Glucan rich nutrition does not increase gut translocation of beta-glucan.


Journal

Mycoses
ISSN: 1439-0507
Titre abrégé: Mycoses
Pays: Germany
ID NLM: 8805008

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 16 06 2020
revised: 01 08 2020
accepted: 07 08 2020
pubmed: 12 8 2020
medline: 20 7 2021
entrez: 12 8 2020
Statut: ppublish

Résumé

(1-3)-b-D-glucan (BDG) is a fungal cell wall component and, in the absence of invasive fungal infection, a novel biomarker for microbial translocation of endogenous fungal products from the gastrointestinal tract into systemic circulation. However, its value as a marker of fungal translocation is limited by a concern that plant BDG-rich food influences blood BDG levels. We conducted a pilot clinical trial to evaluate the impact of a standardised oral BDG challenge on blood BDG levels in participants with and without elevated microbial translocation. We enrolled 14 participants including 8 with HIV infection, 2 with advanced liver cirrhosis, and 4 healthy controls. After obtaining a baseline blood sample, participants received a standardised milkshake containing high levels of BDG followed by serial blood samples up to 8 hours after intake. The standardised oral BDG challenge approach did not change the blood BDG levels over time in all participants. We found consistently elevated blood BDG levels in one participant with advanced liver cirrhosis and a single person with HIV with a low CD4 count of 201 cells/mm Our findings indicate that BDG blood levels were not influenced by plant origin BDG-rich nutrition in PWH, people with advanced liver cirrhosis, or healthy controls. Future studies are needed to analyse gut mycobiota populations in individuals with elevated blood BDG levels.

Sections du résumé

BACKGROUND BACKGROUND
(1-3)-b-D-glucan (BDG) is a fungal cell wall component and, in the absence of invasive fungal infection, a novel biomarker for microbial translocation of endogenous fungal products from the gastrointestinal tract into systemic circulation. However, its value as a marker of fungal translocation is limited by a concern that plant BDG-rich food influences blood BDG levels.
METHODS METHODS
We conducted a pilot clinical trial to evaluate the impact of a standardised oral BDG challenge on blood BDG levels in participants with and without elevated microbial translocation. We enrolled 14 participants including 8 with HIV infection, 2 with advanced liver cirrhosis, and 4 healthy controls. After obtaining a baseline blood sample, participants received a standardised milkshake containing high levels of BDG followed by serial blood samples up to 8 hours after intake.
RESULTS RESULTS
The standardised oral BDG challenge approach did not change the blood BDG levels over time in all participants. We found consistently elevated blood BDG levels in one participant with advanced liver cirrhosis and a single person with HIV with a low CD4 count of 201 cells/mm
CONCLUSION CONCLUSIONS
Our findings indicate that BDG blood levels were not influenced by plant origin BDG-rich nutrition in PWH, people with advanced liver cirrhosis, or healthy controls. Future studies are needed to analyse gut mycobiota populations in individuals with elevated blood BDG levels.

Identifiants

pubmed: 32780885
doi: 10.1111/myc.13161
pmc: PMC7736360
mid: NIHMS1651176
doi:

Substances chimiques

Biomarkers 0
Glucans 0
beta-Glucans 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

24-29

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007036
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI147821
Pays : United States
Organisme : NIH HHS
ID : AI036214
Pays : United States
Organisme : NIH HHS
ID : MH113477
Pays : United States
Organisme : CIHR
ID : PTJ 166049
Pays : Canada
Organisme : NIAID NIH HHS
ID : P30 AI036214
Pays : United States
Organisme : CIHR
ID : HOP 103230
Pays : Canada
Organisme : NIAID NIH HHS
ID : P01 AI131385
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH113477
Pays : United States
Organisme : NICHD NIH HHS
ID : R21 HD094646
Pays : United States
Organisme : NIDA NIH HHS
ID : DP2 DA051915
Pays : United States

Informations de copyright

© 2020 Wiley-VCH GmbH.

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Auteurs

Martin Hoenigl (M)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.
Section of Infectious Diseases and Tropical Medicine, Medical University of Graz, Graz, Austria.

John Lin (J)

Chronic Viral Illness Service, McGill University Health Centre, Montreal, QC, Canada.
Infectious Diseases and Immunity in Global Health Program, Research Institute of McGill University Health Centre, Montreal, QC, Canada.

Malcolm Finkelman (M)

Clinical Development, Associates of Cape Cod, Inc, Falmouth, MA, USA.

Yonglong Zhang (Y)

Clinical Development, Associates of Cape Cod, Inc, Falmouth, MA, USA.

Maile Y Karris (MY)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.

Scott L Letendre (SL)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.

Ronald J Ellis (RJ)

Department of Neurosciences, University of California San Diego, San Diego, CA, USA.

Leah Burke (L)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.

Byron Richard (B)

Nutritional Services, University of California San Diego, San Diego, CA, USA.

Thaidra Gaufin (T)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.

Stéphane Isnard (S)

Chronic Viral Illness Service, McGill University Health Centre, Montreal, QC, Canada.
Infectious Diseases and Immunity in Global Health Program, Research Institute of McGill University Health Centre, Montreal, QC, Canada.

Jean-Pierre Routy (JP)

Chronic Viral Illness Service, McGill University Health Centre, Montreal, QC, Canada.
Infectious Diseases and Immunity in Global Health Program, Research Institute of McGill University Health Centre, Montreal, QC, Canada.

Sara Gianella (S)

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, San Diego, CA, USA.

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Classifications MeSH