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Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach
BACKGROUND: Novel vaccine candidates against Schistosoma japonicum are required, and antigens present in the vulnerable larval developmental stage are attractive targets. Post-genomic technologies are now available which can contribute to such antigen discovery. METHODS: A schistosome-specific prote...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080988/ https://www.ncbi.nlm.nih.gov/pubmed/24964958 http://dx.doi.org/10.1186/1756-3305-7-290 |
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author | McWilliam, Hamish EG Driguez, Patrick Piedrafita, David McManus, Donald P Meeusen, Els NT |
author_facet | McWilliam, Hamish EG Driguez, Patrick Piedrafita, David McManus, Donald P Meeusen, Els NT |
author_sort | McWilliam, Hamish EG |
collection | PubMed |
description | BACKGROUND: Novel vaccine candidates against Schistosoma japonicum are required, and antigens present in the vulnerable larval developmental stage are attractive targets. Post-genomic technologies are now available which can contribute to such antigen discovery. METHODS: A schistosome-specific protein microarray was probed using the local antibody response against migrating larvae. Antigens were assessed for their novelty and predicted larval expression and host-exposed features. One antigen was further characterised and its sequence and structure were analysed in silico. Real-time polymerase chain reaction was used to analyse transcript expression throughout development, and immunoblotting and enzyme-linked immunosorbent assays employed to determine antigen recognition by antibody samples. RESULTS: Several known and novel antigens were discovered, two of which showed up-regulated transcription in schistosomula. One novel antigen, termed S. japonicum Ly-6-like protein 1 (Sj-L6L-1), was further characterised and shown to share structural and sequence features with the Ly-6 protein family. It was found to be present in the worm tegument and expressed in both the larval and adult worms, but was found to be antigenic only in the lungs that the larvae migrate to and traverse. CONCLUSIONS: This study represents a novel approach to vaccine antigen discovery and may contribute to schistosome vaccine development against this important group of human and veterinary pathogens. |
format | Online Article Text |
id | pubmed-4080988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40809882014-07-04 Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach McWilliam, Hamish EG Driguez, Patrick Piedrafita, David McManus, Donald P Meeusen, Els NT Parasit Vectors Research BACKGROUND: Novel vaccine candidates against Schistosoma japonicum are required, and antigens present in the vulnerable larval developmental stage are attractive targets. Post-genomic technologies are now available which can contribute to such antigen discovery. METHODS: A schistosome-specific protein microarray was probed using the local antibody response against migrating larvae. Antigens were assessed for their novelty and predicted larval expression and host-exposed features. One antigen was further characterised and its sequence and structure were analysed in silico. Real-time polymerase chain reaction was used to analyse transcript expression throughout development, and immunoblotting and enzyme-linked immunosorbent assays employed to determine antigen recognition by antibody samples. RESULTS: Several known and novel antigens were discovered, two of which showed up-regulated transcription in schistosomula. One novel antigen, termed S. japonicum Ly-6-like protein 1 (Sj-L6L-1), was further characterised and shown to share structural and sequence features with the Ly-6 protein family. It was found to be present in the worm tegument and expressed in both the larval and adult worms, but was found to be antigenic only in the lungs that the larvae migrate to and traverse. CONCLUSIONS: This study represents a novel approach to vaccine antigen discovery and may contribute to schistosome vaccine development against this important group of human and veterinary pathogens. BioMed Central 2014-06-25 /pmc/articles/PMC4080988/ /pubmed/24964958 http://dx.doi.org/10.1186/1756-3305-7-290 Text en Copyright © 2014 McWilliam et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research McWilliam, Hamish EG Driguez, Patrick Piedrafita, David McManus, Donald P Meeusen, Els NT Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title | Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title_full | Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title_fullStr | Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title_full_unstemmed | Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title_short | Discovery of novel Schistosoma japonicum antigens using a targeted protein microarray approach |
title_sort | discovery of novel schistosoma japonicum antigens using a targeted protein microarray approach |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080988/ https://www.ncbi.nlm.nih.gov/pubmed/24964958 http://dx.doi.org/10.1186/1756-3305-7-290 |
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