Skip to main content
. 2005 May;43(5):2241–2245. doi: 10.1128/JCM.43.5.2241-2245.2005

TABLE 1.

Nucleotide sequences of oligonucleotides used for PCR amplifications and sequencing of blaOXA-23-like, blaOXA-24-like, blaIMP-type, and blaVIM-type genes

Primer (orientation)a Accession no. of blab Sequence (5′→3′) Annealing sitec Amplicon size (bp)d
OXA-23F (F) AJ132105 GATGTGTCATAGTATTCGTCGT −108 to −87 1,058
OXA-23R (R) AF201828 TCACAACAACTAAAAGCACTGT +929 to +950 (OXA-23F/-23R)
OXA-24F (F) AJ239129, AF201826 ATGAAAAAATTTATACTTCCTATATTCAGC +1 to +30 825
OXA-24R (R) AF201827, AF509241 TTAAATGATTCCAAGATTTTCTAGC +801 to +825 (OXA-24F/-24R)
IMP-F (F) S71931, AB010417, AF290912 CATGGTTTGGTGGTTCTTGT +154 to +173 488
IMP-R (R) AB040994, AB074433 ATAATTTGGCGGACTTTGGC +582 to +601 (IMP-1F/-1R)    
VIM-F (F) AF191564, AF300454, AY165025 ATTGGTCTATTTGACCGCGTC +24 to +44 780
VIM-R (R) AY524987, AY524988, AY524989 TGCTACTCAACGACTGAGCG +784 to +803 (VIM-2F/-2R)    
a

Orientation of each primer: F, forward; R, reverse.

b

β-lactamase genes (bla) used in the multiple sequence alignment for designing each primer pair.

c

Positions of annealing sites are with respect to the first nucleotide of the coding region (+1).

d

The primer pair for PCR amplification is indicated in parentheses.