# Characteristics of individual cyp51A SNPs and combinations thereof impacting the azole phenotype in TR34-mediated resistance genotypes of Aspergillus fumigatus

## TL;DR

This study examines how specific genetic mutations in Aspergillus fumigatus affect resistance to antifungal drugs, particularly azoles.

## Contribution

The study identifies novel SNP combinations in cyp51A that influence azole resistance and validates their impact through molecular modeling and in vitro testing.

## Key findings

- Combination mutations in cyp51A significantly increase azole MICs compared to wild-type strains.
- The TR34/L98H/T289A/I364V/G448S genotype shows high resistance to voriconazole but remains susceptible to itraconazole.
- Molecular dynamics simulations correlate with in vitro phenotypes, supporting the structure–function relationship of cyp51A mutations.

## Abstract

The World Health Organization has flagged the rise of drug resistance in Aspergillus fumigatus as a critical concern. Elevated mutation rates in this pathogen contribute to the rapid development of resistance, complicating treatment efforts. We conducted a study on the prevalence of azole resistance among clinical A. fumigatus isolates in the Netherlands from 1994 to 2022 and identified 34 cyp51A variants. To investigate the impact of individual single-nucleotide polymorphisms (SNPs) and combinations thereof on the azole phenotype in TR34-mediated resistance genotypes, we focused on novel, recent mutations and explored the effects of SNPs L98H, T289A, I364V, and G448S and the combination of the mutations TR34/L98H, TR34/L98H/T289A/G448S, and TR34/L98H/T289A/I364V/G448S on azole affinity and susceptibility. We created the three-dimensional protein model of the Cyp51A protein with azoles, and the mutation was introduced to the wild-type cyp51A A. fumigatus strain by the CRISPR-Cas9 gene editing technique. Finally, in vitro susceptibility testing of A. fumigatus strains carrying the mutations was conducted to confirm the azole phenotypes observed in clinical isolates. The MICs of all four azoles against the mutated cyp51A strains, which harbored combination mutations, were higher than those of the wild type, with highly elevated MICs of itraconazole, voriconazole, and isavuconazole. Genotypes TR34/L98H/T289A/I364V/G448S mutant showed a consistent phenotype to the clinical strains, which are highly resistant to voriconazole but susceptible to itraconazole. In this study, we show that molecular dynamics simulations of amino acid substitutions in the cyp51A gene correlate to the structure–function relationship of in vitro phenotype.