Evidence map›Paper›PMID 28798904›Full record

ReviewFrontiers in cellular and infection microbiology2017

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

Mária Kazimírová, Saravanan Thangamani, Pavlína Bartíková, Meghan Hermance, Viera Holíková, Iveta Štibrániová, Patricia A Nuttall

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 136 citations in OpenAlex.

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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 3 countries.

Mária KazimírováDepartment of Medical Zoology, Institute of Zoology, Slovak Academy of SciencesBratislava, Slovakia.
Saravanan ThangamaniDepartment of Pathology, University of Texas Medical BranchGalveston, TX, United States.
Pavlína BartíkováBiomedical Research Center, Institute of Virology, Slovak Academy of SciencesBratislava, Slovakia.
Meghan HermanceDepartment of Pathology, University of Texas Medical BranchGalveston, TX, United States.
Viera HolíkováBiomedical Research Center, Institute of Virology, Slovak Academy of SciencesBratislava, Slovakia.
Iveta ŠtibrániováBiomedical Research Center, Institute of Virology, Slovak Academy of SciencesBratislava, Slovakia.
Patricia A NuttallDepartment of Zoology, University of OxfordOxford, United Kingdom.
Institute of Virology of the Slovak Academy of Sciences · SKThe University of Texas Medical Branch at Galveston · USBiomedical Research Center of the Slovak Academy of Sciences · SKInstitute of Zoology of the Slovak Academy of Sciences · SKUniversity of Oxford · GB

Funding

TICK DETERMINANTS OF POWASSAN VIRUS TRANSMISSIONR01AI127771 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI THANGAMANI, SARAVANAN · 2017 to 2021
$2.0M
Development of a Tick Transmission Model for Heartland Virus PathogenesisR21AI113128 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI THANGAMANI, SARAVANAN · 2015 to 2016
$426k
NIAID NIH HHS R01 AI127771NIAID NIH HHS R21 AI113128
6 · The paper itself

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.

Indexed as

Host-Pathogen InteractionsImmune EvasionVirus ReplicationAnimalsArthropod VectorsHumansTick-Borne DiseasesTicksVirusesarbovirusimmunomodulationskinticktransmissionvaccines

Identifiers

PMID28798904
PMCPMC5526847
OpenAlexW2736180687

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.