1958
DOI: 10.3168/jds.s0022-0302(58)91072-5
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Factors Influencing Growth and Toxin Production in Cheese Inoculated with Spores of Clostridium Botulinum Types A and B. I. Studies with Surface-Ripened Cheese Type I

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Cited by 18 publications
(14 citation statements)
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“…botulinum type B proteolytic is well able to grow in the cheese spread used in this example. Considering the good safety record of processed cheese ( Wagenaar and Dack 1958; Collins‐Thompson and Wood 1993), it is assumed that prevalence is very low, but quantitative estimation of prevalence ( P e ) was not possible with the available information. For that reason, risk was estimated with P e ranging from 10 −20 to 1 ( Table 6, row 4).…”
Section: Resultsmentioning
confidence: 99%
“…botulinum type B proteolytic is well able to grow in the cheese spread used in this example. Considering the good safety record of processed cheese ( Wagenaar and Dack 1958; Collins‐Thompson and Wood 1993), it is assumed that prevalence is very low, but quantitative estimation of prevalence ( P e ) was not possible with the available information. For that reason, risk was estimated with P e ranging from 10 −20 to 1 ( Table 6, row 4).…”
Section: Resultsmentioning
confidence: 99%
“…However, they received 0.2% locust bean gum powder as stabilizer, a substance that is routinely added to many cheese products to prevent separation of brine water from the product. The addition of 0.2% locust bean gum had no effect on growth and toxin production of C. botulin~rn in experimental cheese preparations (Wagenaar and Dack, 1958).…”
Section: Methodsmentioning
confidence: 99%
“…Cheese preparations. Cheese preparations were made as described by Wagenaar and Dack (1958) from type I cheese, a soft surface-ripened cheese the flora of which was made up of bacteria and yeasts. Approximately 10% water was added to the cheese to yield a NaCl-brine concentration favorable to growth of C. botuli?tu~z in the basic product.…”
Section: Methodsmentioning
confidence: 99%
“…The viable count was based on heating the final dilutions in flowing steam for 15 min and on using a deep-tube counting procedure with 10 replicates per dilution. The counting medium consisted of 5% Trypticase (Baltimore Biological Laboratory, Baltimore, Maryland), 0.5% Peptone (Difco) and 1.5% Noble Agar (Difco) as adapted from Wagenaar and Dack (1958). Colony counts were made after approximately 40 h of incubation at 30°C.…”
Section: Preparation and Standardization Of Spore Suspensionmentioning
confidence: 99%