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The ATP-dependent RNA helicase HrpB plays an important role in motility and biofilm formation in Xanthomonas citri subsp. citri

Identifieur interne : 000612 ( Pmc/Curation ); précédent : 000611; suivant : 000613

The ATP-dependent RNA helicase HrpB plays an important role in motility and biofilm formation in Xanthomonas citri subsp. citri

Auteurs : Laís Moreira Granato ; Simone Cristina Picchi ; Maxuel De Oliveira Andrade [États-Unis] ; Marco Aurélio Takita ; Alessandra Alves De Souza ; Nian Wang [États-Unis] ; Marcos Antonio Machado

Source :

RBID : PMC:4804567

Abstract

Background

RNA helicases are enzymes that catalyze the separation of double-stranded RNA (dsRNA) using the free energy of ATP binding and hydrolysis. DEAD/DEAH families participate in many different aspects of RNA metabolism, including RNA synthesis, RNA folding, RNA-RNA interactions, RNA localization and RNA degradation. Several important bacterial DEAD/DEAH-box RNA helicases have been extensively studied. In this study, we characterize the ATP-dependent RNA helicase encoded by the hrpB (XAC0293) gene using deletion and genetic complementation assays. We provide insights into the function of the hrpB gene in Xanthomonas citri subsp. citri by investigating the roles of hrpB in biofilm formation on abiotic surfaces and host leaves, cell motility, host virulence of the citrus canker bacterium and growth in planta.

Results

The hrpB gene is highly conserved in the sequenced strains of Xanthomonas. Mutation of the hrpB gene (∆hrpB) resulted in a significant reduction in biofilms on abiotic surfaces and host leaves. ∆hrpB also exhibited increased cell dispersion on solid medium plates. ∆hrpB showed reduced adhesion on biotic and abiotic surfaces and delayed development in disease symptoms when sprayed on susceptible citrus leaves. Quantitative reverse transcription-PCR assays indicated that deletion of hrpB reduced the expression of four type IV pili genes. The transcriptional start site of fimA (XAC3241) was determined using rapid amplification of 5′-cDNA Ends (5′RACE). Based on the results of fimA mRNA structure predictions, the fimA 5′ UTR may contain three different loops. HrpB may be involved in alterations to the structure of fimA mRNA that promote the stability of fimA RNA.

Conclusions

Our data show that hrpB is involved in adherence of Xanthomonas citri subsp. citri to different surfaces. In addition, to the best of our knowledge, this is the first time that a DEAH RNA helicase has been implicated in the regulation of type IV pili in Xanthomonas.

Electronic supplementary material

The online version of this article (doi:10.1186/s12866-016-0655-1) contains supplementary material, which is available to authorized users.


Url:
DOI: 10.1186/s12866-016-0655-1
PubMed: 27005008
PubMed Central: 4804567

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Laís Moreira Granato
<affiliation>
<nlm:aff id="Aff1">Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
</affiliation>
<affiliation>
<nlm:aff id="Aff2">Universidade Estadual de Campinas/UNICAMP, Instituto de Biologia, P.O. Box 6010, Campinas, SP 13083-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13083-970 Brazil</wicri:noCountry>
</affiliation>
Laís Moreira Granato
<affiliation>
<nlm:aff id="Aff2">Universidade Estadual de Campinas/UNICAMP, Instituto de Biologia, P.O. Box 6010, Campinas, SP 13083-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13083-970 Brazil</wicri:noCountry>
</affiliation>
Simone Cristina Picchi
<affiliation>
<nlm:aff id="Aff1">Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
</affiliation>
Marco Aurélio Takita
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<nlm:aff id="Aff1">Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
</affiliation>
Alessandra Alves De Souza
<affiliation>
<nlm:aff id="Aff1">Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
</affiliation>
Marcos Antonio Machado
<affiliation>
<nlm:aff id="Aff1">Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</nlm:aff>
<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
</affiliation>

Le document en format XML

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<title xml:lang="en" level="a" type="main">The ATP-dependent RNA helicase HrpB plays an important role in motility and biofilm formation in
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
</title>
<author>
<name sortKey="Granato, Lais Moreira" sort="Granato, Lais Moreira" uniqKey="Granato L" first="Laís Moreira" last="Granato">Laís Moreira Granato</name>
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<name sortKey="Picchi, Simone Cristina" sort="Picchi, Simone Cristina" uniqKey="Picchi S" first="Simone Cristina" last="Picchi">Simone Cristina Picchi</name>
<affiliation>
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<wicri:noCountry code="subfield">SP 13490-970 Brazil</wicri:noCountry>
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<author>
<name sortKey="Andrade, Maxuel De Oliveira" sort="Andrade, Maxuel De Oliveira" uniqKey="Andrade M" first="Maxuel De Oliveira" last="Andrade">Maxuel De Oliveira Andrade</name>
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<name sortKey="De Souza, Alessandra Alves" sort="De Souza, Alessandra Alves" uniqKey="De Souza A" first="Alessandra Alves" last="De Souza">Alessandra Alves De Souza</name>
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<name sortKey="Wang, Nian" sort="Wang, Nian" uniqKey="Wang N" first="Nian" last="Wang">Nian Wang</name>
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<affiliation>
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<div type="abstract" xml:lang="en">
<sec>
<title>Background</title>
<p>RNA helicases are enzymes that catalyze the separation of double-stranded RNA (dsRNA) using the free energy of ATP binding and hydrolysis. DEAD/DEAH families participate in many different aspects of RNA metabolism, including RNA synthesis, RNA folding, RNA-RNA interactions, RNA localization and RNA degradation. Several important bacterial DEAD/DEAH-box RNA helicases have been extensively studied. In this study, we characterize the ATP-dependent RNA helicase encoded by the
<italic>hrpB</italic>
(XAC0293) gene using deletion and genetic complementation assays. We provide insights into the function of the
<italic>hrpB</italic>
gene in
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
by investigating the roles of
<italic>hrpB</italic>
in biofilm formation on abiotic surfaces and host leaves, cell motility, host virulence of the citrus canker bacterium and growth
<italic>in planta</italic>
.</p>
</sec>
<sec>
<title>Results</title>
<p>The
<italic>hrpB</italic>
gene is highly conserved in the sequenced strains of
<italic>Xanthomonas</italic>
. Mutation of the
<italic>hrpB</italic>
gene (
<italic>∆hrpB</italic>
) resulted in a significant reduction in biofilms on abiotic surfaces and host leaves.
<italic>∆hrpB</italic>
also exhibited increased cell dispersion on solid medium plates.
<italic>∆hrpB</italic>
showed reduced adhesion on biotic and abiotic surfaces and delayed development in disease symptoms when sprayed on susceptible citrus leaves. Quantitative reverse transcription-PCR assays indicated that deletion of
<italic>hrpB</italic>
reduced the expression of four type IV pili genes. The transcriptional start site of
<italic>fimA</italic>
(XAC3241) was determined using rapid amplification of 5′-cDNA Ends (5′RACE). Based on the results of
<italic>fimA</italic>
mRNA structure predictions, the
<italic>fimA</italic>
5′ UTR may contain three different loops. HrpB may be involved in alterations to the structure of
<italic>fimA</italic>
mRNA that promote the stability of
<italic>fimA</italic>
RNA.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Our data show that
<italic>hrpB</italic>
is involved in adherence of
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
to different surfaces. In addition, to the best of our knowledge, this is the first time that a DEAH RNA helicase has been implicated in the regulation of type IV pili in
<italic>Xanthomonas</italic>
.</p>
</sec>
<sec>
<title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/s12866-016-0655-1) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
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<name sortKey="Sambrook, J" uniqKey="Sambrook J">J Sambrook</name>
</author>
<author>
<name sortKey="Fritsch, E" uniqKey="Fritsch E">E Fritsch</name>
</author>
<author>
<name sortKey="Maniatis, T" uniqKey="Maniatis T">T Maniatis</name>
</author>
</analytic>
</biblStruct>
<biblStruct></biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Souza, Dp" uniqKey="Souza D">DP Souza</name>
</author>
<author>
<name sortKey="Andrade, Mo" uniqKey="Andrade M">MO Andrade</name>
</author>
<author>
<name sortKey="Alvarez Martinez, Ce" uniqKey="Alvarez Martinez C">CE Alvarez-Martinez</name>
</author>
<author>
<name sortKey="Arantes, Gm" uniqKey="Arantes G">GM Arantes</name>
</author>
<author>
<name sortKey="Farah, Cs" uniqKey="Farah C">CS Farah</name>
</author>
<author>
<name sortKey="Salinas, Rk" uniqKey="Salinas R">RK Salinas</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Li, J" uniqKey="Li J">J Li</name>
</author>
<author>
<name sortKey="Wang, N" uniqKey="Wang N">N Wang</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">BMC Microbiol</journal-id>
<journal-id journal-id-type="iso-abbrev">BMC Microbiol</journal-id>
<journal-title-group>
<journal-title>BMC Microbiology</journal-title>
</journal-title-group>
<issn pub-type="epub">1471-2180</issn>
<publisher>
<publisher-name>BioMed Central</publisher-name>
<publisher-loc>London</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">27005008</article-id>
<article-id pub-id-type="pmc">4804567</article-id>
<article-id pub-id-type="publisher-id">655</article-id>
<article-id pub-id-type="doi">10.1186/s12866-016-0655-1</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Research Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>The ATP-dependent RNA helicase HrpB plays an important role in motility and biofilm formation in
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Granato</surname>
<given-names>Laís Moreira</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
<xref ref-type="aff" rid="Aff2"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Picchi</surname>
<given-names>Simone Cristina</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Andrade</surname>
<given-names>Maxuel de Oliveira</given-names>
</name>
<xref ref-type="aff" rid="Aff3"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Takita</surname>
<given-names>Marco Aurélio</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>de Souza</surname>
<given-names>Alessandra Alves</given-names>
</name>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Nian</given-names>
</name>
<xref ref-type="aff" rid="Aff3"></xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-9780-3990</contrib-id>
<name>
<surname>Machado</surname>
<given-names>Marcos Antonio</given-names>
</name>
<address>
<email>marcos@centrodecitricultura.br</email>
</address>
<xref ref-type="aff" rid="Aff1"></xref>
</contrib>
<aff id="Aff1">
<label></label>
Centro de Citricultura Sylvio Moreira/IAC, Rodovia Anhanguera Km 158, Cordeirópolis, SP 13490-970 Brazil</aff>
<aff id="Aff2">
<label></label>
Universidade Estadual de Campinas/UNICAMP, Instituto de Biologia, P.O. Box 6010, Campinas, SP 13083-970 Brazil</aff>
<aff id="Aff3">
<label></label>
Citrus Research and Educational Center, Department of Microbiology and Cell Science, University of Florida, IFAS, 700 Experiment Station Road, Lake Alfred, FL 33850 USA</aff>
</contrib-group>
<pub-date pub-type="epub">
<day>23</day>
<month>3</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>23</day>
<month>3</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="collection">
<year>2016</year>
</pub-date>
<volume>16</volume>
<elocation-id>55</elocation-id>
<history>
<date date-type="received">
<day>30</day>
<month>6</month>
<year>2015</year>
</date>
<date date-type="accepted">
<day>2</day>
<month>3</month>
<year>2016</year>
</date>
</history>
<permissions>
<copyright-statement>© Granato et al. 2016</copyright-statement>
<license license-type="OpenAccess">
<license-p>
<bold>Open Access</bold>
This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/publicdomain/zero/1.0/">http://creativecommons.org/publicdomain/zero/1.0/</ext-link>
) applies to the data made available in this article, unless otherwise stated.</license-p>
</license>
</permissions>
<abstract id="Abs1">
<sec>
<title>Background</title>
<p>RNA helicases are enzymes that catalyze the separation of double-stranded RNA (dsRNA) using the free energy of ATP binding and hydrolysis. DEAD/DEAH families participate in many different aspects of RNA metabolism, including RNA synthesis, RNA folding, RNA-RNA interactions, RNA localization and RNA degradation. Several important bacterial DEAD/DEAH-box RNA helicases have been extensively studied. In this study, we characterize the ATP-dependent RNA helicase encoded by the
<italic>hrpB</italic>
(XAC0293) gene using deletion and genetic complementation assays. We provide insights into the function of the
<italic>hrpB</italic>
gene in
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
by investigating the roles of
<italic>hrpB</italic>
in biofilm formation on abiotic surfaces and host leaves, cell motility, host virulence of the citrus canker bacterium and growth
<italic>in planta</italic>
.</p>
</sec>
<sec>
<title>Results</title>
<p>The
<italic>hrpB</italic>
gene is highly conserved in the sequenced strains of
<italic>Xanthomonas</italic>
. Mutation of the
<italic>hrpB</italic>
gene (
<italic>∆hrpB</italic>
) resulted in a significant reduction in biofilms on abiotic surfaces and host leaves.
<italic>∆hrpB</italic>
also exhibited increased cell dispersion on solid medium plates.
<italic>∆hrpB</italic>
showed reduced adhesion on biotic and abiotic surfaces and delayed development in disease symptoms when sprayed on susceptible citrus leaves. Quantitative reverse transcription-PCR assays indicated that deletion of
<italic>hrpB</italic>
reduced the expression of four type IV pili genes. The transcriptional start site of
<italic>fimA</italic>
(XAC3241) was determined using rapid amplification of 5′-cDNA Ends (5′RACE). Based on the results of
<italic>fimA</italic>
mRNA structure predictions, the
<italic>fimA</italic>
5′ UTR may contain three different loops. HrpB may be involved in alterations to the structure of
<italic>fimA</italic>
mRNA that promote the stability of
<italic>fimA</italic>
RNA.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Our data show that
<italic>hrpB</italic>
is involved in adherence of
<italic>Xanthomonas citri</italic>
subsp.
<italic>citri</italic>
to different surfaces. In addition, to the best of our knowledge, this is the first time that a DEAH RNA helicase has been implicated in the regulation of type IV pili in
<italic>Xanthomonas</italic>
.</p>
</sec>
<sec>
<title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/s12866-016-0655-1) contains supplementary material, which is available to authorized users.</p>
</sec>
</abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>RNA helicase</kwd>
<kwd>
<italic>Xanthomonas citri</italic>
</kwd>
<kwd>Biofilm</kwd>
<kwd>Citrus canker</kwd>
<kwd>Type IV pili</kwd>
</kwd-group>
<custom-meta-group>
<custom-meta>
<meta-name>issue-copyright-statement</meta-name>
<meta-value>© The Author(s) 2016</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
</record>

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