed |
description | BACKGROUND: Co-circulating respiratory pathogens can interfere with or promote each other, leading to important effects on disease epidemiology. Estimating the magnitude of pathogen-pathogen interactions from clinical specimens is challenging because sampling from symptomatic individuals can create biased estimates. METHODS: We conducted an observational, cross-sectional study using samples collected by the Seattle Flu Study between 11 November 2018 and 20 August 2021. Samples that tested positive via RT-qPCR for at least one of 17 potential respiratory pathogens were included in this study. Semi-quantitative cycle threshold (Ct) values were used to measure pathogen load. Differences in pathogen load between monoinfected and coinfected samples were assessed using linear regression adjusting for age, season, and recruitment channel. RESULTS: 21,686 samples were positive for at least one potential pathogen. Most prevalent were rhinovirus (33·5%), Streptococcus pneumoniae (SPn, 29·0%), SARS-CoV-2 (13.8%) and influenza A/H1N1 (9·6%). 140 potential pathogen pairs were included for analysis, and 56 (40%) pairs yielded significant Ct differences (p < 0.01) between monoinfected and co-infected samples. We observed no virus-virus pairs showing evidence of significant facilitating interactions, and found significant viral load decrease among 37 of 108 (34%) assessed pairs. Samples positive with SPn and a virus were consistently associated with increased SPn load. CONCLUSIONS: Viral load data can be used to overcome sampling bias in studies of pathogen-pathogen interactions. When applied to respiratory pathogens, we found evidence of viral-SPn facilitation and several examples of viral-viral interference. Multipathogen surveillance is a cost-efficient data collection approach, with added clinical and epidemiological informational value over single-pathogen testing, but requires careful analysis to mitigate selection bias. |
format | Online Article Text |
id | pubmed-8845514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-88455142022-02-16 Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data Burstein, Roy Althouse, Benjamin M. Adler, Amanda Akullian, Adam Brandstetter, Elizabeth Cho, Shari Emanuels, Anne Fay, Kairsten Gamboa, Luis Han, Peter Huden, Kristen Ilcisin, Misja Izzo, Mandy Jackson, Michael L. Kim, Ashley E. Kimball, Louise Lacombe, Kirsten Lee, Jover Logue, Jennifer K. Rogers, Julia Chung, Erin Sibley, Thomas R. Van Raay, Katrina Wenger, Edward Wolf, Caitlin R. Boeckh, Michael Chu, Helen Duchin, Jeff Rieder, Mark Shendure, Jay Starita, Lea M. Viboud, Cecile Bedford, Trevor Englund, Janet A. Famulare, Michael medRxiv Article BACKGROUND: Co-circulating respiratory pathogens can interfere with or promote each other, leading to important effects on disease epidemiology. Estimating the magnitude of pathogen-pathogen interactions from clinical specimens is challenging because sampling from symptomatic individuals can create biased estimates. METHODS: We conducted an observational, cross-sectional study using samples collected by the Seattle Flu Study between 11 November 2018 and 20 August 2021. Samples that tested positive via RT-qPCR for at least one of 17 potential respiratory pathogens were included in this study. Semi-quantitative cycle threshold (Ct) values were used to measure pathogen load. Differences in pathogen load between monoinfected and coinfected samples were assessed using linear regression adjusting for age, season, and recruitment channel. RESULTS: 21,686 samples were positive for at least one potential pathogen. Most prevalent were rhinovirus (33·5%), Streptococcus pneumoniae (SPn, 29·0%), SARS-CoV-2 (13.8%) and influenza A/H1N1 (9·6%). 140 potential pathogen pairs were included for analysis, and 56 (40%) pairs yielded significant Ct differences (p < 0.01) between monoinfected and co-infected samples. We observed no virus-virus pairs showing evidence of significant facilitating interactions, and found significant viral load decrease among 37 of 108 (34%) assessed pairs. Samples positive with SPn and a virus were consistently associated with increased SPn load. CONCLUSIONS: Viral load data can be used to overcome sampling bias in studies of pathogen-pathogen interactions. When applied to respiratory pathogens, we found evidence of viral-SPn facilitation and several examples of viral-viral interference. Multipathogen surveillance is a cost-efficient data collection approach, with added clinical and epidemiological informational value over single-pathogen testing, but requires careful analysis to mitigate selection bias. Cold Spring Harbor Laboratory 2022-02-06 /pmc/articles/PMC8845514/ /pubmed/35169816 http://dx.doi.org/10.1101/2022.02.04.22270474 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Burstein, Roy Althouse, Benjamin M. Adler, Amanda Akullian, Adam Brandstetter, Elizabeth Cho, Shari Emanuels, Anne Fay, Kairsten Gamboa, Luis Han, Peter Huden, Kristen Ilcisin, Misja Izzo, Mandy Jackson, Michael L. Kim, Ashley E. Kimball, Louise Lacombe, Kirsten Lee, Jover Logue, Jennifer K. Rogers, Julia Chung, Erin Sibley, Thomas R. Van Raay, Katrina Wenger, Edward Wolf, Caitlin R. Boeckh, Michael Chu, Helen Duchin, Jeff Rieder, Mark Shendure, Jay Starita, Lea M. Viboud, Cecile Bedford, Trevor Englund, Janet A. Famulare, Michael Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title | Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title_full | Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title_fullStr | Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title_full_unstemmed | Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title_short | Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
title_sort | interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845514/ https://www.ncbi.nlm.nih.gov/pubmed/35169816 http://dx.doi.org/10.1101/2022.02.04.22270474 |
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