<?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>1659-1321</journal-id>
<journal-title><![CDATA[Agronomía Mesoamericana]]></journal-title>
<abbrev-journal-title><![CDATA[Agron. Mesoam]]></abbrev-journal-title>
<issn>1659-1321</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Costa Rica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1659-13212025000100023</article-id>
<article-id pub-id-type="doi">10.15517/am.2025.62815</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Molecular methods for the specific detection of Colletotrichum sansevieriae]]></article-title>
<article-title xml:lang="es"><![CDATA[Métodos moleculares para la detección específica de Colletotrichum sansevieriae]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sandoval-Ruiz]]></surname>
<given-names><![CDATA[Rebeca]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Brenes-Angulo]]></surname>
<given-names><![CDATA[Arturo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gómez-Alpízar]]></surname>
<given-names><![CDATA[Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad of Costa Rica Agronomy School Center for Agricultural Research]]></institution>
<addr-line><![CDATA[Montes de Oca San José]]></addr-line>
<country>Costa Rica</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad of Costa Rica Agronomy School Center for Agricultural Research]]></institution>
<addr-line><![CDATA[Montes de Oca San José]]></addr-line>
<country>Costa Rica</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Universidad of Costa Rica Agronomy School Center for Agricultural Research]]></institution>
<addr-line><![CDATA[Montes de Oca San José]]></addr-line>
<country>Costa Rica</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2025</year>
</pub-date>
<volume>36</volume>
<numero>1</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S1659-13212025000100023&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S1659-13212025000100023&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S1659-13212025000100023&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract  Introduction. Sansevieria anthracnose, caused by Colletotrichum sansevieriae, represents a significant risk to the cultivation and export of this ornamental plant. Effective and rapid identification methods for this pathogen are crucial for implementing control measures to prevent its spread to uninfected areas. Objective. To implement and optimize molecular methods for the rapid and reliable identification of C. sansevieriae. Materials and methods. During 2016, a &#946;-tubulin-2 (&#946;-tub2) gene fragment of C. sansevieriae isolated from a local farm in Alajuela, Costa Rica, was analyzed. PCR-RFLP of the partial &#946;-tubulin-2 (&#946;-tub2) gene fragment was implemented using the enzyme MseI (Tru1I). In addition, species-specific primers for C. sansevieriae detection and PCR-RFLP analysis of the amplified fragment were applied. Results. The digestion consistently produced a two-band restriction pattern specific to C. sansevieriae. The designed primers successfully amplified a 383 bp fragment of the &#946;-tub2 from all C. sansevieriae strains tested. No amplification was observed from other Colletotrichum species within the C. gloeosporioides and C. acutatum complexes, as well as from C. truncatum and Fusarium oxysporum isolates. Moreover, this restriction site, located within the amplicon generated by the species-specific primers for C. sansevieriae, enabled successful validation of the species through digestion. Conclusions. Both PCR based methods demonstrated sufficient sensitivity to detect C. sansevieriae in naturally and artificially infected Sansevieria leaves without the need to isolate the pathogen in pure cultures, making the diagnostic process more efficient and accessible.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen  Introducción.  La antracnosis de Sansevieria, causada por Colletotrichum sansevieriae, representa un riesgo significativo para el cultivo y la exportación de esta planta ornamental. Los métodos efectivos y rápidos de identificación de este patógeno son cruciales para implementar medidas de control que prevengan su propagación a áreas no infestadas. Objetivo. Implementar y optimizar métodos moleculares para la identificación rápida y confiable de C. sansevieriae. Materiales y métodos. Durante 2016, se analizó un fragmento del gen &#946;-tubulina-2 (&#946;-tub2) de C. sansevieriae aislado de una finca local en Alajuela, Costa Rica. Se implementó PCR-RFLP del fragmento parcial del gen &#946;-tubulina-2 (&#946;-tub2) con la enzima MseI (Tru1I). Además, se aplicaron cebadores específicos para la detección de C. sansevieriae y análisis PCR-RFLP del fragmento amplificado. Resultados. La digestión produjo de manera consistente un patrón de restricción de dos bandas específico para C. sansevieriae. Los cebadores diseñados amplificaron con éxito un fragmento de 383 pb del &#946;-tub2 de todas las cepas de C. sansevieriae probadas. No se observó amplificación de otras especies de Colletotrichum dentro de los complejos C. gloeosporioides y C. acutatum, ni de aislamientos de C. truncatum y Fusarium oxysporum. Además, este sitio de restricción, ubicado dentro del amplicón generado por los cebadores específicos para C. sansevieriae, permitió la validación exitosa de la especie mediante digestión. Conclusiones. Ambos métodos basados en PCR demostraron ser lo suficientemente sensibles como para detectar C. sansevieriae en hojas de Sansevieria infectadas de manera natural y artificial sin necesidad de aislar el patógeno en cultivos puros, lo que hace que el proceso diagnóstico sea más eficiente y accesible.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[RFLP]]></kwd>
<kwd lng="en"><![CDATA[anthracnose]]></kwd>
<kwd lng="en"><![CDATA[plant disease]]></kwd>
<kwd lng="en"><![CDATA[&#946;-tubulin gene]]></kwd>
<kwd lng="en"><![CDATA[plant pathogen]]></kwd>
<kwd lng="en"><![CDATA[fungal diagnostics]]></kwd>
<kwd lng="es"><![CDATA[RFLP]]></kwd>
<kwd lng="es"><![CDATA[antracnosis]]></kwd>
<kwd lng="es"><![CDATA[enfermedad vegetal]]></kwd>
<kwd lng="es"><![CDATA[gen &#946;-tubulina]]></kwd>
<kwd lng="es"><![CDATA[patógeno vegetal]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico fúngico]]></kwd>
</kwd-group>
</article-meta>
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