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Journal of Clinical Microbiology, April 2006, p. 1567-1570, Vol. 44, No. 4
0095-1137/06/$08.00+0 doi:10.1128/JCM.44.4.1567-1570.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Center for the Study of Emerging and Reemerging Pathogens,1 Division of Infectious Diseases, Department of Internal Medicine,2 Department of Microbiology and Molecular Genetics, The University of Texas Medical School at Houston, Houston, Texas 77030,3 Area de Bioquímica y Biología Molecular, Universidad de La Rioja, 26006 Logroño, Spain,4 Bacterial Molecular Genetics Unit, Universidad El Bosque, Transv 9aA Bis No. 133-25, Bogotá, D.C., Colombia5
Received 19 November 2005/ Returned for modification 23 January 2006/ Accepted 9 February 2006
During an evaluation of PCR for identification of isolates of Enterococcus hirae, a homologue with 82% identity to E. hirae mur-2 was identified in Enterococcus durans and was named mur-2ed. PCR using primers for two genes (copY and murG) of E. hirae strains showed amplification with E. hirae strains only. PCR (under high-stringency conditions) with primers for the mur-2ed gene gave the expected amplification product only with E. durans strains. A combination of murG and mur-2ed primers in a multiplex PCR assay differentiated E. hirae from E. durans in all cases. PCR using these primers appears to be a rapid alternative for identification of E. hirae and E. durans isolates.
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