4.5 Article

Deorphanization and target validation of cross-tick species conserved novel Amblyomma americanum tick saliva protein

Journal

INTERNATIONAL JOURNAL FOR PARASITOLOGY
Volume 43, Issue 6, Pages 439-451

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ijpara.2012.12.012

Keywords

Amblyomma americanum tick feeding biology; Highly conserved tick saliva protein; Anticoagulant function

Categories

Funding

  1. National Institute of Allergy and Infectious Diseases National Institutes of Health (NIAID/NIH), USA [AI081093]
  2. Brazilian National Council for Scientific and Technological Development (CNPq)

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We previously identified a cross-tick species conserved tick feeding stimuli responsive Amblyomma americanum (Aam) AV422 gene. This study demonstrates that AamAV422 belongs to a novel group of arthropod proteins that is characterized by 14 cysteine amino acid residues: C-23-X-7/9-C-33-X-23/24-C-58-X-8-C-67-X-7-C-75-X-23-C-99-X-15-C-115-X-10-C-126-X-24/25/33-(CC151)-C-150-X-7-C-159-X-8-C-168-X-23/24-C-192-X-9/10-C-202 predicted to form seven disulfide bonds. We show that AamAV422 protein is a ubiquitously expressed protein that is injected into the host within the first 24 h of the tick attaching onto the host as revealed by Western blotting analyses of recombinant (r)AamAV422, tick saliva and dissected tick organ protein extracts using antibodies to 24 and 48 h tick saliva proteins. Native AamAV422 is apparently involved with mediating tick anti-hemostasis and anti-complement functions in that rAamAV422 delayed plasma clotting time in a dose responsive manner by up to similar to 160 s, prevented platelet aggregation by up to similar to 16% and caused similar to 24% reduction in production of terminal complement complexes. Target validation analysis revealed that rAamAV422 is a potential candidate for a cocktail or multivalent tick vaccine preparation in that RNA interference (RNAi)-mediated silencing of AamAV422 mRNA caused a statistically significant (similar to 44%) reduction in tick engorgement weights, which is proxy for amounts of ingested blood. We speculate that AamAV422 is a potential target antigen for development of the highly desired universal tick vaccine in that consistent with high conservation among ticks, antibodies to 24 h Ixodes scapularis tick saliva proteins specifically bound rAamAV422. We discuss data in this study in the context of advancing the biology of tick feeding physiology and discovery of potential target antigens for tick vaccine development. (C) 2013 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

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