Ampelomyces strains isolated from diverse powdery mildew hosts in Japan: Their phylogeny and mycoparasitic activity, including timing and quantifying mycoparasitism of Pseudoidium neolycopersici on tomato.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 15 12 2020
accepted: 27 04 2021
entrez: 11 5 2021
pubmed: 12 5 2021
medline: 26 10 2021
Statut: epublish

Résumé

A total of 26 Ampelomyces strains were isolated from mycelia of six different powdery mildew species that naturally infected their host plants in Japan. These were characterized based on morphological characteristics and sequences of ribosomal DNA internal transcribed spacer (rDNA-ITS) regions and actin gene (ACT) fragments. Collected strains represented six different genotypes and were accommodated in three different clades of the genus Ampelomyces. Morphology of the strains agreed with that of other Ampelomyces strains, but none of the examined characters were associated with any groups identified in the genetic analysis. Five powdery mildew species were inoculated with eight selected Ampelomyces strains to study their mycoparasitic activity. In the inoculation experiments, all Ampelomyces strains successfully infected all tested powdery mildew species, and showed no significant differences in their mycoparasitic activity as determined by the number of Ampelomyces pycnidia developed in powdery mildew colonies. The mycoparasitic interaction between the eight selected Ampelomyces strains and the tomato powdery mildew fungus (Pseudoidium neolycopersici strain KTP-03) was studied experimentally in the laboratory using digital microscopic technologies. It was documented that the spores of the mycoparasites germinated on tomato leaves and their hyphae penetrated the hyphae of Ps. neolycopersici. Ampelomyces hyphae continued their growth internally, which initiated the atrophy of the powdery mildew conidiophores 5 days post inoculation (dpi); caused atrophy 6 dpi; and complete collapse of the parasitized conidiphores 7 dpi. Ampelomyces strains produced new intracellular pycnidia in Ps. neolycopersici conidiophores ca. 8-10 dpi, when Ps. neolycopersici hyphae were successfully destroyed by the mycoparasitic strain. Mature pycnidia released spores ca. 10-14 dpi, which became the sources of subsequent infections of the intact powdery mildew hyphae. Mature pycnidia contained each ca. 200 to 1,500 spores depending on the mycohost species and Ampelomyces strain. This is the first detailed analysis of Ampelomyces strains isolated in Japan, and the first timing and quantification of mycoparasitism of Ps. neolycopersici on tomato by phylogenetically diverse Ampelomyces strains using digital microscopic technologies. The developed model system is useful for future biocontrol and ecological studies on Ampelomyces mycoparasites.

Identifiants

pubmed: 33974648
doi: 10.1371/journal.pone.0251444
pii: PONE-D-20-39222
pmc: PMC8112701
doi:

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0251444

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Márk Z Németh (MZ)

Centre for Agricultural Research, Plant Protection Institute, Eötvös Loránd Research Network, Budapest, Hungary.

Yuusaku Mizuno (Y)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.

Hiroki Kobayashi (H)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.

Diána Seress (D)

Centre for Agricultural Research, Plant Protection Institute, Eötvös Loránd Research Network, Budapest, Hungary.

Naruki Shishido (N)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.

Yutaka Kimura (Y)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.

Susumu Takamatsu (S)

Faculty of Bioresources, Mie University, Mie, Japan.

Tomoko Suzuki (T)

Department of Chemical Biological Sciences, Faculty of Science, Japan Women's University, Tokyo, Japan.

Yoshihiro Takikawa (Y)

Plant Center, Institute of Advanced Technology, Kindai University, Wakayama, Japan.

Koji Kakutani (K)

Pharmaceutical Research and Technology Institute, Kindai University, Osaka, Japan.

Yoshinori Matsuda (Y)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.

Levente Kiss (L)

Centre for Agricultural Research, Plant Protection Institute, Eötvös Loránd Research Network, Budapest, Hungary.
Centre for Crop Health, University of Southern Queensland, Toowoomba, Australia.

Teruo Nonomura (T)

Laboratory of Phytoprotection, Science and Technology, Faculty of Agriculture, Kindai University, Nara, Japan.
Agricultural Technology and Innovation Research Institute, Kindai University, Nara, Japan.

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Classifications MeSH