Evidence map›Paper›PMID 33835201›Full record

ArticleApplied microbiology and biotechnology2021

Application of portable real-time recombinase-aided amplification (rt-RAA) assay in the clinical diagnosis of ASFV and prospective DIVA diagnosis.

Zhao-Hua Wang, Pei Li, Xiao Lin, Hong Jia, Yi-Tong Jiang, Xiao-Jia Wang, Shao-Hua Hou

Abstract read
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In one paragraph

Article in Applied microbiology and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Zhao-Hua WangBeijing Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Pei LiNingbo Jiangshen Biotechnology Co., Ltd, Ningbo, Zhejiang, 315000, China.
Xiao LinNanning Phagepharm Bio-techn Co., Ltd, Nanning, Guangxi, 530001, China.
Hong JiaBeijing Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Yi-Tong JiangBeijing Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Xiao-Jia WangKey Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.
Shao-Hua HouBeijing Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Beijing, 100193, China. houshaohua@126.com.
Chinese Academy of Agricultural Sciences · CNChina Agricultural University · CN

Funding

Chinese Academy of Agricultural Sciences basic scientific research operating expenses Y2019YJ07-05The National Key R & D Program of China 2017YFD0502300The National Key R & D Program of China 2018YFC0840400
6 · The paper itself

Abstract

African swine fever, a serious infectious disease, has been found in many countries around the world over the last nearly 100 years, and causes untold damage to the economy wherever it occurs. Diagnosis is currently performed by real-time PCR, which is highly sensitive but can only be carried out in a diagnostic laboratory environment with sophisticated equipment and expertise. A sensitive, rapid diagnostic method that can be implemented in agricultural settings is thus urgently needed for the detection and control of African swine fever virus (ASFV) infection. In this study, we developed an isothermal amplification technology to achieve molecular diagnosis of ASFV in clinical samples, using recombinase-aided amplification (RAA) assay combined with a portable instrument. This assay method avoids the limitations of traditional real-time PCR and offers detection times within 20 min, enabling detection of as few as 10 copies of ASFV DNA molecules per reaction without cross-reaction with other common swine viruses. We evaluated clinical performance using 200 clinical blood samples. The coincidence rate of the detection results between rt-RAA and RT-qPCR was 96.94% positive, 100% negative, and 97.50% total. We have also developed an rt-RAA system for the detection of ASFV targeting the EP402R gene, with detection of as few as 10 copies of DNA per reaction; this offers the possibility of DIVA (differentiating infected from vaccinated animals) diagnosis, because CD2V gene-deleted ASFV could soon be approved to be the leading candidate for live attenuated vaccine in China. The rt-RAA assay is a reliable, rapid, highly sensitive method, and it offers a reasonable alternative to RT-qPCR for point-of-care detection of ASFV. KEY POINTS: • The RT-RAA assay can detect as few as 10 copies of ASFV genome per reaction within 20 min. • The rt-RAA assay system targeting different genes can achieve differentiating infected from vaccinated diagnosis.

Indexed as

African Swine FeverAfrican Swine Fever VirusAnimalsChinaNucleic Acid Amplification TechniquesProspective StudiesReal-Time Polymerase Chain ReactionRecombinasesSensitivity and SpecificitySwineRecombinasesAfrican swine fever virusClinical diagnosisDIVA diagnosisPortable instrumentReal-time recombinase-aided amplification

Identifiers

PMID33835201
OpenAlexW3144882856

What OpenQuestion holds

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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.