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Development of a new multiplex PCR to detect prevalent species of house dust mites in house dust.
Oliveira, Ana Sofia; Gaspar, Carlos; Rolo, Joana; Pereira, Cristiana Costa; Palmeira-de-Oliveira, Rita; Teixeira, João Paulo; Martinez-de-Oliveira, José; Palmeira-de-Oliveira, Ana.
Afiliación
  • Oliveira AS; Health Sciences Research Centre (CICS-UBI), University of Beira Interior Av. Infante D. Henrique, Covilhã, Portugal.
  • Gaspar C; Faculty of Health Sciences,University of Beira Interior, Av. Infante D. Henrique, Covilhã, Portugal.
  • Rolo J; Health Sciences Research Centre (CICS-UBI), University of Beira Interior Av. Infante D. Henrique, Covilhã, Portugal.
  • Pereira CC; Faculty of Health Sciences,University of Beira Interior, Av. Infante D. Henrique, Covilhã, Portugal.
  • Palmeira-de-Oliveira R; Labfit - Health Products Research and Development Lda, UBImedical, Estrada Nacional, Covilhã, Portugal.
  • Teixeira JP; Health Sciences Research Centre (CICS-UBI), University of Beira Interior Av. Infante D. Henrique, Covilhã, Portugal.
  • Martinez-de-Oliveira J; National Institute of Health,Environmental Health Department, Rua Alexandre Herculano, Porto, Portugal.
  • Palmeira-de-Oliveira A; EPIUnit, EPIUnit - Instituto de Saúde Pública da Universidade do Porto, Rua das Taipas, Porto, Portugal.
Int J Environ Health Res ; 32(7): 1500-1512, 2022 Jul.
Article en En | MEDLINE | ID: mdl-33685302
ABSTRACT
Dermatophagoides pteronyssinus and Dermatophagoides farinae are the most common House Dust Mite (HDM) species in home environments worldwide and responsible for HDM allergy. Since the prevalence of HDM-related clinical conditions is linked to exposure to the mite itself, the detection of HDM in the human households gains importance. We aimed to develop a fast and accessible multiplex PCR to detect and distinguish two relevant HDM species in house dust. New primers were designed, and sensitivity analysis was performed. Sequencing of PCR products was also performed to confirm the method's specificity. The limit of detection of the multiplex PCR for both species was as low as 30 pg µL-1. The application of the multiplex PCR to dust samples also resulted in the identification of both species with high sensitivity. The protocol required small amount of template, reagents and a short reaction time thus presenting an alternative to classically used techniques for HDM identification.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pyroglyphidae / Reacción en Cadena de la Polimerasa Multiplex Tipo de estudio: Guideline / Prevalence_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Int J Environ Health Res Asunto de la revista: SAUDE AMBIENTAL Año: 2022 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pyroglyphidae / Reacción en Cadena de la Polimerasa Multiplex Tipo de estudio: Guideline / Prevalence_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Int J Environ Health Res Asunto de la revista: SAUDE AMBIENTAL Año: 2022 Tipo del documento: Article País de afiliación: Portugal