Volume 110, Issue 12 pp. 869-874

Modified pulsed-field gel electrophoresis protocol for typing of enterococci

BAHARAK SAEEDI

BAHARAK SAEEDI

Divisions of Clinical Microbiology and

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ANITA HÄLLGREN

ANITA HÄLLGREN

Divisions of Clinical Microbiology and

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JON JONASSON

JON JONASSON

Divisions of Clinical Microbiology and

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LENNART E. NILSSON

LENNART E. NILSSON

Divisions of Clinical Microbiology and

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HÅKAN HANBERGER

HÅKAN HANBERGER

Infectious Diseases, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, Linköping, Sweden

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BARBRO ISAKSSON

BARBRO ISAKSSON

Divisions of Clinical Microbiology and

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First published: 22 April 2003
Citations: 30
Baharak Saeedi, Division of Clinical Microbiology, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, S-581 85 Linköping, Sweden. e-mail: [email protected]

Received May 13, 2002.

Accepted October 4, 2002.

Abstract

Controlling the spread of vancomycin-resistant enterococci (VRE) is an important task in hospital epidemiology. Pulsed-field gel electrophoresis (PFGE) has become the golden standard for molecular epidemiological characterisation of enterococcal isolates. For separation of DNA fragments by PFGE, different electrophoresis conditions have been recommended, but none of these protocols allows a satisfactory separation of both small and large DNA fragments of enterococci simultaneously. In this study we have speeded up the preparation of chromosomal DNA and defined new electrophoresis conditions that enhance separation of small and large DNA fragments for subtyping of enterococci with a 24 h PFGE.

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