ArticleVeterinary research communications2025
Molecular detection and phylogenetic analysis of lumpy skin disease virus in Yunnan Province, China from 2019 to 2023.
Article in Veterinary research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Development of a Duplex TaqMan-MGB qPCR Assay for Differential Detection of Chinese Epidemic Lumpy Skin Disease Virus Strains and Goatpox Virus.Animals : an open access journal from MDPI · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
Abstract
The lumpy skin disease (LSD), caused by the lumpy skin disease virus (LSDV), represents an emerging infectious disease that poses substantial economic losses to the cattle industries in China. This study aimed to investigate the epidemiological characteristics of LSDV in Yunnan Province, Southwest China, from 2019 to 2023. A Taqman-probe-based real-time PCR (qPCR) assay was developed for the molecular detection of LSDV nucleotides. In total, 2495 samples were collected and tested using the established method. LSDV-positive samples were further analyzed by amplifying and sequencing the GPCR and p32 genes. In addition, Viral isolation was performed to explore the biological characterisitics of the isolate. The developed qPCR assay demonstrated high sensitivity, with a limit of detection of 4.83 copies/µL. Six samples (0.24%) tested positive for LSDV, all originating from skin scabs. Molecular and phylogenetic analyses of the GPCR and p32 genes revealed that these six LSDV strains were genetically related to strains previously reported from China, Russia, and Thailand. One LSDV strain, designated YUN-LSDV, was successfully isolated in primary sheep testicular (PST) cells; while the isolate exhibited insensitivity to Madin-Darby bovine kidney cells. Collectively, this study represents the first report on the epidemiological characteristics of LSDV in cattle in Yunnan Province and contributes to the development of effective prevention and control strategies for LSD.
Indexed as
Identifiers
40900257What OpenQuestion holds
Registered trials
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.