Evidence of Pneumocystis jiroveci in human clinical samples in southwestern Slovakia over a 10-year period (2001–2010)

• Published in: Biológia 2013-08, Vol.68 (4), p.662-666
• Main Authors: Boldiš, Vojtech, Ondriska, František, Kováč, Ľubor, Nohýnková, Eva, pitalská, Eva
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Cell Biology; cell walls; death; DNA; DNA-directed DNA polymerase; fungi; Human immunodeficiency virus; humans; immunocompromised patients; immunocompromised population; Life Sciences; lupus erythematosus; Microbiology; microscopy; nucleotide sequences; parasites; parasitoses; pathogens; patients; people; Plant Sciences; Pneumocystis; Pneumocystis jiroveci; pneumocystis pneumonia; pneumonia; polymerase chain reaction; Protozoa; risk; Section Zoology; taxonomic revisions; therapeutics; Zoology
• ISSN: 0006-3088; 1336-9563
• DOI: 10.2478/s11756-013-0199-x

In the past, Pneumocystis jiroveci (formerly P. carinii) belonged to the Protozoa group, but the studies on structure of the cell wall and nucleotide sequence resulted in the reclassification of this organism in the kingdom Fungi. P. jiroveci is an opportunistic pathogen, responsible for pneumocystis pneumonia with frequent complications of immunocompromised patients. Delayed initiation of appropriate therapy increases the risk of death in immunocompromised patient. The aim of this work was to determine the prevalence of P. jiroveci from patients suspected of having respiratory tract infections in southwestern Slovakia over a 10-year period. Due to the increasing number of immunosuppressed persons, the diagnostic of P. jiroveci in patients with pulmonary complications is essential to improve recovery onsets. Effective diagnosis is currently based on microscopic examination and detection of parasite DNA by polymerase chain reaction (PCR) in bronchoalveolar lavage (BAL) and induced sputum. In total, 386 clinical samples originated from patients suspected of pneumocystis infection were tested within ten years. Requirements for diagnosis of the pathogen were growing during the period. Three hundred and sixteen BALs, 59 induced sputa, 10 lung biopsies and 1 liquor were subjected to the detection of P. jiroveci. P. jiroveci DNA was detected in 30 patients using PCR, but cysts of microorganism were present only in 4 cases by microscopy. The pathogen was confirmed in 24 BALs and 6 sputa samples. The presence of P. jiroveci has been demonstrated mainly in immunocompromised individuals with cancer (20), but also in patients with pneumonia (6+1 HIV), with unspecified parasitic diseases (1+1HIV) and with systemic lupus erythematosus (1).