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. 2010 Nov 15;55(2):904–909. doi: 10.1128/AAC.00962-10

TABLE 1.

Sequences of primers used for specific gene detection

Targeta Primer nameb Primer sequence (5′ to 3′) Size (bp) Ta (°C)c Source or reference
armA armA-F AGGTTGTTTCCATTTCTGAG 405 51 This work
armA-R ACCTATACTTTATCGTCGTC
rmtA rmtA-F CGTGACATAACATCTGTATG 333 51 This work
rmtA-R TTCAAATTCATCAGGCAGTG
rmtB rmtB-F ATTGGGATTTTACCTTTGCC 290 51 This work
rmtB-R TATAAGTTCTGTTCCGATGG
rmtC rmtC-F AGATACCAAATCCAACTACG 369 51 This work
rmtC-R TAAGTAGAAGATCACTCTCG
rmtD rmtD-F TCAAAAAGGAAAAGGACGTG 500 51 This work
rmtD-R CGATGCGACGATCCATTC
rmtD-F2d ATGAGCGAACTGAAGGAAAAAC 744 57 This work
rmtD-R2d TCATTTTCGTTTCAGCACGTAAA
npmA npmA-F CTCAAAGGAACAAAGACGG 641 51 7
npmA-R GAAACATGGCCAGAAACTC
blaTEM tem1-F ATGAGTATTCAACATTTTCGTG 861 55 This work
tem1-R TTACCAATGCTTAATCAGTGAG
blaSHV shv1-F ATGCGTTATATTCGCCTGTG 861 55 This work
shv1-R TTAGCGTTGCCAGTGCTCG
blaCTX-M ctx-MU1 ATGTGCAGYACCAGTAARGT 803 55 13
ctx-MU2 TGGGTRAARTARGTSACCAG
blaKPC Uni-KPC-F ATGTCACTGTATCGCCGTCT 882 55 17
Uni-KPC-R TTACTGCCCGTTGACGCCC
qnrB qnrB-F CCGACCTGAGCGGCACTGA 523 55 18
qnrB-R CGCTCCATGAGCAACGATGCCT
a

rmtE was reported after the conclusion of this work, and its analysis was not included.

b

F, forward; R, reverse.

c

Ta, PCR annealing temperature.

d

Primers to amplify the complete rmtD gene.