• JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
  • JoomlaWorks Simple Image Rotator
 
  Bookmark and Share
 
 
Doctoral Thesis
DOI
10.11606/T.42.2013.tde-18032014-163426
Document
Author
Full name
Halyka Luzorio Franzotti Vasconcellos
Institute/School/College
Knowledge Area
Date of Defense
Published
São Paulo, 2013
Supervisor
Committee
Silva, Wilmar Dias da (President)
Baptistão, Carla Cristina Squaiella
Calich, Vera Lucia Garcia
Elias Junior, Waldir Pereira
Rodriguez, Dunia Del Carmen
Title in Portuguese
Desenvolvimento de cepas de Mycobacterium bovis Calmette-Guérin (BCG) e Mycobacterium smegmatis que expressam fatores de virulência de Escherichia coli enteropatogênica (EPEC).
Keywords in Portuguese
Escherichia coli
Clonagem
Diarréia infantil
Vacinas
Virulência
Abstract in Portuguese
Escherichia coli enteropatogênica (EPEC) é uma importante causa de diarreia infantil. EPEC adere no epitélio intestinal e causa uma lesão conhecida como attaching and effacing (A/E). Cepas recombinantes de Mycobacterium smegmatis (Smeg) e Mycobacterium bovis (BCG) foram construídas para expressar BfpA ou Intimina. Os genes dessas proteínas foram amplificadas por PCR do DNA genômico de EPEC e inseridos nos sítios de BamHI/KpnI do vetor pMIP12. Os plasmídeos construídos pMIP-bfpA e pMIP-intimina foram introduzidos, separadamente,nas cepas de Smeg e BCG. Clones recombinantes foram selecionados baseado na resistência a kanamicina e nomeados como rSmeg pMIP (bfpA ou intimina) and rBCG pMIP (bfpA ou intimina). A expressão dos genes bfpA e intimina foram detectados por Western blotting usando anticorpos primários policonais anti-BfpA e anti-intimina. A imunogenicidade dessas proteínas foi avaliada em camundongos C57BL/6 pela presença de anticorpos anti-BfpA e anti-intimina IgA e IgG nas fezes e soro, respectivamente. TNF-a e INF-g foram produzidas in vitro por céulas do baço de camundongos imunizados com a vacina recombinante com BfpA e Intimina. A adesão de EPEC (E2348/69) em células alvo Hep-2 foi bloqueada pelos anticorpos IgA ou IgG de camundongos imunizados com as vacinas recombinantes, mas não por anticorpos de animais não imunizados. Vacinas recombinantes contendo as proteínas BfpA e Intimina de EPEC podem ser candidatas promissoras.
Title in English
Generation of recombinant bacillus Calmette Guérin and Mycobacterium smegmatis expressing BfpA and intimin as vaccine vectors against enteropathogenic Escherichia coli.
Keywords in English
Escherichia coli
Cloning
Infant diarrhea
Vaccines
Virulence
Abstract in English
Enteropathogenic Escherichia coli (EPEC) is an important cause of diarrhea in children. EPEC adheres to the intestinal epithelium and causes attaching and effacing (A/E) lesions. Recombinant Mycobacterium smegmatis (Smeg) and Mycobacterium bovis BCG strains were constructed to express either BfpA or intimin. The entire bfpA gene and a portion of the intimin gene were amplified by PCR from EPEC genomic DNA and inserted into the pMIP12 vector at the BamHI/KpnI sites. The pMIP bfpA and pMIP intimin vectors were introduced separately into Smeg and BCG. Recombinant clones were selected based on kanamycin resistance and designated rSmeg pMIP (bfpA or intimin) and rBCG pMIP (bfpA or intimin). The expres-sion of bfpA and intimin was detected by Western blotting using polyclonal anti-BfpA and anti-intimin primary antibodies. The immunogenicity of these proteins was assessed in C57BL/6 mice by assaying the feces and serum for the presence of anti-BfpA and anti-intimin IgA and IgG antibodies. TNF-a and INF-g were produced in vitro by spleen cells from mice immunized with recombinant BfpA, whereas TNF-g was produced in mice immunized with recombinant intimin. The adhesion of EPEC (E2348/69) to Hep-2 target cells was blocked by IgA or IgG antibodies from mice immunized with recombinant BfpA or intimin but not by antibodies from non-immunized mice. Immunogenic non-infectious vectors containing relevant EPEC virulence genes may be promising vaccine candidates.
 
WARNING - Viewing this document is conditioned on your acceptance of the following terms of use:
This document is only for private use for research and teaching activities. Reproduction for commercial use is forbidden. This rights cover the whole data about this document as well as its contents. Any uses or copies of this document in whole or in part must include the author's name.
Publishing Date
2014-03-29
 
WARNING: Learn what derived works are clicking here.
All rights of the thesis/dissertation are from the authors
Centro de Informática de São Carlos
Digital Library of Theses and Dissertations of USP. Copyright © 2001-2021. All rights reserved.