Hormographiella aspergillata: an emerging basidiomycete in the clinical setting? A case report and literature review.


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
11 Dec 2020
Historique:
received: 31 07 2020
accepted: 02 12 2020
entrez: 14 12 2020
pubmed: 15 12 2020
medline: 8 1 2021
Statut: epublish

Résumé

Filamentous basidiomycetes are mainly considered to be respiratory tract colonizers but the clinical significance of their isolation in a specimen is debatable. Hormographiella aspergillata was first reported as a human pathogen in 1971. We discuss the role of this mold as a pathogen or colonizer and give an update on diagnostic tools and in vitro antifungal susceptibility. We identified three cases of H. aspergillata with respiratory symptoms in a short period of time. One invasive infection and two colonizations were diagnosed. Culture supernatants showed that H. aspergillata can produce galactomannan and β-D-glucan but not glucuronoxylomannan. For the first time, isavuconazole susceptibility was determined and high minimum inhibitory concentrations (MICs) were found. Liposomal amphotericin B and voriconazole have the lowest MICs. To date, 22 invasive infections involving H. aspergillata have been reported. On isolation of H. aspergillata, its pathogenic potential in clinical settings can be tricky. Molecular identification and antifungal susceptibility testing are essential considering high resistance against several antifungal therapies.

Sections du résumé

BACKGROUND BACKGROUND
Filamentous basidiomycetes are mainly considered to be respiratory tract colonizers but the clinical significance of their isolation in a specimen is debatable. Hormographiella aspergillata was first reported as a human pathogen in 1971. We discuss the role of this mold as a pathogen or colonizer and give an update on diagnostic tools and in vitro antifungal susceptibility.
CASE PRESENTATION METHODS
We identified three cases of H. aspergillata with respiratory symptoms in a short period of time. One invasive infection and two colonizations were diagnosed. Culture supernatants showed that H. aspergillata can produce galactomannan and β-D-glucan but not glucuronoxylomannan. For the first time, isavuconazole susceptibility was determined and high minimum inhibitory concentrations (MICs) were found. Liposomal amphotericin B and voriconazole have the lowest MICs.
CONCLUSION CONCLUSIONS
To date, 22 invasive infections involving H. aspergillata have been reported. On isolation of H. aspergillata, its pathogenic potential in clinical settings can be tricky. Molecular identification and antifungal susceptibility testing are essential considering high resistance against several antifungal therapies.

Identifiants

pubmed: 33308180
doi: 10.1186/s12879-020-05679-z
pii: 10.1186/s12879-020-05679-z
pmc: PMC7731474
doi:

Substances chimiques

Antifungal Agents 0
liposomal amphotericin B 0
Amphotericin B 7XU7A7DROE

Types de publication

Case Reports Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

945

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Auteurs

Maxime Moniot (M)

Laboratoire de Parasitologie-Mycologie, CHU Clermont-Ferrand, CHU Gabriel Montpied, 58 rue Montalembert, 3IHP, 63003, Clermont-Ferrand Cedex 1, France. mmoniot@chu-clermontferrand.fr.
Equipe Interactions Hôte-Parasite, Laboratoire Microorganismes : Génome et Environnement, CNRS, Université Clermont-Auvergne, Clermont-Ferrand, France. mmoniot@chu-clermontferrand.fr.

Rose-Anne Lavergne (RA)

Laboratoire de Parasitologie-Mycologie, Département de Mycologie Médicale, Hôpitaux Universitaires de Nantes, Universités Nantes Atlantique, EA1155-IICiMed, Institut de Recherche en Santé 2, Nantes, France.

Thomas Morel (T)

Laboratoire de Parasitologie-Mycologie, CHU Clermont-Ferrand, CHU Gabriel Montpied, 58 rue Montalembert, 3IHP, 63003, Clermont-Ferrand Cedex 1, France.

Romain Guieze (R)

Service d'Hématologie Clinique, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Florent Morio (F)

Laboratoire de Parasitologie-Mycologie, Département de Mycologie Médicale, Hôpitaux Universitaires de Nantes, Universités Nantes Atlantique, EA1155-IICiMed, Institut de Recherche en Santé 2, Nantes, France.

Philippe Poirier (P)

Laboratoire de Parasitologie-Mycologie, CHU Clermont-Ferrand, CHU Gabriel Montpied, 58 rue Montalembert, 3IHP, 63003, Clermont-Ferrand Cedex 1, France.
Equipe Interactions Hôte-Parasite, Laboratoire Microorganismes : Génome et Environnement, CNRS, Université Clermont-Auvergne, Clermont-Ferrand, France.

Céline Nourrisson (C)

Laboratoire de Parasitologie-Mycologie, CHU Clermont-Ferrand, CHU Gabriel Montpied, 58 rue Montalembert, 3IHP, 63003, Clermont-Ferrand Cedex 1, France.
Equipe Interactions Hôte-Parasite, Laboratoire Microorganismes : Génome et Environnement, CNRS, Université Clermont-Auvergne, Clermont-Ferrand, France.

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Classifications MeSH