| Literature DB >> 31816416 |
Larissa Almeida Martins1, Jan Kotál2, Chaima Bensaoud1, Jindřich Chmelař3, Michail Kotsyfakis4.
Abstract
Ticks must durably suppress vertebrate host responses (hemostasis, inflammation, immunity) to avoid rejection and act as vectors of many pathogenic microorganisms that cause disease in humans and animals. Transcriptomics and proteomics studies have been used to study tick-host-pathogen interactions and have facilitated the systematic characterization of salivary composition and molecular dynamics throughout tick feeding. Tick saliva contains a complement of protease inhibitors that are differentially produced during feeding, many of which inhibit blood coagulation, platelet aggregation, vasodilation, and immunity. Here we focus on two major groups of protease inhibitors, the small molecular weight Kunitz inhibitors and cystatins. We discuss their role in tick-host-pathogen interactions, how they mediate the interaction between ticks and their hosts, and how they might be exploited both by pathogens to invade hosts and as candidates for the treatment of various human pathologies.Entities:
Keywords: Cystatins; Kunitz-domain proteins; Protease inhibitor; Saliva; Salivary gland; Sialomes; Tick-host-pathogen
Year: 2019 PMID: 31816416 DOI: 10.1016/j.bbapap.2019.140336
Source DB: PubMed Journal: Biochim Biophys Acta Proteins Proteom ISSN: 1570-9639 Impact factor: 3.036