羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立

›› 2011, Vol. 38 ›› Issue (3): 199-203.

羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立

孙春辉1,2，郎需龙2，杨艳玲1,2，王秀然1,2，李晓燕2，卜昭阳2，王兴龙2,3

（1.吉林大学畜牧兽医学院，吉林长春 130062； 2.中国人民解放军军事医学科学院军事兽医研究所，吉林长春 130122； 3.吉林省人兽共患病控制与预防中心，吉林长春 130062）

收稿日期:1900-01-01 修回日期:2010-12-16 出版日期:2011-03-20 发布日期:2011-03-20
通讯作者: 王兴龙

Eestablishment of Model that Virulent Brucella melitensi strain 16M Infect Mouse Macrophages

SUN Chun-hui1,2，LANG Xu-long2，YANG Yan-ling1,2，WANG Xiu-ran1,2，LI Xiao-yan2，BU Zhao-yang2，WANG Xing-long2,3

(1.College of Animal Science and Veterinary Medicine，Jilin University，Changchun 130062，China；2.Military Veterinary Institute，Academy of Military Medical Sciences,PLA，Changchun 130122，China；3.Key Laboratory of Jilin Province for Zoonosis Prevention and Control，Changchun 130062，China）

Received:1900-01-01 Revised:2010-12-16 Online:2011-03-20 Published:2011-03-20
Contact: WANG Xing-long

摘要/Abstract

摘要： 巨噬细胞是机体抗吞噬能力最强的细胞，但布鲁氏菌不但不能被巨噬细胞杀死，反而能在胞内大量繁殖，因此，本研究建立其感染模型，为下一步继续研究布鲁氏菌与其宿主细胞表面相关膜蛋白之间的作用和胞内寄生机制奠定基础。用羊布鲁氏菌强毒株16M感染巨噬细胞系264.7（细胞和细菌比例为1∶500），感染时间为4 h，建立布鲁氏菌感染巨噬细胞模型，做间接免疫荧光试验和透射电镜试验。间接免疫荧光试验中一抗与二抗最佳稀释度分别为1∶80和1∶80，电镜下观察到细菌侵入细胞时膜凹陷，形态发生变化，形成内吞小体。本试验减少感染过程所涉及的环境因素，优化了间接免疫荧光试验所需的一抗和二抗浓度比，成功建立感染模型。

关键词: 羊布鲁氏菌强毒株16M; 巨噬细胞系RAW264.7; 间接免疫荧光试验; 透射电镜试验

Abstract: Macrophage was the strongest anti-body cells of phagocytosis，while，Brucella could multiply in the cell and could not be killed. Therefor，we established the infection model，for continuous research Brucella and it’s the host cell，and the interaction of baceria cell and host cell surface-associated membrane protein，discovering the intracellular interaction mechanism for next step. Infection of mouse macrophage cell line RAW264.7 with Brucella melitensi virulent strain 16M were performed 4 h at a cell/bacteria ratio of 1∶500. Brucella-infected marophages were examined by indirect immunofluorescence assay and transmission electron microscopy assay. The optimal concentration ratio of primary antibody and secondary antibody in indirect immunofluorescence assay were 1∶80 and 1∶80，and the membrane depression and the endocytosis bodies were observed by transmission electron microscope. Expriment reduced the environmental factors of the infection process, optimized concentration ratio of primary and secondary antibodies in indirect immunofluorescence assay，established infection model.

Key words: virulent Brucella melitensi strain 16M; macrophage cell line RAW264.7; indirect immunofluorescence assay; electron microscope assay

中图分类号:

S852.61⁺4

孙春辉;;郎需龙;杨艳玲;;王秀然;;李晓燕;卜昭阳;王兴龙;. 羊布鲁氏菌强毒株16M感染小鼠巨噬细胞模型的建立[J]. , 2011, 38(3): 199-203.

SUN Chun-hui;;LANG Xu-long;YANG Yan-ling;;WANG Xiu-ran;;LI Xiao-yan;BU Zhao-yang;WANG Xing-long;. Eestablishment of Model that Virulent Brucella melitensi strain 16M Infect Mouse Macrophages[J]. China Animal Husbandry & Veterinary Medicine, 2011, 38(3): 199-203.

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