Evidence mapPaperPMID 42554767Full record

ArticleFunctional & integrative genomics2026

Whole genome sequencing and annotation of a non-pathogenic Fusarium brachygibbosum TZ1MST22 strain isolated from Medicago sativa in Southern Tunisian oases.

Amani Ben Alaya, Abdelmalek Lekired, Manel Chaouachi, Bilel Khiari, Imen Ben Slimene, Naceur Djébali

Abstract read
PubMed Publisher
In one paragraph

Article in Functional & integrative genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Amani Ben AlayaLaboratory of Bioactive Substances, Center of Biotechnology of Borj Cedria, BP 901, 2050, Hammam-Lif, Tunisia. amani.ben.alaya@gmail.com.
Abdelmalek LekiredCenter for Evolutionary and Theoretical Immunology, Department of Biology, University of New Mexico, Albuquerque, NM, USA.
Manel ChaouachiLaboratory of Bioactive Substances, Center of Biotechnology of Borj Cedria, BP 901, 2050, Hammam-Lif, Tunisia.
Bilel KhiariLaboratory of Bioactive Substances, Center of Biotechnology of Borj Cedria, BP 901, 2050, Hammam-Lif, Tunisia.
Imen Ben SlimeneLaboratory of Bioactive Substances, Center of Biotechnology of Borj Cedria, BP 901, 2050, Hammam-Lif, Tunisia.
Naceur DjébaliLaboratory of Bioactive Substances, Center of Biotechnology of Borj Cedria, BP 901, 2050, Hammam-Lif, Tunisia. naceur.djebali@cbbc.rnrt.tn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fusarium sambucinum species complex (FSAMSC) includes not only major mycotoxin-producing pathogens but also non-pathogenic endophytic species that can promote plant growth and stress tolerance. However, the molecular mechanisms underlying these contrasting lifestyles remain poorly understood, underscoring the need for deeper molecular studies. A non-pathogenic endophytic Fusarium strain, TZ1MST22, isolated from Medicago sativa plants in the Tozeur region of Southern Tunisia, was sequenced using the Illumina NovaSeq 6000 sequencing technology. Here, we report a 39.8 Mb draft genome of TZ1MST22, comprising 160 contigs. Genome completeness was assessed using Benchmarking Universal Single-Copy Orthologs (BUSCO) analysis, which yielded 99.4% completeness. Molecular phylogenetic analysis showed that TZ1MST22 was a Fusarium brachygibbosum belonging to F. sambucinum species complex (FSAMSC). In total, 12396 protein-coding genes were predicted. Of these, 769 genes were annotated as encoding CAZymes, including 46 cellulose-degrading, 62 hemicellulose-degrading, and 38, 25, 8, and 31 chitin/chitosan-, glucan-, lignin-, and pectin-degrading enzymes, respectively, as well as 74 sugar-, poly-, and oligosaccharide-degrading enzymes, and 61 others, including cutinases. In addition, 38 secondary metabolism gene clusters were identified, mainly including terpenes, T1 polyketide synthase genes, and non-ribosomal peptide synthase genes. Comparative genomic analyses revealed that F. brachygibbosum TZ1MST22 harbors more biomass-degrading enzymes than other pathogenic and endophytic Fusarium species. These results expand our genetic knowledge of Fusarium brachygibbosum, as this genome represents the third published genome of this species and the first non-pathogenic one. Our comprehensive whole-genome analysis provides a valuable resource for future studies on gene expression, regulation, function, evolution, and will support efforts to optimize its cultivation for the high-yield production of useful metabolites.

Indexed as

FusariumGenome, FungalMedicago sativaFungal ProteinsMolecular Sequence AnnotationPhylogenyTunisiaWhole Genome SequencingFungal ProteinsCAZymesFusarium species complexLegumesNon-pathogenic FusariumWhole-genome sequencing

Identifiers

PMID42554767

What Socratic 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 Socratic graph.