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1.
Med Mycol ; 57(2): 260-263, 2019 Feb 01.
Article in English | MEDLINE | ID: mdl-29669009

ABSTRACT

Chromoblastomycosis (CBM) is a chronic cutaneous and subcutaneous infection caused by melanized fungal species. We quantified the extractable melanin of 77 strains of CBM agents distributed within five genera. Moreover, resistance to oxidative stress was evaluated in strains exposed or not to the melanin inhibitor tricyclazole. The median percentage of melanin mass extracted from dry fungal mass varied from 0.69 (Rhinocladiella similis) to 3.81 (Phialophora americana). Inhibition of melanin synthesis decreased survival rates to hydrogen peroxide. Together, these data highlight the importance of melanin in CBM agents.


Subject(s)
Ascomycota/chemistry , Ascomycota/physiology , Chromoblastomycosis/microbiology , Melanins/analysis , Oxidative Stress , Antifungal Agents/pharmacology , Ascomycota/drug effects , Ascomycota/isolation & purification , Humans , Hydrogen Peroxide/pharmacology , Melanins/biosynthesis , Microbial Viability/drug effects , Oxidative Stress/drug effects , Phialophora/chemistry , Phialophora/drug effects , Phialophora/isolation & purification , Phialophora/physiology , Species Specificity , Spores, Fungal/physiology , Thiazoles/pharmacology
2.
World J Microbiol Biotechnol ; 33(4): 77, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28341906

ABSTRACT

A comprehensive understanding of the presence and role of yeasts in bottled wines helps to know and control the organoleptic quality of the final product. The South Region of Brazil is an important wine producer, and the state of "Rio Grande do Sul" (RS) accounts for 90% of Brazilian wines. The state of "Santa Catarina" (SC) started the production in 1975, and is currently the fifth Brazilian producer. As there is little information about yeasts present in Brazilian wines, our main objective was to assess the composition of culturable yeasts associated to bottled wines produced in RS and SC, South of Brazil. We sampled 20 RS and 29 SC bottled wines produced between 2003 and 2011, and we isolated culturable yeasts in non-selective agar plates. We identified all isolates by sequencing of the D1/D2 domain of LSU rDNA or ITS1-5.8 S-ITS2 region, and comparison with type strain sequences deposited in GenBank database. Six yeast species were shared in the final product in both regions. We obtained two spoilage yeast profiles: RS with Zygosaccharomyces bailii and Pichia membranifaciens (Dekkera bruxellensis was found only in specific table wines); and SC with Dekkera bruxellensis and Pichia manshurica. Knowledge concerning the different spoilage profiles is important for winemaking practices in both regions.


Subject(s)
Sequence Analysis, DNA/methods , Wine/microbiology , Yeasts/classification , Yeasts/isolation & purification , Brazil , DNA, Fungal/analysis , Dekkera/classification , Dekkera/genetics , Dekkera/isolation & purification , Food Microbiology , Pichia/classification , Pichia/genetics , Pichia/isolation & purification , Saccharomyces cerevisiae/classification , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/isolation & purification , Yeasts/genetics , Zygosaccharomyces/classification , Zygosaccharomyces/genetics , Zygosaccharomyces/isolation & purification
3.
PLoS One ; 9(8): e105870, 2014.
Article in English | MEDLINE | ID: mdl-25171185

ABSTRACT

In microbiology, identification of all isolates by sequencing is still unfeasible in small research laboratories. Therefore, many yeast diversity studies follow a screening procedure consisting of clustering the yeast isolates using MSP-PCR fingerprinting, followed by identification of one or a few selected representatives of each cluster by sequencing. Although this procedure has been widely applied in the literature, it has not been properly validated. We evaluated a standardized protocol using MSP-PCR fingerprinting with the primers (GTG)5 and M13 for the discrimination of wine associated yeasts in South Brazil. Two datasets were used: yeasts isolated from bottled wines and vineyard environments. We compared the discriminatory power of both primers in a subset of 16 strains, choosing the primer (GTG)5 for further evaluation. Afterwards, we applied this technique to 245 strains, and compared the results with the identification obtained by partial sequencing of the LSU rRNA gene, considered as the gold standard. An array matrix was constructed for each dataset and used as input for clustering with two methods (hierarchical dendrograms and QAPGrid layout). For both yeast datasets, unrelated species were clustered in the same group. The sensitivity score of (GTG)5 MSP-PCR fingerprinting was high, but specificity was low. As a conclusion, the yeast diversity inferred in several previous studies may have been underestimated and some isolates were probably misidentified due to the compliance to this screening procedure.


Subject(s)
DNA Fingerprinting/methods , DNA Primers/genetics , Polymerase Chain Reaction/methods , Wine/microbiology , Yeasts/genetics , Cluster Analysis , DNA, Fungal/genetics , Genetic Variation , Phylogeny , RNA, Ribosomal/genetics , Sequence Analysis, DNA , Species Specificity , Yeasts/classification , Yeasts/isolation & purification
4.
Med Mycol ; 52(1): 56-64, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23964828

ABSTRACT

Sporotrichosis is a subacute or chronic mycosis caused worldwide by the dimorphic species complex, Sporothrix schenckii. We studied 85 isolates recovered in Brazil to verify their identification and evaluate their in vitro antifungal susceptibility patterns. Based on phenotypic tests (microscopic features, ability to grow at 30°C and 37°C, colony diameters, as well as assimilation of sucrose and raffinose) and molecular assays (amplification of a fragment of the calmodulin gene), the strains were identified as S. schenckii, S. brasiliensis and S. globosa, with a predominance of S. schenckii isolates. There was 37.7% disagreement between the phenotypic and genotypic identification methodologies. In general, terbinafine was the most active drug, followed by ketoconazole and itraconazole, and the less active fluconazole and voriconazole. Five isolates (one S. globosa and four S. schenckii) were found to be itraconazole-resistant strains but, in general, there were no differences in the in vitro antifungal susceptibility profiles among the Sporothrix species.


Subject(s)
Antifungal Agents/pharmacology , Sporothrix/classification , Sporotrichosis/microbiology , Brazil , Humans , Microbial Sensitivity Tests , Molecular Typing , Mycological Typing Techniques , Sporothrix/genetics , Sporothrix/isolation & purification , Sporothrix/physiology
5.
Mycopathologia ; 176(1-2): 139-44, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23645135

ABSTRACT

Chromoblastomycosis is a chronic cutaneous and subcutaneous mycosis. The management of this infection continues to be challenging because there is no consensus on the therapeutic regimen. We report here a case of a 69-year-old male patient with cauliflower-like lesions on his left leg and foot. He had already been treated with itraconazole at a dose of 200 mg/day for 5 months, with mycological cure for all the affected areas. However, the lesions relapsed at both sites, and treatment with itraconazole was resumed at the dose previously used. Initially, direct mycological examination, cultural, and microculture slide observation were performed. Afterward, sequencing of the ITS1-5.8S rDNA-ITS2 region of the fungal DNA and evaluation of its susceptibility to antifungal agents alone and in combination were performed. In direct mycological examination, the presence of sclerotic cells was verified, and the fungus was identified as Fonsecaea based on cultural and microscopic examinations. Identification as Fonsecaea monophora was confirmed after sequencing of the ITS region and phylogenetic analysis. The isolate was susceptible to itraconazole and terbinafine. The combinations of amphotericin B and terbinafine and terbinafine and voriconazole were synergistic. The use of drugs for which the causative agent is susceptible to singly or in combination may be an alternative for the treatment of mycosis. Furthermore, the identification of the agent by molecular techniques is important for epidemiological purposes. To the best of our knowledge, this is the first case of relapsed chromoblastomycosis caused by F. monophora in Brazil.


Subject(s)
Antifungal Agents/pharmacology , Ascomycota/drug effects , Ascomycota/isolation & purification , Chromoblastomycosis/diagnosis , Chromoblastomycosis/microbiology , Aged , Ascomycota/classification , Ascomycota/genetics , Brazil , Chromoblastomycosis/pathology , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Drug Synergism , Humans , Male , Microbial Sensitivity Tests , Microbiological Techniques , RNA, Ribosomal, 5.8S/genetics , Recurrence , Sequence Analysis, DNA
6.
Med Mycol Case Rep ; 1(1): 72-5, 2012.
Article in English | MEDLINE | ID: mdl-24371743

ABSTRACT

We report a case of an 80-year-old Brazilian man, farmer, with lesions on the dorsum of the hand. A direct mycological examination, cultivation and microculture slide observation was performed. The sequencing of ITS1-5.8S rDNA-ITS2 region was carried out and the etiological agent confirmed as Exophiala spinifera. The in vitro susceptibility of this isolate to antifungal agents alone and in combination was evaluated. This is the third case of phaeohyphomycosis caused by Exophiala spinifera in Brazil.

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