Effect of Glucose on Listeria monocytogenes Survival under Sequential Sublethal Stresses of Gamma Irradiation and NaCl

  • Yoon, Yo-Han (Team for Radiation Food Science and Biotechnology, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute) ;
  • Kim, Gyeong-Yeol (Division of Applied Life Science, Graduate School of Gyeongsang National University) ;
  • Nam, Min-Ji (Division of Applied Life Science, Graduate School of Gyeongsang National University) ;
  • Shim, Won-Bo (Division of Applied Life Science, Graduate School of Gyeongsang National University) ;
  • Seo, Eun-Kyoung (Division of Applied Life Science, Graduate School of Gyeongsang National University) ;
  • Kim, Jae-Hun (Team for Radiation Food Science and Biotechnology, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute) ;
  • Lee, Ju-Woon (Team for Radiation Food Science and Biotechnology, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute) ;
  • Byun, Myung-Woo (Team for Radiation Food Science and Biotechnology, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute) ;
  • Chung, Duck-Hwa (Team for Radiation Food Science and Biotechnology, Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute)
  • Published : 2009.02.28

Abstract

This study evaluated glucose effect on Listeria monocytogenes survival under gamma irradiation and NaCl stress. L. monocytogenes in phosphate buffered saline (PBS) plus glucose (0-4%) was treated with gamma irradiation (0-0.5 kGy), and the samples were then exposed to NaCl (0-9%) in tryptic soy agar plus 0.6% yeast extract. $D_{10}$ and $t_{3D}$ values were determined, and a model for prediction of $D_{10}$ values was developed. Cell counts of L. monocytogenes reduced as irradiation dose increased, and L. monocytogenes in PBS (no glucose) was more sensitive to irradiation and NaCl compared to those in PBS (2 or 4% glucose). $D_{10}$ values were 0.07-0.1, 0.12-0.16, and 0.13-0.15 kGy for 0, 2, and 4% glucose, respectively. The $t_{3D}$ values were 0.22-0.3 (0% glucose), 0.35-0.48 (2% glucose), and 0.40-0.44 (4% glucose). A model performance was acceptable. These results indicate that glucose in foods would increase the resistance of L. monocytogenes to gamma irradiation and NaCl stress.

Keywords

References

  1. Farber JM, Peterkin PI. Listeria monocytogenes, a food-borne pathogen. Microbiol. Rev. 55: 476-511 (1991)
  2. Mead PS, Slutsker L, Dietz V, McCaig LF, Bresee JS, Shapiro C, Griffin PM, Tauxe RV. Food-related illness and death in the United States. Emerg. Infect. Dis. 5: 607-625 (1999) https://doi.org/10.3201/eid0505.990502
  3. Sofos JS, Yoon Y. Safer food using predictive modeling. Fleischwirtschaft Int. 3: 16-19 (2006)
  4. Tompkin RB. Control of Listeria monocytogenes in the food processing environment. J. Food Protect. 65: 709-725 (2002) https://doi.org/10.4315/0362-028X-65.4.709
  5. U.S. Department of Agriculture-Food Safety and Inspection Service. Control of Listeria monocytogenes in ready-to-eat-meat and poultry products; final rule. Fed. Reg. 68: 34208-34254 (2003)
  6. Barmpalia IM, Geornaras I, Belk KE, Scanga JA, Kendall PA, Smith GC, Sofos JN. Control of Listeria monocytogenes on frankfurters with antimicrobials in the formulation and by dipping in organic acid solutions. J. Food Protect. 67: 2456-2464 (2004) https://doi.org/10.4315/0362-028X-67.11.2456
  7. Barmpalia IM, Koutsoumanis KP, Geomaras I, Belk KE, Scanga JA, Kendall PA, Smith GC, Sofos JN. Effect of antimicrobials as ingredients of pork bologna for Listeria monocytogenes control during storage at 4 or 10${^{\circ}C}$. Food Microbiol. 22: 205-211 (2005) https://doi.org/10.1016/j.fm.2004.08.003
  8. Bedie GK, Samelis J, Sofos JN, Belk KE, Scanga JA, Smith GC. Antimicrobials in the formulation to control Listeria monocytogenes postprocessing contamination on frankfurters stored at 4${^{\circ}C}$ in vacuum packages. J. Food Protect. 64: 1949-1955 (2001) https://doi.org/10.4315/0362-028X-64.12.1949
  9. Geornaras I, Belk KE, Scanga JA, Kendall PA, Smith GC, Sofos JN. Postprocessing antimicrobial treatments to control Listeria monocytogenes in commercial vacuum-packaged bologna and ham stored at 10${^{\circ}C}$. J. Food Protect. 68: 991-998 (2005) https://doi.org/10.4315/0362-028X-68.5.991
  10. Geornaras I, Skandamis PN, Belk KE, Scanga JA, Kendall PA, Smith GC, Sofos JN. Postprocess control of Listeria monocytogenes on commercial frankfurters formulated with and without antimicrobials and stored at 10${^{\circ}C}$. J. Food Protect. 69: 53-61 (2006) https://doi.org/10.4315/0362-028X-69.1.53
  11. Geornaras I, Skandamis PN, Belk KE, Scanga JA, Kendall PA, Smith GC, Sofos IN. Post-processing application of chemical solutions for control of Listeria monocytogenes, cultured under different conditions, on commercial smoked sausage formulated with and without potassium lactate-sodium diacetate. Food Microbiol. 23:762-771 (2006) https://doi.org/10.1016/j.fm.2006.01.008
  12. Samelis J, Sofos JN, Kain ML, Scanga JA, Belk KE, Smith GC. Organic acids and their salts as dipping solutions to control Listeria monocytogenes inoculated following processing to sliced pork bologna stored at 4${^{\circ}C}$ in vacuum packages. J. Food Protect. 64:1722-1729 (2001) https://doi.org/10.4315/0362-028X-64.11.1722
  13. Samelis J, Bedie GK, Sofos IN, Belk KE, Scanga JA, Smith GC. Control of Listeria monocytogenes with combined antimicrobials after postprocess contamination and extended storage of frankfurters at 4${^{\circ}C}$ in vacuum packages. J. Food Protect. 65: 299-307 (2002) https://doi.org/10.4315/0362-028X-65.2.299
  14. Samelis J, Bedie GK, Sofos IN, Belk KE, Scanga JA, Smith GC. Combinations of nisin with organic acids or salts to control Listeria monocytogenes on sliced pork bologna stored at 4${^{\circ}C}$ in vacuum packages. Lebensm.-Wiss. Technol. 38: 21-28 (2005) https://doi.org/10.1016/j.lwt.2004.04.012
  15. Glass KA, Doyle MP. Fate of Listeria monocytogenes in processed meat products during refrigerated storage, Appl. Environ. Microb. 55: 1565-1569(1989)
  16. Mbandi E, Shelef LA. Enhanced antimicrobial effects of combination of lactate and diacetate on Listeria monocytogenes and Salmonella spp. in beef bologna. Int. J. Food Microbiol. 76: 191-198 (2002) https://doi.org/10.1016/S0168-1605(02)00026-0
  17. Fan X, Niemira BA, Prakash A. Irradiation of flesh fruits and vegetables. Food Technol.-Chicago 62: 36-43 (2008)
  18. WHO. High dose irradiation. pp. 9-37. In: Wholesomeness of Food Irradiated with Doses above 10 kGy. WHO Technical Report Series 890. World Health Organization, Geneva, Switzerland (1999)
  19. Abu-Tarboush HM, AI-Kahtani HA, Abou-Arab AA, Baijaber AS, El-Mojadid MA. Sensory and microbial quality of chicken as affected by irradiation and post-irradiation storage at 4${^{\circ}C}$. J. Food Protect. 60: 761-770 (1996) https://doi.org/10.4315/0362-028X-60.7.761
  20. Thayer DW, Rajkowski KT. Developments in irradiation of fresh fruits and vegetables. Food Technol.-Chicago 53: 62-65 (1999)
  21. Mayer-Miebach E. Food irradiation-a means of controlling pathogenic microorganisms in food. Lebensm. -Wiss. Technol. 26: 493-497(1993) https://doi.org/10.1006/fstl.1993.1098
  22. Sommers CH, Thayer DW. Survival of surface-inoculated Listeria monocytogenes on commercially available frankfurters following gamma irradiation. J. Food Safety 20: 127-137 (2000) https://doi.org/10.1111/j.1745-4565.2000.tb00293.x
  23. Faleiro ML, Andrew PW, Powder D. Stress response of Listeria monocytogenes isolated from cheese and other foods. Int. J. Food Microbiol. 84: 207-216 (2003) https://doi.org/10.1016/S0168-1605(02)00422-1
  24. Jorgensen F, Stephens PJ, Knochel S. The effect of osmotic shock and subsequent adaptation on the thermotolerance and cell morphology of Listeria monocytogenes. J. Appl. Microbiol. 79: 274-281 (1995) https://doi.org/10.1111/j.1365-2672.1995.tb03137.x
  25. Samelis J, Kendall PA, Smith GC, Sofos JN. Acid tolerance of acid-adapted and nonadapted Escherichia coli 0157:H7 following habituation (10${^{\circ}C}$) in fresh beef decontamination runoff fluids of different pH values. J. Food Protect. 67: 638-645 (2004) https://doi.org/10.4315/0362-028X-67.4.638
  26. Jo C, Lee NY, Kang HJ, Hong SP, Kim YH, Kim HJ, Byun MW. Radio-sensitivity of pathogens in inoculated prepared foods of animal origin. Food Microbiol. 22: 329-336 (2005) https://doi.org/10.1016/j.fm.2004.09.003
  27. Edelson-Mammel SG, Whiting RC, Joseph SW, Buchanan RL. Effect of prior growth conditions on the thermal inactivation of 13 strains of Listeria monocytogenes in two heating menstrual. J. Food Microbiol. 68: 168-172 (2005)
  28. Sharma M, Adler BB, Harrison MD, Beuchat LR. Thermal tolerance of acid-adapted and unadapted Salmonella, Escherichia coli 0157:H7, and Listeria monocytogenes in cantaloupe juice and watermelon juice. Lett. Appl. Microbiol. 41: 448-453 (2005) https://doi.org/10.1111/j.1472-765X.2005.01797.x
  29. Samelis J, Ikeda JS, Sofos JN. Evaluation of the pH-dependent, stationary-phase acid tolerance in Listeria monocytogenes and Salmonella Typhimurium DT104 induced by culturing in media with 1% glucose: A comparative study with Escherichia coli O157:H7. J. Appl. Microbiol. 95: 563-575 (2003) https://doi.org/10.1046/j.1365-2672.2003.02013.x
  30. Skandamis PN, Yoon Y, Stopforth JD, Kendall PA, Sofos JN. Heat and acid tolerance of Listeria monocytogenes after exposure to single and multiple sublethal stresses. Food Microbiol. 25: 294-303 (2008) https://doi.org/10.1016/j.fm.2007.10.008
  31. Song H-P, Kim D-H, Jo C, Lee C-H, Kim K-S, Byun M-W. Effect of gamma irradiation on the microbiological quality and antioxidant activity of fresh vegetable juice. Food Microbiol. 23: 372-378 (2006) https://doi.org/10.1016/j.fm.2005.05.010
  32. Urbain MW. Biological effects of ionizing radiation. pp. 83-117. In:Food Irradiation. Food Science and Technology Series. Academic Press, London, UK (1986)