2015
DOI: 10.1111/exd.12884
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Experimental white piedra: a robust approach to ultrastructural analysis, scanning electron microscopy and etiological discoveries

Abstract: White piedra is a fungal infection characterized by nodules comprised of Trichosporon species and restricted to the extrafollicular portion of the hair shaft. The diagnosis is based on clinical and mycological characteristics, and must be confirmed with a precise identification of the etiological agent. This research aimed to develop an in vitro infection model of white piedra and analyze its morphological and ultra-structural aspects. In the process, hair infection was induced using eight isolates of the genu… Show more

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Cited by 11 publications
(5 citation statements)
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References 16 publications
(21 reference statements)
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“…In electron microscopy studies, a well-organized mass of microorganisms is observed, sometimes with a bacterial coating that probably helps to establish the nodule and that it is mainly constituted by Corynebacterium sp. and other con­stituent microorganisms of the microbiota [4, 13-15]. In our study, an association with S. aureus was verified in 2 cases.…”
Section: Discussionsupporting
confidence: 58%
“…In electron microscopy studies, a well-organized mass of microorganisms is observed, sometimes with a bacterial coating that probably helps to establish the nodule and that it is mainly constituted by Corynebacterium sp. and other con­stituent microorganisms of the microbiota [4, 13-15]. In our study, an association with S. aureus was verified in 2 cases.…”
Section: Discussionsupporting
confidence: 58%
“…Biochemical analysis of white piedra nodules has shown them to be composed of carbon, oxygen, sodium, and magnesium. The nodules of black piedra have sulphur in addition, which could be responsible for their hardness [7].…”
Section: Discussionmentioning
confidence: 99%
“…The DNA was extracted according to Inácio et al, (2016), where the biological samples were transferred to extraction tubes containing a glass bead matrix and 500µL of the extraction buffer (CTAB 2%, NaCl 1.5 M, 100mM Tris-HCl , 20mM EDTA, 1% polyvinylpyrrolidone) previously heated to 65°C. After extraction, the DNA products were assembled in parafilm (5µL of the extraction product, 2µL GLB and 2 µL GelRed), using the Lambda DNA marker as standard.…”
Section: Species-specific Diagnosismentioning
confidence: 99%