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. 2022 Mar 29;10:e13177. doi: 10.7717/peerj.13177

Table 1. PCR primers, annealing temperatures, and amplicon size used to detect the putative virulence genes in the isolates.

Primers Sequences (5’–3’) Tm (°C) Amplicon size (bp) References
Ace Ace-F: CAGGCCAACATCAAGCAACA 65 125 Al-Talib et al. (2015)
Ace-R: GCTTGCCTCGCCTTCTACAA
Agg Agg-F: AAGAAAAAGAAGTAGACCAAC 53 1553 Espeche et al. (2012)
Agg-R: AAACGGCAAGACAAGTAAATA
Asa1 Asa1-F: GCACGCTATTACGAACTATGA 56 375 Vankerckhoven et al. (2004)
Asa-R: TAAGAAAGAACATCACCACGA
Cpd Cpd-F: TGGTGGGTTATTTTTCAATTC 50 782 Eaton & Gasson (2001)
Cpd-R: TACGGCTCTGGCTTACTA
CylA CylA-F: ACTCGGGGATTGATAGGC 60 688 Vankerckhoven et al. (2004)
CylA-R: GCTGCTAAAGCTGCGCTT
ClyB ClyB-F: ATTCCTACCTATGTTCTGTTA 56 843 Vankerckhoven et al. (2004)
ClyB-R: AATAAACTCTTCTTTTCCAAC
EfaAfs EfaAfs-F: GACAGACCCTCACGAATA 56 705 Eaton & Gasson (2001)
EfaAfs-R: AGTTCATCATGCTGTAGTA
GelE GelE-F: CGAAGTTGGAAAAGGAGGC 50 372 Al-Talib et al. (2015)
GelE-R: GGTGAAGAAGTTACTCTGA