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Infect Immun. 1977 Mar;15(3):704-12. doi: 10.1128/iai.15.3.704-712.1977.
2
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本文引用的文献

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Experimental cholera in infant rabbits: a method for chemotherapeutic investigation.幼兔实验性霍乱:一种化疗研究方法。
Br J Pharmacol Chemother. 1955 Jun;10(2):153-9. doi: 10.1111/j.1476-5381.1955.tb00074.x.
2
PATHOGENESIS EXPERIMENTAL CHOLERA IN INFANT RABBITS. I. OBSERVATIONS ON THE INTRAINTESTINAL INFECTION AND EXPERIMENTAL CHOLERA PRODUCED WITH CELL-FREE PRODUCTS.幼兔实验性霍乱的发病机制。I. 关于无细胞产物引起的肠道内感染及实验性霍乱的观察
J Infect Dis. 1964 Jun;114:203-16. doi: 10.1093/infdis/114.3.203.
3
Vibrio cholerae infection in the embryonated egg.鸡胚中的霍乱弧菌感染。
J Infect Dis. 1963 May-Jun;112:264-72. doi: 10.1093/infdis/112.3.264.
4
Role of cholera a toxin in experimental cholera.霍乱毒素在实验性霍乱中的作用。
J Bacteriol. 1959 Oct;78(4):594-5. doi: 10.1128/jb.78.4.594-595.1959.
5
Enterotoxicity of bacteria-free culture-filtrate of Vibrio cholerae.霍乱弧菌无细胞培养滤液的肠毒性
Nature. 1959 May 30;183(4674):1533-4. doi: 10.1038/1831533a0.
6
An experimental study of the mechanism of action of Vibriod cholerae on the intestinal mucous membrane.霍乱弧菌对肠黏膜作用机制的实验研究
J Pathol Bacteriol. 1953 Oct;66(2):559-62. doi: 10.1002/path.1700660228.
7
Experimental cholera in humans.人类实验性霍乱
Br Med J. 1966 Jan 15;1(5480):140-2. doi: 10.1136/bmj.1.5480.140.
8
A permeability factor (toxin) found in cholera stools and culture filtrates and its neutralization by convalescent cholera sera.在霍乱粪便和培养滤液中发现的一种通透因子(毒素)及其被霍乱恢复期血清中和的情况。
Nature. 1965 Aug 7;207(997):614-6. doi: 10.1038/207614a0.
9
Experimental canine cholera. II. Production by cell-free culture filtrates of Vibrio cholerae.实验性犬霍乱。II. 霍乱弧菌无细胞培养滤液所致感染
J Infect Dis. 1969 Feb;119(2):150-7. doi: 10.1093/infdis/119.2.150.
10
Experimental canine cholera. I. Development of the model.实验性犬霍乱。I. 模型的建立。
J Infect Dis. 1969 Feb;119(2):138-49. doi: 10.1093/infdis/119.2.138.

用霍乱弧菌或霍乱毒素对幼鼠进行口服激发诱导肠液积聚。

Intestinal fluid accumulation induced by oral challenge with Vibrio cholerae or cholera toxin in infant mice.

作者信息

Baselski V, Briggs R, Parker C

出版信息

Infect Immun. 1977 Mar;15(3):704-12. doi: 10.1128/iai.15.3.704-712.1977.

DOI:10.1128/iai.15.3.704-712.1977
PMID:870427
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC421427/
Abstract

The diarrheal response of orally inoculated infant mice to viable Vibrio cholerae and purified cholera toxin was quantitated by means of a fluid accumulation (FA) ratio. The FA ratio is defined as the gut weight/remaining body weight. FA ratios were determined in relation to time of exposure and dose. Onset of fluid accumulation with viable cells of strains CA401 and 569B occurred 8 h postinoculation and reached a near maximum of 16 h. A dose of 4 x 10(6) colony-forming units of strain CA401 was required for a positive response 16 to 18 h postinoculation. Several other classical cholera strains demonstrated a similar dose-related response. Strain 569B, however, required a 100-fold higher dose to give a positive response. Several mutant cholera strains were decreased virulence in other model systems elicited FA ratios decreased from wild-type values. Onset of fluid accumulation which cholera toxin occurred 6 to 8 h postinoculation and reached a maximum by 10 h. A dose of 0.5 microng was required for a positive response 10 to 12 h postinoculation. The positive response to toxin could be inhibited by preincubation with specific antitoxin.

摘要

通过液体蓄积(FA)比值对口服接种的幼鼠对活霍乱弧菌和纯化霍乱毒素的腹泻反应进行定量。FA比值定义为肠道重量与剩余体重之比。根据暴露时间和剂量确定FA比值。CA401和569B菌株的活细胞在接种后8小时开始出现液体蓄积,并在16小时达到接近最大值。接种后16至18小时出现阳性反应需要4×10⁶个CA401菌株的菌落形成单位剂量。其他几种经典霍乱菌株表现出类似的剂量相关反应。然而,569B菌株需要高100倍的剂量才能产生阳性反应。在其他模型系统中,几种突变霍乱菌株的毒力降低,其引起的FA比值从野生型值下降。霍乱毒素引起的液体蓄积在接种后6至8小时开始,并在10小时达到最大值。接种后10至12小时出现阳性反应需要0.5微克剂量。毒素的阳性反应可通过与特异性抗毒素预孵育来抑制。