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. 2011 Dec;55(12):5493–5499. doi: 10.1128/AAC.05118-11

Table 2.

Pairs of primers used in the PCR mapping assay analyzing the pKpQIL-like plasmids

Primer Sequence (5′ → 3′) Annealing positionsa Product size (bp) pKpQIL fragment analyzeda Resultb
RepAF GCTGAGCGTAAATCTCAC 4439–4456 159 IncFIIK replicon region (FIIKrepA gene) +
RepAR CTCAACCTCACGCTTCAG 4580–4597
RepAF GCTGAGCGTAAATCTCAC 4439–4456 1,497 Junction between the FIIK replicon region and the pNYC-derived region +
ORF8R CAGACGTGATTTTCTGACCAC 5915–5935
ORF11R GCATGTTTGAACTGGTCAG 8347–8365 682 Junction between Tn4401 and its 5′ flank within the pNYC region +
tnpRF CGACGTCGATGTATTTGCATG 9008–9028
IS26LF GTCGGTGGTGATAAAC 25556–25571 2,847 IS26 insertion within 1331 the pKPN4-derived Tn +/−
TEM-F TTACTGTCATGCCATCC 28386–28402
OXA-9F CTGCTGCATATGTTGGTG 26542–26559 1,861 Junction between blaOXA-9 and blaTEM-1 within the pKPN4 Tn1331 +/−
TEM-F TTACTGTCATGCCATCC 28386–28402
rep2R TCTGCTGGTTATTGGGTGAG 53337–53356 312 FIB-like repA gene within the pKPN4 region +
rep2F GTCTTCGCAGCACAACTATC 53629–53648
TraXF CGCAATGTTCTATGCTGTG 112918–112936 1,576 Junction between the pKPN4 region (traX gene) and the FIIK replicon region +/−
ORF2R CAGAATAACTGCTGCTCAG 838–856
a

Position numbering and the description of plasmid regions is according to reference 25 and the pKpQIL sequence (GenBank accession no. GU595196).

b

Symbols: +, PCR worked with all plasmids analyzed; +/−, PCR worked, but not with all plasmids analyzed.