ABSTRACT
The influence of chemical diluents on the antimicrobial activity of plant essential oil (EO) vapors was evaluated. We first determined if vapors generated from 22 chemical diluents not containing EO had antimicrobial activities. Ethyl ether vapor retarded the growth of S. aureus. The minimal inhibitory concentrations (MICs) and the minimal lethal concentrations (MLCs) of cinnamon bark EO vapor, which was diluted in and generated from 21 diluents, against S. aureus and S. enterica were determined. Cinnamon bark EO vapor showed significantly (P ≤ 0.05) lower MICs against S. aureus when diluted in dimethyl sulfoxide (DMSO), ethanol, ethyl acetate, or jojoba oil, and against S. enterica when diluted in DMSO, ethanol, or jojoba oil, compared to those in other diluents. We compared antimicrobial activities of cinnamon bark EO vapor diluted in DMSO, ethanol, ethyl acetate, or jojoba oil against S. aureus and S. enterica on beef jerky as a food model. Antimicrobial activity was significantly (P ≤ 0.05) higher when vaporized from DMSO. These results indicate that antimicrobial activity of cinnamon bark EO vapor may vary significantly (P ≤ 0.05) depending on the type of diluent from which it is vaporized. These observations provide basic information when developing food and food-contact surface decontamination strategies using EO vapors.
Subject(s)
Anti-Infective Agents , Oils, Volatile , Salmonella enterica , Animals , Cattle , Staphylococcus aureus , Cinnamomum zeylanicum , Dimethyl Sulfoxide , Plant Bark , Oils, Volatile/pharmacology , Plant Oils/pharmacology , Gases , Anti-Infective Agents/pharmacology , Ethanol , Microbial Sensitivity TestsABSTRACT
AIM: This study was done to determine the effects of temperature, pH and sodium chloride (NaCl) on antimicrobial activity of magnesium oxide (MgO) nanoparticles (NPs) against E. coli O157:H7. METHODS AND RESULTS: Culture conditions were established by varying the pH (5.0, 7.2 and 9.0), NaCl concentration (0.5, 2.0, 3.5 and 5.0%, w/v), and incubation temperatures (4, 12, 22 and 37°C). At each condition, the antimicrobial activities of MgO-NPs (0, 1, 2 and 4 mg/ml) against E. coli O157:H7 were measured. Four-way analysis of variance indicated interactions among all factors had a significant effect (p ≤ 0.05) on the antimicrobial activity of MgO-NPs. The concentration of MgO-NPs necessary to cause a 5-log reduction of E. coli O157:H7 under the most inhibitory conditions (37°C, pH 9.0, and 5.0% NaCl) was 0.50 mg/ml of MgO-NPs. CONCLUSION: The antimicrobial activity of the MgO-NPs increased significantly (p ≤ 0.05) with increased temperature, pH and NaCl concentration in TSB. SIGNIFICANCE AND IMPACT OF THE STUDY: The influence of intrinsic and extrinsic factors on antimicrobial activity of MgO-NPs we found will contribute to the development of microbial decontamination strategies using MgO in the food industry.
Subject(s)
Anti-Infective Agents , Escherichia coli O157 , Nanoparticles , Anti-Infective Agents/pharmacology , Colony Count, Microbial , Food Microbiology , Hydrogen-Ion Concentration , Magnesium Oxide/pharmacology , Sodium Chloride/pharmacology , TemperatureABSTRACT
AIM: This study was done to develop a seed decontamination treatment for organic seeds against plant pathogens (Acidovorax citrulli and Xanthomonas campestris) using essential oil (EO) vapours without affecting the seeds' germination rate. METHODS AND RESULTS: By using a diffusion assay and determining minimum inhibitory and lethal concentrations, we screened two EO vapours which were most inhibitory to A. citrulli (cinnamon bark and garlic EO vapours) and X. campestris (onion and garlic EO vapours). After 48 h of exposure to EO vapours at 25°C and 43% or 85% relative humidity (RH), no significant decrease (p > 0.05) in germination rates was observed compared with those of control seeds. It was observed that EO vapour treatment at 25°C and 43% or 85% RH for 48 h caused significant population reductions (p ≤ 0.05) (ca. 0.3-2.6 log colony forming unit/g) compared to those of untreated seeds. CONCLUSION: Applications of EO vapours showed significant (p ≤ 0.05) antimicrobial effects against A. citrulli and X. campestris on both laboratory mediums and plant seeds without decreasing the germination rate of seeds. SIGNIFICANCE AND IMPACT OF THE STUDY: This study provides useful information for the development of natural seed sterilization treatments using EO vapours.
Subject(s)
Anti-Infective Agents , Brassicaceae , Cucurbitaceae , Oils, Volatile , Solanaceae , Xanthomonas campestris , Comamonadaceae , Oils, Volatile/pharmacology , Plant Oils/pharmacology , SeedsABSTRACT
This study was done to develop a method to inactivate Escherichia coli O157:H7 on radish and cabbage seeds using simultaneous treatments with gaseous chlorine dioxide (ClO2) and heat at high relative humidity (RH) without decreasing seeds' viability. Gaseous ClO2 was spontaneously vaporized from a solution containing hydrochloric acid (HCl, 1 N) and sodium chlorite (NaClO2, 100,000 ppm). Using a sealed container (1.8 L), an equation (y = 5687×, R2 = 0.9948) based on the amount of gaseous ClO2 generated from HCl-NaClO2 solution at 60 °C and 85% RH was developed. When radish or cabbage seeds were exposed to gaseous ClO2 at concentrations up to 3,000 ppm for 120 min, germination rates did not significantly decrease (P > 0.05). When seeds inoculated with E. coli O157:H7 were treated with 2,000 or 3,000 ppm of gaseous ClO2 in an atmosphere with 85% RH at 60 °C, populations (6.8-6.9 log CFU/g) on both types of seeds were decreased to below the detection limit for enrichment (-0.5 log CFU/g) within 90 min. This study provides useful information for developing a decontamination method to control E. coli O157:H7 and perhaps other foodborne pathogens on plant seeds by simultaneous treatment with gaseous ClO2 and heat at high RH.
Subject(s)
Brassica/growth & development , Chlorine Compounds/pharmacology , Decontamination/methods , Disinfectants/pharmacology , Escherichia coli O157/drug effects , Oxides/pharmacology , Raphanus/growth & development , Seeds/microbiology , Brassica/microbiology , Chlorine/pharmacology , Escherichia coli O157/growth & development , Germination/drug effects , Hot Temperature , Humidity , Microbial Viability/drug effects , Raphanus/microbiology , Seeds/chemistry , Seeds/growth & developmentABSTRACT
Nuts, including almonds, are occasionally contaminated with Salmonella spp. In this study, we used chlorine dioxide (ClO2) gas to inactivate S. enterica subsp. Enterica serovar Enteritidis on almonds. Almonds inoculated with a single strain of S. Enteritidis (8.95 log cfu/mL) were exposed to ClO2 gas generated from 1.0 or 1.5 mL ClO2 solution in a sealed container at 50 or 60 °C (43% relative humidity) for up to 10 h. The concentration of ClO2 gas peaked at 354-510 and 750-786 ppm within 0.5 h upon deposition of 1.0 and 1.5 mL of aqueous ClO2, respectively, and gradually decreased thereafter. Population of S. Enteritidis on almonds treated at 50 °C decreased to 1.70-2.32 log cfu/sample within 1 h of exposure to ClO2 gas and decreased to below the detection limit (1.7 log cfu/sample) at all ClO2 concentrations after 8 h. At 60 °C, the microbial population fell below the detection limit within 1 h, regardless of the volume of ClO2 solution supplied. Microbial survival on almonds treated with ClO2 gas and stored at 12 or 25 °C was observed for up to 8 weeks and the organism was not recovered from the almonds treated for 10 h and stored at 12 °C for 2-8 weeks. The lightness (L value) and redness (a value) of almonds treated for 10 h were not changed by ClO2 gas treatment, but yellowness (b value) increased. Results showed that Salmonella on almonds was successfully inactivated by ClO2 gas treatment and the microbial survival did not occur during storage.
Subject(s)
Chlorine Compounds/pharmacology , Food Preservation/methods , Food Preservatives/pharmacology , Oxides/pharmacology , Prunus dulcis/microbiology , Salmonella enteritidis/drug effects , Chlorine Compounds/chemistry , Food Preservation/instrumentation , Food Storage , Gases/pharmacology , Microbial Viability/drug effects , Nuts/microbiology , Oxides/chemistry , Salmonella enteritidis/growth & developmentABSTRACT
This study investigated the antimicrobial activities of organic acid vapors against a phytopathogen (Acidovorax citrulli) and foodborne pathogens (Salmonella enterica, Escherichia coli O157:H7, and Listeria monocytogenes) on the surface of Cucurbitaceae seeds. Germination percentages of cucumber, honeydew melon and watermelon seeds treated with acetic and propionic acid vapors (100 mg/L) at 50 °C and 43% or 85% relative humidity (RH) for up to 2 h did not significantly (P > 0.05) decrease. Treatment with formic acid significantly (P ≤ 0.05) decreased the germination percentage. The antimicrobial activities of acetic and propionic acid vapors (100 mg/L; 50 °C; 43% or 85% RH) were determined. A. citrulli was inactivated within 1 h on cucumber and watermelon seeds, regardless of type of organic acid or RH. The phytopathogen was reduced to levels below the detection limit (-0.5 log CFU/g) for enrichment on honeydew melon seeds treated with acetic acid vapor. S. enterica and L. monocytogenes were inactivated within 2 h at 85% RH on honeydew melon and watermelon seeds treated with acetic acid and propionic acid vapors. E. coli O157: H7 was inactivated by treatment with acetic acid vapor at 85% RH. This study provides useful information for developing a method to decontaminate Curcurbitaceae seeds using organic acid vapors as lethal agents.
Subject(s)
Acids/pharmacology , Anti-Bacterial Agents/pharmacology , Cucurbitaceae/microbiology , Escherichia coli O157/drug effects , Listeria monocytogenes/drug effects , Salmonella enterica/drug effects , Acetic Acid/chemistry , Acetic Acid/pharmacology , Acids/chemistry , Anti-Bacterial Agents/chemistry , Comamonadaceae/drug effects , Comamonadaceae/growth & development , Cucurbitaceae/growth & development , Escherichia coli O157/growth & development , Formates/chemistry , Formates/pharmacology , Germination , Listeria monocytogenes/growth & development , Propionates/chemistry , Propionates/pharmacology , Salmonella enterica/growth & development , Seeds/growth & development , Seeds/microbiologyABSTRACT
This study was done to identify combinations of essential oils (EOs) that elicit synergistic antimicrobial effects against Leuconostoc citreum, a spoilage bacterium in vegetable and fruit juices. Twenty-four EOs were tested for antimicrobial activity against L. citreum using an agar well diffusion assay. Ten EOs showed relatively strong antimicrobial activity. Among those, cinnamon bark, oregano, and thyme thymol EOs showed the strongest activity (minimal inhibitory concentration = 1.25 µL/mL). It was confirmed that a combination of oregano and thyme thymol EOs had a synergistic antimicrobial activity (fractional inhibitory concentration index = 0.3750) using a checkerboard assay. This combination also had a synergistic antimicrobial activity against L. citreum in tomato juice. An initial population of L. citreum in tomato juice (5.3 log CFU/mL) increased to ≥ 8.6 log CFU/mL within 48 h at 15 °C and 24 h at 25 °C. Populations reached 6.8-7.2 log CFU/mL in tomato juice containing either 0.156 mL/mL oregano or thyme thymol. However, in the presence of both EOs (0.156 µL/mL in total), populations of L. citreum were significantly lower (5.7-6.5 log CFU/mL) (P ≤ 0.05). Findings will be useful when developing non-thermal food preservation technologies to increase the shelf-life of juices and other foods not containing synthetic preservatives.
Subject(s)
Anti-Infective Agents/pharmacology , Fruit and Vegetable Juices/microbiology , Leuconostoc/drug effects , Oils, Volatile/pharmacology , Origanum/chemistry , Plant Oils/pharmacology , Thymol/pharmacology , Cinnamomum zeylanicum/chemistry , Culture Media/chemistry , Culture Media/pharmacology , Drug Synergism , Food Microbiology/methods , Food Preservation/methods , Solanum lycopersicum/microbiology , Microbial Sensitivity Tests , Thymus Plant/chemistryABSTRACT
We investigated combinations of gaseous essential oils (EO gases) for their synergistic inhibitory activities against Listeria monocytogenes on a laboratory medium and radish sprouts. The minimum inhibitory concentrations and minimum lethal concentrations of oregano, thyme thymol, and cinnamon bark EO gases against L. monocytogenes were 0.0781⯵L/mL on nutrient agar supplemented with glucose and bromocresol purple (NGBA). A checkerboard assay showed that combinations of oregano and thyme thymol EO gases and of oregano and cinnamon bark EO gases exert the strongest synergistic antilisterial activity (fractional inhibitory concentration index [FICI]â¯=â¯0.3750). A combination of thyme thymol and cinnamon bark EO gases also had a synergistic effect (FICIâ¯=â¯0.5000) on L. monocytogenes on NGBA. Combinations of oregano and thyme thymol EO gases were tested for synergistic antimicrobial activity against L. monocytogenes on radish sprouts. A combination of these gases, each at 0.313⯵L/mL, caused a significant (Pâ¯≤â¯0.05) reduction in the number of L. monocytogenes on radish sprouts compared with reductions caused by treatment with oregano or thyme thymol EO gas alone at the same concentration. Our findings provide information that will be useful when developing antimicrobial applications using EO gases to control L. monocytogenes in the food industry.
Subject(s)
Anti-Bacterial Agents/pharmacology , Listeria monocytogenes/drug effects , Oils, Volatile/pharmacology , Origanum/chemistry , Raphanus/microbiology , Thymol/pharmacology , Thymus Plant/chemistry , Anti-Bacterial Agents/chemistry , Cinnamomum zeylanicum/chemistry , Culture Media/chemistry , Culture Media/metabolism , Drug Synergism , Gases/pharmacology , Listeria monocytogenes/growth & development , Microbial Sensitivity Tests , Oils, Volatile/chemistry , Plant Oils/chemistry , Plant Oils/pharmacology , Raphanus/growth & development , Thymol/chemistryABSTRACT
The aim of this study was to use chlorine dioxide (ClO2) gas to inactivate Aspergillus flavus on green coffee beans. Green coffee beans inoculated with A. flavus were exposed to ClO2 gas generated from 0.75, 1, 1.25, or 1.5â¯mL of ClO2 solution in a sealed container at 25 or 50⯰C (100% relative humidity [RH]) for up to 10â¯h. Numbers of A. flavus on beans treated at 25⯰C decreased by 1.1-2.2 log cfu/bean within 1â¯h of exposure to ClO2 and decreased to below the detection limit (≤1.0 log cfu/bean) at all ClO2 concentrations after 10â¯h. At 50⯰C, the microbial population reached the detection limit within 0.5â¯h regardless of the ClO2 solution concentration. Beans exposed to gas for 10â¯hâ¯at 25⯰C were stored for 14 days under conditions of 43, 75, or 100% RH and 4, 12, or 25⯰C. At 4⯰C, visible mold growth was not established regardless of RH. After 12 days, mold was observed only at 25⯰C. At 100% RH, beans stored under the same conditions without ClO2 gas treatment showed mold formation at 13 and 4 days at 12 and 25⯰C, respectively.
Subject(s)
Aspergillus flavus/drug effects , Chlorine Compounds/pharmacology , Chlorine/pharmacology , Coffea/microbiology , Food Preservation/methods , Oxides/pharmacology , Aspergillus flavus/growth & development , Chlorine Compounds/chemistry , Colony Count, Microbial , Oxides/chemistry , Seeds/microbiologyABSTRACT
BACKGROUND: Acidovorax citrulli is a plant pathogen causing bacterial fruit blotch in Cucurbitaceae family. Applying high concentration of disinfectants to seeds containing plant pathogen may substantially decrease the germination rate of seeds. Therefore, it is necessary to develop a hurdle technology which can inactivate plant pathogens without decreasing seed viability. This study was conducted to develop a decontamination method to inactivate the plant pathogen Acidovorax citrulli on Cucurbitaceae seeds by sequential treatments with aqueous chlorine dioxide (ClO2 ), drying, and dry heat. RESULTS: The maximum ClO2 concentration that did not lower germination rates of cucumber, honeydew melon, and watermelon seeds was ca. 100 µg mL-1 of ClO2 for 5 min. Optimal incubation conditions for drying seeds that had been treated with aqueous ClO2 were determined as 25 °C and 43% relative humidity (RH) for 48 h. The maximum dry-heat temperature that did not reduce germination rates of seeds, which had been treated with ClO2 and dried at 25 °C, was 60 °C at 43% RH for 24 h. When seeds containing A. citrulli (6.4-7.0 log CFU g-1 ) were treated with aqueous ClO2 (50 µg mL-1 , 5 min), dried (25 °C, 43% RH, 24 h), and dry heated (60 °C, 43% RH, 24 h), the pathogen was inactivated to below the detection limit from all three seed types (<-0.5 log CFU g-1 ). CONCLUSION: The decontamination conditions to inactivate A. citrullii from Cucurbitaceae seeds without decreasing the seed viability were determined (sequential treatment with ClO2 [50 µg mL-1 , 5 min], dried [25 °C, 43% RH, 24 h], and dry heated [60 °C, 43% RH, 24 h]). The results of this study may also be applicable to other plant pathogens on other types of seeds. © 2019 Society of Chemical Industry.
Subject(s)
Comamonadaceae/drug effects , Cucurbitaceae/microbiology , Decontamination/methods , Seeds/growth & development , Chlorine Compounds/pharmacology , Comamonadaceae/growth & development , Cucurbitaceae/growth & development , Decontamination/instrumentation , Desiccation , Disinfectants/pharmacology , Germination , Oxides/pharmacology , Plant Diseases/microbiology , Plant Diseases/prevention & control , Seeds/microbiologyABSTRACT
Of the 1648 microbial isolates from 133 soil samples collected from 30 diverse locations in the Republic of Korea, two isolates exhibited strong antilisterial activity and ability to grow to high populations (>8.0 log CFU/ml) in Bennett's broth. Isolates were identified as Streptomyces lactacystinicus (strain Samnamu 5-15) and Streptomyces purpureus (strain Chamnamu-sup 4-15). Both isolates formed biofilms on the surface of stainless steel coupons (SSCs) immersed in Bennett's broth within 24â¯hâ¯at 25⯰C. Cells retained antilisterial activity after biofilm formation and showed significantly (Pâ¯≤â¯0.05) enhanced resistance against dry conditions (43% relative humidity [RH]) compared to the cells not in biofilm. An initial population (ca. 3.2 log CFU/cm2) of Listeria monocytogenes inoculated on SSCs lacking Streptomyces biofilm decreased to 1.4 log CFU/cm2 within 48â¯hâ¯at 25⯰C and 43% RH. In contrast, L. monocytogenes (3.3 log CFU/cm2) inoculated on SSCs containing Streptomyces biofilm decreased to populations below the theoretical detection limit (0.5 log CFU/cm2) within 24â¯h. The results indicate that biofilms formed by the Streptomyces spp. inhibitory to L. monocytogenes showed enhanced resistance to desiccation condition (43% RH) and effectively inhibited the growth of L. monocytogenes on the surfaces of SSCs. Antilisterial biofilms developed in this study may be applicable on desiccated environmental surfaces in food related environments such as food storage, handling, and processing facilities to enhance the microbiological safety of foods.
Subject(s)
Antibiosis , Biofilms , Listeria monocytogenes/growth & development , Stainless Steel/analysis , Streptomyces/physiology , Colony Count, Microbial , Desiccation , Food Handling , Food Microbiology , Republic of Korea , Soil Microbiology , Streptomyces/growth & development , Streptomyces/isolation & purificationABSTRACT
This study was done to determine the antifungal activities of essential oil (EO) vapours of 97 plants against Penicillium corylophilum and to test combinations of EO vapours for synergistic antifungal effects. Among 97 commercially available EOs extracted from plant parts, garlic, cinnamon bark, may chang (mountain pepper), citronella, thyme thymol, oregano, spearmint, and thyme linalool EO vapours exhibited relatively strong antifungal activities. The minimal inhibitory concentrations of these EO vapours were 0.0390-0.6250⯵L/mL. A combination of cinnamon bark, citronella, and may chang EO vapours, as well as a combination of cinnamon bark and citronella EO vapours, showed synergistic inhibitory activities to P. corylophilum on a laboratory medium. A combination of cinnamon bark, citronella, and may chang EO vapours had synergistic activity in inhibiting growth of P. corylophilium on beef jerky. Observations reported here provide basic information valuable when developing strategies to inhibit the growth of P. corylophilum and possibly other moderately xerophilic molds on intermediate-moisture foods.
Subject(s)
Antifungal Agents/pharmacology , Meat Products/microbiology , Oils, Volatile/pharmacology , Penicillium/drug effects , Acyclic Monoterpenes , Cymbopogon/chemistry , Drug Synergism , Food Contamination/prevention & control , Food Microbiology , Mentha spicata/chemistry , Microbial Sensitivity Tests , Monoterpenes/pharmacology , Origanum/chemistry , Thymus Plant/chemistryABSTRACT
Chili pepper (Capsicum annuum L.) powder and other powdered spices containing chili peppers are occasionally contaminated with foodborne pathogens. We applied chlorine dioxide (ClO2) gas treatment to chili peppers prior to drying to inactivate Salmonella Typhimurium. Chili peppers inoculated with S. Typhimurium were exposed to ClO2 gas generated from 0.77â¯mL of aqueous ClO2 for 6â¯hâ¯at 25⯰C and 100% relative humidity, followed by air drying at 55⯰C for up to 24â¯h. Populations of S. Typhimurium and total aerobic bacteria (TAB) on peppers, chromaticity values, and moisture content were determined after various treatment times. S. Typhimurium (ca. 5.6 log cfu/g) was reduced to <0.7 log cfu/g of peppers treated with ClO2 gas for 0.5â¯hâ¯at 25⯰C, but was detected by enrichment (>1â¯cfu/10.8â¯g) after treatment for 4â¯h. The pathogen was not detected after treatment with ClO2 gas for 6â¯h. S. Typhimurium did not decrease significantly (Pâ¯>â¯0.05) on peppers exposed to air at 25⯰C for 6â¯h, but rapidly decreased to 1.6 log cfu/g after subsequent drying for 6â¯hâ¯at 55⯰C. The initial number of TAB (ca. 6.5 log cfu/g) decreased to 1.4 log cfu/g after treatment with ClO2 gas for 0.5â¯h and was less than the detection limit (0.7 log cfu/g) after 2â¯h. TAB counts were not reduced by treating peppers with air for 6â¯h, but decreased to <0.7 log cfu/g after subsequent drying for 24â¯hâ¯at 55⯰C. The lightness (L value) of treated and untreated chili peppers did not change during drying, but redness (a value) and yellowness (b value) decreased. Results showed that treatment of chili peppers containing S. Typhimurium (5.6 log cfu/g) with ClO2 gas for 6â¯h prior to drying at 55⯰C reduced the population toâ¯<â¯1â¯cfu/10.8â¯g.
Subject(s)
Capsicum/microbiology , Chlorine Compounds/pharmacology , Desiccation , Microbial Viability/drug effects , Oxides/pharmacology , Salmonella typhimurium/drug effects , Colony Count, Microbial , Color , Food Microbiology , Gases/pharmacology , Salmonella typhimurium/pathogenicity , Salmonella typhimurium/physiologyABSTRACT
Non-pathogenic bacterial biofilms were developed on the surface of stainless steel possessing desiccation tolerance and antimicrobial activity against Salmonella enterica. Three bacteria exhibiting strong antimicrobial activities against S. enterica were isolated from various soils, foods, and food-contact surfaces. Isolates were identified as Pseudomonas extremorientalis (strain Lettuce-28), Paenibacillus peoriae (strain Lettuce-7), and Streptomyces cirratus (strain Geumsan-207). These bacteria grew rapidly and formed biofilms within 24 h on the surface of stainless steel coupons (SSCs) immersed in laboratory media (tryptic soy broth or Bennet's broth) at 25 °C. Cells in biofilms had enhanced tolerance to desiccation (exposure to 43% atmospheric relative humidity [RH]) and retained antimicrobial activity against S. enterica. Populations of S. enterica deposited on SSCs containing biofilm formed by Ps. extremorientalis strain Lettuce-28, for example, decreased by > 2.5 log CFU/coupon within 24 h at 25 °C and 43% RH, while the number of cells inoculated on SSCs lacking biofilm decreased by 1.5 log CFU/coupon. Antimicrobial activities of the three antagonistic bacteria against S. enterica persisted in desiccated biofilms. This study provides insights to developing strategies to inactivate Salmonella and perhaps other foodborne pathogens on abiotic surfaces using non-pathogenic antagonistic bacteria.
Subject(s)
Biofilms , Pseudomonas/physiology , Salmonella enterica/physiology , Stainless Steel/analysis , Antibiosis , Food Microbiology , Pseudomonas/growth & development , Pseudomonas/isolation & purification , Salmonella enterica/growth & development , Soil MicrobiologyABSTRACT
The aim of this study was to evaluate the antimicrobial activities of gaseous essential oils (EO gases) against Listeria monocytogenes on the surfaces of a laboratory medium and radish sprouts. We determined the minimal inhibitory concentration (MIC) and minimal lethal concentration (MLC) values of EO gases from eight EOs extracted from basil leaves, carrot seed, cinnamon bark, cinnamon leaves, clove flower buds, oregano leaves, thyme flowers (linalool), and thyme leaves (thymol) against L. monocytogenes on a nutrient agar supplemented with 1% glucose and 0.025% bromocresol purple (NGBA). Oregano, thyme thymol, and cinnamon bark EO gases showed the strongest antilisterial activities (MIC and MLC, 78.1µL/L). We also investigated the inhibitory and lethal activities of these gases against L. monocytogenes on the surface of radish sprouts. The number of L. monocytogenes after exposure to EO gases at ≥156µL/L was significantly (P≤0.05) lower than that of untreated L. monocytogenes. For example, the initial number of L. monocytogenes on the surface of radish sprouts (ca. 6.3logCFU/g) decreased by 1.4logCFU/g within 24h at 30°C and 43% relative humidity (RH) without EO gas treatment, whereas the number of L. monocytogenes after exposure to oregano, thyme thymol, and cinnamon bark EO gases at 156µL/L decreased by 2.1, 2.1, and 1.8logCFU/g, respectively, after 24h. Although EO gases exerted greater lethal activities at higher concentrations (312 and 625µL/L), L. monocytogenes on the surface of radish sprouts was not completely inactivated. The number of L. monocytogenes on sprouts treated with oregano, thyme thymol, and cinnamon bark EO gases at 625µL/L decreased by 2.7-3.0logCFU/g after 24h at 30°C and 43% RH. Results indicate that EO gases that showed antilisterial activities on a laboratory medium also exhibited reduced lethal activity on the surface of radish sprouts. These findings will be useful when developing strategies to inactivate L. monocytogenes and possibly other foodborne pathogens on sprouts and perhaps other foods using EO gases.
Subject(s)
Anti-Bacterial Agents/pharmacology , Foodborne Diseases/prevention & control , Gases/pharmacology , Listeria monocytogenes/drug effects , Oils, Volatile/pharmacology , Plant Preparations/pharmacology , Raphanus/microbiology , Acyclic Monoterpenes , Cinnamomum zeylanicum/chemistry , Food Microbiology , Foodborne Diseases/microbiology , Microbial Sensitivity Tests , Monoterpenes/chemistry , Origanum/chemistry , Thymus Plant/chemistryABSTRACT
Halloysite nanotubes (HNTs), which are natural nanomaterials, have a hollow tubular structure with about 15 nm inner and 50 nm outer diameters. Because of their tubular shape, HNTs loaded with various materials have been investigated as functional nanocapsules. In this study, thyme essential oil (TO) was encapsulated successfully in HNTs using vacuum pulling methods, followed by end-capping or a layer-by-layer surface coating process for complete encapsulation. Nanocapsules loaded with TO were mixed with flexographic ink and coated on a paper for applications as food packaging materials. Scanning electron microscopy and transmission electron microscopy were used to characterize the morphology of the nanocapsules and to confirm the TO loading of the nanocapsules. Fourier transform infrared spectroscopy and thermogravimetric analyses analysis were used to complement the structural information. In addition, the controlled release of TO from the nanocapsules showed sustained release properties over a period of many days. The results reveal that the release properties of TO in these nanocapsules could be controlled by surface modifications such as end-capping and/or surface coating of bare nanocapsules. The packaging paper with TO-loaded HNT capsules was effective in eliminating against Escherichia coli during the first 5 d and showed strong antibacterial activity for about 10 d.
Subject(s)
Aluminum Silicates/chemistry , Food Packaging/instrumentation , Nanocapsules/chemistry , Oils, Volatile/chemistry , Plant Extracts/chemistry , Thymus Plant/chemistry , Anti-Bacterial Agents/chemistry , Clay , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Spectroscopy, Fourier Transform Infrared , ThermogravimetryABSTRACT
The effect of a combined treatment using aqueous chlorine dioxide (ClO2 ) and hot-air drying to inactivate Bacillus cereus spores on red chili peppers was evaluated. Ten washed and dried pepper samples, each comprising half of a single pepper (Capsicum annuum L.), were inoculated with B. cereus spore suspension. The inoculated samples were washed with sodium hypochlorite (NaOCl; 50, 100, or 200 µg/mL) or ClO2 (50, 100, or 200 µg/mL) solution for 1 min and then air-dried (25 ± 1 °C, 47 ± 1% relative humidity), which was followed by drying with hot air at 55 °C for up to 48 h. The spore populations on the samples were enumerated and their aw and chromaticity values were measured. The spore numbers immediately after treatment with NaOCl and ClO2 were not significantly different. A more rapid reduction in spore numbers was observed in the samples treated with ClO2 than those treated with NaOCl during drying. A combined treatment of ClO2 and hot-air drying significantly reduced the spore populations to below the detection limit (1.7 log CFU/sample). B. cereus spores on chili peppers were successfully inactivated by washing with ClO2 solution followed by hot-air drying whereas the pepper color was maintained.
Subject(s)
Bacillus cereus/drug effects , Capsicum/microbiology , Chlorine Compounds/pharmacology , Food Preservation/methods , Oxides/pharmacology , Bacillus cereus/growth & development , Capsicum/chemistry , Colony Count, Microbial , Desiccation , Food Preservation/instrumentation , Sodium Hypochlorite/pharmacology , Spores, Bacterial/drug effects , Spores, Bacterial/growth & developmentABSTRACT
Food-grade galactooligosaccharide (GOS) with low water activity (aw of ca. 0.7) is used as an ingredient in various foods. We evaluated heat tolerances of Salmonella, Cronobacter sakazakii, and Pediococcus acidilactici at temperatures (70 to 85°C) used during the saturation process of GOS by comparing decimal reduction time (D-values) and thermal resistance constants (z-values). To determine the D- and z-values, GOS containing Salmonella (5.1 to 5.8 log CFU/g) or C. sakazakii (5.3 to 5.9 log CFU/g) was heat treated at 70, 77.5, or 85°C for up to 40, 25, or 15 s, respectively, and GOS containing P. acidilactici (6.1 to 6.5 log CFU/g) was heat treated at 70, 77.5, or 85°C for up to 150, 75, or 40 s, respectively. The D-values were calculated using a linear model for heating time versus microbial population for each bacterium. When the D-values for Salmonella, C. sakazakii, and P. acidilactici in GOS were compared, the thermal resistance of all bacteria decreased as the temperature increased. Among the three bacteria, P. acidilactici had higher D-values than did Salmonella and C. sakazakii. The z-values of Salmonella, C. sakazakii, and P. acidilactici were 30.10, 33.18, and 13.04°C, respectively. Overall order of thermal resistance was P. acidilactici > Salmonella ≈ C. sakazakii. These results will be useful for selecting appropriate heat treatment conditions for the decontamination of pathogenic microorganisms during GOS manufacturing.
Subject(s)
Cronobacter sakazakii/growth & development , Hot Temperature , Pediococcus acidilactici/growth & development , Salmonella/growth & development , Colony Count, Microbial , Food Handling , Food Microbiology , ThermotoleranceABSTRACT
An effective bactericidal cold-marinating method for beef products is described, exploiting the synergism between soy sauce and natural compounds (carvacrol, CV or thymol, TM) to reduce microbiological risks. Beef slices inoculated with Escherichia coli O157:H7, Listeria monocytogenes, and Salmonella Typhimurium (3.1-3.5logCFU/g) were marinated in a teriyaki sauce with or without CV and TM (0.3 and 0.5%). After 1, 3, and 7days at 4°C, indigenous microflora population, color, lipid oxidation, marinade uptake, and pH of marinated beef and leftover marinade samples were examined. Teriyaki sauce alone did not reduce or inhibit any of the target pathogens or indigenous bacteria, while 0.5% CV- or TM-containing teriyaki sauce inactivated all inocula without recovery within 7days (p<0.05). The pathogens relocated from the beef into the leftover marinade (3.0-3.4logCFU/mL) were also completely inactivated. The treatment inhibited growth of indigenous aerobic bacteria (p<0.05) and inactivated coliform bacteria. Physicochemical parameters were not significantly affected (p>0.05).
Subject(s)
Escherichia coli O157/drug effects , Listeria monocytogenes/drug effects , Monoterpenes/pharmacology , Red Meat/microbiology , Salmonella typhimurium/drug effects , Thymol/pharmacology , Animals , Anti-Bacterial Agents/pharmacology , Cattle , Color , Cymenes , Escherichia coli O157/growth & development , Food Handling/methods , Food Microbiology , Hydrogen-Ion Concentration , Listeria monocytogenes/growth & development , Salmonella typhimurium/growth & developmentABSTRACT
The aim of this study was to investigate the lethal effects of simultaneous treatments with gaseous chlorine dioxide (ClO2) and mild wet heat (55 °C at 100% relative humidity [RH]) on Salmonella enterica in chicken feces on the surface of eggshells. Gaseous ClO2 production decreased significantly (P ≤ 0.05) as the RH (23, 43, 68, 85, and 100%) at 25 °C was increased. The lethality of gaseous ClO2 against S. enterica in feces on eggshells increased significantly (P ≤ 0.05) as RH increased. For example, when treated with gaseous ClO2 at 85 and 100% RH at 25 °C, S. enterica (5.9 log CFU/egg) was inactivated within 4 h. In contrast, at 23, 43, and 68% RH, the pathogen remained at 5.1, 5.0, and 2.8 log CFU/egg, respectively, after 6 h. Finally, when eggshells surface-contaminated with S. enterica (5.8 log CFU/egg) were treated with gaseous ClO2 (peak concentration of ClO2: 185.6 ppm) at 100% RH and 55 °C, inactivation occurred within 1 h. These results indicate that treatment of surface-contaminated shell eggs with gaseous ClO2 at elevated RH and temperature is effective in inactivating S. enterica. These observations will be useful when developing an effective sanitation program to enhance the microbiological safety of shell eggs.