Influence of cinnamon and clove essential oils on the D- and z-values of Escherichia coli O157:H7 in apple cider.

Escherichia coli O157:H7 has become a concern within the apple cider industry. The purpose of this study was to screen several essential oils and isolated components for antimicrobial activity against E. coli O157:H7 in tryptic soy broth at neutral and acidic pH and to assess the effect of these additives on the D-value of E. coli O157:H7 in apple cider in combination with mild heat treatments. Cinnamon oil and clove oil strongly inhibited the growth of E. coli O157:H7 at neutral and acidic pH, (R)-(-)-carvone and (S)-(-)-perillaldehyde were moderately inhibitory at both pH 7.2 and pH 4.5, and citral and geraniol displayed moderate activity at pH 4.5 only. Lemon oil, methyl jasmonate, and p-anisaldehyde displayed little or no antibacterial activity. A synergistic effect between the essential oils and the lower pH of the growth medium was evident by consistently lower MICs at pH 4.5. Cinnamon and clove oils (0.01%, vol/vol) were further tested in apple cider in combination with mild heat treatments for the practical control of E. coli O157:H7 in apple cider. The addition of either essential oil resulted in lower D-values than those for cider alone, suggesting a synergistic effect and the potential efficacy of a mild heat treatment for apple cider.

Growth pH does not affect the initial physiological state parameter (pO) of Listeria monocytogenes.

It has proven difficult to develop adequate mathematical models for the lag phase (lambda) which characterizes the adaptation period prior to the initiation of exponential growth by microorganisms. This is due, in part, to our incomplete understanding of the nature of the initial physiological state of cells (defined as h0 or p0 depending on the model), and changes taking place during adaptation. The objectives of the present study were to characterize p0 using data from growth of Listeria monocytogenes in an automated turbidimetric instrument (Bioscreen), and to determine the influence of limiting growth pH. A model was developed for individual cells which combined a continuous adaptation phase (defined by p0) with a discrete step marking the transition to a continuous exponential growth phase (the CDC model). Parameters of the new model were: p0; the specific growth rate (mu); the initial cell number (N0); and the maximum cell density (Nmax). Progressive reduction of the growth pH in the Bioscreen to 4.7 decreased the p. It was noted that the regression lines for all trials at all pH values appeared to have a common x-intercept (20.086+/-1.092), and it was deduced that, when the Bioscreen detection limit (15.07 In cfu well(-1)) was subtracted, the resulting value represented the "true" value for the initial physiological state of the cells.

Proposal of a novel parameter to describe the influence of pH on the lag phase of Listeria monocytogenes.

Predictive models for lag phase duration (lambda) have been less reliable than specific growth rate (mu) models due, in part, to the influence of the pre-growth environment on lambda. A discrete modelling approach was taken to more completely define the response of individual cells to new environments. Time to detection (td) data was obtained from serial twofold dilutions of Listeria monocytogenes growing in a Bioscreen at 30 degrees C. Comparison of the inoculum densities required to achieve maximum td at growth pH values from 7.2 to 4.7 revealed that, as the growth pH decreased, fewer cells were capable of making the transition to the exponential phase. The proportion of these cells (termed "adaptable cells") in the original inoculum was used to define a new parameter (r0) which, when combined with the constant mean individual cell physiological state parameter (p0), the variation in p0 (SDp0), the inital inoculum (N0) and the maximum population density (Nmax) was able to simulate a complete growth curve. Power transformations with rescaled explanatory variables provided suitable models for the influence of pH on mu, r0, and SDp0, (r2>0.70).

Growth and survival of various strains of enterohemorrhagic Escherichia coli in hydrochloric and acetic acid.

Nineteen strains of enterohemorrhagic Escherichia coli isolated from humans and foods were examined for their ability to grow and survive at low pH in organic (acetic) and mineral (HCl) acids. Strains were subcultured in tryptic soy broth adjusted to various pH values (3.75 to 4.75 for HCl and 4.75 to 5.75 for acetic acid) and incubated for 72 h at 37 degrees C to determine the minimum growth pH value. Minimum pH values for growth of 4.25 and 5.5 were found for HCl and acetic acid, respectively. Strains were also exposed to pH 2.0 (HCl) and pH 4.0 (acetic acid) for up to 24 h at 37 degrees C to assess their ability to survive. HCl was a more effective inhibitor after 6 h of exposure, whereas acetic acid was more effective after 24 h. Outbreak strains survived acid treatment significantly (P < or = 0.05) better than strains isolated from fermented or high-pH foods or animal or human isolates. Significant (P < or = 0.05) differences among serotypes and between O157:H7 and other serotypes were apparent after 3 or 6 h of exposure to acids.

Nisin reduces the thermal resistance of Listeria monocytogenes Scott A in liquid whole egg.

D-values (decimal reduction times) and z-values (increase in temperature required for a 1-log change in D-value) for Listeria monocytogenes Scott A were determined in liquid whole egg with nisin (0 or 10 microg ml(-1)) and NaCl (0 or 10%) by a submerged glass ampoule procedure. Samples were plated onto nonselective agar at appropriate intervals, and D-values were determined using a modified biphasic logistic equation. Addition of NaCl increased D-values at all temperatures tested. The addition of nisin to unsalted liquid whole egg resulted in a rapid 4-log reduction in viable counts within the first hour. Nisin significantly (P < or = 0.05) decreased D-values at lower (< 58 degrees C) temperatures in both unsalted and salted liquid whole egg but had little effect on the D-values at current minimum U.S. and Canadian pasteurization temperatures (60 degrees C without NaCl; 63 degrees C with NaCl). However, when nisin was added 2 h prior to heat treatment, D-values were significantly (P < or = 0.05) reduced at these temperatures. Inhibitory levels of nisin were detected in the liquid whole egg postpasteurization. Nisin could have a favorable impact on the control of L. monocytogenes in pasteurized liquid egg products.