Evidence map›Paper›PMID 28865007›Full record

ArticleMicrobial ecology2018

Cryphonectria hypovirus 1-Induced Epigenetic Changes in Infected Phytopathogenic Fungus Cryphonectria parasitica.

Lucija Nuskern, Marin Ježić, Zlatko Liber, Jelena Mlinarec, Mirna Ćurković-Perica

Abstract read
PubMed Publisher
In one paragraph

Article in Microbial ecology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Laccase Activity in FungusJournal of fungi (Basel, Switzerland) · 2021
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

5 authors at 1 institution in 1 country.

Lucija NuskernDepartment of Biology, Faculty of Science, University of Zagreb, Marulićev trg 9a, HR-10 000, Zagreb, Croatia.
Marin JežićDepartment of Biology, Faculty of Science, University of Zagreb, Marulićev trg 9a, HR-10 000, Zagreb, Croatia.
Zlatko LiberDepartment of Biology, Faculty of Science, University of Zagreb, Marulićev trg 9a, HR-10 000, Zagreb, Croatia.
Jelena MlinarecDepartment of Biology, Faculty of Science, University of Zagreb, Marulićev trg 9a, HR-10 000, Zagreb, Croatia.
Mirna Ćurković-PericaDepartment of Biology, Faculty of Science, University of Zagreb, Marulićev trg 9a, HR-10 000, Zagreb, Croatia. mirna.curkovic-perica@biol.pmf.hr.
University of Zagreb · HR

Funding

Hrvatska Zaklada za Znanost 5381Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (CH) IZ73Z0_152525/1
6 · The paper itself

Abstract

Biotic stress caused by virus infections induces epigenetic changes in infected plants and animals, but this is the first report on methylation pattern changes in a fungus after mycovirus infection. As a model pathosystem for mycovirus-host interactions, we used Cryphonectria hypovirus 1 (CHV1) and its host fungus Cryphonectria parasitica, in which deregulation of methylation cycle enzymes upon virus infection was observed previously. Six CHV1 strains of different subtypes were transferred into three different C. parasitica isolates in order to assess the effect of different CHV1 strains and/or subtypes on global cytosine methylation level in infected fungus, using methylation-sensitive amplification polymorphism (MSAP). Infection with CHV1 affected the methylation pattern of the C. parasitica genome; it increased the number and diversity of methylated, hemi-methylated, and total MSAP markers found in infected fungal isolates compared to virus-free controls. The increase in methylation levels correlated well with the CHV1-induced reduction of fungal growth in vitro, indicating that C. parasitica genome methylation upon CHV1 infection, rather than being the defensive mechanism of the fungus, is more likely to be the virulence determinant of the virus. Furthermore, the severity of CHV1 effect on methylation levels of infected C. parasitica isolates depended mostly on individual CHV1 strains and on the combination of host and virus genomes, rather than on the virus subtype. These novel findings broaden our knowledge about CHV1 strains which could potentially be used in human-aided biocontrol of chestnut blight, a disease caused by C. parasitica in chestnut forest ecosystems and orchards.

Indexed as

Epigenesis, GeneticAscomycotaDNA, FungalDNA MethylationEpigenomicsFungal VirusesGenes, FungalGenome, ViralHost-Pathogen InteractionsPest Control, BiologicalPlant DiseasesVirulence FactorsDNA, FungalVirulence FactorsBiocontrolBiotic stressChestnut blightFungus-mycovirus interactionMSAP epigenotyping

Identifiers

PMID28865007
OpenAlexW2751262133

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.