Evidence map›Paper›PMID 36146726›Full record

ArticleViruses2022

Deletion of the CD2v Gene from the Genome of ASFV-Kenya-IX-1033 Partially Reduces Virulence and Induces Protection in Pigs.

Johanneke D Hemmink, Emmanuel M Khazalwa, Hussein M Abkallo, Bernard Oduor, Jeremiah Khayumbi, Nicholas Svitek, Sonal P Henson, Sandra Blome, Günther Keil, Richard P Bishop and 1 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 36 citations in OpenAlex.

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  12. Towards Safe African Swine Fever Vaccines: TheAnimals : an open access journal from MDPI · 2024
    Article
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  17. Identification ofFrontiers in microbiology · 2024
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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

11 authors at 3 institutions in 3 countries.

Johanneke D HemminkAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0001-8764-4156
Emmanuel M KhazalwaAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0001-6233-483X
Hussein M AbkalloAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0002-5594-4418
Bernard OduorAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.
Jeremiah KhayumbiAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.
Nicholas SvitekAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0002-4539-5806
Sonal P HensonAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0002-2002-5462
Sandra BlomeInstitute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, Insel Riems, 17493 Greifswald, Germany.ORCID 0000-0001-5465-5609
Günther KeilInstitute of Diagnostic Virology, Friedrich-Loeffler-Institut, Suedufer 10, Insel Riems, 17493 Greifswald, Germany.ORCID 0000-0001-5141-1916
Richard P BishopInternational Livestock Research Institute, Nairobi 00100, Kenya.
Lucilla SteinaaAnimal and Human Health Program, International Livestock Research Institute, Nairobi 00100, Kenya.ORCID 0000-0003-3691-3971
International Livestock Research Institute · KEFriedrich-Loeffler-Institut · DEUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infection of pigs with the African swine fever virus (ASFV) leads to a devastating hemorrhagic disease with a high mortality of up to 100%. In this study, a CD2v gene deletion was introduced to a genotype IX virus from East Africa, ASFV-Kenya-IX-1033 (ASFV-Kenya-IX-1033-∆CD2v), to investigate whether this deletion led to reduced virulence in domestic pigs and to see if inoculation with this LA-ASFV could induce protective immunity against parental virus challenge. All pigs inoculated with ASFV-Kenya-IX-1033-ΔCD2v survived inoculation but presented with fever, reduced appetite and lethargy. ASFV genomic copies were detected in only one animal at one time point. Seven out of eight animals survived subsequent challenge with the pathogenic parental strain (87.5%) but had mild to moderate clinical symptoms and had a gross pathology compatible with chronic ASFV infection. All mock-immunised animals developed acute ASF upon challenge with ASFV-Kenya-IX-1033 and were euthanised upon meeting the humane endpoint criteria. ASFV genome copy numbers after challenge were similar in the two groups. ASFV-Kenya-IX-1033-∆CD2v is therefore a useful tool to investigate the development of immunity to ASFV genotype IX, but safety concerns preclude its use as a candidate vaccine without further attenuation.

Indexed as

African Swine FeverAfrican Swine Fever VirusViral VaccinesAnimalsGene DeletionKenyaSus scrofaSwineVirulenceViral VaccinesAfrican swine feverCD2vgene deletionvaccine

Identifiers

PMID36146726
PMCPMC9503863
OpenAlexW4293724104

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.