Category Archives: Food Technology

Research – Inactivation of viruses related to foodborne infections using cold plasma technology

Wiley Online

Globally, there is a rise in day-to-day demand for minimally processed foods to supply nutritious, wholesomeness and safe foods to the consumers. Contamination of food by pathogens is a serious problem resulting in several outbreaks. Food pathogens like molds, bacteria were detectable and can be inactivated. The virus detection in foods is always a difficult task as their presence could not alter any noticeable change in the quality. Norovirus, Hepatitis A viruses are well-known for their foodborne outbreaks and illnesses. Enveloped viruses are resistant and have the stability to the current traditional preservation methods due to the presence of a protective capsid layer and an envelope. The current thermal processing has shown significant effect on the product quality. The use of chemical disinfestation compounds is not suitable for food commodities. There is a need for alternative nonthermal food processing technologies for decontamination of food and food packages and preserving the food quality as well. Cold plasma is one of the emerging nonthermal, chemical-free residues, and eco-friendly technology widely being applied to the different food sectors. The main antiviral mechanism is the disruption of the capsid protein layer, the oxidation and denaturation of viral proteins. The method has also caused damage to the envelope layer and genetic material. This review focuses on cold plasma inactivation efficiency on different viruses.

Canada – Certain Tri-Star Seafood Supply Ltd. brand Live Spot Prawns recalled due to Norovirus

CFIA

Food Borne Illness - Norovirus -CDC Photo

Summary

Product
Certain Live Spot Prawns
Issue
Food – Microbial Contamination – Norovirus
What to do

Do not consume, use, sell, serve, or distribute the recalled product

Affected products

Issue

Tri-Star Seafood Supply Ltd. is recalling certain Tri-Star Seafood Supply Ltd. brand Live Spot Prawns from the marketplace due to possible norovirus contamination.

The recalled product has been sold in British Columbia, Alberta, Manitoba, and Ontario, and may have been distributed in other provinces and territories.

What you should do

  • If you think you became sick from consuming a recalled product, call your doctor
  • Check to see if you have the recalled product in your home or establishment
  • Do not consume the recalled product
  • Do not serve, use, sell, or distribute the recalled product
  • Recalled products should be thrown out or returned to the location where they were purchased
  • Consumers who are unsure if they have purchased the affected product are advised to contact their retailer

People with norovirus illness usually develop symptoms of gastroenteritis within 24 to 48 hours, but symptoms can start as early as 12 hours after exposure. The illness often begins suddenly. Even after having the illness, you can still become re-infected by norovirus. The main symptoms of norovirus illness are diarrhea, vomiting (children usually experience more vomiting than adults), nausea and stomach cramps. Other symptoms may include low-grade fever, headache, chills, muscle aches and fatigue (a general sense of tiredness).  Most people feel better within one or two days, with symptoms resolving on their own, and experience no long-term health effects. As with any illness causing diarrhea or vomiting, people who are ill should drink plenty of liquids to replace lost body fluids and prevent dehydration. In severe cases, patients may need to be hospitalized and given fluids intravenously.

Research – Comparison of Selected Phenotypic Features of Persistent and Sporadic Strains of Listeria monocytogenes Sampled from Fish Processing Plants

MDPI

(1) Background: The main source of transmission of Listeria monocytogenes is contaminated food, e.g., fish and meat products and raw fruit and vegetables. The bacteria can remain for 13 years on machines in food processing plants, including fish plants.

(2) Methods: A total of 720 swabs were collected from a salmon filleting line. The research material consisted of 62 (8.6%) L. monocytogenes isolates. Pulsed Field Gel Electrophoresis (PFGE) allowed detecting a pool of persistent strains. All persistent strains (n = 6) and a parallel group of strains collected sporadically (n = 6) were characterized by their ability to invade HT-29 cells, biofilm formation ability, and minimum bactericidal concentrations (MBC) of selected disinfectants.

(3) Results: Among the obtained isolates, 38 genetically different strains were found, including 6 (15.8%) persistent strains. The serogroup 1/2a-3a represented 28 strains (73.7%), including the persistent ones. There were no significant differences in invasiveness between the persistent and sporadic strains. The persistent strains tolerated higher concentrations of the tested disinfectants, except for iodine-based compounds. The persistent strains initiated the biofilm formation process faster and formed it more intensively.

(4) Conclusions: The presence of persistent strains in the food processing environment is a great challenge for producers to ensure consumer safety. This study attempts to elucidate the phenotypic characteristics of persistent L. monocytogenes strains. View Full-Text

Research – Application of ultra-fine bubble technology to reduce Listeria monocytogenes contamination of fresh produce

Center for Produce Safety

Summary

Water used for washing or hydrocooling can act as a source of produce contamination with Listeria monocytogenes. Since this could lead to human infections, controlling L. monocytogenes in hydrocooling water and produce is critical for food safety. Commercial disinfectants (chlorine, quaternary ammonium compounds) are not completely effective in killing L. monocytogenes in wash water or on produce, especially in presence of organic load.

This proposal aims to investigate the potential of a new technology that employs water containing ultra-fine gas bubbles (size ~ 1 micrometer or less) for washing produce (celery, gala apples, romaine lettuce). We will generate ultra-fine ozone (UFO) bubbles in water using a high energy shear method and test the potential of resulting solution to rapidly kill (in 30 to 60 sec) L. monocytogenes in wash water and on produce surface. In addition, the efficacy of UFO bubble water to synergistically improve the Listeria killing potential of aforementioned commercial disinfectants will be tested. The anti-listerial efficacy of UFO bubble water will also be tested in presence of organic load. Successful completion of this project will provide the produce industry with novel antimicrobial treatment for disinfecting wash water and produce in single pass or re- circulated hydrocooling systems.

Technical Abstract

The widespread distribution of Listeria monocytogenes in agricultural environments such as soil, manure and water results in frequent contamination of food processing areas. Although good agricultural practices partially reduce contamination, however, due to the open nature of farming, it is extremely difficult to completely prevent pathogen influx. Water used for washing or hydrocooling can act as a source of equipment and produce contamination with L. monocytogenes. Since this could lead to human infections, controlling L. monocytogenes in hydrocooling water and on the surface of fresh produce is critical for food safety. Currently used commercial disinfectants (chlorine, peracetic acid, quaternary ammonium compounds) are not completely effective in killing L. monocytogenes in wash water or on the surface of produce, especially in presence of organic load. Moreover, the presence of chemical residues and the formation of harmful organochlorine compounds is an occupational concern due to associated health risks, including cancer. Therefore, there is a need for developing novel strategies that could be employed (either alone or in combination with currently used commercial disinfectants) to control L. monocytogenes in wash water and on surface of fresh produce, vegetables and fruits.

This proposal aims to investigate the potential of a new technology that employs water containing ultra-fine gas bubbles (size ~ 1 micrometer or less) for washing produce (celery, gala apples, romaine lettuce). We will generate ultra-fine ozone (UFO) bubbles in water using a high energy shear method and test the potential of resulting solution to rapidly kill (in 30 to 60 sec) L. monocytogenes in wash water and on produce surface. In addition, the efficacy of UFO bubble water to synergistically improve the Listeria killing potential of aforementioned commercial disinfectants will be tested. The anti-listerial efficacy of UFO bubble water will also be tested in presence of organic load.

Potential impact from anticipated outcomes: Successful completion of this project will provide the produce industry with novel antimicrobial treatment for disinfecting wash water and produce in dump tanks, and single pass or re-circulated hydrocooling systems. This intervention will translate into increased microbiological safety of fresh produce.

Research – Microbial Safety and Sensory Analyses of Cold-Smoked Salmon Produced with Sodium-Reduced Mineral Salts and Organic Acid Salts

MDPI

Cold-smoked (CS) salmon contains high levels of sodium salts, and excess dietary sodium intake is associated with an array of health complications. CS salmon may also represent a food safety risk due to possible presence and growth of the foodborne pathogen Listeria monocytogenes which may cause fatal human infections. Here we determine how reformulated CS salmon using commercial sodium-reduced salt replacers containing KCl (e.g., Nutek, Smart Salt, SOLO-LITE) and acetate-based preservative salts (Provian K, proviant NDV) affect sensory properties, quality, and microbial safety. Initial sensory screening of sodium-reduced CS salmon was followed by L. monocytogenes growth analyses in selected variants of reformulated CS salmon, and finally by analyses of CS salmon variants produced in an industrial smokehouse. Projective mapping indicated overall minor sensory changes in sodium-replaced samples compared with a conventional product with NaCl. Growth of L. monocytogenes was temperature-dependent (4 °C vs. 8 °C storage) with similar growth in sodium-reduced and conventional CS salmon. The addition of 0.9% of the preservative salts Provian K or Provian NDV gave up to 4 log lower L. monocytogenes counts in both sodium-reduced and conventional cold-smoked salmon after 29 days of chilled storage. No changes in pH (range 6.20–6.33), aw levels (range 0.960–0.973), or weight yield (96.8 ± 0.2%) were evident in CS salmon with salt replacers or Provian preservative salts. Analyses of CS salmon produced with selected mineral salt and preservative salt combinations in an industrial salmon smokery indicated marginal differences in sensory properties. Samples with the preservative salt Provian NDV provided L. monocytogenes growth inhibition and low-level total viable counts (<2.8 log/g) dominated by Photobacterium and Carnobacterium during storage. Production of sodium-reduced CS salmon with inhibiting salts provides a simple method to achieve a healthier food product with increased food safety.

Research – Removal of Ochratoxin A from Grape Juice by Clarification: A Response Surface Methodology Study

MDPI

This study achieved maximum removal of ochratoxin A (OTA) during the grape juice clarification process with minimal reduction in antioxidant compounds (phenolic acid, flavonoids, and antioxidant capacity by FRAP) by the RSM method. Independent variables included three types of clarifiers—gelatin, bentonite, and diatomite (diatomaceous earth)—at a concentration level of 0.25–0.75% and clarification time of 1–3 h. OTA was measured by high-performance liquid chromatography with fluorescence detection. Clarifying agent concentration and clarification time affected the reduction amount of OTA and antioxidant compounds in grape juice. There was a direct linear correlation between the reduction amounts of OTA and antioxidant compounds and capacity with the concentration of bentonite, gelatin, and diatomite, and the clarification time. The reduction amount of OTA and antioxidant capacity followed the linear mode. However, the decreased phenolic acid and flavonoid values followed the quadratic model. The study results showed that if the concentrations of bentonite, gelatin, and diatomite and clarification time were 0.45, 0.62, 0.25%, and 1 h, respectively, the maximum amount of OTA reduction (41.67%) occurred. Furthermore, the phenolic acid, flavonoid, and antioxidant activity decrease amounts were at their lowest levels, i.e., 23.86, 7.20, and 17.27%, respectively. View Full-Text

Research – Inactivation of Foodborne Pathogens on Inshell Walnuts by UV-C Radiation

Journal of Food Protection

Inshell walnuts could be contaminated with pathogens through direct contact or cross-contamination during harvesting and postharvest hulling, drying, or storage. This study aimed to assess the efficacy of ultraviolet–C (UV–C) radiation in inactivating foodborne pathogens on inshell walnut surfaces. Intact inshell walnut surfaces were inoculated separately with Salmonella spp., Escherichia coli O157:H7, Listeria monocytogenes , and Staphylococcus aureus , and then subjected to UV–C radiation at doses of 29.4, 147.0, 294.0, 588.0, and 882.0 mJ/cm 2 . UV–C radiation inactivated the inoculated pathogens in a dose-dependent manner, and a tailing effect was observed for the inactivation of pathogens. UV–C radiation at 29.4 mJ/cm 2 and 882.0 mJ/cm 2 reduced the populations of  S . Enteritidis PT 30, S . Typhimurium, E. coli O157:H7, L. monocytogenes , and S. aureus on inshell walnut surfaces by 0.82–1.25 and 1.76–2.41 log CFU/walnut, respectively. Scanning electron photomicrographs showed pathogenic bacterial cells in the cracks and crevices of the inshell walnut surface, and the shielding of microorganisms by the cracks and crevices may have contributed to the tailing effect observed during UV–C inactivation. No significant changes ( p  > 0.05) were found in walnut lipid oxidation following UV–C radiation at doses up to 882.0 mJ/cm 2 . Together, the results indicate that UV–C radiation could be a potential technology for reducing the populations of various foodborne pathogens on inshell walnut surfaces while maintaining the quality of walnuts.

Research – Attachment and survival of Salmonella enterica and Listeria monocytogenes on tomatoes (Solanum lycopersicum) as affected by relative humidity, temperature and time of storage 

Journal of Food Protection

Tomatoes (Solanum lycopersicum) are one of the most consumed fruits worldwide. The fruit can become contaminated with Salmonella and Listeria monocytogenes at different stages of the production and supply chain, and these pathogens may survive under different storage conditions. The effect of relative humidity, temperature and time of storage on the attachment and survival characteristics of both pathogens on the surface of tomatoes was investigated. Fresh whole Roma tomatoes were inoculated with a cocktail of Salmonella or L. monocytogenes and stored at 5, 12, 25, 30, or 35 ºC for 10 days. Every day during storage, relative humidity and temperature were measured and tomatoes were removed to enumerate cells of these pathogens that were loosely attached (LA, cells detached from the tomato surface by simple rinse) and strongly attached (SA, cells that required sonication to detach. Enumeration was achieved by spread-plate method. Surviving populations of LA and SA cells were obtained and the attachment strength (SR) was calculated to express the proportion of SA cells on the tomato surface. The LA initial counts of Salmonella and L. monocytogenes on the surface of the fruit after inoculation were 6.6 and 6.5 log CFU/tomato, and for SA were 5.1 and 5.6 log CFU/tomato, respectively. For both pathogens, the LA counts were higher (p < 0.05) than the SA counts. Also, the LA and SA counts varied significantly as a function of temperature, relative humidity and time of storage. The S R for Salmonella was affected by the time but not the temperature of storage, while the S R for L. monocytogenes was affected by the temperature, relative humidity and time of storage (p < 0.05). Understanding the attachment and survival of Salmonella and L. monocytogenes on tomatoes stored at different temperature conditions may be useful in determining ways to prevent/reduce the establishment of pathogens and designing improved decontamination methods for tomatoes.

Research – The effectiveness and safety of high pressure food treatment

asca

Definition and applicable regulations

Type of food treated and processing conditions

Intrinsic and extrinsic factors of food that influence the effectiveness of high pressure treatment

Possible chemical and microbiological hazards associated with high pressure treatment

High pressure treatment as an alternative to pasteurization of milk

Efficacy of high pressure treatment for the control of Listeria monocytogenes in ready-to-eat foods

Research – Possible explanation for limited reduction of pathogens on radish microgreens after spray application of chlorinated water during growth with disperse contamination spread of abiotic surrogate on leaves

Wiley Online

The purpose of this study was to determine the efficacy of spray application of chlorinated water before harvest on the population of Salmonella enterica Typhimurium and Escherichia coli O157:H7 on radish microgreens. The transfer of abiotic surrogate to radish microgreens was also evaluated to track possible pathogen contamination spread by inoculating seed and growth media. During growth, microgreens inoculated with strains of pathogens were sprayed with chlorinated water at three different concentrations (0.50, 1.00, and 2.00 ± 0.05 ppm free chlorine). Spray application of chlorinated water was performed on microgreens once (day 9), twice (day 8 and 9), three (day 7, 8, and 9), and four times (day 6, 7, 8, and 9). Microgreens were harvested 12 hr after the last application of chlorinated water. Salmonella and E. coli O157:H7 populations were reduced with the increase in chlorine concentration. Chlorinated water reduced Salmonella and E. coli O157:H7 populations up to 1.1 log CFU/g (p < .05) and 0.9 log CFU/g (p > .05), respectively. Images taken under UV illumination provided the visualization of abiotic surrogate spread on cotyledon and upper hypocotyl (all edible parts) of radish microgreen plants regardless of seed or growth media inoculation. Scanning Electron Microscopy showed the presence of abiotic surrogate and generic E. coli on microgreen leaves. Spray application of chlorinated water during microgreen growth may help to reduce microbial load but cannot be used as the only control measure.