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Single-tube four-target lateral flow assay detects human papillomavirus types associated with majority of cervical cancers.
Barra, Maria; Chang, Megan; Salcedo, Mila P; Schmeler, Kathleen; Scheurer, Michael; Maza, Mauricio; Lopez, Leticia; Alfaro, Karla; Richards-Kortum, Rebecca.
Afiliação
  • Barra M; Department of Bioengineering, Rice University, Houston, TX, USA.
  • Chang M; Department of Bioengineering, Rice University, Houston, TX, USA.
  • Salcedo MP; Department of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Schmeler K; Department of Gynecologic Oncology & Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Scheurer M; Department of Pediatrics Hematology/Oncology, Baylor College of Medicine, Houston, TX, USA.
  • Maza M; Basic Health International, San Salvador, El Salvador.
  • Lopez L; Basic Health International, San Salvador, El Salvador.
  • Alfaro K; Basic Health International, San Salvador, El Salvador.
  • Richards-Kortum R; Department of Bioengineering, Rice University, Houston, TX, USA. Electronic address: rkortum@rice.edu.
Anal Biochem ; 688: 115480, 2024 May.
Article em En | MEDLINE | ID: mdl-38331373
ABSTRACT
Isothermal nucleic acid amplification methods have many advantages for use at the point of care. However, there is a lack of multiplexed isothermal amplification tests to detect multiple targets in a single reaction, which would be valuable for many diseases, such as infection with high-risk human papillomavirus (hrHPV). In this study, we developed a multiplexed loop-mediated isothermal amplification (LAMP) reaction to detect the three most common hrHPV types that cause cervical cancer (HPV16, HPV18, and HPV45) and a cellular control for sample adequacy. First, we characterized the assay limit of detection (LOD) in a real-time reaction with fluorescence readout; after 30 min of amplification the LOD was 100, 10, and 10 copies/reaction of HPV16, HPV18, and HPV45, respectively, and 0.1 ng/reaction of human genomic DNA (gDNA). Next, we implemented the assay on lateral flow strips, and the LOD was maintained for HPV16 and HPV18, but increased to 100 copies/reaction for HPV45 and to 1 ng/reaction for gDNA. Lastly, we used the LAMP test to evaluate total nucleic acid extracted from 38 clinical samples; compared to qPCR, the LAMP test had 89% sensitivity and 95% specificity. When integrated with sample preparation, this multiplexed LAMP assay could be useful for point-of-care testing.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo do Útero / Infecções por Papillomavirus / Papillomavirus Humano 18 Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Anal Biochem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Colo do Útero / Infecções por Papillomavirus / Papillomavirus Humano 18 Tipo de estudo: Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Anal Biochem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos