Beyond <i>Fumigatus</i> : a molecular portrait of clinical <i>Aspergillus</i> diversity, pathogenicity, and antifungal resistance

<i>Aspergillus</i> infection poses a major clinical challenge, particularly in immunocompromised individuals, with invasive diseases associated with high mortality. While <i>Aspergillus fumigatus</i> remains the predominant species causing human infections, recent studies highlight the growing clinical significance of lesser-known and cryptic <i>Aspergillus</i> species, which often exhibit reduced susceptibility to standard antifungal therapies. In this study, we analyzed 196 clinical <i>Aspergillus</i> isolates from 107 patients treated at the NIH Clinical Center between 2019 and 2022. A total of 38 <i>Aspergillus</i> species across 11 taxonomic sections were identified, with non-<i>fumigatus</i> and cryptic species accounting for 77.1% of all isolates. The most frequently recovered species were <i>A. fumigatus sensu stricto</i> (22.9%), <i>A. sydowii</i> (8.7%), <i>A. calidoustus</i> (7.1%), <i>A. nidulans</i> (6.6%), <i>A. tanneri</i> (6.1%), and <i>A. terreus</i> (5.6%). Species-level identification was achieved in 43% of isolates using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). In contrast, PCR sequencing confirmed species identity in over 88% of isolates by targeting the internal transcribed spacer (ITS) region of rDNA, 81% using the β-tubulin gene, and 68% using the calmodulin gene. The most common underlying clinical conditions among patients were bronchiectasis (35%), chronic granulomatous disease (22%), and pulmonary non-tuberculous mycobacterial infection (17%). Out of 107 patients, eight died (8/107, 7.5%); six of these deaths occurred in patients with chronic granulomatous disease (CGD) and two in patients with RAG1 deficiency. Antifungal susceptibility testing showed that olorofim had the lowest minimal inhibitory concentrations across species. In contrast, the activity of triazoles and amphotericin B was variable, particularly against <i>A. tanneri</i>, <i>A. calidoustus</i>, and <i>A. sydowii</i>. This study presents one of the largest species-level data sets of <i>Aspergillus</i> isolates to date, underscoring the diversity, pathogenic potential, and resistance profiles of non-<i>fumigatus</i> species. Accurate species identification plays an important role in guiding appropriate antifungal therapy and improving clinical outcomes, although further studies are needed to elucidate its direct impact on treatment decisions.

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Journal
Antimicrobial Agents and Chemotherapy
Published
2026-01-13
DOI
https://doi.org/10.1128/aac.01184-25
Primary Topic
Antifungal resistance and susceptibility
Type
article
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article

Beyond Fumigatus : a molecular portrait of clinical Aspergillus diversity, pathogenicity, and antifungal resistance

A. Freeman, Christa Zerbe, Kevin P. Fennelly, K J Kwon-Chung et al.
Antimicrobial Agents and Chemotherapy
Antifungal resistance and susceptibility
article

Beyond Fumigatus : a molecular portrait of clinical Aspergillus diversity, pathogenicity, and antifungal resistance

A. Freeman, Christa Zerbe, Kevin P. Fennelly, K J Kwon-Chung, Sherin S. Shahegh, Steven Holland, Chioma I. Aneke, Amir Seyedmousavi
article en

Abstract

<i>Aspergillus</i> infection poses a major clinical challenge, particularly in immunocompromised individuals, with invasive diseases associated with high mortality. While <i>Aspergillus fumigatus</i> remains the predominant species causing human infections, recent studies highlight the growing clinical significance of lesser-known and cryptic <i>Aspergillus</i> species, which often exhibit reduced susceptibility to standard antifungal therapies. In this study, we analyzed 196 clinical <i>Aspergillus</i> isolates from 107 patients treated at the NIH Clinical Center between 2019 and 2022. A total of 38 <i>Aspergillus</i> species across 11 taxonomic sections were identified, with non-<i>fumigatus</i> and cryptic species accounting for 77.1% of all isolates. The most frequently recovered species were <i>A. fumigatus sensu stricto</i> (22.9%), <i>A. sydowii</i> (8.7%), <i>A. calidoustus</i> (7.1%), <i>A. nidulans</i> (6.6%), <i>A. tanneri</i> (6.1%), and <i>A. terreus</i> (5.6%). Species-level identification was achieved in 43% of isolates using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). In contrast, PCR sequencing confirmed species identity in over 88% of isolates by targeting the internal transcribed spacer (ITS) region of rDNA, 81% using the β-tubulin gene, and 68% using the calmodulin gene. The most common underlying clinical conditions among patients were bronchiectasis (35%), chronic granulomatous disease (22%), and pulmonary non-tuberculous mycobacterial infection (17%). Out of 107 patients, eight died (8/107, 7.5%); six of these deaths occurred in patients with chronic granulomatous disease (CGD) and two in patients with RAG1 deficiency. Antifungal susceptibility testing showed that olorofim had the lowest minimal inhibitory concentrations across species. In contrast, the activity of triazoles and amphotericin B was variable, particularly against <i>A. tanneri</i>, <i>A. calidoustus</i>, and <i>A. sydowii</i>. This study presents one of the largest species-level data sets of <i>Aspergillus</i> isolates to date, underscoring the diversity, pathogenic potential, and resistance profiles of non-<i>fumigatus</i> species. Accurate species identification plays an important role in guiding appropriate antifungal therapy and improving clinical outcomes, although further studies are needed to elucidate its direct impact on treatment decisions.

Antimicrobial Agents and ChemotherapyVol. 70(2)
National Institutes of Health (US), National Heart, Lung, and Blood Institute (US), National Institute of Allergy and Infectious Diseases (US), National Institutes of Health Clinical Center (US)
Openalex Percentile: Top 86%
Antifungal resistance and susceptibility
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