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Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection

Extracellular vesicles (EVs) are increasingly appreciated as a mechanism of communication among cells that contribute to many physiological processes. Although EVs can promote either antiviral or proviral effects during viral infections, the role of EVs in virus-associated polymicrobial infections r...

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Autores principales: Hendricks, Matthew R., Lane, Sidney, Melvin, Jeffrey A., Ouyang, Yingshi, Stolz, Donna B., Williams, John V., Sadovsky, Yoel, Bomberger, Jennifer M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918795/
https://www.ncbi.nlm.nih.gov/pubmed/33503419
http://dx.doi.org/10.1016/j.celrep.2020.108672
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author Hendricks, Matthew R.
Lane, Sidney
Melvin, Jeffrey A.
Ouyang, Yingshi
Stolz, Donna B.
Williams, John V.
Sadovsky, Yoel
Bomberger, Jennifer M.
author_facet Hendricks, Matthew R.
Lane, Sidney
Melvin, Jeffrey A.
Ouyang, Yingshi
Stolz, Donna B.
Williams, John V.
Sadovsky, Yoel
Bomberger, Jennifer M.
author_sort Hendricks, Matthew R.
collection PubMed
description Extracellular vesicles (EVs) are increasingly appreciated as a mechanism of communication among cells that contribute to many physiological processes. Although EVs can promote either antiviral or proviral effects during viral infections, the role of EVs in virus-associated polymicrobial infections remains poorly defined. We report that EVs secreted from airway epithelial cells during respiratory viral infection promote secondary bacterial growth, including biofilm biogenesis, by Pseudomonas aeruginosa. Respiratory syncytial virus (RSV) increases the release of the host iron-binding protein transferrin on the extravesicular face of EVs, which interact with P. aeruginosa biofilms to transfer the nutrient iron and promote bacterial biofilm growth. Vesicular delivery of iron by transferrin more efficiently promotes P. aeruginosa biofilm growth than soluble holo-transferrin delivered alone. Our findings indicate that EVs are a nutrient source for secondary bacterial infections in the airways during viral infection and offer evidence of transkingdom communication in the setting of polymicrobial infections.
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spelling pubmed-79187952021-03-01 Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection Hendricks, Matthew R. Lane, Sidney Melvin, Jeffrey A. Ouyang, Yingshi Stolz, Donna B. Williams, John V. Sadovsky, Yoel Bomberger, Jennifer M. Cell Rep Article Extracellular vesicles (EVs) are increasingly appreciated as a mechanism of communication among cells that contribute to many physiological processes. Although EVs can promote either antiviral or proviral effects during viral infections, the role of EVs in virus-associated polymicrobial infections remains poorly defined. We report that EVs secreted from airway epithelial cells during respiratory viral infection promote secondary bacterial growth, including biofilm biogenesis, by Pseudomonas aeruginosa. Respiratory syncytial virus (RSV) increases the release of the host iron-binding protein transferrin on the extravesicular face of EVs, which interact with P. aeruginosa biofilms to transfer the nutrient iron and promote bacterial biofilm growth. Vesicular delivery of iron by transferrin more efficiently promotes P. aeruginosa biofilm growth than soluble holo-transferrin delivered alone. Our findings indicate that EVs are a nutrient source for secondary bacterial infections in the airways during viral infection and offer evidence of transkingdom communication in the setting of polymicrobial infections. 2021-01-26 /pmc/articles/PMC7918795/ /pubmed/33503419 http://dx.doi.org/10.1016/j.celrep.2020.108672 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hendricks, Matthew R.
Lane, Sidney
Melvin, Jeffrey A.
Ouyang, Yingshi
Stolz, Donna B.
Williams, John V.
Sadovsky, Yoel
Bomberger, Jennifer M.
Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title_full Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title_fullStr Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title_full_unstemmed Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title_short Extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
title_sort extracellular vesicles promote transkingdom nutrient transfer during viral-bacterial co-infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918795/
https://www.ncbi.nlm.nih.gov/pubmed/33503419
http://dx.doi.org/10.1016/j.celrep.2020.108672
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