Purpose
Bacterial or virus co-infections with SARS-CoV-2 have been reported in many studies; however, the knowledge on
Aspergillus
co-infection among patients with COVID-19 was limited. This study was conducted to identify and isolate fungal agents and to evaluate the prevalence of pulmonary aspergillosis (CAPA) as well as antifungal susceptibility patterns of
Aspergillus
species in patients with COVID-19 admitted to Shahid Beheshti Hospital, Kashan, Iran.
Methods
The study involved 119 patients with severe COVID-19 pneumonia referred to the Shahid Beheshti Hospital, Kashan, Iran. A total of 17
Aspergillus
spp. that were isolated from COVID-19 patients suspected of CAPA were enrolled in the study. CAPA was defined using ECMM/ISHAM consensus criteria. The PCR amplification of the β-tubulin gene was used to identify the species. The antifungal activities of fluconazole, itraconazole, voriconazole, amphotericin B against
Aspergillus
spp. were evaluated according to the Clinical and Laboratory Standards Institute manual (M38-A3).
Results
From the 119 patients with severe COVID-19 pneumonia, CAPA was confirmed in 17 cases (14.3%). Of these, 12 (70.6%) were males and 5 (29.4%) were females; the mean age at presentation was 73.8 years (range: 45–88 years; median = 77; IQR = 18).
Aspergillus fumigatus
(9/17; 52.9%),
Aspergillus flavus
(5/17; 29.4%),
Aspergillus oryzae
(3/17, 17.6%), were identified as etiologic agents of CAPA, using the molecular techniques. Voriconazole and amphotericin B showed more activity against all isolates. Moreover, the MIC of fluconazole, itraconazole varied with the tested isolates. For 3 clinical isolates of
A. fumigatus,
2 isolate of
A. flavus
and 3
A. oryzae
, the MIC of fluconazole and itraconazole were ≥ 16 µg/mL.
Conclusions
We observed a high incidence (14.3%) of probable aspergillosis in 119 patients with COVID-19, which might indicate the risk for developing IPA in COVID-19 patients. When comparing patients with and without CAPA regarding baseline characteristics, CAPA patients were older (
p
=0 .024), had received more frequent systemic corticosteroids (
p
= 0.024), and had a higher mortality rate (
p
= 0.018). The outcome of CAPA is usually poor, thus emphasis shall be given to screening and/or prophylaxis in COVID-19 patients with any risk of developing CAPA.