Detailed Information on Publication Record
2019
Detection and identification of fungi in bronchoalveolar lavage fluid from immunocompromised patients using panfungal PCR
ŘÍČNÁ, Dita, Martina LENGEROVÁ, Matěj BEZDÍČEK, Iva KOCMANOVÁ, Lubos DRGONA et. al.Basic information
Original name
Detection and identification of fungi in bronchoalveolar lavage fluid from immunocompromised patients using panfungal PCR
Authors
ŘÍČNÁ, Dita (203 Czech Republic, belonging to the institution), Martina LENGEROVÁ (203 Czech Republic, belonging to the institution), Matěj BEZDÍČEK (203 Czech Republic, belonging to the institution), Iva KOCMANOVÁ (203 Czech Republic), Lubos DRGONA (703 Slovakia), Barbora WEINBERGEROVÁ (203 Czech Republic, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution) and Zdeněk RÁČIL (203 Czech Republic, belonging to the institution)
Edition
Folia microbiologica, Dordrecht, Springer, 2019, 0015-5632
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 1.730
RIV identification code
RIV/00216224:14110/19:00108353
Organization unit
Faculty of Medicine
UT WoS
000468847600014
Keywords in English
fungal pneumonia
Tags
International impact, Reviewed
Změněno: 12/7/2019 16:43, Soňa Böhmová
Abstract
V originále
Rapid diagnostics of fungal pneumonia and initiation of appropriate therapy are still challenging. In this study, we used two panfungal assays to test bronchoalveolar lavage fluid (BALF) samples to prove their ability to confirm invasive fungal disease diagnosis and identify causative agents. Two methods targeting different fungal rDNA regions were used, and the obtained PCR products were sequenced directly or after cloning. In total, 106 BALF samples from 104 patients were tested. After sequencing, we obtained 578 sequences. Four hundred thirty-seven sequences were excluded from further analysis due to duplication (n=335) or similarity with sequences detected in the extraction control sample (n=102); 141 unique sequences were analyzed. Altogether, 23/141 (16%) of the fungi detected belonged to pathogenic species, and 63/141 (45%) were identified as various yeasts; a variety of environmental or very rare fungal human pathogens represented 29/141 (21%) of the total and 26/141 (18%) were described as uncultured fungus. Panfungal PCR detected fungal species that would be missed by specific methods in only one case (probable cryptococcosis). Panfungal PCR followed by sequencing has limited use for testing BALF samples due to frequent commensal or environmental fungal species pickup.
Links
MUNI/A/1105/2018, interní kód MU |
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TE02000058, research and development project |
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