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. 2012 Mar;56(3):1635–1638. doi: 10.1128/AAC.06182-11

Table 2.

blaKPC excision patterns in additional Tn4401-bearing strains

Strain Species InC type(s)a MLSTb KPC Tn4401 variantc Size(s) of Tn4401 deletion pattern(s) (bp)d
1 K. pneumoniae N, FIIs 63 KPC-4 b 160, 278, 430
2 K. pneumoniae Unk 76 KPC-3 a 155, 217
3 K. pneumoniae FIIs 234 KPC-2 a 289
4 K. pneumoniae FIIs 258 KPC-2 a 278, 430
5 K. pneumoniae FIIs 258 KPC-3 b 186, 278, 430
6 K. pneumoniae N, A/C 258 KPC-2 a 215, 278, 430
7 K. pneumoniae Unk 258 KPC-2 a 191, 278, 430
8 K. pneumoniae FIIs 258 KPC-3 b 278, 430
9 K. pneumoniae FIIs 258 KPC-3 −68 255
10 K. pneumoniae A/C 486 KPC-2 b 278, 430
11 E. coli L1, N, Y, FIA, FIB, FIIs 2 KPC-2 b 278, 430
12 E. coli L1, N, Y, FIA, FIB, FIIs 2 KPC-3 b 278, 430
13 E. coli L1, FIA, FIB, FIIs 43 KPC-2 a 278, 430
14 E. coli FIB, A/C, Frep 33 KPC-2 a 278, 430
15 E. coli A/C 35 KPC-3 b 278
a

Plasmid replicon typing was performed using a method previously described by Carattoli et al. (2). Unk, unknown.

b

MLST for K. pneumoniae was performed using the method described by Diancourt et al. (9); MLST for E. coli was performed using the Institut Pasteur MLST scheme (http://www.pasteur.fr/recherche/genopole/PF8/mlst/EColi.html).

c

Tn4401 variants were identified by PCR (6), followed by DNA sequencing. “−68” indicates the previously described variant with a 68-bp deletion upstream of blaKPC (13).

d

Tn4401 deletion patterns were identified by nested PCR and are expressed as the PCR product length resulting from amplification with primer set F2/R2.