Evidence map›Paper›PMID 31051010›Full record

ArticlePloS one2019

Differential gene expression and physiological changes during acute or persistent plant virus interactions may contribute to viral symptom differences.

Réka Pesti, Levente Kontra, Kenny Paul, Imre Vass, Tibor Csorba, Zoltán Havelda, Éva Várallyay

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.2field-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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Global expression patterns ofFrontiers in plant science · 2023
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  8. Silver Nanoparticles Prepared UsingJournal of fungi (Basel, Switzerland) · 2022
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  9. Review
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  13. Article
  14. Article
  15. Article
  16. Microarray analysis ofPhysiology and molecular biology of plants : an international journal of functional plant biology · 2021
    Article
  17. 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 2 institutions in 1 country.

Réka PestiDiagnostic Group, Department of Genomics, Agricultural Biotechnology Research Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Levente KontraDiagnostic Group, Department of Genomics, Agricultural Biotechnology Research Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Kenny PaulInstitute of Plant Biology, Biological Research Centre, Szeged, Hungary.
Imre VassInstitute of Plant Biology, Biological Research Centre, Szeged, Hungary.
Tibor CsorbaVirology Group, Department of Plant Biotechnology, Agricultural Biotechnology Research Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Zoltán HaveldaPlant Developmental Biology Group, Department of Plant Biotechnology, Agricultural Biotechnology Research Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.
Éva VárallyayDiagnostic Group, Department of Genomics, Agricultural Biotechnology Research Institute, National Agricultural Research and Innovation Centre, Gödöllő, Hungary.ORCID 0000-0002-9085-942X
National Agricultural Research and Innovation Centre · HUHUN-REN Szegedi Biológiai Kutatóközpont · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses have different strategies for infecting their hosts. Fast and acute infections result in the development of severe symptoms and may cause the death of the plant. By contrast, in a persistent interaction, the virus can survive within its host for a long time, inducing only mild symptoms. In this study, we investigated the gene expression changes induced in CymRSV-, crTMV-, and TCV-infected Nicotiana benthamiana and in PVX- and TMV-U1-infected Solanum lycopersicum plants after the systemic spread of the virus by two different high-throughput methods: microarray hybridization or RNA sequencing. Using these techniques, we were able to clearly differentiate between acute and persistent infections. We validated the gene expression changes of selected genes by Northern blot hybridization or by qRT-PCR. We show that, in contrast to persistent infections, the drastic shut-off of housekeeping genes, downregulation of photosynthesis-related transcripts and induction of stress genes are specific outcomes with acute infections. We also show that these changes are not a consequence of host necrosis or the presence of a viral silencing suppressor. Thermal imaging data and chlorophyll fluorescence measurements correlated very well with the molecular changes. We believe that the molecular and physiological changes detected during acute infections mostly contribute to virus symptom development. The observed characteristic physiological changes associated with economically more dangerous acute infections could serve as a basis for the elaboration of remote monitoring systems suitable for detecting developing virus infections in crops. Moreover, as molecular and physiological changes are characteristics of different types of virus lifestyles, this knowledge can support risk assessments of recently described novel viruses.

Indexed as

Gene Expression Regulation, PlantHost-Pathogen InteractionsNicotianaPlant DiseasesPlant LeavesPlant ProteinsPlant VirusesSolanum lycopersicumVirus ReplicationPlant Proteins

Identifiers

PMID31051010
PMCPMC6499435
OpenAlexW2943273635

What OpenQuestion holds

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LicenceCC BY
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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.