Comparison of real-time PCR, conventional PCR, and galactomannan antigen detection by enzyme-linked immunosorbent assay using bronchoalveolar lavage fluid samples from hematology patients for diagnosis of invasive pulmonary aspergillosis

J Clin Microbiol. 2003 Aug;41(8):3922-5. doi: 10.1128/JCM.41.8.3922-3925.2003.

Abstract

An iCycler iQ real-time PCR assay targeting 18S rRNA Aspergillus-specific sequences was developed for the diagnosis of invasive pulmonary aspergillosis (IPA). Positive findings were obtained for 18 of 20 (90%) bronchoalveolar lavage (BAL) fluid specimens from patients with probable or confirmed IPA and were obtained for none of the 24 BAL samples from patients with no clinical evidence of aspergillosis. These results were concordant with those of a nested PCR assay, which detected 90% of the patients with IPA, while galactomannan ELISA revealed positivity for 100% of these patients, suggesting that combined use of methods might improve the diagnosis of IPA.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens, Fungal / analysis
  • Aspergillosis, Allergic Bronchopulmonary / diagnosis*
  • Aspergillosis, Allergic Bronchopulmonary / mortality
  • Aspergillus / genetics
  • Aspergillus / isolation & purification*
  • Bronchoalveolar Lavage Fluid / chemistry
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Galactose / analogs & derivatives
  • Humans
  • Male
  • Mannans / analysis*
  • Middle Aged
  • Polymerase Chain Reaction / methods*
  • Survival Analysis

Substances

  • Antigens, Fungal
  • Mannans
  • galactomannan
  • Galactose