Mycobacterium bovis Δmce2 double deletion mutant protects cattle against challenge with virulent M. bovis

被引:30
|
作者
Carlos Blanco, Federico [1 ]
Veronica Bianco, Maria [1 ]
Garbaccio, Sergio [2 ]
Meikle, Virginia [1 ]
Jose Gravisaco, Maria [1 ]
Montenegro, Valeria [1 ]
Alfonseca, Edgar [3 ]
Singh, Mahavir
Barandiaran, Soledad [4 ]
Canal, Ana [5 ]
Vagnoni, Lucas [6 ]
Buddle, Bryce Malcom [7 ]
Bigi, Fabiana [1 ]
Cataldi, Angel [1 ]
机构
[1] INTA, Inst Biotecnol, RA-1686 Buenos Aires, DF, Argentina
[2] INTA, Inst Patobiol, RA-1686 Buenos Aires, DF, Argentina
[3] Univ Nacl Autonoma Mexico, Fac Med Vet & Zootecnia, Mexico City, DF, Mexico
[4] Univ Buenos Aires, Sch Vet, Buenos Aires, DF, Argentina
[5] Univ Nacl Litoral, Fac Ciencias Vet, Catedra Patol Basica, Esperanza, Argentina
[6] INTA, Ctr Invest Vet & Agron, RA-1686 Buenos Aires, DF, Argentina
[7] AgResearch, Hopkirk Res Inst, Palmerston North, New Zealand
关键词
Bovine tuberculosis; Mycobacterium bovis; Live vaccine; mce; ENHANCED PROTECTION; INFECTED CATTLE; MOUSE MODEL; TUBERCULOSIS; VACCINES; MICE; BCG; IMMUNOGENICITY; VACCINATION; EXPRESSION;
D O I
10.1016/j.tube.2013.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A Mycobacterium bovis strain deleted in mce2A and mce2B genes (M. bovis Delta mce2) was tested as an experimental vaccine in cattle challenged with a virulent M. bovis strain. Three-and-a-half-month old calves (n = 5 to 6 per group) were vaccinated and challenged with a virulent strain of M. bovis by the intratracheal route 9 weeks after vaccination. A non-vaccinated group and a group vaccinated with BCG were included as controls. Blood samples were collected to measure IFN-gamma by an interferon-gamma release assay (IGRA), cytometry and cytokine responses of bovine purified protein derivative (PPD) restimulated peripheral blood mononuclear cells (PBMCs). The IGRA test showed IFN-gamma values similar to pre-vaccination except for the animals vaccinated with M. bovis Dmce2, where a significant increase was observed at 30 days post-vaccination. The expression of IL-2R on CD4+ cells in response to PPD from the animals vaccinated with Dmce2 increased at 15 days post-vaccination compared to cells from non-vaccinated group. Vaccination of cattle with M. bovis Dmce2 induced the highest (P < 0.05) expression of IFN-gamma and IL-17 mRNA upon PPD stimulation of PBMCs compared to vaccination with BCG or that for the non-vaccinated group. There was a weak positive correlation between the production of these proinflammatory cytokines post-vaccination and reduced pathology scores post-challenge. The animals were euthanized and necropsied 100 days after challenge. The group vaccinated with M. bovis Dmce2 displayed a significantly lower histopathological score for lesions in lungs and pulmonary lymph nodes than for the other groups (P < 0.05). A marked positive reaction to tuberculin intradermal test was observed post-vaccination in animals vaccinated with M. bovis Dmce2 compared to those vaccinated with BCG or the non-vaccinated group. In contrast, after challenge, non-vaccinated animals had greater skin test responses than the vaccinated animals. In summary, M. bovis Dmce2 is a promising vaccine candidate to control M. bovis pathogenesis in cattle. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:363 / 372
页数:10
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