A Reverse Transcription Loop-mediated Isothermal Amplification (RT-LAMP) method was developed to detect Zika. The primers were designed based on the NS5 region of 64 complete genomes. Lyophilized LAMP reagent was used. Initially, seven different arboviruses were tested and only Zika samples tested positive. Additionally, serial dilutions of one of Zika's RNA were compared using RT-LAMP and qRT-PCR, demonstrating that RT-LAMP is 1,000 times more sensitive. We also evaluated 300 serum samples with RT-LAMP comparing the results with standard qRT-PCR methods, and we obtained a 99.3% sensitivity, 100% specificity, 100% positive predictive value, and 99.3% negative predictive value. In conclusion, this method provides a low-cost, high-performance, viable, and reliable alternative for the rapid diagnosis of Zika in primary health-care facilities.
|Título traducido de la contribución||Development and validation of loop-mediated isothermal amplification for the detection of the zika virus|
|Número de páginas||6|
|Publicación||Revista Peruana de Medicina de Experimental y Salud Publica|
|Estado||Publicada - 2019|
Nota bibliográficaPublisher Copyright:
© 2019, Instituto Nacional de Salud. All rights reserved.
- Polymerase chain reaction (source: MeSH NLM)
- RNA-directed DNA polymerase
- Zika virus