Incidence and genetic variability of Listeria species from three milk processing plants

The presence of Listeria in three milk processing environments as a potential source of milk contamination was assessed. Swab samples (n = 210) taken from milk processing plants were examined. Sample sites included the milk processing equipment, besides areas handling raw and pasteurized milk. The USDA Listeria-selective enrichment procedure was used to process the samples. Forty one (19.52%) Listeria isolates were recovered. The isolates were further subjected to biochemical and genotypic characterization. Out of 41 isolates, 16 (7.62%) were confirmed as Listeria monocytogenes, 2 (0.95%) as L. ivanovii, 19 (9.05%) as L. innocua. 1 (0.48%) as L. seeligeri and 3 (1.43%) as L. grayi. All the L. monocytogenes isolates were positive for the hlyA gene. PCR based serotyping revealed all L. monocytogenes to be of 1/2a, 1/2c, 3a and 3c serovar group. AscI and ApaI restriction analysis yielded four PFGE clusters for 16 L. monocytogenes isolates obtained from raw milk collector, milk silos, buttermilk mixer, cheese and other milk product processor. No predominant PFGE cluster was observed among these L. monocytogenes isolates. The main sources of L. monocytogenes were found to be raw milk collector and milk silos. In the present study L. monocytogenes was isolated from milk and milk products processing plants which could cross-contaminate the processed products and may possess a potential threat to public health.     

Prevalence and antimicrobial resistance patterns of Listeria species isolated from poultry products marketed in Iran

In the present study, a total of 402 poultry product samples composed of raw, ready-to-cook (RTC) and ready-to-eat (RTE) products were examined for the presence of Listeria spp. The total contamination rate with Listeria spp. in poultry products was 33.3% with a higher rate of contamination in warm seasons than in cold seasons. The most species recovered was Listeria innocua (46.3%); the remaining isolates were Listeria monocytogenes (38.8%), Listeria ivanovii (9.7%) and Listeria seeligeri (5.22%). L. monocytogenes was detected in 14.1%, 12.2% and 11.4% of raw, RTC and RTE poultry products, respectively. Serotype 4b (44.9%) was the predominant serotype of L. monocytogenes isolates followed by 1/2a (40.8%), 1/2b (10.2%) and 1/2c (4.08%). Considering seasonal variability, 1/2a was the most prevalent serotype in warm seasons, while 4b was predominant in cold seasons. The Listeria spp. particularly L. monocytogenes isolates were highly resistant to ampicillin, penicillin, fluroquinolones and tetracycline. The results indicate that high prevalence of Listeria spp. especially L. monocytogenes in poultry products, and resistance of the isolates to the antimicrobials commonly used to treat human listeriosis could be a potential health hazard for consumers. In addition, prevalence of L. monocytogenes serotype 4b that involved in the majority of foodborne outbreaks of human listeriosis is a public health concern.     

Simultaneous detection of Listeria species isolated from meat processed foods using multiplex PCR

Listeriosis is a foodborne disease caused by the pathogenic Listeria monocytogenes and is considered as a serious health problem due to the severity of symptoms and its high mortality rate. Listeria genus is divided into six species and especially L. monocytogenes is an important foodborne pathogen in humans and livestock. Recently, other Listeria species are reported as pathogenic strains in decayed foods and environments as well. High mortality rate of listeriosis demands for rapid methods to detect the potential presence of the food pathogens in the food industry. We have developed a multiplex PCR for rapid and simultaneous detection of six Listeria species including Listeria grayi, Listeria innocua, Listeria ivanovii, L. monocytogenes, Listeria seeligeri and Listeria welshimeri to identify specific Listeria species in processed foods. The optimized multiplex PCR in this study utilized one Listeria genus specific and each Listeria species-specific primer pairs. Each primer pair yields the products of 370-bp for Listeria genus-specific, 201-bp for L. grayi-specific, 749-bp for L. innocua-specific, 463-bp for L. ivanovii-specific, 509-bp for L. monocytogenes-specific, 673-bp for L. seeligeri-specific and 281-bp for L. welshimeri-specific. We have successfully applied multiplex PCR strategy to 93 Listeria isolates from processed meat products to determine specific Listeria species and out of which 81 strains of L. monocytogenes, 10 strains of L. innocua and 2 strains of L. welshimeri were identified. This established multiplex PCR provides rapid and reliable results and will be useful for the detection of Listeria species in contaminated food products and clinical samples.     

Prevalence of Listeria spp. in ready to eat foods (RTE) from Algiers (Algeria)

The aim of this study was to establish the occurrence of Listeria spp., especially Listeria monocytogenes in ready to eat RTE food marketed in Algiers (Algeria).A total of 227 samples were collected from different producers and retailers.All samples were analyzed using a conventional cultivation method AFNOR V08-055.Out of 227 samples tested, 21 (9.3%) tested positive for Listeria spp. among them, 6 (2.6%) tested positive for L. monocytogenes. L. innocua was the most common Listeria species found being detected in 11 samples (4.8%), although both Listeria ivanovii and Listeria welshimeri were detected in 3 (1.3%) and 1 (0.4%) food samples respectively.The study of the antimicrobial sensitivity of Listeria monocytogenes strains showed no resistance.The study has enabled us to detect these contaminants in a wide range of RTE foods, to suggest that contamination likely occurs after heat treatment, and to assess the danger represented by this category of food for populations at risk.     

Increase over time in the prevalence of multiple antibiotic resistance among isolates of Listeria monocytogenes from poultry in Spain

The aim of this study was to determine and compare the antibiotic resistance profiles of Listeria monocytogenes isolates obtained from poultry in North-Western Spain in 1993 and 2006. The prevalence of Listeria spp. and L. monocytogenes was also investigated. A total of 202 samples were analysed (100 in 1993 and 102 in 2006). Samples taken in 1993 and 2006 showed a similar (P > 0.05) prevalence for both Listeria spp. (95.0% and 92.1%, respectively) and L. monocytogenes (32.0% and 24.5%). In both 1993 and 2006 the species most frequently detected was Listeria innocua, followed by L. monocytogenes. Other species isolated were Listeria welshimeri, Listeria grayi and Listeria ivanovii. L. monocytogenes isolates (68) were tested by disc diffusion assay for their resistance to 15 drugs currently used in veterinary and human therapy. All isolates displayed resistance to at least one antibiotic. Excluding nalidixic acid, to which most strains are intrinsically resistant, 37.2% of strains in 1993 and 96.0% in 2006 showed resistance to at least one antibiotic. Multi-resistance (resistance to two or more antibiotics) was less common in 1993 than in 2006 (18.6% and 84.0%, respectively; P < 0.001). The average number of antibiotics to which the strains were resistant was lower (P < 0.001) in 1993 (1.6) than in 2006 (4.2). An increase (P < 0.05) in the percentage of resistant strains was observed between 1993 and 2006 for six different drugs: gentamicin, streptomycin, neomycin, enrofloxacin, ciprofloxacin and furazolidone. In this research, the prevalence and the antibiotic susceptibility of L. monocytogenes in poultry samples from the same origin in North-Western Spain in the 1990s and the 2000s were compared for the first time. The increase in antibiotic resistance from 1993 to 2006 constitutes a matter for concern and confirms a general worldwide pattern among many groups of bacteria. The high prevalence of L. monocytogenes in poultry suggests the crucial role of food handlers in preventing listeriosis in consumers. Reducing the prevalence of L. monocytogenes in poultry and preventing the emergence or selection of antibiotic-resistant strains are also highlighted.     

Listeria monocytogenes prevalence, contamination levels and strains characterization throughout the Parma ham processing chain

In order to estimate prevalence, levels and patterns of Listeria monocytogenes contamination, a total of 774 swine carcasses were traced along the Parma ham production chain. Analyses were conducted on isolates originated from the same carcass, collected at different stages during processing, resulting in 0.2% (faeces at intestine removal from carcasses), 3.0% (swabbing of carcasses), 12.5% (fresh hams) and 2.0% prevalence (dry-cured hams). The highest contamination levels of L. monocytogenes were reached in fresh hams after cutting and were followed by a marked decrease during the subsequent processing stages. All the 132 isolates were characterized by serotyping and Pulsed-Field Gel Electrophoresis (PFGE). Transfer of L. monocytogenes between different stages of the processing chain was not reported, whereas processing itself has proved to be an important cause of contamination. The sole isolate of fecal origin belonged to a pulsotype that was uncommon to any of those recovered in carcasses, fresh hams and dry-cured hams, indicating that contaminations from farms does not significantly affect Parma ham production. For the majority of the strains isolated from the same production plants, PFGE profiles were highly similar. In several cases, the same pulsotypes were recurrently detected, over time, in carcasses and fresh ham samples sharing the same processing environment. A_w levels were also measured, showing that drying of the ham surface was able to induce a considerable decrease of the contamination levels, although unable to ultimately remove L. monocytogenes.     

Prevalence and characterization of Listeria monocytogenes isolated from retail food in Henan,China

Listeria monocytogenes, an important foodborne pathogen, is the causal agent of listeriosis. In this study, a total of 954 food samples originating from raw meat, cooked meat products, seafood, and vegetables purchased from supermarkets and open-air markets in Henan province, China, were analyzed for the presence of L. monocytogenes. All L. monocytogenes isolates were subjected to serotyping, pulsed-field gel electrophoresis (PFGE), and antimicrobial resistance. The overall percentage of L. monocytogenes prevalence was 6.2% (n = 59) with the highest rate of 7.4% for cooked meat products followed by raw meat (6.7%). The isolates belonged to five serotypes (1/2a, 1/2b, 1/2c, 4b, and 4c), with serotype 1/2a being predominant (55.9%). PFGE revealed a low genetic diversity among the isolates, irrespective of their sources, suggesting that dominant clones are widespread in different food products in Henan. Resistance to cefotaxime (30.5%) and ciprofloxacin (13.5%) was most often, whereas resistance to tetracycline, trimethoprim/sulfamethoxazole, and erythromycin was observed less frequently. The presence of L. monocytogenes in food products and antimicrobial resistance among the isolates represents a potential public health risk. Our results indicate that effective hygienic measures and bacteriological controls are necessary in China to reduce the contamination of retail food samples by L. monocytogenes.     

Prevalence and characterization of Listeria monocytogenes isolated from retail-level ready-to-eat foods in South China

Listeria monocytogenes is an important food-borne pathogen causing meningitis, meningoencephalitis and abortion. To assess the potential risk to consumer health, the presence of L. monocytogenes was investigated using qualitative and quantitative methods. Ten (6.33%) of 158 retail RTE food samples were positive for L. monocytogenes and the contamination levels were less than 10 MPN/g,while none of 65 dairy products was positive for L. monocytogenes. The 37 strains were grouped into five clusters and two singletons, five clusters and two singletons, and three clusters and one singleton by enterobacterial repetitive intergenic consensus-polymerase chain reaction (ERIC-PCR) and RAPD fingerprint respectively, at similarity coefficient of 80%. The susceptibility test showed that 83.8% were susceptible to 15 antimicrobials; two were penicillin-resistant, and one was multidrug-resistant to kanamycin, tetracycline, sulfamethoxazole, rifampin, gentamycin, penicillin, and ampicillin. Virulent L. monocytogenes that possess partial antimicrobial resistance, and serotypes frequently associated with listeriosis were recovered from RTE foods. Consumers may, therefore, be exposed to potential risks of L. monocytogenes infection in South China. This study contributed to the prevalence and contamination levels of L. monocytogenes in RTE foods in South China for the first time, providing baseline information for Chinese regulatory authorities to formulate a regulatory framework for controlling L. monocytogenes to improve the microbiological safety of RTE foods.     

Occurrence of Listeria spp. in dairy plants in Southern Italy and molecular subtyping of isolates using AFLP

We report the detection of Listeria spp. and Listeria monocytogenes in 34 dairy plants. In total, 547 of food, product contact surface and floor drain samples were collected along the product lines. Nineteen cheese factories (55.8%) were contaminated by Listeria spp. Of these 20.6% were L. monocytogenes positive. Listeria spp. was found in 6.8% of food samples, 11.3% of product contact surfaces and 40.6% of floor drains. L. monocytogenes was found in 2.4% of food samples, 4.9% of product contact surfaces and 18.8% of floor drains. Twentyfive L. monocytogenes isolates were serotyped using commercial specific antisera and genotyped using Amplified Fragment Length Polymorphism (AFLP) analysis. AFLP genotyping discriminated the four species of Listeria isolated and different genotypes for each species, moreover it could identify persistent genotypes in some dairy facilities. Listeria spp. and L. monocytogenes are widely spread in the dairy sector and probably contaminate foods during the production process. Facility-based monitoring can identify possible routes of transmission and thus allow establishment of more effective strategies to prevent food contamination.     

Prevalence of Listeria spp. at a poultry processing plant in Brazil and a phage test for rapid confirmation of suspect colonies

Sites and occurrence of Listeria contamination in an industrial poultry processing plant were investigated by sampling carcasses at varying stages of processing and testing the hands and gloves of food handlers as well as the chilling water used in the process. In the course of nine visits to a local processing plant we collected a total of 121 samples: 66 from carcasses, 37 from workers' hands and gloves and 18 from the water used for chilling. Except for the water samples Listeria was isolated at all sampling sites. The species most often isolated was Listeria innocua, which accounted for 28 of the 31 (90.3%) isolates. The frequency of Listeria in the chicken carcasses was similar at bleeding, defeathering and end of evisceration stages (33.3%), reduced during scalding (16.7%), and rose immediately after initial evisceration stage (50%) to peak after packaging (76.2%). The carcasses were contaminated by L. monocytogenes serotypes 1b and 1c only during packaging. The prevalence of Listeria spp. on workers' hands and gloves was 46% mostly with L. innocua (40.5%) followed by L. monocytogenes 1b (11.8%). Chilling water presented more than 100 ppm of chlorine, which could explain why the samples were negative to Listeria. As the contamination by Listeria in the carcasses progressively rose both in number, species and strains during processing it seems reasonable to conclude that those carcasses become contaminated at the processing level. Improvement and innovation measures to control bacteria in general at the processing plant level are necessary to effectively reduce final product contamination by L. monocytogenes. In the course of this work we introduced a bacteriophage susceptibility test to confirm suspected Listeria colonies which was able to reduce the time of analysis to a minimum of 30 h depending on the isolation technique employed.     

A 12-month longitudinal study of Listeria monocytogenes contamination and persistence in pork retail markets in China

Listeria monocytogenes is a foodborne pathogen frequently isolated from raw pork meat. This study was designed to investigate the prevalence and molecular characteristics of L. monocytogenes in raw pork from open markets in China. The survey was conducted monthly over a 12-month period in Zigong, China. L. monocytogenes was isolated from 262 of 1641 samples collected (16.0%) including minced meat samples (131/608, 21.5%), pork pieces samples (111/857, 13.0%) and environmental swabs (20/176, 11.4%). The isolation rates in spring and winter were significantly higher than those in summer and autumn (X² = 68.85, P < 0.05). All isolates were subjected to serotyping, multi-locus sequence typing (MLST) and AscI pulsed-field gel electrophoresis (PFGE). The 262 isolates were subtyped into five serotypes: 1/2b (43.1%), 1/2c (35.5%), 1/2a (19.1%), 4b (1.1%), 3a (1.1%); 20 sequence types (STs) with four most frequent STs, being ST9 (35.9%), ST87 (19.8%), ST3 (16.0%) and ST8 (14.1%); and 39 pulsotypes (PTs) with PT4 (26.3%), PT30 (14.5%) and PT11 (12.6%) being most frequent. Two primary pulsotypes from pork pieces were previously isolated from clinical listeriosis cases in the local hospitals. The six markets from different districts differed in the level of contamination and strain types. Persistent contamination of L. monocytogenes was found in the markets especially in meat mincers, which were found to be one likely source of continuous cross contamination. These findings will help develop strategies to reduce L. monocytogenes contamination in open markets for better public health control and prevention of foodborne L. monocytogenes infections.     

Prevalence,antibiotic resistance and genetic diversity of Listeria monocytogenes isolated from retail ready-to-eat foods in China

Listeria monocytogenes is a major foodborne pathogen that is well known as high mortality rate upon infected. This study aimed to investigate the prevalence of L. monocytogenes isolates from retail ready-to-eat (RTE) foods in China and characterize the isolates of L. monocytogenes by antibiotic resistance, serotyping, ERIC-PCR and REP-PCR subtyping analyses. From September 2012 to January 2014, a total of 364 retail RTE foods were obtained. Using the qualitative and quantitative methods, 25 samples (6.87%) were positive for L. monocytogenes. The identity of isolates of L. monocytogenes was confirmed by PCR. All 80 isolates in this survey were sensitive to penicillin and mezlocillin, the highest resistance is clindamycin (51.25%), followed by cephalothin (23.75%) and ampicillin (12.5%). Twenty-seven isolates were susceptible to all 14 tested antibiotics; seventeen isolates were resistant to more than two antibiotics, including six multiresistent strains resist to more than 10 antibiotics. L. monocytogenes isolates belonged to serovar types 1/2a (3a), 4b (4d, 4e), 1/2b (3b, 7) and 1/2c (3c). 29 L. monocytogenes isolates were selected by serotyping. At the relative similarity coefficient of 0.80, it grouped 29 isolates and 5 reference strains into 2 clusters and 3 singletons, 4 clusters and 1 singleton by ERIC-PCR and REP-PCR, respectively. Our study reflects the potential risk of L. monocytogenes infection in China. We also provide a comprehensive surveillance on its incidence on the RTE foods of L. monocytogenes and ensure more accurate treatment of human listeriosis with effective antibiotics.     

Presence of Listeria monocytogenes in Chilean food matrices

ObjectivesTo compare Listeria monocytogenes strains obtained from food matrices with those from environmental samples in the same food processing plant.Methods and resultsBetween 2008 and 2012 the presence of L. monocytogenes was evaluated in 2647 food samples. A total of 448 work surfaces and 92 equipment's were also evaluated from 6 plants which produce ready-to-eat (RTE) foods in Santiago, Chile. An additional selected sample of hand and nails samples was also obtained from 13 food handlers working in a sausage elaboration plant.As a whole L. monocytogenes was present in 265 (10%) food samples and 22 (4%) environmental samples. The foods with highest recovery were red meats 14/60 (23%), poultry 223/1196 (19%), the remaining samples accounted a total of 27/1391 (2%). The environmental samples positive for L. monocytogenes were obtained from two food plants both the cheese 8/8 (100%) and from a fresh peaches exporter 3/3 (100%). Finally L. monocytogenes was isolated from 5/13 (38%) food handlers studied.ConclusionsThe study confirms the presence of L. monocytogenes in different matrices, especially in meat and RTE products. Analyses conducted on work surfaces revealed that contamination comes mostly from both raw materials and surfaces in indirect contact with foods.Significance and impact of studyThe study reinforces the need for companies to apply regulations related to food quality and safety systems (HACCP, Hazard Analysis & Critical Control Points) to prevent L. monocytogenes contamination from food processing plants.     

Successful management of Listeria spp. in an avocado processing facility

Listeria monocytogenes can grow and multiply in various food matrices and cause severe human illness. Apart from the influence on consumer health, L. monocytogenes contamination of ready-to-eat (RTE) food products causes major economic losses due to product recalls. Control of foodborne pathogens in RTE food products is a challenge, specifically in foods that cannot undergo a heat-treatment during processing. The aim of this study was to develop control strategies for the management of L. monocytogenes in an avocado processing facility, additional to a quality control system. An in-house monitoring system (IMS) was established to test specifically for Listeria spp. in the final products and processing environment, including floors, equipment, work areas and personnel. Guacamole and environmental samples were collected and tested on-site for Listeria with the ISO 11290-1 method. Based on the prevalence of Listeria, the facility introduced new strategies in processing to counter cross contamination. Results from the 2014 guacamole production season showed almost complete eradication of Listeria spp. in final products (0.17%, n = 1170) and the processing facility (0.79%, n = 1520). This is a major achievement since the highest incidence of Listeria spp. over a period of five years was measured at 11.39% (n = 948) in the final product during the 2013 season and 13.44% (n = 1927) in the processing facility in 2011. These results indicate that successful management of Listeria spp. in an avocado processing facility can be accomplished with in-house monitoring of the listerial population and subsequent adjustments to the processing system.     

Investigation on prevalence of Listeria spp. and Listeria monocytogenes in animal-derived foods by multiplex PCR assay targeting novel genes

Chilled and frozen animal-derived food can be contaminated by Listeria spp., emerging foodborne pathogens in food industry. The objective of this study was to mine novel target genes by comparative genomics approach for multiplex PCR detection and differentiation of Listeria monocytogenes and other Listeria spp. in food. Multiplex PCR assay targeting the genetic markers LMOf2365_2721, AX25_00730, lin1814, int, lwe1673, and Oxidoreductase gene, resulted in the amplification of DNA fragments of 583 bp, 703 bp, 421 bp, 994 bp, 345 bp, and 201 bp from L. monocytogenes, Listeria ivanovii, Listeria innocua, Listeria seeligeri, Listeria welshimeri, and Listeria grayi, respectively. The detection limits of the multiplex assays were as low as 89 fg/μL genomic DNA and 910 CFU/mL of bacterial culture. The prevalence of Listeria spp. was determined using the developed multiplex PCR assay and standard microbiological method in a total of 200 food samples collected from different supermarkets and traditional agri-product markets in Nanjing, China. A total of 28 samples were found to be positive for the presence of Listeria, including 10.9% (6/55) of livestock meat samples, 22% (11/50) of poultry samples, 15% (6/40) of shellfish samples, 13.3% (4/30) of octopus samples and 4% (1/25) of freshwater fish samples. Of these, 13 isolates were classified as L. monocytogenes, 11 were classified as L. innocua, 2 were classified as L. ivanovii and 3 were classified as L. welshimeri. These results demonstrate that the multiplex PCR assay based on novel target genes is able to rapidly detect the Listeria spp. in 12 h with high accuracy and sensitivity, which may be used in the future for detection of Listeria spp. in animal-derived food products.     

Foodborne transmission of Listeria monocytogenes via ready-to-eat salad: A nationwide outbreak in Switzerland, 2013–2014

From 26 October 2013 to 23 April 2014, 32 cases of listeriosis infected with an Listeria monocytogenes strain serovar 4b, sequence type 4 and belonging to a single distinct PFGE pulsotype were registered in patients from several cantons of Switzerland. L. monocytogenes was detected in blood (75%), CSF (16%), ascites (6%) and in joint fluid (3%) samples. By the end of March 2014, a food producing company reported an L. monocytogenes contamination of ready-to-eat salads to the authorities after detecting the pathogen through its in-house routine quality control. Product and environmental samples collected during subsequent investigations yielded isolates, matching the outbreak strain, thus confirming that ready-to-eat salad from this company was most likely the outbreak source. The cause for the product contamination was related to a design-inherent hygienic problem of one specific product-feeding belt. Complementary patient interviews also identified ready-to-eat green salads bought at one retailer as the likely outbreak source.     

Listeria detection in microscale solid state inoculation with minimal selective agents

The food industry needs a simple, reliable, and cost-effective primary screening protocol for routine inspection of bacterial contamination. Microscale inoculation technique is proposed as an alternative method for Listeria detection. This proposed novel technique shows a good correlation with standard spread plate technique for the enumeration of pure Listeria cultures (R² = 0.96, P < 0.0001). The commonly used selective agents in Listeria media (PALCAM, MOX, and OCLA) were assessed for their inhibitory effect on Listeria monocytogenes, Listeria innocua, and Listeria ivanovii using the microscale inoculation technique. The concentration of selective agents was lowered to inhibit competitive bacteria with minimum impact on the growth of Listeria. At the standard concentration, all three media showed less inhibition on L. monocytogenes and L. innocua than on L. ivanovii. OCLA had less inhibitory effect on the three species than did MOX and PALCAM. The comparison between ISO 11290-1 and microscale with 25% of selective agent concentration on detection of Listeria in 36 naturally contaminated food samples revealed that the microscale technique agreed well with the ISO method (Cohen KAPPA = 0.83). Reduction of selective agent concentration to 25% of the conventional formulas resulted in substantial improvement in detectability of Listeria spp. without significantly reducing specificity. The detection sensitivity of the Listeria colonies in food samples was significantly improved by microscale inoculation with 25% of the inhibitors on the three selective media at 24 and 48 h incubation (ANOVA, P = 0.039). At 48 h incubation the improvement was from 95%, 90%, and 85% (ISO method with regular strength inhibitors) to 100%, 100%, and 90% (microscale) on OCLA, MOX, and PALCAM respectively. There was no discrepancy between the microscale and the ISO method in detection of L. monocytogenes in the food samples. The optimization of Listeria detection improves sensitivity of detection as well as reducing media volume which may reduce costs and waste generated.     

Prevalence,genetic diversity and antimicrobial susceptibility of Listeria monocytogenes isolated from open-air food markets in Greece

A total of 210 food samples originating from milk products, ready-to-eat salads, raw meat and raw meat products purchased in ten open-air market places in Thessaloniki, Greece, were analyzed for the presence of Listeria monocytogenes. Thirty (14.3%) contained L. monocytogenes with the highest prevalence in raw meat (27.5%), raw meat products (18%) and cheese (8%). The strains were susceptible to 16 antimicrobials as determined by microbroth dilution, except one strain which displayed resistance to tetracycline (MIC > 32 μg/ml). This strain carried the tetracycline resistance gene tet(M). Pulsed-field gel electrophoresis (PFGE) revealed a low genetic diversity among the isolates, irrespective of their origin. This suggests that dominant L. monocytogenes clones are widespread in different food product types in open-air food markets in Greece. The high prevalence of L. monocytogenes in these products indicates that appropriate hygienic measures and periodic bacteriological controls are also necessary in open-air food markets to reduce contamination with food-borne pathogens. Greek specialties made with raw meat and raw milk may contain L. monocytogenes and should not be consumed by persons at risk.     

Antimicrobial resistance profiles of Listeria monocytogenes isolated from ready-to-eat products in Poland in 2007–2011

The aim of the study was to characterize strains of Listeria monocytogenes isolated from ready to eat (RTE) products collected as part of official food control and monitoring in Poland. A total of 105 L. monocytogenes isolates from RTE products: 54- cakes and 51 – delicatessen products were examined. The presence L. monocytogenes in cakes and delicatessen products was 0.4% and 0.7% respectively suggesting the level of contamination of RTE products with L. monocytogenes is very low.     

Occurrence and antibiotic resistance profiles of Listeria monocytogenes isolated from seafood products and market and processing environments in Iran

This study was designed to determine the occurrence of Listeria monocytogenes in popular seafood products and their market and processing environments. The frequency of L. monocytogenes contamination was found to be 4.83% in raw and 14.5% in RTE seafood products. In raw products, the prevalence of L. monocytogenes was significantly higher (P < 0.05) in freshwater fish (11.4%) than in seawater fish (1.80%) and shrimp (1.69%). Cold-smoked fish had the highest frequency of L. monocytogenes contamination among the RTE products. The microbial load of L. monocytogenes in seafood products was in the range of <0.3 to 1100 MPN/g; and did not exceed 100 MPN/g in most of the examined samples. The incidence of L. monocytogenes in environmental and personnel samples was 17.1% and 16.2% in markets, and 21.3% and 18.2% in processing plants, respectively. It was found that contamination of processed fish fillets and shrimp flesh with L. monocytogenes mainly originated from the processing environments, rather than the raw materials. In addition, the implemented cleaning procedures were insufficient to eliminate L. monocytogenes from the market and processing environments. Serological examinations revealed that serotype 1/2a (45.7%) was the predominant serotype of L. monocytogenes followed by 4b (40.3%), 1/2c (5.39%), 1/2b (4.68%), and 4c (3.96%). Regarding seasonal variability, 1/2a was the dominant serotype during warm seasons, whereas 4b was the most prevalent serotype during cold seasons. The isolates of L. monocytogenes were highly resistant to penicillin, ampicillin, tetracycline, and vancomycin. The results indicate that prevalence of L. monocytogenes serotypes 1/2a and 4b, which are associated with foodborne outbreaks of human listeriosis; and their resistance to commonly used antibiotics for treatment of human listeriosis could be a public health concern.