Category Archives: microbial contamination

Research – Researchers turn to air sampling to detect Campylobacter in chicken flocks

Food Safety News

 

A project led by the National Food Institute, Technical University of Denmark, has developed a test method to improve the likelihood of identifying Campylobacter-positive chicken flocks.

Being able to identify Campylobacter-positive flocks before they arrive at the slaughterhouse allows them to be slaughtered after the negative flocks to avoid cross-contamination along the production line.

The method was worked on in the EU project, AIR-SAMPLE, which began in January 2018 and runs until June 2020. Other partners are the Istituto Zooprofilattico Sperimentale dell’Abruzzo e del Molise “Giuseppe Caporale” in Italy, Veterinary Research Institute in the Czech Republic, National Veterinary Research Institute in Poland and Norwegian Veterinary Institute.

The aim was to develop and validate air sampling as a low-cost and multi-purpose alternative to fecal droppings or boot swabs for surveillance, monitoring and eradication of Campylobacter in confined and biosecured broiler production operations.

RASFF Alert -Animal Feed – Aflatoxin – Groundnut Kernels

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RASFF – aflatoxins (B1 = 64.8 µg/kg – ppb) in groundnut kernels from India in the UK

RASFF Aleret – Animal Feed – Ergot Alkaloids – Triticale

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RASFF – ergot (Claviceps purpurea) alkaloids (3.5 g/kg) in triticale from France in Belgium

Tanzania – Fast-Track East African Community Aflatoxin Law to End Toxic Menace

All Africa

The war on aflatoxins in East Africa is intensifying as member-states of the East African Community (EAC) strategise through regular consultative meetings on how best to surmount the malady in the region.

Aflatoxins are a family of toxins produced by certain fungi which include – but are by no means limited to – ‘Aspergillus flavus’ and ‘Aspergillus parasiticus,’ that are abundant in warm and humid regions across the world. The highly-carcinogenic toxins are mostly found on agricultural crops such as maize, as well as cottonseeds, peanuts, cashew nuts, walnuts, pine nuts, coconuts, almonds, etc.

What with maize being a staple food in the region – and nuts being popular ingestibles for all age groups – aflatoxins are a huge threat to humanity. Hence the concerns and dire need to wipe out aflatoxins in our region and the African continent as a whole…

 

Kenya – Aflatoxin Levels in Maize Worry Kebs and Millers

All Africa

The Kenya Bureau of Standards (Kebs) and millers have raised concerns over high levels of aflatoxin in maize.

They say most of the maize contains unacceptable levels of the toxin, making it unfit for human consumption.

Poor storage facilities and heavy rains in maize-growing zones have contributed to the problem, said Dr Henry Rotich, the director of meteorology and testing at Kebs.

“Regular inspections and tests for aflatoxin are carried out to ensure maize flour and other products meet recommended standards,” he said.

“In Kenya, the allowable aflatoxin level in maize is 10 parts per billion. Anything above that is unacceptable.”

Research – Compatibility of commercially produced protective cultures with common cheesemaking cultures and their antagonistic effect on foodborne pathogens

JFP

The documented survival of pathogenic bacteria including Listeria monocytogenes (LM), shiga toxin-producing Escherichia coli (STEC), and Salmonella during the manufacture and aging of some cheeses highlights the need for additional interventions to enhance food safety. Unfortunately, few interventions are compliant with the Standards of Identity for cheese. Protective bacterial cultures (PC) represent actionable, natural interventions. However, supportive data for commercially produced PCs regarding their efficacy against pathogens and potential antagonism with each other and cheesemaking cultures are scant, thereby impeding their potential use by the cheese industry. The overall objective of this study was to identify commercially produced PCs that exert antimicrobial activity towards pathogens with minimal impact on beneficial cheese microbes. Direct antagonism and agar well diffusion assays were used to determine the impact of 10 commercially produced PCs on the growth of starter cultures and cultures of ripening bacteria and fungi. Deferred antagonism was used to evaluate the potential for antimicrobial effects against LM, STEC, and Salmonella. PCs and starter cultures were co-cultured in UHT milk to determine the effects of co-culture on starter acidification profiles when incubated according to a simulated cheese-making temperature profile (4 h at 35°C followed by 20 h at 20°C). Compatibility assays suggest that PC antagonism is microbe and strain specific. Only one PC negatively impacted the acidification of the starters tested. PC antagonism of ripening bacteria and fungi growth varied but was consistent within species. All PCs displayed deferred inhibition of LM, STEC, and Salmonella growth but to varying degrees. These data identify commercial PCs with potential for the control of pathogens and characterize their compatibility with cheesemaking cultures for future use by cheesemakers and investigations of their efficacy in the production of cheese.

Research – Biofilm formation by South African non-O157 Shiga toxigenic Escherichia coli on stainless steel coupons

NRC

This study examined the biofilm-forming ability of six non-O157 Shiga-toxin-producing Escherichia coli (STEC) strains: O116:H21, wzx-Onovel5:H19, O129:H21, O129:H23, O26:H11, and O154:H10 on stainless steel coupons after 24, 48, and 72 h of incubation at 22 °C and after 168 h at 10 °C. The results of crystal violet staining revealed that strains O129:H23 and O154:H10 were able to form biofilms on both the submerged surface and the air–liquid interface of coupons, whereas strains O116:H21, wzx-Onovel5:H19, O129:H21, and O26:H11 formed biofilm only at the air–liquid interface. Viable cell counts and scanning electron microscopy showed that biofilm formation increased (p < 0.05) over time. The biofilm-forming ability of non-O157 STEC was strongest (p < 0.05) at 22 °C after 48 h of incubation. The strongest biofilm former regardless of temperature was O129:H23. Generally, at 10 °C, weak to no biofilm was observed for isolates O154:H10, O116:H21, wzx-Onovel5:H19, O26:H11, and O129:H21 after 168 h. This study found that temperature affected the biofilm-forming ability of non-O157 STEC strains. Overall, our data indicate a high potential for biofilm formation by the isolates at 22 °C, suggesting that non-O157 STEC strains could colonize stainless steel within food-processing facilities. This could serve as a potential source of adulteration and promote the dissemination of these potential pathogens in food.

Research – Survival and histamine production by histamine forming bacteria exposed to low doses of gamma irradiation

JFP

Histamine fish poisoning occurs when fish containing high amount of histamine are consumed. Since histamine is thermally stable, control of histamine forming bacteria in seafood is a good strategy to prevent the formation of histamine. One of the potential ways to do this is to apply gamma radiation on the histamine formers. In order to understand the effect of gamma radiation on the histamine forming bacteria, laboratory isolates of prolific histamine forming bacteria namely Morganella morganii, Klebsiella variicola and Proteus vulgaris were exposed to different doses of gamma radiation in nutrient broth and in tuna muscle spiked with histamine formers. None of the test bacteria survived in tuna muscle radiated at 2.0 kGy. Among the selected histamine formers, Klebsiella variicola was highly sensitive to gamma radiation and was eliminated at a dose of 1.5 kGy. Histamine production levels were also reduced as radiation dose increased. These results suggest that gamma irradiation can effectively eliminate histamine forming bacteria and the threat of histamine poisoning in seafood.

Scotland – New research into Campylobacter infection in Scotland

HPS

campy2

Image CDC

17 March 2020

Article: 54/1104

Food Standards Scotland (FSS) has published new research on Campylobacter, the most common cause of bacterial food poisoning in Scotland, which provides evidence concerning those at greater risk of infection and severe illness, and the estimated healthcare cost of infection. Conducted between 2013 and 2019, this research was undertaken by Health Protection Scotland (HPS) and the University of Aberdeen, on behalf of FSS.

The research confirmed that, while a higher number of cases are reported in more affluent areas of Scotland, those living in the most deprived areas are at an increased risk of developing serious illness and being hospitalised.

The results showed that overall, around 14% of Campylobacter cases lead to hospitalisation, with hospital admissions more likely to have one or more of the following risk factors:

  • being 65 years or older
  • having an underlying medical condition
  • being prescribed with proton pump inhibitor to reduce stomach acid production in the 90 days prior to infection

The findings from this research have enabled public health authorities to estimate that, with approximately 6,000 cases reported per year, Scotland’s total annual healthcare cost for Campylobacter infections is approximately three million pounds.

Research – Combination of ultraviolet light‐C and clove essential oil to inactivate Salmonella Typhimurium biofilms on stainless steel

Wiley Online

Abstract

Salmonella typhimurium is able to form biofilms as a resistance mechanism against antimicrobials; therefore, it represents a problem for assuring food safety and highlights the importance of research on anti‐biofilm technologies. In this study, S. typhimurium biofilms were inactivated with the combination of clove essential oil (CEO) and ultraviolet light (UV‐C). The volatile composition of the CEO determined by gas chromatography showed eugenol as the major constituent (82%). A combination of CEO with UV‐C achieved a complete bacterial reduction (6.8 log/cm2) on biofilms with doses of 1.2 mg/ml and 76.41 mJ/cm2, respectively. Individually, the CEO at 1.2 mg/ml caused a reduction of 1.8 log CFU/cm2 of attached bacteria cells on stainless steel, while UV‐C individually used at 620.4 mJ/cm2 caused a 2.9 log CFU/cm2 reduction compared to control biofilms. In conclusion, this study demonstrated a synergistic effect of combining CEO and UV‐C irradiation to inactivate biofilms of S. typhimurium.