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1.
Microorganisms ; 11(9)2023 Sep 18.
Artigo em Inglês | MEDLINE | ID: mdl-37764179

RESUMO

In an attempt to determine the mating type of different Sporothrix schenckii sensu stricto isolates that remained viable after a long period of preservation in a culture collection and to correlate them with the degree of virulence/pathogenicity, a PCR technique using primers designed for the sequences of MAT1-1-1 and MAT1-2-1 genes and a murine experimental model were used. The results showed that there was no correlation between the mating type and virulence among the isolates. Furthermore, different degrees of virulence/pathogenicity, ranging from high to low, were found among them based on different virulence parameters. It was assumed that the long period of preservation favored the changes, yielding the isolation of variants. Thus, we believe that new technologies for studies on factors can improve our knowledge of the pathogenesis of sporotrichosis.

2.
Physiotherapy ; 97(4): 273-7, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22051582

RESUMO

OBJECTIVES: To evaluate the presence of fungi on contact electrodes and ultrasound transducers from physiotherapy clinics. DESIGN: Quantitative study conducted at the Laboratory of Microbiology and Immunology, Faculty of Health Sciences and Technology of Piauí - NOVAFAPI, Teresina, Brazil. SETTING: Sample collection was performed in 10 clinics (20 ultrasound transducers and 20 contact electrodes). MAIN OUTCOME MEASURES: Swabs were soaked with saline solution, inoculated in culture and incubated for filamentous fungi and yeast growth. RESULTS: Fourteen taxons were identified: Acremomium hyalinulum (Sacc.), Aspergillus terreus, Candida albicans, Cladosporium cladosporioides, Cladosporium elatum, Cladosporium oxysporum, Cladosporium sphaerospermum, Cladosphialophora bantiana, Curvularia clavata, Curvularia senegalensis, Fusarium oxysporum, Penicillium decumbens, Scopulariopsis candida and Sporothrix schenckii. Aspergillus terreus, Cladosporium oxysporum, Sporothrix shenckii and Candida albicans were found most often on contact electrodes, and Penicillium decumbens and Cladosporium cladosporioides were found most often on ultrasound transducers. CONCLUSION: Fungi were found on all of the contact electrodes and ultrasound transducers. Physiotherapy professionals need to improve the disinfection procedures for this equipment.


Assuntos
Terapia por Estimulação Elétrica/instrumentação , Contaminação de Equipamentos , Fungos/isolamento & purificação , Terapia por Ultrassom/instrumentação , Instituições de Assistência Ambulatorial , Brasil , Eletrodos/microbiologia , Humanos , Transdutores/microbiologia
3.
Mycoses ; 53(2): 130-7, 2010 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-19389074

RESUMO

We have developed a two-step PCR assay that amplifies a region of the ceja-1 sequence that is specific for virulent strains of Paracoccidioides brasiliensis. An internal region of the ceja-1 sequence was chosen for designing primers that were utilised in a single tube heminested PCR protocol to amplify DNA from six virulent strains. PCR specificity was determined by the absence of amplified products with genomic DNA from four non-virulent strains of P. brasiliensis and from eight fungal pathogens, one bacterium, two protozoa, one worm and mouse and human genomic DNA (leucocytes). The fact that the PCR product was only obtained with the genetic material from virulent isolates of P. brasiliensis suggested that this partial amplified sequence might be a marker of virulence for this fungus. The diagnostic potential of this PCR was confirmed by the successful amplification of this fragment with genomic DNA obtained in lymph node aspirate from a patient with paracoccidioidomycosis.


Assuntos
Micologia/métodos , Paracoccidioides/genética , Paracoccidioides/isolamento & purificação , Paracoccidioidomicose/diagnóstico , Reação em Cadeia da Polimerase/métodos , Animais , Biomarcadores , Primers do DNA/genética , DNA Fúngico/química , DNA Fúngico/genética , Humanos , Camundongos , Dados de Sequência Molecular , Sensibilidade e Especificidade , Análise de Sequência de DNA
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