From Cecilie, Pukall Rudiger, Schumann Peter, Hormazábal Víctor, Granum Per Einar
Department of Food Safety and Infection Biology, Norwegian School of Veterinary Science, PO Box 8146, Dep, NO-0033 Oslo, Norway.
Appl Environ Microbiol. 2005 Mar;71(3):1178-83. doi: 10.1128/AEM.71.3.1178-1183.2005.
A total of 333 Bacillus spp. isolated from foods, water, and food plants were examined for the production of possible enterotoxins and emetic toxins using a cytotoxicity assay on Vero cells, the boar spermatozoa motility assay, and a liquid chromatography-mass spectrometry method. Eight strains produced detectable toxins; six strains were cytotoxic, three strains produced putative emetic toxins (different in size from cereulide), and one strain produced both cytotoxin(s) and putative emetic toxin(s). The toxin-producing strains could be assigned to four different species, B. subtilis, B. mojavensis, B. pumilus, or B. fusiformis, by using a polyphasic approach including biochemical, chemotaxonomic, and DNA-based analyses. Four of the strains produced cytotoxins that were concentrated by ammonium sulfate followed by dialysis, and two strains produced cytotoxins that were not concentrated by such a treatment. Two cultures maintained full cytotoxic activity, two cultures reduced their activity, and two cultures lost their activity after boiling. The two most cytotoxic strains (both B. mojavensis) were tested for toxin production at different temperatures. One of these strains produced cytotoxin at growth temperatures ranging from 25 to 42 degrees C, and no reduction in activity was observed even after 24 h of growth at 42 degrees C. The strains that produced putative emetic toxins were tested for the influence of time and temperature on the toxin production. It was shown that they produced putative emetic toxin faster or just as fast at 30 as at 22 degrees C. None of the cytotoxic strains produced B. cereus-like enterotoxins as tested by PCR or by immunological methods.
共对从食品、水和食用植物中分离出的333株芽孢杆菌属菌株进行了检测,采用Vero细胞毒性试验、公猪精子活力试验和液相色谱-质谱法检测其是否产生可能的肠毒素和呕吐毒素。8株菌株产生了可检测到的毒素;6株具有细胞毒性,3株产生假定的呕吐毒素(大小与蜡样芽胞杆菌溶血素不同),1株同时产生细胞毒素和假定的呕吐毒素。通过包括生化、化学分类和基于DNA分析的多相方法,产毒菌株可分为4个不同的种,即枯草芽孢杆菌、莫哈韦芽孢杆菌、短小芽孢杆菌或梭状芽孢杆菌。其中4株产生的细胞毒素经硫酸铵浓缩后再透析,2株产生的细胞毒素未经此种处理浓缩。两种培养物保持了完全的细胞毒性活性,两种培养物活性降低,两种培养物煮沸后失去活性。对毒性最强的两株菌株(均为莫哈韦芽孢杆菌)在不同温度下进行了产毒测试。其中一株在25至42摄氏度的生长温度下产生细胞毒素,即使在42摄氏度下生长24小时后,活性也未降低。对产生假定呕吐毒素的菌株进行了时间和温度对产毒影响的测试。结果表明,它们在30摄氏度下产生假定呕吐毒素的速度与在22摄氏度下一样快或更快。通过PCR或免疫方法检测,所有细胞毒性菌株均未产生蜡样芽孢杆菌样肠毒素。