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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
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.
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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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