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. 2011 Jan 7;77(5):1601–1607. doi: 10.1128/AEM.02506-10

TABLE 1.

PCR primer sequences and conditions used in this study

Target Primers Sequences (5′-3′) PCR conditions Expected amplicon size (bp) Reference
16S rRNA genes 16s8F/16s806R AGAGTTTGATCCTGGCTCAG/GGACTACCAGGGTATCTAATCC 94°C, 5 min; 30 cycles of 94°C, 30 s, 62°C, 30 s, 72°C, 90 s 800 19
Integrase 1 gene (intl1) Int1F/Int1R CCTCCCGCACGATGATC/TCCACGCATCGTCAGGC 94°C, 5 min; 33 cycles of 94°C, 45 s, 64°C, 30 s, 72°C, 1 min 280 16
Integrase 2 gene (intI2) RB201/RB202 GCAAACGCAAGCATTCATTA/ACGGATATGCGACAAAAAGG 300 3
Class 1 gene cassette GC1_RLF/GC1_RLR GGCATCCAAGCAGCAAG/AAGCAGACTTGACCTGA 95°C, 5 min; 35 cycles of 94°C, 1 min, 55°C, 1 min, 72°C, 1.5 min Variable 5
CTX-M (blaCTX-M) CTX-M/F/CTX-M/R TTTGCGATGTGCAGTACCAGTAA/CTCCGCTGCCGGTTTTATC 95°C, 5 min; 35 cycles of 94°C, 1 min, 55°C, 1 min, 72°C, 1.5 min 500 11
CTX-M-1 (blaCTX-M-1) CTX-M-1-MP-F/CTX-M-1-MP-R AAAAATCACTGCGCCAGTTC/AGCTTATTCATCGCCACGTT 415 31
TEM (blaTEM) T1/T2 CCGTGTCGCCCTTATTCC/AGGCACCTATCTCAGCGA 800 32