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. 2010 Jul 23;76(18):6085–6100. doi: 10.1128/AEM.00447-10

TABLE 2.

List of loci and primers used for PCR amplification

Locus Expected product size (bp)a Hot startb Primer name and sequence (5′-3′)
Forward Reverse
ldh 921 No HdB35ldhF, CAAAAAATTATTTTAGTTGGCGACGGAGCAGTTGG HdB36ldhR, TTGTTTCATTGCRTCGTCWAG
lmo0490 791 Yes HdB37LMO490F, GCCACTCCAATCAGACACAGTTTATCACCAAC HdB38LMO490R, ACTGGCATTTCTTTGTGTGTCCAAATTTCGAAAGC
prs 809 No HdB40prsF, CCAAATTAACATTGAAGAAAGTATCCGTGGTTGTC HdB41prsR, GAACTTACAGAWGCATTYTCATGWAC
sigB 841 Yes Lm sigB15, AATATATTAATGAAAAGCAGGTGGAG Lm sigB16, ATAAATTATTTGATTCAACTGCCTT
polC 968 No HdB14polCF, CAAGCWGCTGATTGGGGWCAYAAAGC HdB15polCR, GCMGCTTGCATYCCTTTTTGCATCATYGCTTCA
rarA 860 No HdB30rarAF, ATGGCAATTCAACCTTTAGCTTACCGRATGCG HdB31rarAR, TCCTCATAWGCCATAACDAGCATTCTCC
LMO1555 712 No HdB32LMO1555F, ATGAKTAAAAAARTTRTTTTAACAAGAGARGC HdB33LMO1555R, CCTCCTGTATTATCAAATCAGCTARGTGCTTCATG
pbpA 1,240 Yes HdB20pbpAF, TCGCAGAAGTTGGAACCGAACGGCGGG HdB21pbpAR, GCAGCATARGCWCCRGCCATTTGCATTGG
addB 845 No HdB26addBF, TGGAAATGGGAAAAAGARGGMGAYTGGAT HdB27addBR, GCTTGYTTAGARCGAATRTAACTACTTTGTTC
LMO2763 1,216 Yes HdB39LMO2763F: GAACACGGCATGGAACGTGTTTTAGTACCAG HdB40LMO2763R, AGCCGACCAGAAGCGCGAGCCAGTTTCCTCCTG
a

The expected product size was calculated based on the respective gene sequence for L. monocytogenes EGD-e.

b

This column indicates whether hot start PCR was performed (hot start PCR was done by manual addition of the Taq polymerase after the initial denaturation step).