Monocytogenes Growth Research Articles

Assessment and Validation of Predictive Growth Models for Locally Isolated Salmonella enterica and Listeria monocytogenes in Alfalfa Sprouts at Various Temperatures

ABSTRACTSprouts are popular due to their high nutritional content, including vitamins, minerals, antioxidants, and enzymes. However, the conditions favorable for sprouting, such as warm and humid environments, are also ideal for the growth of bacteria, including food‐borne pathogens. Here, we analyzed the growth and developed predictive models of locally isolated and commercial strains of Salmonella enterica and Listeria monocytogenes in alfalfa sprouts under various constant temperatures, ranging from 5°C to 25°C. Our findings indicated that these pathogens could grow at 5°C in sprouts, albeit with a low growth rate. A rapid increase in concentration occurred at temperatures of 10°C and above. The fitted models demonstrated high performance, with R2 values ranging from 0.964 to 0.997 and RMSE values ranging from 0.15 to 0.51, respectively. Based on the fitted values, bias factor (Af) values varied between 1.01 and 1.06, with all accuracy factor (Bf) values at 1.00. Acceptable prediction zone (APZ) values ranged from 81.8% to 100%. Validation of the models under dynamic temperature conditions for specific strains showed acceptable performance. This study enhances our understanding of S. enterica and L. monocytogenes growth in alfalfa sprouts. The findings of this study could be used to improve the risk assessment of these pathogens in alfalfa sprouts.

Assessing Listeria monocytogenes Growth in Artificially Inoculated Sea-Farmed Product—Raw Sea Bass (Dicentrarchus labrax) Fillet, Produced in Greece

Listeria monocytogenes (Lm) is responsible for listeriosis, a serious foodborne disease, with high hospitalization and mortality rates worldwide. The main cause of listeriosis in humans is the consumption of ready-to-eat (RTE) foods; Commission Regulation (EC) No 2073/2005 establishes microbiological criteria for Lm in RTE foods. Raw fish products are widely consumed, e.g., in sushi and various seafood recipes (e.g., carpaccio, sashimi, maki, nigiri, tartare, etc.), but are not subjected to RTE food safety criteria. The aim of our study was to assess the growth potential of Lm in raw sea bass fillets obtained from a leading aquaculture company in Greece. In order to assess the growth of Lm in raw sea bass fillets, we applied the “challenge test”, a scientific experiment designed to assess the growth of Lm within a specific food product under controlled conditions. According to our results, and taking into consideration the health risk for the listeriosis-vulnerable population, raw fish products utilized in the preparation of RTE foods, including sushi and an array of seafood dishes, should be incorporated in the Category of Safety Criteria of Regulation (EC) No 2073/2005 “Ready-to-eat food able to support the growth of Listeria monocytogenes”.

Bacteriocin characterization of Enterococcus faecium isolates and evaluation of their in situ anti-Listerial activity in Beyaz cheese

Nowadays, as the interest in natural preservatives increases, research on bioprotective cultures that produce bacteriocins and studies on the use of these cultures in foods are also increasing day by day. Present study aimed to investigate bacteriocin characterization and safety of Enterococcus faecium H108, H206 isolates and their potential utilization in the reduction of Listeria monocytogenes ATCC7644 in Beyaz cheese. Enterocin producing E. faecium H108 and H206 strains were isolated from raw cow's milk and identified by 16S rRNA sequencing. Enterocin containing supernatants of E. faecium H108 and H206 were found to be stable to heat various chemicals used in food industry, wide pH range, lysozyme and catalase enzymes. On the other hand, activity of enterocins were inactivated by proteolytic enzymes. Maximum activity of E. faecium H108 was 6400 AU/mL, while that of H206 was 12800 AU/mL, and the activities remained stable for 24 h. Supernatant of both E. faecium H108 and H206 inhibited L. monocytogenes growth in vitro. E. faecium H108 and H206 did not show haemolytic and DN-ase activities and were susceptible to most of the antibiotics tested. The isolates were used in Beyaz cheese and were found to significantly, but not completely inhibit L. monocytogenes growth. The findings of this research suggest that E. faecium H108 and H206 isolates, after a detailed safety assessment, might be employed as bioprotective cultures in Beyaz cheese with starter culture or hurdle technologies.

Antibacterial activity and mechanism of the sesquiterpene δ-cadinene against Listeria monocytogenes

Listeria monocytogenes is a food-borne pathogen that seriously threatens human health. We analyzed the antibacterial activity and mechanism of δ-cadinene against L. monocytogenes. The effect of δ-cadinene on L. monocytogenes gene expression was investigated using RNA sequencing. δ-Cadinene inhibited L. monocytogenes growth at a minimum inhibitory concentration of 5 μL/mL and a minimum bactericidal concentration of 10 μL/mL. In addition, δ-cadinene suppressed biofilm formation, altered cell morphology, and damaged the cell membrane of L. monocytogenes, enhancing membrane permeability and affecting the membrane potential. Of note, "plasma membrane" and "membrane" were the most significantly enriched Gene Ontology terms. Sixteen differentially expressed genes were strongly correlated with biofilm formation, protein and nucleic acid leakage, and membrane potential. The growth of L. monocytogenes in milk was effectively controlled with 10 μL/mL δ-cadinene, especially at 4 °C. In conclusion, treatment with δ-cadinene could be a potential strategy for controlling the contamination of foods by L. monocytogenes.

Modelling the Growth of Listeria monocytogenes on Fresh-Cut Cucumbers at Various Storage Temperatures

The primary objective of this study was to investigate the behavior of Listeria monocytogenes (L. monocytogenes) on fresh-cut cucumbers. Fresh-cut cucumber samples were inoculated with a mixture of six strains of L. monocytogenes. The inoculated samples were stored at 5, 10, 15, 20, 25, 30, and 35 °C. The results demonstrated that L. monocytogenes was able to grow on fresh-cut cucumbers at all the evaluated temperatures, although its growth decreased but was not inhibited at 5 °C. An extreme storage temperature of 35 °C considerably reduced the lag time. L. monocytogenes growth on fresh-cut cucumbers was controlled for several days by storage at a low temperature, mainly at 5 °C. Thus, this product should only be stored at low temperatures. The growth process was fitted by the Baranyi model, with the specific growth rates equally well-fitted to the Ratkowsky square-root model. The R-square and mean square error values for the corresponding Ratkowsky square-root models were 0.97 (R2 > 0.95) and 0.02, respectively. The Baranyi and Ratkowsky square-root models exhibited good relevancy. The predictive models developed in this study can be used to estimate the risk assessment of L. monocytogenes on fresh-cut cucumber.

In vitro antimicrobial activity of ginseng extract against Staphylococcus aureus, Salmonella Typhimurium and Listeria monocytogenes and its inhibitory effects on these pathogens in cooked ground beef

Present study is focused on exploring in vitro antimicrobial activity of ginseng extract (GE) against Staphylococcus aureus, Salmonella Typhimurium and Listeria monocytogenes and their biofilm forming ability, then determining its antimicrobial efficiency during the storage (4 and 10 °C) of cooked ground beef contaminated with these pathogens. Results revealed that the minimum inhibitory concentration (MIC) for S. aureus, S. typhimurium and L. monocytogenes were 90, 70 and 40 mg/mL, respectively. GE was also able to inhibit biofilm production by S. aureus and L. monocytogenes, whereas S. typhimurium did not produce biofilm with or without GE application. On the other hand, the results of GE aplication in ground beef indicated that GE incorporation at 0.5% or more reduced S. aureus and S. Typhmurium counts in cooked ground beef at the end of 30 d storage at 4 °C (P < 0.05). Using 1% or more GE totally inhibited S. Typhmurium after 15 d storage at 4 °C (P < 0.05). However, GE application did not affect S. aureus or S. Typhmurium counts in cooked ground beef stored at 10 °C. Furthermore, incorporation of 0.5% or more GE generally inhibited L. monocytogenes growth in cooked ground beef at the end of storage at both 4 and 10 °C (P < 0.05). In general, pH was lower in samples with GE than those without GE regardless of differences in the type of tested pathogen, storage time and temperatures (P < 0.05). Although similar aw was generally obtained on processing day, lower aw was observed in GE containing groups at the end of storage for both storage temperatures (P < 0.05). Oxidation reduction potential (ORP) in all groups generally increased during storage at both storage temperatures (P < 0.05). In conclusion, our results demonstrated that GE has an important role in controlling growth of tested pathogens and may be used as a natural agent by the meat industry to inhibit the growth of food-borne pathogens in cooked processed meat products during storage.

Antilisterial activity of olive-derived polyphenols: an experimental study on meat preparations

Pork meat and processed pork products have been linked to multiple listeriosis outbreaks worldwide during the past years. Specifically, it has been highlighted that minced pork meat is easily perishable and may increase the growth of Listeria monocytogenes, which could be harmful to the general public's health. This study aimed to investigate the potential application of olive oil mill wastewater polyphenolic and red beet extracts as natural antimicrobial agents for L. monocytogenes growth control in burgers. The minced pork meat was mixed with the extracts and experimentally inoculated with L. monocytogenes, then molded into vacuum-packaged and cold-stored (4±1°C) burgers kept under alternating exposure to fluorescent light. The L. monocytogenes enumeration was performed on burgers at 0, 2, 5, and 10 days of shelf life. In uninoculated burgers, physicochemical (pH, water activity, color) and sensory determination (descriptive sensory analysis) were also conducted. At the end of storage, the samples treated with olive-derived extract showed the lowest value of L. monocytogenes (approximately 1.3 Log CFU/g). The physicochemical and sensory traits of burgers have benefited from the addition of both olive-derived and red beet extracts. Results suggest that olive mill wastewater polyphenolic extracts could be added to minced pork meat products to act as a natural antimicrobial agent.

Inactivation efficacy of four commercial post-process treatments against Listeria monocytogenes and impact on the commercial quality of leafy greens

The problem of product contamination with human pathogenic microorganisms is still unsolved. Although prevention through the implementation of good agricultural practices and good manufacturing practices is the gold standard, product decontamination strategies can be used to complement preventive measures. Different bioprotective treatments have been suggested to reduce the risk of listeriosis in fresh produce, but more information is needed before industrial implementation. This study focused on the efficacy of four commercial treatments against Listeria monocytogenes growth and their effect on the organoleptic quality of baby spinach, cut romaine, cut iceberg, and shredded cabbage. The treatments included SafePro® (CHR Hansen, DK) and Holdbac® (DowDuPont, US), based on the use of lactic acid bacteria (LAB) cultures as well as two different bacteriophage solutions, ListShield (Intralytix, US) and PhageGuard Listex™ (PhageGuard, US). The selected treatments were tested under simulated commercial conditions. The application was performed after processing and before packaging using a fine mist spray. In all the trials, Listex™ showed the best results in reducing L. monocytogenes growth during shelf life in the four leafy greens chosen. Microbial reductions were close to 2 log units. L. monocytogenes reductions were observed 1 day after Listex™ application and the efficacy was maintained during storage (15 days at 7 °C). Organoleptic quality, including flavor, texture, browning/yellowing, decay, and visual appearance of the four leafy greens was not significantly affected by the application of Listex™ when compared to the untreated products. Post-process treatment with Listex™ based on bacteriophages effectively reduced L. monocytogenes and can be recommended as a control tool to reduce the risks for the presence of L. monocytogenes in leafy greens.

Extension of the gamma concept to handle changing environment during shelf-life. Applied to an example with Listeria monocytogenes in salads with changing pH.

Prediction of microbial growth is the main topic within the area of predictive microbiology. A commonly used framework is the so-called gamma concept which is to view the bacterial growth rate as a product of a bacteria- and medium specific maximum instantaneous factor, and several environmental factors. Traditionally environmental factors are assumed to be constant, leading to exponential growth. In the current study, we expand the gamma concept to include changing dynamic environmental factors, exemplified by pH, and show how this might affect estimates for Listeria monocytogenes growth rates and thereby predicted shelf-life. The study shows how substantial environmental changes might lead to large biases for the estimated growth and shelf-life, if not accounted for in the model. Finally, the study shed some light on how accuracy for the growth rate estimates might be improved by allocating more weight to observations prone to favorable than unfavorable environmental conditions.

Growth Control of Listeria monocytogenes in Raw Sausage via Bacteriocin-Producing Leuconostoc carnosum DH25.

The current study addresses the critical issue of Listeria monocytogenes growth in raw sausage/meat products leading to human infections, most commonly listeriosis, which is known for its high fatality rate. This research focuses on the isolation, identification, and screening of lactic acid bacteria from various meat and fish products in Switzerland. In total, 274 lactic acid bacteria strains were isolated from 30 different products and were screened for their ability to inhibit Listeria monocytogenes growth, with 51 isolates demonstrating anti-Listeria activity at 8 °C, 15 °C, 25 °C, and 37 °C. Further experiments, using a meat model and a raw sausage challenge test, demonstrated that Leuconostoc carnosum DH25 significantly inhibited Listeria monocytogenes growth during the ripening and storage of the tested meat/sausage. This inhibitory effect was found to be attributed to the bacteriocins produced by Leuconostoc carnosum DH25 rather than factors like pH or water activity. The stability of the anti-Listeria substances was examined, revealing their resistance to temperature and pH changes, making Leuconostoc carnosum DH25 a promising protective culture for raw sausages. The genome sequencing of this strain confirms its safety, with no antibiotic resistance genes or virulence factors detected, and reveals the presence of the structural genes for the production of the bacteriocin LeucocinB-Ta11a. This study underscores the potential of LAB strains and their bacteriocins as effective tools for enhancing food safety and preventing Listeria monocytogenes growth in meat products, offering valuable insights into biocontrol strategies in the food industry.

Prior freezing impact on the growth kinetics of Listeria monocytogenes in hot dog sausages

Listeria monocytogenes adapts to low-temperature environments and grows rapidly at room temperature. This bacterium is associated with several foodborne outbreaks due to cold chain breaks, particularly ready-to-eat foods such as sausages. The present study evaluated how frozen storage (-10 °C) for 30 and 90 days of hot dog sausages influences the bacterial growth kinetics between 7 and 30 °C under isothermal conditions. L. monocytogenes growth measurements were based on the ISO 11290-2 standard, and the mathematical model of Baranyi and Roberts was used to describe the bacterial growth. The sausages were incubated with around 2 log CFU/cm2, remaining constant for up to 90 days. However, prior freezing periods influenced bacterial growth behavior, mainly at chilled conditions (7 and 10 °C), increasing the maximum specific growth rate by 60%, lag phase time by 72%, and physiological state of the cells by 166%. The maximum population was not influenced by prior freezing. The proposed model fits the isothermal conditions studied. L. monocytogenes, after food thawing, grows at the same or higher rate than before freezing, which could represent a risk if the manufacturer's recommendations are not followed.

Vγ9+Vδ2+ T cell control of Listeria monocytogenes growth in infected epithelial cells requires butyrophilin 3A genes

Intracellular bacteria produce antigens, which serve as potent activators of γδ T cells. Phosphoantigens are presented via a complex of butyrophilins (BTN) to signal infection to human Vγ9+Vδ2+ T cells. Here, we established an in vitro system allowing for studies of Vγ9+Vδ2+ T cell activity in coculture with epithelial cells infected with the intracellular bacterial pathogen Listeria monocytogenes. We report that the Vγ9+Vδ2+ T cells efficiently control L. monocytogenes growth in such cultures. This effector function requires the expression of members of the BTN3A family on epithelial cells. Specifically, we observed a BTN3A1-independent BTN3A3 activity to present antigen to Vγ9+Vδ2+ T cells. Since BTN3A1 is the only BTN3A associated with phosphoantigen presentation, our study suggests that BTN3A3 may present different classes of antigens to mediate Vγ9+Vδ2+ T cell effector function against L. monocytogenes-infected epithelia.

Effect of Commercial and Autochthonous Bioprotective Cultures for Controlling Listeria monocytogenes Contamination of Pecorino Sardo Dolce PDO Cheese.

The composition and physicochemical characteristics of short-aged Pecorino Sardo PDO (Protected Designation of Origin) cheese makes it permissive to Listeria monocytogenes growth. The PDO product specification stipulates that this cheese is produced with whole sheep's milk inoculated with cultures from the area of origin. Therefore, the use of bioprotective cultures for the inhibition of pathogens in PDO cheeses is allowed only if autochthonous microorganisms are used. Furthermore, bioprotective cultures are generally used on the cheese surface to prevent the outgrowth of L. monocytogenes, the application of which can be time-consuming and require specialist technical knowledge. In this study, we examine the direct addition of bioprotective cultures to the cheese vat and compare the activity of a commercial bioprotective culture (Lactiplantibacillus plantarum) and an autochthonous lactic acid bacterium with bioprotective properties (Lactobacillus delbruekii sups. sunkii), for the inhibition of L. monocytogenes in Pecorino Sardo PDO cheese. Three types of Pecorino Sardo PDO cheese were made with bioprotective cultures added directly to the cheese milk along with the starter inoculum: PSA, with the commercial bioprotective culture; PSB, with the autochthonous bioprotective culture; and a CTRL cheese with no bioprotective culture. A challenge test was performed on each of these cheeses by artificially contaminating the cheese surface with L. monocytogenes (2 Log10 CFU/g). Three batches of each cheese type were analyzed to enumerate mesophilic and thermophilic lactic acid bacteria and to investigate the growth potential of L. monocytogenes during manufacturing, at the end of ripening, at the end of shelf-life, and after 180 days from cheese production. Both bioprotective cultures tested in this study showed inhibitory action against the pathogen with 0.3-1.8 Log10 CFU/g (colony-forming unit per gram) reduction levels. The autochthonous organism, L. sunkii, was as effective as the commercially supplied culture, and the addition of the bioprotective cultures to the cheese-making procedure offered protection against L. monocytogenes. The direct addition of bioprotective cultures to the making procedure of Pecorino Sardo PDO cheese is a potentially innovative strategy to improve the safety of this product.

Effects of sodium nitrite reduction, removal or replacement on cured and cooked meat for microbiological growth, food safety, colon ecosystem, and colorectal carcinogenesis in Fischer 344 rats

Epidemiological and experimental evidence indicated that processed meat consumption is associated with colorectal cancer risks. Several studies suggest the involvement of nitrite or nitrate additives via N-nitroso-compound formation (NOCs). Compared to the reference level (120 mg/kg of ham), sodium nitrite removal and reduction (90 mg/kg) similarly decreased preneoplastic lesions in F344 rats, but only reduction had an inhibitory effect on Listeria monocytogenes growth comparable to that obtained using the reference nitrite level and an effective lipid peroxidation control. Among the three nitrite salt alternatives tested, none of them led to a significant gain when compared to the reference level: vegetable stock, due to nitrate presence, was very similar to this reference nitrite level, yeast extract induced a strong luminal peroxidation and no decrease in preneoplastic lesions in rats despite the absence of NOCs, and polyphenol rich extract induced the clearest downward trend on preneoplastic lesions in rats but the concomitant presence of nitrosyl iron in feces. Except the vegetable stock, other alternatives were less efficient than sodium nitrite in reducing L. monocytogenes growth.

Modeling the effects of temperature and pH on Listeria monocytogenes growth in Mexican-style pork chorizo

Temperature abuse often occurs during the elaboration and storage of Mexican-style pork chorizo that usually is prepared following a diversity of recipes with variations of the ingredients mainly the amount of vinegar added, causing fluctuation in the final pH of the product. The objective of this work was to study the effect and interaction of temperature (5-30°C) and pH (4.5-6.5) on the lag phase (LP), generation time (GT), and exponential growth rate (EGR) of Listeria monocytogenes inoculated in pork chorizo using response surface methodology. Regression models were developed to predict growth parameters. Predictive models were significant (p < 0.05), had no lack of fit (p > 0.05) and had an R2 > 0.94. These criteria indicate that the models satisfactorily describe the experimental data and can be used to estimate the LP, GT, and EGR of L. monocytogenes in pork chorizo as a function of pH and temperature within the studied limits. By simulating the growth of L. monocytogenes under temperature abuse storage and inadequate product's pH level, risk scenarios were identified. The optimal pH and temperature that maximize LP and GT, and minimize EGR were pH = 4.79 and temperature = 8.66 °C. Under these conditions, LP = 142 h, GT = 22.3 h, and EGR = 0.0135 Log (CFU/g)/h were predicted. Pork chorizo producers can use the models generated in this study to estimate the potential risk of L. monocytogenes growth as a function of the pH and temperature within the range established in this work.

Shelf-life boundaries of Listeria monocytogenes in cold smoked salmon during refrigerated storage and temperature abuse

Cold smoked salmon (CSS) is a high-value ready-to-eat product, but it generally has a short shelf-life even under refrigeration and can support the growth of Listeria monocytogenes. Therefore, the objective of this study was to examine the growth and survival of L. monocytogenes in CSS during refrigerated storage and temperature abuse.The growth and survival data of L. monocytogenes (116 records, 465 data points) were retrieved from ComBase (https://www.combase.cc). All records contained storage time and temperature, but other information (aw, pH, and salt) was not fully documented. Each data point, normalized with the initial population to calculate relative growth (RG, log CFU/g), was used to classify the probability of growth. Eighty percent (80%) of the data were randomly sampled for examining the effect of storage time and temperature on growth of L. monocytogenes, while the remaining 20% were set aside for model validation.Logistic regression was used to develop a model for classifying L. monocytogenes growth according to 7 different control thresholds (CT), ranging from 0 to 3 log CFU/g in RG. A probability threshold was set to judge if the bacterial growth has exceeded a CT. The validation showed > 89% of true negative rate for not exceeding the control thresholds. A dynamic method was then developed and demonstrated to predict the growth probabilities under fluctuating temperature conditions. The result of this study suggested that storage time and temperature could be used to predict the growth of L. monocytogenes in CSS and to control listeriosis using a risk-based strategy. It can be used by the retailers and consumers to determine if a packaged product is safe to consume based on its time and temperature history.

Assessing Listeria monocytogenes growth kinetics in rice pudding at different storage temperatures

Rice pudding is a popular artisanal dairy dessert highly consumed in the main rice-producing countries, including Egypt. This study aimed to evaluate and model the growth of Listeria monocytogenes in rice pudding dessert stored at different temperatures (4–25 °C) over its shelf-life. Lab-scale rice pudding samples were prepared following a traditional Egyptian recipe and inoculated with a three-strain cocktail of L. monocytogenes (ca. 3 × 102 cfu/g). Inoculated rice pudding samples (pH = 6.67 ± 0.06 and aw = 0.99 ± 0.002) were stored at different isothermal conditions (4, 8, 12, 18, and 25 °C) and microbiologically analysed for up to 30 days for pathogen quantification by plate count methodology. Global regression analysis was used to fit the Baranyi model coupled with the Ratkowsky model to growth data, relating L. monocytogenes concentrations (N, log cfu/g) with storage temperature (°C) and times (d). Model validation was performed using published independent data. L. monocytogenes growth potential increased by increasing storage temperature. The estimated Ratkowsky model parameters were b = 0.0819 ± 0.0017 log cfu/d·°C and Tmin = −3.28 ± 0.20 °C. The indices RMSE = 0.39 and R2adj = 0.97 indicated a good agreement between the experimental data and the model predictions. The estimated maximum growth rate (μmax) values ranged between 0.355 and 5.363 log cfu/d from 4 to 25 °C. The model was successfully validated using published L. monocytogenes Scott A and California strains growth data in rice pudding samples stored at 5, 12 and 22 °C, as evidenced by the assessed statistical indices. The predictive model developed and validated in this study will aid in decision-making regarding the microbiological safety of rice pudding dessert with respect to L. monocytogenes growth, considering a wide range of storage temperatures.

Antilisterial activity of cinnamon essential oil, pomegranate extract, or strawberry tree extract against Listeria monocytogenes in slices of dry-cured ham and pork loin.

Owing to concerns about the antimicrobial resistance of agents that can prevent the growth of Listeria monocytogenes in meat, researchers have investigated natural preservatives with antilisterial effects. However, in vivo application of essential oils and plant extracts usually results in reduced antimicrobial activity in meat products when compared to in vitro studies. This study aimed to evaluate the in vivo antimicrobial activity of cinnamon essential oil, pomegranate, and strawberry tree extracts in slices of dry-cured ham and pork loin against L. monocytogenes. Fragments of sterile dry-cured ham were inoculated with 100 μL cinnamon oil 0.5%, pomegranate, or strawberry crude extract. After 10 min, 100 μL of L. monocytogenes serotype 4b (104 colony-forming unit [CFU]/mL) was inoculated, and samples were incubated at 7 °C for 7 d to simulate the processing and storage temperature conditions of dry-cured meat products. L. monocytogenes was detected and quantified. Only strawberry extract presented significant differences (P < 0.05) from the control; thus, it was selected for the assay with 2% and 4% salt-treated pork loin. The strawberry tree extract significantly (P < 0.05) reduced the growth of L. monocytogenes in dry-cured ham. However, it could not reduce L. monocytogenes growth in pork loin, regardless of the salt concentration. This is the first report on the antimicrobial effect of strawberry tree leaf extract against L. monocytogenes in dry-cured ham.

A potential probiotic Enterococcus faecium isolated from camel rumen, fatty acids biotransformation, antilisteria activity and safety assessment

The probiotic features of a new Enterococcus faecium strain isolated from camel rumen were investigated. The isolate identified as E. faecium 96B4 exhibited notable tolerance to gastrointestinal conditions, with high cell viability at pH 1.5 after 3 h (about 7.48 log10 cfu mL−1). Besides complete inhibition of Listeria monocytogenes growth, E. faecium 96B4 showed high hydrophobicity, auto- and co-aggregations abilities. It showed 76.33% cholesterol assimilation ability and boosted the extracellular unsaturated fatty acid content up to 25.53% in the presence of soybean oil as a substrate. Moreover, 96.17 ± 3.52 μg mL−1 conjugated linoleic acid production and 2.56 fold increase in oleic acid content were highlighted. Significant diacetyl production ability was also demonstrated. E. faecium 96B4 passed the safety assessment successfully. The association between the microbiome and host health makes the camel, as a unique animal, a rich source of beneficial microorganism candidates for designing future foods.

Microbiome and Physicochemical Features Associated with Differential Listeria monocytogenes Growth in Soft, Surface-Ripened Cheeses.

Soft-ripened cheeses (SRCs) are at a higher risk for the growth of the foodborne pathogen Listeria monocytogenes due to favorable moisture content and pH compared to other cheeses. L. monocytogenes growth is not consistent across SRCs, however, and may be affected by physicochemical and/or microbiome characteristics of the cheeses. Therefore, the purpose of this study was to investigate how the physicochemical and microbiome profiles of SRCs may affect L. monocytogenes growth. Forty-three SRCs produced from raw (n = 12) or pasteurized (n = 31) milk were inoculated with L. monocytogenes (103 CFU/g), and the pathogen growth was monitored over 12 days at 8°C. In parallel, the pH, water activity (aw), microbial plate counts, and organic acid content of cheeses were measured, and the taxonomic profiles of the cheese microbiomes were measured using 16S rRNA gene targeted amplicon sequencing and shotgun metagenomic sequencing. L. monocytogenes growth differed significantly between cheeses (analysis of variance [ANOVA]; P < 0.001), with increases ranging from 0 to 5.4 log CFU (mean of 2.5 ± 1.2 log CFU), and was negatively correlated with aw. Raw milk cheeses showed significantly lower L. monocytogenes growth than pasteurized-milk cheeses (t test; P = 0.008), possibly due to an increase in microbial competition. L. monocytogenes growth in cheeses was positively correlated with the relative abundance of Streptococcus thermophilus (Spearman correlation; P < 0.0001) and negatively correlated with the relative abundances of Brevibacterium aurantiacum (Spearman correlation; P = 0.0002) and two Lactococcus spp. (Spearman correlation; P < 0.01). These results suggest that the cheese microbiome may influence the food safety in SRCs. IMPORTANCE Previous studies have identified differences in L. monocytogenes growth between SRCs, but no clear mechanism has yet been elucidated. To the best of our knowledge, this is the first study to collect a wide range of SRCs from retail sources and attempt to identify key factors associated with pathogen growth. A key finding in this research was the positive correlation between the relative abundance of S. thermophilus and the growth of L. monocytogenes. The inclusion of S. thermophilus as a starter culture is more common in industrialized SRC production, suggesting that industrial production of SRC may increase the risk of L. monocytogenes growth. Overall, the results of this study further our understanding of the impact of aw and the cheese microbiome on the growth of L. monocytogenes in SRCs, hopefully leading toward the development of SRC starter/ripening cultures that can prevent L. monocytogenes growth.