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一种高效的流产布鲁氏菌2308Δery活疫苗可区分自然感染和疫苗接种感染。

A potent Brucella abortus 2308 Δery live vaccine allows for the differentiation between natural and vaccinated infection.

作者信息

Zhang Junbo, Yin Shuanghong, Guo Fei, Meng Ren, Chen Chuangfu, Zhang Hui, Li Zhiqiang, Fu Qiang, Shi Huijun, Hu Shengwei, Ni Wei, Li Tiansen, Zhang Ke

机构信息

College of Animal Science and Technology, Shihezi University, Shihezi, 832003, P. R. China.

出版信息

J Microbiol. 2014 Aug;52(8):681-8. doi: 10.1007/s12275-014-3689-9. Epub 2014 Jul 4.

DOI:10.1007/s12275-014-3689-9
PMID:24994009
Abstract

Brucellosis is a globally distributed zoonotic disease that causes animal and human diseases. However, the current Brucella abortus vaccines (S19 and RB51) are deficient; they can cause abortion in pregnant animals. Moreover, when the vaccine S19 is used, tests cannot differentiate natural from vaccinated infection. Therefore, a safer and more potent vaccine is needed. A Brucella abortus 2308 ery promoter mutant (Δery) was constructed to overcome these drawbacks. The growth of the Δery mutant was significantly attenuated in macrophages and mice and induced high protective immunity in mice. Moreover, Δery induced an anti-Brucella-specific IgG (immunoglobulin G) response and stimulated the expression of interferon-gamma (INF-γ) and interleukin-4 (IL-4). Furthermore, the expression of EryA antigen allowed for the serological differentiation between natural and vaccinated infection in mice. These results indicate that the Δery mutant is a potential attenuated live vaccine candidate against virulent Brucella abortus 2308 (S2308) infection.

摘要

布鲁氏菌病是一种全球分布的人畜共患病,可导致动物和人类发病。然而,目前的牛布鲁氏菌疫苗(S19和RB51)存在缺陷;它们可导致怀孕动物流产。此外,使用疫苗S19时,检测无法区分自然感染和疫苗接种感染。因此,需要一种更安全、效力更强的疫苗。构建了牛布鲁氏菌2308 ery启动子突变体(Δery)以克服这些缺点。Δery突变体在巨噬细胞和小鼠中的生长显著减弱,并在小鼠中诱导了高度的保护性免疫。此外,Δery诱导了抗布鲁氏菌特异性IgG(免疫球蛋白G)反应,并刺激了干扰素-γ(INF-γ)和白细胞介素-4(IL-4)的表达。此外,EryA抗原的表达使得能够在小鼠中区分自然感染和疫苗接种感染。这些结果表明,Δery突变体是一种潜在的减毒活疫苗候选物,可用于预防强毒牛布鲁氏菌2308(S2308)感染。

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A potent Brucella abortus 2308 Δery live vaccine allows for the differentiation between natural and vaccinated infection.一种高效的流产布鲁氏菌2308Δery活疫苗可区分自然感染和疫苗接种感染。
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Intradermal immunization with outer membrane protein 25 protects Balb/c mice from virulent B. abortus 544.经皮免疫外膜蛋白 25 可保护 Balb/c 小鼠免受强毒 B. abortus 544 的侵害。
Mol Immunol. 2012 Jun;51(2):159-68. doi: 10.1016/j.molimm.2012.02.126. Epub 2012 Mar 30.
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Expression of the soybean allergenic protein P34 in Escherichia coli and its indirect ELISA detection method.大豆过敏原蛋白 P34 在大肠杆菌中的表达及其间接 ELISA 检测方法。
Appl Microbiol Biotechnol. 2012 Jun;94(5):1337-45. doi: 10.1007/s00253-012-4006-3. Epub 2012 Mar 25.
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The 16MΔvjbR as an ideal live attenuated vaccine candidate for differentiation between Brucella vaccination and infection.
布鲁氏菌病疫苗评估:全面综述
Front Vet Sci. 2022 Jul 18;9:925773. doi: 10.3389/fvets.2022.925773. eCollection 2022.
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Meta-Analysis and Advancement of Brucellosis Vaccinology.布鲁氏菌病疫苗学的Meta分析与进展
PLoS One. 2016 Nov 15;11(11):e0166582. doi: 10.1371/journal.pone.0166582. eCollection 2016.
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Expression and regulation of the operon of in human trophoblast cells.人滋养层细胞中[具体物质]操纵子的表达与调控 。 (你原文中“of the operon of in”这里第二个“of”后面应该少了具体内容,我按照正常翻译逻辑补充了“[具体物质]”,你可根据实际情况修改)
Exp Ther Med. 2016 Oct;12(4):2723-2728. doi: 10.3892/etm.2016.3688. Epub 2016 Sep 8.
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Protection efficacy of the Brucella abortus ghost vaccine candidate lysed by the N-terminal 24-amino acid fragment (GI24) of the 36-amino acid peptide PMAP-36 (porcine myeloid antimicrobial peptide 36) in murine models.在小鼠模型中,由36个氨基酸的肽PMAP - 36(猪髓样抗菌肽36)的N端24个氨基酸片段(GI24)裂解的布鲁氏菌流产株候选菌苗的保护效力。
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The Brucella melitensis M5-90 phosphoglucomutase (PGM) mutant is attenuated and confers protection against wild-type challenge in BALB/c mice.布鲁氏菌M5-90磷酸葡萄糖变位酶(PGM)突变体在BALB/c小鼠中减毒,并能提供针对野生型攻击的保护作用。
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Inactivation of formyltransferase (wbkC) gene generates a Brucella abortus rough strain that is attenuated in macrophages and in mice.缺失形式转移酶(wbkC)基因可使布鲁氏菌粗糙型菌株丧失活力,该突变株在巨噬细胞和小鼠中减毒。
Vaccine. 2010 Aug 2;28(34):5627-34. doi: 10.1016/j.vaccine.2010.06.023. Epub 2010 Jun 19.
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J Clin Microbiol. 2009 Jul;47(7):2084-9. doi: 10.1128/JCM.02159-08. Epub 2009 May 6.
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