Evidence map›Paper›PMID 41593665›Full record

ArticleBMC veterinary research2026

Establishment and application of EmDEA, a rapid on-site nucleic acid detection method for parrot bornavirus type 4.

Yanhong Qian, Yao Wu, Jing Chen, Pian Zhang, Mei Yin, Xiaoxiao Zhang, Fumin Wang, Jiejian Zou, Wu Chen, Fen Shan and 6 more

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Yanhong Qian *Guangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Yao Wu *GeneVide Biotech Co., Ltd, Suzhou, 215028, China.
Jing Chen *Guangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Pian ZhangGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Mei YinGuangdong Provincial Wildlife Rescue Center, Guangzhou, 510520, China.
Xiaoxiao ZhangGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Fumin WangGuangdong Provincial Wildlife Rescue Center, Guangzhou, 510520, China.
Jiejian ZouGuangdong Provincial Wildlife Rescue Center, Guangzhou, 510520, China.
Wu ChenGuangzhou Zoo & Guangzhou Wildlife Research Center, Guangzhou, 510070, China.
Fen ShanGuangzhou Zoo & Guangzhou Wildlife Research Center, Guangzhou, 510070, China.
Gang WangGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Hua XiangGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China.
Qiushi LiGeneVide Biotech Co., Ltd, Suzhou, 215028, China.
Zhenxin HuGeneVide Biotech Co., Ltd, Suzhou, 215028, China. zhenxin.hu@genevide.com.
Shengjun LuoGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China. 422368881@qq.com.
Xiaohu WangGuangdong Province Key Laboratory of Livestock Disease Prevention, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases, Provincial Observation and Research Station for Animal Disease, Institute of Animal Health, Ministry of Agriculture and Rural Affairs, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China. wangxiaohu2020@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parrot bornavirus (PaBV) is a neurotropic virus that causes chronic infection in parrots, affecting their nervous and gastrointestinal systems and often resulting in high mortality in captive populations. It is a major threat to the parrot breeding industry and the ornamental bird trade. We used Enzyme-Mediated Dual Exponential Amplification (EmDEA) rapid nucleic acid detection technology to create a novel, simple, and highly sensitive method for detecting parrot bornavirus type 4 (PaBV-4). Primers and probes specific to the M gene of PaBV-4 were designed. After two rounds of screening and optimization, the optimal primer pair was identified as F4R7RNA1. The assay was tested for specificity, sensitivity, and clinical usefulness. The test showed no cross-reactivity with H5N2, H7N9, H9N2, NDV, IBV, or IBDV. It had a detection limit of 5 copies/µL and a repeatability coefficient of variation of less than 5%. Among 270 clinical tissue samples from parrots, the assay achieved a 100% positive concordance rate and an overall agreement of 97.03% with conventional RT-PCR results. The entire detection process takes only 30 min and allows for direct RNA detection of PaBV-4. The method is simple to use, fast, sensitive, and accurate, making it an invaluable tool for on-site detection of PaBV-4.

Indexed as

Bird DiseasesBornaviridaeMononegavirales InfectionsNucleic Acid Amplification TechniquesParrotsAnimalsRapid Diagnostic TestsRNA, ViralSensitivity and SpecificityRNA, ViralClinical applicationEmEDAIsothermal amplificationParrot bornavirus type 4Rapid on-site testing

Identifiers

PMID41593665
PMCPMC12973659

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LicenceCC BY-NC-ND
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Registered trials

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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.