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引用本文的文献

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Challenges of Diphtheria Toxin Detection.白喉毒素检测的挑战。
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2
Rapid, direct tissue culture test for toxigenicity of Corynebacterium diphtheriae.白喉棒状杆菌产毒性的快速直接组织培养检测
Appl Microbiol. 1973 May;25(5):709-12. doi: 10.1128/am.25.5.709-712.1973.
3
Diphtheria: a possible foodborne outbreak in Hodeida, Yemen Arab Republic.白喉:阿拉伯也门共和国荷台达可能发生的食源性疫情。
Bull World Health Organ. 1985;63(2):287-93.
4
Modified culture technique for Corynebacterium diphtheriae isolation from desiccated swabs.从干燥拭子中分离白喉棒状杆菌的改良培养技术。
J Clin Microbiol. 1978 Feb;7(2):137-8. doi: 10.1128/jcm.7.2.137-138.1978.
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Rapid determination of Corynebacterium diphtheriae toxigenicity by counterimmunoelectrophoresis.用对流免疫电泳快速检测白喉棒状杆菌产毒性
J Clin Microbiol. 1978 May;7(5):493-4. doi: 10.1128/jcm.7.5.493-494.1978.

本文引用的文献

1
The plate virulence test for diphtheria.白喉平板毒力试验
J Clin Pathol. 1949 Nov;2(4):250-8. doi: 10.1136/jcp.2.4.250.
2
Titration of diphtheria toxin, antitoxin and toxoid in tissue culture.组织培养中白喉毒素、抗毒素和类毒素的滴定
Acta Microbiol Acad Sci Hung. 1961;8:389-96.
3
[Diagnosis of diphtheria on tissue culture].
Ann Inst Pasteur (Paris). 1960 Aug;99:179-87.
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The effect of diphtheria toxin on the metabolism of HeLa cells.白喉毒素对海拉细胞代谢的影响。
J Exp Med. 1959 Feb 1;109(2):145-63. doi: 10.1084/jem.109.2.145.
5
Action of diphtheria toxin on cells cultivated in vitro.白喉毒素对体外培养细胞的作用。
Proc Soc Exp Biol Med. 1957 Aug-Sep;95(4):700-2. doi: 10.3181/00379727-95-23335.
6
[Contribution to the titration of diphtheria toxin-antitoxin on tissue cultures].
Arch Roum Pathol Exp Microbiol. 1964 Dec;23(4):1017-24.
7
Tissue culture method for the titration of diphtheria antitoxin in human sera.人体血清中白喉抗毒素滴定的组织培养方法。
Health Lab Sci. 1967 Jul;4(3):181-8.

白喉棒状杆菌产毒性检测的组织培养方法

Tissue culture method for toxigenicity testing of Corynebacterium diphtheriae.

作者信息

Schubert J H, Bickham S T, Wiggins G L

出版信息

Appl Microbiol. 1968 Nov;16(11):1748-52. doi: 10.1128/am.16.11.1748-1752.1968.

DOI:10.1128/am.16.11.1748-1752.1968
PMID:4973065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC547753/
Abstract

A method for toxigenicity testing of Corynebacterium diphtheriae in tissue cultures was developed. Results were obtained by comparing destruction of the monkey kidney or, preferably, rabbit kidney monolayer by 0.1 ml of the C. diphtheriae culture in Elek's broth containing 20% rabbit serum with the appearance after the addition of 0.2 ml of a mixture of the C. diphtheriae culture and diphtheria antitoxin. The mixture of C. diphtheriae broth culture and 10 antitoxin units per ml was incubated for 1 hr at room temperature before it was added to the tissue cultures which were then incubated as long as 5 days; most results, however, were read in 72 hr. Elek's broth medium was superior to heart infusion broth for toxin production by C. diphtheriae. Addition of 20% rabbit serum improved toxin production in either broth. Numerous toxigenic and atoxigenic C. diphtheriae cultures were tested for toxigenicity in primary rabbit and monkey kidney tissue cultures. If properly controlled, this in vitro method appeared to have an advantage over the in vitro agar gel method; its results were comparable with the rabbit intradermal test. With the wider use of tissue cultures in most laboratories, we believe that the tissue culture method for toxigenicity would be more economical and easier to perform than the animal intradermal method.

摘要

开发了一种在组织培养中对白喉棒状杆菌进行产毒试验的方法。通过比较含有20%兔血清的Elek肉汤中0.1 ml白喉棒状杆菌培养物对猴肾或更理想的兔肾单层细胞的破坏情况,与加入0.2 ml白喉棒状杆菌培养物和白喉抗毒素混合物后的外观来获得结果。白喉棒状杆菌肉汤培养物与每毫升10个抗毒素单位的混合物在室温下孵育1小时后再加入组织培养物中,然后孵育长达5天;然而,大多数结果在72小时读取。Elek肉汤培养基在白喉棒状杆菌产毒方面优于心脏浸液肉汤。在任何一种肉汤中添加20%兔血清均可提高产毒量。对大量产毒和无毒白喉棒状杆菌培养物在原代兔肾和猴肾组织培养中进行了产毒试验。如果得到适当控制,这种体外方法似乎比体外琼脂凝胶法具有优势;其结果与兔皮内试验相当。鉴于大多数实验室更广泛地使用组织培养,我们认为产毒的组织培养方法比动物皮内方法更经济且更易于操作。