Your browser doesn't support javascript.
loading
Nested PCR for Detection of Malassezia Species from Patient Skin Scales and Clinical Strains / 대한피부과학회지
Korean Journal of Dermatology ; : 446-452, 2008.
Artículo en Coreano | WPRIM | ID: wpr-29337
ABSTRACT

BACKGROUND:

Due to recent identification of new Malassezia (M.) species, M. dermatis, and M. equi, the genus Malassezia was revised into eleven species that have been isolated from human and animal skin. This has further substantiated the need for molecular techniques to distinguish the various Malassezia species.

OBJECTIVE:

We aimed to make the nested polymerase chain reaction (PCR) using species-specific primers with specificity and sensitivity as a diagnostic tool for differentiating the various Malassezia species from skin scales and fungal cells rapidly and accurately. In addition, we evaluated the common causative Malassezia species in the patients with seborreheic dermatitis, pityriasis versicolor or pityrisporum folliculitis.

METHODS:

Malassezia species-specific primers were designed based on DNA sequencing of the ribosomal RNA gene. The standard strains of eight members of the genus Malassezia such M. pachydermatis, M. furfur, M. sympodialis, M. globosa, M. obtuse, M. restricta, M. slooffiae, and M. dermatis were used for positive control. Each Malassezia species was cultured separately and two or three standard species were cultured together on Modified Leeming and Notman agar (MLNA) media plates. In addition, twenty-five clinical strains of Malassezia species isolated from the skin of patients with dermatological conditions and twenty-three samples of skin scale were used as well.

RESULTS:

The nested PCR assay with primers for all eight Malassezia species were species-specific since it amplified DNA only from the target Malassezia species, and could differentiate mixed, that is, the two or three Malassezia species of all standard strains grown on MLNA medium precisely. Detection of Malassezia species from clinical strains and patient skin scales using the nested PCR assay was 96% (24/25) and 87% (20/23), respectively. M. globosa, M. sympodialis, M. restricta were the most common causative Malassezia species in patients with pityriasis versicolor, pityrosporum folliculitis, seborrheic dermatitis, respectively.

CONCLUSION:

Nested PCR using species-specific primers is useful and reliable in the detection of various Malassezia species from patient skin scales as well as cultured fungal cells.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Tiña Versicolor / Pesos y Medidas / ADN / Reacción en Cadena de la Polimerasa / Sensibilidad y Especificidad / Análisis de Secuencia de ADN / Dermatitis Seborreica / Genes de ARNr / Agar Tipo de estudio: Estudio diagnóstico Límite: Animales / Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Año: 2008 Tipo del documento: Artículo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Piel / Tiña Versicolor / Pesos y Medidas / ADN / Reacción en Cadena de la Polimerasa / Sensibilidad y Especificidad / Análisis de Secuencia de ADN / Dermatitis Seborreica / Genes de ARNr / Agar Tipo de estudio: Estudio diagnóstico Límite: Animales / Humanos Idioma: Coreano Revista: Korean Journal of Dermatology Año: 2008 Tipo del documento: Artículo