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1.
J Mycol Med ; 29(1): 24-27, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30616967

ABSTRACT

AIM: The aim of this study was to investigate the collection of avian Aspergillus fumigatus isolates for the presence of triazole resistance. MATERIAL AND METHOD: The study was performed on 60 A. fumigatus isolates cultured from lung tissue samples from chicken (25), geese (17), turkeys (13) and ducks (5). The samples were obtained from 40 different farms located in the Southwest Poland and were collected in the period of September 2015 to November 2016. The EUCAST microdilution method, with the use of three concentrations of itraconazole (ITR) (1, 0.5, and 0.25mg/L), was used to screen the susceptibility of all isolates. Additionally, the selected 20 isolates were tested with eleven concentrations ranging 0.015-16mg/L of ITR, voriconazole, posaconazole and isavuconazole. RESULTS: Most tested isolates (59/60) were susceptible to ITR (MIC≤0.5mg/L). One isolate showed elevated MIC for ITR (16mg/L), as well as voriconazole (4mg/L), izavuconazole (4mg/L), and posaconazole (0.5mg/L). This isolate was identified on the basis of DNA analysis as A. fumigatus carrying TR34/L98H mutation. All of the ITR-susceptible isolates under study were also susceptible to other triazoles. CONCLUSION: Obtained results indicated a low frequency (1.6%) of A. fumigatus resistant to triazoles among avian isolates from the Southwest regions of Poland.


Subject(s)
Antifungal Agents/pharmacology , Aspergillus fumigatus/drug effects , Drug Resistance, Fungal , Itraconazole/pharmacology , Poultry/microbiology , Animals , Aspergillus fumigatus/isolation & purification , Chickens/microbiology , Ducks/microbiology , Farms , Fungal Proteins/genetics , Geese/microbiology , Lung/microbiology , Microbial Sensitivity Tests , Poland , Poultry Diseases/microbiology , Turkeys/microbiology
2.
J Eur Acad Dermatol Venereol ; 30(10): 1819-1822, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27306227

ABSTRACT

OBJECTIVES: The identification of species in the Arthroderma otae complex is essential to determine the origin of infection and to eliminate the risk of transmission. Microsporum canis is a zoophilic species, whereas Microsporum audouinii and Microsporum ferrugineum are anthropophilic species. In this paper, we propose alternative methods that permit species-specific identification of both anthropophilic and zoophilic members of the A. otae complex METHODS: Two PCR assays were designed based on differences in the DNA fragment encoding ß-tubulin and were applied in both traditional and real-time PCR using DNA isolated by rapid method from culture. RESULT: The two assays presented in this study enable the identification of M. canis and M. audouinii/M. ferrugineum with 100% sensitivity and specificity by both traditional and real-time PCR. CONCLUSION: We developed a new diagnostic assay using specific primers and both traditional and real-time PCR reactions that can be applied in routine laboratory praxis as well as in epidemiological studies to detect M. canis and M. audouinii/M. ferrugineum DNA from a pure culture.


Subject(s)
Arthrodermataceae/genetics , Microsporum/genetics , Polymerase Chain Reaction/methods , Humans , Species Specificity
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