Literature DB >> 20351187

The protein moiety of Brucella abortus outer membrane protein 16 is a new bacterial pathogen-associated molecular pattern that activates dendritic cells in vivo, induces a Th1 immune response, and is a promising self-adjuvanting vaccine against systemic and oral acquired brucellosis.

Karina A Pasquevich1, Clara García Samartino, Lorena M Coria, Silvia M Estein, Astrid Zwerdling, Andrés E Ibañez, Paula Barrionuevo, Fernanda Souza de Oliveira, Natalia Barbosa Carvalho, Julia Borkowski, Sergio Costa Oliveira, Heribert Warzecha, Guillermo H Giambartolomei, Juliana Cassataro.   

Abstract

Knowing the inherent stimulatory properties of the lipid moiety of bacterial lipoproteins, we first hypothesized that Brucella abortus outer membrane protein (Omp)16 lipoprotein would be able to elicit a protective immune response without the need of external adjuvants. In this study, we demonstrate that Omp16 administered by the i.p. route confers significant protection against B. abortus infection and that the protective response evoked is independent of the protein lipidation. To date, Omp16 is the first Brucella protein that without the requirement of external adjuvants is able to induce similar protection levels to the control live vaccine S19. Moreover, the protein portion of Omp16 (unlipidated Omp16 [U-Omp16]) elicits a protective response when administered by the oral route. Either systemic or oral immunization with U-Omp16 elicits a Th1-specific response. These abilities of U-Omp16 indicate that it is endowed with self-adjuvanting properties. The adjuvanticity of U-Omp16 could be explained, at least in part, by its capacity to activate dendritic cells in vivo. U-Omp16 is also able to stimulate dendritic cells and macrophages in vitro. The latter property and its ability to induce a protective Th1 immune response against B. abortus infection have been found to be TLR4 dependent. The facts that U-Omp16 is an oral protective Ag and possesses a mucosal self-adjuvanting property led us to develop a plant-made vaccine expressing U-Omp16. Our results indicate that plant-expressed recombinant U-Omp16 is able to confer protective immunity, when given orally, indicating that a plant-based oral vaccine expressing U-Omp16 could be a valuable approach to controlling this disease.

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Year:  2010        PMID: 20351187     DOI: 10.4049/jimmunol.0902209

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  28 in total

1.  TLR2 and TLR4 signaling pathways are required for recombinant Brucella abortus BCSP31-induced cytokine production, functional upregulation of mouse macrophages, and the Th1 immune response in vivo and in vitro.

Authors:  Jia-Yun Li; Yuan Liu; Xiao-Xue Gao; Xiang Gao; Hong Cai
Journal:  Cell Mol Immunol       Date:  2014-04-28       Impact factor: 11.530

Review 2.  The role of NLRP3 and AIM2 in inflammasome activation during Brucella abortus infection.

Authors:  Fernanda M Marim; Miriam M Costa Franco; Marco Tulio R Gomes; Maria Cruz Miraglia; Guillermo H Giambartolomei; Sergio C Oliveira
Journal:  Semin Immunopathol       Date:  2016-07-12       Impact factor: 9.623

3.  Oral delivery of Brucella spp. recombinant protein U-Omp16 abrogates the IgE-mediated milk allergy.

Authors:  Paola Lorena Smaldini; Andrés Esteban Ibañez; Carlos Alberto Fossati; Juliana Cassataro; Guillermo Horacio Docena
Journal:  Hum Vaccin Immunother       Date:  2014       Impact factor: 3.452

4.  Invasive Escherichia coli vaccines expressing Brucella melitensis outer membrane proteins 31 or 16 or periplasmic protein BP26 confer protection in mice challenged with B. melitensis.

Authors:  V K Gupta; G Radhakrishnan; J Harms; G Splitter
Journal:  Vaccine       Date:  2012-04-28       Impact factor: 3.641

5.  Immunization with Brucella VirB proteins reduces organ colonization in mice through a Th1-type immune response and elicits a similar immune response in dogs.

Authors:  Cora N Pollak; María Magdalena Wanke; Silvia M Estein; M Victoria Delpino; Norma E Monachesi; Elida A Comercio; Carlos A Fossati; Pablo C Baldi
Journal:  Clin Vaccine Immunol       Date:  2014-12-24

6.  Toll-like receptor 4-linked Janus kinase 2 signaling contributes to internalization of Brucella abortus by macrophages.

Authors:  Jin Ju Lee; Dong Hyeok Kim; Dae Geun Kim; Hu Jang Lee; Wongi Min; Man Hee Rhee; Jae Youl Cho; Masahisa Watarai; Suk Kim
Journal:  Infect Immun       Date:  2013-04-29       Impact factor: 3.441

7.  Antigen-specific acquired immunity in human brucellosis: implications for diagnosis, prognosis, and vaccine development.

Authors:  Anthony P Cannella; Renee M Tsolis; Li Liang; Philip L Felgner; Mayuko Saito; Alessandro Sette; Eduardo Gotuzzo; Joseph M Vinetz
Journal:  Front Cell Infect Microbiol       Date:  2012-02-01       Impact factor: 5.293

Review 8.  The role of innate immune signals in immunity to Brucella abortus.

Authors:  Marco Túlio R Gomes; Priscila C Campos; Leonardo A de Almeida; Fernanda S Oliveira; Miriam Maria S Costa; Fernanda M Marim; Guilherme S M Pereira; Sergio C Oliveira
Journal:  Front Cell Infect Microbiol       Date:  2012-10-25       Impact factor: 5.293

9.  The immunomodulatory activity of meningococcal lipoprotein Ag473 depends on the conformation made up of the lipid and protein moieties.

Authors:  Ching-Liang Chu; Yen-Ling Yu; Yueh-Chen Kung; Pei-Yu Liao; Ko-Jiunn Liu; Yen-Tzu Tseng; Yuan-Chuen Lin; Steve Shih-Yang Hsieh; Pele Choi-Sing Chong; Chiou-Ying Yang
Journal:  PLoS One       Date:  2012-07-23       Impact factor: 3.240

10.  Caspase-2-dependent dendritic cell death, maturation, and priming of T cells in response to Brucella abortus infection.

Authors:  Xinna Li; Yongqun He
Journal:  PLoS One       Date:  2012-08-22       Impact factor: 3.240

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