摘要：Infections due to triazole-resistant
Aspergillus fumigatus are increasingly reported worldwide and are associated with treatment failure and mortality. The principal class of azole-resistant isolates is characterized by tandem repeats of 34 bp or 46 bp within the promoter region of the
cyp51A gene. Loop-mediated isothermal amplification (LAMP) is a widely used nucleic acid amplification system that is fast and specific. Here we describe a LAMP assay method to detect the 46 bp tandem repeat insertion in the
cyp51A gene promoter region based on novel LAMP primer sets
. It also differentiated strains with TR
46 tandem repeats from those with TR
34 tandem repeats. These results showed this TR
46-LAMP method is specific, rapid, and provides crucial insights to develop novel antifungal therapeutic strategies against severe fungal infections due to
A. fumigatus with TR
46 tandem repeats.
