Ixodes scapularis salivary gland protein P11 facilitates migration of Anaplasma phagocytophilum from the tick gut to salivary glands

被引:49
作者
Liu, Lei [1 ]
Narasimhan, Sukanya [1 ]
Dai, Jianfeng [1 ]
Zhang, Lili [1 ]
Cheng, Gong [1 ]
Fikrig, Erol [1 ,2 ]
机构
[1] Yale Univ, Infect Dis Sect, Dept Internal Med, Sch Med, New Haven, CT 06520 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家卫生研究院;
关键词
Anaplasma; haemocytes; Ixodes ticks; salivary gland protein; HUMAN GRANULOCYTIC EHRLICHIOSIS; MECHANISMS; DROSOPHILA; HEMOCYTES; RICINUS;
D O I
10.1038/embor.2011.177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ixodes ticks harbour several human pathogens belonging to the order Rickettsiales, including Anaplasma phagocytophilum, the agent of human anaplasmosis. When ticks feed on A. phagocytophilum-infected mice, the pathogen enters the ticks' gut. The bacteria then migrate from the gut to infect the salivary glands of the ticks and are transmitted to the next host via the saliva. The molecular mechanisms that enable the migration of A. phagocytophilum from the gut to the salivary glands are poorly understood. Here we show that a secreted tick protein, P11, is important in this process. We show that P11 enables A. phagocytophilum to infect tick haemocytes, which are required for the migration of A. phagocytophilum from the gut to the salivary glands. Silencing of p11 impaired the A. phagocytophilum infection of tick haemocytes in vivo and consequently decreased pathogen infection of the salivary glands. In vitro experiments showed that P11 could bind to A. phagocytophilum and thus facilitate its infection of tick cells. This report provides new insights into A. phagocytophilum infection of ticks and reveals new avenues to interrupt the life cycle of Anaplasma and related Rickettsial pathogens.
引用
收藏
页码:1196 / 1203
页数:8
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