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Infect Immun. 1994 Aug;62(8):3206-12. doi: 10.1128/iai.62.8.3206-3212.1994.
2
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3
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4
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5
Comparison of immune responses and resistance to brucellosis in mice vaccinated with Brucella abortus 19 or RB51.用流产布鲁氏菌19株或RB51株接种的小鼠对布鲁氏菌病的免疫反应和抵抗力比较。
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6
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Booster vaccination with safe, modified, live-attenuated mutants of Brucella abortus strain RB51 vaccine confers protective immunity against virulent strains of B. abortus and Brucella canis in BALB/c mice.用安全的、经过改造的流产布鲁氏菌RB51疫苗减毒活突变体进行加强免疫,可使BALB/c小鼠对流产布鲁氏菌和犬布鲁氏菌的强毒株产生保护性免疫。
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Evaluation of serologic responses, lymphocyte proliferative responses, and clearance from lymphatic organs after vaccination of bison with Brucella abortus strain RB51.用布鲁氏菌流产菌株RB51对野牛进行疫苗接种后,对血清学反应、淋巴细胞增殖反应以及从淋巴器官清除情况的评估。
Am J Vet Res. 1998 Apr;59(4):410-5.
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PLoS One. 2015 Sep 9;10(9):e0136696. doi: 10.1371/journal.pone.0136696. eCollection 2015.
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In situ microscopy analysis reveals local innate immune response developed around Brucella infected cells in resistant and susceptible mice.原位显微镜分析揭示了在抗性和易感小鼠中,围绕布鲁氏菌感染细胞发展的局部先天免疫反应。
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Laboratory animal models for brucellosis research.用于布鲁氏菌病研究的实验动物模型。
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7
DeltaznuADeltapurE Brucella abortus 2308 mutant as a live vaccine candidate.德尔塔兹努 A 德尔塔普鲁 E 布鲁氏菌 abortus 2308 突变体作为活疫苗候选物。
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Brucellosis: the case for live, attenuated vaccines.布鲁氏菌病:减毒活疫苗的情况
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Deletion of znuA virulence factor attenuates Brucella abortus and confers protection against wild-type challenge.锌摄取蛋白A(znuA)毒力因子的缺失减弱了牛布鲁氏菌的毒力,并赋予机体抵抗野生型菌株攻击的保护作用。
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Protective properties of rifampin-resistant rough mutants of Brucella melitensis.羊种布鲁氏菌耐利福平粗糙突变株的保护特性
Infect Immun. 2005 Jul;73(7):4198-204. doi: 10.1128/IAI.73.7.4198-4204.2005.

本文引用的文献

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Interactions between mononuclear phagocytes and Brucella abortus strains of different virulence.单核吞噬细胞与不同毒力的流产布鲁氏菌菌株之间的相互作用。
Proc Soc Exp Biol Med. 1958 Feb;97(2):393-7. doi: 10.3181/00379727-97-23752.
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Immune responses and protection against infection and abortion in cattle experimentally vaccinated with mutant strains of Brucella abortus.用流产布鲁氏菌突变株对牛进行实验性疫苗接种后的免疫反应及对感染和流产的保护作用。
Am J Vet Res. 1993 Oct;54(10):1591-7.
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Serologic responses in diagnostic tests for brucellosis in cattle vaccinated with Brucella abortus 19 or RB51.用流产布鲁氏菌19或RB51疫苗接种的牛布鲁氏菌病诊断试验中的血清学反应。
J Clin Microbiol. 1994 Apr;32(4):1065-6. doi: 10.1128/jcm.32.4.1065-1066.1994.
4
Macrophage activation during experimental murine brucellosis. III. Do macrophages exert feedback control during brucellosis?实验性小鼠布鲁氏菌病期间的巨噬细胞激活。III. 巨噬细胞在布鲁氏菌病期间是否发挥反馈控制作用?
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Outer membrane proteins from rough strains of four Brucella species.四种布鲁氏菌粗糙菌株的外膜蛋白。
Infect Immun. 1984 Oct;46(1):188-94. doi: 10.1128/iai.46.1.188-194.1984.
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Human brucellosis.人类布鲁氏菌病
Rev Infect Dis. 1983 Sep-Oct;5(5):821-42. doi: 10.1093/clinids/5.5.821.
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Monoclonal antibodies to Brucella surface antigens associated with the smooth lipopolysaccharide complex.针对与光滑脂多糖复合物相关的布鲁氏菌表面抗原的单克隆抗体。
Am J Vet Res. 1984 May;45(5):967-71.
8
Survival of rough and smooth strains of Brucella abortus in bovine mammary gland macrophages.牛流产布鲁氏菌粗糙型和平滑型菌株在牛乳腺巨噬细胞中的存活情况。
Am J Vet Res. 1988 Jul;49(7):1092-7.
9
Identification of Brucella abortus in formalin-fixed, paraffin-embedded tissues of cows, goats, and mice with an avidin-biotin-peroxidase complex immunoenzymatic staining technique.运用抗生物素蛋白-生物素-过氧化物酶复合物免疫酶染色技术在牛、山羊和小鼠的福尔马林固定、石蜡包埋组织中鉴定流产布鲁氏菌。
Am J Vet Res. 1986 Oct;47(10):2147-50.
10
Comparison of living and nonliving vaccines for Brucella abortus in BALB/c mice.BALB/c小鼠中布鲁氏菌活疫苗与灭活疫苗的比较。
Infect Immun. 1986 Aug;53(2):245-51. doi: 10.1128/iai.53.2.245-251.1986.

感染流产布鲁氏菌19、RB51或2308的小鼠的免疫和病理反应。

Immune and pathologic responses in mice infected with Brucella abortus 19, RB51, or 2308.

作者信息

Stevens M G, Olsen S C, Pugh G W, Palmer M V

机构信息

Brucellosis Research Unit, National Animal Disease Center, USDA Agricultural Research Service, Ames, Iowa 50010.

出版信息

Infect Immun. 1994 Aug;62(8):3206-12. doi: 10.1128/iai.62.8.3206-3212.1994.

DOI:10.1128/iai.62.8.3206-3212.1994
PMID:8039890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC302947/
Abstract

Immune and pathologic responses were measured for 20 weeks after infection of mice with Brucella abortus 19, RB51, or 2308. Live bacteria and bacterial antigens of 19 and RB51 persisted in spleens for 10 and 4 weeks after infection, respectively, whereas 2308 bacteria and bacterial antigens persisted for at least 20 weeks. Small germinal centers and profound lymphoid depletion occurred in spleens of mice during the first 4 weeks of infection with strain 19 or 2308; however, mice infected with strain RB51 had much larger germinal centers but no lymphoid depletion. At 4 weeks, only spleen cells from RB51-infected mice proliferated when incubated with 2308 bacteria. Large germinal centers in the spleen and spleen cell proliferative responses to 2308 did not appear in strain 19-infected mice until 6 weeks or in strain 2308-infected mice until 10 weeks. Similar proliferative responses to 2308 occurred in mice infected with strain 19 or RB51 at 6 weeks and in mice infected with strain 19, RB51, or 2308 at 10 weeks. However, at 20 weeks, spleen cell proliferative responses to 2308 occurred in mice infected with strain 19 or 2308 but not in mice infected with strain RB51. Mice infected with strain RB51 had lower and less persistent antibody titers to 2308 than did mice infected with strain 19 or 2308. Collectively, these results indicate that RB51-infected mice have less persistent immune responses to 2308 than do mice infected with 19 or 2308. The shorter duration of the responses probably resulted because RB51 is considerably less pathogenic and is cleared more rapidly from mice than are 19 and 2308.

摘要

在用流产布鲁氏菌19、RB51或2308感染小鼠后,对其免疫和病理反应进行了20周的监测。19型和RB51型的活菌及细菌抗原分别在感染后10周和4周持续存在于脾脏中,而2308型细菌及细菌抗原持续存在至少20周。在用19型或2308型菌株感染小鼠的前4周,脾脏中出现小生发中心和严重的淋巴细胞耗竭;然而,感染RB51型菌株的小鼠生发中心大得多,但没有淋巴细胞耗竭。在4周时,仅RB51感染小鼠的脾细胞与2308型细菌一起孵育时会增殖。直到6周,19型感染小鼠的脾脏中才出现大生发中心以及脾细胞对2308型的增殖反应,而2308型感染小鼠直到10周才出现。19型或RB51型感染小鼠在6周时以及19型、RB51型或2308型感染小鼠在10周时,对2308型有类似的增殖反应。然而,在20周时,19型或2308型感染小鼠的脾细胞对2308型有增殖反应,而RB51型感染小鼠则没有。与感染19型或2308型的小鼠相比,感染RB51型的小鼠对2308型的抗体滴度更低且持续时间更短。总体而言,这些结果表明,与感染19型或2308型的小鼠相比,感染RB51型的小鼠对2308型的免疫反应持续时间更短。反应持续时间较短可能是因为RB51的致病性相当低,并且比19型和2308型从小鼠体内清除得更快。