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Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System

Bovine anaplasmosis or cattle-tick fever is a tick-borne haemolytic disease caused by the rickettsial haemoparasite Anaplasma marginale in tropical and subtropical areas of the world. While difficult to express, the proteins VirB9-1 and VirB10 are immunogenic components of the outer membrane type IV...

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Autores principales: Zhang, Bing, Cavallaro, Antonio S., Mody, Karishma T., Zhang, Jun, Deringer, James R., Brown, Wendy C., Mahony, Timothy J., Yu, Chengzhong, Mitter, Neena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245741/
https://www.ncbi.nlm.nih.gov/pubmed/28335329
http://dx.doi.org/10.3390/nano6110201
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author Zhang, Bing
Cavallaro, Antonio S.
Mody, Karishma T.
Zhang, Jun
Deringer, James R.
Brown, Wendy C.
Mahony, Timothy J.
Yu, Chengzhong
Mitter, Neena
author_facet Zhang, Bing
Cavallaro, Antonio S.
Mody, Karishma T.
Zhang, Jun
Deringer, James R.
Brown, Wendy C.
Mahony, Timothy J.
Yu, Chengzhong
Mitter, Neena
author_sort Zhang, Bing
collection PubMed
description Bovine anaplasmosis or cattle-tick fever is a tick-borne haemolytic disease caused by the rickettsial haemoparasite Anaplasma marginale in tropical and subtropical areas of the world. While difficult to express, the proteins VirB9-1 and VirB10 are immunogenic components of the outer membrane type IV secretion system that have been identified as candidate antigens for vaccines targeting of A. marginale. Soluble VirB9-1 and VirB10 were successfully expressed using Pichia pastoris. When formulated with the self-adjuvanting silica vesicles, SV-100 (diameter: 50 nm, and pore entrance size: 6 nm), 200 µg of VirB9-1 and VirB10 were adsorbed per milligram of nanoparticle. The VirB9-1 and VirB10, SV-100 formulations were shown to induce higher antibody responses in mice compared to the QuilA formulations. Moreover, intracellular staining of selected cytokines demonstrated that both VirB9-1 and VirB10 formulations induced cell-mediated immune responses in mice. Importantly, the SV-100 VirB9-1 and VirB10 complexes were shown to specifically stimulate bovine T-cell linages derived from calves immunised with A. marginale outer membrane fractions, suggesting formulations will be useful for bovine immunisation and protection studies. Overall this study demonstrates the potential of self-adjuvanting silica vesicle formulations to address current deficiencies in vaccine delivery applications.
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spelling pubmed-52457412017-03-21 Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System Zhang, Bing Cavallaro, Antonio S. Mody, Karishma T. Zhang, Jun Deringer, James R. Brown, Wendy C. Mahony, Timothy J. Yu, Chengzhong Mitter, Neena Nanomaterials (Basel) Article Bovine anaplasmosis or cattle-tick fever is a tick-borne haemolytic disease caused by the rickettsial haemoparasite Anaplasma marginale in tropical and subtropical areas of the world. While difficult to express, the proteins VirB9-1 and VirB10 are immunogenic components of the outer membrane type IV secretion system that have been identified as candidate antigens for vaccines targeting of A. marginale. Soluble VirB9-1 and VirB10 were successfully expressed using Pichia pastoris. When formulated with the self-adjuvanting silica vesicles, SV-100 (diameter: 50 nm, and pore entrance size: 6 nm), 200 µg of VirB9-1 and VirB10 were adsorbed per milligram of nanoparticle. The VirB9-1 and VirB10, SV-100 formulations were shown to induce higher antibody responses in mice compared to the QuilA formulations. Moreover, intracellular staining of selected cytokines demonstrated that both VirB9-1 and VirB10 formulations induced cell-mediated immune responses in mice. Importantly, the SV-100 VirB9-1 and VirB10 complexes were shown to specifically stimulate bovine T-cell linages derived from calves immunised with A. marginale outer membrane fractions, suggesting formulations will be useful for bovine immunisation and protection studies. Overall this study demonstrates the potential of self-adjuvanting silica vesicle formulations to address current deficiencies in vaccine delivery applications. MDPI 2016-11-05 /pmc/articles/PMC5245741/ /pubmed/28335329 http://dx.doi.org/10.3390/nano6110201 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Bing
Cavallaro, Antonio S.
Mody, Karishma T.
Zhang, Jun
Deringer, James R.
Brown, Wendy C.
Mahony, Timothy J.
Yu, Chengzhong
Mitter, Neena
Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title_full Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title_fullStr Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title_full_unstemmed Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title_short Nanoparticle-Based Delivery of Anaplasma marginale Membrane Proteins; VirB9-1 and VirB10 Produced in the Pichia pastoris Expression System
title_sort nanoparticle-based delivery of anaplasma marginale membrane proteins; virb9-1 and virb10 produced in the pichia pastoris expression system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5245741/
https://www.ncbi.nlm.nih.gov/pubmed/28335329
http://dx.doi.org/10.3390/nano6110201
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