Food Protection Trends

Abstracts - August 2007

Detection of Nonpathogenic and Pathogenic Listeria Species by Use of a Chromogenic Agar
 

Removal of Bacteria from Fingertips and the Residual Amount Remaining on the Hand Washing Nailbrush 

Survey of Consumer Attitudes and the Effectiveness of Hand Cleansers in the Home  


Detection of Nonpathogenic and Pathogenic Listeria Species by Use of a Chromogenic Agar

Lawrence Restaino, Elon W. Frampton, Wiliam C. Lionberg, and Anthony L. Restaino

R & F Laboratories, 2725 Curtiss St., Downers Grove, IL 60515, USA

SUMMARY
A selective and differential chromogenic plating medium (R & F Listeria spp./Listeria monocytogenes Plating Medium [LSPM]) has been developed that simultaneously differentiates presumptive colonies of both the nonpathogenic Listeria species (L. innocua, L. seeligeri, L. welshimeri, and L. grayi) and the pathogenic species (L. monocytogenes and L. ivanovii) on a single plate in 42–48 h at 35ºC. Unlike chromogenic media that produce only a single color in detecting the presence of all Listeria species on the basis of ß-glucosidase activity, or those that specifically detect the two pathogenic species by phosphatidylinositol-specific-phospholipase C activities (PI-PLC), LSPM contains a combination of indoxyl-derivative chromogenic substrates with which colonies of nonpathogenic Listeria species are pink because of their β-glucosidase activity, and pathogenic species are blue-green to blue-violet, depending on the strain-specific balance of β-glucosidase and PI-PLC activities on an agar with an opaque white background. On LSPM, 39 pure culture strains of L. monocytogenes yielded blue-green to blue-violet colonies 1–2 mm in diameter with or without surrounding precipitates in 42–48 h, and 4 strains of L. ivanovii yielded dark blue-green colonies with dark precipitates, whereas all of the nonpathogenic Listeria strains yielded pink colonies 1–2 mm diameter without precipitates. The ability to differentiate Listeria spp. from L. monocytogenes over a broad range on the same plate of LSPM was demonstrated at ratios of 1:1 to 100:1 of L. innocua to L. monocytogenes. Additionally, a high level of selectivity by this plating medium was evidenced by the lack of growth by common species of five gram-positive genera (Bacillus, Staphylococcus, Lactobacillus, Pediococcus, and Enterococcus), and eight gram-negative genera (Escherichia, Enterobacter, Citrobacter, Shigella, Morganella, Providencia, Pantoea, and Klebsiella). Two yeast genera, Zygosaccharomyces and Candida, also failed to grow at 35ºC.

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Removal of Bacteria from Fingertips and the Residual Amount Remaining on the Hand Washing Nailbrush

O. Peter Snyder, Jr.

Hospitality Institute of Technology and Management, 670 Transfer Road, Suite 21A, St. Paul, MN 55114, USA

SUMMARY
The purpose of this study, which utilized 3 volunteer participants, was to measure the effectiveness of the double hand-washing procedure for removing non-pathogenic surrogate Escherichia coli organisms from fingertips and to measure the residual E. coli remaining on the nailbrush. Data from the experiment show that use of the nailbrush during hand and fingertip washing (Wash #1) reduced an inoculum of E. coli on fingertips by 2.98 log10 CFU/ml, an almost 1,000–fold reduction. When Wash #1 was followed by a 10-s wash without the nailbrush (Wash #2), there was an additional reduction of 1.72 log10 CFU/ ml, an approximately 50–fold reduction. Added together, there was a total average reduction of 4.70 log10 CFU/ml. Thus, the double hand-wash method was shown to reduce bacteria on fingers and to offer a validated solution for the foodservice operation that wishes to use the FDA Food Code provision of §3-301.11(D)(6) as an alternative to gloving. The average E. coli population remaining on the nailbrush after use during Wash #1 was measured, and it was found that retention was less than 1 in 107 of the initial bacterial inoculum.

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Survey of Consumer Attitudes and the Effectiveness of Hand Cleansers in the Home

Janice M. Brown-1*, John S. Avens-2, Patricia A. Kendall-2, Dorene R. Hyatt-3, and Martha B. Stone-2

1-Dept. of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA
2-Dept. of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523-1571, USA
3-Dept. of Microbiology Immunology & Pathology, Colorado State University, Fort Collins, CO 80523-1644, USA

SUMMARY
Although frequent hand washing reduces microbial load, the best handcleansing agents and hand washing methodologies to employ to reduce microbial load on hands are not obvious. The objectives of this study were to determine public attitudes about available hand cleansers and to determine the effectiveness of three hand cleansers in reducing bacteria on hands. A survey was distributed to ascertain the rationale used to select specific hand cleansers for use in the home. Most respondents believed that regular hand soaps (no active ingredient) were not as effective as antibacterial soaps in reducing bacteria on hands. Liquid hand soap, antibacterial liquid hand soap, and an alcohol gel sanitizer were evaluated to determine their effectiveness in reducing bacteria on hands. Comparisons made between pre-wash agar touch plates and post-wash agar touch plates showed that all three hand cleansers reduced bacteria on hands when a 20 s hand wash procedure was used. No significant differences (P > 0.05) were detected between relative colony numbers (RCN), defined as a visible range of bacterial or fungal colonies, obtained with liquid hand soap with antibacterial ingredients and liquid hand soap without
such ingredients. However, alcohol gel significantly reduced (P ≤ 0.05) RCN on hands, compared to results with liquid hand soap and antibacterial hand soap.


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