Evidence map›Paper›PMID 32883295›Full record

ArticleVirology journal2020

First detection of African swine fever (ASF) virus genotype X and serogroup 7 in symptomatic pigs in the Democratic Republic of Congo.

Patrick N Bisimwa, Juliette R Ongus, Christian K Tiambo, Eunice M Machuka, Espoir B Bisimwa, Lucilla Steinaa, Roger Pelle

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
7.9field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Patrick N BisimwaDepartment of Molecular Biology and Biotechnology, Pan African University, Institute of Basic Sciences, Technology and Innovation, Nairobi, Kenya.
Juliette R OngusDepartment of Molecular Biology and Biotechnology, Pan African University, Institute of Basic Sciences, Technology and Innovation, Nairobi, Kenya.
Christian K TiamboBiosciences eastern and central Africa-International Livestock Research Institute (BecA-ILRI) Hub, Naivasha Road, P.O. Box 30709, Nairobi, 00100, Kenya.
Eunice M MachukaBiosciences eastern and central Africa-International Livestock Research Institute (BecA-ILRI) Hub, Naivasha Road, P.O. Box 30709, Nairobi, 00100, Kenya.
Espoir B BisimwaDepartment of Animal Science and Production, Université Evangélique en Afrique, Bukavu, Democratic Republic of the Congo.
Lucilla SteinaaInternational Livestock Research Institute, Animal and Human Health, Nairobi, Kenya.
Roger PelleBiosciences eastern and central Africa-International Livestock Research Institute (BecA-ILRI) Hub, Naivasha Road, P.O. Box 30709, Nairobi, 00100, Kenya. r.pelle@cgiar.org.ORCID 0000-0003-1053-085X
International Livestock Research Institute · KEUniversité Evangélique en Afrique · CDJomo Kenyatta University of Agriculture and Technology · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfrican swine fever (ASF) is a highly contagious and severe hemorrhagic viral disease of domestic pigs. The analysis of variable regions of African swine fever virus (ASFV) genome led to more genotypic and serotypic information about circulating strains. The present study aimed at investigating the genetic diversity of ASFV strains in symptomatic pigs in South Kivu province of the Democratic Republic of Congo (DRC). MATERIALS AND

methodsBlood samples collected from 391 ASF symptomatic domestic pigs in 6 of 8 districts in South Kivu were screened for the presence of ASFV, using a VP73 gene-specific polymerase chain reaction (PCR) with the universal primer set PPA1-PPA2. To genotype the strains, we sequenced and compared the nucleotide sequences of PPA-positive samples at three loci: the C-terminus of B646L gene encoding the p72 protein, the E183L gene encoding the p54 protein, and the central hypervariable region (CVR) of the B602L gene encoding the J9L protein. In addition, to serotype and discriminate between closely related strains, the EP402L (CD2v) gene and the intergenic region between the I73R and I329L genes were analyzed.

resultsASFV was confirmed in 26 of 391 pigs tested. However, only 19 and 15 PPA-positive samples, respectively, were successfully sequenced and phylogenetically analyzed for p72 (B646L) and p54 (E183L). All the ASFV studied were of genotype X. The CVR tetrameric repeat clustered the ASFV strains in two subgroups: the Uvira subgroup (10 TRS repeats, AAAABNAABA) and another subgroup from all other strains (8 TRS repeats, AABNAABA). The phylogenetic analysis of the EP402L gene clustered all the strains into CD2v serogroup 7. Analyzing the intergenic region between I73R and I329L genes revealed that the strains were identical but contained a deletion of a 33-nucleotide internal repeat sequence compared to ASFV strain Kenya 1950.

conclusionASFV genotype X and serogroup 7 was identified in the ASF disease outbreaks in South Kivu province of DRC in 2018-2019. This represents the first report of ASFV genotype X in DRC. CVR tetrameric repeat sequences clustered the ASFV strains studied in two subgroups. Our finding emphasizes the need for improved coordination of the control of ASF.

Indexed as

African Swine FeverAfrican Swine Fever VirusAnimalsBase SequenceDemocratic Republic of the CongoDisease OutbreaksDNA, ViralGenotypePhylogenySequence Analysis, DNASerogroupSus scrofaSwineViral ProteinsDNA, ViralViral ProteinsAfrican swine fever virusDomestic pigsDR CongoGenotype-serogroupPhylogenySouth Kivu province

Identifiers

PMID32883295
PMCPMC7468181
OpenAlexW3081932298

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.