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Responses of different geographic populations of two potato tuber moth species to genetic variants of Phthorimaea operculella granulovirus

Identifieur interne : 000721 ( Istex/Corpus ); précédent : 000720; suivant : 000722

Responses of different geographic populations of two potato tuber moth species to genetic variants of Phthorimaea operculella granulovirus

Auteurs : Jean-Louis Zeddam ; Xavier Léry ; Yannery G Mez-Bonilla ; Carlos Espinel-Correal ; David Páez ; François Rebaudo ; Miguel L Pez-Ferber

Source :

RBID : ISTEX:4896240E6EEC105278D1CAB8FA55E932129599EA

English descriptors

Abstract

Phthorimaea operculella granulovirus (PhopGV) belongs to the genus Betabaculovirus of the arthropod‐infecting Baculoviridae. PhopGV is able to infect several gelechiid species. Among them are the potato tuber moths Phthorimaea operculella Zeller and Tecia solanivora Povolny (both Lepidoptera: Gelechiidae). In various South American countries, PhopGV‐based biopesticides are used to control either P. operculella or T. solanivora. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various PhopGV isolates and various populations of P. operculella and T. solanivora. Virus isolates from P. operculella were more pathogenic against their original host species than against T. solanivora. A PhopGV isolated from T. solanivora was less efficient against P. operculella. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same PhopGV isolate. This was the case for both host species and for five PhopGV isolates. Comparative restriction fragment length polymorphism (RFLP) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of PhopGV, corresponding to the regions of open reading frame PhopGV046, gene PhopGV129 (egt), and repeat 9 (located between open reading frames PhopGV083 and PhopGV084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate, JLZ9f. The results are discussed in the context of the production and use of PhopGV as a biological agent against these two pest species.

Url:
DOI: 10.1111/eea.12115

Links to Exploration step

ISTEX:4896240E6EEC105278D1CAB8FA55E932129599EA

Le document en format XML

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<div type="abstract">Phthorimaea operculella granulovirus (PhopGV) belongs to the genus Betabaculovirus of the arthropod‐infecting Baculoviridae. PhopGV is able to infect several gelechiid species. Among them are the potato tuber moths Phthorimaea operculella Zeller and Tecia solanivora Povolny (both Lepidoptera: Gelechiidae). In various South American countries, PhopGV‐based biopesticides are used to control either P. operculella or T. solanivora. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various PhopGV isolates and various populations of P. operculella and T. solanivora. Virus isolates from P. operculella were more pathogenic against their original host species than against T. solanivora. A PhopGV isolated from T. solanivora was less efficient against P. operculella. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same PhopGV isolate. This was the case for both host species and for five PhopGV isolates. Comparative restriction fragment length polymorphism (RFLP) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of PhopGV, corresponding to the regions of open reading frame PhopGV046, gene PhopGV129 (egt), and repeat 9 (located between open reading frames PhopGV083 and PhopGV084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate, JLZ9f. The results are discussed in the context of the production and use of PhopGV as a biological agent against these two pest species.</div>
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<abstract>Phthorimaea operculella granulovirus (PhopGV) belongs to the genus Betabaculovirus of the arthropod‐infecting Baculoviridae. PhopGV is able to infect several gelechiid species. Among them are the potato tuber moths Phthorimaea operculella Zeller and Tecia solanivora Povolny (both Lepidoptera: Gelechiidae). In various South American countries, PhopGV‐based biopesticides are used to control either P. operculella or T. solanivora. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various PhopGV isolates and various populations of P. operculella and T. solanivora. Virus isolates from P. operculella were more pathogenic against their original host species than against T. solanivora. A PhopGV isolated from T. solanivora was less efficient against P. operculella. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same PhopGV isolate. This was the case for both host species and for five PhopGV isolates. Comparative restriction fragment length polymorphism (RFLP) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of PhopGV, corresponding to the regions of open reading frame PhopGV046, gene PhopGV129 (egt), and repeat 9 (located between open reading frames PhopGV083 and PhopGV084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate, JLZ9f. The results are discussed in the context of the production and use of PhopGV as a biological agent against these two pest species.</abstract>
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hthorimaea operculella granulovirus</hi>
(Phop
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) belongs to the genus
<hi rend="italic">
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etabaculovirus</hi>
of the arthropod‐infecting
<hi rend="fc">B</hi>
aculoviridae. Phop
<hi rend="fc">GV</hi>
is able to infect several gelechiid species. Among them are the potato tuber moths
<hi rend="italic">
<hi rend="fc">P</hi>
hthorimaea operculella </hi>
<hi rend="fc">Z</hi>
eller and
<hi rend="italic">
<hi rend="fc">T</hi>
ecia solanivora </hi>
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ovolny (both
<hi rend="fc">L</hi>
epidoptera:
<hi rend="fc">G</hi>
elechiidae). In various
<hi rend="fc">S</hi>
outh
<hi rend="fc">A</hi>
merican countries, Phop
<hi rend="fc">GV</hi>
‐based biopesticides are used to control either
<hi rend="italic">
<hi rend="fc">P</hi>
. operculella</hi>
or
<hi rend="italic">
<hi rend="fc">T</hi>
. solanivora</hi>
. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various Phop
<hi rend="fc">GV</hi>
isolates and various populations of
<hi rend="italic">
<hi rend="fc">P</hi>
. operculella</hi>
and
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. solanivora</hi>
. Virus isolates from
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. operculella</hi>
were more pathogenic against their original host species than against
<hi rend="italic">
<hi rend="fc">T</hi>
. solanivora</hi>
. A Phop
<hi rend="fc">GV</hi>
isolated from
<hi rend="italic">
<hi rend="fc">T</hi>
. solanivora</hi>
was less efficient against
<hi rend="italic">
<hi rend="fc">P</hi>
. operculella</hi>
. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same Phop
<hi rend="fc">GV</hi>
isolate. This was the case for both host species and for five Phop
<hi rend="fc">GV</hi>
isolates. Comparative restriction fragment length polymorphism (
<hi rend="fc">RFLP</hi>
) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of Phop
<hi rend="fc">GV</hi>
, corresponding to the regions of open reading frame Phop
<hi rend="fc">GV</hi>
046, gene
<hi rend="italic">Phop
<hi rend="fc">GV</hi>
129</hi>
(
<hi rend="italic">egt</hi>
), and repeat 9 (located between open reading frames Phop
<hi rend="fc">GV</hi>
083 and Phop
<hi rend="fc">GV</hi>
084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate,
<hi rend="fc">JLZ</hi>
9f. The results are discussed in the context of the production and use of Phop
<hi rend="fc">GV</hi>
as a biological agent against these two pest species.</p>
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<correspondenceTo>Correspondence and present address: Jean‐Louis Zeddam, IRD‐DER, 911, Avenue Agropolis, BP 64501, Montpellier 34394, France. E‐mail:
<email>jean-louis.zeddam@ird.fr</email>
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<contentMeta>
<titleGroup>
<title type="main">Responses of different geographic populations of two potato tuber moth species to genetic variants of
<i>
<fc>P</fc>
hthorimaea operculella granulovirus</i>
</title>
<title type="shortAuthors">
<i>Zeddam</i>
et al.</title>
</titleGroup>
<creators>
<creator affiliationRef="#eea12115-aff-0001 #eea12115-aff-0002" corresponding="yes" creatorRole="author" noteRef="#eea12115-note-0001" xml:id="eea12115-cr-0001">
<personName>
<givenNames>Jean‐Louis</givenNames>
<familyName>Zeddam</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0002 #eea12115-aff-0003" creatorRole="author" noteRef="#eea12115-note-0001" xml:id="eea12115-cr-0002">
<personName>
<givenNames>Xavier</givenNames>
<familyName>Léry</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0004" creatorRole="author" xml:id="eea12115-cr-0003">
<personName>
<givenNames>Yannery</givenNames>
<familyName>Gómez‐Bonilla</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0005" creatorRole="author" xml:id="eea12115-cr-0004">
<personName>
<givenNames>Carlos</givenNames>
<familyName>Espinel‐Correal</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0001" creatorRole="author" xml:id="eea12115-cr-0005">
<personName>
<givenNames>David</givenNames>
<familyName>Páez</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0001 #eea12115-aff-0002" creatorRole="author" xml:id="eea12115-cr-0006">
<personName>
<givenNames>François</givenNames>
<familyName>Rebaudo</familyName>
</personName>
</creator>
<creator affiliationRef="#eea12115-aff-0006" creatorRole="author" xml:id="eea12115-cr-0007">
<personName>
<givenNames>Miguel</givenNames>
<familyName>López‐Ferber</familyName>
</personName>
</creator>
</creators>
<affiliationGroup>
<affiliation countryCode="EC" type="organization" xml:id="eea12115-aff-0001">
<orgDiv>Pontificia Universidad Católica del Ecuador</orgDiv>
<orgName>Facultad de Ciencias Naturales y Biológicas</orgName>
<address>
<city>Quito</city>
<country>Ecuador</country>
</address>
</affiliation>
<affiliation countryCode="FR" type="organization" xml:id="eea12115-aff-0002">
<orgDiv>IRD</orgDiv>
<orgDiv>Institut de Recherche pour le Développement</orgDiv>
<orgDiv>Laboratoire Evolution</orgDiv>
<orgDiv>Génomes et Spéciation</orgDiv>
<orgDiv>Centre National de la Recherche Scientifique (CNRS)</orgDiv>
<orgName>UR 072</orgName>
<orgName>UPR 9034</orgName>
<address>
<street>91198 Gif‐sur‐Yvette Cedex, France; et Université Paris‐Sud 11</street>
<city>Orsay Cedex</city>
<postCode>91405</postCode>
<country>France</country>
</address>
</affiliation>
<affiliation countryCode="FR" type="organization" xml:id="eea12115-aff-0003">
<orgDiv>Centre de Recherche</orgDiv>
<orgDiv>IRD</orgDiv>
<orgName>UR072</orgName>
<address>
<city>Saint‐Christol‐les‐Alès</city>
<postCode>30380</postCode>
<country>France</country>
</address>
</affiliation>
<affiliation countryCode="CR" type="organization" xml:id="eea12115-aff-0004">
<orgName>Instituto National de Investigación y Transferencia de Technología Agropecuaria (INTA)</orgName>
<address>
<city>San José</city>
<country>Costa Rica</country>
</address>
</affiliation>
<affiliation countryCode="CO" type="organization" xml:id="eea12115-aff-0005">
<orgDiv>Centro de Biotecnología y Bioindustria</orgDiv>
<orgName>CORPOICA</orgName>
<address>
<street>km 14 vía Mosquera</street>
<city>Cundinamarca</city>
<country>Colombia</country>
</address>
</affiliation>
<affiliation countryCode="FR" type="organization" xml:id="eea12115-aff-0006">
<orgDiv>Ecole des Mines d'Alès</orgDiv>
<orgName>Centre LGEI</orgName>
<address>
<street>6 Avenue de Clavières</street>
<city>Alès</city>
<postCode>30100</postCode>
<country>France</country>
</address>
</affiliation>
</affiliationGroup>
<keywordGroup type="author">
<keyword xml:id="eea12115-kwd-0001">
<i>
<fc>B</fc>
etabaculovirus</i>
</keyword>
<keyword xml:id="eea12115-kwd-0002">insect virus</keyword>
<keyword xml:id="eea12115-kwd-0003">bioassay</keyword>
<keyword xml:id="eea12115-kwd-0004">pathogenicity</keyword>
<keyword xml:id="eea12115-kwd-0005">viral variant</keyword>
<keyword xml:id="eea12115-kwd-0006">
<i>
<fc>T</fc>
ecia solanivora</i>
</keyword>
<keyword xml:id="eea12115-kwd-0007">
<fc>L</fc>
epidoptera</keyword>
<keyword xml:id="eea12115-kwd-0008">
<fc>G</fc>
elechiidae</keyword>
<keyword xml:id="eea12115-kwd-0009">Phop
<fc>GV</fc>
</keyword>
<keyword xml:id="eea12115-kwd-0010">
<fc>B</fc>
aculoviridae</keyword>
</keywordGroup>
<fundingInfo>
<fundingAgency>McKnight Foundation's Collaborative Crop Research Program</fundingAgency>
</fundingInfo>
<abstractGroup>
<abstract type="main" xml:id="eea12115-abs-0001">
<title type="main">Abstract</title>
<p>
<i>
<fc>P</fc>
hthorimaea operculella granulovirus</i>
(Phop
<fc>GV</fc>
) belongs to the genus
<i>
<fc>B</fc>
etabaculovirus</i>
of the arthropod‐infecting
<fc>B</fc>
aculoviridae. Phop
<fc>GV</fc>
is able to infect several gelechiid species. Among them are the potato tuber moths
<i>
<fc>P</fc>
hthorimaea operculella </i>
<fc>Z</fc>
eller and
<i>
<fc>T</fc>
ecia solanivora </i>
<fc>P</fc>
ovolny (both
<fc>L</fc>
epidoptera:
<fc>G</fc>
elechiidae). In various
<fc>S</fc>
outh
<fc>A</fc>
merican countries, Phop
<fc>GV</fc>
‐based biopesticides are used to control either
<i>
<fc>P</fc>
. operculella</i>
or
<i>
<fc>T</fc>
. solanivora</i>
. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various Phop
<fc>GV</fc>
isolates and various populations of
<i>
<fc>P</fc>
. operculella</i>
and
<i>
<fc>T</fc>
. solanivora</i>
. Virus isolates from
<i>
<fc>P</fc>
. operculella</i>
were more pathogenic against their original host species than against
<i>
<fc>T</fc>
. solanivora</i>
. A Phop
<fc>GV</fc>
isolated from
<i>
<fc>T</fc>
. solanivora</i>
was less efficient against
<i>
<fc>P</fc>
. operculella</i>
. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same Phop
<fc>GV</fc>
isolate. This was the case for both host species and for five Phop
<fc>GV</fc>
isolates. Comparative restriction fragment length polymorphism (
<fc>RFLP</fc>
) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of Phop
<fc>GV</fc>
, corresponding to the regions of open reading frame Phop
<fc>GV</fc>
046, gene
<i>Phop
<fc>GV</fc>
129</i>
(
<i>egt</i>
), and repeat 9 (located between open reading frames Phop
<fc>GV</fc>
083 and Phop
<fc>GV</fc>
084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate,
<fc>JLZ</fc>
9f. The results are discussed in the context of the production and use of Phop
<fc>GV</fc>
as a biological agent against these two pest species.</p>
</abstract>
</abstractGroup>
</contentMeta>
<noteGroup xml:id="eea12115-ntgp-0001">
<note xml:id="eea12115-note-0001">Both authors contributed equally to this work.</note>
</noteGroup>
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<title>Responses of different geographic populations of two potato tuber moth species to genetic variants of Phthorimaea operculella granulovirus</title>
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<title>Responses of different geographic populations of two potato tuber moth species to genetic variants of Phthorimaea operculella granulovirus</title>
</titleInfo>
<name type="personal">
<namePart type="given">Jean‐Louis</namePart>
<namePart type="family">Zeddam</namePart>
<affiliation>Pontificia Universidad Católica del Ecuador, Facultad de Ciencias Naturales y Biológicas, Quito, Ecuador</affiliation>
<affiliation>IRD, Institut de Recherche pour le Développement, Laboratoire Evolution, Génomes et Spéciation, Centre National de la Recherche Scientifique (CNRS), UR 072, UPR 9034, 91198 Gif‐sur‐Yvette Cedex, France; et Université Paris‐Sud 11, 91405, Orsay Cedex, France</affiliation>
<description>Both authors contributed equally to this work.</description>
<affiliation>E-mail: jean-louis.zeddam@ird.fr</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Xavier</namePart>
<namePart type="family">Léry</namePart>
<affiliation>IRD, Institut de Recherche pour le Développement, Laboratoire Evolution, Génomes et Spéciation, Centre National de la Recherche Scientifique (CNRS), UR 072, UPR 9034, 91198 Gif‐sur‐Yvette Cedex, France; et Université Paris‐Sud 11, 91405, Orsay Cedex, France</affiliation>
<affiliation>Centre de Recherche, IRD, UR072, 30380, Saint‐Christol‐les‐Alès, France</affiliation>
<description>Both authors contributed equally to this work.</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Yannery</namePart>
<namePart type="family">Gómez‐Bonilla</namePart>
<affiliation>Instituto National de Investigación y Transferencia de Technología Agropecuaria (INTA), San José, Costa Rica</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Carlos</namePart>
<namePart type="family">Espinel‐Correal</namePart>
<affiliation>Centro de Biotecnología y Bioindustria, CORPOICA, km 14 vía Mosquera, Cundinamarca, Colombia</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">David</namePart>
<namePart type="family">Páez</namePart>
<affiliation>Pontificia Universidad Católica del Ecuador, Facultad de Ciencias Naturales y Biológicas, Quito, Ecuador</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">François</namePart>
<namePart type="family">Rebaudo</namePart>
<affiliation>Pontificia Universidad Católica del Ecuador, Facultad de Ciencias Naturales y Biológicas, Quito, Ecuador</affiliation>
<affiliation>IRD, Institut de Recherche pour le Développement, Laboratoire Evolution, Génomes et Spéciation, Centre National de la Recherche Scientifique (CNRS), UR 072, UPR 9034, 91198 Gif‐sur‐Yvette Cedex, France; et Université Paris‐Sud 11, 91405, Orsay Cedex, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Miguel</namePart>
<namePart type="family">López‐Ferber</namePart>
<affiliation>Ecole des Mines d'Alès, Centre LGEI, 6 Avenue de Clavières, 30100, Alès, France</affiliation>
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<abstract>Phthorimaea operculella granulovirus (PhopGV) belongs to the genus Betabaculovirus of the arthropod‐infecting Baculoviridae. PhopGV is able to infect several gelechiid species. Among them are the potato tuber moths Phthorimaea operculella Zeller and Tecia solanivora Povolny (both Lepidoptera: Gelechiidae). In various South American countries, PhopGV‐based biopesticides are used to control either P. operculella or T. solanivora. Many trials have indicated that a particular viral isolate can exhibit very distinct pathogenicity when infecting different host species or different populations of one host species. In this study, we compared host–pathogen interactions using various PhopGV isolates and various populations of P. operculella and T. solanivora. Virus isolates from P. operculella were more pathogenic against their original host species than against T. solanivora. A PhopGV isolated from T. solanivora was less efficient against P. operculella. In addition, virus isolates differed in pathogenicity toward their hosts (i.e., lethal concentrations of isolates ranged from low to high). Unexpectedly, we also found that host populations of one species from distinct geographic origins did not differ significantly in susceptibility to the same PhopGV isolate. This was the case for both host species and for five PhopGV isolates. Comparative restriction fragment length polymorphism (RFLP) analyses of 11 isolates including those used in bio‐assays indicated three main regions of variation in the genome of PhopGV, corresponding to the regions of open reading frame PhopGV046, gene PhopGV129 (egt), and repeat 9 (located between open reading frames PhopGV083 and PhopGV084). Comparison of the nucleotide sequences of the insertions/deletions present in these regions were carried out for the most variable isolate, JLZ9f. The results are discussed in the context of the production and use of PhopGV as a biological agent against these two pest species.</abstract>
<note type="funding">McKnight Foundation's Collaborative Crop Research Program</note>
<subject>
<genre>keywords</genre>
<topic>Betabaculovirus</topic>
<topic>insect virus</topic>
<topic>bioassay</topic>
<topic>pathogenicity</topic>
<topic>viral variant</topic>
<topic>Tecia solanivora</topic>
<topic>Lepidoptera</topic>
<topic>Gelechiidae</topic>
<topic>PhopGV</topic>
<topic>Baculoviridae</topic>
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