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本文引用的文献

1
Pertussis control: time for something new?百日咳控制:是时候采取新措施了?
Trends Microbiol. 2012 May;20(5):211-3. doi: 10.1016/j.tim.2012.03.003. Epub 2012 Apr 9.
2
Unexpectedly limited durability of immunity following acellular pertussis vaccination in preadolescents in a North American outbreak.在北美的一次疫情中,未预料到的是,亚单位百日咳疫苗在青春期前儿童中的免疫持久性有限。
Clin Infect Dis. 2012 Jun;54(12):1730-5. doi: 10.1093/cid/cis287. Epub 2012 Mar 15.
3
Pertussis vaccines: where to now?百日咳疫苗:何去何从?
Expert Rev Vaccines. 2011 Nov;10(11):1497-500. doi: 10.1586/erv.11.147.
4
Laboratory adaptation of Bordetella pertussis is associated with the loss of type three secretion system functionality.实验室适应的百日咳博德特氏菌与 III 型分泌系统功能丧失有关。
Infect Immun. 2011 Sep;79(9):3677-82. doi: 10.1128/IAI.00136-11. Epub 2011 Jul 5.
5
Differential expression of type III effector BteA protein due to IS481 insertion in Bordetella pertussis.由于 IS481 的插入,百日咳博德特氏菌中 III 型效应子 BteA 蛋白的差异表达。
PLoS One. 2011 Mar 10;6(3):e17797. doi: 10.1371/journal.pone.0017797.
6
What to do and what not to do in serological diagnosis of pertussis: recommendations from EU reference laboratories.在百日咳血清学诊断中应该做什么和不应该做什么:欧盟参考实验室的建议。
Eur J Clin Microbiol Infect Dis. 2011 Mar;30(3):307-12. doi: 10.1007/s10096-010-1104-y. Epub 2010 Nov 11.
7
The present and future control of pertussis.百日咳的当前及未来防控
Clin Infect Dis. 2010 Sep 15;51(6):663-7. doi: 10.1086/655826.
8
The epidemiology of pertussis in Germany: past and present.德国百日咳的流行病学:过去与现在。
BMC Infect Dis. 2009 Feb 25;9:22. doi: 10.1186/1471-2334-9-22.
9
Virulence factor secretion and translocation by Bordetella species.博德特氏菌属细菌的毒力因子分泌与转运
Curr Opin Microbiol. 2009 Feb;12(1):88-93. doi: 10.1016/j.mib.2009.01.001. Epub 2009 Jan 29.
10
Bordetella Bsp22 forms a filamentous type III secretion system tip complex and is immunoprotective in vitro and in vivo.博德特氏菌Bsp22形成丝状III型分泌系统顶端复合物,在体外和体内均具有免疫保护作用。
Mol Microbiol. 2009 Jan;71(2):492-504. doi: 10.1111/j.1365-2958.2008.06543.x. Epub 2008 Dec 5.

百日咳博德特氏菌 III 型分泌系统尖端复合蛋白 Bsp22 不是保护性抗原,并且在人类和小鼠感染期间不能引起血清抗体反应。

The Bordetella pertussis type III secretion system tip complex protein Bsp22 is not a protective antigen and fails to elicit serum antibody responses during infection of humans and mice.

机构信息

Institute of Microbiology of the ASCR, Prague, Czech Republic.

出版信息

Infect Immun. 2013 Aug;81(8):2761-7. doi: 10.1128/IAI.00353-13. Epub 2013 May 20.

DOI:10.1128/IAI.00353-13
PMID:23690400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719584/
Abstract

The type III secretion system (T3SS) of pathogenic bordetellae employs a self-associating tip complex protein Bsp22. This protein is immunogenic during infections by Bordetella bronchiseptica and could be used as a protective antigen to immunize mice against B. bronchiseptica challenge. Since low-passage clinical isolates of the human pathogen Bordetella pertussis produce a highly homologous Bsp22 protein (97% homology), we examined its vaccine and diagnostic potential. No Bsp22-specific antibodies were, however, detected in serum samples from 36 patients with clinically and serologically confirmed whooping cough disease (pertussis syndrome). Moreover, although the induction of Bsp22 secretion by the laboratory-adapted 18323 strain in the course of mice lung infection was observed, the B. pertussis 18323-infected mice did not mount any detectable serum antibody response against Bsp22. Furthermore, immunization with recombinant Bsp22 protein yielded induction of high Bsp22-specific serum antibody titers but did not protect mice against an intranasal challenge with B. pertussis 18323. Unlike for B. bronchiseptica, hence, the Bsp22 protein is nonimmunogenic, and/or the serum antibody response to it is suppressed, during B. pertussis infections of humans and mice.

摘要

病原菌博德特氏菌的 III 型分泌系统(T3SS)使用一种自聚集尖端复合蛋白 Bsp22。该蛋白在支气管败血博德特氏菌感染期间具有免疫原性,可用作保护性抗原,以免疫小鼠抵抗博德特氏菌的攻击。由于人类病原体百日咳博德特氏菌的低传代临床分离株产生高度同源的 Bsp22 蛋白(97%同源性),我们研究了其疫苗和诊断潜力。然而,在 36 名经临床和血清学证实患有百日咳病(百日咳综合征)的患者的血清样本中,未检测到针对 Bsp22 的特异性抗体。此外,尽管在小鼠肺部感染过程中观察到实验室适应的 18323 株诱导 Bsp22 分泌,但感染百日咳博德特氏菌 18323 的小鼠未针对 Bsp22 产生任何可检测到的血清抗体反应。此外,用重组 Bsp22 蛋白免疫产生了高 Bsp22 特异性血清抗体滴度,但不能保护小鼠免受鼻内百日咳博德特氏菌 18323 的攻击。因此,与博德特氏菌支气管败血亚种不同,Bsp22 蛋白在人类和小鼠的百日咳感染期间是非免疫原性的,和/或针对它的血清抗体反应受到抑制。