Affiliations 

  • 1 Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia. howingsze86@hotmail.com
  • 2 State Key Laboratory for Microbial Metabolism and School of Life Sciences & Biotechnology, Shanghai Jiaotong University, 200030, Shanghai, China. hyou@sjtu.edu.cn
  • 3 Biomedical Research Centre, Faculty of Medicine, Universiti Sultan Zainal Abidin, 20400, Kuala Terengganu, Malaysia. yeocc@unisza.edu.my
  • 4 Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia. thongkl@um.edu.my
BMC Genomics, 2015;16:199.
PMID: 25879448 DOI: 10.1186/s12864-015-1421-8

Abstract

Strains of Escherichia coli that are non-typeable by pulsed-field gel electrophoresis (PFGE) due to in-gel degradation can influence their molecular epidemiological data. The DNA degradation phenotype (Dnd(+)) is mediated by the dnd operon that encode enzymes catalyzing the phosphorothioation of DNA, rendering the modified DNA susceptible to oxidative cleavage during a PFGE run. In this study, a PCR assay was developed to detect the presence of the dnd operon in Dnd(+) E. coli strains and to improve their typeability. Investigations into the genetic environments of the dnd operon in various E. coli strains led to the discovery that the dnd operon is harboured in various diverse genomic islands.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.