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. 2020 Dec 1;20:909. doi: 10.1186/s12879-020-05534-1

Table 2.

Primer sequences, fragment size, and PCR conditions for detection of virulence genes in Pseudomonas aeruginosa

Gene Primer sequence (5′➔3′) Fragment size (bp) Annealing T (°C)
algD F: AAGGCGGAAATGCCATCTCC 290 60
R: AGGGAAGTTCCGGGCGTTTG
exoY F: TATCGACGGTCATCGTCAGGT 1035
R: TTGATGCACTCGACCAGCAAG
plcH F: GCACGTGGTCATCCTGATGC 608
R: TCCGTAGGCGTCGACGTAC
rhIR F: TGCATTTTATCGATCAGGGC 133 57
R: CACTTCCTTTTCCAGGACG
lasI F: CGTGCTCAAGTGTTCAAGG 295
R: TACAGTCGGAAAAGCCCAG
apr F: TGTCCAGCAATTCTCTTGC 1017
R: CGTTTTCCACGGTGACC
exoT F: CAATCATCTCAGCAGAACCC 1159
R: TGTCGTAGAGGATCTCCTG
rhII F: TTCATCCTCCTTTAGTCTTCCC 155
R: TTCCAGCGATTCAGAGAGC
exoS F: CGTCGTGTTCAAGCAGATGGTGCTG 444 65
R: CCGAACCGCTTCACCAGGC
plcN F: TCCGTTATCGCAACCAGCCCTACG 481
R: TCGCTGTCGAGCAGGTCGAAC
lasB F: GGAATGAACGAAGCGTTCTCCGAC 284
R: TGGCGTCGACGAACACCTCG
lasR F: AAGTGGAAAATTGGAGTGGAG 130
R: GTAGTTGCCGACGACGATGAAG
algU F: CGCGAACCGCACCATCGCTC 1500 66
R: GCCGCACGTCACGAGC
exoU F: TACCAGGTACGGCCATGTTC 575 59
R: ACGCTCTGAAGCCTGAAGAC

Bp Base pairs; F Forward; R Reverse; T Temperature

PCR was performed following the manufacturer’s instructions