Evidence map›Paper›PMID 26314305›Full record

ArticleGenome biology and evolution2015

Comparative Genomics Including the Early-Diverging Smut Fungus Ceraceosorus bombacis Reveals Signatures of Parallel Evolution within Plant and Animal Pathogens of Fungi and Oomycetes.

Rahul Sharma, Xiaojuan Xia, Kai Riess, Robert Bauer, Marco Thines

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Article in Genome biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 21 citations in OpenAlex.

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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 3 institutions in 1 country.

Rahul SharmaBiodiversity and Climate Research Centre (BiK-F), Frankfurt (Main), Germany Department for Biological Sciences, Institute of Ecology, Evolution and Diversity, Goethe University, Frankfurt (Main), Germany Senckenberg Gesellschaft für Naturforschung, Frankfurt (Main), Germany Cluster for Integrative Fungal Research (IPF), Frankfurt (Main), Germany.
Xiaojuan XiaBiodiversity and Climate Research Centre (BiK-F), Frankfurt (Main), Germany Department for Biological Sciences, Institute of Ecology, Evolution and Diversity, Goethe University, Frankfurt (Main), Germany Senckenberg Gesellschaft für Naturforschung, Frankfurt (Main), Germany.
Kai RiessPlant Evolutionary Ecology, Institute of Evolution and Ecology, University of Tübingen, Germany.
Robert BauerPlant Evolutionary Ecology, Institute of Evolution and Ecology, University of Tübingen, Germany.
Marco ThinesBiodiversity and Climate Research Centre (BiK-F), Frankfurt (Main), Germany Department for Biological Sciences, Institute of Ecology, Evolution and Diversity, Goethe University, Frankfurt (Main), Germany Senckenberg Gesellschaft für Naturforschung, Frankfurt (Main), Germany Cluster for Integrative Fungal Research (IPF), Frankfurt (Main), Germany marco.thines@senckenberg.de.
Senckenberg Society for Nature Research · DEUniversity of Tübingen · DESenckenberg Biodiversity and Climate Research Centre · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ceraceosorus bombacis is an early-diverging lineage of smut fungi and a pathogen of cotton trees (Bombax ceiba). To study the evolutionary genomics of smut fungi in comparison with other fungal and oomycete pathogens, the genome of C. bombacis was sequenced and comparative genomic analyses were performed. The genome of 26.09 Mb encodes for 8,024 proteins, of which 576 are putative-secreted effector proteins (PSEPs). Orthology analysis revealed 30 ortholog PSEPs among six Ustilaginomycotina genomes, the largest groups of which are lytic enzymes, such as aspartic peptidase and glycoside hydrolase. Positive selection analyses revealed the highest percentage of positively selected PSEPs in C. bombacis compared with other Ustilaginomycotina genomes. Metabolic pathway analyses revealed the absence of genes encoding for nitrite and nitrate reductase in the genome of the human skin pathogen Malassezia globosa, but these enzymes are present in the sequenced plant pathogens in smut fungi. Interestingly, these genes are also absent in cultivable oomycete animal pathogens, while nitrate reductase has been lost in cultivable oomycete plant pathogens. Similar patterns were also observed for obligate biotrophic and hemi-biotrophic fungal and oomycete pathogens. Furthermore, it was found that both fungal and oomycete animal pathogen genomes are lacking cutinases and pectinesterases. Overall, these findings highlight the parallel evolution of certain genomic traits, revealing potential common evolutionary trajectories among fungal and oomycete pathogens, shaping the pathogen genomes according to their lifestyle.

Indexed as

Evolution, MolecularGenome, FungalBasidiomycotaFungal ProteinsGenes, FungalGenomicsHyphaeMetabolic Networks and PathwaysOomycetesPhylogenySelection, GeneticFungal Proteinscomparative genomicsconvergent evolutionevolutionary biologymetabolic pathwayspositive selectionsmut fungiUstilaginomycotina

Identifiers

PMID26314305
PMCPMC4607519
OpenAlexW2192691337

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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.