Evidence map›Paper›PMID 34432124›Full record

ArticleCurrent genetics2021

Genetic response to nitrogen starvation in the aggressive Eucalyptus foliar pathogen Teratosphaeria destructans.

Minette Havenga, Brenda D Wingfield, Michael J Wingfield, Léanne L Dreyer, Francois Roets, Janneke Aylward

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Current genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Minette HavengaDepartment of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa. havenga.minette@fabi.up.ac.za.ORCID http://orcid.org/0000-0001-5870-3778
Brenda D WingfieldDepartment of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0002-6189-1519
Michael J WingfieldDepartment of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0001-9346-2009
Léanne L DreyerDepartment of Botany and Zoology, Stellenbosch University, Stellenbosch, South Africa.ORCID http://orcid.org/0000-0001-7579-1028
Francois RoetsDepartment of Conservation Ecology and Entomology, Stellenbosch University, Stellenbosch, South Africa.ORCID http://orcid.org/0000-0003-3849-9057
Janneke AylwardDepartment of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, South Africa.ORCID http://orcid.org/0000-0002-9038-9595
Stellenbosch University · ZAUniversity of Pretoria · ZA

Funding

national research foundation of south africa 11824sarchi chair in fungal genomics 98353
6 · The paper itself

Abstract

Teratosphaeria destructans is one of the most aggressive foliar pathogens of Eucalyptus. The biological factors underpinning T. destructans infections, which include shoot and leaf blight on young trees, have never been interrogated. Thus, the means by which the pathogen modifies its host environment to overcome host defences remain unknown. By applying transcriptome sequencing, the aim of this study was to compare gene expression in a South African isolate of T. destructans grown on nitrogen-deficient and complete media. This made it possible to identify upregulated genes in a nitrogen-starved environment, often linked to the pathogenicity of the fungus. The results support the hypothesis that nitrogen starvation in T. destructans likely mirrors an in planta genetic response. This is because 45% of genes that were highly upregulated under nitrogen starvation have previously been reported to be associated with infection in other pathogen systems. These included several CAZymes, fungal effector proteins, peptidases, kinases, toxins, lipases and proteins associated with detoxification of toxic compounds. Twenty-five secondary metabolites were identified and expressed in both nitrogen-deficient and complete conditions. Additionally, the most highly expressed genes in both growth conditions had pathogenicity-related functions. This study highlights the large number of expressed genes associated with pathogenicity and overcoming plant defences. As such, the generated baseline knowledge regarding pathogenicity and aggressiveness in T. destructans is a valuable reference for future in planta work.

Indexed as

Gene Expression Regulation, FungalHost-Pathogen InteractionsAscomycotaComputational BiologyEucalyptusFungal ProteinsGene Expression ProfilingNitrogenPlant DiseasesRNA-SeqSecondary MetabolismTranscriptomeFungal ProteinsNitrogenEnzyme secretionFungal pathogenicity factorsRNAseqTranscriptomicsVirulence

Identifiers

PMID34432124
OpenAlexW3195537009

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.