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F型肉毒梭菌孢子暴露于亚致死剂量的γ射线对其生长和毒素产生的影响。

Effects on growth and toxin production of exposure of spores of Clostridium botulinum type F to sublethal doses of gamma irradiation.

作者信息

Williams-Walls N J

出版信息

Appl Microbiol. 1969 Jan;17(1):128-34. doi: 10.1128/am.17.1.128-134.1969.

Abstract

Spores of the Langeland strain of Clostridium botulinum type F were grown at 30 or 10 C after exposure to 0.0, 0.1, or 0.2 megarad of cesium-137 gamma irradiation. When incubated at 30 C, cultures irradiated at the 0.2-megarad level reached the stationary growth phase 15 hr earlier than the 0.0 or 0.1 megarad-irradiated cultures. This was not the result of earlier or more frequent germination of the irradiated spores, the formation of larger individual cells, filament formation, or cell clumping. It appeared to result from elimination of a lytic phenomenon noted in 0.0 and 0.1 megarad-irradiated cultures after 26 and 29 hr of incubation, respectively, which was followed by a second exponential-growth response 5 hr later in these cultures. The time of toxin appearance in culture supernatant fractions was independent of prior irradiation treatment and occurred after 36 hr of incubation. Toxin release was essentially logarithmic until maximal titers were reached and maximal toxin titers were higher in irradiated than in unirradiated cultures. The higher toxin level was sustained over a period of 23 days of 30 C. Toxin produced in the 30 C cultures could not be trypsin-activated. An incubation temperature of 10 C resulted in no outgrowth of spores subjected to 0.2 megarad of irradiation, although spore germination did occur. At 10 C, outgrowth of the 0.1-megarad culture was faster with slightly higher quantities of a more stable toxin than was seen in the unirradiated control. At 10 C, trypsinization was necessary to demonstrate the toxin present in the cultures.

摘要

将肉毒杆菌F型兰格兰德菌株的孢子在暴露于0.0、0.1或0.2兆拉德的铯-137γ射线照射后,于30℃或10℃下培养。当在30℃培养时,接受0.2兆拉德照射的培养物比接受0.0或0.1兆拉德照射的培养物提前15小时到达稳定生长期。这不是照射后孢子更早或更频繁萌发、形成更大的单个细胞、形成丝状或细胞聚集的结果。这似乎是由于消除了分别在培养26小时和29小时后在接受0.0和0.1兆拉德照射的培养物中观察到的一种溶解现象,随后这些培养物在5小时后出现第二次指数生长反应。培养上清液组分中毒素出现的时间与先前的照射处理无关,且在培养36小时后出现。毒素释放基本呈对数关系,直到达到最大滴度,且照射培养物中的最大毒素滴度高于未照射培养物。在30℃下,较高的毒素水平持续了23天。在30℃培养物中产生的毒素不能被胰蛋白酶激活。10℃的培养温度导致接受0.2兆拉德照射的孢子没有生长,尽管孢子确实发生了萌发。在10℃下,接受0.1兆拉德照射的培养物生长更快,产生的毒素量略高且更稳定,比未照射的对照培养物中的情况要好。在10℃下,需要用胰蛋白酶处理才能证明培养物中存在毒素。

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