Aqueous Matrix Compositions and pH Influence Feline Calicivirus Inactivation by High Pressure Processing

Authors: Kingsley, David H.1; Chen, Haiqiang2

Source: Journal of Food Protection®, Number 8, August 2008, pp. 1544-1741 , pp. 1598-1603(6)

Publisher: International Association for Food Protection

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Abstract:

The individual effects of pH (pH 3 to 8), NaCl (0 to 21%), sucrose (0 to 70%), and whey protein (0 to 2%) on pressure resistance of feline calicivirus (FCV) in Dulbecco's modified Eagle medium with 10% fetal bovine serum were determined. At pH 3 through 8, the virus was more resistant to pressure at a pH of ≤5.2. For FCV samples with sucrose (up to 40%) or NaCl (up to 12%), the amount of FCV inactivated by pressure was inversely proportional to the sucrose or NaCl concentration. For example, a treatment of 250 MPa at 20°C for 5 min reduced the FCV titer by 5.1 log PFU/ml without added sucrose and by 0.9 log PFU/ml with 40% sucrose. Reduced pressure sensitivity with increasing NaCl and sucrose concentrations was not a simple function of water activity. Different PFU reductions were observed for NaCl and sucrose samples with equivalent water activity. Whey protein at concentrations up to 2% did not provide a protective effect. The combined effect of NaCl and sucrose at 4 and 20°C on pressure resistance of FCV also was examined. When both NaCl and sucrose were added to the FCV stock, they had an additive effect on increasing the pressure resistance of FCV. The individual (6% NaCl or 20% sucrose) and combined (6% NaCl plus 20% sucrose) resistance effects did not abrogate enhanced inactivation for pressure treatments at 4°C compared with those at 20°C. Aqueous matrix compositions, in particular different concentrations of NaCl and sucrose or different pH values, can substantially alter the efficiency of virus inactivation by high pressure processing.

Document Type: Research Article

Affiliations: 1: U.S. Department of Agriculture, Agricultural Research Service, Microbial Food Safety Research Unit, W. W. Baker Center, Delaware State University, Dover, Delaware 19901, USA 2: Department of Animal & Food Sciences, University of Delaware, Newark, Delaware 19716-2150, USA

Publication date: August 1, 2008

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