Evidence map›Paper›PMID 23849788›Full record

ArticleVirology2013

Host cell tropism mediated by Australian bat lyssavirus envelope glycoproteins.

Dawn L Weir, Ina L Smith, Katharine N Bossart, Lin-Fa Wang, Christopher C Broder

Open access · greenAbstract read
In one paragraph

Article in Virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Pseudotyped Viruses for Lyssavirus.Advances in experimental medicine and biology · 2023
    Article
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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

5 authors at 3 institutions in 3 countries.

Dawn L WeirDepartment of Microbiology, Uniformed Services University, Bethesda, MD 20814, USA. dawn.weir@usuhs.edu
Ina L Smith
Katharine N Bossart
Lin-Fa Wang
Christopher C Broder
Commonwealth Scientific and Industrial Research Organisation · AUUniformed Services University of the Health Sciences · USBoston University · US

Funding

Vaccine strategy for broad spectrum protection agains non-typhoidal salmonellU54AI057168 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI WHITE, JUDITH M. · 2003 to 2013
$91.5M
NIAID NIH HHS AI057168NIAID NIH HHS U54 AI057168
6 · The paper itself

Abstract

Australian bat lyssavirus (ABLV) is a rhabdovirus of the lyssavirus genus capable of causing fatal rabies-like encephalitis in humans. There are two variants of ABLV, one circulating in pteropid fruit bats and another in insectivorous bats. Three fatal human cases of ABLV infection have been reported with the third case in 2013. Importantly, two equine cases also arose in 2013; the first occurrence of ABLV in a species other than bats or humans. We examined the host cell entry of ABLV, characterizing its tropism and exploring its cross-species transmission potential using maxGFP-encoding recombinant vesicular stomatitis viruses that express ABLV G glycoproteins. Results indicate that the ABLV receptor(s) is conserved but not ubiquitous among mammalian cell lines and that the two ABLV variants can utilize alternate receptors for entry. Proposed rabies virus receptors were not sufficient to permit ABLV entry into resistant cells, suggesting that ABLV utilizes an unknown alternative receptor(s).

Indexed as

Viral TropismVirus InternalizationAnimalsChiropteraGenes, ReporterGreen Fluorescent ProteinsHorsesHumansLyssavirusRhabdoviridae InfectionsStaining and LabelingVesiculovirusViral Envelope ProteinsGreen Fluorescent ProteinsViral Envelope ProteinsAustralian bat lyssavirusEmergingEncephalitisEnvelope glycoproteinRabies virusReceptorRhabdovirusTropismViral entryZoonosis

Identifiers

PMID23849788
PMCPMC6183051
OpenAlexW2022533019

What OpenQuestion holds

Textmetadata
LicenceTDM
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.