<?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>0120-548X</journal-id>
<journal-title><![CDATA[Acta Biológica Colombiana]]></journal-title>
<abbrev-journal-title><![CDATA[Acta biol.Colomb.]]></abbrev-journal-title>
<issn>0120-548X</issn>
<publisher>
<publisher-name><![CDATA[Universidad Nacional de Colombia, Facultad de Ciencias, Departamento de Biología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-548X2015000100005</article-id>
<article-id pub-id-type="doi">10.15446/abc.v20n1.41673</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[AVALIAÇÃO DA ATIVIDADE ANTIBACTERIANA E MODULADORA DE AMINOGLICOSÍDEOS DO ÓLEO ESSENCIAL DE Cymbopogon citratus (DC.) Stapf]]></article-title>
<article-title xml:lang="es"><![CDATA[Evaluación de la Actividad Antibacteriana y Moduladora de Aminoglucósidos de Aceite Escencial de Cymbopogon Citratus (DC.) Stapf]]></article-title>
<article-title xml:lang="en"><![CDATA[Evaluation of Antibacterial Activity of Aminoglycosides and Modulating the Essential Oil of Cymbopogon citratus (DC.) Stapf]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[F. LUCENA]]></surname>
<given-names><![CDATA[Bruno F]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[TINTINO]]></surname>
<given-names><![CDATA[Saulo R]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[FIGUEREDO]]></surname>
<given-names><![CDATA[Fernando G]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[DE M. OLIVEIRA]]></surname>
<given-names><![CDATA[Cícera Datiane]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[DOS S. AGUIAR]]></surname>
<given-names><![CDATA[José J]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[DO N. CARDOSO]]></surname>
<given-names><![CDATA[Edmilson]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[A. DE AQUINO]]></surname>
<given-names><![CDATA[Pedro E]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[ANDRADE]]></surname>
<given-names><![CDATA[Jacqueline C]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[M. COUTINHO]]></surname>
<given-names><![CDATA[Henrique D]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[F. MATIAS]]></surname>
<given-names><![CDATA[Ednardo F]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidade Regional do Cariri  ]]></institution>
<addr-line><![CDATA[Crato CE]]></addr-line>
<country>Brasil</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Laboratorio de Microbiologia Faculdade Leão Sampaio ]]></institution>
<addr-line><![CDATA[Juazeiro do Norte CE]]></addr-line>
<country>Brasil</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Universidade Regional do Cariri  ]]></institution>
<addr-line><![CDATA[Crato CE]]></addr-line>
<country>Brasil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>01</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>01</month>
<year>2015</year>
</pub-date>
<volume>20</volume>
<numero>1</numero>
<fpage>39</fpage>
<lpage>45</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-548X2015000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-548X2015000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-548X2015000100005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Vários trabalhos vêm demonstrando a importância do estudo de produtos naturais como fonte alternativa para novos antimicrobianos ou que venham potencializar os já existentes. Neste contexto este trabalho teve como objetivo investigar a atividade antibacteriana e as possíveis interações entre o óleo essencial de Cymbopogon citratus combinados a aminoglicosídeos frente a linhagens padrões e multirresistentes de S. aureus, E. coli e de P. aeruginosa provenientes de isolados clínicos. Um ensaio de microdiluição foi realizado para verificar a atividade antibacteriana e as possíveis interacções entre o produto natural e os antibióticos, utilizando uma concentração sub-inibitória. Através dos resultados foi constatado a interferência sinérgica dos aminoglicosídeos quando associados com o óleo essencial em uma concentração de CIM/8, com redução das CIMs em até quatro pontos frente às linhagens de S. aureus 358, E. coli 27 e P. aeruginosa-143. Mas nenhuma atividade modificadora foi observada frente a P. aeruginosa 78 e P. aeruginosa 91. Através dos resultados pode-se concluir que o óleo essencial de Cymbopogon citratus pode ser uma fonte alternativa de produtos naturais com atividade antibacteriana.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Varios trabajos están demostrando la importancia del estudio de productos naturales como una fuente alternativa para nuevos antimicrobianos o que puedan mejorar los ya existentes. En este contexto, el objetivo de este trabajo fue investigar la actividad antibacteriana y las posibles interacciones entre el aceite esencial de Cymbopogon citratus aminoglucósido combinado frente de linajes y patrones de S. aureus multirresistente, E. coli y P. aeruginosa provenientes de aislamientos clínicos. Se realizó una prueba de microdilución para verificar la actividad antibacteriana y posibles interacciones entre el producto natural y antibióticos, usando una concentración sub-inibitória. A través de los resultados se observan interferencia sinérgica de los aminoglucósidos cuando se asocian con el aceite esencial en una concentración de CIM/8, con reducción de CIMs de hasta cuatro puntos contra las cepas de S. aureus 358, E. coli 27 y P. aeruginosa 143. Pero no se observó ninguna actividad modificadora contra P. aeruginosa 78 y P. aeruginosa 91. A través de los resultados se puede concluir que el aceite esencial de Cymbopogon citratus puede ser una fuente alternativa de productos naturales con actividad antibacteriana.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Several works demonstrated the importance of the study of natural products as an alternative source for new antimicrobial drugs or for modulators for these ones. In this point, the aim of this was to investigate the antibacterial activity and the possible interactions between the essential oil of Cymbopogon citratus alone and in association with aminoglycosides against standard and clinically isolated strains of multidrug-resistant bacteria such as S. aureus, E. coli and P. aeruginosa by microdilution method. The results indicated a synergism between the antibiotics and the essential oil with a subinhibitory concentration (MIC/8), reducing the minimal inhibitory concentration (MIC) sixteen times against the multidrug-resistant strains of S. aureus 358, E. coli 27 and P. aeruginosa 143, but none modulatory activity was observed against P. aeruginosa 78 and P. aeruginosa 91 strains. By our results, can be concluded that the essential oil of Cymbopogon citratus can be an interesting source of natural products with antibacterial and/or modulatory antibiotic activities.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Cymbopogon citratus]]></kwd>
<kwd lng="pt"><![CDATA[Escherichia coli]]></kwd>
<kwd lng="pt"><![CDATA[óleo essencial]]></kwd>
<kwd lng="pt"><![CDATA[Pseudomonas aeruginosa]]></kwd>
<kwd lng="pt"><![CDATA[Staphylococcus aureus]]></kwd>
<kwd lng="es"><![CDATA[Cymbopogon citratus]]></kwd>
<kwd lng="es"><![CDATA[Escherichia coli]]></kwd>
<kwd lng="es"><![CDATA[aceite esencial]]></kwd>
<kwd lng="es"><![CDATA[Pseudomonas aeruginosa]]></kwd>
<kwd lng="es"><![CDATA[Staphylococcus aureus]]></kwd>
<kwd lng="en"><![CDATA[Cymbopogon citratus]]></kwd>
<kwd lng="en"><![CDATA[Escherichia coli]]></kwd>
<kwd lng="en"><![CDATA[essential oil]]></kwd>
<kwd lng="en"><![CDATA[Pseudomonas aeruginosa]]></kwd>
<kwd lng="en"><![CDATA[Staphylococcus aureus]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[   <font size="2" face="Verdana">      <P>doi:<a href="http://dx.doi.org/10.15446/abc.v20n1.41673" target="_blank">10.15446/abc.v20n1.41673</a>.</P>      <P align="right">Art&iacute;culo de investigaci&oacute;n</P>      <P align="center"><font size="4" face="Verdana"><B>AVALIA&Ccedil;&Atilde;O DA ATIVIDADE ANTIBACTERIANA E MODULADORA DE AMINOGLICOS&Iacute;DEOS DO &Oacute;LEO ESSENCIAL DE <I>Cymbopogon citratus</I> (DC.) Stapf </B></font></P>      <P align="center"><font size="3" face="Verdana"><B>Evaluaci&oacute;n de la Actividad Antibacteriana y Moduladora de Aminogluc&oacute;sidos de Aceite Escencial de <I>Cymbopogon Citratus</I> (DC.) Stapf </B></font></P>      <P align="center"><font size="3" face="Verdana"><B>Evaluation of Antibacterial Activity of Aminoglycosides and Modulating the Essential Oil of<I> Cymbopogon citratus</I> (DC.) Stapf </B></font></P>      <P><B>Bruno F. F. LUCENA<Sup>2</Sup>, Saulo R. TINTINO<Sup>1</Sup>*, Fernando G. FIGUEREDO<Sup>1,2</Sup>, C&iacute;cera Datiane DE M. OLIVEIRA<Sup>3</Sup>, Jos&eacute; J. DOS S. AGUIAR<Sup>1</Sup>, Edmilson DO N. CARDOSO<Sup>2</Sup>, Pedro E. A. DE AQUINO<Sup>2</Sup>, Jacqueline C. ANDRADE<Sup>1</Sup>, Henrique D. M. COUTINHO<Sup>1</Sup>, Ednardo F. F. MATIAS<Sup>1</Sup>.</B></P>      <P><Sup>1</Sup> Laborat&oacute;rio de Microbiologia e Biologia Molecular, Universidade Regional do Cariri. Rua Cel. Antonio Luis, 1161, Pimenta, 63105-000. Crato, CE, Brasil.    <BR> <Sup>2</Sup> Laboratorio de Microbiologia, Faculdade Le&atilde;o Sampaio. Av. Le&atilde;o Sampaio, Km 3, CEP 63000-000,Juazeiro do Norte, CE, Brasil.    <BR> <Sup>3</Sup> Laborat&oacute;rio de Farmacologia e Qu&iacute;mica Medicinal, Universidade Regional do Cariri. Rua Cel. Antonio Luis, 1161, Pimenta, 63105-000. Crato, CE, Brasil</B>.    ]]></body>
<body><![CDATA[<BR> *<B><I>For correspondence.</I></B> <a href="mailto:saulorelison@gmail.com">saulorelison@gmail.com</a> </P>      <P>Received 22th January 2014, Returned for revision 27th April 2014, accepted 29th April 2014.</P>      <P><B>Citation / Citar este art&iacute;culo como:</B> Lucena BFF, Tintino SR, Figueredo FG, Oliveira CDM, Aguiar JJS, Cardoso EN, Aquino PEA, Andrade JC, Coutinho HDM, Matias EFF. Avalia&ccedil;&atilde;o da atividade antibacteriana e moduladora de aminoglicos&iacute;deos do &oacute;leo essencial de <I>Cymbopogon citratus</I> (DC.) Stapf. Acta biol. Colomb. 2015;20(1):39-45. doi: <a href="http://dx.doi.org/10.15446/abc.v20n1.41673" target="_blank">http://dx.doi.org/10.15446/abc.v20n1.41673</a>.</P>  <HR>      <P><B>RESUMO </B></P>      <P>V&aacute;rios trabalhos v&ecirc;m demonstrando a import&acirc;ncia do estudo de produtos naturais como fonte alternativa para novos antimicrobianos ou que venham potencializar os j&aacute; existentes. Neste contexto este trabalho teve como objetivo investigar a atividade antibacteriana e as poss&iacute;veis intera&ccedil;&otilde;es entre o &oacute;leo essencial de <I>Cymbopogon citratus </I>combinados a aminoglicos&iacute;deos frente a linhagens padr&otilde;es e multirresistentes de <I>S. aureus, E. coli </I>e de <I>P. aeruginosa </I>provenientes de isolados cl&iacute;nicos. Um ensaio de microdilui&ccedil;&atilde;o foi realizado para verificar&nbsp;a atividade antibacteriana e as poss&iacute;veis interac&ccedil;&otilde;es entre&nbsp;o produto natural&nbsp;e os antibi&oacute;ticos,&nbsp;utilizando uma concentra&ccedil;&atilde;o&nbsp;sub-inibit&oacute;ria. Atrav&eacute;s dos resultados foi constatado a interfer&ecirc;ncia sin&eacute;rgica dos aminoglicos&iacute;deos quando associados com o &oacute;leo essencial em uma concentra&ccedil;&atilde;o de CIM/8, com redu&ccedil;&atilde;o das CIMs em at&eacute; quatro pontos frente &agrave;s linhagens de <I>S. aureus </I>358, <I>E. coli </I>27 e <I>P. aeruginosa-</I>143. Mas nenhuma atividade modificadora foi observada frente a <I>P. aeruginosa</I> 78 e <I>P. aeruginosa </I>91. Atrav&eacute;s dos resultados pode-se concluir que o &oacute;leo essencial de <I>Cymbopogon citratus </I>pode ser uma fonte alternativa de produtos naturais com atividade antibacteriana.</P>      <P><B>Palavras&#150;chave: </B><I>Cymbopogon citratus</I>, <I>Escherichia coli,</I> &oacute;leo essencial,<I> Pseudomonas aeruginosa, Staphylococcus aureus. </I></P>      <P><B>RESUMEN </B></P>      <P>Varios trabajos est&aacute;n demostrando la importancia del estudio de productos naturales como una fuente alternativa para nuevos antimicrobianos o que puedan mejorar los ya existentes. En este contexto, el objetivo de este trabajo fue investigar la actividad antibacteriana y las posibles interacciones entre el aceite esencial de <I>Cymbopogon citratus</I> aminogluc&oacute;sido combinado frente de linajes y patrones de <I>S. aureus</I> multirresistente, <I>E. coli </I>y <I>P. aeruginosa</I> provenientes de aislamientos cl&iacute;nicos. Se realiz&oacute; una prueba de microdiluci&oacute;n para verificar la actividad antibacteriana y posibles interacciones entre el producto natural y antibi&oacute;ticos, usando una concentraci&oacute;n sub-inibit&oacute;ria. A trav&eacute;s de los resultados se observan interferencia sin&eacute;rgica de los aminogluc&oacute;sidos cuando se asocian con el aceite esencial en una concentraci&oacute;n de CIM/8, con reducci&oacute;n de CIMs de hasta cuatro puntos contra las cepas de <I>S. aureus </I> 358, <I>E. coli </I>27 y <I>P. aeruginosa</I> 143. Pero no se observ&oacute; ninguna actividad modificadora contra <I>P. aeruginosa </I>78 y P. aeruginosa 91. A trav&eacute;s de los resultados se puede concluir que el aceite esencial de <I>Cymbopogon citratus</I> puede ser una fuente alternativa de productos naturales con actividad antibacteriana.</P>      <P><B>Palabras clave: </B><I>Cymbopogon citratus</I>, <I>Escherichia coli</I>, aceite esencial, <I>Pseudomonas aeruginosa</I>, <I>Staphylococcus aureus. </I></P>      <P><B>ABSTRACT </B></P>      ]]></body>
<body><![CDATA[<P>Several works demonstrated the importance of the study of natural products as an alternative source for new antimicrobial drugs or for modulators for these ones. In this point, the aim of this was to investigate the antibacterial activity and the possible interactions between the essential oil of&nbsp;<I>Cymbopogon citratus </I>alone and in association with aminoglycosides against standard and clinically isolated strains of multidrug-resistant bacteria such as&nbsp;<I>S. aureus, E. coli&nbsp;</I>and&nbsp;<I>P. aeruginosa </I>by microdilution method. The results indicated a synergism between the antibiotics and the essential oil with a subinhibitory concentration (MIC/8), reducing the minimal inhibitory concentration (MIC) sixteen times against the multidrug-resistant strains of&nbsp;<I>S. aureus&nbsp;</I>358,&nbsp;<I>E. coli&nbsp;</I>27 and&nbsp;<I>P. aeruginosa&nbsp;</I>143, but none modulatory activity was observed against&nbsp;<I>P. aeruginosa </I>78 and&nbsp;<I>P. aeruginosa&nbsp;</I>91 strains. By our results, can be concluded that the essential oil of&nbsp;<I>Cymbopogon citratus&nbsp;</I>can be an interesting source of natural products with antibacterial and/or modulatory antibiotic activities.</P>      <P><B>Keywords:</B><I> Cymbopogon citratus</I>, <I>Escherichia coli,</I> essential oil,<I> Pseudomonas aeruginosa, Staphylococcus aureus. </I></P>  <HR>      <P><B>INTRODU&Ccedil;&Atilde;O </B></P>      <P>Em todo o mundo, h&aacute; um grande n&uacute;mero de cepas bacterianas resistentes a m&uacute;ltiplas drogas, principalmente no ambiente hospitalar, aumentando a morbidade, custos inerentes a cuidados de sa&uacute;de, e as taxas de mortalidade devido a infec&ccedil;&otilde;es (Dias e Monteiro, 2010). A maioria das bact&eacute;rias t&ecirc;m m&uacute;ltiplos mecanismos de resist&ecirc;ncia a qualquer droga e, uma vez resistente, pode rapidamente dar origem a um grande n&uacute;mero de descendentes resistentes (Gold e Moellering, 1996). A resist&ecirc;ncia bacteriana pode ser transferida por mecanismos diversos, podendo estabelecerse entre microrganismos de uma mesma popula&ccedil;&atilde;o ou de diferentes popula&ccedil;&otilde;es, como da microbiota animal para humana e vice-versa (Baccaro <I>et al</I>., 2002).</P>      <P>A capacidade de desenvolver resist&ecirc;ncia aos agentes antibacterianos &eacute; uma caracter&iacute;stica observada entre os microorganismos em geral. Enquanto isso, as bact&eacute;rias s&atilde;o capazes de desenvolver diferentes mecanismos de resist&ecirc;ncia, os quais s&atilde;o codificados geneticamente, em que os genes de resist&ecirc;ncia podem ser adquiridos atrav&eacute;s de muta&ccedil;&atilde;o e de transfer&ecirc;ncia de material gen&eacute;tico (Carneiro, 2006). O desenvolvimento de infec&ccedil;&otilde;es em seres humanos, incluem uma diversidade de bact&eacute;rias Gram-positivas e Gram-negativas, conforme descrito abaixo, mostrando resist&ecirc;ncia aos agentes antibacterianos.</P>      <P>As bact&eacute;rias do g&ecirc;nero <I>Staphylococcus</I> s&atilde;o distribu&iacute;das na natureza, bem como na microbiota normal da pele e das mucosas de animais e aves. Algumas esp&eacute;cies de <I>Staphylococcus</I> s&atilde;o geralmente reconhecidos como agentes etiol&oacute;gicos de infec&ccedil;&otilde;es oportunistas em muitos animais e seres humanos (Nostro <I>et al</I>., 2004; Coutinho <I>et al</I>., 2009). <I>Staphylococcus aureus, S. epidermidis, S. saprophyticus </I>e <I>S. haemolyticus</I> s&atilde;o as esp&eacute;cies que s&atilde;o os agentes causadores mais importantes de infec&ccedil;&otilde;es humanas e hospitalares. Al&eacute;m de causar diferentes tipos de intoxica&ccedil;&otilde;es, <I>S. aureus </I>representa o agente etiol&oacute;gico mais comum de infec&ccedil;&otilde;es purulentas (por exemplo, fur&uacute;nculo, carb&uacute;nculo, abcesso, miocardite, endocardite, pneumonia, meningite, artrite bacteriana) (Verhoeff <I>et al</I>., 1999).</P>      <P>A esp&eacute;cie <I>Pseudomonas aeruginosa </I>&eacute; respons&aacute;vel por uma variedade de infec&ccedil;&otilde;es, tais como aquelas que atacam a pele, trato urin&aacute;rio, olhos e ouvidos. A ampla distribui&ccedil;&atilde;o ambiental de <I>Pseudomonas</I> &eacute; assegurada por seus requisitos n&atilde;o-exigentes de seu crescimento, al&eacute;m de ter in&uacute;meros fatores estruturais, enzimas e toxinas que potencializam a sua virul&ecirc;ncia, tornando-se resistentes aos antibi&oacute;ticos mais comuns (Murray <I>et al</I>., 2004).</P>      <P>A <I>Escherichia coli</I> &eacute; uma das principais bact&eacute;rias causadoras de doen&ccedil;as infecciosas em seres humanos. &Eacute; conhecida por sua produ&ccedil;&atilde;o de enterotoxinas, cujas propriedades t&ecirc;m sido amplamente investigadas, sendo que a atividade de suas citotoxinas e seu papel na infec&ccedil;&atilde;o humana foram identificados principalmente em infec&ccedil;&otilde;es do trato urin&aacute;rio (Matias <I>et al</I>., 2010).</P>      <P>No que diz respeito &agrave; crescente import&acirc;ncia dada &agrave; infec&ccedil;&otilde;es bacterianas em comunidades hospitalares e para o desenvolvimento progressivo da resist&ecirc;ncia antimicrobiana, um grande n&uacute;mero de estudos t&ecirc;m sido realizados com produtos naturais em busca de uma nova perspectiva no tratamento de infec&ccedil;&otilde;es bacterianas. Muitas plantas foram avaliadas n&atilde;o apenas pela sua atividade antimicrobiana direta, mas tamb&eacute;m como um agente modificador de resist&ecirc;ncia (Gibbons, 2004). A utiliza&ccedil;&atilde;o de &oacute;leos essenciais de plantas como agentes antimicrobianos mostra uma possibilidade de que os microrganismos ir&atilde;o adquirir baixa resist&ecirc;ncia para a sua a&ccedil;&atilde;o, por serem misturas complexas, tornando muito dif&iacute;cil adapta&ccedil;&atilde;o microbiana (Daferera <I>et al</I>., 2003).</P>      <P>V&aacute;rios compostos de produtos qu&iacute;micos, de fontes naturais ou sint&eacute;ticas, tais como a partir de fenotiazinas ou produtos naturais, possuem atividade direta contra muitas esp&eacute;cies de bact&eacute;rias, aumentam a atividade de um antibi&oacute;tico espec&iacute;fico, invertem a resist&ecirc;ncia natural de bact&eacute;rias espec&iacute;ficas a determinados antibi&oacute;ticos, promovem a elimina&ccedil;&atilde;o de plasm&iacute;deos a partir de bact&eacute;rias e inibem a fun&ccedil;&atilde;o de transporte da membrana de plasma no que se refere a determinados antibi&oacute;ticos (Gunics <I>et al</I>., 2002).</P>      ]]></body>
<body><![CDATA[<P>Nessa perspectiva, o uso de produtos naturais como esp&eacute;cie <I>Cymbopogon citratus</I> (DC.) Stapf no controle da resist&ecirc;ncia bacteriana, torrna-se uma alternativa relevante. Ela &eacute; uma herb&aacute;cea e pertence a classe <I>Liliopsida,</I> a ordem <I>Poales </I>e &agrave; fam&iacute;lia <I>Poaceae </I>(Lorenzi e Matos, 2002; Santos <I>et al</I>., 2009). Esp&eacute;cie vegetal conhecida popularmente no Brasil como capim-santo, capim-lim&atilde;o, capim-cheiroso, capimcidreira, capim-cidr&atilde;o, citronela-de-java, erva-cidreira e capim-cidr&oacute;. Seu uso principal &eacute; como anti-hipertensivo, antiasm&aacute;tico, antit&eacute;rmico, antiss&eacute;ptico, antiparasit&aacute;rio, antirreum&aacute;tico, miorrelaxante e antiespasm&oacute;dico. Este trabalho foi desenvolvido com o objetivo de evidenciar atividade antibacteriana e moduladora de antibi&oacute;tico, pelo &oacute;leo essencial de <I>Cymbopogon citratus</I>, atrav&eacute;s da t&eacute;cnica de microdilui&ccedil;&atilde;o contra cepas padr&otilde;es e multirresistentes de <I>Escherichia coli, Staphylococcus aureus </I>e<I> Pseudomonas aeruginosa. </I></P>      <P><B>MATERIAL E M&Eacute;TODOS    <BR> Microrganismos </B></P>      <P>As linhagens bacterianas utilizadas foram: <I>E. coli:</I> EC&#150; ATCC 10536, EC&#150;27; <I>S. aureus: </I>SA&#150;ATCC 25923, SA&#150;358; <I>P. aeruginosa</I>: PA&#150;ATCC 15442, PA&#150;91, PA&#150;143 e PA&#150;78 com perfil de resist&ecirc;ncia identificado na <a href="#tab1">Tabela 1</a>. Todas as linhagens foram mantidas em infus&atilde;o de cora&ccedil;&atilde;o em Agar (HIA, Difco Laboratories Ltda.). Antes dos ensaios, as linhagens foram cultivadas por 24h a 35#&#186;C em caldo de infus&atilde;o de c&eacute;rebro e cora&ccedil;&atilde;o (BHI, Difco Laboratories Ltda).</P>      <p align="center"><a name="tab1"><img src="img/revistas/abc/v20n1/v20n1a05tab1.jpg"></a></p>      <P>Folhas de <I>Cymbopogon citratus </I>foram coletadas &agrave;s 8h30min, no S&iacute;tio Gavi&atilde;o, distrito do munic&iacute;pio de Juazeiro do Norte, Cear&aacute;, Brasil no m&ecirc;s de dezembro/2011. O material vegetal foi identificado e uma exsicata foi depositada em herb&aacute;rio Caririense D&aacute;rdano de Andrade-Lima (HCDAL) do Departamento de Ci&ecirc;ncias Biol&oacute;gicas (URCA), sob registro n#&#186; 4018.</P>      <P><B>Obten&ccedil;&atilde;o do &oacute;leo essencial de <I>Cymbopogon citratus </I></B></P>      <P>O &oacute;leo essencial foi obtido utilizando-se o sistema de hidrodestila&ccedil;&atilde;o em aparelho tipo Clevenger modificado por Gottlieb e Magalh&atilde;es (1960). As folhas frescas de <I>C. citratus </I>foram colocadas em bal&atilde;o de vidro de 5L, acrescida de 3L de &aacute;gua destilada e aquecidas por 2h. Ap&oacute;s esse per&iacute;odo, a mistura &aacute;gua/&oacute;leo obtida foi separada, tratada com sulfato de s&oacute;dio anidro, filtrada e o &oacute;leo obtido (OECC) foi mantido sob refrigera&ccedil;&atilde;o at&eacute; o momento das an&aacute;lises. Para os testes foi utilizado solu&ccedil;&atilde;o preparadas a partir do &oacute;leo essencial sob uma concentra&ccedil;&atilde;o de 10 mg/mL, dissolvidos em DMSO (Dimetilsulf&oacute;xido, Sigma-Aldrich&reg;), em seguida dilu&iacute;dos com &aacute;gua destilada est&eacute;ril para uma concentra&ccedil;&atilde;o de 1024 &mu;g/mL.</P>      <P><B>Teste de atividade antibacteriana e atividade modulat&oacute;ria do antibi&oacute;tico </B></P>      <P>A Concentra&ccedil;&atilde;o Inibit&oacute;ria M&iacute;nima (CIM) foi determinada em ensaio de micro-dilui&ccedil;&atilde;o em caldo (NCCLS, 2003) utilizando-se um inoculo de 100 &mu;L de cada linhagem, suspensas em caldo BHI que apresentava uma concentra&ccedil;&atilde;o de 10<Sup>5</Sup> UFC/mL em placas de micro-titula&ccedil;&atilde;o com 96 po&ccedil;os, com dilui&ccedil;&otilde;es em s&eacute;rie &frac12;. Em cada po&ccedil;o foi adicionado 100&mu;L de solu&ccedil;&atilde;o de cada amostra. As concentra&ccedil;&otilde;es finais do produto natural variaram entre 512 &#150; 8 &mu;g/mL. Para os controles foram utilizados os antibi&oacute;ticos padr&otilde;es amicacina, neomicina e gentamicina cujas concentra&ccedil;&otilde;es finais variaram entre 2500 &mu;g/mL &#150; 2,44&mu;g/mL. As CIMs foram registradas como as menores concentra&ccedil;&otilde;es para a inibi&ccedil;&atilde;o do crescimento.</P>      ]]></body>
<body><![CDATA[<P>Para avaliar o &oacute;leo essencial como modulador da a&ccedil;&atilde;o antibi&oacute;tica, a CIM de antibi&oacute;ticos da classe dos aminoglicos&iacute;deos, foram avaliados na presen&ccedil;a e na aus&ecirc;ncia do &oacute;leo essencial em micro-placas est&eacute;reis. Os antibi&oacute;ticos foram avaliados nas concentra&ccedil;&otilde;es variando de 2500 &mu;g/mL &#150; 2,4 &mu;g/mL.</P>      <P>As amostras foram misturadas em caldo BHI 10% em concentra&ccedil;&otilde;es sub-inibit&oacute;rias, obtidos e determinados ap&oacute;s a realiza&ccedil;&atilde;o de teste de avalia&ccedil;&atilde;o da CIM, sendo que para o teste de modula&ccedil;&atilde;o a concentra&ccedil;&atilde;o da solu&ccedil;&atilde;o do &oacute;leo essencial foi reduzida 8 (oito) vezes (CIM/8). A prepara&ccedil;&atilde;o das solu&ccedil;&otilde;es de antibi&oacute;ticos foi realizada com a adi&ccedil;&atilde;o de &aacute;gua destilada est&eacute;ril em concentra&ccedil;&atilde;o dobrada (5000&micro;g/mL) em rela&ccedil;&atilde;o &agrave; concentra&ccedil;&atilde;o inicial definida e volumes de 100&mu;L dilu&iacute;dos seriadamente 1:1 em caldo BHI 10%. Em cada cavidade com 100&mu;L do meio de cultura continha a suspens&atilde;o bacteriana dilu&iacute;da a 10<Sup>5</Sup> UFC/mL (1:10). Os mesmos controles utilizados na avalia&ccedil;&atilde;o da CIM para o &oacute;leo foram utilizados durante a modula&ccedil;&atilde;o (Coutinho <I>et al</I>., 2009). As placas preenchidas e incubadas a 35#&#186;C por 24 horas e ap&oacute;s esse per&iacute;odo a leitura foi evidenciada pelo uso de rezazurina. Os ensaios foram realizados em triplicada e os resultados foram expressos como m&eacute;dia das repeti&ccedil;&otilde;es.</P>      <P><B>RESULTADOS </B></P>      <P>O &oacute;leo essencial avaliado no presente trabalho, ap&oacute;s todo o procedimento de prepara&ccedil;&atilde;o, apresentou rendimento de 0,49%. Alguns trabalhos demonstraram que as temperaturas elevadas influenciam na qualidade do &oacute;leo essencial do <I>Cymbopogon citratus</I>, por mostrarem concentra&ccedil;&otilde;es mais elevadas do citral no hor&aacute;rio de 08h &agrave;s 13h e que o rendimento desse &oacute;leo &eacute; de 0,28 a 0,50% da massa de folhas tanto secas como frescas (Nascimento <I>et al</I>., 2000).</P>      <P>Um ensaio piloto utilizando apenas o DMSO foi realizado, mas nenhuma atividade antibacteriana ou moduladora foi verificada, indicando n&atilde;o apresentar toxicidade.</P>      <P>A <a href="#tab3">tabela 3</a> mostra a interfer&ecirc;ncia do &oacute;leo sobre a atividade de aminoglicos&iacute;deos frente &agrave;s linhagens de SA&#150;358 e a EC&#150;27, demonstrando uma interfer&ecirc;ncia na atividade dos antibi&oacute;ticos, com redu&ccedil;&atilde;o das CIMs. Os efeitos mais representativos foram na associa&ccedil;&atilde;o do OECC na concentra&ccedil;&atilde;o de 128 &mu;g/mL (CIM 1/8) com os antibi&oacute;ticos, observando modula&ccedil;&atilde;o da atividade da amicacina associada ao OECC frente &agrave; EC&#150;27, com redu&ccedil;&atilde;o da CIM de 312,50 para 39,06&mu;g/mL e frente a SA&#150;358 com redu&ccedil;&atilde;o da CIM de 78,12 para 4,88 &mu;g/mL.</P>      <p align="center"><a name="tab3"><img src="img/revistas/abc/v20n1/v20n1a05tab3.jpg"></a></p>      <P>J&aacute; a <a href="#tab4">tabela 4</a> mostra a interfer&ecirc;ncia do &oacute;leo sobre a atividade de aminoglicos&iacute;deos frente &agrave; linhagem de <I>P. aeruginosa</I>, demonstrando uma interfer&ecirc;ncia na atividade dos antibi&oacute;ticos, com redu&ccedil;&atilde;o das CIMs frente a <I>P. aeruginosa</I> 91. O efeito mais representativo foi na associa&ccedil;&atilde;o do OECC na concentra&ccedil;&atilde;o de 128 &mu;g/mL (CIM 1/8) com os antibi&oacute;ticos no meio de cultura, observando um refor&ccedil;o na atividade da amicacina associada ao OECC frente &agrave; EC&#150;27 com redu&ccedil;&atilde;o da CIM de 312,5 para 39,06 &mu;g/mL. No entanto, n&atilde;o foi obsevado interfer&ecirc;ncia da atividade antibi&oacute;tica quando associado &agrave;s outras duas linhagens de <I>P. aeruginosa. </I>Resultado este que corrobora com de Bassol&eacute; (2011), que n&atilde;o avaliou modula&ccedil;&atilde;o da atividade antibacteriana pela t&eacute;cnica de difus&atilde;o em disco.</P>      <p align="center"><a name="tab4"><img src="img/revistas/abc/v20n1/v20n1a05tab4.jpg"></a></p>      <P><B>DISCUSS&Atilde;O </B></P>      ]]></body>
<body><![CDATA[<P>Segundo pesquisas j&aacute; realizadas, &oacute;leo essencial de <I>C. citratus </I>apresenta diversas classes de metab&oacute;litos secund&aacute;rios que apresentam uma ampla variedade de atividades biol&oacute;gicas como a antimicrobiana (Shah <I>et al</I>., 2011). A elucida&ccedil;&atilde;o do &oacute;leo segundo Shah <I>et al</I>., (2011), demonstrou a presen&ccedil;a de diversos compostos potencialmente bioativos no &oacute;leo, como fen&oacute;is, terpenos, alco&oacute;is, cetonas, &eacute;steres e principalmente alde&iacute;dos tem sido constantemente registrado. Al&eacute;m do isolamento, foram identificados novos triterpen&oacute;ides das folhas de <I>C. citratus</I> que s&atilde;o o cymbopogone e o cymbopogonol. Flavon&oacute;ides e compostos fen&oacute;licos como luteolin, isoorientin 2&#39;&#39;-O-rhamnoside, quercetina, kaempferol e apiginina. Os componentes fen&oacute;licos elimicina, catecol, &aacute;cido clorog&ecirc;nico, &aacute;cido cafeico e hidro-quinona tamb&eacute;m foram isolados (Shah <I>et al</I>., 2011). Possui o citral e mirceno como principais compostos (Ming <I>et al</I>., 1996).</P>      <P>Na determina&ccedil;&atilde;o da Concentra&ccedil;&atilde;o Inibit&oacute;ria M&iacute;nima (CIM) do &oacute;leo essencial testado contra linhagens padr&otilde;es e multiresistentes de <I>E. coli, S. aureus </I>e<I> P. aeruginos</I>, como demonstrado na <a href="#tab2">tabela 2</a>, foi verificado que o &oacute;leo apresentou a mesma CIM frente as linhagens testadas de &ge;1024 &mu;g/mL com exce&ccedil;&atilde;o da CIM de 512 &mu;g/mL frente a SA &#150; ATCC 25923, n&atilde;o demonstrando atividade cl&iacute;nica relevante de acordo com os limites estabelecidos pelo protocolo (Houghton <I>et al</I>., 2007). No entanto, a amostra associada aos aminoglicos&iacute;deos demonstrou modula&ccedil;&atilde;o da atividade antibacteriana dos antibi&oacute;ticos.</P>      <p align="center"><a name="tab2"><img src="img/revistas/abc/v20n1/v20n1a05tab2.jpg"></a></p>      <P>Os mecanismos pelos quais os produtos naturais podem inibir o crescimento de microorganismos s&atilde;o diversos, e pode ser em parte devido &agrave; natureza hidrof&oacute;bica de determinados componentes. Esses referidos componentes podem interagir com a dupla camada lip&iacute;dica da membrana celular e afetar a cadeia respirat&oacute;ria e a produ&ccedil;&atilde;o de energia (Nicolson e Evans, 1999), ou at&eacute; mesmo tornar a c&eacute;lula mais perme&aacute;vel aos antibi&oacute;ticos, levando &agrave; suspens&atilde;o da atividade vital da celular (Burt, 2004). A interfer&ecirc;ncia com os sistemas de enzim&aacute;ticos de bact&eacute;rias pode ser tamb&eacute;m um potencial mecanismo de a&ccedil;&atilde;o (Wendakoon e Sakaguchi, 1995). Podem ser obtidos tais mecanismos de a&ccedil;&atilde;o pela combina&ccedil;&atilde;o de extrato com antibi&oacute;ticos &agrave; concentra&ccedil;&atilde;o sub-inibit&oacute;ria aplicada diretamente ao meio de cultura (Coutinho <I>et al</I>., 2010a).</P>      <P>Produtos naturais derivados de plantas medicinais v&ecirc;m sendo utilizados como fonte de novos compostos bioativos em especial para o tratamento de doen&ccedil;as infecciosas. Portanto, &eacute; real a possibilidade de utilizar plantas como fonte de novos compostos bioativos que sejam eficazes contra bact&eacute;rias resistentes aos antibi&oacute;ticos convencionais (Butler e Buss, 2006). Sejam esses produtos de origem vegetal ou animal, podem alterar o efeito de antibi&oacute;ticos, seja aumentando ou reduzindo suas atividades, podendo assim, serem denominados modificadores da atividade antibi&oacute;tica (Rodrigues <I>et al</I>., 2009; Tintino <I>et al., </I>2013).</P>      <P>A atividade sin&eacute;rgica observada pode ser devido &agrave; presen&ccedil;a de dois dos tr&ecirc;s principais componentes do &oacute;leo, os componentes &alpha;-citral (geranial) e &beta;-citral (neral) que apresentam uma reconhecida atividade antibacteriana frente a linhagens Gram-positivas e Gram-negativas, j&aacute; o terceiro principal componente do &oacute;leo o mirceno, n&atilde;o apresentou nenhuma atividade antibacteriana observ&aacute;vel (Martins <I>et al</I>., 2004). O citral &eacute; tido como sendo o respons&aacute;vel pelas atividades inseticidas e germicidas. No cultivo brasileiro, o teor de citral nos &oacute;leos essenciais de <I>C. citratus</I> est&aacute; em torno de 75 a 86% (Martins <I>et al</I>., 2004). Os taninos e os flavonoides s&atilde;o sintetizados por plantas em resposta a infec&ccedil;&otilde;es microbianas (Ho <I>et al</I>., 2001; Figueredo <I>et al</I>., 2013), sendo capazes de alterar a parede celular ou destruir a membrana plasm&aacute;tica facilitando absor&ccedil;&atilde;o das drogas (Matias <I>et al</I>., 2010; Figueredo <I>et al</I>., 2013).</P>      <P>A diferen&ccedil;a na atividade moduladora do &oacute;leo essencial contra as linhagens de <I>P. aeruginosa, </I>possivelmente se deve a presen&ccedil;a de mecanismos de resist&ecirc;ncia como bomba de efluxo, produ&ccedil;&atilde;o de enzimas que clivam o anel <I>&szlig;-</I>lact&acirc;mico (<I>&szlig;</I>-lactamases), mudan&ccedil;as nas PBP, entre outros (Bush, 2002; Enright <I>et al</I>., 2002).</P>      <P>A atua&ccedil;&atilde;o dos produtos naturais potencializando a a&ccedil;&atilde;o de antibi&oacute;ticos frente a bact&eacute;rias multirresistentes tem sido demonstrado em v&aacute;rios estudos (Coutinho <I>et al.</I>, 2009; Coutinho <I>et al.</I>, 2010a; Coutinho <I>et al.</I>, 2010b). A &quot;herbal shotgum&quot; ou &#151; &quot;synergistic multi-effect targeting&quot; &eacute; uma estrat&eacute;gia que refere ao uso de plantas e drogas em uma abordagem usando extratos combinados afetando diversos alvos do microrganismo ao mesmo tempo, com elementos terap&ecirc;uticos colaborando sinergicamente ou antagonicamente. Isto tem sido demonstrado n&atilde;o apenas a partir da combina&ccedil;&atilde;o de extratos, mas tamb&eacute;m de produtos naturais ou extratos e produtos sint&eacute;ticos ou antibi&oacute;ticos (Wagner e Ulrich-Merzenich, 2009).</P>      <P><B>CONCLUS&Atilde;O </B></P>      <P>Os resultados obtidos neste trabalho, indicam que o &oacute;leo essencial de <I>Cymbopogon citratus &eacute;</I> uma fonte alternativa de produto natural com a&ccedil;&atilde;o antibacteriana, j&aacute; que possui a presen&ccedil;a de compostos com reconhecida atividade antibacteriana como terpenos, al&eacute;m de indicar a possibilidade do uso desse &oacute;leo combinado a antibi&oacute;ticos utilizados na cl&iacute;nica frente a linhagens Gram-positivas e Gram-negativas.</P>      ]]></body>
<body><![CDATA[<P><B>AGRADECIMENTOS </B></P>      <P>A Faculdade Le&atilde;o Sampaio, ao CNPq e Funcap pelo apoio financeiro e &agrave; Universidade Regional do Cariri pela disponibiliza&ccedil;&atilde;o de materiais e espa&ccedil;o f&iacute;sico.</P>  <HR>      <P><B>REFER&Ecirc;NCIAS </B></P>      <!-- ref --><P>Baccaro MR, Moreno AM, Corr&ecirc;a A, Ferreira AJP, Calderaro FF. Resist&ecirc;ncia antimicrobiana de amostras de <I>Escherichia coli </I>isoladas de fezes de leit&otilde;es com diarreia. Arq Inst Biol. 2002;69(2):15-18.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000066&pid=S0120-548X201500010000500001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>      <!-- ref --><P>Bassol&eacute; IHN, Lamien-Meda A, Bayala B, Obame LC, Ilboudo AJ, Franz C, <I>et al</I>. Chemical composition and antimicrobial activity of <I>Cymbopogon citratus </I>and <I>Cymbopogon giganteus</I> essential oils alone and in combination. Phytomedicine. 2011;18(12):1070-1074. Doi: <a href="http://dx.doi.org/10.1016/j.phymed.2011.05.009" target="_blank">10.1016/j.phymed.2011.05.009</a> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000068&pid=S0120-548X201500010000500002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><P>Burt S. Essential oils: their antibacterial properties and potential applicationsin foods &#150;a review. Int J Food Microbiol. 2004;94(3):223-253. Doi: <a href="http://dx.doi.org/10.1016/j.ijfoodmicro.2004.03.022" target="_blank">http://dx.doi.org/10.1016/j.ijfoodmicro.2004.03.022</a>.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000069&pid=S0120-548X201500010000500003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>      <!-- ref --><P>Bush K. The impact of beta-lactamases on the development of novel antimicrobial agents. Curr Opin Invest Drugs. 2002;3(9):1284-1290.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000071&pid=S0120-548X201500010000500004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>      ]]></body>
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<ref-list>
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<person-group person-group-type="author">
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