Cargando…

Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels

Black spot disease, caused by Alternaria brassicicola in Brassica species, is one of the most devastating diseases all over the world, especially since there is no known fully resistant Brassica cultivar. In this study, the visualization of black spot disease development on Brassica oleracea var. ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Macioszek, Violetta Katarzyna, Gapińska, Magdalena, Zmienko, Agnieszka, Sobczak, Mirosław, Skoczowski, Andrzej, Oliwa, Jakub, Kononowicz, Andrzej Kiejstut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593931/
https://www.ncbi.nlm.nih.gov/pubmed/33092216
http://dx.doi.org/10.3390/cells9102329
_version_ 1783601509155471360
author Macioszek, Violetta Katarzyna
Gapińska, Magdalena
Zmienko, Agnieszka
Sobczak, Mirosław
Skoczowski, Andrzej
Oliwa, Jakub
Kononowicz, Andrzej Kiejstut
author_facet Macioszek, Violetta Katarzyna
Gapińska, Magdalena
Zmienko, Agnieszka
Sobczak, Mirosław
Skoczowski, Andrzej
Oliwa, Jakub
Kononowicz, Andrzej Kiejstut
author_sort Macioszek, Violetta Katarzyna
collection PubMed
description Black spot disease, caused by Alternaria brassicicola in Brassica species, is one of the most devastating diseases all over the world, especially since there is no known fully resistant Brassica cultivar. In this study, the visualization of black spot disease development on Brassica oleracea var. capitata f. alba (white cabbage) leaves and subsequent ultrastructural, molecular and physiological investigations were conducted. Inter- and intracellular hyphae growth within leaf tissues led to the loss of host cell integrity and various levels of organelle disintegration. Severe symptoms of chloroplast damage included the degeneration of chloroplast envelope and grana, and the loss of electron denseness by stroma at the advanced stage of infection. Transcriptional profiling of infected leaves revealed that photosynthesis was the most negatively regulated biological process. However, in infected leaves, chlorophyll and carotenoid content did not decrease until 48 hpi, and several chlorophyll a fluorescence parameters, such as photosystem II quantum yield (F(v)/F(m)), non-photochemical quenching (NPQ), or plant vitality parameter (Rdf) decreased significantly at 24 and 48 hpi compared to control leaves. Our results indicate that the initial stages of interaction between B. oleracea and A. brassicicola are not uniform within an inoculation site and show a complexity of host responses and fungal attempts to overcome host cell defense mechanisms. The downregulation of photosynthesis at the early stage of this susceptible interaction suggests that it may be a part of a host defense strategy, or, alternatively, that chloroplasts are targets for the unknown virulence factor(s) of A. brassicicola. However, the observed decrease of photosynthetic efficiency at the later stages of infection is a result of the fungus-induced necrotic lesion expansion.
format Online
Article
Text
id pubmed-7593931
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-75939312020-10-30 Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels Macioszek, Violetta Katarzyna Gapińska, Magdalena Zmienko, Agnieszka Sobczak, Mirosław Skoczowski, Andrzej Oliwa, Jakub Kononowicz, Andrzej Kiejstut Cells Article Black spot disease, caused by Alternaria brassicicola in Brassica species, is one of the most devastating diseases all over the world, especially since there is no known fully resistant Brassica cultivar. In this study, the visualization of black spot disease development on Brassica oleracea var. capitata f. alba (white cabbage) leaves and subsequent ultrastructural, molecular and physiological investigations were conducted. Inter- and intracellular hyphae growth within leaf tissues led to the loss of host cell integrity and various levels of organelle disintegration. Severe symptoms of chloroplast damage included the degeneration of chloroplast envelope and grana, and the loss of electron denseness by stroma at the advanced stage of infection. Transcriptional profiling of infected leaves revealed that photosynthesis was the most negatively regulated biological process. However, in infected leaves, chlorophyll and carotenoid content did not decrease until 48 hpi, and several chlorophyll a fluorescence parameters, such as photosystem II quantum yield (F(v)/F(m)), non-photochemical quenching (NPQ), or plant vitality parameter (Rdf) decreased significantly at 24 and 48 hpi compared to control leaves. Our results indicate that the initial stages of interaction between B. oleracea and A. brassicicola are not uniform within an inoculation site and show a complexity of host responses and fungal attempts to overcome host cell defense mechanisms. The downregulation of photosynthesis at the early stage of this susceptible interaction suggests that it may be a part of a host defense strategy, or, alternatively, that chloroplasts are targets for the unknown virulence factor(s) of A. brassicicola. However, the observed decrease of photosynthetic efficiency at the later stages of infection is a result of the fungus-induced necrotic lesion expansion. MDPI 2020-10-20 /pmc/articles/PMC7593931/ /pubmed/33092216 http://dx.doi.org/10.3390/cells9102329 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Macioszek, Violetta Katarzyna
Gapińska, Magdalena
Zmienko, Agnieszka
Sobczak, Mirosław
Skoczowski, Andrzej
Oliwa, Jakub
Kononowicz, Andrzej Kiejstut
Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title_full Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title_fullStr Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title_full_unstemmed Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title_short Complexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levels
title_sort complexity of brassica oleracea–alternaria brassicicola susceptible interaction reveals downregulation of photosynthesis at ultrastructural, transcriptional, and physiological levels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7593931/
https://www.ncbi.nlm.nih.gov/pubmed/33092216
http://dx.doi.org/10.3390/cells9102329
work_keys_str_mv AT macioszekviolettakatarzyna complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT gapinskamagdalena complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT zmienkoagnieszka complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT sobczakmirosław complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT skoczowskiandrzej complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT oliwajakub complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels
AT kononowiczandrzejkiejstut complexityofbrassicaoleraceaalternariabrassicicolasusceptibleinteractionrevealsdownregulationofphotosynthesisatultrastructuraltranscriptionalandphysiologicallevels