Abstract
Polymerase chain reaction (PCR) is a sensitive method for detection of Aspergillus DNA in bronchoalveolar lavage fluid, but it has not yet been able to distinguish infection from contamination. We have established a technique to quantify Aspergillus DNA using a real-time PCR method to resolve this problem, and we report herein a successful application of real-time PCR to diagnose invasive pulmonary aspergillosis by comparing the amount of Aspergillus DNA in bronchial lavage fluid from an affected area to that from an unaffected area. This novel tool will provide rapid, sensitive, and specific diagnosis of pulmonary aspergillosis.
Copyright 2002 Wiley-Liss, Inc.
Publication types
-
Case Reports
-
Comparative Study
-
Evaluation Study
MeSH terms
-
Adult
-
Aspergillosis / diagnosis*
-
Aspergillosis / etiology
-
Aspergillosis / genetics
-
Aspergillosis / pathology
-
Aspergillus fumigatus / genetics
-
Aspergillus fumigatus / isolation & purification*
-
Bone Marrow Transplantation / adverse effects
-
Bronchoalveolar Lavage Fluid / chemistry*
-
Computer Systems
-
Cryptogenic Organizing Pneumonia / etiology
-
DNA, Fungal / analysis*
-
Female
-
Graft vs Host Disease / etiology
-
Humans
-
Immunosuppressive Agents / adverse effects
-
Immunosuppressive Agents / therapeutic use
-
Leukemia, Myeloid, Acute / complications
-
Lung Diseases, Fungal / diagnosis*
-
Lung Diseases, Fungal / etiology
-
Lung Diseases, Fungal / genetics
-
Lung Diseases, Fungal / pathology
-
Opportunistic Infections / diagnosis
-
Opportunistic Infections / etiology
-
Opportunistic Infections / genetics
-
Opportunistic Infections / pathology
-
Polymerase Chain Reaction*
-
Sensitivity and Specificity
-
Transplantation, Homologous
Substances
-
DNA, Fungal
-
Immunosuppressive Agents