Evidence map›Paper›PMID 40103407›Full record

ArticleThe veterinary quarterly2025

Evaluation of recombinant extracellular enveloped virion protein candidates for the detection of serological responses to lumpy skin disease virus in cattle.

Kitipong Angsujinda, Phatpimol Kitchanakan, Nabhasbhichayabha Daewang, Lerdchai Chintapitaksakul, Saruda Wanganurakkul, Sudkate Chaiyo, Nanthika Khongchareonporn, Timothy J Mahony, Wanchai Assavalapsakul

Abstract read
In one paragraph

Article in The veterinary quarterly, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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

9 authors.

Kitipong AngsujindaAquatic Resources Research Institute, Chulalongkorn University, Bangkok, Thailand.
Phatpimol KitchanakanDepartment of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
Nabhasbhichayabha DaewangDepartment of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
Lerdchai ChintapitaksakulNational Institute of Animal Health, Department of Livestock Development, Bangkok, Thailand.
Saruda WanganurakkulVeterinary Research and Development Center (Eastern Region), Department of Livestock Development, Chonburi, Thailand.
Sudkate ChaiyoThe Institute of Biotechnology and Genetic Engineering, Chulalongkorn University, Bangkok, Thailand.
Nanthika KhongchareonpornThe Institute of Biotechnology and Genetic Engineering, Chulalongkorn University, Bangkok, Thailand.
Timothy J MahonyQueensland Alliance for Agriculture and Food Innovation, The University of Queensland, Brisbane, Australia.ORCID 0000-0003-4573-7906
Wanchai AssavalapsakulDepartment of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lumpy skin disease virus (LSDV) is a significant threat to cattle, particularly in countries like Thailand, where outbreaks have necessitated the importation of diagnostic kits and vaccines. This study aimed to evaluate several recombinant extracellular enveloped virion (EEV) protein candidates, including F13L, A33R, A34R, and B5R, for their potential use in serological detection assays for LSDV specific antibodies in cattle. Given the challenges associated with LSDV research, such as its classification as a Class III biological agent in Thailand, gene synthesis was employed to produce these proteins. The recombinant proteins were expressed in a prokaryotic system and analyzed using SDS-PAGE and Western blotting. Among the candidates, F13L demonstrated the highest correlation with the results from a commercially available and validated ELISA, yielding 85.7%, and 75% positive for the infected and vaccinated groups, respectively, identifying it a promising candidate for serosurveillance activities during active LSDV outbreaks. Sequence analysis confirmed a 100% match between the F13L designed from the Neethling type strain 2490 and various Thai LSDV strains from the 2021 outbreaks, underscoring its potential as a conserved diagnostic marker. The availability of recombinant F13L and its reactivity with cattle sera from LSDV infected or vaccinated animals, demonstrated in this study, suggests it could also serve as a potential candidate for vaccine development. The study concludes that recombinant F13L shows great promise for the development of LSDV serological assays, though further optimization and validation are necessary to harness its diagnostic potential.

Indexed as

Lumpy Skin DiseaseLumpy skin disease virusViral Envelope ProteinsAnimalsAntibodies, ViralCattleEnzyme-Linked Immunosorbent AssayRecombinant ProteinsSerologic TestsThailandVirionAntibodies, ViralRecombinant ProteinsViral Envelope ProteinsF13LLumpy skin disease viruspalmitoylated EEV proteinrecombinant proteinserological detection

Identifiers

PMID40103407
PMCPMC11924265

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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.