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:1513-1</font></em></font></strong></font></td></tr><tr><td colspan=2><br><br><table align=center width=700><tr><td>Área: <b>Imunologia Clínica e Diagnóstico ( Divisão F )</b><p align=justify><strong><P>SEROLOGIC DIAGNOSIS OF PSEUDOMONAS AERUGINOSA PULMONARY INFECTION IN CHILDREN WITH CYSTIC FIBROSIS</P></strong></p><p align=justify><b>Aline da Costa Cruz </b> (<i>UERJ</i>); <b>Tânia Folescu </b> (<i>UERJ</i>); <b>Laurinda Higa </b> (<i>UERJ</i>); <b>Elisabeth Andrade Marques </b> (<i>UERJ</i>); <b>Bianca Cruz Neves </b> (<i>UERJ</i>); <b>Lucimar Gonçalves Milagres </b> (<i>UERJ</i>)<br><br></p><b><font size=2>Resumo</font></b><p align=justify class=tres><font size=2><P class=MsoNormal style="MARGIN: 0cm 0cm 0pt; TEXT-INDENT: 35.45pt; TEXT-ALIGN: justify"><FONT face="Times New Roman, Times, serif"><SPAN lang=EN-US style="FONT-SIZE: 12pt; COLOR: black; mso-ansi-language: EN-US">Cystic Fibrosis (CF) is a lethal disease of autosomal recessive character, which affects people of different ethnicities. The disease is characterized by the involvement of systemic exocrine glands and in most patients, the lung disease becomes the predominant pathology. The infection with <I style="mso-bidi-font-style: normal">P. aeruginosa</I> is the leading cause of mortality in patients with CF. The Type III Secretion System (TTSS) of bacteria is expressed during acute disease and injects cytotoxic proteins inside the host cell. There is a great interesting in investigate the antibody response to <I style="mso-bidi-font-style: normal">P. aeruginosa</I> in CF patients in order to diagnose a pulmonary infection or colonization before the culture. Then, preventive antibiotic treatment can be initiated before the installation of chronic lung infection. We investigated the antibody response (IgG + IgA + IgM) against TTSS proteins of <I style="mso-bidi-font-style: normal">P. aeruginosa </I>by Western-blot. The study included 51 patients with CF, from 1.1 to 16.8 years </SPAN><SPAN lang=EN-US style="FONT-SIZE: 12pt; mso-ansi-language: EN-US">attending the Pediatric Pulmonology Unit of Fernandes Figueira Institute (IFF)  FIOCRUZ, <?xml:namespace prefix = st1 ns = "urn:schemas-microsoft-com:office:smarttags" /><st1:City w:st="on"><st1:place w:st="on">Rio de Janeiro</st1:place></st1:City>,<SPAN style="COLOR: black"> for a period of approximately 2 years. </SPAN>Most patients had or 4 blood samples collected for antibody analyses. Samples were obtained with a<SPAN style="COLOR: black"> mean interval of 6 months. The negative control group consisted of 28 non-CF individuals, from 2 to 17 years, attended at <st1:place w:st="on"><st1:PlaceName w:st="on">Pedro</st1:PlaceName> <st1:PlaceName w:st="on">Ernesto</st1:PlaceName> <st1:PlaceName w:st="on">University</st1:PlaceName> <st1:PlaceType w:st="on">Hospital</st1:PlaceType></st1:place> - HUPE - UERJ. The TTSS proteins were extracted from strains PAO1 and PAOÄExsA (regulator of TTSS proteins expression) of <I style="mso-bidi-font-style: normal">P. aeruginosa</I>. Positive and negative controls were used in all reactions. For the identification of TTSS proteins in the reaction we used antisera from mice immunized with the recombinant protein PcrV. Twelve (75%) of 16 CF patients considered not infected by <I style="mso-bidi-font-style: normal">P. aeruginosa </I>had their first serology positive for "PopB" and 15 (93.75%) for "ExoS/ExoT . These results indicated that these patients were colonized or infected by <I style="mso-bidi-font-style: normal">P. aeruginosa</I>. </SPAN><SPAN style="mso-bidi-font-weight: bold">About 25% e 35,7% of negative control sera showed a weak reactivity with  PopB or  ExoS , respectively.</SPAN><SPAN style="COLOR: black"> The time between the first positive serology and the first isolation of <I style="mso-bidi-font-style: normal">P. aeruginosa</I> in these patients ranged from 18 to 30 months. In conclusion, it is possible to make a serological diagnosis of pulmonary infection by<I style="mso-bidi-font-style: normal"> P. aeruginosa </I>before the isolation of the bacterium by culture.<?xml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /><o:p></o:p></SPAN></SPAN></FONT></P></font></p><br><b>Palavras-chave: </b>&nbsp;Cystic Fibrosis, Pseudomonas aeruginosa, Pulmonary infection, Serologic diagnosis, TTSS</td></tr></table></tr></td></table></body></html>