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Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax
BACKGROUND: Malaria parasites form intracellular membranes that separate the parasite from the internal space of erythrocytes, and membrane proteins from the parasites are exported to the host via the membrane. In our previous study, Plasmodium vivax early transcribed membrane protein (PvETRAMP) 11....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921578/ https://www.ncbi.nlm.nih.gov/pubmed/31856917 http://dx.doi.org/10.1186/s13071-019-3846-4 |
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author | Lee, Seong-Kyun Han, Jin-Hee Park, Ji-Hoon Ha, Kwon-Soo Park, Won Sun Hong, Seok-Ho Na, Sunghun Cheng, Yang Han, Eun-Taek |
author_facet | Lee, Seong-Kyun Han, Jin-Hee Park, Ji-Hoon Ha, Kwon-Soo Park, Won Sun Hong, Seok-Ho Na, Sunghun Cheng, Yang Han, Eun-Taek |
author_sort | Lee, Seong-Kyun |
collection | PubMed |
description | BACKGROUND: Malaria parasites form intracellular membranes that separate the parasite from the internal space of erythrocytes, and membrane proteins from the parasites are exported to the host via the membrane. In our previous study, Plasmodium vivax early transcribed membrane protein (PvETRAMP) 11.2, an intracellular membrane protein that is highly expressed in blood-stage parasites, was characterized as a highly immunogenic protein in P. vivax malaria patients. However, the other PvETRAMP family proteins have not yet been investigated. In this study, PvETRAMPs were expressed and evaluated to determine their immunological profiles. METHODS: The protein structure and amino acid alignment were carried out using bioinformatics analysis software. A total of six PvETRAMP family proteins were successfully expressed and purified using a wheat germ cell free protein expression system and the purified proteins were used for protein microarray and immunization of mice. The localization of the protein was determined with serum against PvETRAMP4. IgG subclasses were assessed from the immunized mice. RESULTS: In silico analysis showed that P. vivax exhibits nine genes encoding the ETRAMP family. The ETRAMP family proteins are relatively small molecules with conserved structural features. A total of 6 recombinant ETRAMP proteins were successfully expressed and purified. The serum positivity of P. vivax malaria patients and healthy individuals was evaluated using a protein microarray method. Among the PvETRAMPs, ETRAMP4 showed the highest positivity rate of 62%, comparable to that of PvETRAMP11.2, which served as the positive control, and a typical export pattern of PvETRAMP4 was observed in the P. vivax parasite. The assessment of IgG subclasses in mice immunized with PvETRAMP4 showed high levels of IgG1 and IgG2b. PvETRAMP family proteins were identified and characterized as serological markers. CONCLUSIONS: The relatively high antibody responses to PvETRAMP4 as well as the specific IgG subclasses observed in immunized mice suggest that the ETRAMP family is immunogenic in pathogens and can be used as a protein marker and for vaccine development. [Image: see text] |
format | Online Article Text |
id | pubmed-6921578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69215782019-12-30 Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax Lee, Seong-Kyun Han, Jin-Hee Park, Ji-Hoon Ha, Kwon-Soo Park, Won Sun Hong, Seok-Ho Na, Sunghun Cheng, Yang Han, Eun-Taek Parasit Vectors Research BACKGROUND: Malaria parasites form intracellular membranes that separate the parasite from the internal space of erythrocytes, and membrane proteins from the parasites are exported to the host via the membrane. In our previous study, Plasmodium vivax early transcribed membrane protein (PvETRAMP) 11.2, an intracellular membrane protein that is highly expressed in blood-stage parasites, was characterized as a highly immunogenic protein in P. vivax malaria patients. However, the other PvETRAMP family proteins have not yet been investigated. In this study, PvETRAMPs were expressed and evaluated to determine their immunological profiles. METHODS: The protein structure and amino acid alignment were carried out using bioinformatics analysis software. A total of six PvETRAMP family proteins were successfully expressed and purified using a wheat germ cell free protein expression system and the purified proteins were used for protein microarray and immunization of mice. The localization of the protein was determined with serum against PvETRAMP4. IgG subclasses were assessed from the immunized mice. RESULTS: In silico analysis showed that P. vivax exhibits nine genes encoding the ETRAMP family. The ETRAMP family proteins are relatively small molecules with conserved structural features. A total of 6 recombinant ETRAMP proteins were successfully expressed and purified. The serum positivity of P. vivax malaria patients and healthy individuals was evaluated using a protein microarray method. Among the PvETRAMPs, ETRAMP4 showed the highest positivity rate of 62%, comparable to that of PvETRAMP11.2, which served as the positive control, and a typical export pattern of PvETRAMP4 was observed in the P. vivax parasite. The assessment of IgG subclasses in mice immunized with PvETRAMP4 showed high levels of IgG1 and IgG2b. PvETRAMP family proteins were identified and characterized as serological markers. CONCLUSIONS: The relatively high antibody responses to PvETRAMP4 as well as the specific IgG subclasses observed in immunized mice suggest that the ETRAMP family is immunogenic in pathogens and can be used as a protein marker and for vaccine development. [Image: see text] BioMed Central 2019-12-19 /pmc/articles/PMC6921578/ /pubmed/31856917 http://dx.doi.org/10.1186/s13071-019-3846-4 Text en © The Author(s) 2019 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Lee, Seong-Kyun Han, Jin-Hee Park, Ji-Hoon Ha, Kwon-Soo Park, Won Sun Hong, Seok-Ho Na, Sunghun Cheng, Yang Han, Eun-Taek Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title | Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title_full | Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title_fullStr | Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title_full_unstemmed | Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title_short | Evaluation of antibody responses to the early transcribed membrane protein family in Plasmodium vivax |
title_sort | evaluation of antibody responses to the early transcribed membrane protein family in plasmodium vivax |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921578/ https://www.ncbi.nlm.nih.gov/pubmed/31856917 http://dx.doi.org/10.1186/s13071-019-3846-4 |
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