Gut mycobiome dysbiosis after sepsis and trauma
Sepsis and trauma are known to disrupt gut bacterial microbiome communities, but the impacts and perturbations in the fungal (mycobiome) community after severe infection or injury, particularly in patients experiencing chronic critical illness (CCI), remain unstudied. We assess persistence of the gu...
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creator | Park, Gwoncheol Munley, Jennifer A Kelly, Lauren S Kannan, Kolenkode B Mankowski, Robert T Sharma, Ashish Upchurch, Gilbert Casadesus, Gemma Chakrabarty, Paramita Wallet, Shannon M Maile, Robert Bible, Letitia E Wang, Bo Moldawer, Lyle L Mohr, Alicia M Efron, Philip A Nagpal, Ravinder |
description | Sepsis and trauma are known to disrupt gut bacterial microbiome communities, but the impacts and perturbations in the fungal (mycobiome) community after severe infection or injury, particularly in patients experiencing chronic critical illness (CCI), remain unstudied.
We assess persistence of the gut mycobiome perturbation (dysbiosis) in patients experiencing CCI following sepsis or trauma for up to two-to-three weeks after intensive care unit hospitalization.
We show that the dysbiotic mycobiome arrays shift toward a pathobiome state, which is more susceptible to infection, in CCI patients compared to age-matched healthy subjects. The fungal community in CCI patients is largely dominated by Candida spp; while, the commensal fungal species are depleted. Additionally, these myco-pathobiome arrays correlate with alterations in micro-ecological niche involving specific gut bacteria and gut-blood metabolites.
The findings reveal the persistence of mycobiome dysbiosis in both sepsis and trauma settings, even up to two weeks post-sepsis and trauma, highlighting the need to assess and address the increased risk of fungal infections in CCI patients. |
doi_str_mv | 10.1186/s13054-023-04780-4 |
format | Article |
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We assess persistence of the gut mycobiome perturbation (dysbiosis) in patients experiencing CCI following sepsis or trauma for up to two-to-three weeks after intensive care unit hospitalization.
We show that the dysbiotic mycobiome arrays shift toward a pathobiome state, which is more susceptible to infection, in CCI patients compared to age-matched healthy subjects. The fungal community in CCI patients is largely dominated by Candida spp; while, the commensal fungal species are depleted. Additionally, these myco-pathobiome arrays correlate with alterations in micro-ecological niche involving specific gut bacteria and gut-blood metabolites.
The findings reveal the persistence of mycobiome dysbiosis in both sepsis and trauma settings, even up to two weeks post-sepsis and trauma, highlighting the need to assess and address the increased risk of fungal infections in CCI patients.</description><identifier>ISSN: 1364-8535</identifier><identifier>EISSN: 1466-609X</identifier><identifier>EISSN: 1364-8535</identifier><identifier>EISSN: 1366-609X</identifier><identifier>DOI: 10.1186/s13054-023-04780-4</identifier><identifier>PMID: 38212826</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Bacteria ; Bioinformatics ; Candida ; Cardiovascular disease ; Critical care ; Data collection ; Dysbiosis - complications ; Dysbiosis - microbiology ; Ethnicity ; Fungi ; Gastrointestinal Microbiome ; Homeostasis ; Hospitalization ; Hospitals ; Humans ; Immune system ; Metabolites ; Mortality ; Multiculturalism & pluralism ; Mycobiome ; Nosocomial infections ; Pathogens ; Sepsis ; Sepsis - complications ; Trauma</subject><ispartof>Critical care (London, England), 2024-01, Vol.28 (1), p.18-18, Article 18</ispartof><rights>2024. The Author(s).</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-42b7df8eeb8de5fa17fb6c4d571dbe4f1d5a32578797f556c3c2998e8389d4083</citedby><cites>FETCH-LOGICAL-c375t-42b7df8eeb8de5fa17fb6c4d571dbe4f1d5a32578797f556c3c2998e8389d4083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38212826$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Gwoncheol</creatorcontrib><creatorcontrib>Munley, Jennifer A</creatorcontrib><creatorcontrib>Kelly, Lauren S</creatorcontrib><creatorcontrib>Kannan, Kolenkode B</creatorcontrib><creatorcontrib>Mankowski, Robert T</creatorcontrib><creatorcontrib>Sharma, Ashish</creatorcontrib><creatorcontrib>Upchurch, Gilbert</creatorcontrib><creatorcontrib>Casadesus, Gemma</creatorcontrib><creatorcontrib>Chakrabarty, Paramita</creatorcontrib><creatorcontrib>Wallet, Shannon M</creatorcontrib><creatorcontrib>Maile, Robert</creatorcontrib><creatorcontrib>Bible, Letitia E</creatorcontrib><creatorcontrib>Wang, Bo</creatorcontrib><creatorcontrib>Moldawer, Lyle L</creatorcontrib><creatorcontrib>Mohr, Alicia M</creatorcontrib><creatorcontrib>Efron, Philip A</creatorcontrib><creatorcontrib>Nagpal, Ravinder</creatorcontrib><title>Gut mycobiome dysbiosis after sepsis and trauma</title><title>Critical care (London, England)</title><addtitle>Crit Care</addtitle><description>Sepsis and trauma are known to disrupt gut bacterial microbiome communities, but the impacts and perturbations in the fungal (mycobiome) community after severe infection or injury, particularly in patients experiencing chronic critical illness (CCI), remain unstudied.
We assess persistence of the gut mycobiome perturbation (dysbiosis) in patients experiencing CCI following sepsis or trauma for up to two-to-three weeks after intensive care unit hospitalization.
We show that the dysbiotic mycobiome arrays shift toward a pathobiome state, which is more susceptible to infection, in CCI patients compared to age-matched healthy subjects. The fungal community in CCI patients is largely dominated by Candida spp; while, the commensal fungal species are depleted. Additionally, these myco-pathobiome arrays correlate with alterations in micro-ecological niche involving specific gut bacteria and gut-blood metabolites.
The findings reveal the persistence of mycobiome dysbiosis in both sepsis and trauma settings, even up to two weeks post-sepsis and trauma, highlighting the need to assess and address the increased risk of fungal infections in CCI patients.</description><subject>Bacteria</subject><subject>Bioinformatics</subject><subject>Candida</subject><subject>Cardiovascular disease</subject><subject>Critical care</subject><subject>Data collection</subject><subject>Dysbiosis - complications</subject><subject>Dysbiosis - microbiology</subject><subject>Ethnicity</subject><subject>Fungi</subject><subject>Gastrointestinal Microbiome</subject><subject>Homeostasis</subject><subject>Hospitalization</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immune system</subject><subject>Metabolites</subject><subject>Mortality</subject><subject>Multiculturalism & pluralism</subject><subject>Mycobiome</subject><subject>Nosocomial infections</subject><subject>Pathogens</subject><subject>Sepsis</subject><subject>Sepsis - 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complications</topic><topic>Dysbiosis - microbiology</topic><topic>Ethnicity</topic><topic>Fungi</topic><topic>Gastrointestinal Microbiome</topic><topic>Homeostasis</topic><topic>Hospitalization</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Immune system</topic><topic>Metabolites</topic><topic>Mortality</topic><topic>Multiculturalism & pluralism</topic><topic>Mycobiome</topic><topic>Nosocomial infections</topic><topic>Pathogens</topic><topic>Sepsis</topic><topic>Sepsis - complications</topic><topic>Trauma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Gwoncheol</creatorcontrib><creatorcontrib>Munley, Jennifer A</creatorcontrib><creatorcontrib>Kelly, Lauren S</creatorcontrib><creatorcontrib>Kannan, Kolenkode B</creatorcontrib><creatorcontrib>Mankowski, Robert T</creatorcontrib><creatorcontrib>Sharma, Ashish</creatorcontrib><creatorcontrib>Upchurch, Gilbert</creatorcontrib><creatorcontrib>Casadesus, Gemma</creatorcontrib><creatorcontrib>Chakrabarty, Paramita</creatorcontrib><creatorcontrib>Wallet, Shannon M</creatorcontrib><creatorcontrib>Maile, Robert</creatorcontrib><creatorcontrib>Bible, Letitia E</creatorcontrib><creatorcontrib>Wang, Bo</creatorcontrib><creatorcontrib>Moldawer, Lyle L</creatorcontrib><creatorcontrib>Mohr, Alicia M</creatorcontrib><creatorcontrib>Efron, Philip A</creatorcontrib><creatorcontrib>Nagpal, Ravinder</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Critical care (London, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Gwoncheol</au><au>Munley, Jennifer A</au><au>Kelly, Lauren S</au><au>Kannan, Kolenkode B</au><au>Mankowski, Robert T</au><au>Sharma, Ashish</au><au>Upchurch, Gilbert</au><au>Casadesus, Gemma</au><au>Chakrabarty, Paramita</au><au>Wallet, Shannon M</au><au>Maile, Robert</au><au>Bible, Letitia E</au><au>Wang, Bo</au><au>Moldawer, Lyle L</au><au>Mohr, Alicia M</au><au>Efron, Philip A</au><au>Nagpal, Ravinder</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gut mycobiome dysbiosis after sepsis and trauma</atitle><jtitle>Critical care (London, England)</jtitle><addtitle>Crit Care</addtitle><date>2024-01-11</date><risdate>2024</risdate><volume>28</volume><issue>1</issue><spage>18</spage><epage>18</epage><pages>18-18</pages><artnum>18</artnum><issn>1364-8535</issn><eissn>1466-609X</eissn><eissn>1364-8535</eissn><eissn>1366-609X</eissn><abstract>Sepsis and trauma are known to disrupt gut bacterial microbiome communities, but the impacts and perturbations in the fungal (mycobiome) community after severe infection or injury, particularly in patients experiencing chronic critical illness (CCI), remain unstudied.
We assess persistence of the gut mycobiome perturbation (dysbiosis) in patients experiencing CCI following sepsis or trauma for up to two-to-three weeks after intensive care unit hospitalization.
We show that the dysbiotic mycobiome arrays shift toward a pathobiome state, which is more susceptible to infection, in CCI patients compared to age-matched healthy subjects. The fungal community in CCI patients is largely dominated by Candida spp; while, the commensal fungal species are depleted. Additionally, these myco-pathobiome arrays correlate with alterations in micro-ecological niche involving specific gut bacteria and gut-blood metabolites.
The findings reveal the persistence of mycobiome dysbiosis in both sepsis and trauma settings, even up to two weeks post-sepsis and trauma, highlighting the need to assess and address the increased risk of fungal infections in CCI patients.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>38212826</pmid><doi>10.1186/s13054-023-04780-4</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Bioinformatics Candida Cardiovascular disease Critical care Data collection Dysbiosis - complications Dysbiosis - microbiology Ethnicity Fungi Gastrointestinal Microbiome Homeostasis Hospitalization Hospitals Humans Immune system Metabolites Mortality Multiculturalism & pluralism Mycobiome Nosocomial infections Pathogens Sepsis Sepsis - complications Trauma |
title | Gut mycobiome dysbiosis after sepsis and trauma |
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