1,721,184 research outputs found
Novel food trends and climate changes: Impact on emerging food-borne bacterial pathogens
No full textRates of infection with foodborne bacterial pathogens and their attendant economic burden remain high in industrialized and developing countries, despite persistent efforts to increase the safety of the food supply from farm to fork. New pathogens, like non-O157 Shiga toxin-producing Escherichia coli (STEC) and Arcobacter butzleri have been isolated during outbreaks; others, like Helicobacter pullorum, are emerging as foodborne human pathogens. Large consumption of fresh produce in healthy diets, increasing worldwide trade in food products and raw materials and climate changes are all among the key factors contributing to shifts in the traditional association of foodborne pathogens from foods of animal origin to other commodities and to the emergence or re-emergence of known and new pathogens
Modelling survival behaviour of Salmonella enterica ser. Enteritidis, Typhimurium and Tennessee on table eggs during storage at different temperatures
No full textQuantitative risk assessment studies on the health risk of Salmonella due to consumption of contaminated table eggs are based on the assumption that Salmonella is inside the egg and that the pathogen belongs to serovar Enteritidis. However different serovars of Salmonella may contaminate the surface of table eggs and spread to other foods at consumer's kitchen due to improper food handling. In the present study the survival behaviour of one strain each from Salmonella enterica serovars Enteritidis, Typhimurium and Tennessee on table egg surface during storage at 4, 8, and 20°C have been described. Besides, in those cases observed data were subjected for modelling; linear, log-linear tail and Weibull models were compared in terms of model fitting and model performance. Overall, in most cases, inactivation kinetics presented a linear trend on Salmonella behaviour so that Weibull and linear models adequately described observed data. Regarding log-linear tail models, though they presented a better fitting, their adequacy could not be assessed given the lack of data in the tail region. Regarding storage temperatures, 4°C was predicted to be the most inhibitory temperature for table eggs externally contaminated by a strain of S.enterica serovar Enteritidis. After 28 days of storage, a reduction of 4 log10cfu/g of eggshell on the S.enterica ser. Enteritidis load was registered at 4°C. S.enterica ser. Typhimurium and Tennessee showed higher survival rates at all tested temperatures. The results highlighted the importance of keeping constant the storage temperature of table eggs in order to reduce the risk of S.enterica ser. Enteritidis contaminating the surface of table eggs. However this temperature might not be the optimal one in view of S.enterica serovars other than Enteritidis
Proposal of sampling protocols to verify possible performance objectives for Campylobacter species control in Italian broiler batches
Full text linkCampylobacteriosis represents the most important food-borne illness in the EU. Broilers, as well as poultry meat, spread the majority of strains responsible for human cases. The main aims of this study were to suggest an approach for the definition of performance objectives (POs) based on prevalence and concentration of Campylobacter species (spp.) in broiler carcasses; moreover, sampling plans to determine the acceptability of broiler batches at the slaughterhouses in relation to such POs were formulated. The dataset used in this study was the one regarding Italy composed during the European Food Safety Authority baseline survey which was performed in the EU in 2008. A total of 393 carcasses obtained from 393 different batches collected from 48 Italian slaughterhouses were included in the analysis. Uncertainty in prevalence and concentration of Campylobacter spp. on carcasses was quantified assuming a beta and log normal distribution. Statistical analysis and distribution fitting were performed in ModelRisk v4.3 (Monte Carlo simulation with 10,000 iterations). By taking the 50th percentile of prevalence distribution as safety limit, sampling plans were subsequently calculated basing on the binomial approach. Final values of number of samples were equal to 4 or 5 to test with qualitative analysis. Considering a limit of quantification of 10 colony forming units/g, a higher number of samples (i.e. 10-13) would be necessary to test using enumeration. An increase of the sensibility of the analytical technique should be necessary to achieve realistic and useful sampling plans based on concentration data
Evaluation of Real-Time PCR to complement ISO 6579:2004 method for the detection of Salmonella in pork cuts
Full text linkAccording to Commission Regulation (EC) No 2073/2005 of 15 November 2005 on microbiological crite-ria for foodstuff , the analytical reference method for the detection of Salmonella in food is ISO 6579:2004. However this long and labor-intensive method is not in line with the short production times of the food industry. In the last years, Real-Time PCR is used more and more by scientists for the relia-ble, fast and specific detection of bacterial pathogens in food. The aim of the present study was to eval-uate the Salmonella detection capability of a validated Real-Time PCR assay on naturally contaminated pork cuts in comparison with the reference method ISO 6579:2004. Three sampling were performed and included 16 pork cut packaging. From each packaging, three aliquots of 10 g each were tested separate-ly by ISO 6579:2004 method and by Real-Time PCR. In particular this molecular method was applied on DNA samples extracted from pre-enrichment broth after 1 and 18 hours of incubation. Within the three sampling periods, Real-Time PCR detected Salmonella in 81%, 100% e 62,5% of pork cut samples respectively, whereas the corresponding percentages of detection of the reference method were 56%, 81% e 62,5% respectively. In conclusion the Real-Time PCR assay used in the present study might be a reliable tool for a fast detection of Salmonella on pork cuts, especially when large number of samples needs to be tested. The reference method might be applied only on positive samples for isolation purpos-es mandatory in epidemiological investigations
Listeria monocytogenes Circulating in Rabbit Meat Products and Slaughterhouses in Italy: Prevalence Data and Comparison among Typing Results
No full textRabbit meat has outstanding dietetic and nutritional properties. However, few data on microbiological hazards associated with rabbit productions are available. In this study, the presence of Listeria monocytogenes was determined in 430 rabbit carcasses, 256 rabbit meat cuts and products, and 599 environmental sponges collected from four Italian rabbit slaughterhouses over a period of 1 year. Prevalence of L. monocytogenes among the 1285 rabbit meat and environmental samples was 11%, with statistically significant differences between slaughterhouses. The highest prevalence (33.6%) was observed in rabbit meat cuts and products; the majority of positive environmental samples were collected from conveyor belts. Overall, 27.9% and 14.3% of rabbit cuts and carcasses, respectively, had L. monocytogenes counts higher than 1 colony-forming unit (CFU)/10 g. A selection of 123 isolates from positive samples was genotyped and serotyped to determine genetic profiles and diversity among L. monocytogenes isolates contaminating different slaughterhouses and classes of products investigated. Discriminatory power and concordance among the results obtained using multilocus variable-number tandem-repeat analysis (MLVA), multilocus sequence typing (MLST), pulsed-field gel electrophoresis (PFGE), automated EcoRI ribotyping, and serotyping were assessed. The isolates selected for typing were classified into serotypes 1/2a (52.8%), 1/2c (32.5%), and 1/2b (14.6%). The majority of the isolates were classified as ST14 (34.1%), ST9 (35.5%), ST121 (17.9%), and ST224 (14.6%). The greatest discriminatory power was observed with the MLVA typing, followed by MLST, PFGE, and ribotyping. The best bidirectional concordance was achieved between PFGE and MLST. There was 100% correlation between both MLST and MLVA with serotype. Moreover, a high unidirectional correspondence was observed between MLVA and both MLST and PFGE, as well as between PFGE and both MLST and serotyping. The results of this study show for the first time in Italy prevalence and genetic profiles of L. monocytogenes isolated in rabbit products and slaughterhouses
Identification and genetic characterisation of orthopaedic Staphylococcus isolates collected in Italy by automated EcoRI ribotyping
No full textSanitisation of fresh-cut celery and radicchio by gas plasma treatments in water medium
Full text linkThe antimicrobial efficacy of dielectric barrier discharge atmospheric gas plasma (DBD) was tested against Listeria monocytogenes and shigatoxin-producing Escherichia coli serogroups O157 and O26. Challenge tests were carried out with samples of cut celery and radicchio leaves inoculated with a mix of five strains of L. monocytogenes or the two strains of E. coli immersed in deionised water. The treatment efficacy was also assessed considering only the contaminated deionised water. For deionised inoculated water alone, a treatment time-dependent strong effect was observed and a pathogens reduction higher than 6LogCFU/mL was obtained after 40min of treatment. With the vegetables presence in the liquid medium, the efficacy appeared reduced and related to the treatment time, microorganism, substrate and storage duration (reduction up to 2.5 and 3.7LogCFU/cm2 for L. monocytogenes and E. coli, respectively). No significant changes were observed on celery visual attributes, soluble solids content and textural parameters. A significant decrease of the chroma colour parameter during storage was noted in treated radicchio samples respect to control ones
Comparison between 16S rRNA and shotgun sequencing data for the taxonomic characterization of the gut microbiota
Full text linkIn this paper we compared taxonomic results obtained by metataxonomics (16S rRNA gene sequencing) and metagenomics (whole shotgun metagenomic sequencing) to investigate their reliability for bacteria profiling, studying the chicken gut as a model system. The experimental conditions included two compartments of gastrointestinal tracts and two sampling times. We compared the relative abundance distributions obtained with the two sequencing strategies and then tested their capability to distinguish the experimental conditions. The results showed that 16S rRNA gene sequencing detects only part of the gut microbiota community revealed by shotgun sequencing. Specifically, when a sufficient number of reads is available, Shotgun sequencing has more power to identify less abundant taxa than 16S sequencing. Finally, we showed that the less abundant genera detected only by shotgun sequencing are biologically meaningful, being able to discriminate between the experimental conditions as much as the more abundant genera detected by both sequencing strategies
Microbiological and Modeling Approach to Derive Performance Objectives for Bacillus cereus Group in Ready-to-Eat Salads
No full textIn this article, the performance objectives (POs) for Bacillus cereus group (BC) in celery, cheese, and spelt added as ingredients in a ready-to-eat mixed spelt salad, packaged under modified atmosphere, were calculated using a Bayesian approach. In order to derive the POs, BC detection and enumeration were performed in nine lots of naturally contaminated ingredients and final product. Moreover, the impact of specific production steps on the BC contamination was quantified. Finally, a sampling plan to verify the ingredient lots' compliance with each PO value at a 95% confidence level (CL) was defined. To calculate the POs, detection results as well as results above the limit of detection but below the limit of quantification (i.e., censored data) were analyzed. The most probable distribution of the censored data was determined and two-dimensional (2D) Monte Carlo simulations were performed. The PO values were calculated to meet a food safety objective of 4 log10 cfu of BC for g of spelt salad at the time of consumption. When BC grows during storage between 0.90 and 1.90 log10 cfu/g, the POs for BC in celery, cheese, and spelt ranged between 1.21 log10 cfu/g for celery and 2.45 log10 cfu/g for spelt. This article represents the first attempt to manage the concept of PO and 2D Monte Carlo simulation in the flow chart of a complex food matrix, including raw and cooked ingredients
- …
