Evidence map›Paper›PMID 35891386›Full record

ArticleViruses2022

Occurrence, Genetic Variability of Tomato Yellow Ring Orthotospovirus Population and the Development of Reverse Transcription Loop-Mediated Isothermal Amplification Assay for Its Rapid Detection.

Aleksandra Zarzyńska-Nowak, Daria Budzyńska, Agnieszka Taberska, Norbert Jędrzejczak, Julia Minicka, Natasza Borodynko-Filas, Beata Hasiów-Jaroszewska

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. 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
0.2field-weighted citation impact, top 34% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

7 authors at 1 institution in 1 country.

Aleksandra Zarzyńska-NowakInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0003-4944-2910
Daria BudzyńskaInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0002-3923-0829
Agnieszka TaberskaInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0002-3059-3041
Norbert JędrzejczakInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.
Julia MinickaInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0002-7773-9079
Natasza Borodynko-FilasInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0002-4217-6421
Beata Hasiów-JaroszewskaInstitute of Plant Protection-National Research Institute, ul. Wł. Węgorka 20, 60-318 Poznań, Poland.ORCID 0000-0002-8267-023X
Institute of Plant Protection · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tomato-infecting viruses have been considered as a serious threat to tomato crops in Poland. Therefore, during 2014-2021, 234 tomato samples delivered directly by greenhouse tomato growers to Plant Disease Clinic of IPP-NRI were tested. Eight virus species: pepino mosaic virus (PepMV), tomato yellow ring orthotospovirus (TYRV), tomato spotted wilt orthotospovirus (TSWV), potato virus Y (PVY), cucumber mosaic virus (CMV), tomato black ring virus (TBRV) and tomato mosaic virus (ToMV) were detected in single or mixed infection in 89 samples. The presence of TYRV was established for the first time in Poland in 2014. Since then, its presence has been observed in single and mixed infection with TSWV and CMV. Here, we analysed the genetic variability of TYRV population based on complete nucleocapsid (N) protein gene sequence of 55 TYRV isolates. Maximum-likelihood reconstruction revealed the presence of three distinct, well-supported phylogroups. Moreover, the effect of host species on virus diversity was confirmed. Therefore, RT-LAMP assay was developed for the rapid and efficient detection of TYRV isolates that can be implemented in field and greenhouse conditions.

Indexed as

CoinfectionCucumovirusCytomegalovirus InfectionsPotyvirusSolanum lycopersicumHumansMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesReverse Transcriptiondiagnosticsevolutionary dynamicsRT-LAMPtomato virusesTYRV

Identifiers

PMID35891386
PMCPMC9323093
OpenAlexW4283640778

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LicenceCC BY
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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.