» Articles » PMID: 28798904

Tick-Borne Viruses and Biological Processes at the Tick-Host-Virus Interface

Overview
Date 2017 Aug 12
PMID 28798904
Citations 63
Authors
Affiliations
Soon will be listed here.
Abstract

Ticks are efficient vectors of arboviruses, although less than 10% of tick species are known to be virus vectors. Most tick-borne viruses (TBV) are RNA viruses some of which cause serious diseases in humans and animals world-wide. Several TBV impacting human or domesticated animal health have been found to emerge or re-emerge recently. In order to survive in nature, TBV must infect and replicate in both vertebrate and tick cells, representing very different physiological environments. Information on molecular mechanisms that allow TBV to switch between infecting and replicating in tick and vertebrate cells is scarce. In general, ticks succeed in completing their blood meal thanks to a plethora of biologically active molecules in their saliva that counteract and modulate different arms of the host defense responses (haemostasis, inflammation, innate and acquired immunity, and wound healing). The transmission of TBV occurs primarily during tick feeding and is a complex process, known to be promoted by tick saliva constituents. However, the underlying molecular mechanisms of TBV transmission are poorly understood. Immunomodulatory properties of tick saliva helping overcome the first line of defense to injury and early interactions at the tick-host skin interface appear to be essential in successful TBV transmission and infection of susceptible vertebrate hosts. The local host skin site of tick attachment, modulated by tick saliva, is an important focus of virus replication. Immunomodulation of the tick attachment site also promotes co-feeding transmission of viruses from infected to non-infected ticks in the absence of host viraemia (non-viraemic transmission). Future research should be aimed at identification of the key tick salivary molecules promoting virus transmission, and a molecular description of tick-host-virus interactions and of tick-mediated skin immunomodulation. Such insights will enable the rationale design of anti-tick vaccines that protect against disease caused by tick-borne viruses.

Citing Articles

Haemaphysalis longicornis subolesin controls the infection and transmission of severe fever with thrombocytopenia syndrome virus.

Yuan C, Sun Y, Chen J, Xu Q, Zhou X, Zou Z NPJ Vaccines. 2025; 10(1):17.

PMID: 39856151 PMC: 11761454. DOI: 10.1038/s41541-024-01061-1.


Tick salivary cystatin Iristatin limits the virus replication in skin of tick-borne encephalitis virus-infected mice.

Langhansova H, Berankova Z, Khanna R, Kotal J, Kotsyfakis M, Palus M Parasitol Res. 2025; 124(1):8.

PMID: 39821815 PMC: 11739226. DOI: 10.1007/s00436-024-08441-5.


Metatranscriptomic analysis reveals the diversity of RNA viruses in ticks in Inner Mongolia, China.

Su S, Cui M, Xing L, Gao R, Mu L, Hong M PLoS Negl Trop Dis. 2024; 18(12):e0012706.

PMID: 39661583 PMC: 11634002. DOI: 10.1371/journal.pntd.0012706.


Detection and prevalence of a novel Bandavirus related to Guertu virus in Amblyomma gemma ticks and human populations in Isiolo County, Kenya.

Koka H, Langat S, Oyola S, Cherop F, Rotich G, Mutisya J PLoS One. 2024; 19(9):e0310862.

PMID: 39302958 PMC: 11414941. DOI: 10.1371/journal.pone.0310862.


GW4869 inhibitor affects vector competence and tick-borne flavivirus acquisition and transmission by blocking exosome secretion.

Sultana H, Ahmed W, Neelakanta G iScience. 2024; 27(8):110391.

PMID: 39108711 PMC: 11301069. DOI: 10.1016/j.isci.2024.110391.


References
1.
Vancova I, Slovak M, Hajnicka V, Labuda M, Simo L, Peterkova K . Differential anti-chemokine activity of Amblyomma variegatum adult ticks during blood-feeding. Parasite Immunol. 2007; 29(4):169-77. DOI: 10.1111/j.1365-3024.2006.00931.x. View

2.
Liu X, Bonnet S . Hard tick factors implicated in pathogen transmission. PLoS Negl Trop Dis. 2014; 8(1):e2566. PMC: 3907338. DOI: 10.1371/journal.pntd.0002566. View

3.
Best S, Morris K, Shannon J, Robertson S, Mitzel D, Park G . Inhibition of interferon-stimulated JAK-STAT signaling by a tick-borne flavivirus and identification of NS5 as an interferon antagonist. J Virol. 2005; 79(20):12828-39. PMC: 1235813. DOI: 10.1128/JVI.79.20.12828-12839.2005. View

4.
Mlera L, Melik W, Bloom M . The role of viral persistence in flavivirus biology. Pathog Dis. 2014; 71(2):137-63. PMC: 4154581. DOI: 10.1111/2049-632X.12178. View

5.
Brown S, WORMS M, Askenase P . Rhipicephalus appendiculatus: larval feeding sites in guinea pigs actively sensitized and receiving immune serum. Exp Parasitol. 1983; 55(1):111-20. DOI: 10.1016/0014-4894(83)90004-8. View