Evidence map›Paper›PMID 29505617›Full record

ArticlePLoS neglected tropical diseases2018

Pathogenesis of bat rabies in a natural reservoir: Comparative susceptibility of the straw-colored fruit bat (Eidolon helvum) to three strains of Lagos bat virus.

Richard Suu-Ire, Lineke Begeman, Ashley C Banyard, Andrew C Breed, Christian Drosten, Elisa Eggerbauer, Conrad M Freuling, Louise Gibson, Hooman Goharriz, Daniel L Horton and 12 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

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  13. Bat-borne virus diversity, spillover and emergence.Nature reviews. Microbiology · 2020
    Review
  14. Article
  15. Article
  16. Novel Insights Into Immune Systems of Bats.Frontiers in immunology · 2020
    Review
  17. Review
  18. Article
  19. Review
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

22 authors at 9 institutions in 5 countries.

Richard Suu-IreInstitute of Zoology, Zoological Society of London, London, United Kingdom.
Lineke BegemanDepartment of Viroscience, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID 0000-0001-8856-9135
Ashley C BanyardWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Andrew C BreedWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Christian DrostenInstitute of Virology, Medical University of Berlin, Berlin, Germany.
Elisa EggerbauerInstitute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Island of Riems, Germany.
Conrad M FreulingInstitute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Island of Riems, Germany.
Louise GibsonInstitute of Zoology, Zoological Society of London, London, United Kingdom.
Hooman GoharrizWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Daniel L HortonSchool of Veterinary Medicine, University of Surrey, Guildford, United Kingdom.
Daisy JenningsWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Ivan V KuzminDepartment of Pathology, University of Texas Medical Branch, Galveston, Texas, United States of America.
Denise MarstonWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Yaa Ntiamoa-BaiduDepartment of Animal Biology and Conservation Science, University of Ghana, Accra, Ghana.
Silke Riesle SbarbaroInstitute of Zoology, Zoological Society of London, London, United Kingdom.
David SeldenWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Emma L WiseWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Thijs KuikenDepartment of Viroscience, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Anthony R FooksWildlife Zoonoses and Vector Borne Disease Research Group, Animal and Plant Health Agency, Addlestone, United Kingdom.
Thomas MüllerInstitute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald, Island of Riems, Germany.
James L N WoodDepartment of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Andrew A CunninghamInstitute of Zoology, Zoological Society of London, London, United Kingdom.
Animal and Plant Health Agency · GBZoological Society of London · GBFriedrich-Loeffler-Institut · DEErasmus University Rotterdam · NLMSB Medical School Berlin · DEThe University of Texas Medical Branch at Galveston · USUniversity of Cambridge · GBUniversity of Ghana · GHUniversity of Surrey · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rabies is a fatal neurologic disease caused by lyssavirus infection. People are infected through contact with infected animals. The relative increase of human rabies acquired from bats calls for a better understanding of lyssavirus infections in their natural hosts. So far, there is no experimental model that mimics natural lyssavirus infection in the reservoir bat species. Lagos bat virus is a lyssavirus that is endemic in straw-colored fruit bats (Eidolon helvum) in Africa. Here we compared the susceptibility of these bats to three strains of Lagos bat virus (from Senegal, Nigeria, and Ghana) by intracranial inoculation. To allow comparison between strains, we ensured the same titer of virus was inoculated in the same location of the brain of each bat. All bats (n = 3 per strain) were infected, and developed neurological signs, and fatal meningoencephalitis with lyssavirus antigen expression in neurons. There were three main differences among the groups. First, time to death was substantially shorter in the Senegal and Ghana groups (4 to 6 days) than in the Nigeria group (8 days). Second, each virus strain produced a distinct clinical syndrome. Third, the spread of virus to peripheral tissues, tested by hemi-nested reverse transcriptase PCR, was frequent (3 of 3 bats) and widespread (8 to 10 tissues positive of 11 tissues examined) in the Ghana group, was frequent and less widespread in the Senegal group (3/3 bats, 3 to 6 tissues positive), and was rare and restricted in the Nigeria group (1/3 bats, 2 tissues positive). Centrifugal spread of virus from brain to tissue of excretion in the oral cavity is required to enable lyssavirus transmission. Therefore, the Senegal and Ghana strains seem most suitable for further pathogenesis, and for transmission, studies in the straw-colored fruit bat.

Indexed as

AnimalsAntibodies, ViralBrainChiropteraDisease ReservoirsHost-Pathogen InteractionsImmunohistochemistryLyssavirusNeuronsRabiesAntibodies, Viral

Identifiers

PMID29505617
PMCPMC5854431
OpenAlexW2791294487

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.