Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula

Ascochyta (Mycosphaerella) blight on cultivated peas is primarily caused by infection through asexual spores (pycnospores) of Mycosphaerella pinodes (Berk. et Blox.) Vestergren [recently renamed Peyronellaea pinodes (Berk. & A. Bloxam) Aveskamp, Gruyter & Verkley]. Using a model path...

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Main Authors: Tomoko Suzuki, Aya Maeda, Masaya Hirose, Yuki Ichinose, Tomonori Shiraishi, Kazuhiro Toyoda
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-06-01
Series:Frontiers in Plant Science
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fpls.2017.01132/full
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spelling doaj-a1637afaeb2249928916fd68d99ba24c2020-11-24T22:42:40ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2017-06-01810.3389/fpls.2017.01132269291Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatulaTomoko Suzuki0Tomoko Suzuki1Aya Maeda2Masaya Hirose3Yuki Ichinose4Tomonori Shiraishi5Kazuhiro Toyoda6Laboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanFaculty of Science, Japan Women’s UniversityBunkyo-ku, JapanLaboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanLaboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanLaboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanLaboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanLaboratory of Plant Pathology and Genetic Engineering, Graduate School of Environmental and Life Science, Okayama UniversityOkayama, JapanAscochyta (Mycosphaerella) blight on cultivated peas is primarily caused by infection through asexual spores (pycnospores) of Mycosphaerella pinodes (Berk. et Blox.) Vestergren [recently renamed Peyronellaea pinodes (Berk. & A. Bloxam) Aveskamp, Gruyter & Verkley]. Using a model pathosystem involving Medicago truncatula and Mycosphaerella pinodes strain OMP-1, we examined the histology and ultrastructure of early infection events and fungal development including penetration by appressoria, vegetative growth of infection hyphae, and host responses. On the susceptible ecotype R108-1, pycnospores germinated and grew over the surface of the epidermis, then formed an appressoria and penetrated the cuticle. Beneath the cuticle, the infection peg expanded into a hyphae that grew within the outer wall of the epidermis. Subsequently, the hyphae penetrated down within mesophyll cells and proliferated vigorously, eventually, forming asexual fruiting bodies (pycnidia). In contrast, successful penetration and subsequent growth of infection hyphae were considerably restricted in the ecotype Caliph. Detected by its reaction with cerium chloride (CeCl3) to generate electron-dense cerium perhydroxides in transmission electron micrographs, hydrogen peroxide (H2O2) accumulated in epidermal and mesophyll cells of Caliph challenged with pycnospores of M. pinodes. This intracellular localization was confirmed by energy-dispersive X-ray spectroscopy. Our observations thus indicate that the oxidative burst reaction leading to the generation of reactive oxygen species is associated with a local host defense response in Caliph, since no clear H2O2 accumulation was detectable in susceptible R108-1. Indeed, aberrant hyphae such as intrahyphal hyphae and dead hyphae, probably due to a local defense elicited by the fungus, were abundant in Caliph but not in R108-1. Our results on the cellular interactions between the fungus and host cells provide additional insights to understand foliar infection by M. pinodes on cultivated peas.http://journal.frontiersin.org/article/10.3389/fpls.2017.01132/fulltransmission electron microscopy (TEM)disease resistanceenergy-dispersive X-ray (EDX) spectroscopyhydrogen peroxide (H2O2)intrahyphal hyphaesusceptibility
collection DOAJ
language English
format Article
sources DOAJ
author Tomoko Suzuki
Tomoko Suzuki
Aya Maeda
Masaya Hirose
Yuki Ichinose
Tomonori Shiraishi
Kazuhiro Toyoda
spellingShingle Tomoko Suzuki
Tomoko Suzuki
Aya Maeda
Masaya Hirose
Yuki Ichinose
Tomonori Shiraishi
Kazuhiro Toyoda
Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
Frontiers in Plant Science
transmission electron microscopy (TEM)
disease resistance
energy-dispersive X-ray (EDX) spectroscopy
hydrogen peroxide (H2O2)
intrahyphal hyphae
susceptibility
author_facet Tomoko Suzuki
Tomoko Suzuki
Aya Maeda
Masaya Hirose
Yuki Ichinose
Tomonori Shiraishi
Kazuhiro Toyoda
author_sort Tomoko Suzuki
title Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
title_short Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
title_full Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
title_fullStr Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
title_full_unstemmed Ultrastructural and Cytological Studies on Mycosphaerella pinodes Infection of the Model Legume Medicago truncatula
title_sort ultrastructural and cytological studies on mycosphaerella pinodes infection of the model legume medicago truncatula
publisher Frontiers Media S.A.
series Frontiers in Plant Science
issn 1664-462X
publishDate 2017-06-01
description Ascochyta (Mycosphaerella) blight on cultivated peas is primarily caused by infection through asexual spores (pycnospores) of Mycosphaerella pinodes (Berk. et Blox.) Vestergren [recently renamed Peyronellaea pinodes (Berk. & A. Bloxam) Aveskamp, Gruyter & Verkley]. Using a model pathosystem involving Medicago truncatula and Mycosphaerella pinodes strain OMP-1, we examined the histology and ultrastructure of early infection events and fungal development including penetration by appressoria, vegetative growth of infection hyphae, and host responses. On the susceptible ecotype R108-1, pycnospores germinated and grew over the surface of the epidermis, then formed an appressoria and penetrated the cuticle. Beneath the cuticle, the infection peg expanded into a hyphae that grew within the outer wall of the epidermis. Subsequently, the hyphae penetrated down within mesophyll cells and proliferated vigorously, eventually, forming asexual fruiting bodies (pycnidia). In contrast, successful penetration and subsequent growth of infection hyphae were considerably restricted in the ecotype Caliph. Detected by its reaction with cerium chloride (CeCl3) to generate electron-dense cerium perhydroxides in transmission electron micrographs, hydrogen peroxide (H2O2) accumulated in epidermal and mesophyll cells of Caliph challenged with pycnospores of M. pinodes. This intracellular localization was confirmed by energy-dispersive X-ray spectroscopy. Our observations thus indicate that the oxidative burst reaction leading to the generation of reactive oxygen species is associated with a local host defense response in Caliph, since no clear H2O2 accumulation was detectable in susceptible R108-1. Indeed, aberrant hyphae such as intrahyphal hyphae and dead hyphae, probably due to a local defense elicited by the fungus, were abundant in Caliph but not in R108-1. Our results on the cellular interactions between the fungus and host cells provide additional insights to understand foliar infection by M. pinodes on cultivated peas.
topic transmission electron microscopy (TEM)
disease resistance
energy-dispersive X-ray (EDX) spectroscopy
hydrogen peroxide (H2O2)
intrahyphal hyphae
susceptibility
url http://journal.frontiersin.org/article/10.3389/fpls.2017.01132/full
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