Multiplex PCR amplification assay for the detection of <i> <sup>bla</sup> </i> SHV, <i> <sup>bla</sup> </i> TEM and <i> <sup>bla</sup> </i> CTX‐M genes in <i>Enterobacteriaceae</i>

H.‐J. MONSTEIN, Maud Nilsson, Måns Nilsson, K. Dornbusch, Lennart E. Nilsson

Apmis · 2007 · 359 citations · 18 references

Concepts

Abstract

Extended-spectrum beta-lactamases (ESBLs) are often mediated by (bla-)SHV, (bla)TEM and (bla)CTX-M genes in Enterobacteriaceae and other Gram-negative bacteria. Numerous molecular typing methods, including PCR-based assays, have been developed for their identification. To reduce the number of PCR amplifications needed we have developed a multiplex PCR assay which detects and discriminates between (bla-)SHV, (bla)TEM and (bla)CTX-M PCR amplicons of 747, 445 and 593 bp, respectively. This multiplex PCR assay allowed the identification of (bla-)SHV, (bla)TEM and (bla)CTX-M genes in a series of clinical isolates of Enterobacteriaceae with previously characterised ESBL phenotype. The presence of (bla)SHV, (bla)TEM and (bla)CTX-M genes was confirmed by partial DNA sequence analysis. Apparently, the universal well-established CTX-M primer pair used here to reveal plasmid-encoded (bla)CTX-M genes would also amplify the chromosomally located K-1 enzyme gene in all Klebsiella oxytoca strains included in the study.

References

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