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本文引用的文献

1
Development of a toxA gene knock-out mutant of Pasteurella multocida and evaluation of its protective effects.多杀性巴氏杆菌toxA基因敲除突变株的构建及其保护效果评估
J Microbiol. 2006 Jun;44(3):320-6.
2
Immunogenicity and efficacy of three recombinant subunit Pasteurella multocida toxin vaccines against progressive atrophic rhinitis in pigs.三种重组亚单位多杀性巴氏杆菌毒素疫苗对猪进行性萎缩性鼻炎的免疫原性和效力
Vaccine. 2006 Jan 9;24(1):27-35. doi: 10.1016/j.vaccine.2005.07.079. Epub 2005 Aug 9.
3
Efficacy of vaccination of calves against hemorrhagic septicemia with a live aroA derivative of Pasteurella multocida B:2 by two different routes of administration.用多杀性巴氏杆菌B:2的aroA基因活衍生物通过两种不同给药途径对犊牛进行出血性败血症疫苗接种的效果。
Infect Immun. 2005 Mar;73(3):1475-81. doi: 10.1128/IAI.73.3.1475-1481.2005.
4
Development of a genetically modified nontoxigenic Pasteurella multocida toxin as a candidate for use in vaccines against progressive atrophic rhinitis in pigs.开发一种基因改造的无毒多杀性巴氏杆菌毒素,作为猪进行性萎缩性鼻炎疫苗的候选物。
Am J Vet Res. 2005 Jan;66(1):113-8. doi: 10.2460/ajvr.2005.66.113.
5
The Pasteurella multocida toxin is encoded within a lysogenic bacteriophage.多杀巴斯德氏菌毒素由一种溶原性噬菌体编码。
Mol Microbiol. 2004 Jan;51(1):255-69. doi: 10.1046/j.1365-2958.2003.03829.x.
6
Expression of a truncated Pasteurella multocida toxin antigen in Bordetella bronchiseptica.截短的多杀性巴氏杆菌毒素抗原在支气管败血波氏杆菌中的表达。
Vet Microbiol. 2003 Jul 30;94(4):313-23. doi: 10.1016/s0378-1135(03)00137-8.
7
Localization of functional domains of the mitogenic toxin of Pasteurella multocida.多杀性巴氏杆菌促有丝分裂毒素功能域的定位
Infect Immun. 2001 Dec;69(12):7839-50. doi: 10.1128/IAI.69.12.7839-7850.2001.
8
Biological activity of a C-terminal fragment of Pasteurella multocida toxin.多杀巴斯德菌毒素C端片段的生物活性
Infect Immun. 2001 Jun;69(6):3628-34. doi: 10.1128/IAI.69.6.3628-3634.2001.
9
Antibody reactions after aerogenous or subcutaneous immunization of pigs with Pasteurella multocida antigens.
Vaccine. 2000 Nov 22;19(7-8):751-7. doi: 10.1016/s0264-410x(00)00263-2.
10
The molecular biology of pasteurella multocida.多杀巴斯德菌的分子生物学
Vet Microbiol. 2000 Mar 1;72(1-2):3-25. doi: 10.1016/s0378-1135(99)00183-2.

多杀性巴氏杆菌毒素4个截短片段的表达及其免疫原性。

Expression of 4 truncated fragments of Pasteurella multocida toxin and their immunogenicity.

作者信息

Seo Jayoung, Pyo Hyoju, Lee Semi, Lee Jaeil, Kim Taejung

机构信息

Biotherapy Human Resources Center, College of Veterinary Medicine, Chonnam National University, Gwangju, Republic of Korea.

出版信息

Can J Vet Res. 2009 Jul;73(3):184-9.

PMID:19794890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2705072/
Abstract

Pasteurella multocida toxin (PMT) is a poor antigen that becomes more immunogenic after its native structure has been destroyed. In contrast, partially truncated PMT proteins, which are predicted to be good antigens when used as a vaccine, might be used to improve the control of atrophic rhinitis in pigs. In this study, 4 truncated PMT fragments were expressed in Escherichia coli, and those 4 fragments were inoculated into mice to produce the polyclonal antibodies. The results of an enzyme-linked immunosorbent assay (ELISA) revealed that #1 and #4 fragments were the most immunogenic. Immunized mice were subsequently challenged intraperitoneally with P. multocida type D. Five of the eight #1 fragment-immunized mice showed some protection against death and bacterial clearance. Pigs immunized with #1 fragment produced no or mild atrophic rhinitis (turbinate conchal score) after challenge, suggesting that this #1 fragment could be a good candidate for a subunit recombinant-type vaccine.

摘要

多杀性巴氏杆菌毒素(PMT)是一种较差的抗原,在其天然结构被破坏后免疫原性会增强。相比之下,部分截短的PMT蛋白在用作疫苗时预计是良好的抗原,可能用于改善猪萎缩性鼻炎的防控。在本研究中,4个截短的PMT片段在大肠杆菌中表达,并将这4个片段接种到小鼠体内以产生多克隆抗体。酶联免疫吸附测定(ELISA)结果显示,#1和#4片段免疫原性最强。随后,用D型多杀性巴氏杆菌对免疫的小鼠进行腹腔攻毒。在8只接种#1片段的小鼠中,有5只表现出对死亡和细菌清除的一定保护作用。用#1片段免疫的猪在攻毒后未出现或仅出现轻度萎缩性鼻炎(鼻甲贝壳状评分),表明该#1片段可能是亚单位重组型疫苗的良好候选物。