Modeling the Germination Kinetics of Clostridium botulinum 56A Spores as Affected by Temperature, pH, and Sodium Chloride†

2000 ◽  
Vol 63 (8) ◽  
pp. 1071-1079 ◽  
Author(s):  
FABIOLA P. CHEA ◽  
YUHUAN CHEN ◽  
THOMAS J. MONTVILLE ◽  
DONALD W. SCHAFFNER

The germination kinetics of proteolytic Clostridium botulinum 56A spores were modeled as a function of temperature (15, 22, 30°C), pH (5.5, 6.0, 6.5), and sodium chloride (0.5, 2.0, 4.0%). Germination in brain heart infusion (BHI) broth was followed with phase-contrast microscopy. Data collected were used to develop the mathematical models. The germination kinetics expressed as cumulated fraction of germinated spores over time at each environmental condition were best described by an exponential distribution. Quadratic polynomial models were developed by regression analysis to describe the exponential parameter (time to 63% germination) (r2 = 0.982) and the germination extent (r2 = 0.867) as a function of temperature, pH, and sodium chloride. Validation experiments in BHI broth (pH: 5.75, 6.25; NaCl: 1.0, 3.0%; temperature: 18, 26°C) confirmed that the model's predictions were within an acceptable range compared to the experimental results and were fail-safe in most cases.

2013 ◽  
Vol 80 (2) ◽  
Author(s):  
Julie Desarnaud ◽  
François Bertrand ◽  
Noushine Shahidzadeh-Bonn

In this study, we show that the key to understand why the same salt can cause damage in some conditions and not in others is the kinetics of crystallization. We present experiments assessing the impact of the recrystallization dynamics of sodium sulfate on damage observed in sandstone after repeated cycles of rewetting/drying and humidification/drying. Macroscopic and microscopic scale experiments using magnetic resonance imaging and phase contrast microscopy demonstrate that sodium sulfate that has both hydrated and anhydrous phases can lead to severe damage in sandstone during rewetting/drying cycles, but not during humidity cycling. During rewetting (a rapid process) in regions (pores) that are highly concentrated in salt, anhydrous microcrystals dissolve only partially, giving rise to a heterogeneous salt solution that is supersaturated with respect to the hydrated phase. The remaining anhydrous crystals then act as seeds for the formation of large amounts of hydrated crystals, creating grape-like structures that expand rapidly. These clusters can generate stresses larger than the tensile strength of the stone, leading to damage. On the other hand, with humidification (a slow process) and after complete deliquescence of salt crystals, the homogeneous sodium sulfate solution can reach high concentrations during evaporation without any nucleation, favoring the formation of isolated anhydrous crystals (thenardite). The crystallization of the anhydrous salt generates only very small stresses compared to the hydrated clusters and therefore causes hardly any damage to the stone.


1992 ◽  
Vol 55 (7) ◽  
pp. 509-513 ◽  
Author(s):  
LAURA L. ZAIKA ◽  
JOHN G. PHILLIPS ◽  
ROBERT L. BUCHANAN

A modified factorial design was used to measure the effects and interactions of temperature (10 to 37°C), pH (5.5 to 7.5), sodium chloride (0.5 to 5.0%), and sodium nitrite (0 to 1000 ppm) on the aerobic growth kinetics of Shigella flexneri in brain heart infusion broth. A total of 592 cultures were analyzed, with growth curves being generated using the Gompertz equation. A quadratic model for growth of S. flexneri in terms of temperature, pH, sodium chloride, and sodium nitrite concentrations was obtained by response surface analysis. This model provides an estimate of bacterial growth in response to any combination of the variables studied within the specified ranges. Estimates obtained with the model compared favorably with growth of S. flexneri in milk.


1985 ◽  
Vol 48 (8) ◽  
pp. 693-696 ◽  
Author(s):  
M. K. WAGNER ◽  
F. F. BUSTA

The influence of 0.4% sodium acid pyrophosphate (SAPP) or 0.26% potassium sorbate (PS) on Clostridium botulinum 52A growth and toxicity from spores was studied at two pH levels 5.55 and 5.85. Absorbancy measurements at 630 nm were used in combination with microscopic evaluations and toxin analysis to compare effects of additives on normal cell development. Treatment cultures containing 0.4% SAPP and 0.26% PS at a higher pH of 5.85 showed no increase in absorbancy and no sign of toxicity, but elongated vegetative cells (≥9 μm) were observed using phase contrast microscopy rather than scanning electron microscopy. The SAPP–PS treatment culture at a lower pH of 5.55 displayed no signs of growth spectrophometrically or microscopically, as well as no toxicity. These data suggest that a SAPP–PS combination in a laboratory medium at pH 5.85 does not halt germination and outgrowth, yet may prevent cell division; whereas, the same treatment at pH 5.55 inhibits normal spore germination.


2005 ◽  
Vol 71 (9) ◽  
pp. 4998-5003 ◽  
Author(s):  
Sandra C. Stringer ◽  
Martin D. Webb ◽  
Susan M. George ◽  
Carmen Pin ◽  
Michael W. Peck

ABSTRACT Knowledge of the distribution of growth times from individual spores and quantification of this biovariability are important if predictions of growth in food are to be improved, particularly when, as for Clostridium botulinum, growth is likely to initiate from low numbers of spores. In this study we made a novel attempt to determine the distributions of times associated with the various stages of germination and subsequent growth from spores and the relationships between these stages. The time to germination (t germ), time to emergence (t emerg), and times to reach the lengths of one (t C1) and two (t C2) mature cells were quantified for individual spores of nonproteolytic C. botulinum Eklund 17B using phase-contrast microscopy and image analysis. The times to detection for wells inoculated with individual spores were recorded using a Bioscreen C automated turbidity reader and were compatible with the data obtained microscopically. The distributions of times to events during germination and subsequent growth showed considerable variability, and all stages contributed to the overall variability in the lag time. The times for germination (t germ), emergence (t emerg − t germ), cell maturation (t C1 − t emerg), and doubling (t C2 − t C1) were not found to be correlated. Consequently, it was not possible to predict the total duration of the lag phase from information for just one of the stages, such as germination. As the variability in postgermination stages is relatively large, the first spore to germinate will not necessarily be the first spore to produce actively dividing cells and start neurotoxin production. This information can make a substantial contribution to improved predictive modeling and better quantitative microbiological risk assessment.


2020 ◽  
Vol 8 (1) ◽  
pp. 8-14
Author(s):  
Adel Rezayi ◽  
Vadood Razavilar ◽  
Zohreh Mashak ◽  
Amirali Anvar

Background: Considering the high fatality of botulism, the control of Clostridium botulinum and its neurotoxins has clinical importance. In this regard, using chemical preservatives, natural essential oils (Eos), and changes in the growth predisposing factors of bacteria are suitable methods to control the growth and toxin producing of C. botulinum in foods. Objective: The current survey was done to assess the effects of Citrus sinensis EO and intrinsic and extrinsic factors on the growth and toxin producing of C. botulinum type A. Materials and Methods: In this experiment with a factorial design, C. sinensis EO (0.0%, 0.015%, 0.03%, and 0.045%), nisin (0, 500, and 1500 IU/mL), nitrite (0, 20, and 60 ppm), pH (5.5 and 6.5), storage temperature (25 and 35° C), and sodium chloride (NaCl, 0.5% and 3%) were used to assess bacterial growth in the brain heart infusion medium. Finally, the mouse bioassay method was also used to assess toxicity. Results: Clostridium sinensis EO with a concentration of 0.045%, as well as the reduction of pH and temperature could significantly delay the growth of bacteria (P≤0.05) in contrast to the use of NaCl and nisin alone. However, all concentrations of sodium chloride (NaCl), nisin, and C. sinensis EO (< 0.045%) in interaction with each other, especially in combination with nitrite, showed good synergistic effects. Conclusion: These results suggested that using certain concentrations of C. sinensis EO and nisin, along with other suboptimal factors caused a significant decrease in the nitrite contents of foods with a significant reduction in the growth and toxin-producing ability of C. botulinum.


1998 ◽  
Vol 37 (4-5) ◽  
pp. 211-214 ◽  
Author(s):  
Linda K. Sawyer ◽  
Slawomir W. Hermanowicz

Growth and detachment rates of an environmental isolate of Aeromonas hydrophila attached to a surface were determined under varying nutrient supply conditions in a complex medium. Growth and detachment of cells were observed in real time using phase contrast microscopy in glass parallel plate flow chambers. Surface shear stress was controlled in all experiments at 3 N m−2. Images were taken every 15 min. Digital image analysis was used to determine specific growth and detachment rates. An observable parameter proportional to the nutrient depletion at the surface due to transfer limitations was used to indicate nutrient limitations. Specific detachment rates increased as the depletion parameter increased, indicating that nutrient limitations cause this bacterium to detach at greater rates.


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 440.1-441
Author(s):  
M. L. Peral ◽  
I. Calabuig ◽  
A. Martín-Carratalá ◽  
M. Andrés ◽  
E. Pascual

Background:Synovial fluid analysis using polarized microscopy is the gold standard for the diagnosis of crystal-related arthritis. In our experience, we have noted that, when calcium pyrophosphate (CPP) crystals are observed, they sometimes appear within intracellular vacuoles. However, this phenomenon is not seen in those samples containing monosodium urate (MSU) crystals. This finding has been scantly reported in the literature, but may be useful in clinical practice to ensure accurate crystal identification.Objectives:Our study aims to assess whether the presence of vacuoles contributes to identifying the type of crystal, and also to gauge the frequency of their presentation.Methods:We conducted an observational study in a rheumatology unit between February and June of 2019. Synovial fluids containing CPP or MSU crystals, obtained in daily clinical practice, were consecutively included for analysis. Two observers simultaneously analyzed the presence of vacuoles by ordinary light and phase contrast microscopy in less than 24 hours after their extraction, using a microscope equipped with two viewing stations. The primary study variable was to determine whether CPP and MSU crystals are seen inside intracellular vacuoles, and to calculate the frequency of this finding for each type of crystal, estimating their 95% confidence interval (95% CI) and comparing rates using Fisher’s exact test.Results:Twenty-one samples were obtained. Data is given in the Table. MSU crystals were present in 7 (33.3%) and CPP crystals in 14 (66.6%). Interestingly, none of the MSU samples showed crystal-containing vacuoles (95% CI 0-35.4%). On the contrary, cytoplasmic vacuoles containing crystals were present in all of the CPP samples (95% CI 78.5-100%). The findings were confirmed by phase-contrast microscopy. Differences were statistically significant (p<0.001).Table.SAMPLES ACCORDING TO TYPE OF MICROCRYSTAL(n=21)SAMPLES WITH VACUOLS(UNDER ORDINARY LIGHT)SAMPLES WITH VACUOLS(UNDER PHASE CONTRAST)CPP (14; 66.6%)14 (100%)(95%CI 78.5-100%)14 (100%)(95%CI 78.5-100%)MSU (7; 33.3%)0 (0%)(95%CI 0-35.4%)0 (0%)(95%CI 0-35.4%)Conclusion:The presence of vacuoles may be a useful and easy way to differentiate MSU and CPP crystals when performing synovial fluid microscopy in clinical practice, since it appears to be a distinctive feature in CPP crystal fluids.References:[1]Kohn NN, Hughes RE, McCarty DJ Jr, Faires JS. The significance of calcium phosphate crystals in the synovial fluid of arthritic patients: the «pseudogout syndrome». II. Identification of crystals. Ann InternMed. 1962 May;56:738-45.[2]Pascual E, Sivera F, Andrés M. Synovial Fluid Analysis for Crystals. CurrOpRheumatol 2011;23:161-169.[3]McCarty DJ, Koopman WJ. Arthritis and allied conditions: A textbook of rheumatology, volumen 1. Lea &amp;Febiger. 1993.[4]Pascual E, Sivera F. Synovial fluid crystal Analysis. En Gout and other crystal arthropathies. Terkeltaub R ed. Elsevier; 2012: p.20-34.[5]Hwang HS, Yang CM, Park SJ, Kim HA. Monosodium Urate Crystal-Induced Chondrocyte Death via Autophagic Process. Int J Mol Sci. 2015 Dec 8;16(12):29265-77.Image 1. Microscopy with ordinary light. Cells with cytoplasmic vacuoles are observed, as well as abundant intra and extracellular CPP crystals.Image 2. Microscopy with phase contrast technique. Cells with intracellular vacuoles are observed inside which have microcrystals with parallelepiped morphology, compatible with CPP.Disclosure of Interests: :None declared


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