Evidence map›Paper›PMID 36350399›Full record

ArticleArchives of microbiology2022

Development of one-step multiplex RT-PCR assay for rapid simultaneous detection of five RNA viruses and Acidovorax citrulli in major cucurbitaceous crops in China.

Zhenxing Zhao, Jun Xiang, Qian Tian, Wenjun Zhao, Tao Zhou, Lixia Zhao, Yongjiang Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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 4 institutions in 2 countries.

Zhenxing ZhaoInstitute of Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, 100176, China.
Jun XiangInstitute of Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, 100176, China.
Qian TianInstitute of Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, 100176, China.
Wenjun ZhaoInstitute of Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, 100176, China.
Tao ZhouState Key Laboratory of Agrobiotechnology and Key Laboratory of Pest Monitoring and Green Management-MOA, Department of Plant Pathology, China Agricultural University, Beijing, 100193, China.
Lixia ZhaoState Key Laboratory of Environmental Chemistry and Eco-Toxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, 100085, China. zlx@rcees.ac.cn.
Yongjiang ZhangInstitute of Plant Quarantine, Chinese Academy of Inspection and Quarantine, Beijing, 100176, China. zhangyjpvi@yeah.net.
Chinese Academy of Inspection and Quarantine · CNChina Agricultural University · CNChinese Academy of Sciences · CNNanjing Agricultural University · CN

Funding

Basic Scientific Research Foundation of the Chinese Academy of Inspection and Quarantine 2020JK017Fellowship of China Postdoc Research Foundation 2021M693037the National Key R&D Program of China No. 2021YFD1400100, 2021YFD1400103
6 · The paper itself

Abstract

Cucurbitaceous fruits and vegetables are important crops. Viral and bacterial diseases cause substantial economic losses to cucurbit crops globally. For rapid detection of these pathogens and improved disease control, a one-step multiplex reverse-transcription polymerase chain reaction (mRT-PCR) system was created. This method allowed for the concurrent detection of Tobacco mosaic virus (TMV), Zucchini yellow mosaic virus (ZYMV), Watermelon mosaic virus (WMV), Cucumber green mottle mosaic virus (CGMMV), Cucumber mosaic virus (CMV), and Acidovorax citrulli. Five pairs of specific primers were created according to the conserved regions around the coat protein (CP) genes of each virus, and one pair was based on the A. citrulli internal transcribed spacer (ITS). To limit false negatives, one pair of primers, created based on the Transcriptional elongation factor 1-α (EF1-α) from the major cucurbitaceous crop species, was put into the mRT-PCR reaction system. Primer concentrations, annealing temperature, extension time, and amplification cycles were optimized. Anticipated fragments of 152 bp (TMV), 205 bp (ZYMV), 318 bp (WMV), 419 bp (CGMMV), 529 bp (CMV), 662 bp (A. citrulli), and 821 bp (EF1-α) were amplified by the multiplex RT-PCR system, and their origin was established via DNA sequencing. This method was successfully used to examine field-collected seed samples of cucurbitaceous crops from China. The results demonstrated that the one-step mRT-PCR technique is a quick, efficient, and sensitive assay for the concurrent detection of six pathogens of cucurbits. It provides a method for monitoring and preventing these diseases.

Indexed as

Cytomegalovirus InfectionsPotyvirusComamonadaceaeDNA PrimersHumansPlant DiseasesReverse Transcriptase Polymerase Chain ReactionTobamovirusDNA PrimersAcidovorax citrulliCucurbitaceous cropsDetectionOne-step mRT-PCRVirus

Identifiers

PMID36350399
OpenAlexW4308752074

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.