<?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>1405-2768</journal-id>
<journal-title><![CDATA[Polibotánica]]></journal-title>
<abbrev-journal-title><![CDATA[Polibotánica]]></abbrev-journal-title>
<issn>1405-2768</issn>
<publisher>
<publisher-name><![CDATA[Instituto Politécnico Nacional, Escuela Nacional de Ciencias Biológicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1405-27682023000100109</article-id>
<article-id pub-id-type="doi">10.18387/polibotanica.55.8</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Evaluación in vitro del efecto antibacteriano de los extractos de Bidens pilosa y Eryngium foetidum]]></article-title>
<article-title xml:lang="en"><![CDATA[In vitro evaluation of the antibacterial efect of extracts of Bidens pilosa y Eryngium foetidum]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chafla-Moina]]></surname>
<given-names><![CDATA[A. L.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Silva-Déley]]></surname>
<given-names><![CDATA[L. M.]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad Estatal Amazónica Facultad de Ciencias de la Tierra ]]></institution>
<addr-line><![CDATA[Pastaza ]]></addr-line>
<country>Ecuador</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Universidad Técnica de Cotopaxi Medicina Veterinaria ]]></institution>
<addr-line><![CDATA[Latacunga ]]></addr-line>
<country>Ecuador</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2023</year>
</pub-date>
<numero>55</numero>
<fpage>109</fpage>
<lpage>119</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_arttext&amp;pid=S1405-27682023000100109&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_abstract&amp;pid=S1405-27682023000100109&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.mx/scielo.php?script=sci_pdf&amp;pid=S1405-27682023000100109&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen El objetivo del estudio fue identificar cualitativamente los metabolitos secundarios y evaluar el efecto antimicrobiano in vitro de las plantas Bidens pilosa y Eryngium foetidum frente a Staphylococcus aureus (C44-02), Escherichia coli (D31-12) y Salmonella typhimurium (D31-15). Esta actividad se observó mediante la técnica modificado de difusión en pocillos en agar Müeller Hinton, se utilizó 5 y 10 mg/mL de extracto por especie vegetal. Se determinó la concentración mínima inhibitoria (CMI) y la concentración mínima bactericida (CBM) mediante difusión en agar, con soluciones del extracto vegetal en concentraciones de 250, 125, 62.5, 31.25 y 15.62 mg/mL para la CMI. El mayor porcentaje de rendimiento del extracto fue con B. pilosa de 1.3% y para la E. foetidum de 0.21%. El análisis fitoquímico reveló la presencia de metabolitos secundarios alcaloides, glúcidos, saponinas, esteroles, fenoles, terpenoides, flavonoides y taninos. El extracto etanólico de E. foetidum (10 mg/mL) presentó mayor actividad antimicrobiana frente aS. aureus con halo de inhibición de 21,0 ± 2,0 mm. y fue más sensible con una CMI 15.62 mg/mL y CMB 31.25 mg/mL, Para B. pilosa frente aS. aureus con CMI 62.5 mg/mL y CMB 125 mg/mL E. coli y S. typhimurium fueron más resistentes con CMI 125 mg/mL y CMB 125 y 250 mg/mL respectivamente. Esta búsqueda sugiere que los principios activos presentes en las plantas pueden jugar un rol significativo en la acción inhibitoria contra elS. aureus y que el etanol presente como solvente no es el responsable de tal efecto.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract The objective of the study was to qualitatively identify secondary metabolites and evaluate the in vitro antimicrobial effect of Bidens pilosa and Eryngium foetidum plants against Staphylococcus aureus (C44-02), Escherichia coli (D31-12) and Salmonella typhimurium (D31-15). This activity was observed by the modified well diffusion technique in Müeller Hinton agar, using 5 and 10 mg/mL of extract per plant species. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) were determined by agar diffusion, with solutions of the plant extract at concentrations of 250, 125, 62.5, 31.25 and 15.62 mg/mL for MIC. The highest percentage extract yield was with B. pilosa of 1.3% and for E. foetidum of 0.21%. Phytochemical analysis revealed the presence of secondary metabolites alkaloids, glucids, saponins, sterols, phenols, terpenoids, flavonoids and tannins. The ethanolic extract of E. foetidum (10 mg/mL) showed higher antimicrobial activity against S. aureus with inhibition halo of 21.0 ± 2.0 mm and was more sensitive with MIC 15. 62 mg/mL and CMB 31.25 mg/mL, For B. pilosa against S. aureus with MIC 62.5 mg/mL and CMB 125 mg/mL E. coli and S. typhimurium were more resistant with MIC 125 mg/mL and CMB 125 and 250 mg/mL respectively. This finding suggests that the active principles present in the plants may play a significant role in the inhibitory action against S. aureus and that the ethanol present as solvent is not responsible for such effect.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Bidens pilosa]]></kwd>
<kwd lng="es"><![CDATA[Eryngium foetidum]]></kwd>
<kwd lng="es"><![CDATA[actividad antibacteriana]]></kwd>
<kwd lng="es"><![CDATA[tamizaje fitoquímico]]></kwd>
<kwd lng="en"><![CDATA[Bidens pilosa]]></kwd>
<kwd lng="en"><![CDATA[Eryngium foetidum]]></kwd>
<kwd lng="en"><![CDATA[antibacterial efect]]></kwd>
<kwd lng="en"><![CDATA[phytochemical screening]]></kwd>
</kwd-group>
</article-meta>
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