Evidence map›Paper›PMID 31878885›Full record

ArticleBMC genomics2019

Network analysis exposes core functions in major lifestyles of fungal and oomycete plant pathogens.

Eswari Pj Pandaranayaka, Omer Frenkel, Yigal Elad, Dov Prusky, Arye Harel

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The Multifaceted Roles of Fungal Cutinases during Infection.Journal of fungi (Basel, Switzerland) · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. 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.

Eswari Pj PandaranayakaDepartment of Vegetable and Field Crops, Institute of Plant Sciences, Volcani Center, Agricultural Research Organization, Rishon LeZion, Israel.
Omer FrenkelDepartment of Plant Pathology and Weed Research, Institute of Plant Protection, Volcani Center, Agricultural Research Organization, Rishon LeZion, Israel.
Yigal EladDepartment of Plant Pathology and Weed Research, Institute of Plant Protection, Volcani Center, Agricultural Research Organization, Rishon LeZion, Israel.
Dov PruskyDepartment of Postharvest Science, Institute of Postharvest and Food Sciences, Volcani Center, Agricultural Research Organization, Rishon LeZion, Israel.
Arye HarelDepartment of Vegetable and Field Crops, Institute of Plant Sciences, Volcani Center, Agricultural Research Organization, Rishon LeZion, Israel. aryeharel@volcani.agri.gov.il.
Agricultural Research Organization · IL

Funding

Israeli Chief Scientist, Ministry of Agriculture, IL 20-10-0069
6 · The paper itself

Abstract

backgroundGenomic studies demonstrate that components of virulence mechanisms in filamentous eukaryotic pathogens (FEPs, fungi and oomycetes) of plants are often highly conserved, or found in gene families that include secreted hydrolytic enzymes (e.g., cellulases and proteases) and secondary metabolites (e.g., toxins), central to the pathogenicity process. However, very few large-scale genomic comparisons have utilized complete proteomes from dozens of FEPs to reveal lifestyle-associated virulence mechanisms. Providing a powerful means for exploration, and the discovery of trends in large-scale datasets, network analysis has been used to identify core functions of the primordial cyanobacteria, and ancient evolutionary signatures in oxidoreductases.

resultsWe used a sequence-similarity network to study components of virulence mechanisms of major pathogenic lifestyles (necrotroph (ic), N; biotroph (ic), B; hemibiotroph (ic), H) in complete pan-proteomes of 65 FEPs and 17 saprobes. Our comparative analysis highlights approximately 190 core functions found in 70% of the genomes of these pathogenic lifestyles. Core functions were found mainly in: transport (in H, N, B cores); carbohydrate metabolism, secondary metabolite synthesis, and protease (H and N cores); nucleic acid metabolism and signal transduction (B core); and amino acid metabolism (H core). Taken together, the necrotrophic core contains functions such as cell wall-associated degrading enzymes, toxin metabolism, and transport, which are likely to support their lifestyle of killing prior to feeding. The biotrophic stealth growth on living tissues is potentially controlled by a core of regulatory functions, such as: small G-protein family of GTPases, RNA modification, and cryptochrome-based light sensing. Regulatory mechanisms found in the hemibiotrophic core contain light- and CO

conclusionsThe selected set of enriched core functions identified in our work can facilitate future studies aimed at controlling FEPs. One interesting example would be to facilitate the identification of the pathogenic potential of samples analyzed by metagenomics. Finally, our analysis offers potential evolutionary scenarios, suggesting that an early-branching saprobe (identified in previous studies) has probably evolved a necrotrophic lifestyle as illustrated by the highest number of shared gene families between saprobes and necrotrophs.

Indexed as

Gene Regulatory NetworksGenomicsEvolution, MolecularFungiOomycetesPlantsBiotrophComparative genomicsCore functionFungus–plant interactionHemibiotrophNecrotrophNetworkPlant pathogenVirulence

Identifiers

PMID31878885
PMCPMC6933724
OpenAlexW2998310894

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.