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. 2016 May 26;11(5):e0156383. doi: 10.1371/journal.pone.0156383

Table 1. PCR primers used in this study.

Target Gene Primer Sequence (5’-3’) Traditional PCR annealing temp. (°C) qPCR annealing temp. (°C) Ampliconsize (bp) Source
blaKPC-2 K-FW ATGTCACTGTATCGCCGTCT 55 - 893 [33]
K-RV TTTTCAGAGCCTTACTGCCC
S-blaKPC-2 SK-FW GCTTCCCACTGTGCAGCTCATTC 66.1 66.1 213 This study
SK-RV CGCCCAACTCCTTCAGCAACAAATTG
S-blaGES-1 SG-FW ATGGCACGTACTGTGGCTAA 56 56 287 This study
SG-RV TGACCGACAGAGGCAACTAAT
blaIMP-1 I-FW GGAATAGAGTGGCTTAAYTCTC 50 50 232 [34]
I-RV GGTTTAAYAAAACAACCACC
blaVIM-2 V-FW GTTTGGTCGCATATCGCAAC 60 - 382 [34]
V-RV AATGCGCAGCACCAGGATAG
blaOXA-48 O-FW GCGTGGTTAAGGATGAACAC 47 47 438 [34]
O-RV CATCAAGTTCAACCCAACCG
16S rRNA 16S-FW CGGTGAATACGTTCYCGG 58 57.5 126 [35]
16S-RV GGWTACCTTGTTACGACTT
16S rRNA 27F AGAGTTTGATCCTGGCTCAG 56 - 1466 [36]
1492R GGTTACCTTGTTACGACTT