Evaluation of AFLP, a high-resolution DNA fingerprinting method, as a tool for molecular subtyping of enterohemorrhagic Escherichia coli O157:H7 isolates

Microbiol Immunol. 1999;43(8):803-6. doi: 10.1111/j.1348-0421.1999.tb02473.x.

Abstract

The amplified fragment-length polymorphism (AFLPTM) technique is based on the selective PCR amplification of restriction fragments. We investigated the utility of AFLP in the molecular subtyping of enterohemorrhagic Escherichia coli serotype O157:H7 isolates. We analyzed a total of 46 isolates of E. coli O157:H7 along with other serotypes, O26:H11, 0114:H19 and 0119:NT. Isolates of E. coli O157:H7 derived from the same outbreak showed an identical AFLP-banding pattern and were subtyped into the same group, giving results almost consistent with those of a pulsed-field gel electrophoresis (PFGE) study, while other serotypes showed clearly different patterns from those of E. coli O157:H7. These results suggest that the AFLP technique has potential as an alternative tool for the molecular epidemiology of E. coli O157:H7.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Typing Techniques*
  • DNA Fingerprinting / methods*
  • DNA Primers
  • DNA, Bacterial / analysis
  • Deoxyribonucleases, Type II Site-Specific
  • Escherichia coli O157 / classification*
  • Escherichia coli O157 / genetics
  • Escherichia coli O157 / isolation & purification
  • Evaluation Studies as Topic
  • Humans

Substances

  • DNA Primers
  • DNA, Bacterial
  • endodeoxyribonuclease MseI
  • Deoxyribonucleases, Type II Site-Specific