Low gamma irradiation of raw meat. II. Bacteriological effects on samples from butcheries

One hundred and twenty samples of raw ground meat, a component of ‘filet américain’ consumed raw in some European countries, were investigated, both directly and after gamma irradiation with a dose of 1 kGy. Moreover, the meat was checked serologically for presence of other type beside beef.Salmonella were isolated from 23 (19.2%) non-irradiated samples, MPN counts ranged from 40 to 2 × 10³ organisms/100 g. Only 1 sample was Salmonella-positive after irradiation, at an amount of 2.3 × 10²/100 g.Yersinia enterocolitica was found in 60 (50%) samples of raw meat but this organism was not isolated from irradiated samples.From none of the investigated samples of raw meat could Campylobacter jejuni be isolated.The average reduction after irradiation of the total aerobic count and Enterobacteriaceae was 2.18 and 4.00 log cycles, respectively.In 5 of 120 samples of raw ground meat intended for preparation of filet américain the presence of pork was demonstrated.Based on the results of this study it may be concluded that irradiation of raw meat with a dose of 1 kGy eliminated of reduced some pathogens of public health concern to acceptable levels.     

The biofilm forming potential of bacterial species in the genus Campylobacter

The biofilm forming abilities of 16 strains representative of 14 of the 16 species comprising the genus Campylobacter were determined on glass, stainless steel, and polystyrene plastic. The formation of biofilms has been suggested as a means by which Campylobacter is able to persist within an inhospitable environment. Of the eight microaerophilic Campylobacter species, including two strains each of Campylobacter jejuni and Campylobacter fetus, only C. jejuni strain 81–176 reliably produced a visible biofilm on multiple surfaces. Alternately, all six strains of the anaerobic Campylobacter species reliably produced visible biofilms on multiple surfaces. Electron micrographs of the individual biofilms showed relatively homogeneous biofilms produced by the anaerobic strains, while the microaerophilic C. jejuni strain 81–176 produced a biofilm containing similar quantities of both the spiral and coccoid forms. This survey suggests a difference in the biofilm forming potentials and the morphologies of the bacteria comprising the biofilms between anaerobic and microaerophilic species of Campylobacter. Additionally, differences observed in the biofilm forming ability of two strains of C. jejuni suggest the need for a further investigation of the biofilm forming potential of this species using a larger number of strains.     

Correlation between astaxanthin amount and a* value in fresh Atlantic salmon (Salmo salar) muscle during different irradiation doses

The amount of astaxanthin and a* value changes in fresh Atlantic salmon light and dark muscle during cold storage was studied for different e-beam doses (0, 1, 1.5, 2 and 3 kGy). Astaxanthin (mg/kg muscle) and a* value decreased with increasing irradiation dose for both fresh light and dark muscle. The level of irradiation dose gave high correlation between a* value and amount of astaxanthin. The reason for the change in colour or decrease in a* value of Atlantic salmon during irradiation could be due to the destruction of astaxanthin. The amount of astaxanthin and a* value of 1 kGy treated salmon fillets were not significantly different (p > 0.05) from that of the control but significantly different (p < 0.05) from other irradiation treatments. The colour (a* value) of salmon muscle was related to the content of astaxanthin, which decreased as irradiation increased. The amount of astaxanthin in light muscle was three to five times greater than dark muscle. This study demonstrated that irradiating salmon fillets at 1 kGy, can be successfully used and leads to no significant change in colour and amount of astaxanthin.     

Low dose gamma irradiation of raw meat. I. Bacteriological and sensory quality effects in artificially contaminated samples

Filet américain, consisting of raw, ground meat (beef) mixed with mayonnaise sauce, and the corresponding raw beef (without sauce) were experimentally contaminated with different strains of Salmonella. Yersinia enterocolitica and Campylobacter jejuni and irradiated with doses up to 1.5 kGy.Radiation resistance (D value) was determined immediately after irradiation. For the evaluation of the irradiaion effect on Y. enterocolitica in relation to storage, a number of samples were stored for a few days at 3°C and the microbiologically examined.D values of S. typhimurium, S. anatum, S. panama and S. stanley (strains isolated from retail filet américain) irradiated in filet américain were found to be 0.37, 0.45, 0.41 and 0.61 kGy and in raw beef 0.55, 0.67, 0.66 and 0.78 kGy, respectively. D values of Y. enterocolitica serotypes 0:3, 0:5, 27 and 0:9 irradiated in filet américain were 0.043, 0.065, and 0.080 kGy and in raw beef, 0.10, 0.16 and 0.21 kGy, respectively. D values of C. jejuni (three strains) irradiated in filet américain were 0.11, 0.08 and 0.09 and in beef 0.15, 0.14 and 0.16 kGy, respectively.It is concluded that doses as low as 1 kGy are effective in reducing Salmonella by approximately 1.6–2.7 log cycles in filet américan and 1.3–1.8 log cycles in ground meat. Numbers of Y. enterocolitica and C. jejuni are always reduced by more than 4 log cycles with this dose.On sensory evaluation 38% of samples of filet américain irradiated directly with 1 kGy were not acceptable for a taste panel; preference was for the unirradiated sample in 82% of the cases. However, when beef was irradiated with the same dose prior to the addition of mayonnaise sauce no significant taste differences could be observed between nonirradiated and irradiated samples.     

Presence of Campylobacter and Arcobacter species in in-line milk filters of farms authorized to produce and sell raw milk and of a water buffalo dairy farm in Italy

The objectives of this study were to investigate the presence of Campylobacter spp. and Arcobacter spp. in dairy herds authorized for the production and sale of raw milk and in a water buffalo dairy farm, and to test the antimicrobial susceptibility of the isolates. A total of 196 in-line milk filters were collected from 14 dairy farms (13 bovine and 1 water buffalo) for detection of Campylobacter spp. and Arcobacter spp. by microbiological culture. For each farm investigated, 1 isolate for each Campylobacter and Arcobacter species isolated was tested using the Etest method (AB Biodisk, Solna, Sweden) to evaluate the susceptibility to ciprofloxacin, tetracycline, chloramphenicol, ampicillin, erythromycin, and gentamicin. A total of 52 isolates were detected in 49 milk filters in 12 farms (85.7%) out of 14 and the isolates were identified as Campylobacter jejuni (6), Campylobacter hyointestinalis ssp. hyointestinalis (8), Campylobacter concisus (1), Campylobacter fetus ssp. fetus (1), Arcobacter butzleri (22), and Arcobacter cryaerophilus (14). The small number of isolates tested for antimicrobial susceptibility precludes any epidemiological consideration but highlights that all Campylobacter isolates were susceptible to macrolides, which are the first-choice drugs for the treatment of campylobacteriosis, and that resistance to fluoroquinolones and tetracycline was detected; for Arcobacter isolates, resistance to ampicillin and chloramphenicol was detected. The sale of raw milk for human consumption by self-service automatic vending machines has been allowed in Italy since 2004 and the presence of C. jejuni in in-line milk filters confirms that raw milk consumption is a significant risk factor for human infection. The high occurrence of emerging Campylobacter spp. and Arcobacter spp. discovered in dairy farms authorized for production and sale of raw milk represents an emerging hazard for human health.     

Combined effect of gamma-irradiation and conventional cooking onAeromonas hydrophila in meatball

Irradiation combined with a conventional cooking procedure was applied to meatball and the effects on bacterial load and inoculatedAeromonas hydrophila were determined. Meatball samples were irradiated by using a⁶⁰Co source at the dose levels of 0, 0.30,0.75,1.50,2.50 kGy and cold stored at 4±1°C for 7 days. Bacterial load and the count ofA. hydrophila decreased when the irradiation dose level increased. A minimum inhibition effect was found at the dose of 0.30 kGy. Irradiation in combination with a conventional cooking procedure was found to be more effective in reducingA. hydrophila and the bacterial load in meatball. This study indicated that a dose of 0.75 kGy was sufficient to destroy approximately 10⁴ cfu/g ofA. hydrophila in meatball.     

Effect of Gamma Radiation on Campylobacter jejuni

Radiation resistance of Campylobacter jejuni in broth, ground beef, and ground turkey meat was determined using dose levels from 0 - 200 Krad at −30 ± 10°C, at 0 - 5°C, and at 30 ± 10°C. Irradiation at −30°C increased radiation resistance of cultures in ground meats; broth cultures were not greatly influenced by temperature. The effect of culture age on radiation resistance was also evaluated using cells in various physiological phases. Age did not have a pronounced effect on radiation resistance. The largest D₁₀ value for C. jejuni was 32 Krad, which was less than D₁₀ values commonly reported for salmonellae.     

Combined effect of gamma-irradiation and conventional cooking onAeromonas hydrophila in meatball

Irradiation combined with a conventional cooking procedure was applied to meatball and the effects on bacterial load and inoculatedAeromonas hydrophila were determined. Meatball samples were irradiated by using a⁶⁰Co source at the dose levels of 0, 0.30,0.75,1.50,2.50 kGy and cold stored at 4±1°C for 7 days. Bacterial load and the count ofA. hydrophila decreased when the irradiation dose level increased. A minimum inhibition effect was found at the dose of 0.30 kGy. Irradiation in combination with a conventional cooking procedure was found to be more effective in reducingA. hydrophila and the bacterial load in meatball. This study indicated that a dose of 0.75 kGy was sufficient to destroy approximately 10⁴ cfu/g ofA. hydrophila in meatball.     

Solid phase extraction (SPE) method for detection of irradiated meats

Solid phase extraction (SPE) has been proposed as an alternative to the currently used florisil column chromatography. The hydrocarbons formed from beef, pork and chicken irradiated with 0-10 kGy were determined by the SPE and quantified by GC/MS. The limit of detection for the hydrocarbons in irradiated meats was 0.5 kGy. The correlation between the irradiation dose and the concentrations of hydrocarbons in beef, pork and chicken was high that linear regression coefficients (r²) were 0.87-0.99. SPE method would be used as the rapid detection of irradiated meats.     

Changes in colour and antioxidant activities of Hizikia fusiformis cooking drips by gamma irradiation

To utilize the cooking drips produced during the seaweed drying process, the effect of gamma irradiation on microbial contamination, colour, and antioxidant activities of Hizikia fusiformis cooking drips (HCD) was investigated. A two log cycles reduction of total aerobic bacteria and yeast and moulds counts was obtained irradiating HCD at 1 kGy. The Hunter L^∗ value of the HCD ethanol extract was increased by the gamma irradiation treatment, but the a^∗ and b^∗ values decreased upon irradiation depending on the absorbed dose. The 1,1-diphenyl-2-picrylhydrazyl radical scavenging and β-carotene bleaching activities of the HCD extracts increased as a result of gamma irradiation, which was rationalized by the observed increase in polyphenolic compounds content. These results suggest that wasted cooking drips can be used as a functional component by the food and cosmetic industries if the irradiation technology were applied.     

Gamma irradiation as a means to eliminate Listeria monocytogenes from frozen chicken meat

Cells of Listeria monocytogenes ATCC 35152 were sensitive to gamma irradiation in phosphate buffer, pH 7.00 (D₁₀, dose required for 10% survival—0.15 kGy) at 0–5°C. The cells showed higher radiation survival when irradiated under frozen condition, with a D₁₀ of 0.3 kGy. The protection offered by shrimp/chicken/kheema homogenates (100 g litre^?1) was evidenced by even higher D₁₀ values (0.5 kGy) at both 0–5°C and cryogenic temperature. Boneless chicken meat samples were artificially inoculated with L monocytogenes ATCC 35152 cells at low (5 × 10³) colony-forming unit (cfu) g^?1 and high (5 × 10⁶ cfu g^?1) concentrations and irradiated at 1, 3, 4, 6 kGy doses under cryogenic conditions. The efficacy of the radiation process was evaluated by detecting L monocytogenes during storage at 2–4°C in the irradiated samples. These studies, when repeated with three other serotypes of L monocytogenes, clearly suggested the need for a dose of 3 kGy for elimination of 10³ cfu cells of L monocytogenes g^?1 from air-packed frozen chicken meat.     

Inhibition of enterotoxicogenic strains Bacillus cereus GT1 and Staphylococcus aureus S1 isolated from double white cream cheese

In this study three different food preservatives (sodium nitrate, sodium benzoate and sodium sorbate) were used to evaluate their effect on two enterotoxicogenic strains (Bacillus cereus GT1 and Staphylococcus aureus S1). A significant decrease in the viability and production of virulence factors was observed. Yet, obvious tolerance to increasing concentrations (from 1 to 6?g/l) of the three preservatives was recorded reflecting possible resistance mechanisms within the tested strains. The two strains were subjected to increasing doses of gamma radiation (1, 2, 3, 4, 5, 6, 7, 8, 9 and 10?kGy). Obvious correlation was observed between the initial counts of bacterial spores contaminating the products and the required dose for their complete elimination. Whereas the eliminating dose of B. cereus GT1 strain was 10?kGy only 4?kGy was sufficient to suppress the growth and virulence of S. aureus S1, reflecting its sensitivity to low doses of gamma irradiation. Also, inhibition of the two strains by probiotic strain Bacillus pumilus G4 was studied both in situ (in cheese) and in vitro (in culture media). The viable cell population of B. cereus GT1 increased from 10⁶ to 2.9?×?10⁸?CFU/g within 60?h in controls but decreased from 2.1?×?10⁶ to 2.3?×?10³?CFU/g after treatment with the probiotic strain. No viable count was observed after 60?h of incubation. Whereas, the viable cell population of S. aureus S1 increased from 10⁶ to 2.5?×?10⁸?CFU/g within 60?h in controls but decreased from 1.5?×?10⁶ to 4.3?×?10²?CFU/g after treatment with the probiotic strain. No viable count was observed after 54?h of incubation.     

电子束辐照对即食凤爪品质的影响

以即食凤爪为试材,研究了电子加速器辐照处理对凤爪品质的影响,分析了不同剂量处理条件下凤爪的脂质氧化TBARS值、总挥发性盐基氮、弹性、汁液流失率、感官品质和菌落的变化情况。结果表明:当辐照剂量达到6.0 kGy时,产品贮藏180 d后其菌落总数为4 300 cfu/g,菌落总数电子束辐照的D10值在1.84～2.22 kGy;辐照剂量大于6.0 kGy时,TBARS值与空白相比有显著差异,而TVB-N则无显著差异;辐照剂量超过8.0 kGy时,则凤爪的弹性与汁液流失率有显著的影响。辐照剂量在一定范围内(8.0 kGy),对产品的感官品质不会产生明显的影响。常温下180 d的贮藏实验结果显示,采用电子束辐照可以显著降低并控制即食凤爪微生物含量,延长产品的货架期。     

Use of low dose e-beam irradiation to reduce E. coli O157:H7, non-O157 (VTEC) E. coli and Salmonella viability on meat surfaces

This study determined the extent that irradiation of fresh beef surfaces with an absorbed dose of 1 kGy electron (e-) beam irradiation might reduce the viability of mixtures of O157 and non-O157 verotoxigenic Escherichia coli (VTEC) and Salmonella. These were grouped together based on similar resistances to irradiation and inoculated on beef surfaces (outside flat and inside round, top and bottom muscle cuts), and then e-beam irradiated. Salmonella serovars were most resistant to 1 kGy treatment, showing a reduction of ≤ 1.9 log CFU/g. This treatment reduced the viability of two groups of non-O157 E. coli mixtures by ≤ 4.5 and ≤ 3.9 log CFU/g. Log reductions of ≤ 4.0 log CFU/g were observed for E. coli O157:H7 cocktails. Since under normal processing conditions the levels of these pathogens on beef carcasses would be lower than the lethality caused by the treatment used, irradiation at 1 kGy would be expected to eliminate the hazard represented by VTEC E. coli.     

Inactivation kinetics of Listeria monocytogenes, Salmonella enterica serovar Typhimurium, and Campylobacter jejuni in ready-to-eat sliced ham using UV-C irradiation

To investigate the applicability of UV-C irradiation on the inactivation of foodborne pathogenic bacteria in ready-to-eat sliced ham, UV-C treatment was evaluated. Irradiation dose required for 90% reduction of the populations of Listeria monocytogenes, Salmonella enterica serovar Typhimurium, and Campylobacter jejuni were determined to be 2.48, 2.39, and 2.18 J/m². Ready-to-eat sliced hams were inoculated with the pathogens and irradiated with UV-C light of 1000, 2000, 4000, 6000, and 8000 J/m². Microbiological data indicated that foodborne pathogen populations significantly (p < 0.05) decreased with increasing UV-C irradiation. In particular, UV-C irradiation at 8000 J/m² reduced the populations of L. monocytogenes, S. Typhimurium, and C. jejuni in the ham by 2.74, 2.02, and 1.72 log CFU/g. The results indicate that UV-C irradiation can be used as a microbial inactivation method for ready-to-eat sliced ham, and inactivation kinetics of the foodborne pathogens fit the Weibull model better than the first-order kinetics model.     

Inhibition of egg and larval development of the Indian meal moth Plodia interpunctella (Hübner) and almond moth Ephestia cautella (Walker) by gamma radiation in decorticated hazelnuts

In this study, inhibition of egg hatching and development of immature stages of the Indian meal moth and almond moth by irradiation in hazelnuts was investigated. Irradiation doses required to inhibit the development of eggs of Plodia interpunctella and Ephestia cautella were 450 and 300 Gy, respectively, and no adults of either species emerged from treated samples (all stages) at 1 kGy of radiation in large-scale tests. The low-dose irradiation treatment did not cause excessive oxidative deterioration and no significant differences were found in organoleptic studies at 0.5-3 kGy in decorticated hazelnuts. However, total tocopherol content decreased depending on irradiation dose.     

Biofilm formation by Campylobacter jejuni in controlled mixed-microbial populations

This study was to screen the ability of biofilm formation by Campylobacter jejuni strains found in New Zealand, and investigate the biofilm growth of C. jejuni in a controlled mixed-microbial population that includes five different bacteria. The ability of C. jejuni to form a biofilm in monoculture and mixed-microbial populations was measured in a laboratory assay using a microtiter plate screening assay. The optical density of the biofilm and cell growth from mixed-microbial populations was converted to a Biofilm Formation Index (BFI). This index was used to standardize the biofilm formation in the mixed-microbial populations. High BFI was observed for Enterococcus faecalis (2.30) and Staphylococcus simulans (3.75) when they were grown with C. jejuni multilocus sequence type ST-474: a dominant poultry and human-associated type in New Zealand. C. jejuni cells were recovered from most of the biofilms containing E. faecalis and/or S. simulans. These results suggest that E. faecalis and S. simulans may play a role in biofilm formation in the poultry environment as both of these microorganisms are found in poultry processing environments and were able to form a biofilm in association with C. jejuni under microaerobic conditions. Understanding the relationships among C. jejuni, E. faecalis and S. simulans in poultry processing plants and farms may help in the design of strategies to reduce the reservoir of contamination of these bacteria and reduce the incidence of campylobacteriosis.     

Effects of γ-irradiation on the α-tocopherol and fatty acids content of raw unpeeled almond kernels (Prunus dulcis)

The present study evaluated fatty acid composition and α-tocopherol content of almond as a function of irradiation dose in order to determine dose levels causing minimal undesirable changes to almonds. Raw unpeeled almonds variety Tuono (Prunus dulcis (Mill.) D. A. Webb) were irradiated using ⁶⁰Co source at dose of 0.5, 1.5, 3, 6, 8 and 10 kGy.     

PorA specific primers for the identification of Campylobacter species in food and clinical samples

Campylobacteriosis is a public health problem with considerable socio-economic impact. As the European Food Safety Authority has emphasized the importance of a surveillance programme for campylobacteriosis, the aim of the present study was the optimization of a specific and sensitive PCR protocol able to detect Campylobacter species responsible for gastrointestinal infections. Raw poultry meat samples were analysed for the presence of Campylobacter sp., by plating onto mCCD (Modified Charcoal-Cefoperazone-Deoxycholate) Agar and Campylobacter Selective Preston Agar and using four sets of species-specific primers for Campylobacter jejuni, Campylobacter coli, Campylobacter upsaliensis and Campylobacter lari designed to bridge the porA gene. The resulting primers demonstrated a sensitivity of 0.01 ng/μl for the C. coli-specific, C. lari-specific, and C. upsaliensis-specific primer sets and 0.5 ng/μl for the C. jejuni-specific primer sets using DNA from pure cultures. Non-specific amplification of non-target DNA was not observed indicating excellent specificity. The primers were useful for the analyses of poultry meat samples both for direct plating onto mCCDA, and for DNA extracted directly from the cells grown for 48 h in Preston enrichment broth. The sets of primers were also useful when used for species identification of human isolates.