Category Archives: food contamination

Research – A Quantitative Risk Assessment of Human Salmonellosis from Consumption of Walnuts in the United States

Journal of Food Protection

We assessed the risk of human salmonellosis from consumption of shelled walnuts in the United States and the impact of 0- to 5-log reduction treatments for Salmonella during processing. We established a baseline model with Salmonella contamination data from 2010 to 2013 surveys of walnuts from California operations to estimate baseline prevalence and levels of Salmonella during preshelling storage and typical walnut processing stages, considered U.S. consumption data, and applied an adapted dose-response model from the Food and Agriculture Organization and the World Health Organization to evaluate risk of illness per serving and per year. Our baseline model predicted 1 case of salmonellosis per 100 million servings (95% confidence interval [CI], 1 case per 3 million to 1 case per 2 billion servings) of walnuts untreated during processing and uncooked by consumers, resulting in an estimated 6 cases of salmonellosis per year (95% CI, <1 to 278 cases) in the United States. A minimum 3-log reduction treatment for Salmonella during processing of walnuts eaten alone or as an uncooked ingredient resulted in a mean risk of <1 case per year. We modeled the impact on risk per serving of three atypical situations in which the Salmonella levels were increased by 0.5 to 1.5 log CFU per unit pretreatment during processing at the float tank or during preshelling storage or posttreatment during partitioning into consumer packages. No change in risk was associated with the small increase in levels of Salmonella at the float tank, whereas an increase in risk was estimated for each of the other two atypical events. In a fourth scenario, we estimated the risk per serving associated with consumption of walnuts with Salmonella prevalence and levels from a 2014 to 2015 U.S. retail survey. Risk per serving estimates were two orders of magnitude larger than those of the baseline model without treatment. Further research is needed to determine whether this finding reflects variability in Salmonella contamination across the supply or a rare event affecting a portion of the supply.

Research – Utility of Whole Genome Sequencing To Describe the Persistence and Evolution of Listeria monocytogenes Strains within Crabmeat Processing Environments Linked to Two Outbreaks of Listeriosis

Journal of Food Protection

This article describes the identification and investigation of two extended outbreaks of listeriosis in which crabmeat was identified as the vehicle of infection. Comparing contemporary and retrospective typing data of Listeria monocytogenes isolates from clinical cases and from food and food processing environments allowed the detection of cases going back several years. This information, combined with the analysis of routinely collected enhanced surveillance data, helped to direct the investigation and identify the vehicle of infection. Retrospective whole genome sequencing (WGS) analysis of isolates provided robust microbiological evidence of links between cases, foods, and the environments in which they were produced and demonstrated that for some cases and foods, identified by fluorescent amplified fragment length polymorphism, the molecular typing method in routine use at the time, were not part of the outbreak. WGS analysis also showed that the strains causing illness had persisted in two food production environments for many years and in one producer had evolved into two strains over a period of around 8 years. This article demonstrates the value of reviewing L. monocytogenes typing data from clinical cases together with that from foods as a means of identifying potential vehicles and sources of infection in outbreaks of listeriosis. It illustrates the importance of reviewing retrospective L. monocytogenes typing alongside enhanced surveillance data to characterize extended outbreaks and inform control measures. Also, this article highlights the advantages of WGS analysis for strain discrimination and clarification of evolutionary relationships that refine outbreak investigations and improve our understanding of L. monocytogenes in the food chain.

Research – Assessment of Microbial Populations in the Manufacture of Vacuum-Packaged Ready-to-Eat Roast Beef and in a Related Production Plant

Journal of Food Protection

Some microbiological criteria were monitored for 6 months in vacuum-packaged roast beef (15 production batches), raw beef (10 batches), and other meat products (12 batches) produced in an Italian small to medium-size enterprise. Fifty-five environmental swab samples also were analyzed. The main bacterial groups were identified by cultural methods according to International Organization for Standardization standards. Listeria monocytogenes was enumerated with the most-probable-number protocol, and species identification was confirmed with a specific PCR assay. Immediately after vacuum packaging, all ready-to-eat (RTE) products had low mean aerobic colony counts (<102 to 2.4 × 102 CFU g−1), anaerobic colony counts (1.6 to 6.5 × 101 CFU g−1), Enterobacteriaceae counts (1.1 to 1.4 × 101 CFU g−1), and Escherichia coli counts (generally below the detection limit). Nevertheless, the prevalence of L. monocytogenes in these samples was 3.7%. In roast beef samples, the aerobic and anaerobic colony counts reached unacceptable levels (>106 CFU g−1) after 14 days of refrigerated storage. Because the prevalence of L. monocytogenes increased to 13.3% during storage, a substantial reduction in the shelf life of these products is recommended. Surfaces without direct contact with food (floors and drains) had the highest mean counts for aerobic colonies (8.0 × 103 to 9.5 × 105 CFU/cm2), anaerobic colonies (2.9 × 103 to 3.2 × 104 CFU/cm2), Enterobacteriaceae (1.5 × 101 to 8.4 × 101 CFU/cm2), and E. coli (6.0 to 7.7 CFU/cm2). The levels of L. monocytogenes on direct food contact surfaces were below the detection limit, but more than 25% of floor samples were contaminated. These results reveal the persistence of L. monocytogenes in food processing environments, although at very low levels, posing a high risk of postcooking recontamination for RTE products. To improve hygienic conditions and reduce cross-contamination, an increase in operator awareness and a reassessment of surface sanitization protocols are needed.

RASFF Alerts – Salmonella – Sesame Seeds – Ground Black Pepper – Chicken Breast Fillets

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RASFF -Salmonella (presence /25g) in sesame seeds hulled from Nigeria, via Turkey in Poland

RASFF-Salmonella (present /25g) in sesame seeds from Nigeria in Poland

RASFF-Salmonella (present /25g) in ground black pepper from Vietnam in Spain

RASFF-Salmonella enterica ser. Typhimurium in frozen chicken breast filletts from the Netherlands in the Netherlands

RASFF Alert – Listeria monocytogenes – Smoked Salmon

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RASFF-Listeria monocytogenes (presence /25g) in chilled smoked Norwegian salmon from Latvia in Italy

 

RASFF Alert – E.coli – Live Mussels

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RASFF -too high count of Escherichia coli (940 MPN/100g) in live mussels (Mytilus edulis) to be purified from Ireland in Ireland

RASFF Alert – Histamine – Chilled mackerel (Scomber scombrus)

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RASFF -histamine (410 mg/kg – ppm) in chilled mackerel (Scomber scombrus) from France in Belgium

RASFF Alerts – Aflatoxin – Peanuts – Pistachios – Groundnuts – Almonds

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RASFF-aflatoxins (B1 = 37.7; Tot. = 44.3 µg/kg – ppb) in peanuts with shell from Egypt in Italy

RASFF-aflatoxins (B1 = 73.8; Tot. = 79 µg/kg – ppb) in pistachios in shell from Syria in Greece

RASFF-aflatoxins (B1 = 21.2; Tot. > 24 µg/kg – ppb) in groundnuts from China in Spain

RASFF-aflatoxins (B1 = 60; Tot. = 71 µg/kg – ppb) in shelled pistachios from the Netherlands in the Netherlands

RASFF-aflatoxins (B1 = 92; Tot. = 110 µg/kg – ppb) in almonds from the United States in the Netherlands

RASFF Alert – Ochratoxin – Sultana Raisins

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RASFF -ochratoxin A (14.6 µg/kg – ppb) in sultana raisins from Turkey in Poland

Information – From leftovers to storing food: How to avoid food poisoning this Christmas

Start Sat 60

Food poisoning impacts more than four million Australians each year and with the Christmas season fast approaching, it’s important to take food safety and food poisoning seriously.

In simple terms, food poisoning is caused because of contamination. This can be caused by food being prepared in unhygienic areas, if food is stored at incorrect temperatures, or if food is simply undercooked. Food poisoning terms many people are familiar with include staphylococcus aureus, listeria, salmonella and bacillus cereus and symptoms and side effects can vary from person to person.

Is food poisoning caused by the last thing I ate?

Despite the myth, food poisoning is not always caused by the last thing a person ate. In fact, the NSW Food Authority states that symptoms such as gastro intestinal cramps and vomiting can be caused by food eaten up to eight hours before symptoms start to show.

Diarrhoea on the other hand can begin between four hours to three days after eating affected food.