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本文引用的文献

1
Pneumococcal pneumolysin and H(2)O(2) mediate brain cell apoptosis during meningitis.肺炎球菌溶血素和H₂O₂在脑膜炎期间介导脑细胞凋亡。
J Clin Invest. 2002 Jan;109(1):19-27. doi: 10.1172/JCI12035.
2
The roles of mucD and alginate in the virulence of Pseudomonas aeruginosa in plants, nematodes and mice.mucD和藻酸盐在铜绿假单胞菌对植物、线虫和小鼠的致病力中的作用。
Mol Microbiol. 2001 Sep;41(5):1063-76. doi: 10.1046/j.1365-2958.2001.02580.x.
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Genetic control of susceptibility to group A streptococcal infection in mice.小鼠对A组链球菌感染易感性的遗传控制
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A simple model host for identifying Gram-positive virulence factors.一种用于鉴定革兰氏阳性菌毒力因子的简单模式宿主。
Proc Natl Acad Sci U S A. 2001 Sep 11;98(19):10892-7. doi: 10.1073/pnas.191378698. Epub 2001 Sep 4.
5
H(2)O(2)-nonproducing Streptococcus pyogenes strains: survival in stationary phase and virulence in chronic granulomatous disease.不产生H(2)O(2)的化脓性链球菌菌株:在稳定期的存活及在慢性肉芽肿病中的毒力
Microbiology (Reading). 2001 Sep;147(Pt 9):2469-2477. doi: 10.1099/00221287-147-9-2469.
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Virulence of group A streptococci in fertile hens eggs is mainly effected by M protein and streptolysin O.
Int J Med Microbiol. 2001 Apr;291(1):45-56. doi: 10.1078/1438-4221-00102.
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Programmed cell death mediated by ced-3 and ced-4 protects Caenorhabditis elegans from Salmonella typhimurium-mediated killing.由ced-3和ced-4介导的程序性细胞死亡可保护秀丽隐杆线虫免受鼠伤寒沙门氏菌介导的杀伤。
Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2735-9. doi: 10.1073/pnas.041613098. Epub 2001 Feb 13.
8
A novel bacterial pathogen, Microbacterium nematophilum, induces morphological change in the nematode C. elegans.一种新型细菌病原体——嗜线虫微杆菌,可诱导秀丽隐杆线虫发生形态变化。
Curr Biol. 2000;10(24):1615-8. doi: 10.1016/s0960-9822(00)00867-8.
9
Caenorhabditis elegans is a model host for Salmonella typhimurium.秀丽隐杆线虫是鼠伤寒沙门氏菌的一种模式宿主。
Curr Biol. 2000 Nov 30;10(23):1543-5. doi: 10.1016/s0960-9822(00)00833-2.
10
Salmonella typhimurium proliferates and establishes a persistent infection in the intestine of Caenorhabditis elegans.鼠伤寒沙门氏菌在秀丽隐杆线虫的肠道中增殖并建立持续感染。
Curr Biol. 2000 Nov 30;10(23):1539-42. doi: 10.1016/s0960-9822(00)00830-7.

化脓性链球菌通过过氧化氢介导对线虫的杀伤作用

Hydrogen peroxide-mediated killing of Caenorhabditis elegans by Streptococcus pyogenes.

作者信息

Jansen W T M, Bolm M, Balling R, Chhatwal G S, Schnabel R

机构信息

GBF-National Research Center for Biotechnology, 38124 Braunschweig, Germany.

出版信息

Infect Immun. 2002 Sep;70(9):5202-7. doi: 10.1128/IAI.70.9.5202-5207.2002.

DOI:10.1128/IAI.70.9.5202-5207.2002
PMID:12183571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC128270/
Abstract

Caenorhabditis elegans is currently introduced as a new, facile, and cheap model organism to study the pathogenesis of gram-negative bacteria such as Pseudomonas aeruginosa and Salmonella enterica serovar Typhimurium. The mechanisms of killing involve either diffusible exotoxins or infection-like processes. Recently, it was shown that also some gram-positive bacteria kill C. elegans, although the precise mechanisms of killing remained open. We examined C. elegans as a pathogenesis model for the gram-positive bacterium Streptococcus pyogenes, a major human pathogen capable of causing a wide spectrum of diseases. We demonstrate that S. pyogenes kills C. elegans, both on solid and in liquid medium. Unlike P. aeruginosa and S. enterica serovar Typhimurium, the killing by S. pyogenes is solely mediated by hydrogen peroxide. Killing required live streptococci; the killing capacity depends on the amount of hydrogen peroxide produced, and killing can be inhibited by catalase. Major exotoxins of S. pyogenes are not involved in the killing process as confirmed by using specific toxin inhibitors and knockout mutants. Moreover, no accumulation of S. pyogenes in C. elegans is observed, which excludes the involvement of infection-like processes. Preliminary results show that S. pneumoniae can also kill C. elegans by hydrogen peroxide production. Hydrogen peroxide-mediated killing might represent a common mechanism by which gram-positive, catalase-negative pathogens kill C. elegans.

摘要

秀丽隐杆线虫目前被作为一种新型、简便且廉价的模式生物引入,用于研究铜绿假单胞菌和鼠伤寒沙门氏菌等革兰氏阴性菌的发病机制。杀伤机制涉及可扩散的外毒素或类似感染的过程。最近研究表明,一些革兰氏阳性菌也能杀死秀丽隐杆线虫,尽管确切的杀伤机制尚不清楚。我们研究了秀丽隐杆线虫作为酿脓链球菌发病机制的模型,酿脓链球菌是一种主要的人类病原体,能够引发多种疾病。我们证明,酿脓链球菌在固体和液体培养基中都能杀死秀丽隐杆线虫。与铜绿假单胞菌和鼠伤寒沙门氏菌不同,酿脓链球菌的杀伤作用完全由过氧化氢介导。杀伤需要活的链球菌;杀伤能力取决于产生的过氧化氢量,并且杀伤作用可被过氧化氢酶抑制。使用特异性毒素抑制剂和基因敲除突变体证实,酿脓链球菌的主要外毒素不参与杀伤过程。此外,未观察到酿脓链球菌在秀丽隐杆线虫中积累,这排除了类似感染过程的参与。初步结果表明,肺炎链球菌也可通过产生过氧化氢杀死秀丽隐杆线虫。过氧化氢介导的杀伤可能是革兰氏阳性、过氧化氢酶阴性病原体杀死秀丽隐杆线虫的一种常见机制。