Autor(es): Oliveira, M. ; Pinto, M. ; Simões, H. ; Gomes, J.P. ; Veríssimo, C. ; Sabino, R.
Data: 2022
Identificador Persistente: http://hdl.handle.net/10400.18/8508
Origem: Repositório Científico do Instituto Nacional de Saúde
Assunto(s): Aspergillusmolecular; Mycobiome; Aspergillosis; Diagnosis; Fungal Infection; Molecular diagnosis; Mycobiome; Infecções Sistémicas e Zoonoses
Objective: Aspergillosis diagnosis depends on the detection of Aspergillus in biological samples ─ usually using cultural and immunoenzyme techniques ─ but their sensitivity and specificity varies. We aimed to study the prevalence of Aspergillus in patients at higher risk of chronic pulmonary aspergillosis (i.e., HIV-infected patients and individuals with active or previous tuberculosis), and to determine the potential role of molecular approaches to increase detection of Aspergillus in respiratory samples. Methods: The DNA extracted from 43 respiratory samples that had been previously analyzed by immunoenzyme and/or cultural techniques was amplified by real-time multiplex PCR, and the results of these methods were compared. We also sequenced the ITS1 region and the calmodulin gene in 10 respiratory samples to perform a pilot metagenomic study to understand the ability of this methodology to detect potential pathogenic fungi in the lung mycobiome. Results: Real-time Aspergillus PCR test exhibited a higher positivity rate than the conventional techniques used for aspergillosis diagnosis, particularly in individuals at risk for chronic pulmonary aspergillosis. The metagenomic analysis allowed for the detection of various potentially pathogenic fungi. Conclusions: Molecular techniques, including metagenomics, have great ability to detect potentially pathogenic fungi rapidly and efficiently in human biological samples.
