The 2-Cys Peroxiredoxin-Deficient Listeria monocytogenes Displays Impaired Growth and Survival in the Presence of Hydrogen Peroxide In Vitro But Not in Mouse Organs

2007 ◽  
Vol 54 (5) ◽  
pp. 382-387 ◽  
Author(s):  
Kwang-Pyo Kim ◽  
Byoung-Kwon Hahm ◽  
Arun K. Bhunia
1998 ◽  
Vol 61 (5) ◽  
pp. 551-556 ◽  
Author(s):  
BENJAMIN J. JUVEN ◽  
SUSAN F. BAREFOOT ◽  
MERLE D. PIERSON ◽  
LINDA H. McCASKILL ◽  
BRIAN SMITH

A culture of the psychrotrophic strain FloraCarn L-2 of Lactobacillus alimentarius was added to ground beef (pH 5.4) inoculated with two isolates of Listeria monocytogenes able to grow in refrigerated ground beef. The ground beef was vacuum-packaged and stored for 9 weeks at 4°C. Populations of inoculated L. monocytogenes initially were 6.3 to 6.4 log10 CFU/g and increased to 7.4 log10 CFU/g in ground beef with no added lactobacilli. Addition of L. alimentarius L-2 or its antibiotic-resistant mutant SRL-2 reduced the final populations of L. monocytogenes to 4.3 or 4.1 log10 CFU/g, respectively. L. alimentarius L-2 did not produce bacteriocins or hydrogen peroxide in vitro. The antilisterial effect of L. alimentarius observed in laboratory media and ground beef is attiibuted to lactic acid (ca. 50 mM) produced by growing cultures.


2010 ◽  
Vol 7 (3) ◽  
pp. 1008-1012
Author(s):  
Farhan Zameer ◽  
Shubha Gopal

The present study aimed to understand the survival strategies adapted byListeria monocytogenesto combat oxidative stress in planktonic and biofilm cells with response to hydrogen peroxide (H2O2). The sensitivity ofL. monocytogenesto H2O2(oxidative stress) was found to vary in growth cycle. Early log phase cells were found to be sensitive to 100 μM H2O2when compared to stationary phase. Biofilm population was found to be resistant to the oxidative stress induced at 4% of H2O2when compared to their planktonic counterpart at 3.5%. This adaptive behavior allows the pathogen to overcome food preservation and safety barriers, which pose a potential risk to human health. The overall results suggest that, H2O2at a concentration of 6% could be used as a potent sanitizer for the elimination of listerial biofilms.


2007 ◽  
Vol 70 (11) ◽  
pp. 2626-2630 ◽  
Author(s):  
R. FIROUZI ◽  
S. S. SHEKARFOROUSH ◽  
A. H. K. NAZER ◽  
Z. BORUMAND ◽  
A. R. JOOYANDEH

The in vitro effects of plant essential oils (EOs) against pathogenic bacteria are well known, yet few studies have addressed the effects of these compounds against pathogens associated with ready-to-cook foods. Experiments were conducted to determine the effectiveness of oregano and nutmeg EOs on the growth and survival of Yersinia enterocolitica and Listeria monocytogenes in broth culture and in Iranian barbecued chicken. Ready-to-cook Iranian barbecued chicken was prepared according to the common practice with 1, 2, and 3 μl/g of oregano and nutmeg EOs. The test and control (without EOs) samples were inoculated with Y. enterocolitica and L. monocytogenes to a final concentration of 6 to 7 log CFU/g and stored at 3, 8, and 20°C. Microorganisms were counted just before and at 24, 48, and 72 h after storage based on growth on Yersinia selective agar supplemented with cefsulodine, igrasan, and novobiocin and on Listeria selective agar supplemented with nalidixic acid and acriflavin. In the broth culture system, the nutmeg EO had a greater effect on L. monocytogenes (MIC = 0.20 μl/ml) than did the oregano EO (MIC = 0.26 μl/ml). However, the oregano EO had a greater effect on Y. enterocolitica (MIC = 0.16 μl/ml) than did the nutmeg EO (MIC = 0.25 μl/ml). In ready-to-cook Iranian barbecued chicken, the log CFU per gram of both bacteria after up to 72 h of incubation was not decreased significantly by various combinations of oregano and nutmeg EOs (1, 2, and 3 μl/g) and storage temperatures (3, 8, and 20°C) when compared with control samples (without EOs). Although examination of spices in culture media can yield accurate microbiological data, without complementary tests in foods these data are of limited value for assessing food safety.


1992 ◽  
Vol 55 (7) ◽  
pp. 542-544 ◽  
Author(s):  
GEORGE THARRINGTON ◽  
KENT M. SORRELLS

Milk culture filtrates from Lactobacillus delbrueckii subsp. lactis were found to be inhibitory to test strains of Listeria monocytogenes. Effective in vitro inhibition was found in broth cultures and well diffusion assays. The causative factor(s) of inhibition was lactic acid and hydrogen peroxide.


2002 ◽  
Vol 65 (6) ◽  
pp. 924-930 ◽  
Author(s):  
DIKE O. UKUKU ◽  
WILLIAM FETT

Attachment and survival of Listeria monocytogenes on external surfaces (rind) of inoculated cantaloupe, resistance of the surviving bacteria to chlorine or hydrogen peroxide treatments, transfer of the pathogen from unsanitized and sanitized rinds to fresh-cut tissues during cutting and growth, and survival of L. monocytogenes on fresh-cut pieces of cantaloupe were investigated. Surface treatment with 70% ethanol to reduce the native microflora on treated melon, followed by immersion in a four-strain cocktail of L. monocytogenes (108 CFU/ml) for 10 min, deposited 4.2 log10 CFU/cm2 and 3.5 log10 CFU/cm2 of L. monocytogenes on treated and untreated cantaloupe rinds, respectively. L. monocytogenes survived on the treated or untreated cantaloupe rinds for up to 15 days during storage at 4 and 20°C, but populations declined by approximately 1 to 2 log10 CFU/cm2. Fresh-cut pieces prepared from inoculated whole cantaloupes stored at 4°C for 24 h after inoculation were positive for L. monocytogenes. Washing inoculated whole cantaloupes in solutions containing 1,000 ppm of chlorine or 5% hydrogen peroxide for 2 min at 1 to 15 days of storage at 4°C after inoculation resulted in a 2.0-to 3.5-log reduction in L. monocytogenes on the melon surface. Fresh-cut pieces prepared from the sanitized melons were negative for L. monocytogenes. After direct inoculation onto fresh-cut pieces, L. monocytogenes survived, but did not grow, during 15 days of storage at 4°C. Growth was evident by 4 h of storage at 8 and 20°C. It is concluded that sanitizing with chlorine or hydrogen peroxide has the potential to reduce or eliminate the transfer of L. monocytogenes on melon surfaces to fresh-cut pieces during cutting.


LWT ◽  
2021 ◽  
pp. 111881
Author(s):  
Jessica Audrey Feijó Corrêa ◽  
João Vitor Garcia dos Santos ◽  
Alberto Gonçalves Evangelista ◽  
Anne Caroline Schoch Marques Pinto ◽  
Renata Ernlund Freitas de Macedo ◽  
...  

Odontology ◽  
2021 ◽  
Author(s):  
Sarita Giri ◽  
Ayuko Takada ◽  
Durga Paudel ◽  
Koki Yoshida ◽  
Masae Furukawa ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Vishal Panchariya ◽  
Vishal Bhati ◽  
Harishkumar Madhyastha ◽  
Radha Madhyastha ◽  
Jagdish Prasad ◽  
...  

AbstractExtraction of biosurfactants from plants is advantageous than from microbes. The properties and robustness of biosurfactant derived from the mesocarp of Balanites aegyptiaca have been reported. However, the dark brown property of biosurfactant and lack of knowledge of its biocompatibility limits its scope. In the present work, the decolorization protocol for this biosurfactant was optimized using hydrogen peroxide. The hemolytic potential and biocompatibility based on cell toxicity and proliferation were also investigated. This study is the first report on the decolorization and toxicity assay of this biosurfactant. For decolorization of biosurfactant, 34 full factorial design was used, and the data were subjected to ANOVA. Results indicate that 1.5% of hydrogen peroxide can decolorize the biosurfactant most efficiently at 40 °C in 70 min at pH 7. Mitochondrial reductase (MTT) and reactive oxygen species (ROS) assays on M5S mouse skin fibroblast cells revealed that decolorized biosurfactant up to 50 µg/mL for 6 h had no significant toxic effect. Hemolysis assay showed ~ 2.5% hemolysis of human RBCs, indicating the nontoxic effect of this biosurfactant. The present work established a decolorization protocol making the biosurfactant chromatically acceptable. Biocompatibility assays confirm its safer use as observed by experiments on M5S skin fibroblast cells under in vitro conditions.


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