Respiratory Treatment and Prevention (Advances in Experimental Medicine and Biology)

(Jacob Rumans) #1

Advs Exp. Medicine, Biology - Neuroscience and Respiration (2016) 27: 27–33
DOI 10.1007/5584_2016_46
#Springer International Publishing Switzerland 2017
Published online: 12 July 2016


Diagnosis of Invasive Pulmonary
Aspergillosis

E. Swoboda-Kopec ́, M. Sikora, K. Piskorska, M. Gołas ́,
I. Netsvyetayeva, D. Przybyłowska, and E. Mierzwin ́ska-
Nastalska

Abstract
Culturing strains from clinical samples is the main method to diagnose
invasive pulmonary aspergillosis. Detecting the galactomannan antigen in
serum samples is an auxiliary examination. The goal of this study was to
determine the frequency with whichAspergillus fumigatuswas cultured in
clinical samples taken from patients hospitalized in the the Infant Jesus
Teaching Hospital in Warsaw, Poland, in the period of 2013–2014.
Specimens from the respiratory tract and blood were cultured for myco-
logical and serological assessments. Strain isolation was performed in
chloramphenicol Sabouraud agar. Species identification was based on
morphological traits in macro-cultures and on microscopic examination.
The galactomannan antigen was detected by ELISA method. Out of 2000
clinical samples with positive mycological results, 200 were obtained
from the respiratory tract.A. fumigatus was cultured in 13 cases from
the respiratory group. Ten cases were cultured out of tracheal aspirates
and three from bronchoalveolar lavage fluid. The galactomannan antigen
was detected in a serum sample from only one out of the 13 patients with
cultures positive forA. fumigatus. It also was detected in serum samples of
three other patients in whomA. fumigatusculture yielded a negative
result. We conclude that culture-confirmed invasive pulmonary aspergil-
losis represents a scarce finding. A. fumigatuscultured from clinical
samples may not always be confirmed by ELISA assay andvice versaa
positive ELISA result does not attest the successful culture.

E. Swoboda-Kopec ́, K. Piskorska (*), M. Gołas ́,
and I. Netsvyetayeva
Department of Medical Microbiology, Medical
University of Warsaw, 5 Chałubin ́skiego St., 02-004
Warsaw, Poland
e-mail:[email protected]


M. Sikora
Department of Dental Microbiology, Medical University
of Warsaw, Warsaw, Poland
D. Przybyłowska and E. Mierzwin ́ska-Nastalska
Department of Prosthodontic, Medical University of
Warsaw, Warsaw, Poland

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