Listeria monocytogenes survival of UV-C radiation is enhanced by presence of sodium chloride, organic food material and by bacterial biofilm formation
Publication: Research - peer-review › Journal article – Annual report year: 2011
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Listeria monocytogenes survival of UV-C radiation is enhanced by presence of sodium chloride, organic food material and by bacterial biofilm formation. / Bernbom, Nete; Vogel, Birte Fonnesbech; Gram, Lone.
In: International Journal of Food Microbiology, Vol. 147, No. 1, 2011, p. 69-73.Publication: Research - peer-review › Journal article – Annual report year: 2011
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TY - JOUR
T1 - Listeria monocytogenes survival of UV-C radiation is enhanced by presence of sodium chloride, organic food material and by bacterial biofilm formation
A1 - Bernbom,Nete
A1 - Vogel,Birte Fonnesbech
A1 - Gram,Lone
AU - Bernbom,Nete
AU - Vogel,Birte Fonnesbech
AU - Gram,Lone
PB - Elsevier BV
PY - 2011
Y1 - 2011
N2 - The bactericidal effect on food processing surfaces of ceiling-mounted UV-C light (wavelength 254nm) was determined in a fish smoke house after the routine cleaning and disinfection procedure. The total aerobic counts were reduced during UV-C light exposure (48h) and the number of Listeria monocytogenes positive samples went from 30 (of 68) before exposure to 8 (of 68). We therefore in a laboratory model determined the L. monocytogenes reduction kinetics by UV-C light with the purpose of evaluating the influence of food production environmental variables, such as presence of NaCl, organic material and the time L. monocytogenes was allowed to adhere to steel before exposure. L. monocytogenes grown and attached in tryptone soy broth (TSB) with glucose were rapidly killed (after 2min) by UV-C light. However, bacteria grown and adhered in TSB with glucose and 5% NaCl were more resistant and numbers declined with 4–5log units during exposure of 8–10min. Bacteria grown in juice prepared from cold-smoked salmon were protected and numbers were reduced with 2–3log when UV-C light was used immediately after attachment whereas numbers did not change at all if bacteria had been allowed to form a biofilm for 7days before exposure. It is not known if this enhanced survival is due to physiological changes in the attached bacterial cells, a physical protection of the cells in the food matrix or a combination. In conclusion, we demonstrate that UV-C light is a useful extra bacteriocidal step and that it, as all disinfecting procedures, is hampered by the presence of organic material.
AB - The bactericidal effect on food processing surfaces of ceiling-mounted UV-C light (wavelength 254nm) was determined in a fish smoke house after the routine cleaning and disinfection procedure. The total aerobic counts were reduced during UV-C light exposure (48h) and the number of Listeria monocytogenes positive samples went from 30 (of 68) before exposure to 8 (of 68). We therefore in a laboratory model determined the L. monocytogenes reduction kinetics by UV-C light with the purpose of evaluating the influence of food production environmental variables, such as presence of NaCl, organic material and the time L. monocytogenes was allowed to adhere to steel before exposure. L. monocytogenes grown and attached in tryptone soy broth (TSB) with glucose were rapidly killed (after 2min) by UV-C light. However, bacteria grown and adhered in TSB with glucose and 5% NaCl were more resistant and numbers declined with 4–5log units during exposure of 8–10min. Bacteria grown in juice prepared from cold-smoked salmon were protected and numbers were reduced with 2–3log when UV-C light was used immediately after attachment whereas numbers did not change at all if bacteria had been allowed to form a biofilm for 7days before exposure. It is not known if this enhanced survival is due to physiological changes in the attached bacterial cells, a physical protection of the cells in the food matrix or a combination. In conclusion, we demonstrate that UV-C light is a useful extra bacteriocidal step and that it, as all disinfecting procedures, is hampered by the presence of organic material.
U2 - 10.1016/j.ijfoodmicro.2011.03.009
DO - 10.1016/j.ijfoodmicro.2011.03.009
JO - International Journal of Food Microbiology
JF - International Journal of Food Microbiology
SN - 0168-1605
IS - 1
VL - 147
SP - 69
EP - 73
ER -