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. 2014 May;80(10):3258–3265. doi: 10.1128/AEM.00231-14

TABLE 1.

Primers and probes for quantitative PCR used in the present study

Name Sequence (5′→3′)a Product size (bp) Annealing temp (°C) Final primer concn (nM) Target Reference
Universal bacteria
    BACT1369F CGGTGAATACGTTCYCGG 123 59 300 rrnS gene 29
    PROK1492R GGWTACCTTGTTACGACTT
    TM1389F HEX-CTTGTACACACCGCCCGTC-BHQ1
erm(B)
    ermB-F AAAACTTACCCGCCATACCA 139 65 400 Erythromycin resistance gene locus B 30
    ermB-R TTTGGCGTGTTTCATTGCTT
str(B)
    strB-F ATCGCTTTGCAGCTTTGTTT 143 61 300 Streptomycin phosphotransferase B 31
    strB-R ATGATGCAGATCGCCATGTA
    strB-P HEX-ATGCCTCGGAACTGCGT-BHQ1
sul1
    sul1-F GACTGCAGGCTGGTGGTTAT 105 64 200 Sulfamethazine resistance gene 1 This study
    sul1-R GAAGAACCGCACAATCTCGT
int1
    Int1F2 TCGTGCGTCGCCATCACA 67 62 400 Integrase class 1 23
    Int1R2 GCTTGTTCTACGGCACGTTTGA
IncW repA
    IncW-F GGCCATCGTATCAACGAGAT 153 61 300 repA gene from plasmid incompatibility group W This study
    IncW-R ATTGGTGCGCTCAAAGTAGC
    IncW-P HEX-AGCTGGCTTAGTCGGCTACA-BHQ1
a

HEX, 2′,4′,5′,7′-tetrachloro-6-carboxy-4,7-dichlorofluorescein succinimidyl ester; BHQ1, black hole quencher 1.