David L. Campos, Angela Perdomo, Kendra Nightingale, Jorge Franco, Luis Jimenez, Mindy M. Brashears
{"title":"乳酸菌的协同作用:静电喷涂、浸渍和配方应用唾液乳杆菌L28和屎肠球菌J19提高奶酪抗单核细胞增生李斯特菌的安全性","authors":"David L. Campos, Angela Perdomo, Kendra Nightingale, Jorge Franco, Luis Jimenez, Mindy M. Brashears","doi":"10.1016/j.jfp.2025.100507","DOIUrl":null,"url":null,"abstract":"<div><div>Recent outbreaks of listeriosis linked to cheese and recalls of cheese contaminated with <em>Listeria monocytogenes</em> have emerged as a significant public health concern due to the ability of this pathogen to grow during refrigerated storage. We hypothesized that a lactic acid bacteria (LAB) intervention applied onto the surface of cheese by electrostatic spray, dipping or formulation of the product with LAB would be effective in controlling <em>L monocytogenes</em> growth during refrigerated storage. The purpose of this study was to utilize two LAB strains, including J19 <em>Enterococcus faecium</em> and L28 <em>Lactobacillus salivarius</em> individually and in combination, to reduce <em>L. monocytogenes</em> on the surface of cheese during a 60 d of refrigerated storage period. We inoculated various cheeses with a five-strain cocktail of <em>L. monocytogenes</em>. After inoculation, the surface of cheeses had a <em>L. monocytogenes</em> concentration of approximately 10<sup>6</sup> CFU/cm<sup>2</sup> on day 0 and the cheeses were subjected to a LAB electrostatic spray or dipping treatment. Electrostatic spray treatments were as follows, (1) L28 at a concentration of 10<sup>8</sup>, (2) J19 at a concentration of 10<sup>8</sup> and (3) a combination of L28 and J19 at a concentration of 10<sup>8</sup> at a 1:1 ratio. Resultant <em>L. monocytogenes</em> populations were enumerated on days 0, 1, 3, 7, 14, 30, 45, and 60. Results indicated that J19 inhibited <em>L. monocytogenes</em>, while the L28 and the combination resulted in little inhibition. When utilizing J19 as an intervention, there was always an immediate reduction of <em>L. monocytogenes</em> on all cheese types on day zero of approximately 1 log10. The use of J19 as a biological intervention in cheese could improve the safety of cheeses that may become contaminated with <em>L. monocytogenes</em>.</div></div>","PeriodicalId":15903,"journal":{"name":"Journal of food protection","volume":"88 6","pages":"Article 100507"},"PeriodicalIF":2.1000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lactic Acid Bacteria Synergy: Electrostatic Spraying, Dipping, and Formulation Applications of Lactobacillus salivarius L28 and Enterococcus faecium J19 to Enhance Cheese Safety Against Listeria monocytogenes\",\"authors\":\"David L. Campos, Angela Perdomo, Kendra Nightingale, Jorge Franco, Luis Jimenez, Mindy M. Brashears\",\"doi\":\"10.1016/j.jfp.2025.100507\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Recent outbreaks of listeriosis linked to cheese and recalls of cheese contaminated with <em>Listeria monocytogenes</em> have emerged as a significant public health concern due to the ability of this pathogen to grow during refrigerated storage. We hypothesized that a lactic acid bacteria (LAB) intervention applied onto the surface of cheese by electrostatic spray, dipping or formulation of the product with LAB would be effective in controlling <em>L monocytogenes</em> growth during refrigerated storage. The purpose of this study was to utilize two LAB strains, including J19 <em>Enterococcus faecium</em> and L28 <em>Lactobacillus salivarius</em> individually and in combination, to reduce <em>L. monocytogenes</em> on the surface of cheese during a 60 d of refrigerated storage period. We inoculated various cheeses with a five-strain cocktail of <em>L. monocytogenes</em>. After inoculation, the surface of cheeses had a <em>L. monocytogenes</em> concentration of approximately 10<sup>6</sup> CFU/cm<sup>2</sup> on day 0 and the cheeses were subjected to a LAB electrostatic spray or dipping treatment. Electrostatic spray treatments were as follows, (1) L28 at a concentration of 10<sup>8</sup>, (2) J19 at a concentration of 10<sup>8</sup> and (3) a combination of L28 and J19 at a concentration of 10<sup>8</sup> at a 1:1 ratio. Resultant <em>L. monocytogenes</em> populations were enumerated on days 0, 1, 3, 7, 14, 30, 45, and 60. Results indicated that J19 inhibited <em>L. monocytogenes</em>, while the L28 and the combination resulted in little inhibition. When utilizing J19 as an intervention, there was always an immediate reduction of <em>L. monocytogenes</em> on all cheese types on day zero of approximately 1 log10. The use of J19 as a biological intervention in cheese could improve the safety of cheeses that may become contaminated with <em>L. monocytogenes</em>.</div></div>\",\"PeriodicalId\":15903,\"journal\":{\"name\":\"Journal of food protection\",\"volume\":\"88 6\",\"pages\":\"Article 100507\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of food protection\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0362028X25000596\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of food protection","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0362028X25000596","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Lactic Acid Bacteria Synergy: Electrostatic Spraying, Dipping, and Formulation Applications of Lactobacillus salivarius L28 and Enterococcus faecium J19 to Enhance Cheese Safety Against Listeria monocytogenes
Recent outbreaks of listeriosis linked to cheese and recalls of cheese contaminated with Listeria monocytogenes have emerged as a significant public health concern due to the ability of this pathogen to grow during refrigerated storage. We hypothesized that a lactic acid bacteria (LAB) intervention applied onto the surface of cheese by electrostatic spray, dipping or formulation of the product with LAB would be effective in controlling L monocytogenes growth during refrigerated storage. The purpose of this study was to utilize two LAB strains, including J19 Enterococcus faecium and L28 Lactobacillus salivarius individually and in combination, to reduce L. monocytogenes on the surface of cheese during a 60 d of refrigerated storage period. We inoculated various cheeses with a five-strain cocktail of L. monocytogenes. After inoculation, the surface of cheeses had a L. monocytogenes concentration of approximately 106 CFU/cm2 on day 0 and the cheeses were subjected to a LAB electrostatic spray or dipping treatment. Electrostatic spray treatments were as follows, (1) L28 at a concentration of 108, (2) J19 at a concentration of 108 and (3) a combination of L28 and J19 at a concentration of 108 at a 1:1 ratio. Resultant L. monocytogenes populations were enumerated on days 0, 1, 3, 7, 14, 30, 45, and 60. Results indicated that J19 inhibited L. monocytogenes, while the L28 and the combination resulted in little inhibition. When utilizing J19 as an intervention, there was always an immediate reduction of L. monocytogenes on all cheese types on day zero of approximately 1 log10. The use of J19 as a biological intervention in cheese could improve the safety of cheeses that may become contaminated with L. monocytogenes.
期刊介绍:
The Journal of Food Protection® (JFP) is an international, monthly scientific journal in the English language published by the International Association for Food Protection (IAFP). JFP publishes research and review articles on all aspects of food protection and safety. Major emphases of JFP are placed on studies dealing with:
Tracking, detecting (including traditional, molecular, and real-time), inactivating, and controlling food-related hazards, including microorganisms (including antibiotic resistance), microbial (mycotoxins, seafood toxins) and non-microbial toxins (heavy metals, pesticides, veterinary drug residues, migrants from food packaging, and processing contaminants), allergens and pests (insects, rodents) in human food, pet food and animal feed throughout the food chain;
Microbiological food quality and traditional/novel methods to assay microbiological food quality;
Prevention of food-related hazards and food spoilage through food preservatives and thermal/non-thermal processes, including process validation;
Food fermentations and food-related probiotics;
Safe food handling practices during pre-harvest, harvest, post-harvest, distribution and consumption, including food safety education for retailers, foodservice, and consumers;
Risk assessments for food-related hazards;
Economic impact of food-related hazards, foodborne illness, food loss, food spoilage, and adulterated foods;
Food fraud, food authentication, food defense, and foodborne disease outbreak investigations.