Elliot Ryser

Dr. Elliot Ryser


Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 May 2009 in Journal of Food Protection
Verified
Journal Article
Closed access
AWAlissa M. Wesche
Alissa M. Wesche
JGJoshua B. Gurtler
Joshua B. Gurtler
BMBradley P. Marks
Bradley P. Marks
ERElliot Ryser
Elliot Ryser
Environmental stress and food preservation methods (e.g., heating, chilling, acidity, and alkalinity) are known to induce adaptive responses within the bacterial cell. Microorganisms that survive a...

1 April 2004 in Journal of Food Protection
Verified
Journal Article
Closed access
ACArzu Cagri
Arzu Cagri
ZUZeynep Ustunol
Zeynep Ustunol
ERElliot Ryser
Elliot Ryser
Increasing consumer demand for microbiologicallysafer foods, greater convenience,smaller packages, and longer product shelf life is forcing the industry to develop new food-processing,cooking, hand...

1 April 2004 in Journal of Food Protection
Verified
Journal Article
Closed access
SRStephanie L. Rodgers
Stephanie L. Rodgers
JCJerry N. Cash
Jerry N. Cash
MSMohammad Siddiq
Mohammad Siddiq
ERElliot Ryser
Elliot Ryser
Ozone (3 ppm), chlorine dioxide (3 and 5 ppm), chlorinated trisodium phosphate (100- and 200-ppm chlorine), and peroxyacetic acid (80 ppm) were assessed for reduction of Escherichia coli O157:H7 an...

1 August 2001 in Journal of Food Science
Verified
Journal Article
Closed access
PDF file
ACA. Cagri
A. Cagri
ZUZ. Ustunol
Z. Ustunol
ERElliot Ryser
Elliot Ryser

1 March 2006 in Journal of Food Protection
Verified
Journal Article
Closed access
KVKeith L. Vorst
Keith L. Vorst
Ewen ToddEwen Todd
Ewen Todd
ERElliot Ryser
Elliot Ryser
A commercial delicatessen slicer was used as the vector for sequential quantitative transfer of Listeria monocytogenes (i) from an inoculated slicer blade (∼108, 105, or 103 CFU per blade) to 30 slices of uninoculated delicatessen turkey, bologna, and salami, (ii) from inoculated product (∼108 CFU/cm2) to the slicer, and (iii) from inoculated product (108, 105, or 103 CFU/cm2) to 30 slices of uninoculated product via the slicer blade. Cutting force and product composition also were assessed for their impact on L. monocytogenes transfer. Five product contact areas on the slicer, which were identified from residue of product bathed in Glow-Germ, were also sampled using a 1-ply composite tissue technique after inoculated product had been sliced. After being sliced with inoculated blades, each product slice was surface or pour plated on modified Oxford agar and/or enriched in University of Vermont medium. Greater transfer (P < 0.05) occurred from inoculated turkey (108 CFU/cm2) to the five slicer contact area...

1 July 2012 in Journal of Food Protection
Verified
Journal Article
Closed access
ABAnnemarie L. Buchholz
Annemarie L. Buchholz
GDGordon R. Davidson
Gordon R. Davidson
BMBradley P. Marks
Bradley P. Marks
Ewen ToddEwen Todd
Ewen Todd
ERElliot Ryser
Elliot Ryser
Postharvest contamination and subsequent spread of Escherichia coli O157:H7 can occur during shredding, conveying, fluming, and dewatering of fresh-cut leafy greens. This study quantified E. coli O157:H7 transfer from leafy greens to equipment surfaces during simulated small-scale commercial processing. Three to five batches (22.7 kg) of baby spinach, iceberg lettuce, and romaine lettuce were dip inoculated with a four-strain cocktail of avirulent, green fluorescent protein-labeled, ampicillinresistant E. coli O157:H7 to contain ∼10(6), 10(4), and 10(2) CFU/g, and then were processed after 1 h of draining at ∼23°C or 24 h of storage at 4°C. Lettuce was shredded using an Urschel TransSlicer at two different blade and belt speeds to obtain normal (5 by 5 cm) and more finely shredded (0.5 by 5 cm) lettuce. Thereafter, the lettuce was step conveyed to a flume tank and was washed and then dried using a shaker table and centrifugal dryer. Product (25-g) and water (40-ml) samples were collected at various points during processing. After processing, product contact surfaces (100 cm(2)) on the shredder (n = 14), conveyer (n = 8), flume tank (n = 11), shaker table (n = 9), and centrifugal dryer (n = 8) were sampled using one-ply composite tissues. Sample homogenates diluted in phosphate or neutralizing buffer were plated, with or without prior 0.45- m m membrane filtration, on Trypticase soy agar containing 0.6% yeast extract supplemented with 100 ppm of ampicillin to quantify green fluorescent protein-labeled E. coli O157:H7 under UV light. During leafy green processing, ∼90% of the E. coli O157:H7 inoculum transferred to the wash water. After processing, E. coli O157:H7 populations were highest on the conveyor and shredder (P<0.05), followed by the centrifugal dryer, flume tank, and shaker table, with ∼29% of the remaining product inoculum lost during centrifugal drying. Overall, less (P<0.05) of the inoculum remained on the product after centrifugally drying iceberg lettuce that was held for 1 h (8.13%) as opposed to 24 h (42.18%) before processing, with shred size not affecting the rate of E. coli O157:H7 transfer.