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. 2020 Sep 15;11(1):1257–1267. doi: 10.1080/21505594.2020.1809329

Table 1.

Primers used for the detection of virulence genes and CRISPR-associated genes.

Gene Primer Sequence (5ʹ–3ʹ) PCR product length (bp) References
esp espF GGAACGCCTTGGTATGCTAAC 95 [46]
espR GCCACTTTATCAGCCTGAACC
cylA cylF ACTCGGGGATTGATAGGC 688 [47]
cylR GCTGCTAAAGCTGCGCTT
hyl hylF ACAGAAGAGCTGCAGGAAATG 276 [11]
hylR GACTGACGTCCAAGTTTCCAA
efaA efaF TGGGACAGACCCTCACGAATA 101 [48]
efaR CGCCTGTTTCTAAGTTCAAGCC
gelE gelF TATGACAATGCTTTTTGGGAT 213 [47]
gelR AGATGCACCCGAAATAATATA
ace aceF GGAGAGTCAAATCAAGTACGTTGGTT 101 [49]
aceR TGTTGACCACTTCCTTGTCGAT
ebpR ebpF AAAAATGATTCGGCTCCAGAA 101 [11]
ebpR TGCCAGATTCGCTCTCAAAG
asa1 asaF GCACGCTATTACGAACTATGA 375 [47]
asaR TAAGAAAGAACATCACCACGA
CRISPR1-cas csn1 For CAGAAGACTATCAGTTGGTG 783 [18]
Rev CCTTCTAAATCTTCTTCATAG
CRISPR1-cas loci For GCGATGTTAGCTGATACAAC 315 [18]
Rev CGAATATGCCTGTGGTGAAA
CRISPR2 loci For CTGGCTCGCTGTTACAGCT variable [18]
Rev GCCAATGTTACAATATCAAACA
CRISPR3-cas csn1 For GCTGAATCTGTGAAGTTACTC 258 [18]
Rev CTGTTTTGTTCACCGTTGGAT
CRISPR3-cas loci For GATCACTAGGTTCAGTTATTTC 224 [18]
Rev CATCGATTCATTATTCCTCCAA