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    • Proszę używać tego identyfikatora do cytowań lub wstaw link do tej pozycji: http://hdl.handle.net/11320/17754
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    Pole DCWartośćJęzyk
    dc.contributor.authorMacioszek, Violetta Katarzyna-
    dc.contributor.authorGapińska, Magdalena-
    dc.contributor.authorZmienko, Agnieszka-
    dc.contributor.authorSobczak, Mirosław-
    dc.contributor.authorSkoczowski, Andrzej-
    dc.contributor.authorOliwa, Jakub-
    dc.contributor.authorKononowicz, Andrzej Kiejstut-
    dc.date.accessioned2024-12-17T08:17:20Z-
    dc.date.available2024-12-17T08:17:20Z-
    dc.date.issued2020-
    dc.identifier.citationCells 2020, Volume 9, Issue 10, p. 1-25pl
    dc.identifier.issn2073-4409-
    dc.identifier.urihttp://hdl.handle.net/11320/17754-
    dc.description.abstractBlack 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 (Fv/Fm), 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.pl
    dc.description.sponsorshipMinistry of Science and Higher Education, Grant No. N N302 3188 33 University of Bialystok, Poland.pl
    dc.description.sponsorshipNational Center of Research and Development, Grant No. ERA-CAPS II/1/2015pl
    dc.description.sponsorshipUniversity of Bialystok, Polandpl
    dc.language.isoenpl
    dc.publisherMDPIpl
    dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Międzynarodowe*
    dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
    dc.subjectAlternaria brassicicolapl
    dc.subjectchlorophyll a fluorescencepl
    dc.subjectchloroplast ultrastructurepl
    dc.subjectdefense responsepl
    dc.subjectmicroarraypl
    dc.subjectphotosynthesispl
    dc.subjectsusceptibilitypl
    dc.titleComplexity of Brassica oleracea–Alternaria brassicicola Susceptible Interaction Reveals Downregulation of Photosynthesis at Ultrastructural, Transcriptional, and Physiological Levelspl
    dc.typeArticlepl
    dc.rights.holder© 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) licensepl
    dc.identifier.doi10.3390/cells9102329-
    dc.description.EmailVioletta Katarzyna Macioszek: v.macioszek@uwb.edu.plpl
    dc.description.EmailMagdalena Gapińska: magdalena.gapinska@biol.uni.lodz.plpl
    dc.description.EmailAgnieszka Zmienko: akisiel@ibch.poznan.plpl
    dc.description.EmailMirosław Sobczak: miroslaw_sobczak@sggw.edu.plpl
    dc.description.EmailAndrzej Skoczowski: andrzej.skoczowski@up.krakow.plpl
    dc.description.EmailJakub Oliwa: jakub.oliwa@gmail.compl
    dc.description.EmailAndrzej Kiejstut Kononowicz: andrzej.kononowicz@biol.uni.lodz.plpl
    dc.description.AffiliationVioletta Katarzyna Macioszek - Laboratory of Plant Physiology, Department of Biology and Plant Ecology, Faculty of Biology, University of Bialystok, 15-245 Bialystok, Polandpl
    dc.description.AffiliationMagdalena Gapińska - Laboratory of Microscopy Imaging and Specialized Biological Techniques, Faculty of Biology and Environmental Protection, University of Lodz, 90-237 Lodz, Polandpl
    dc.description.AffiliationAgnieszka Zmienko - Department of Molecular and Systems Biology, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznan, Polandpl
    dc.description.AffiliationMirosław Sobczak - Department of Botany, Institute of Biology, Warsaw University of Life Sciences (SGGW), 02-787 Warsaw, Polandpl
    dc.description.AffiliationAndrzej Skoczowski - Institute of Biology, Pedagogical University in Krakow, 30-084 Krakow, Polandpl
    dc.description.AffiliationJakub Oliwa - Department of Chemistry and Biochemistry, Institute of Basic Sciences, University of Physical Education in Krakow, 31-571 Krakow, Polandpl
    dc.description.AffiliationAndrzej Kiejstut Kononowicz - Department of Plant Ecophysiology, Faculty of Biology and Environmental Protection, University of Lodz, 90-237 Lodz, Polandpl
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    dc.description.volume9pl
    dc.description.issue10pl
    dc.description.firstpage1pl
    dc.description.lastpage25pl
    dc.identifier.citation2Cellspl
    dc.identifier.orcid0000-0002-5143-4226-
    dc.identifier.orcid0000-0002-3125-7920-
    dc.identifier.orcid0000-0002-9128-7996-
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