<?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>1010-2752</journal-id>
<journal-title><![CDATA[Revista de Protección Vegetal]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Protección Veg.]]></abbrev-journal-title>
<issn>1010-2752</issn>
<publisher>
<publisher-name><![CDATA[Centro Nacional de Sanidad Agropecuaria]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1010-27522020000100003</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Actividad antimicrobiana de extractos crudos bioactivos de raíces de Morinda royoc L. crecidas en Cuba]]></article-title>
<article-title xml:lang="en"><![CDATA[Antimicrobial activity of bioactive crude extracts of Morinda royoc L. roots grown in Cuba]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cid Valdés]]></surname>
<given-names><![CDATA[Geeisy Angela]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Linares Rivero]]></surname>
<given-names><![CDATA[Claudia]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rivas Paneca]]></surname>
<given-names><![CDATA[Maribel]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Quiñones-Gálvez]]></surname>
<given-names><![CDATA[Janet]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Capdesuñer Ruiz &#8224;]]></surname>
<given-names><![CDATA[Yanelis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de Ciego de Ávila &#8220;Máximo Gómez Báez&#8221; Centro de Bioplantas ]]></institution>
<addr-line><![CDATA[ Ciego de Ávila]]></addr-line>
<country>Cuba</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>04</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>04</month>
<year>2020</year>
</pub-date>
<volume>35</volume>
<numero>1</numero>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S1010-27522020000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S1010-27522020000100003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S1010-27522020000100003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN Este trabajo tuvo como objetivo determinar la actividad antimicrobiana in vitro de extractos crudos de raíces de Morinda royoc L., ricos en antraquinonas bioactivas, sobre dos bacterias fitopatógenas (Xanthomonas campestris p.v. phaseoli y Pectobacterium carotovorum subsp. carotovorum), dos bacterias patógenas de humanos (Bacillus licheniformis y Stenotrophomonas maltophilia) y tres hongos fitopatógenos (Rhizoctonia solani K&#971;hn, Stemphylium solani Webber y Sarocladium oryzae Sawada). El extracto se preparó a una concentración de 10 mg·ml-1, previamente obtenido por el método de extracción en Soxhlet. Para la evaluación de la actividad antimicrobiana se utilizó el método de difusión en agar para las bacterias y el de microdilución para los hongos. Los resultados obtenidos en este estudio demostraron que el extracto fue efectivo para inhibir más del 50 % del crecimiento de Xanthomonas campestris sin diferencias significativas entre las diferentes dosis usadas. Bajo las mismas condiciones, se alcanzó una inhibición ca. del 50 % del crecimiento de las bacterias Bacillus licheniformis y Stenotrophomonas maltophilia a las 48 horas de exposición a las dosis 150 y 450 µg respectivamente. Por otro lado, los hongos estudiados mostraron susceptibilidad al extracto después de las 48 horas de incubación. La mayor actividad antifúngica se logró frente a Rhizoctonia solani, con una reducción ca. 50 % de su crecimiento frente a las concentraciones 1,25 y 2,5 mg·ml-1 sin diferencias significativas. Después de 72 horas de incubación no se observó actividad inhibitoria del extracto en el crecimiento de los hongos. De todos los patógenos estudiados en este trabajo, Pectobacterium carotovorum fue el único que no mostró susceptibilidad frente a las dosis de extracto usadas.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT The aim of this work was to determine the in vitro antimicrobial activity of the anthraquinone-rich crude extract of Morinda royoc L. roots. Its inhibitory activity was tested on two plant-pathogen bacteria (Xanthomonas campestris pv phaseoli and Pectobacterium carotovorum subsp. carotovorum), two human-pathogen bacteria (Bacillus licheniformis and Stenotrophomonas maltophilia) and three plant-pathogen fungi (Rhizoctonia solani K&#971;hn, Stemphylium solani Webber and Sarocladium oryzae Sawada). The extract was prepared at 10 mg·ml-1, previously obtained by Soxhlet extraction method. To evaluate the antimicrobial activity on bacteria, the agar diffusion method was used, whereas the microdilution method was developed to evaluate the inhibitory activity against fungi. The results obtained from this study demonstrated that the anthraquinone-rich extract was effective in inhibiting more than 50 % of Xanthomonas campestris growth without significant differences between the different doses. After 48 hours and under the same conditions, growth inhibition ca. 50 % of Bacillus licheniformis and Stenotrophomonas maltophilia was observed at the doses of 150 and 450 µg, respectively. On the other hand, all the selected fungi in this study showed susceptibility to the extract after 48 hours of incubation. The highest antifungal activity was achieved on Rhizoctonia solani, with a growth reduction ca. 50 % at concentrations of 1.25 and 2.5 mg·ml-1. After 72 hours of incubation, no significant differences were observed in the growth of any of the three fungi. From all the pathogens selected for this study, only Pectobacterium carotovorum showed no susceptibility to any of the evaluated doses of the extract.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[extractos crudos]]></kwd>
<kwd lng="es"><![CDATA[patógenos]]></kwd>
<kwd lng="es"><![CDATA[actividad inhibitoria]]></kwd>
<kwd lng="es"><![CDATA[porcentaje de inhibición]]></kwd>
<kwd lng="es"><![CDATA[antraquinonas bioactivas]]></kwd>
<kwd lng="en"><![CDATA[crude extracts]]></kwd>
<kwd lng="en"><![CDATA[pathogens]]></kwd>
<kwd lng="en"><![CDATA[inhibitory activity]]></kwd>
<kwd lng="en"><![CDATA[inhibition percentage]]></kwd>
<kwd lng="en"><![CDATA[bioactive anthraquinones]]></kwd>
</kwd-group>
</article-meta>
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