This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Macovei, L.
Right arrow Articles by Zurek, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Macovei, L.
Right arrow Articles by Zurek, L.
Agricola
Right arrow Articles by Macovei, L.
Right arrow Articles by Zurek, L.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, November 2007, p. 6740-6747, Vol. 73, No. 21
0099-2240/07/$08.00+0     doi:10.1128/AEM.01444-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Influx of Enterococci and Associated Antibiotic Resistance and Virulence Genes from Ready-To-Eat Food to the Human Digestive Tract{triangledown}

Lilia Macovei and Ludek Zurek*

Department of Diagnostic Medicine and Pathobiology,1 Department of Entomology, Kansas State University, Manhattan, Kansas 665062

Received 28 June 2007/ Accepted 23 August 2007

The influx of enterococcal antibiotic resistance (AR) and virulence genes from ready-to-eat food (RTEF) to the human digestive tract was assessed. Three RTEFs (chicken salad, chicken burger, and carrot cake) were sampled from five fast-food restaurants five times in summer (SU) and winter (WI). The prevalence of enterococci was significantly higher in SU (92.0% of salad samples and 64.0% of burger samples) than in WI (64.0% of salad samples and 24.0% of burger samples). The overall concentrations of enterococci during the two seasons were similar (~103 CFU/g); the most prevalent were Enterococcus casseliflavus (41.5% of isolates) and Enterococcus hirae (41.5%) in WI and Enterococcus faecium (36.8%), E. casseliflavus (27.6%), and Enterococcus faecalis (22.4%) in SU. Resistance in WI was detected primarily to tetracycline (50.8%), ciprofloxacin (13.8%), and erythromycin (4.6%). SU isolates were resistant mainly to tetracycline (22.8%), erythromycin (22.1%), and kanamycin (13.0%). The most common tet gene was tet(M) (35.4% of WI isolates and 11.9% of SU isolates). The prevalence of virulence genes (gelE, asa1, cylA, and esp) and marker genes for clinical isolates (EF_0573, EF_0592, EF_0605, EF_1420, EF_2144, and pathogenicity island EF_0050) was low (≤12.3%). Genotyping of E. faecalis and E. faecium using pulsed-field gel electrophoresis revealed that the food contamination likely originated from various sources and that it was not clonal. Our conservative estimate (single AR gene copy per cell) for the influx of tet genes alone to the human digestive tract is 3.8 x 105 per meal (chicken salad). This AR gene influx is frequent because RTEFs are commonly consumed and that may play a role in the acquisition of AR determinants in the human digestive tract.


* Corresponding author. Mailing address: Department of Diagnostic Medicine and Pathobiology and Department of Entomology, Kansas State University, Manhattan, KS 66506. Phone: (785) 532-4731. Fax: (785) 532-6232. E-mail: lzurek{at}ksu.edu

{triangledown} Published ahead of print on 31 August 2007.


Applied and Environmental Microbiology, November 2007, p. 6740-6747, Vol. 73, No. 21
0099-2240/07/$08.00+0     doi:10.1128/AEM.01444-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.