Evidence map›Paper›PMID 26084502›Full record

ArticleBMC genomics2015

Distinctive expansion of gene families associated with plant cell wall degradation, secondary metabolism, and nutrient uptake in the genomes of grapevine trunk pathogens.

Abraham Morales-Cruz, Katherine C H Amrine, Barbara Blanco-Ulate, Daniel P Lawrence, Renaud Travadon, Philippe E Rolshausen, Kendra Baumgartner, Dario Cantu

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

82 citing papers in PubMed, 188 citations in OpenAlex.

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22 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 1 country.

Abraham Morales-CruzDepartment of Viticulture and Enology, University of California Davis, Davis, CA, 95616, USA. abmora@ucdavis.edu.
Katherine C H AmrineDepartment of Viticulture and Enology, University of California Davis, Davis, CA, 95616, USA. kcamrine@ucdavis.edu.
Barbara Blanco-UlateDepartment of Viticulture and Enology, University of California Davis, Davis, CA, 95616, USA. bblanco@ucdavis.edu.
Daniel P LawrenceDepartment of Plant Pathology, University of California Davis, Davis, CA, 95616, USA. dlawrence@ucdavis.edu.
Renaud TravadonDepartment of Plant Pathology, University of California Davis, Davis, CA, 95616, USA. rtravadon@ucdavis.edu.
Philippe E RolshausenDepartment of Botany and Plant Sciences, University of California Riverside, Riverside, CA, 92521, USA. philrols@ucr.edu.
Kendra BaumgartnerUnited States Department of Agriculture - Agricultural Research Service, Crops Pathology and Genetics Research Unit, Davis, CA, 95616, USA. kbaumgartner@ucdavis.edu.
Dario CantuDepartment of Viticulture and Enology, University of California Davis, Davis, CA, 95616, USA. dacantu@ucdavis.edu.
University of California, Davis · USUnited States Department of Agriculture · USUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrunk diseases threaten the longevity and productivity of grapevines in all viticulture production systems. They are caused by distantly-related fungi that form chronic wood infections. Variation in wood-decay abilities and production of phytotoxic compounds are thought to contribute to their unique disease symptoms. We recently released the draft sequences of Eutypa lata, Neofusicoccum parvum and Togninia minima, causal agents of Eutypa dieback, Botryosphaeria dieback and Esca, respectively. In this work, we first expanded genomic resources to three important trunk pathogens, Diaporthe ampelina, Diplodia seriata, and Phaeomoniella chlamydospora, causal agents of Phomopsis dieback, Botryosphaeria dieback, and Esca, respectively. Then we integrated all currently-available information into a genome-wide comparative study to identify gene families potentially associated with host colonization and disease development.

resultsThe integration of RNA-seq, comparative and ab initio approaches improved the protein-coding gene prediction in T. minima, whereas shotgun sequencing yielded nearly complete genome drafts of Dia. ampelina, Dip. seriata, and P. chlamydospora. The predicted proteomes of all sequenced trunk pathogens were annotated with a focus on functions likely associated with pathogenesis and virulence, namely (i) wood degradation, (ii) nutrient uptake, and (iii) toxin production. Specific patterns of gene family expansion were described using Computational Analysis of gene Family Evolution, which revealed lineage-specific evolution of distinct mechanisms of virulence, such as specific cell wall oxidative functions and secondary metabolic pathways in N. parvum, Dia. ampelina, and E. lata. Phylogenetically-informed principal component analysis revealed more similar repertoires of expanded functions among species that cause similar symptoms, which in some cases did not reflect phylogenetic relationships, thereby suggesting patterns of convergent evolution.

conclusionsThis study describes the repertoires of putative virulence functions in the genomes of ubiquitous grapevine trunk pathogens. Gene families with significantly faster rates of gene gain can now provide a basis for further studies of in planta gene expression, diversity by genome re-sequencing, and targeted reverse genetic approaches. The functional validation of potential virulence factors will lead to a more comprehensive understanding of the mechanisms of pathogenesis and virulence, which ultimately will enable the development of accurate diagnostic tools and effective disease management.

Indexed as

Cell WallFoodFungiGenomicsMycosesPlant CellsPlant DiseasesProteomeSecondary MetabolismVirulenceVirulence FactorsVitisWoodProteomeVirulence Factors

Identifiers

PMID26084502
PMCPMC4472170
OpenAlexW1642117298

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.