Real-Time PCR Coupled with Automated DNA Extraction and Detection of Galactomannan Antigen in Serum by Enzyme-Linked Immunosorbent Assay for Diagnosis of Invasive Aspergillosis

Author:

Costa Catherine1,Costa Jean-Marc12,Desterke Christophe1,Botterel Françoise1,Cordonnier Catherine3,Bretagne Stéphane1

Affiliation:

1. Laboratoire de Parasitologie-Mycologie and UMR BIPAR 956

2. Laboratoire de Biologie Moléculaire, Hôpital Américain de Paris, Neuilly, France

3. Service d'Hématologie Clinique, Hôpital H. Mondor-APHP, 94010 Créteil

Abstract

ABSTRACT To improve the diagnosis of invasive aspergillosis (IA), we developed a LightCycler PCR assay targeted to Aspergillus fumigatus and A. flavus mitochondrial DNA. To avoid contamination, fully automated nucleic acid extraction with the MagNA Pure LC apparatus was used. The linearity of the results was achieved over a 6-log range of input A. fumigatus DNA, from 0.3 ng to 3 fg/10 μl of water. We retrospectively compared the LightCycler PCR and an enzyme-linked immunosorbent assay for the detection of galactomannan (GM) in serum from 14 patients with IA. The GM assay was more frequently positive (57 of 109; 52%) than the PCR assay (49 of 109; 45%). The LightCycler PCR assay, combined with automated DNA extraction, could be used in association with the GM assay to improve the reliability of IA diagnosis.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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