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一种用于食品中金黄色葡萄球菌计数的改良猪血浆琼脂。

A modified pork plasma agar for the enumeration of Staphylococcus aureus in foods.

作者信息

Hauschild A H, Park C E, Hilsheimer R

出版信息

Can J Microbiol. 1979 Sep;25(9):1052-7. doi: 10.1139/m79-161.

Abstract

The coagulase reaction of Staphylococcus aureus on the PPSA (pork plasma for S. aureus) agar of Devoyod et al. was found to be fibrinogen-deficient. By including bovine fibrinogen (BFG) in the medium, the fibrin halos around S. aureus colonies became more distinct, preparations of pork plasma previously unacceptable for inclusion in the original PPSA agar were performing well, and the amount of pork plasma required in PPSA agar could be reduced by nearly 90%. In the modified medium, designated PPF (pork plasma fibrinogen) agar, the agar base (Baird-Parker agar without egg yolk) was unchanged. After surface plating, the base was covered with 8 mL of a modified overpour agar: 2.5% pork plasma, 0.38% BFG, and 0.0015% soy trypsin inhibitor in 0.7% Bacto agar. Most S. aureus strains could be enumerated after 24 h of incubation at 35 degrees C; the others required 44 h. Without soy trypsin inhibitor, a number of strains showed considerable fibrinolysis between 24 and 44 h of growth; this activity was neutralized by the inhibitor. The S. aureus counts of 27 food samples on PPF agar were essentially the same as the confirmed S. aureus counts obtained by the Baird-Parker method.

摘要

发现金黄色葡萄球菌在德沃约德等人的PPSA(用于金黄色葡萄球菌的猪肉血浆)琼脂上的凝固酶反应缺乏纤维蛋白原。通过在培养基中加入牛纤维蛋白原(BFG),金黄色葡萄球菌菌落周围的纤维蛋白光环变得更加明显,以前不能用于原始PPSA琼脂的猪肉血浆制剂表现良好,并且PPSA琼脂中所需的猪肉血浆量可减少近90%。在改良培养基(称为PPF(猪肉血浆纤维蛋白原)琼脂)中,琼脂基础(不含蛋黄的贝尔德-帕克琼脂)保持不变。表面接种后,在基础上覆盖8 mL改良的倾注上层琼脂:2.5%猪肉血浆、0.38%BFG和0.0015%大豆胰蛋白酶抑制剂于0.7%细菌琼脂中。大多数金黄色葡萄球菌菌株在35℃培养24小时后可计数;其他菌株需要44小时。如果没有大豆胰蛋白酶抑制剂,一些菌株在生长24至44小时之间表现出相当程度的纤维蛋白溶解;这种活性被抑制剂中和。PPF琼脂上27份食品样品的金黄色葡萄球菌计数与通过贝尔德-帕克方法获得的确认金黄色葡萄球菌计数基本相同。

相似文献

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Enumeration of vital and thermally stressed Staphylococcus aureus in foods using Baird-Parker pig plasma agar (BPP).
J Appl Bacteriol. 1980 Feb;48(1):101-13. doi: 10.1111/j.1365-2672.1980.tb05212.x.

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