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Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro

East Coast fever (ECF) caused by Theileria parva kills cattle in East, Central and Southern Africa leading to significant economic losses. Vaccination is used as a control strategy against ECF and is presently dependent on deliberate infection with live sporozoites and simultaneous treatment with a...

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Autores principales: Nyagwange, James, Nene, Vishvanath, Mwalimu, Stephen, Henson, Sonal, Steinaa, Lucilla, Nzau, Benjamin, Tijhaar, Edwin, Pelle, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Scientific 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956992/
https://www.ncbi.nlm.nih.gov/pubmed/29678234
http://dx.doi.org/10.1016/j.vetimm.2018.03.004
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author Nyagwange, James
Nene, Vishvanath
Mwalimu, Stephen
Henson, Sonal
Steinaa, Lucilla
Nzau, Benjamin
Tijhaar, Edwin
Pelle, Roger
author_facet Nyagwange, James
Nene, Vishvanath
Mwalimu, Stephen
Henson, Sonal
Steinaa, Lucilla
Nzau, Benjamin
Tijhaar, Edwin
Pelle, Roger
author_sort Nyagwange, James
collection PubMed
description East Coast fever (ECF) caused by Theileria parva kills cattle in East, Central and Southern Africa leading to significant economic losses. Vaccination is used as a control strategy against ECF and is presently dependent on deliberate infection with live sporozoites and simultaneous treatment with a long-acting oxytetracycline. Although effective, this method has serious limitations; the immunity is parasite strain specific and immunized cattle can become life-long asymptomatic carriers of the parasite, posing risk for the spread of the disease. In efforts to develop a subunit vaccine, the role of antibodies in the neutralization of T. parva sporozoites infection of host cells has been investigated and a circumsporozoite protein, p67, is able to induce such neutralizing antibodies. However, the p67 protein only protects a proportion of immunized cattle against T. parva challenge and such protection might be improved by inclusion of additional parasite antigens that neutralize sporozoite infection. In an attempt to identify such antigens, we searched the re-annotated T. parva genome for genes predicted to contain GPI anchor signals, since they are likely to be located on the cell surface, and expressed fragments of six of the selected genes in E. coli. The recombinant proteins were used to raise antisera in mice. Antisera to two proteins, TpMuguga_01g00876 and TpMuguga_01g00939, neutralized sporozoite infectivity to a high degree, while antisera to two additional proteins, TpMuguga_01g00095 and TpMuguga_04g00437, exhibited moderate neutralizing capacity. We conclude that these four antigens are potential vaccine candidates, which should be evaluated further in cattle.
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spelling pubmed-59569922018-05-17 Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro Nyagwange, James Nene, Vishvanath Mwalimu, Stephen Henson, Sonal Steinaa, Lucilla Nzau, Benjamin Tijhaar, Edwin Pelle, Roger Vet Immunol Immunopathol Article East Coast fever (ECF) caused by Theileria parva kills cattle in East, Central and Southern Africa leading to significant economic losses. Vaccination is used as a control strategy against ECF and is presently dependent on deliberate infection with live sporozoites and simultaneous treatment with a long-acting oxytetracycline. Although effective, this method has serious limitations; the immunity is parasite strain specific and immunized cattle can become life-long asymptomatic carriers of the parasite, posing risk for the spread of the disease. In efforts to develop a subunit vaccine, the role of antibodies in the neutralization of T. parva sporozoites infection of host cells has been investigated and a circumsporozoite protein, p67, is able to induce such neutralizing antibodies. However, the p67 protein only protects a proportion of immunized cattle against T. parva challenge and such protection might be improved by inclusion of additional parasite antigens that neutralize sporozoite infection. In an attempt to identify such antigens, we searched the re-annotated T. parva genome for genes predicted to contain GPI anchor signals, since they are likely to be located on the cell surface, and expressed fragments of six of the selected genes in E. coli. The recombinant proteins were used to raise antisera in mice. Antisera to two proteins, TpMuguga_01g00876 and TpMuguga_01g00939, neutralized sporozoite infectivity to a high degree, while antisera to two additional proteins, TpMuguga_01g00095 and TpMuguga_04g00437, exhibited moderate neutralizing capacity. We conclude that these four antigens are potential vaccine candidates, which should be evaluated further in cattle. Elsevier Scientific 2018-05 /pmc/articles/PMC5956992/ /pubmed/29678234 http://dx.doi.org/10.1016/j.vetimm.2018.03.004 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nyagwange, James
Nene, Vishvanath
Mwalimu, Stephen
Henson, Sonal
Steinaa, Lucilla
Nzau, Benjamin
Tijhaar, Edwin
Pelle, Roger
Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title_full Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title_fullStr Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title_full_unstemmed Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title_short Antibodies to in silico selected GPI-anchored Theileria parva proteins neutralize sporozoite infection in vitro
title_sort antibodies to in silico selected gpi-anchored theileria parva proteins neutralize sporozoite infection in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5956992/
https://www.ncbi.nlm.nih.gov/pubmed/29678234
http://dx.doi.org/10.1016/j.vetimm.2018.03.004
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