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Filamentous Phytophthora Pathogens Deploy Effectors to Interfere With Bacterial Growth and Motility.

Identifieur interne : 000166 ( Main/Exploration ); précédent : 000165; suivant : 000167

Filamentous Phytophthora Pathogens Deploy Effectors to Interfere With Bacterial Growth and Motility.

Auteurs : Ji Wang [République populaire de Chine] ; Danyu Shen [République populaire de Chine] ; Chengcheng Ge [République populaire de Chine] ; Yaxin Du [République populaire de Chine] ; Long Lin [République populaire de Chine] ; Jin Liu [République populaire de Chine] ; Tian Bai [République populaire de Chine] ; Maofeng Jing [République populaire de Chine] ; Guoliang Qian [République populaire de Chine] ; Daolong Dou [République populaire de Chine]

Source :

RBID : pubmed:33101256

Abstract

Phytophthora comprises a group of filamentous plant pathogens that cause serious crop diseases worldwide. It is widely known that a complex effector repertoire was secreted by Phytophthora pathogens to manipulate plant immunity and determine resistance and susceptibility. It is also recognized that Phytophthora pathogens may inhabit natural niches within complex environmental microbes, including bacteria. However, how Phytophthora pathogens interact with their cohabited microbes remains poorly understood. Here, we present such an intriguing case by using Phytophthora-bacteria interaction as a working system. We found that under co-culture laboratory conditions, several Phytophthora pathogens appeared to block the contact of an ecologically relevant bacterium, including Pseudomonas fluorescence and a model bacterium, Escherichia coli. We further observed that Phytophthora sojae utilizes a conserved Crinkler (CRN) effector protein, PsCRN63, to impair bacterial growth. Phytophthora capsici deploys another CRN effector, PcCRN173, to interfere with bacterial flagellum- and/or type IV pilus-mediated motility whereas a P. capsici-derived RxLR effector, PcAvh540, inhibits bacterial swimming motility, but not twitching motility and biofilm formation, suggesting functional diversification of effector-mediated Phytophthora-bacteria interactions. Thus, our studies provide a first case showing that the filamentous Phytophthora pathogens could deploy effectors to interfere with bacterial growth and motility, revealing an unprecedented effector-mediated inter-kingdom interaction between Phytophthora pathogens and bacterial species and thereby uncovering ecological significance of effector proteins in filamentous plant pathogens besides their canonical roles involving pathogen-plant interaction.

DOI: 10.3389/fmicb.2020.581511
PubMed: 33101256
PubMed Central: PMC7554372


Affiliations:


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<div type="abstract" xml:lang="en">
<i>Phytophthora</i>
comprises a group of filamentous plant pathogens that cause serious crop diseases worldwide. It is widely known that a complex effector repertoire was secreted by
<i>Phytophthora</i>
pathogens to manipulate plant immunity and determine resistance and susceptibility. It is also recognized that
<i>Phytophthora</i>
pathogens may inhabit natural niches within complex environmental microbes, including bacteria. However, how
<i>Phytophthora</i>
pathogens interact with their cohabited microbes remains poorly understood. Here, we present such an intriguing case by using
<i>Phytophthora</i>
-bacteria interaction as a working system. We found that under co-culture laboratory conditions, several
<i>Phytophthora</i>
pathogens appeared to block the contact of an ecologically relevant bacterium, including
<i>Pseudomonas fluorescence</i>
and a model bacterium,
<i>Escherichia coli</i>
. We further observed that
<i>Phytophthora sojae</i>
utilizes a conserved Crinkler (CRN) effector protein, PsCRN63, to impair bacterial growth.
<i>Phytophthora capsici</i>
deploys another CRN effector, PcCRN173, to interfere with bacterial flagellum- and/or type IV pilus-mediated motility whereas a
<i>P. capsici</i>
-derived RxLR effector, PcAvh540, inhibits bacterial swimming motility, but not twitching motility and biofilm formation, suggesting functional diversification of effector-mediated
<i>Phytophthora</i>
-bacteria interactions. Thus, our studies provide a first case showing that the filamentous
<i>Phytophthora</i>
pathogens could deploy effectors to interfere with bacterial growth and motility, revealing an unprecedented effector-mediated inter-kingdom interaction between
<i>Phytophthora</i>
pathogens and bacterial species and thereby uncovering ecological significance of effector proteins in filamentous plant pathogens besides their canonical roles involving pathogen-plant interaction.</div>
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<i>Phytophthora</i>
comprises a group of filamentous plant pathogens that cause serious crop diseases worldwide. It is widely known that a complex effector repertoire was secreted by
<i>Phytophthora</i>
pathogens to manipulate plant immunity and determine resistance and susceptibility. It is also recognized that
<i>Phytophthora</i>
pathogens may inhabit natural niches within complex environmental microbes, including bacteria. However, how
<i>Phytophthora</i>
pathogens interact with their cohabited microbes remains poorly understood. Here, we present such an intriguing case by using
<i>Phytophthora</i>
-bacteria interaction as a working system. We found that under co-culture laboratory conditions, several
<i>Phytophthora</i>
pathogens appeared to block the contact of an ecologically relevant bacterium, including
<i>Pseudomonas fluorescence</i>
and a model bacterium,
<i>Escherichia coli</i>
. We further observed that
<i>Phytophthora sojae</i>
utilizes a conserved Crinkler (CRN) effector protein, PsCRN63, to impair bacterial growth.
<i>Phytophthora capsici</i>
deploys another CRN effector, PcCRN173, to interfere with bacterial flagellum- and/or type IV pilus-mediated motility whereas a
<i>P. capsici</i>
-derived RxLR effector, PcAvh540, inhibits bacterial swimming motility, but not twitching motility and biofilm formation, suggesting functional diversification of effector-mediated
<i>Phytophthora</i>
-bacteria interactions. Thus, our studies provide a first case showing that the filamentous
<i>Phytophthora</i>
pathogens could deploy effectors to interfere with bacterial growth and motility, revealing an unprecedented effector-mediated inter-kingdom interaction between
<i>Phytophthora</i>
pathogens and bacterial species and thereby uncovering ecological significance of effector proteins in filamentous plant pathogens besides their canonical roles involving pathogen-plant interaction.</AbstractText>
<CopyrightInformation>Copyright © 2020 Wang, Shen, Ge, Du, Lin, Liu, Bai, Jing, Qian and Dou.</CopyrightInformation>
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