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Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents

Endobronchial stents are increasingly used to treat airway complications in multiple conditions including lung transplantation but little is known about the biofilms that form on these devices. We applied deep sequencing to profile luminal biofilms of 46 endobronchial stents removed from 20 subjects...

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Autores principales: McGinniss, John E., Imai, Ize, Simon-Soro, Aurea, Brown, Melanie C., Knecht, Vincent R., Frye, Laura, Ravindran, Priyanka M., Dothard, Marisol I., Wadell, Dylan A., Sohn, Michael B., Li, Hongzhe, Christie, Jason D., Diamond, Joshua M., Haas, Andrew R., Lanfranco, Anthony R., DiBardino, David M., Bushman, Frederic D., Collman, Ronald G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541290/
https://www.ncbi.nlm.nih.gov/pubmed/31141557
http://dx.doi.org/10.1371/journal.pone.0217306
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author McGinniss, John E.
Imai, Ize
Simon-Soro, Aurea
Brown, Melanie C.
Knecht, Vincent R.
Frye, Laura
Ravindran, Priyanka M.
Dothard, Marisol I.
Wadell, Dylan A.
Sohn, Michael B.
Li, Hongzhe
Christie, Jason D.
Diamond, Joshua M.
Haas, Andrew R.
Lanfranco, Anthony R.
DiBardino, David M.
Bushman, Frederic D.
Collman, Ronald G.
author_facet McGinniss, John E.
Imai, Ize
Simon-Soro, Aurea
Brown, Melanie C.
Knecht, Vincent R.
Frye, Laura
Ravindran, Priyanka M.
Dothard, Marisol I.
Wadell, Dylan A.
Sohn, Michael B.
Li, Hongzhe
Christie, Jason D.
Diamond, Joshua M.
Haas, Andrew R.
Lanfranco, Anthony R.
DiBardino, David M.
Bushman, Frederic D.
Collman, Ronald G.
author_sort McGinniss, John E.
collection PubMed
description Endobronchial stents are increasingly used to treat airway complications in multiple conditions including lung transplantation but little is known about the biofilms that form on these devices. We applied deep sequencing to profile luminal biofilms of 46 endobronchial stents removed from 20 subjects primarily with lung transplantation-associated airway compromise. Microbial communities were analyzed by bacterial 16S rRNA and fungal ITS marker gene sequencing. Corynebacterium was the most common bacterial taxa across biofilm communities. Clustering analysis revealed three bacterial biofilm types: one low diversity and dominated by Corynebacterium; another was polymicrobial and characterized by Staphylococcus; and the third was polymicrobial and associated with Pseudomonas, Streptococcus, and Prevotella. Biofilm type was significantly correlated with stent material: covered metal with the Staphylococcus-type biofilm, silicone with the Corynebacterium-dominated biofilm, and uncovered metal with the polymicrobial biofilm. Subjects with sequential stents had frequent transitions between community types. Fungal analysis found Candida was most prevalent, Aspergillus was common and highly enriched in two of three stents associated with airway anastomotic dehiscence, and fungal taxa not typically considered pathogens were highly enriched in some stents. Thus, molecular analysis revealed a complex and dynamic endobronchial stent biofilm with three bacterial types that associate with stent material, a central role for Corynebacterium, and that both expected and unexpected fungi inhabit this unique niche. The current work provides a foundation for studies to investigate the relationship between stent biofilm composition and clinical outcomes, mechanisms of biofilm establishment, and strategies for improved stent technology and use in airway compromise.
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spelling pubmed-65412902019-06-05 Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents McGinniss, John E. Imai, Ize Simon-Soro, Aurea Brown, Melanie C. Knecht, Vincent R. Frye, Laura Ravindran, Priyanka M. Dothard, Marisol I. Wadell, Dylan A. Sohn, Michael B. Li, Hongzhe Christie, Jason D. Diamond, Joshua M. Haas, Andrew R. Lanfranco, Anthony R. DiBardino, David M. Bushman, Frederic D. Collman, Ronald G. PLoS One Research Article Endobronchial stents are increasingly used to treat airway complications in multiple conditions including lung transplantation but little is known about the biofilms that form on these devices. We applied deep sequencing to profile luminal biofilms of 46 endobronchial stents removed from 20 subjects primarily with lung transplantation-associated airway compromise. Microbial communities were analyzed by bacterial 16S rRNA and fungal ITS marker gene sequencing. Corynebacterium was the most common bacterial taxa across biofilm communities. Clustering analysis revealed three bacterial biofilm types: one low diversity and dominated by Corynebacterium; another was polymicrobial and characterized by Staphylococcus; and the third was polymicrobial and associated with Pseudomonas, Streptococcus, and Prevotella. Biofilm type was significantly correlated with stent material: covered metal with the Staphylococcus-type biofilm, silicone with the Corynebacterium-dominated biofilm, and uncovered metal with the polymicrobial biofilm. Subjects with sequential stents had frequent transitions between community types. Fungal analysis found Candida was most prevalent, Aspergillus was common and highly enriched in two of three stents associated with airway anastomotic dehiscence, and fungal taxa not typically considered pathogens were highly enriched in some stents. Thus, molecular analysis revealed a complex and dynamic endobronchial stent biofilm with three bacterial types that associate with stent material, a central role for Corynebacterium, and that both expected and unexpected fungi inhabit this unique niche. The current work provides a foundation for studies to investigate the relationship between stent biofilm composition and clinical outcomes, mechanisms of biofilm establishment, and strategies for improved stent technology and use in airway compromise. Public Library of Science 2019-05-29 /pmc/articles/PMC6541290/ /pubmed/31141557 http://dx.doi.org/10.1371/journal.pone.0217306 Text en © 2019 McGinniss et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McGinniss, John E.
Imai, Ize
Simon-Soro, Aurea
Brown, Melanie C.
Knecht, Vincent R.
Frye, Laura
Ravindran, Priyanka M.
Dothard, Marisol I.
Wadell, Dylan A.
Sohn, Michael B.
Li, Hongzhe
Christie, Jason D.
Diamond, Joshua M.
Haas, Andrew R.
Lanfranco, Anthony R.
DiBardino, David M.
Bushman, Frederic D.
Collman, Ronald G.
Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title_full Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title_fullStr Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title_full_unstemmed Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title_short Molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
title_sort molecular analysis of the endobronchial stent microbial biofilm reveals bacterial communities that associate with stent material and frequent fungal constituents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541290/
https://www.ncbi.nlm.nih.gov/pubmed/31141557
http://dx.doi.org/10.1371/journal.pone.0217306
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