Year prepared: 2013
Rapid and quantitative detection of Aspergillus from clinical samples may facilitate an early diagnosis of invasive pulmonary aspergillosis (IPA). As nucleic acid-based detection is a viable option, we demonstrate that Aspergillus burdens can be rapidly and accurately detected by a novel real-time nucleic acid assay other than qPCR by using the combination of nucleic acid sequence-based amplification (NASBA) and the molecular beacon (MB) technology. Here, we detail a real-time NASBA assay to determine quantitative Aspergillus burdens in lungs and bronchoalveolar lavage (BAL) fluids of rats with experimental IPA.
Laboratory Protocols
-
Title
Type
-
Assaying antifungal levels
-
Fungal Molecular Biology
-
Fungal Molecular Biology
-
Detection in clinical samples
-
More protocol collections
-
Methods for DNA sequencing
-
Using Non-homologous End-Joining-Deficient Strains for Functional Gene Analyses in Filamentous Fungi
Fungal Molecular Biology