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.     

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.     

Occurrence and traceability of Listeria monocytogenes strains isolated from sheep's milk cheese-making plants environment

The aim of the study was to conduct an extensive survey on Listeria monocytogenes and Listeria spp. environmental contamination in 13 cheese-making plants. A total of 409 environmental and food samples were collected during years 2011–2013. Listeria spp. contamination was observed in all the facilities, while L. monocytogenes was recovered from 12 facilities with a prevalence ranging between 3.0% and 22.6%. Floor drains were the most contaminated sampling sites (48.8% of positive samples), serving as harbourage site for subsequent contamination. Out of 616 isolates, 277 (45.0%) were Listeria innocua, 274 (44.5%) L. monocytogenes, 41 (6.6%) Listeria ivanovii, 14 (2.3%) Listeria welshimeri and 10 (1.6%) Listeria gravyi. Serotyping carried out by PCR and agglutination method for L. monocytogenes revealed that 169 strains (61.7%) were serotype 1/2a, 65 (23.7%) 4b, 20 (7.3%) 1/2b, 10 (3.6%) 3a, 7 (2.5%) 1/2c and 3 (1.1%) 3b. PFGE conducted on L. monocytogenes isolates using AscI and ApaI restriction enzymes, yielded 6 clusters. Two predominant PFGE clusters were observed including respectively 36 and 32 strains. Within cheese-making plants, L. monocytogenes showed wide variability with strains distributed up to 4 different clusters. Pulsotypes isolated from raw milk filter were never detected in the processing environment, indicating that the contamination originated from sources other than raw milk. The isolation of strains with similar profile from different sampling sites, within and among cheese-making plants, indicated the possible transfer of L. monocytogenes contamination along production lines and from one facility to another. Strains recovered from food were confirmed as originating from the processing environment.     

Genotypic characterization and antimicrobial resistance of Listeria monocytogenes from ready-to-eat foods

Listeria monocytogenes is an important foodborne pathogen. The aims of this study were to determine genetic relatedness of L. monocytogenes isolated from ready-to-eat (RTE) foods in Malaysia. L. monocytogenes isolates from RTE foods were characterized by multiplex-PCR serotyping, REP-PCR, BOX-PCR, RAPD, PFGE, virulotyping and antibiotyping. Of the 32 L. monocytogenes isolates analyzed, 21 (65.6%) were assigned to serogroup “1/2a, 3a”, seven (21.9%) serogroup “1/2c, 3c”, and four (12.5%) serogroup “4b, 4d, 4e”. All the L. monocytogenes harbored inlA, inlB, inlC and inlJ virulence genes. More than half (53%) L. monocytogenes isolates were resistant to penicillin G, followed by tetracycline (15.6%), amoxicillin-clavulanic acid (12.5%), vancomycin (9.4%) erythromycin (6.3%), clindamycin, streptomycin, kanamycin, and chloramphenicol (each 3.1%). REP-PCR, BOX-PCR, RAPD and PFGE generated 28 (D = 0.992), 31 (D = 0.998), 32 (D = 1), and 20 (D = 0.916) patterns, respectively. These results indicate that L. monocytogenes isolates from RTE food were heterogeneous. There was no correlation between antibiograms and serogroups or pulsotypes or PCR-typing and/or sources of isolates. Since different subtyping methods often give different discriminatory powers, the use of more than one subtyping approach is necessary in providing a more accurate picture of the genetic diversity of L. monocytogenes. In conclusion, L. monocytogenes isolates from RTE possess the internalin genes and are genetically diverse. Furthermore, the occurrence of resistant isolates belonging to epidemiologically important serogroups “1/2a, 3a” and “4b, 4d, 4e” in RTE foods is a matter of public health concern.     

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 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.     

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.     

Comparison of antibiotic resistance patterns in Listeria monocytogenes and Salmonella enterica strains pre-exposed and exposed to poultry decontaminants

Recent opinions expressed by European Union Scientific Committees suggest there is a potential for poultry decontaminants to increase resistance to antibiotics. At this moment there is no scientific information available to estimate this risk accurately. Four strains (Listeria monocytogenes serovar 1/2a, Listeria monocytogenes serovar 4b, Salmonella enterica serotype Typhimurium and Salmonella enterica serotype Enteritidis) were repeatedly exposed to increasing sub-inhibitory concentrations of decontaminants (trisodium phosphate, acidified sodium chlorite, citric acid, chlorine dioxide or peroxyacetic acid) and tested against 15 antibiotics by means of a standard disc-diffusion technique (NCCLS). The antibiotic resistance patterns of strains were compared before and after exposure to decontaminants. Intra-specific differences in antibiotic resistance patterns were found among strains. Increases in resistance to various antibiotics were observed in L. monocytogenes and S. enterica strains after exposure to chemicals (especially ASC). These results raise concerns over the application of certain poultry decontaminants, since they could contribute to the development of microbial resistance mechanisms. However, these are preliminary results derived from laboratory-based experiments. Additional studies under practical field conditions would be needed to substantiate these findings.     

Polymerase chain reaction detection of Listeria monocytogenes using oligonucleotide primers targeting actA gene

A polymerase chain reaction (PCR) assay targeting the gene encoding actA was developed for detecting Listeria monocytogenes in pure cell cultures and on artificially contaminated pork, water and milk. 827-bp PCR product was detected in all 51 L. monocytogenes strains belonging to four different sero-groups (1/2a, 1/2b, 1/2c, and 4b). In contrast, the PCR product was not detected both in all other Listeria spp., including Listeria innocua, Listeria ivanovill, Listeria seelingeri, Listeria welshimeri, or Listeria grayi and in non-Listeria bacteria, indicating that the primer set we use was highly specific for L. monocytogenes. The detection limit of the PCR assay for pure cell cultures was 10⁵ cfu per ml pure cell culture. However, the assay could detect as few as 10¹ cfu of L. monocytogenes in 25 g of pork and 25 ml milk and water following 16 h of enrichment in Listeria Enrichment broth (LEB) at 30 °C. Only a large number of dead L. monocytogenes cells can cause false positivity, as determined using model pork, milk and water samples artificially contaminated with decimal dilutions of dead L. monocytogenes. The total assay time including enrichment was approximately 18 h. These results suggest that the PCR assay based on amplifying actA gene can used to rapidly detect L. monocytogenes on pork, milk, water and possibly other types of food products.     

Sardinian goat’s milk as source of bacteriocinogenic potential protective cultures

Goat breeding in Sardinia constitutes an important source of income for farming and shepherding activities. In this study 170 LAB strains were isolated from Sardinian goat’s milk and tested for bacteriocins production against several food-borne pathogenic microorganisms. Four isolates (SD1, SD2, SD3 and SD4) were selected for their effective inhibition on Listeria monocytogenes. The strains were classified as members of Enterococcus genus, according to their biochemical and physiological characteristics, and then genetically identified as Enterococcus faecium. In MRS broth at 37 °C, bacteriocins SD1 and SD2 were produced at much higher levels (51200 AU/ml) compared to bacteriocin SD3 (3200 AU/ml) and bacteriocin SD4 (800 AU/ml). Their peptides were inactivated by proteolytic enzymes, but not when treated with α-amylase, catalase and lipase. The four bacteriocins remained stable at pH from 2.0 to 12.0, after exposure to 100 °C for 120 min and were not affected by the presence of surfactants and salts (N-Laourylsarcosine, NaCl, SDS, Triton X-100, Tween 20, Tween 80 and urea). Their molecular size was determined to be approximately 5 kDa by tricine-SDS-PAGE.Since the strains exhibited a strong antimicrobial activity against 21 L. monocytogenes strains and 6 Salmonella spp. isolates, they should be considered as potential bio-preservatives cultures for fermented food productions. Moreover, due to their technological features, the four strains could be taken in account for using as adjunct NSLAB (non-starter lactic acid bacteria) rather than as starter culture.     

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.     

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.     

Evolution of Listeria monocytogenes populations during the ripening of naturally contaminated raw ewe’s milk cheese

The aim of this work was to study, in loco, the evolution of Listeria monocytogenes populations, during ripening (7, 42, 60 and 120 days) of naturally contaminated raw ewe’s milk cheese. Two batches of cheese consisting of 20 or 16 cheeses were obtained from two farmstead cheesemakers, respectively. A significant increase in numbers of L. monocytogenes was observed for both batches, from 7 to 42 days of ripening. These results suggest that this type of cheese has potential to support the survival of L. monocytogenes, while stressing the importance of cheese contamination in the dairies by resident strains.     

Antilisterial activity and stability of nanovesicle-encapsulated antimicrobial peptide P34 in milk

Bacillus sp. P34, a strain isolated from aquatic environments of Brazilian Amazon basin, produces a bacteriocin-like substance (BLS) which was encapsulated in nanovesicles prepared from partially purified soy lecithin. The efficiency of free and encapsulated BLS P34 to control the development of L. monocytogenes and maintenance of antimicrobial activity was assessed over time in milk. The antimicrobial activity of free and encapsulated BLS P34 decreased approximately 50% after 4 days of storage (<4 °C) in skim and whole milk. After this period there was not significant loss of activity up to 21 days. The viable counts of Listeria monocytogenes in skim and whole milk containing 3200 AU/ml of free or encapsulated BLS P34 were always lower than those observed in controls without bacteriocin at both 30 °C and 7 °C. At 1600 AU/ml concentration, free and encapsulated BLS P34 were inhibitory to L. monocytogenes in skim milk, when compared with the control at 7 days. Nanovesicle-encapsulated and free BLS P34 shows potential use as biopreservative for application in milk-derived 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.     

Effect of temperature and salt on thermal inactivation of Listeria monocytogenes in salmon roe

Listeria monocytogenes is a potentially fatal foodborne pathogen that can be found in ready-to-eat seafood products, such as fresh salmon roe. Once contaminated, salmon roe must be decontaminated prior to human consumption. This study was conducted to determine the thermal inactivation kinetics of L. monocytogenes in raw salmon roe as affected by bacterial strain, temperature, and salt concentration. Three different strains of L. monocytogenes, including serotype 4b (F2365), 1/2b (F4260), and 1/2a (V7), were individually inoculated to salmon roe supplemented with salt (0–4.5%), and heated under different temperatures (57.5–65.0 °C) to evaluate the survival of the bacterium during heating and determine the D-values. Results showed that the thermal resistance (log D) of L. monocytogenes was significantly affected by bacterial strain, temperature, and salt and by their interactive effects, with strain F2365 being the most heat-resistant among all three strains tested. Salt added to salmon roe significantly increased the thermal resistance of the bacteria. For L. monocytogenes F2365, the z value of the bacterium in salmon roe was 5.99 °C, and its heat resistance increased with the level of salt in a linear manner. The results of kinetic analysis and the models obtained in this study may be used by the seafood industry to develop proper thermal processes to eliminate L. monocytogenes in raw salmon roe and to ensure microbial safety and prevent foodborne illness.     

Is Listeria innocua 2030c,a tetracycline-resistant strain,a suitable marker for replacing L. monocytogenes in challenge studies with cold-smoked fish?

The suitability of Listeria innocua 2030c, a tetracycline-resistant strain, to be used as an indicator for replacing Listeria monocytogenes in challenge studies with cold-smoked fish was ascertained. L. innocua 2030c was compared to serovars 4b and 1/2c of L. monocytogenes, the major types isolated from Portuguese cold-smoked fish products. Growth curves at 30°C, growth/survival patterns at 30°C under exposure to different times and concentrations of ozone and sensitivity to Carnobacterium divergens V41 and C. piscicola V1 and their bacteriocins V41 and V1, were determined. No important differences between L. innocua 2030c and L. monocytogenes 4b and 1/2c were found, therefore L. innocua 2030c can be considered a suitable indicator for replacing those L. monocytogenes strains in challenge studies.     

Lactic acid bacteria biodiversity in Italian marinated seafood salad and their interactions on the growth of Listeria monocytogenes

The aim of this research was to study the biodiversity of lactic acid bacteria (LAB) in marinated seafood salad (pH 5.0) and their interaction on the growth of Listeria monocytogenes. LAB were highly present in the samples considered in this study, reaching values of 8.0 log cfu/g at the end of product’s shelf-life. A high biodiversity in terms of LAB species and strains was detected by means of RAPD–PCR within the 171 bacterial isolates collected. Among them Lactobacillus curvatus, Lactobacillus sanfranciscensis and Enterococcus were present in all the salad batches considered. Three challenge tests against L. monocytogenes were carried out in order to assess the growth of this pathogen in the presence of dominant populations of LAB. L. monocytogenes tended to decrease in time, suggesting that a stable concentration of LAB inhibits the development of this pathogenic micro-organism.     

Inactivation of Listeria monocytogenes and Salmonella enterica serovar Senftenberg 775W inoculated into fruit juice by means of ultra high pressure homogenisation

The inactivation of Listeria monocytogenes and Salmonella enterica serovar Senftenberg 775 W by ultra high pressure homogenisation (UHPH) was evaluated in grape and orange juices inoculated at a concentration of approximately 7 log CFU/ml. The fluid inlet temperature used was 6 °C and the pressure levels assayed were 200, 300 and 400 MPa. Viable and injured bacterial counts were obtained 2 h after the UHPH treatments and after 5, 8, and 15 days of storage at 4 °C. Pressure level had a significant impact on the lethal effect of UHPH and complete inactivation of S. enterica serovar Senftenberg 775 W was achieved at 400 MPa. L. monocytogenes showed more resistance than S. enterica serovar Senftenberg 775 W to the UHPH treatments and no significant differences were observed between 300 and 400 MPa treatments in both juices. Sublethal injuries were not detected in any case. During the storage at 4 °C viable counts of both strains showed a decreasing trend. L. monocytogenes viable counts became undetectable in UHPH treated and also in control samples of grape juice which could be attributed to the presence of natural compounds with antilisterial effect.     

Multiple regression model for thermal inactivation of Listeria monocytogenes in liquid food products

A multiple regression model was constructed for thermal inactivation of Listeria monocytogenes in liquid food products, based on 802 sets of data with 51 different strains and 6 cocktails of strains published from 1984 to 2010. Significant variables, other than inactivation temperature, were pH, sodium chloride content, sugar content, the temperature of growth or storage before inactivation, in addition to a heat shock before inactivation. The constructed model for thermal inactivation of L. monocytogenes has a reduced variability as these variables are known to influence the thermal resistance (and these are known or controllable in practice). Mean simulation results of inactivation of L. monocytogenes during pasteurisation (20 s, 76 °C) of raw milk (calculated mean level after growth 14 cfu/l) were comparable with results of a single regression model constructed from inactivation data found in experiments in milk only (175 data sets, 18 strains/cocktails). Both models predicted a probability of survival of less than 1 in a billion litres. The study shows that multiple regression modelling can be used to obtain a model from all data available, with a limited and realistic uncertainty level, while retaining the variability of heat resistance due to the 51 strains and 6 cocktails of strains (unknown and not controllable in practice).