ÿþ<HTML><HEAD><TITLE>25º Congresso Brasileiro de Microbiologia </TITLE><link rel=STYLESHEET type=text/css href=css.css></HEAD><BODY aLink=#ff0000 bgColor=#FFFFFF leftMargin=0 link=#000000 text=#000000 topMargin=0 vLink=#000000 marginheight=0 marginwidth=0><table align=center width=700 cellpadding=0 cellspacing=0><tr><td align=left bgcolor=#cccccc valign=top width=550><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=3><font size=1>25º Congresso Brasileiro de Microbiologia </font></font></strong><font face=Verdana size=1><b><br></b></font><font face=Verdana, Arial,Helvetica, sans-serif size=1><strong> </strong></font></font></td><td align=right bgcolor=#cccccc valign=top width=150><font face=arial size=2><strong><font face=Verdana, Arial, Helvetica, sans-serif size=1><font size=1>ResumoID:487-2</font></em></font></strong></font></td></tr><tr><td colspan=2><br><br><table align=center width=700><tr><td>Área: <b>Microbiologia Clinica ( Divisão A )</b><p align=justify><strong>HIGH LEVEL RESISTANCE IN <EM>KLEBSIELLA PNEUMONIAE </EM>ISOLATES HARBOURING SIMULTANEOUSLY KPC AND ESBL GENES</strong></p><p align=justify><b><u>Anna Carolina Soares Almeida </u></b> (<i>UPE</i>); <b>Felipe Lira de Sá Cavalcanti </b> (<i>UFPE</i>); <b>Marinalda Anselmo Vilela </b> (<i>UPE</i>); <b>Marcos Antonio de Morais Júnior </b> (<i>UFPE</i>); <b>Márcia Maria Camargo de Morais </b> (<i>UPE</i>)<br><br></p><b><font size=2>Resumo</font></b><p align=justify class=tres><font size=2><SPAN lang=EN-US style="FONT-SIZE: 12pt; LINE-HEIGHT: 115%; FONT-FAMILY: Arial; mso-fareast-language: EN-US; mso-fareast-font-family: Calibri; mso-ansi-language: EN-US; mso-bidi-language: AR-SA">Carbapenem are regarded as the drugs of choice for serious infections with ESBL-producing organisms. For this reason, KPC carbapenemases represent a serious public health problem. KPC-producing <I style="mso-bidi-font-style: normal">K. pneumoniae</I> became a frequent nosocomial pathogen, specially in bloodstream infections. Reports on production of multiple beta-lactamases in a single pathogen are increasing, as well as, the occurrence of other integron-borne resistance determinants. The ten strains used in this study showed decreased susceptibility to third-generation cephalosporin and were isolated from bloodstream infections from patients hospitalized in a teaching university hospital (HUOC), in Recife, Brazil. Susceptibilities were determined by the disk-diffusion method; screening for the ESBL and class A carbapenemase-producing phenotypes were performed and evaluated according to CLSI (2009) criteria. The presence of <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC</SUB>, <I style="mso-bidi-font-style: normal">bla</I><SUB>CTX-M</SUB>, <I style="mso-bidi-font-style: normal">bla</I><SUB>TEM</SUB> and class 1 integrase was determined by specific PCR. The positive PCR product for <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC </SUB>was purified using the PCR Purification Kit (Promega). Sequencing was performed with the BigDye Terminator Cycle Sequencing Kit in ABI Prisma 3100 DNA sequencer (Applied Biosystems). Sequences were compared with database of GenBank. The results exhibited that the isolates were positive for ESBL (80%) and carbapenemase (60%) production; the presence of the <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC</SUB> was confirmed by sequencing. Antimicrobial susceptibility testing showed high resistance levels (more than 80%) to extended-spectrum cephalosporin, ertapenem, aminoglicosydes, monobactam, quinolones and beta-lactam/beta-lactamase inhibitor. Molecular investigations showed that all the isolates harbored class 1 integron. Moreover, 84%, 50% e 33% of the isolates exhibited simultaneous presence of <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC</SUB>/<I style="mso-bidi-font-style: normal">bla</I><SUB>CTX</SUB>, <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC</SUB>/<I style="mso-bidi-font-style: normal">bla</I><SUB>TEM</SUB>, and <I style="mso-bidi-font-style: normal">bla</I><SUB>KPC</SUB>/<I style="mso-bidi-font-style: normal">bla</I><SUB>CTX/</SUB><I style="mso-bidi-font-style: normal">bla</I><SUB>TEM</SUB>, respectively. The isolates showed a high rate of resistance to beta-lactam and non-beta-lactam antibiotics. This profile should be probably an effect of association of two or more <I style="mso-bidi-font-style: normal">bla</I> genes, in addition to other gene cassetes inserted in class 1 integron. Our finding exhibited </SPAN><SPAN lang=EN-US style="FONT-SIZE: 12pt; LINE-HEIGHT: 115%; FONT-FAMILY: Arial; mso-fareast-language: PT-BR; mso-fareast-font-family: Calibri; mso-ansi-language: EN-US; mso-bidi-language: AR-SA">the coexistence of multiple resistant genes in the same isolate</SPAN><SPAN lang=EN-US style="FONT-SIZE: 12pt; LINE-HEIGHT: 115%; FONT-FAMILY: Arial; mso-fareast-language: EN-US; mso-fareast-font-family: Calibri; mso-ansi-language: EN-US; mso-bidi-language: AR-SA">. Methods of surveillance should be implanting to control the spread of these MDR phenotypes.</SPAN></font></p><br><b>Palavras-chave: </b>&nbsp;Carbapenemase, KPC, ESBL, Klebsiella pneumoniae</td></tr></table></tr></td></table></body></html>