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培养条件对丝裂霉素C介导的噬菌体诱导及沙门氏菌毒素释放的影响

Influence of cultural conditions on mitomycin C-mediated bacteriophage induction and release of Salmonella toxin.

作者信息

Peterson J W, Houston C W, Koo F C

出版信息

Infect Immun. 1981 Apr;32(1):232-42. doi: 10.1128/iai.32.1.232-242.1981.

Abstract

Several isolates of Salmonella were examined for the capacity to synthesize and release a cholera toxin-like toxin that exerted a biological effect on Chinese hamster ovary cells. Measurements of this Salmonella toxin, which was contained in cell sonic extracts and culture filtrates, were expressed in cholera toxin equivalents (nanograms), since the Chinese hamster ovary cell responses of the cholera toxin and the Salmonella toxin were indistinguishable. Comparative titrations of Salmonella preparations were also performed by using an enzyme-linked immunosorbent assay specific for cholera toxin antigen. The amount of Salmonella toxin synthesized was low (nanogram levels), but the toxin was detectable in cell sonic extracts as early as 6 h after culture inoculation and reached maximal levels by 12 h. Salmonella toxin antigen was not detectable in control culture filtrates until 48 h, but the addition of mitomycin C at 8.5 h resulted in the sudden appearance of toxin antigen at 10 to 12 h, and the toxin antigen level reached a maximum at 14 h. A large peak of Chinese hamster ovary cell activity was observed at 48 h in the control culture, but significant Chinese hamster ovary cell activity was detected as early as 14 h. A larger amount of Chinese hamster ovary cell-reactive material was observed as early as 10 h in cultures grown with mitomycin C. The mechanism of the mitomycin-mediated phenomenon that yielded more toxin in culture filtrates was associated with bacteriophage induction. A bacteriophage plaque assay with a susceptible Salmonella strain revealed that there were free bacteriophage in mitomycin-treated culture filtrates (but not control culture filtrates) at 12 h. Toxin production was greatest when cultures were grown at 30 to 37 degrees C and lowest when cultures were grown at 25 degrees C. The inoculum size and degree of culture aeration (agitation) had little effect on synthesis of the toxin, and toxin production occurred during anaerobic growth.

摘要

对几种沙门氏菌分离株进行了检测,以确定其合成并释放一种霍乱毒素样毒素的能力,该毒素对中国仓鼠卵巢细胞具有生物学效应。由于霍乱毒素和沙门氏菌毒素对中国仓鼠卵巢细胞的反应无法区分,因此对细胞超声提取物和培养滤液中所含的这种沙门氏菌毒素的测量结果以霍乱毒素当量(纳克)表示。还使用针对霍乱毒素抗原的酶联免疫吸附测定法对沙门氏菌制剂进行了比较滴定。沙门氏菌毒素的合成量较低(纳克水平),但在培养接种后6小时,细胞超声提取物中即可检测到该毒素,到12小时达到最高水平。对照培养滤液中直到48小时才检测到沙门氏菌毒素抗原,但在8.5小时添加丝裂霉素C后,毒素抗原在10至12小时突然出现,毒素抗原水平在14小时达到最大值。在对照培养中,48小时观察到中国仓鼠卵巢细胞活性出现一个大峰值,但早在14小时就检测到了显著的中国仓鼠卵巢细胞活性。在用丝裂霉素C培养的培养物中,早在10小时就观察到了更多的中国仓鼠卵巢细胞反应性物质。丝裂霉素介导的现象导致培养滤液中产生更多毒素的机制与噬菌体诱导有关。对一株敏感沙门氏菌菌株进行的噬菌体噬斑测定表明,在12小时时,丝裂霉素处理的培养滤液(而非对照培养滤液)中有游离噬菌体。当培养物在30至37摄氏度下生长时,毒素产生量最大,而在25摄氏度下生长时,毒素产生量最低。接种量和培养通气程度(搅拌)对毒素合成影响不大,并且在厌氧生长期间会产生毒素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cc3/350612/08244d807750/iai00162-0247-a.jpg

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