Molecular Interactions that Enable Movement of the Lyme Disease Agent from the Tick Gut into the Hemolymph

PLoS Pathogens

Sarojini Adusumilli¹  Jianfeng Dai²  Sukanya Narasimhan²  Yang O. Zhao²  Lei Liu²  Erol Fikrig²  Lili Zhang²  Yue Zhang² 

[1] Howard Hughes Medical Institute, Chevy Chase, Maryland, United States of America;Section of Infectious Diseases, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America

关键词: Spirochetes;    Salivary gl;    s;    Borrelia infection;    Borrelia burgdorferi;    Nymphs;    Immune serum;    Ticks;    Borrelia;   

DOI  :  10.1371/journal.ppat.1002079

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

Borrelia burgdorferi, the causative agent of Lyme disease, is transmitted to humans by bite of Ixodes scapularis ticks. The mechanisms by which the bacterium is transmitted from vector to host are poorly understood. In this study, we show that the F(ab)2 fragments of BBE31, a B.burgdorferi outer-surface lipoprotein, interfere with the migration of the spirochete from tick gut into the hemolymph during tick feeding. The decreased hemolymph infection results in lower salivary glands infection, and consequently attenuates mouse infection by tick-transmitted B. burgdorferi. Using a yeast surface display approach, a tick gut protein named TRE31 was identified to interact with BBE31. Silencing tre31 also decreased the B. burgdorferi burden in the tick hemolymph. Delineating the specific spirochete and arthropod ligands required for B. burgdorferi movement in the tick may lead to new strategies to interrupt the life cycle of the Lyme disease agent.

【 授权许可】

CC BY