Skip to main content
. 2019 Aug 28;93(18):e00705-19. doi: 10.1128/JVI.00705-19

TABLE 1.

Primers used for RT-PCR detection and RT-qPCR quantification of DENV-1, ZIKV, CFAV, and Aedes aegypti housekeeping genes rp49 and rps7

Genome Genomic region Application Direction Primer sequence (5′ → 3′) Length of PCR product (bp) Annealing temp (°C)
DENV-1 NS5 Detection Forward GGAAGGAGAAGGACTCCACA 105 60
DENV-1 NS5 Detection Reverse ATCCTTGTATCCCATCCGGCT 105 60
ZIKV NS1 Detection Forward GTATGGAATGGAGATAAGGCCCA 191 60
ZIKV NS2A Detection Reverse ACCAGCACTGCCATTGATGTGC 191 60
CFAV NS3 Quantification Forward ACACGAGTGAAGCTGGTTGA 92 56
CFAV NS3 Quantification Reverse ACATACGTTCCTGGTTCCCG 92 56
CFAV E Detection Forward GCTTCAAGTGGGGGATTGGA 345 62
CFAV E Detection Reverse CAACTTTCTCCATGCCGTGC 345 62
CFAV 5′ UTRa Genomic cDNA amplification Forward AGTTTATAAAAACTTCGGCTTGGCT 10,696 60
CFAV 3′ UTR RT, genomic cDNA amplification Reverse AGCGCATCTATGGTATAGAAAAGA 10,696 60
Aedes aegypti rp49 Housekeeping gene quantification Forward ACAAGCTTGCCCCCAACT 97 60
Aedes aegypti rp49 Housekeeping gene quantification Reverse CCGTAACCGATGTTTGGC 97 60
Aedes aegypti rps7 Housekeeping gene detection Forward GGGACAAATCGGCCAGGCTATC 292 64
Aedes aegypti rps7 Housekeeping gene detection Reverse TCGTGGACGCTTCTGCTTGTTG 292 64
a

UTR, untranslated region.