Persistence of Escherichia coli O157:H7 on the rhizosphere and phyllosphere of lettuce

Lett Appl Microbiol. 2009 Dec;49(6):784-90. doi: 10.1111/j.1472-765X.2009.02745.x. Epub 2009 Sep 22.

Abstract

Aims: The major objective of this study was to determine the effects of low levels of Escherichia coli O157:H7 contamination on plant by monitoring the survival of the pathogen on the rhizosphere and leaf surfaces of lettuce during the growth process.

Methods and results: Real-time PCR and plate counts were used to quantify the survival of E. coli O157:H7 in the rhizosphere and leaf surfaces after planting. Real-time PCR assays were designed to amplify the stx1, stx2 and the eae genes of E. coli O157:H7. The detection limit for E. coli O157:H7 quantification by real-time PCR was 2.4 x 10(3) CFU g(-1) of starting DNA in rhizosphere and phyllosphere samples and about 10(2) CFU g(-1) by plate count. The time for pathogens to reach detection limits on the leaf surface by plate counts was 7 days after planting in comparison with 21 days in the rhizosphere. However, real-time PCR continued to detect stx1, stx2 and the eae genes throughout the experimental period.

Conclusion: Escherichia coli O157:H7 survived throughout the growth period as was determined by real-time PCR and by subsequent enrichment and immunomagnetic separation of edible part of plants.

Significance and impact of the study: The potential presence of human pathogens in vegetables grown in soils contaminated with E. coli O157:H7 is a serious problem to our national food supply as the pathogen may survive on the leaf surface as they come in contact with contaminated soil during germination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Colony Count, Microbial
  • DNA, Bacterial / analysis
  • Escherichia coli O157 / genetics
  • Escherichia coli O157 / growth & development*
  • Food Contamination / analysis*
  • Food Microbiology*
  • Immunomagnetic Separation
  • Lactuca / microbiology*
  • Limit of Detection
  • Plant Leaves / microbiology
  • Polymerase Chain Reaction / methods
  • Soil Microbiology

Substances

  • DNA, Bacterial