Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici

The oomycete vegetable pathogen Phytophthora capsici causes significant losses of important vegetable crops worldwide. Calcium and other plant nutrients have been used in disease management of oomycete pathogens. Calcium homeostasis and signalling is essential for numerous biological processes, and...

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Main Authors: Peiqing Liu, jie gong, xueling ding, Yue Jiang, guoliang chen, benjin li, qiyong weng, Qinghe Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01236/full
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spelling doaj-b1648344edc9486b87ade36e9757c58a2020-11-24T23:21:12ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2016-08-01710.3389/fmicb.2016.01236210241Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsiciPeiqing Liu0jie gong1xueling ding2Yue Jiang3guoliang chen4benjin li5qiyong weng6Qinghe Chen7Fujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesFujian Academy of Agricultural SciencesThe oomycete vegetable pathogen Phytophthora capsici causes significant losses of important vegetable crops worldwide. Calcium and other plant nutrients have been used in disease management of oomycete pathogens. Calcium homeostasis and signalling is essential for numerous biological processes, and Ca2+ channel blockers prevent excessive Ca2+ influx into the fungal cell. However, it is not known whether voltage-gated Ca2+ channel blockers improve control over oomycete pathogens. In the present study, we compared the inhibitory effects of CaCl2 and the extracellular Ca2+ chelator EDTA on mycelial growth and found that calcium assimilation plays a key role in P. capsici mycelial growth. Next, we involved the voltage-gated Ca2+ channel blockers verapamil (VP) and nifedipine (NFD) to analyse the effect of Ca2+ channel blockers on mycelial growth and sporulation; the results suggested that NFD, but not VP, caused significant inhibition. Ion rescue in an NFD-induced inhibition assay suggested that NFD-induced inhibition is calcium-dependent. In addition, NFD increased P. capsici sensitivity to H2O2 in a calcium-dependent manner, and extracellular calcium rescued it. Furthermore, NFD inhibited the virulence and gene expression related to its pathogenicity. These results suggest that NFD inhibits mycelial growth, sporulation, and virulence of P. capsici.http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01236/fullNifedipineVirulenceH2O2Phytophthora capsicicalcium rescue
collection DOAJ
language English
format Article
sources DOAJ
author Peiqing Liu
jie gong
xueling ding
Yue Jiang
guoliang chen
benjin li
qiyong weng
Qinghe Chen
spellingShingle Peiqing Liu
jie gong
xueling ding
Yue Jiang
guoliang chen
benjin li
qiyong weng
Qinghe Chen
Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
Frontiers in Microbiology
Nifedipine
Virulence
H2O2
Phytophthora capsici
calcium rescue
author_facet Peiqing Liu
jie gong
xueling ding
Yue Jiang
guoliang chen
benjin li
qiyong weng
Qinghe Chen
author_sort Peiqing Liu
title Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
title_short Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
title_full Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
title_fullStr Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
title_full_unstemmed Title: The L-type Ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of Phytophthora capsici
title_sort title: the l-type ca2+ channel blocker nifedipine inhibits mycelial growth, sporulation, and virulence of phytophthora capsici
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2016-08-01
description The oomycete vegetable pathogen Phytophthora capsici causes significant losses of important vegetable crops worldwide. Calcium and other plant nutrients have been used in disease management of oomycete pathogens. Calcium homeostasis and signalling is essential for numerous biological processes, and Ca2+ channel blockers prevent excessive Ca2+ influx into the fungal cell. However, it is not known whether voltage-gated Ca2+ channel blockers improve control over oomycete pathogens. In the present study, we compared the inhibitory effects of CaCl2 and the extracellular Ca2+ chelator EDTA on mycelial growth and found that calcium assimilation plays a key role in P. capsici mycelial growth. Next, we involved the voltage-gated Ca2+ channel blockers verapamil (VP) and nifedipine (NFD) to analyse the effect of Ca2+ channel blockers on mycelial growth and sporulation; the results suggested that NFD, but not VP, caused significant inhibition. Ion rescue in an NFD-induced inhibition assay suggested that NFD-induced inhibition is calcium-dependent. In addition, NFD increased P. capsici sensitivity to H2O2 in a calcium-dependent manner, and extracellular calcium rescued it. Furthermore, NFD inhibited the virulence and gene expression related to its pathogenicity. These results suggest that NFD inhibits mycelial growth, sporulation, and virulence of P. capsici.
topic Nifedipine
Virulence
H2O2
Phytophthora capsici
calcium rescue
url http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01236/full
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