Bacteriophage strain typing by rapid single molecule analysis

Nucleic Acids Res. 2015 Oct 15;43(18):e117. doi: 10.1093/nar/gkv563. Epub 2015 May 27.

Abstract

Rapid characterization of unknown biological samples is under the focus of many current studies. Here we report a method for screening of biological samples by optical mapping of their DNA. We use a novel, one-step chemo-enzymatic reaction to covalently bind fluorophores to DNA at the four-base recognition sites of a DNA methyltransferase. Due to the diffraction limit of light, the dense distribution of labels results in a continuous fluorescent signal along the DNA. The amplitude modulations (AM) of the fluorescence intensity along the stretched DNA molecules exhibit a unique molecular fingerprint that can be used for identification. We show that this labelling scheme is highly informative, allowing accurate genotyping. We demonstrate the method by labelling the genomes of λ and T7 bacteriophages, resulting in a consistent, unique AM profile for each genome. These profiles are also successfully used for identification of the phages from a background phage library. Our method may provide a facile route for screening and typing of various organisms and has potential applications in metagenomics studies of various ecosystems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteriophage Typing / methods*
  • Bacteriophages / classification
  • Bacteriophages / genetics
  • DNA Barcoding, Taxonomic
  • Fluorescent Dyes
  • Genome, Viral
  • Molecular Typing / methods
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)

Substances

  • Fluorescent Dyes
  • DNA modification methylase TaqI
  • Site-Specific DNA-Methyltransferase (Adenine-Specific)