Abstract
A diagnosis system for the early detection of Dengue virus was carried out by amplification of the NS1 gene portion using RT-PCR. Results obtained from clinical samples corresponded to previous RT-PCR works aimed at the structural region of the virion. Dengue cDNA from one of the sera samples was then cloned and sequenced. Comparison by nucleotide sequence analysis with other reference strains determined that this viral strain was Dengue serotype 1.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have