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PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica

Phytophthora parasitica is a notorious oomycete pathogen that causes severe disease in a wide variety of crop species. Infection of plants involves mainly its asexual life stage, including papillate sporangia and biflagellated zoospores, which are the primary dispersal and infection agents of this p...

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Autores principales: Hwu, Fang-Yu, Lai, Ming-Wei, Liou, Ruey-Fen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395580/
https://www.ncbi.nlm.nih.gov/pubmed/28469602
http://dx.doi.org/10.3389/fmicb.2017.00610
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author Hwu, Fang-Yu
Lai, Ming-Wei
Liou, Ruey-Fen
author_facet Hwu, Fang-Yu
Lai, Ming-Wei
Liou, Ruey-Fen
author_sort Hwu, Fang-Yu
collection PubMed
description Phytophthora parasitica is a notorious oomycete pathogen that causes severe disease in a wide variety of crop species. Infection of plants involves mainly its asexual life stage, including papillate sporangia and biflagellated zoospores, which are the primary dispersal and infection agents of this pathogen. Calcium signaling has been thought as the key regulator for sporangium formation and zoospore differentiation. However, not much is known about the molecular players involved in these processes. In Saccharomyces cerevisiae, mating pheromone-induced death 1 (MID1) encodes a component of a putative calcium channel. Here, we identified and characterized the function of PpMID1, an MID1 homolog from P. parasitica. The expression of PpMID1 was high in sporangia. Gene silencing of PpMID1 resulted in the formation of sporangia that lacked papilla and showed a tendency for direct germination. Notably, in response to cold shock to induce zoospore formation, these sporangia showed no sign of cytoplasmic cleavage and thereby failed to form zoospores. Nonetheless, the addition of CaCl(2) or MgCl(2) partially recovered the silenced sporangia phenotype, with the formation of papillate sporangia similar to those of the wild type and the release of zoospores upon cold shock. As well, virulence toward Nicotiana benthamiana was reduced in the PpMID1-silenced transformants. These results indicate a role of PpMID1 in the asexual development and virulence of P. parasitica.
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spelling pubmed-53955802017-05-03 PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica Hwu, Fang-Yu Lai, Ming-Wei Liou, Ruey-Fen Front Microbiol Microbiology Phytophthora parasitica is a notorious oomycete pathogen that causes severe disease in a wide variety of crop species. Infection of plants involves mainly its asexual life stage, including papillate sporangia and biflagellated zoospores, which are the primary dispersal and infection agents of this pathogen. Calcium signaling has been thought as the key regulator for sporangium formation and zoospore differentiation. However, not much is known about the molecular players involved in these processes. In Saccharomyces cerevisiae, mating pheromone-induced death 1 (MID1) encodes a component of a putative calcium channel. Here, we identified and characterized the function of PpMID1, an MID1 homolog from P. parasitica. The expression of PpMID1 was high in sporangia. Gene silencing of PpMID1 resulted in the formation of sporangia that lacked papilla and showed a tendency for direct germination. Notably, in response to cold shock to induce zoospore formation, these sporangia showed no sign of cytoplasmic cleavage and thereby failed to form zoospores. Nonetheless, the addition of CaCl(2) or MgCl(2) partially recovered the silenced sporangia phenotype, with the formation of papillate sporangia similar to those of the wild type and the release of zoospores upon cold shock. As well, virulence toward Nicotiana benthamiana was reduced in the PpMID1-silenced transformants. These results indicate a role of PpMID1 in the asexual development and virulence of P. parasitica. Frontiers Media S.A. 2017-04-19 /pmc/articles/PMC5395580/ /pubmed/28469602 http://dx.doi.org/10.3389/fmicb.2017.00610 Text en Copyright © 2017 Hwu, Lai and Liou. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hwu, Fang-Yu
Lai, Ming-Wei
Liou, Ruey-Fen
PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title_full PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title_fullStr PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title_full_unstemmed PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title_short PpMID1 Plays a Role in the Asexual Development and Virulence of Phytophthora parasitica
title_sort ppmid1 plays a role in the asexual development and virulence of phytophthora parasitica
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395580/
https://www.ncbi.nlm.nih.gov/pubmed/28469602
http://dx.doi.org/10.3389/fmicb.2017.00610
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