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Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples
Published on: December 22, 2014
Mycobiome analyses of critically ill COVID-19 patients
Danielle Weaver1, Sara Gago1, Matteo Bassetti2,3
1University of Manchester, Manchester, United Kingdom.
Abstract:
Coronavirus disease 2019 (COVID-19)-associated pulmonary aspergillosis (CAPA) is a life-threatening complication in patients with severe COVID-19. Previously, acute respiratory distress syndrome in patients with COVID-19 has been associated with lung fungal dysbiosis, evidenced by reduced microbial diversity and Candida colonization. Increased fungal burden in the lungs of critically ill COVID-19 patients is linked to prolonged mechanical ventilation and increased mortality. However, specific mycobiome signatures associated with severe COVID-19 in the context of survival and antifungal drug prophylaxis have not yet been determined, and such knowledge could have an important impact on treatment. To understand the composition of the respiratory mycobiome in critically ill COVID-19 patients with and without CAPA and the impact of antifungal use in patient outcome, we performed a multinational study of 39 COVID-19 patients in intensive care units (ICUs). Respiratory mycobiome was profiled using internal transcribed spacer 1 sequencing, and Aspergillus fumigatus burden was further validated using quantitative PCR. Fungal communities were investigated using alpha diversity, beta diversity, taxa predominance, and taxa abundances. Respiratory mycobiomes of COVID-19 patients were dominated by Candida and Aspergillus. There was no significant association with corticosteroid use or CAPA diagnosis and respiratory fungal communities. Increased A. fumigatus burden was associated with mortality and, the use of azoles at ICU admission was linked with an absence of A. fumigatus. Our findings suggest that mold-active antifungal treatment at ICU admission may be linked with reduced A. fumigatus-associated mortality in severe COVID-19. However, further studies are warranted on this topic.IMPORTANCEInvasive fungal infections are a serious complication affecting up to a third of patients with severe COVID-19. Nevertheless, our understanding of the fungal communities in the lungs during critically ill COVID-19 remains limited. Evidence suggests a higher fungal burden is associated with prolonged ventilation and higher mortality, although the particular organisms responsible for this link are unclear. Antifungal prophylaxis may be beneficial for reducing the burden of fungal co-infections in COVID-19 intensive care. However, the composition of the fungal microbiome in severe COVID-19 in relation to prophylactic antifungals, as well as how this is associated with survival outcomes, is yet to be studied. Our study provides insights into the lung fungal microbiome in severe COVID-19 and has found antifungal treatment to be associated with lower Aspergillus fumigatus burden and that higher levels of this pathogen are associated with mortality. Therefore, our study suggests mold-active antifungal prophylaxis may be beneficial in severe COVID-19.
Insights
Antifungal treatment in intensive care units may reduce mortality in severe COVID-19 patients by lowering Aspergillus fumigatus burden. Further research is needed to confirm these findings on COVID-19-associated pulmonary aspergillosis.
Area of Science:
- Medical Microbiology
- Infectious Diseases
- Pulmonology
Background:
- COVID-19-associated pulmonary aspergillosis (CAPA) is a severe complication.
- Fungal dysbiosis and increased fungal burden in COVID-19 are linked to poor outcomes.
- Limited understanding of mycobiome signatures and antifungal prophylaxis impact in severe COVID-19.
Purpose of the Study:
- To analyze respiratory mycobiome composition in critically ill COVID-19 patients.
- To investigate the impact of antifungal use on patient outcomes.
- To identify mycobiome signatures associated with survival and CAPA.
Main Methods:
- Multinational study of 39 COVID-19 ICU patients.
- Respiratory mycobiome profiling using ITS1 sequencing.
- Quantification of Aspergillus fumigatus burden via qPCR.
Main Results:
- Respiratory mycobiomes were dominated by Candida and Aspergillus.
- No significant association between corticosteroid use, CAPA, and fungal communities.
- Increased A. fumigatus burden correlated with mortality.
- Azole use at ICU admission was linked to absence of A. fumigatus.
Conclusions:
- Mold-active antifungal treatment at ICU admission may reduce A. fumigatus-associated mortality in severe COVID-19.
- Further studies are warranted to validate these findings and inform treatment strategies.
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