Evidence map›Paper›PMID 26502988›Full record

ArticleVirology journal2015

Efficient self-assembly and protective efficacy of infectious bursal disease virus-like particles by a recombinant baculovirus co-expressing precursor polyprotein and VP4.

Hyun-Jeong Lee, Ji-Ye Kim, Soo-Jeong Kye, Hee-Jung Seul, Suk-Chan Jung, Kang-Seuk Choi

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 15 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

6 authors at 1 institution in 1 country.

Hyun-Jeong LeeAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. hyunjlee@korea.kr.
Ji-Ye KimAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. jiyekim@korea.kr.
Soo-Jeong KyeAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. cessna70@korea.kr.
Hee-Jung SeulAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. glwjd82@korea.kr.
Suk-Chan JungAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. brujung@korea.kr.
Kang-Seuk ChoiAvian Disease Division, Animal and Plant Quarantine Agency, 175 Anyangro, Anyang, Gyeonggi, 430-757, Republic of Korea. kchoi0608@korea.kr.
Animal and Plant Quarantine Agency · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVirus-like particle (VLP) technology is considered one of the most promising approaches in animal vaccines, due to the intrinsic immunogenic properties as well as high safety profile of VLPs. In this study, we developed a VLP vaccine against infectious bursal disease virus (IBDV), which causes morbidity and mortality in chickens, by expressing a baculovirus in insect cells.

methodsTo improve the self-proteolytic processing of precursor polyprotein (PP), we constructed a recombinant baculovirus transfer vector that co-expresses PP and the VP4 protease gene of IBDV.

resultsExpression and VLP assembly of recombinant proteins and antigenicity of the VLP were examined by Western blotting, ELISA, and transmission electron microscopy. In animal experiments, vaccination with the recombinant VLP induced strong and uniform humoral immunity and provided complete protection against challenge with very virulent (vv) IBDV in SPF chickens (n = 12). As determined by the bursa of Fabricius (BF)/body weight (B/BW) ratio, the protection against post-challenge bursal atrophy was significantly higher (P < 0.001) in VLP-vaccinated birds than in non-vaccinated controls.

conclusionsSince the protective efficacy of the VLP vaccine was comparable to that of a commercially available inactivated vaccine, the recombinant VLP merits further investigation as an alternative means of protection against vvIBD.

Indexed as

AnimalsAntibodies, ViralBaculoviridaeBirnaviridae InfectionsBlotting, WesternBursa of FabriciusCell LineChickensEnzyme-Linked Immunosorbent AssayGenetic VectorsInfectious bursal disease virusInsectaMicroscopy, Electron, TransmissionPolyproteinsPoultry DiseasesProtein MultimerizationAntibodies, ViralPolyproteinsVaccines, Virus-Like ParticleViral Structural ProteinsViral VaccinesVirosomesVP4 protein, infectious bursal disease virus

Identifiers

PMID26502988
PMCPMC4621879
OpenAlexW1870883039

What OpenQuestion holds

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LicenceCC BY
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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.