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Chitosan nano-structure loaded with recombinant E. coli O157:H7 antigens as a vaccine candidate can effectively increase immunization capacity.
Khanifar, Jaleh; Salmanian, Ali Hatef; Haji Hosseini, Reza; Amani, Jafar; Kazemi, Rohoallah.
Afiliação
  • Khanifar J; a Department of Biology, Payame Noor University , Tehran , Iran.
  • Salmanian AH; b Department of Agricultural Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB) , Tehran , Iran.
  • Haji Hosseini R; a Department of Biology, Payame Noor University , Tehran , Iran.
  • Amani J; c Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences , Tehran , Iran.
  • Kazemi R; d Department of Molecular Biology, Green Gene Company , Tehran , Iran.
Artif Cells Nanomed Biotechnol ; 47(1): 2593-2604, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31240960
ABSTRACT
Escherichia coli O157H7 is considered as emerging foodborne pathogens that occur globally. Three major virulence protein factors; EspA(E), intimin(I), Tir(T) and Stx2 toxin have been found to be highly associated with bloody diarrhoea or, Haemolytic Uremic Syndrome. In this study, a trivalent recombinant EIT in combination with the binding domain of STX toxin were encapsulated with chitosan nanoparticles as a combination vaccine candidate. Mice were immunized either subcutaneously or orally with these antigens and challenged with E. coli O157H7. Results of the binding inhibition assay with caco2 cell monolayer show a significant reduction in the adhesion percentage of pre-treated E. coli O157H7 with immunized mice sera. Evaluation of neutralizing abilities of immune sera pre-incubated with CD50 dose of STX2 by Vero cells cytotoxicity neutralization assay shows less morphological reforms in comparison with the control groups. Results of mice mortality challenge with STX2 demonstrate around 66% of survived in immunized mice. In a challenge experiment with E. coli O157H7, all the immunized mice showed a significant decrease in bacterial colonization and shedding. The results indicate that the use of multiple recombinant proteins in combination with natural nanostructure effectively evocated strong humoral and mucosal response, increasing the protection capacity of the synthetic antigen.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Imunização / Escherichia coli O157 / Quitosana / Nanopartículas / Antígenos de Bactérias Limite: Animals Idioma: En Revista: Artif Cells Nanomed Biotechnol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Portadores de Fármacos / Imunização / Escherichia coli O157 / Quitosana / Nanopartículas / Antígenos de Bactérias Limite: Animals Idioma: En Revista: Artif Cells Nanomed Biotechnol Ano de publicação: 2019 Tipo de documento: Article