Pharyngeal Microbial Signatures Are Predictive of the Risk of Fungal Pneumonia in Hematologic Patients

Autor: Luca Facchini, Luigina Romani, Daniela Valente, Antonio Spadea, Katerina Coufalikova, Lukas Englmaier, Katia Codeluppi, Monica Borghi, Matteo Puccetti, Teresa Zelante, Angelica Spolzino, Zdenek Spacil, Giulia Dragonetti, Melissa Palmieri, Francesco Merli, Gianpaolo Nadali, Giuseppe Lomurno, Claudio Costantini, Emilia Nunzi, Francesco Marchesi, Roberta Spaccapelo, Franco Aversa, Marina M. Bellet, Vincenzo Nicola Talesa, Enzo Acerbi, Stefano Giovagnoli, Lorella Melillo, Giorgia Renga, Livio Pagano, Gessica Marchesini
Přispěvatelé: Singapore Centre for Environmental Life Sciences and Engineering
Rok vydání: 2021
Předmět:
0301 basic medicine
Indole-3aldehyde
Antifungal Agents
Hematological malignancies
invasive fungal infection
airway microbiome
metabolomics
tryptophan
indole-3-aldehyde
antibiotics

Antibiotics
invasive fungal infection
antibiotics
Hematological malignancies
Mice
0302 clinical medicine
Risk Factors
Antimicrobial stewardship
airway microbiome
biology
Microbiota
Biological sciences [Science]
Host-Associated Microbial Communities
metabolomics
3. Good health
Infectious Diseases
Hematologic Neoplasms
030220 oncology & carcinogenesis
Metabolic profile
medicine.drug_class
Hematological Malignancies
Immunology
Risk Assessment
Microbiology
03 medical and health sciences
medicine
Animals
Humans
tryptophan
Clostridiales
Airway Microbiome
Bacteroidetes
indole-3-aldehyde
Pneumonia
biology.organism_classification
Fungal pneumonia
medicine.disease
Hematologic Diseases
Disease Models
Animal

Settore MED/15 - MALATTIE DEL SANGUE
030104 developmental biology
Mycoses
Murine model
Metagenome
Pharynx
Parasitology
Metagenomics
Dysbiosis
Zdroj: Infect Immun
ISSN: 1098-5522
0019-9567
DOI: 10.1128/iai.00105-21
Popis: The ability to predict invasive fungal infections (IFI) in patients with hematological malignancies is fundamental for successful therapy. Although gut dysbiosis is known to occur in hematological patients, whether airway dysbiosis also contributes to the risk of IFI has not been investigated. Nasal and oropharyngeal swabs were collected for functional microbiota characterization in 173 patients with hematological malignancies recruited in a multicenter, prospective, observational study and stratified according to the risk of developing IFI. A lower microbial richness and evenness were found in the pharyngeal microbiota of high-risk patients that were associated with a distinct taxonomic and metabolic profile. A murine model of IFI provided biologic plausibility for the finding that loss of protective anaerobes, such as Clostridiales and Bacteroidetes, along with an apparent restricted availability of tryptophan, is causally linked to the risk of IFI in hematologic patients and indicates avenues for antimicrobial stewardship and metabolic reequilibrium in IFI. This work was supported by FunMeta Project (ERC-2011-AdG 293714), MicroTher(ERC-2018-PoC-813099), and Gilead (IN-IT-131-4525-518872.9) to L.R. and the GrantAgency of the Czech Republic (GACR No 17-24592Y) and the Czech Ministry ofEducation, Youth and Sports (CETOCOEN PLUS CZ.02.1.01/0.0/0.0/15_003/0000469;LM2015051 and CETOCOEN EXCELLENCE Teaming 2 project CZ.02.1.01/0.0/0.0/18_046/0015975; and Horizon2020 project 857560) to Z.S.
Databáze: OpenAIRE