Efficacy of ATP Monitoring for Measuring Organic Matter on Postharvest Food Contact Surfaces

2020 ◽  
Vol 83 (10) ◽  
pp. 1829-1837
Author(s):  
KRISTIN LANE ◽  
LYNNE A. McLANDSBOROUGH ◽  
WESLEY R. AUTIO ◽  
AMANDA J. KINCHLA

ABSTRACT The Food Safety Modernization Act, specifically the Produce Safety Rule, requires growers to clean and sanitize food contact surfaces to protect against produce contamination. An ATP monitoring device is a potential sanitation tool to monitor the efficacy of an on-farm cleaning and sanitation program that could help growers meet regulatory expectations mandated by the Produce Safety Rule. This ATP monitoring device uses bioluminescence to detect all ATP (found in bacteria and produce matter cells) from a swabbed surface. Because little work has been done to test the efficacy of these tools under postharvest conditions, the present study evaluated ATP measurement for postharvest food contact surface cleanliness evaluation. Concentrations of leafy greens (spinach, romaine, and red cabbage, with or without Listeria innocua) were used as organic matter applied to stainless steel, high-density polyethylene plastic, and bamboo wood coupons to represent postharvest food contact surfaces. The ATP levels on the coupons were then measured by using swabs and an ATP monitoring device. Results showed that the concentration of L. innocua and leafy greens on a food contact surface had a highly significant effect on the ATP monitoring device reading (P < 0.0001). The ATP monitoring device had a lower limit of detection for L. innocua at 4.5 log CFU per coupon. The type of leafy green on a food contact surface did not affect the ATP reading (P = 0.88). Leafy greens with added L. innocua had a higher ATP reading when compared with saline and L. innocua, demonstrating the presence of leafy green matter contributes to ATP reading when combined with L. innocua. The different food contact surfaces had different ATP response readings (P = 0.03), resulting in no detectable levels of bacteria and/or leafy green material from bamboo wood surfaces (P = 0.16). On the basis of our results, the ATP measurement is an appropriate tool to measure produce or bacterial contamination on stainless steel or high-density polyethylene plastic surfaces; however, it is not recommended for wood surfaces. HIGHLIGHTS

1980 ◽  
Vol 43 (6) ◽  
pp. 447-449 ◽  
Author(s):  
K. E. EUGSTER ◽  
B. J. SKURA ◽  
W. D. POWRIE

A rapid method for detection and quantitation of lipid-containing food soils on food-contact surfaces has been developed to ascertain whether these surfaces have been properly cleaned. The method is based on transfer of lipid-based soils from a food-contact surface to a polyethylene film and subsequent quantitation of the lipid, at 1750 cm−1, by infrared spectrophotometry. Peak height at 1750 cm−1 is linearly related to the quantity of lipid on the polyethylene surface. Standard curves for peak-height against lipid distribution on the polyethylene film were constructed for stainless steel, glass and three types of plastic cutting board material (high density polyethylene, smooth nylotrol and rough nylotro).


2001 ◽  
Vol 64 (9) ◽  
pp. 1430-1434 ◽  
Author(s):  
BALDEV R. GULATI ◽  
PAUL B. ALLWOOD ◽  
CRAIG W. HEDBERG ◽  
SAGAR M. GOYAL

Norwalk and Norwalk-like viruses (NLVs) are important causes of foodborne gastroenteritis in restaurant-related outbreaks. Efficacy of common disinfection methods against these viruses on food-contact surfaces and fresh produce is not known partially because of their nonculturability. Seven commercial disinfectants for food-contact surfaces and three sanitizers for fruits and vegetables were tested against cultivable feline calicivirus (FCV). Disks of stainless steel, strawberry, and lettuce were contaminated with known amounts of FCV. The disinfectants were applied at one, two, and four times the manufacturer's recommended concentrations for contact times of 1 and 10 min. The action of disinfectant was stopped by dilution, and the number of surviving FCVs was determined by titration in cell cultures. An agent was considered effective if it reduced the virus titer by at least 3 log10 from an initial level of 107 50% tissue culture infective dose. None of the disinfectants was effective when used at the manufacturer's recommended concentration for 10 min. Phenolic compounds, when used at two to four times the recommended concentration, completely inactivated FCV on contact surfaces. A combination of quaternary ammonium compound and sodium carbonate was effective on contact surfaces at twice the recommended concentration. Rinsing of produce with water alone reduced virus titer by 2 log10. On artificially contaminated strawberry and lettuce, peroxyacetic acid and hydrogen peroxide was the only effective formulation when used at four times the manufacturers' recommended concentration for 10 min. These findings suggest that FCV and perhaps NLVs are very resistant to commercial disinfectants. However, phenolic compounds at two to four times their recommended concentrations appear to be effective at decontaminating environmental surfaces and may help control foodborne outbreaks of calicivirus in restaurants.


1974 ◽  
Vol 37 (7) ◽  
pp. 361-368 ◽  
Author(s):  
J. D. Baldock

Procedures for microbiological assessment of bacterial contamination on surfaces of equipment and foods are reviewed. The procedures for food-contact surfaces include the following categories: swab contact, surface rinse, direct contact, agar and impression methods, and vacuum probe. Three categories of methods to estimate bacterial numbers on food surfaces are discussed. The importance of knowledge about the various techniques, design of sampling, their limitations and variations are emphasized. Design of sampling and interpretation of results are also considered.


2003 ◽  
Vol 66 (9) ◽  
pp. 1587-1594 ◽  
Author(s):  
ALESSANDRA DE CESARE ◽  
BRIAN W. SHELDON ◽  
KATIE S. SMITH ◽  
LEE-ANN JAYKUS

Although many cases of Campylobacter and Salmonella enteritis have been attributed to the undercooking of poultry and other foods, cross-contamination between raw and cooked foods via food contact surfaces and worker contact has also been identified as a significant risk factor. Cross-contamination may be particularly important in relation to the high prevalence of contamination in raw poultry products and other foods and the low infectious doses that have been reported for Campylobacter species. Lag phase and decimal reduction times (D-values at 27°C [81°F] and 60 to 62% relative humidity) were determined for Campylobacter jejuni and Salmonella species (five-strain pools) suspended in either a phosphate-buffered saline (PBS) solution or Trypticase soy broth (TSB) and then inoculated (0.1-ml drop per surface) on 5-cm2 samples of Formica laminate (F), glazed ceramic tile (CT), 304 polished stainless steel (SS), and 100% cotton dishcloth (D). Triplicate samples were collected from each contact surface periodically, and the populations of surviving organisms were enumerated on Campy Cefex and brain heart infusion agars for C. jejuni and Salmonella species, respectively. Lag time and rate of inactivation were influenced by organism type, contact surface, and suspending medium. Initial mean lag times ranging from 60 to 190 min were followed by log-linear (r2 > 0.94) decreases in cell populations that varied across contact surfaces. D-values of 12.5, 19.1, 24.1, and 29.7 min and of 23.7, 10.5, 12.7, and 13.9 min were calculated for C. jejuni suspended in PBS and TSB and then spotted on D, F, SS, and CT surfaces, respectively. The times required to produce a 3-log reduction in population with PBS and TSB ranged from 102 (D) to 247 (F) min and from 112 (CT) to 167 (F) min, respectively. C. jejuni cells suspended in the nutritionally enriched medium (TSB) and spotted on the hard surfaces were inactivated about 1.4 times as fast as cells suspended in PBS. For the Salmonella test strains, D-values of 17.1, 426.6, 118.6, and 41.9 min and of 48.2, 1363.2, 481.8, and 134.2 min were calculated for cells suspended in PBS and TSB and then spotted on D, F, SS, and CT surfaces, respectively. In contrast to C. jejuni, Salmonella serotypes were 1.7 to 3.3 times more persistent when suspended in TSB than when suspended in PBS and were 1.2 to 25.3 times more persistent than C. jejuni, depending on the contact surface and the type of suspension fluid (i.e., overall time required to achieve a 3-log reduction in population, lag time + 3 × D). These findings indicate that both the contact surface and the level of organic matter can influence the survival and persistence of C. jejuni and Salmonella species on food contact surfaces.


2019 ◽  
Vol 3 (2) ◽  
Author(s):  
S. Sirdesai ◽  
B. De Vegt ◽  
R. Peterson ◽  
A. Moncho ◽  
J. Van Mierlo

ObjectivesListeria is a pathogenic bacterium that is widespread in nature and can enter food processing plants through many vectors, like raw materials, process waste and personnel. Food processors work hard to keep Listeria out of the environment, but it can at times be found from food contact surfaces to floor drains. The sanitation can be compounded when equipment is pitted or cracked creating a harborage or niche in which Listeria can grow. Many control strategies for cleaning and biofilm removal have been put into place but may not suffice in eliminating Listeria from the food contact surface or environment. Bacteriophages are now being used to tackle these pathogens in food processing environments. Since they only target specific bacteria, they are harmless to humans, animals and plants, while effectively eliminating Listeria.This study determines the efficacy of a commercially available bacteriophage product, PhageGuard Listex, against Listeria on commonly found materials in food processing plants (stainless steel and UHMW polyethylene). Efficacy was determined by applying two phage concentrations, as well as two exposure times.Materials and MethodsOvernight cultures of L. monocytogenes ATCC13832 and L. innocua ATCC51742 were mixed in equal parts to create a Listeria cocktail (2 × 109 CFU/cm2). Sterile coupons (100 cm2) of stainless steel or UHMW polyethylene were artificially inoculated with the cocktail at 2.5ML/cm2 and left to dry at 37°C until completely dry. Subsequently, coupons were treated with 2 × 107 or 1 × 108 Plaque Forming Units (PFU)/cm2 using a spray system and incubated at room temperature for 1 and 3 h, before retrieval and enumeration of bacteria on selective agar plates. Sample size n:3. Results were analyzed using two-way ANOVA, with Dunnett’s multiple comparisons test on the normalized data.ResultsA dose dependent response to the phage treatment was observed, where an increasing phage concentration resulted in an increase in Listeria kill on both surfaces. On stainless steel, a treatment dose of 2 × 107 PFU/cm2 resulted in a statistically significant bacterial reduction of 1.27 log after 1 h (p value < 0.0001), while application of 1 × 108 PFU/cm2 showed a 2.16 log reduction (p value < 0.0001). On UHMW polyethylene, a bacterial reduction of 0.47 log was observed 1 h after applying 2 × 107 PFU/cm2, while the application of 1 × 108 PFU/cm2 led to a reduction of 1.95 log. However, these reductions were not statistically significant (p value > 0.05). After 3 h of treatment, the reductions were slightly higher in both materials (Table 3). After this time, the difference between control and 5% treatment on UHMW polyethylene obtained a p-value < 0.05.ConclusionPhage technology is an easy and safe intervention which can be used as an additional tool to control Listeria in processing environments. The above results indicate that the commercially available phage solution, PhageGuard Listex, can reduce Listeria contamination on food contact surfaces by 0.4 to 3.4 logs after 3 h of treatment.Table 3Log reduction of Listeria cells after applicatio nof two bacteriophage concentrations, measured at 1 and 3 h post phage treatment


Pathogens ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 717
Author(s):  
Niels Demaître ◽  
Geertrui Rasschaert ◽  
Lieven De Zutter ◽  
Annemie Geeraerd ◽  
Koen De Reu

The purpose of this study was to investigate the L. monocytogenes occurrence and genetic diversity in three Belgian pork cutting plants. We specifically aim to identify harborage sites and niche locations where this pathogen might occur. A total of 868 samples were taken from a large diversity of food and non-food contact surfaces after cleaning and disinfection (C&D) and during processing. A total of 13% (110/868) of environmental samples tested positive for L. monocytogenes. When looking in more detail, zone 3 non-food contact surfaces were contaminated more often (26%; 72/278) at typical harborage sites, such as floors, drains, and cleaning materials. Food contact surfaces (zone 1) were less frequently contaminated (6%; 25/436), also after C&D. PFGE analysis exhibited low genetic heterogeneity, revealing 11 assigned clonal complexes (CC), four of which (CC8, CC9, CC31, and CC121) were predominant and widespread. Our data suggest (i) the occasional introduction and repeated contamination and/or (ii) the establishment of some persistent meat-adapted clones in all cutting plants. Further, we highlight the importance of well-designed extensive sampling programs combined with genetic characterization to help these facilities take corrective actions to prevent transfer of this pathogen from the environment to the meat.


Foods ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1459
Author(s):  
Alexandra Calle ◽  
Mariana Fernandez ◽  
Brayan Montoya ◽  
Marcelo Schmidt ◽  
Jonathan Thompson

Ultraviolet (UV-C) light-emitting diode (LED) light at a wavelength of 250–280 nm was used to disinfect skinless chicken breast (CB), stainless steel (SS) and high-density polyethylene (HD) inoculated with Salmonella enterica. Irradiances of 2 mW/cm2 (50%) or 4 mW/cm2 (100%) were used to treat samples at different exposure times. Chicken samples had the lowest Salmonella reduction with 1.02 and 1.78 Log CFU/cm2 (p ≤ 0.05) after 60 and 900 s, respectively at 50% irradiance. Higher reductions on CB were obtained with 100% illumination after 900 s (>3.0 Log CFU/cm2). Salmonella on SS was reduced by 1.97 and 3.48 Log CFU/cm2 after 60 s of treatment with 50% and 100% irradiance, respectively. HD showed a lower decrease of Salmonella, but still statistically significant (p ≤ 0.05), with 1.25 and 1.77 Log CFU/cm2 destruction for 50 and 100% irradiance after 60 s, respectively. Longer exposure times of HD to UV-C yielded up to 99.999% (5.0 Log CFU/cm2) reduction of Salmonella with both irradiance levels. While UV-C LED treatment was found effective to control Salmonella on chicken and food contact surfaces, we propose three mechanisms contributing to reduced efficacy of disinfection: bacterial aggregation, harboring in food and work surface pores and light absorption by fluids associated with CB.


Food Control ◽  
2021 ◽  
Vol 125 ◽  
pp. 107988
Author(s):  
Zi Hua ◽  
Frank Younce ◽  
Juming Tang ◽  
Dojin Ryu ◽  
Barbara Rasco ◽  
...  

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