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Serine Protease Inhibitors in Ticks: An Overview of Their Role in Tick Biology and Tick-Borne Pathogen Transmission

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Date 2017 Jun 8
PMID 28589099
Citations 29
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Abstract

New tick and tick-borne pathogen control approaches that are both environmentally sustainable and which provide broad protection are urgently needed. Their development, however, will rely on a greater understanding of tick biology, tick-pathogen, and tick-host interactions. The recent advances in new generation technologies to study genomes, transcriptomes, and proteomes has resulted in a plethora of tick biomacromolecular studies. Among these, many enzyme inhibitors have been described, notably serine protease inhibitors (SPIs), whose importance in various tick biological processes is only just beginning to be fully appreciated. Among the multiple active substances secreted during tick feeding, SPIs have been shown to be directly involved in regulation of inflammation, blood clotting, wound healing, vasoconstriction and the modulation of host defense mechanisms. In light of these activities, several SPIs were examined and were experimentally confirmed to facilitate tick pathogen transmission. In addition, to prevent coagulation of the ingested blood meal within the tick alimentary canal, SPIs are also involved in blood digestion and nutrient extraction from the meal. The presence of SPIs in tick hemocytes and their involvement in tick innate immune defenses have also been demonstrated, as well as their implication in hemolymph coagulation and egg development. Considering the involvement of SPIs in multiple crucial aspects of tick-host-pathogen interactions, as well as in various aspects of the tick parasitic lifestyle, these molecules represent highly suitable and attractive targets for the development of effective tick control strategies. Here we review the current knowledge regarding this class of inhibitors in tick biology and tick-borne pathogen transmission, and their potential as targets for future tick control trials.

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References
1.
Koh C, Kazimirova M, Trimnell A, Takac P, Labuda M, Nuttall P . Variegin, a novel fast and tight binding thrombin inhibitor from the tropical bont tick. J Biol Chem. 2007; 282(40):29101-13. DOI: 10.1074/jbc.M705600200. View

2.
Porter L, Radulovic Z, Kim T, Braz G, da Silva Vaz Jr I, Mulenga A . Bioinformatic analyses of male and female Amblyomma americanum tick expressed serine protease inhibitors (serpins). Ticks Tick Borne Dis. 2014; 6(1):16-30. PMC: 4252504. DOI: 10.1016/j.ttbdis.2014.08.002. View

3.
Ehebauer M, Mans B, Gaspar A, Neitz A . Identification of extrinsic blood coagulation pathway inhibitors from the tick Ornithodoros savignyi (Acari: Argasidae). Exp Parasitol. 2002; 101(2-3):138-48. DOI: 10.1016/s0014-4894(02)00102-9. View

4.
Rodriguez-Valle M, Vance M, Moolhuijzen P, Tao X, Lew-Tabor A . Differential recognition by tick-resistant cattle of the recombinantly expressed Rhipicephalus microplus serine protease inhibitor-3 (RMS-3). Ticks Tick Borne Dis. 2012; 3(3):159-69. DOI: 10.1016/j.ttbdis.2012.03.002. View

5.
Imamura S, Namangala B, Tajima T, Tembo M, Yasuda J, Ohashi K . Two serine protease inhibitors (serpins) that induce a bovine protective immune response against Rhipicephalus appendiculatus ticks. Vaccine. 2005; 24(13):2230-7. DOI: 10.1016/j.vaccine.2005.10.055. View