Genomic and Phenotypic Analysis of COVID-19-Associated Pulmonary Aspergillosis Isolates of Aspergillus fumigatus.
Aged
Antifungal Agents
Aspergillus
Aspergillus fumigatus
/ classification
COVID-19
/ complications
Female
Genomics
Humans
Male
Metabolomics
Microbial Sensitivity Tests
Middle Aged
Mutation
Phenotype
Polymorphism, Single Nucleotide
Pulmonary Aspergillosis
/ complications
SARS-CoV-2
Secondary Metabolism
/ genetics
Virulence
/ genetics
Aspergillus
COVID-19
acute respiratory distress syndrome
aspergillosis
coinfection
pathogenicity
secondary infection
superinfection
virulence factors
Journal
Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614
Informations de publication
Date de publication:
03 09 2021
03 09 2021
Historique:
pubmed:
10
6
2021
medline:
18
9
2021
entrez:
9
6
2021
Statut:
ppublish
Résumé
The ongoing global pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for coronavirus disease 2019 (COVID-19), first described in Wuhan, China. A subset of COVID-19 patients has been reported to have acquired secondary infections by microbial pathogens, such as opportunistic fungal pathogens from the genus Aspergillus. To gain insight into COVID-19-associated pulmonary aspergillosis (CAPA), we analyzed the genomes and characterized the phenotypic profiles of four CAPA isolates of Aspergillus fumigatus obtained from patients treated in the area of North Rhine-Westphalia, Germany. By examining the mutational spectrum of single nucleotide polymorphisms, insertion-deletion polymorphisms, and copy number variants among 206 genes known to modulate A. fumigatus virulence, we found that CAPA isolate genomes do not exhibit significant differences from the genome of the Af293 reference strain. By examining a number of factors, including virulence in an invertebrate moth model, growth in the presence of osmotic, cell wall, and oxidative stressors, secondary metabolite biosynthesis, and the MIC of antifungal drugs, we found that CAPA isolates were generally, but not always, similar to A. fumigatus reference strains Af293 and CEA17. Notably, CAPA isolate D had more putative loss-of-function mutations in genes known to increase virulence when deleted. Moreover, CAPA isolate D was significantly more virulent than the other three CAPA isolates and the A. fumigatus reference strains Af293 and CEA17, but similarly virulent to two other clinical strains of A. fumigatus. These findings expand our understanding of the genomic and phenotypic characteristics of isolates that cause CAPA.
Identifiants
pubmed: 34106569
doi: 10.1128/Spectrum.00010-21
pmc: PMC8552514
doi:
Substances chimiques
Antifungal Agents
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0001021Subventions
Organisme : NIAID NIH HHS
ID : R56 AI146096
Pays : United States
Commentaires et corrections
Type : UpdateOf
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