Cristin-resultat-ID: 863509
Sist endret: 1. desember 2011, 16:43
Resultat
Vitenskapelig artikkel
2005

Morphological, chemical and molecular differentiation of Fusarium equiseti isolated from Norwegian cereals

Bidragsytere:
  • Barbara Kosiak
  • Arne Holst-Jensen
  • Thomas Rundberget
  • Maria Teresa Gonzalez Jaen og
  • Mona Torp

Tidsskrift

International journal of food microbiology
ISSN 0168-1605
e-ISSN 1879-3460
NVI-nivå 2

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2005
Volum: 99
Hefte: 2
Sider: 195 - 206

Importkilder

Scopus-ID: 2-s2.0-13944255114

Beskrivelse Beskrivelse

Tittel

Morphological, chemical and molecular differentiation of Fusarium equiseti isolated from Norwegian cereals

Sammendrag

The morphological variation, secondary metabolite profiles and restriction fragment length polymorphisms (RFLPs) of PCR amplified intergenic spacer (IGS) ribosomal DNA (rDNA) were studied in 27 isolates of Fusarium equiseti, 25 isolated from Norwegian cereals and 2 from soil obtained from the IBT culture collection (BioCentrum, Technical University of Denmark). All 27 isolates were tested for production of fusarochromanone (FUSCHR), zearalenone (ZEA) and the trichothecenes: 15- monoacetoxy-scirpentriol (MAS), diacetoxy-scirpenol (DAS), T-2 and HT-2 toxins, T2-triol, neosolaniol (NEO), deoxynivalenol (DON), nivalenol (NIV) and 4-acetylnivalenol (Fus-X). The trichothecenes were analysed by GC-MS in a selected ion monitoring mode, while FUSCHR was determined by ion pair HPLC with fluorometric detection and production of ZEA by TLC. For amplification of IGS rDNA primers CNL12 and CNS1 were applied. IGS rDNA was digested with the four restriction enzymes: AvaII, CfoI, EcoRI and Sau3A. In addition, we sequenced the IGS rDNA region of three of the Norwegian isolates. There were two morphological types among the Norwegian strains of F. equiseti, type I with short apical cells (dominating) and type II with long apical cells, with four haplotypes identified based on the RFLP data. Variation in secondary metabolite profiles within and between the morphological groups was observed and the levels of produced toxins were: FUSCHR 3000–42,500 and 25–30 ng/g, NIV 20–2500 and 120–700 ng/g, FUS-X 20–15,000 and 0 ng/g, DAS 30–7500 and 0–600 ng/g, and MAS 10– 600 and 0–500 ng/g, for strains with short and long apical cells, respectively. NEO was detected in 16/27 strains tested (all morphotype I). All but four strains of type I (these four lacked a restriction site for EcoRI) had identical RFLP profiles. The isolates of type II had two haplotypes. The IGS sequence similarity data indicated differences between these morphotypes corresponding to two separate lineages apparently at the species level.

Bidragsytere

Barbara Kosiak

  • Tilknyttet:
    Forfatter
Aktiv cristin-person

Arne Holst-Jensen

Bidragsyterens navn vises på dette resultatet som Arne Holst-Jensen
  • Tilknyttet:
    Forfatter
    ved Forskningsgruppe dyrehelse ved Veterinærinstituttet

Jan Thomas Rundberget

Bidragsyterens navn vises på dette resultatet som Thomas Rundberget
  • Tilknyttet:
    Forfatter
    ved Kjemi ved Veterinærinstituttet

Maria Teresa Gonzalez Jaen

  • Tilknyttet:
    Forfatter
    ved Universidad Complutense de Madrid

Mona Torp

  • Tilknyttet:
    Forfatter
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