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Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes
BACKGROUND: Trichinella spiralis infection induces protective immunity against re-infection in animal models. Identification of the antigens eliciting acquired immunity during infection is important for vaccine development against Trichinella infection and immunodiagnosis. METHODS AND FINDINGS: The...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545582/ https://www.ncbi.nlm.nih.gov/pubmed/26288365 http://dx.doi.org/10.1371/journal.pone.0136189 |
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author | Bi, Kuo Yang, Jing Wang, Lei Gu, Yuan Zhan, Bin Zhu, Xinping |
author_facet | Bi, Kuo Yang, Jing Wang, Lei Gu, Yuan Zhan, Bin Zhu, Xinping |
author_sort | Bi, Kuo |
collection | PubMed |
description | BACKGROUND: Trichinella spiralis infection induces protective immunity against re-infection in animal models. Identification of the antigens eliciting acquired immunity during infection is important for vaccine development against Trichinella infection and immunodiagnosis. METHODS AND FINDINGS: The T. spiralis adult cDNA library was immunoscreened with sera from pigs experimentally infected with 20,000 infective T. spiralis larvae. Total 43 positive clones encoding for 28 proteins were identified; one of the immunodominant proteins was 20 kDa Ts-ES-1 secreted by Trichinella stichocytes and existing in the excretory/secretory (ES) products of T. spiralis adult and muscle larval worms. Ts-ES-1 contains 172 amino acids with a typical signal peptide in the first 20 amino acids. The expression of Ts-ES-1 was detected in both the adult and muscle larval stages at the mRNA and protein expression levels. Mice immunized with recombinant Ts-ES-1 (rTs-ES-1) formulated with ISA50v2 adjuvant exhibited a significant worm reduction in both the adult worm (27%) and muscle larvae burden (42.1%) after a challenge with T. spiralis compared to the adjuvant control group (p<0.01). The rTs-ES-1-induced protection was associated with a high level of specific anti-Ts-ES-1 IgG antibodies and a Th1/Th2 mixed immune response. CONCLUSION: The newly identified rTs-ES-1 is an immunodominant protein secreted by Trichinella stichocytes during natural infection and enables to the induction of partial protective immunity in vaccinated mice against Trichinella infection. Therefore, rTs-ES-1 is a potential candidate for vaccine development against trichinellosis. |
format | Online Article Text |
id | pubmed-4545582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45455822015-09-01 Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes Bi, Kuo Yang, Jing Wang, Lei Gu, Yuan Zhan, Bin Zhu, Xinping PLoS One Research Article BACKGROUND: Trichinella spiralis infection induces protective immunity against re-infection in animal models. Identification of the antigens eliciting acquired immunity during infection is important for vaccine development against Trichinella infection and immunodiagnosis. METHODS AND FINDINGS: The T. spiralis adult cDNA library was immunoscreened with sera from pigs experimentally infected with 20,000 infective T. spiralis larvae. Total 43 positive clones encoding for 28 proteins were identified; one of the immunodominant proteins was 20 kDa Ts-ES-1 secreted by Trichinella stichocytes and existing in the excretory/secretory (ES) products of T. spiralis adult and muscle larval worms. Ts-ES-1 contains 172 amino acids with a typical signal peptide in the first 20 amino acids. The expression of Ts-ES-1 was detected in both the adult and muscle larval stages at the mRNA and protein expression levels. Mice immunized with recombinant Ts-ES-1 (rTs-ES-1) formulated with ISA50v2 adjuvant exhibited a significant worm reduction in both the adult worm (27%) and muscle larvae burden (42.1%) after a challenge with T. spiralis compared to the adjuvant control group (p<0.01). The rTs-ES-1-induced protection was associated with a high level of specific anti-Ts-ES-1 IgG antibodies and a Th1/Th2 mixed immune response. CONCLUSION: The newly identified rTs-ES-1 is an immunodominant protein secreted by Trichinella stichocytes during natural infection and enables to the induction of partial protective immunity in vaccinated mice against Trichinella infection. Therefore, rTs-ES-1 is a potential candidate for vaccine development against trichinellosis. Public Library of Science 2015-08-19 /pmc/articles/PMC4545582/ /pubmed/26288365 http://dx.doi.org/10.1371/journal.pone.0136189 Text en © 2015 Bi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bi, Kuo Yang, Jing Wang, Lei Gu, Yuan Zhan, Bin Zhu, Xinping Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title | Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title_full | Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title_fullStr | Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title_full_unstemmed | Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title_short | Partially Protective Immunity Induced by a 20 kDa Protein Secreted by Trichinella spiralis Stichocytes |
title_sort | partially protective immunity induced by a 20 kda protein secreted by trichinella spiralis stichocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545582/ https://www.ncbi.nlm.nih.gov/pubmed/26288365 http://dx.doi.org/10.1371/journal.pone.0136189 |
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