PubMed Health⌕ Search

Biomedical subjects

Micha Peleg

Publications and source records attributed to Micha Peleg.

10 recordsLinked to original sources

An expanded Fermi solution for microbial risk assessment.

'Fermi solution' refers to an estimate of a quantity of interest derived from a sequence of guesses about factors of which detailed knowledge is unavailable. When one makes such guesses, it is unlikely that the large majority of them will be either too high or too low. Most probably, some of the overestimates will be offset by some of the underestimates, and the final result will be often close to the correct value. The method has been popularized as recreational physics but it has also been applied in risk assessment, where the factors involved, but not their exact magnitudes, are known. The concept has potential application in certain types of food poisoning risk assessments, and in estimating the number victims of a bioterrorist attack on the food or water supply, where some guessing is inevitable because of the absence of accurate relevant data. We consider a version of the method in which ranges instead of single values are entered as the factors' estimates. For simplicity, the risk to be assessed is taken to be the product of the factors, and their true values are regarded as being uniformly distributed over their respective ranges. The risk itself is therefore construed as a random variable with a probability distribution whose parameters are explicitly determined by the individual factors' ranges and which can often be approximated by a lognormal distribution. The mode of this lognormal distribution is taken to be the "best guess" of the risk, and a credible interval is constructed with a specified level of "confidence". The best guess and credible interval are shown to be robust against small perturbations of the ranges. Thus, even if the ranges are misspecified to some degree, assessments based on the best guess or credible interval will not be substantially altered. This can help to achieve consensus among assessors in situations where very little hard knowledge exists. The calculation procedure has been automated in software that has been made freely available over the Internet. The concept is demonstrated with two hypothetical problems: predicting the number of persons who would come down with acute food poisoning after consuming a contaminated dish, and estimating the number of daily salmonellosis cases in a large metropolitan area.

Confidence Intervals↗

On modeling and simulating transitions between microbial growth and inactivation or vice versa.

Resumed growth of the survivors of a heat or chemical treatment after cooling or a disinfectant dissipation is not an uncommon phenomenon. Similarly, the inverse, the onset of mortality in a growing microbial population as a result of exposure to increasing temperature or concentration of an antimicrobial agent, is also a familiar scenario. Provided that in either regime, the organism has no time to adapt biologically, the continuous transition from growth to inactivation or vice versa can be simulated with conventional growth and inactivation models, whose rate constant is allowed to change sign. Where both the growth and inactivation follow first-order kinetics, the sign change has no effect on the model equation's solutions. The same applies when the growth and inactivation patterns are described by a rate model, like the differential logistic equation or its various variants. However, determination of such models' coefficients from experimental isothermal growth and inactivation data can be difficult for technical reasons, unless the model can be integrated analytically. If not, or when the model itself is unknown a priori, then the rate equation would have to be derived from the fit of empirical models like the Weibull, modified versions of the logistic function and the like. But this may create a new kind of problem as a result of that the log and certain power operations cannot be used for negative numbers. For certain models at least, the problem can be solved through modification of the procedure by which the rate equation is solved numerically. This is demonstrated in simulated transitions between growth and inactivation and between inactivation and growth based on the log linear and Weibullian-power law models and three logistic patterns based on a shifted logistic function, the Baranyi-Roberts model and a shifted arctan model.

Bacteria↗

Linear and non-linear kinetics in the synthesis and degradation of acrylamide in foods and model systems.

Isothermal acrylamide formation in foods and asparagine-glucose model systems has ubiquitous features. On a time scale of about 60 min, at temperatures in the approximate range of 120-160 degrees C, the acrylamide concentration-time curve has a characteristic sigmoid shape whose asymptotic level and steepness increases with temperature while the time that corresponds to the inflection point decreases. In the approximate range of 160-200 degrees C, the curve has a clear peak, whose onset, height, width and degree of asymmetry depend on the system's composition and temperature. The synthesis-degradation of acrylamide in model systems has been recently described by traditional kinetic models. They account for the intermediate stages of the process and the fate of reactants involved at different levels of scrutiny. The resulting models have 2-6 rate constants, accounting for both the generation and elimination of the acrylamide. Their temperature dependence has been assumed to obey the Arrhenius equation, i.e., each step in the reaction was considered as having a fixed energy of activation. A proposed alternative is constructing the concentration curve by superimposing a Fermian decay term on a logistic growth function. The resulting model, which is not unique, has five parameters: a hypothetical uninterrupted generation-level, two steepness parameters; of the concentration climbs and fall and two time characteristics; of the acrylamide synthesis and elimination. According to this model, peak concentration is observed only when the two time constants are comparable. The peak's shape and height are determined by the gap between the two time constants and the relative magnitudes of the two "rate" parameters. The concept can be extended to create models of non-isothermal acrylamide formation. The basic assumption, which is yet to be verified experimentally, is that the momentary rate of the acrylamide synthesis or degradation is the isothermal rate at the momentary temperature, at a time that corresponds to its momentary concentration. The theoretical capabilities of a model of this kind are demonstrated with computer simulations. If the described model is correct, then by controlling temperature history, it is possible to reduce the acrylamide while still accomplishing much of the desirable effects of a heat process.

Acrylamide↗

Modeling and predicting non-isothermal microbial growth using general purpose software.

Published experimental isothermal growth curves of Clostridium perfringens cells in ground ham were fitted with a modified three-parameter version of the logistic equation as a primary model and the temperature dependence of the three parameters by ad hoc empirical secondary models. These were used to predict the organism's non-isothermal growth curves under three different cooling regimes. The assumption has been that the organism's instantaneous (or momentary) non-isothermal growth rate is the isothermal rate at the given temperature at a time that corresponds to its instantaneous population size. This could be translated into a differential rate model equation, whose coefficients are constructed from terms that reflect the changing growth parameters with temperature and hence with time. The continuous rate equation, however, can be solved incrementally by a numerical procedure that can be implemented in similar purpose software like Microsoft Excel(R). In all three cases, there was good agreement between the growth curves predicted by the model and those found experimentally. This demonstrated that the procedure can be used to generate growth curves under complicated thermal histories that may include regular and irregular temperature oscillations.

Animals↗

Statistical analysis of the fluctuating counts of fecal bacteria in the water of Lake Kinneret.

Counts of E. coli, Enteroccoci and fecal coliforms in four sites around Lake Kinneret (The Sea of Galilee), collected every 2-4 weeks for about 5 years during 1995-2002 showed irregular fluctuations punctuated by aperiodic outbursts of variable magnitude. Because of the haphazard nature of fecal contamination and large intervals between successive counts, these patterns were described by probabilistic models, based on the truncated Laplace or Extreme Value distribution. Their applicability was tested by comparing the predicted frequencies of counts exceeding different levels calculated from the first half of each record with those actually observed in its second half. Despite the records imperfections and minor violations of the underlying models' assumptions, there was a reasonable agreement between the estimated and actual frequencies. This demonstrated that it is possible to translate the irregular fluctuation pattern into a set of probabilities of future high counts. In principle, such probabilities can be used to quantify the water's fecal contamination pattern and as a tool to assess the efficacy of preventive measures to reduce it.

Enterobacteriaceae↗

Calculating microbial survival parameters and predicting survival curves from non-isothermal inactivation data.

Irrespective of whether the isothermal semi-logarithmic survival curves of heat inactivated microbial cells or spores are linear or nonlinear, it is theoretically possible to numerically calculate their survival parameters from inactivation data obtained under non-isothermal conditions. A method to do the calculation, when the temperature history ('profile') is expressed algebraically, is demonstrated with simulated survival curves. It has been tested with the published survival data of Salmonella, whose nonlinear semi-logarithmic isothermal survival curves can be described by a power law model. The reported survival ratios of Salmonella, determined during non-isothermal heat treatments in a broth and in ground chicken breast, were used to estimate its isothermal survival parameters in the two media and their temperature dependence. These, in turn, were used to predict the cells' survival curves under different temperature 'profiles.' There was a good agreement between the predicted and the reported experimental survival curves in the broth case and reasonable agreement in the ground chicken breasts, where the database was considerably smaller The development of a mathematical method to calculate survival parameters from non-isothermal inactivation data will eliminate the need to determine these parameters under isothermal conditions, which can only be approximated and are technically difficult to perform. In many cases, the proposed method will also enable the determination of the survival parameters in the actual food or medium of interest, which may contain particles, or is too viscous to be heated and cooled effectively using the currently available experimental procedures. In principle, the described mathematical method can also be used to assess organisms' survival parameters in nonthermal inactivation processes, such as exposure to a dissipating chemical agent or the application of ultra high-pressure.

Animals↗

Demonstration of the applicability of the Weibull-log-logistic survival model to the isothermal and nonisothermal inactivation of Escherichia coli K-12 MG1655.

Published isothermal semilogarithmic survival curves of Escherichia coli K-12 MG1655, in the range of 49.8 to 60.6 degrees C, all had noticeable downward concavity. They could be described by the model log S(t) = -b(T)t n, where S(t) = N(t)/N0, N(t) and N0 being the momentary and initial number of organisms, respectively; b(T) is a temperature-dependent rate parameter; and n is a constant found to be about 1.5. The temperature dependence of b(T) could be described by the log-logistic model, b(T) = ln[1 + exp[k(T - Tc)]], which had an almost perfect fit, with k = 0.88 degrees C(-1) and Tc = 60.5 degrees C. The constants, n, k, and Tc were considered the organism's survival parameters in the particular medium. They were incorporated into a rate equation on the assumption that in nonisothermal heating, the momentary inactivation rate is the isothermal rate at the momentary temperature at a time that corresponds to the momentary survival ratio. This model's estimates matched the actual survival curves obtained in the same work under two different nonisothermal heating profiles, lending support to the notion that the Weibull-log-logistic model combination can be used not only to describe isothermal inactivation mathematically, but also to predict survival patterns under nonisothermal conditions.

Colony Count, Microbial↗

Estimating microbial inactivation parameters from survival curves obtained under varying conditions--the linear case.

When the isothermal semi-logarithmic survival curves of heat inactivated microbial cells or spores are known to be linear it is possible to calculate their survival parameters from curves obtained under nonisothermal conditions, provided that the temperature history ('profile') satisfies certain simple mathematical requirements. These requirements have been identified. The concept was tested by retrieving the survival parameters of a Listeria-like organism from generated survival curves for linear and nonlinear heating profiles on which noise had been superimposed. The availability of such a procedure eliminates the need to determine the survival parameters under perfect isothermal conditions, which are difficult to create for technical reasons. It will also enable determination of the survival parameters in the actual medium of interest, which may contain particles or may be too viscous to be treated in a capillary or narrow tube as is currently done. The method can also be used to assess survival parameters in nonthermal inactivation. A treatment with a dissipating chemical agent or anti-microbial is an example. In principle, the concept can be extended to the more general situation where the isothermal or iso-concentration semi-logarithmic survival curves are clearly nonlinear, but this will require a modification of the model and a different numerical calculation procedure.

Computer Simulation↗

Calculation of the non-isothermal inactivation patterns of microbes having sigmoidal isothermal semi-logarithmic survival curves.

Sigmoidal isothermal semi-logarithmic survival curves are of two main types; starting with a downward and changing to upward concavity and vice versa. Both can be described by a variety of mathematical models having 3-4 adjustable parameters. The temperature dependence of these models' parameters can be described by empirical models, which account for the progressive change in the sigmoidal shape, including its disappearance at either high or low temperatures. If the temperature history of a heat-treated population of microbial cells or spores ('temperature profile') can be described algebraically, then there is a way to estimate the survival pattern under these non-isothermal conditions without invoking the traditional D and z values, which require forcing straight lines through the curved experimental data. The described method is based on the assumption that the local slope of the non-isothermal survival curve is that of the isothermal curve at the momentary temperature, at a time, which corresponds to the momentary survival ratio. It is similar to the method previously proposed for microbial populations with a 'power law' type isothermal survival curves, except that the time, which corresponds to the momentary survival ratio, is calculated either symbolically or numerically as a procedure incorporated in the governing differential equation. The method's capabilities are demonstrated with simulated survival curves under temperature histories that resemble thermal processing of foods. They include heating to different target temperatures and starting the cooling at different times.

Animals↗

Squeezing flow viscometry for nonelastic semiliquid foods--theory and applications.

In most conventional rheometers, notably the coaxial cylinders and capillary viscometers, the food specimen is pressed into a narrow gap and its structure is altered by uncontrolled shear. Also, most semiliquid foods exhibit slip, and consequently the measurements do not always reflect their true rheological properties. A feasible solution to these two problems is squeezing flow viscometry where the specimen, practically intact and with or without suspended particles, is squeezed between parallel plates. The outward flow pattern mainly depends on the friction between the fluid and plates or its absence ("lubricated squeezing flow"). Among the possible test geometries, the one of constant area and changing volume is the most practical for foods. The test can be performed at a constant displacement rate using common Universal Testing Machines or under constant loads (creep array). The tests output is in the form of a force-height, force-time, or height-time relationship, from which several rheological parameters can be derived. With the current state of the art, the method can only be applied at small displacement rates. Despite the method's crudeness, its results are remarkably reproducible and sensitive to textural differences among semiliquid food products. The flow patterns observed in foods do not always follow the predictions of rheological models originally developed for polymer melts because of the foods' unique microstructures. The implications of these discrepancies and the role that artifacts may play are evaluated in light of theoretical and practical considerations. The use of squeezing flow viscometry to quantify rheological changes that occur during a product's handling and to determine whether they are perceived sensorily is suggested.

Elasticity↗