Literature DB >> 20943134

Genetic variability and mycohost association of Ampelomyces quisqualis isolates inferred from phylogenetic analyses of ITS rDNA and actin gene sequences.

Mi-Jeong Park1, Young-Joon Choi, Seung-Beom Hong, Hyeon-Dong Shin.   

Abstract

Ampelomyces quisqualis complex is well known as the most common and widespread hyperparasite of the family Erysiphaceae, the cause of powdery mildew diseases. As commercial biopesticide products it is widely used to control the disease in field and plastic houses. Although genetic diversity within Ampelomyces isolates has been previously recognized, a single name A. quisqualis is still applied to all pycnidial intracellular hyperparasites of powdery mildew fungi. In this study, the phylogenetic relationships among Ampelomyces isolates originating from various powdery mildew fungi in Korea were inferred from Bayesian and maximum parsimony analyses of the sequences of ITS rDNA region and actin gene. In the phylogenetic trees, the Ampelomyces isolates could be divided into four distinct groups with high sequence divergences in both regions. The largest group, Clade 1, mostly accommodated Ampelomyces isolates originating from the mycohost Podosphaera spp. (sect. Sphaerotheca). Clade 2 comprised isolates from several genera of powdery mildews, Golovinomyces, Erysiphe (sect. Erysiphe), Arthrocladiella, and Phyllactinia, and was further divided into two subclades. An isolate obtained from Podosphaera (sect. Sphaerotheca) pannosa was clustered into Clade 3, with those from powdery mildews infecting rosaceous hosts. The mycohosts of Ampelomyces isolates in Clade 4 mostly consisted of species of Erysiphe (sect. Erysiphe, sect. Microsphaera, and sect. Uncinula). The present phylogenetic study demonstrates that Ampelomyces hyperparasite is indeed an assemblage of several distinct lineages rather than a sole species. Although the correlation between Ampelomyces isolates and their mycohosts is not obviously clear, the isolates show not only some degree of host specialization but also adaptation to their mycohosts during the evolution of the hyperparasite.
Copyright © 2010 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20943134     DOI: 10.1016/j.funbio.2010.01.003

Source DB:  PubMed          Journal:  Fungal Biol


  9 in total

1.  Molecular phylogeny of endophytic isolates of Ampelomyces from Iran based on rDNA ITS sequences.

Authors:  Samad Jamali
Journal:  Mol Biol Rep       Date:  2014-09-23       Impact factor: 2.316

2.  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.

Authors:  Márk Z Németh; Yuusaku Mizuno; Hiroki Kobayashi; Diána Seress; Naruki Shishido; Yutaka Kimura; Susumu Takamatsu; Tomoko Suzuki; Yoshihiro Takikawa; Koji Kakutani; Yoshinori Matsuda; Levente Kiss; Teruo Nonomura
Journal:  PLoS One       Date:  2021-05-11       Impact factor: 3.240

3.  Host phenology and geography as drivers of differentiation in generalist fungal mycoparasites.

Authors:  Alexandra Pintye; Jeanne Ropars; Nick Harvey; Hyeon-Dong Shin; Christel Leyronas; Philippe C Nicot; Tatiana Giraud; Levente Kiss
Journal:  PLoS One       Date:  2015-03-24       Impact factor: 3.240

4.  Morpho-Molecular Characterization of Two Ampelomyces spp. (Pleosporales) Strains Mycoparasites of Powdery Mildew of Hevea brasiliensis.

Authors:  Kapila K Liyanage; Sehroon Khan; Siraprapa Brooks; Peter E Mortimer; Samantha C Karunarathna; Jianchu Xu; Kevin D Hyde
Journal:  Front Microbiol       Date:  2018-01-19       Impact factor: 5.640

5.  Local adaptation at higher trophic levels: contrasting hyperparasite-pathogen infection dynamics in the field and laboratory.

Authors:  Steven R Parratt; Benoit Barrès; Rachel M Penczykowski; Anna-Liisa Laine
Journal:  Mol Ecol       Date:  2016-12-24       Impact factor: 6.185

Review 6.  Fungal evolution: major ecological adaptations and evolutionary transitions.

Authors:  Miguel A Naranjo-Ortiz; Toni Gabaldón
Journal:  Biol Rev Camb Philos Soc       Date:  2019-04-25

7.  The role of internal transcribed spacer 2 secondary structures in classifying mycoparasitic Ampelomyces.

Authors:  Rosa E Prahl; Shahjahan Khan; Ravinesh C Deo
Journal:  PLoS One       Date:  2021-06-30       Impact factor: 3.240

8.  A hyperparasite affects the population dynamics of a wild plant pathogen.

Authors:  C Tollenaere; B Pernechele; H S Mäkinen; S R Parratt; M Z Németh; G M Kovács; L Kiss; A J M Tack; A-L Laine
Journal:  Mol Ecol       Date:  2014-10-08       Impact factor: 6.185

9.  The "Bipartite" Structure of the First Genome of Ampelomyces quisqualis, a Common Hyperparasite and Biocontrol Agent of Powdery Mildews, May Point to Its Evolutionary Origin from Plant Pathogenic Fungi.

Authors:  Lauren Huth; Gavin J Ash; Alexander Idnurm; Levente Kiss; Niloofar Vaghefi
Journal:  Genome Biol Evol       Date:  2021-08-03       Impact factor: 3.416

  9 in total

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