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. 2018 Oct 19;263:75–80. doi: 10.1016/j.jviromet.2018.10.015

Table 1.

Oligonucleotides used for RV SIBA assay.

Name Sequence 5'→3'
RV-A F-primer TGCACTAGCTGCAGGGTTA
RV-A R-primer GTGTGCTCACTTTGAG
RV-B F-primer GTCTCAAGGCTCCAGGGTTT
RV-B R-primer GTGTGCTTAATTCTGAG
RV-A IO CCCCCCCCCCCCCCCAGGGTTAAGGTTAGCCACATTCAGGGGmCmCmGmGmAmGmGmAmCmUmCmA
RV-B IO CCCCCCCCCCCCCCCAGGGTTTAGGTTAGCCGCATTCAGGGGmCmCmGmGmAmGmGmAmCmUmCmA

For invasion oligonucleotide (IO), bold sequences denote non-homologous seeding regions. mA, mC, mG, and mU denote 2′-O-methyl RNA nucleotides. F, forward; R, reverse; RV, human Rhinovirus; SIBA, strand invasion–based amplification; RV-A assay is designed to detect the sequence between position 421 and 483 within the genome of the human rhinovirus 60 strain ATCC VR-1473 (GenBank: FJ445133.1); RV-B assay is designed to detect the sequence between position 429 and 493 within the genome of the human rhinovirus 17 (GenBank: AF542419.1).