<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0185-3309</journal-id>
<journal-title><![CDATA[Revista mexicana de fitopatología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. mex. fitopatol]]></abbrev-journal-title>
<issn>0185-3309</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Mexicana de Fitopatología A.C.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0185-33092024000200103</article-id>
<article-id pub-id-type="doi">10.18781/r.mex.fit.2311-2</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Variabilidad genética de dos aislados mexicanos de Tomato brown rugose fruit virus y expresión de síntomas en jitomate y chile]]></article-title>
<article-title xml:lang="en"><![CDATA[Genetic variability of two Mexican Tomato brown rugose fruit virus isolates and expression of symptoms in tomato and pepper]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ávila-Alistac]]></surname>
<given-names><![CDATA[Norma]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mora-Aguilera]]></surname>
<given-names><![CDATA[Gustavo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Lozoya-Saldaña]]></surname>
<given-names><![CDATA[Héctor]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zamora-Macorra]]></surname>
<given-names><![CDATA[Erika J.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hernández-Juárez]]></surname>
<given-names><![CDATA[Camilo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Colegio de Postgraduados  ]]></institution>
<addr-line><![CDATA[Texcoco Edo. México]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Colegio de Postgraduados  ]]></institution>
<addr-line><![CDATA[Texcoco Edo. México]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad Autónoma Chapingo  ]]></institution>
<addr-line><![CDATA[Texcoco Edo. México]]></addr-line>
<country>Mexico</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Universidad Autónoma Chapingo  ]]></institution>
<addr-line><![CDATA[Texcoco Edo. México]]></addr-line>
<country>Mexico</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2024</year>
</pub-date>
<volume>42</volume>
<numero>2</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S0185-33092024000200103&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S0185-33092024000200103&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S0185-33092024000200103&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Objetivo/Antecedentes. El objetivo fue analizar la variabilidad de dos aislados mexicanos de ToBRFV posterior a un proceso de inoculación y multiplicación en diferentes variedades comerciales y criollos mexicanos de jitomate (Solanum lycopersicum) (15 materiales) y chile (Capsicum annuum) (20 materiales), y evaluar la expresión de síntomas en condiciones de invernadero.  Materiales y métodos. En invernadero, se analizó la variabilidad postinfección de dos aislados: EM-JI2021 (Edo. de México) y C-JI2021 (Colima) en 15 genotipos de jitomate y 20 de chile. Cada aislado se inoculó mecánicamente en cinco plantas por genotipo con un total de 150 plantas (56 días de edad) de jitomate y 200 de chile. Se emplearon tres plantas por genotipo como testigos. Sesenta y un días después de inoculación se colectó una hoja por planta para RT-PCR. Se registró incidencia y expresión de síntomas. La extracción de ARN fue por CTAB 2 %. Se utilizó oligos ToBRFV-F/ToBRFV-R que amplifican 475pb del gen RpRd (SENASICA-CNRF). Se secuenciaron 24 productos RT-PCR, se limpiaron y alinearon con registros del Genbank NCBI mediante MEGAv11.0.13. Con criterio epidemiológico, se seleccionaron 34 secuencias del GenBank para análisis de variabilidad.  Resultados. Diez días después de la inoculación, los genotipos de jitomate exhibieron mosaico severo, leve, reducción del área foliar. En chile se observaron síntomas diferenciados por genotipo, incluyendo reacción de hipersensibilidad, deformación foliar, necrosis en tallo, mosaico, amarillamiento, lesiones necróticas y condición asintomática. Entre la posición 2,124 al 2,500 pb se tuvo 99.74 % de homología con el primer reporte de ToBRFV en Jordania (KT383474.1). Se encontró homología &gt;99.74 % con aislados de USA (MT002973.1) y Canadá (OQ674195.1). C-JI2021 no exhibió variabilidad, mientras que EM-JI2021 generó tres haplotipos: En Mulato (chile) y Don R (jitomate) se detectó cambio de un nucleótido (c.2,355T&gt;C), mientras que en Santawest, Altius, Sahariana y Nebula (jitomate) se detectaron dos sustituciones (c.2,278A&gt;T; c.2,355T&gt;C).  Conclusión. La intensidad patogénica de ToBRFV varió de asintomática a severa según combinación de hospedero, genotipo y haplotipo. En periodos cortos de infección se detectaron tres haplotipos lo que sugiere capacidad mutagénica del virus en función del hospedero.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Objective/Background. The objective was to analyze the variability of two Mexican isolates of ToBRFV after a process of inoculation and multiplication in different commercial and Mexican landraces of tomato (Solanum lycopersicum) (15 materials) and pepper (Capsicum annuum) (20 materials), and to evaluate the expression of symptoms under greenhouse conditions.  Materials and Methods. In greenhouses, the post-infection variability of two isolates was analyzed: EM-JI2021 (State of Mexico) and C-JI2021 (Colima) in 15 genotypes of tomato and 20 of pepper. Each isolate was mechanically inoculated on five plants per genotype with a total of 150 plants (56 days old) of tomato and 200 of pepper. Three plants per genotype were used as controls. Sixty-one days after inoculation, one leaf per plant was collected for RT-PCR. Incidence and symptom expression were recorded. RNA extraction was by 2% CTAB. ToBRFV-F/ ToBRFV-R primers amplifying 475 bpb of the RpRd gene were used (SENASICACNRF). 24 RT-PCR products were sequenced, cleaned and aligned with NCBI Genbank records using MEGAv11.0.13. Based on epidemiological criteria, 34 sequences were selected from GenBank for variability analysis.  Results. Ten days after inoculation, tomato genotypes exhibited severe mosaic, mild mosaic, and reduced leaf area. In pepper, symptoms differentiated by genotype were observed, including hypersensitivity reaction, leaf deformation, stem necrosis, mosaic, yellowing, necrotic lesions, and asymptomatic condition. Between position 2,124 to 2,500 bp there was 99.74 % homology with the first report of ToBRFV in Jordan (KT383474.1). Homology &gt;99.74 % was found with isolates from USA (MT002973.1) and Canada (OQ674195.1). C-JI2021 exhibited no variability, while EM-JI2021 generated three haplotypes: One nucleotide change (c.2,355T&gt;C) was detected in Mulato (pepper) and Don R (tomato), while two substitutions (c.2,278A&gt;T; c.2,355T&gt;C) were detected in Santawest, Altius, Sahariana and Nebula (tomato).  Conclusion. The pathogenic intensity of ToBRFV varied from asymptomatic to severe depending on the combination of host, genotype, and haplotype. In short periods of infection, three haplotypes were detected, suggesting host-dependent mutagenic capacity of the virus.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Solanum lycopersicum]]></kwd>
<kwd lng="es"><![CDATA[Capsicum annuum]]></kwd>
<kwd lng="es"><![CDATA[ToBRFV]]></kwd>
<kwd lng="es"><![CDATA[aislados.]]></kwd>
<kwd lng="en"><![CDATA[Solanum lycopersicum]]></kwd>
<kwd lng="en"><![CDATA[Capsicum annuum]]></kwd>
<kwd lng="en"><![CDATA[ToBRFV]]></kwd>
<kwd lng="en"><![CDATA[isolates.]]></kwd>
</kwd-group>
</article-meta>
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<page-range>2</page-range></nlm-citation>
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<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zhi-Yong]]></surname>
<given-names><![CDATA[Y.]]></given-names>
</name>
<name>
<surname><![CDATA[Mei-sheng]]></surname>
<given-names><![CDATA[Z.]]></given-names>
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<surname><![CDATA[Hua-yu]]></surname>
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<surname><![CDATA[Ling-zhi]]></surname>
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<surname><![CDATA[Guang-ling]]></surname>
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<article-title xml:lang=""><![CDATA[Biological and molecular characterization of tomato brown rugose fruit virus and development of quadruplex RT-PCR detection]]></article-title>
<source><![CDATA[Journal of Integrative Agriculture]]></source>
<year>2021</year>
<volume>20</volume>
<numero>7</numero>
<issue>7</issue>
<page-range>1871-9</page-range></nlm-citation>
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</article>
