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Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1
In Plasmodium, the membrane of intracellular parasites is initially formed during invasion as an invagination of the red blood cell surface, which forms a barrier between the parasite and infected red blood cells in asexual blood stage parasites. The membrane proteins of intracellular parasites of P...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444142/ https://www.ncbi.nlm.nih.gov/pubmed/26011536 http://dx.doi.org/10.1371/journal.pone.0127500 |
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author | Cheng, Yang Lu, Feng Lee, Seong-Kyun Kong, Deok-Hoon Ha, Kwon-Soo Wang, Bo Sattabongkot, Jetsumon Tsuboi, Takafumi Han, Eun-Taek |
author_facet | Cheng, Yang Lu, Feng Lee, Seong-Kyun Kong, Deok-Hoon Ha, Kwon-Soo Wang, Bo Sattabongkot, Jetsumon Tsuboi, Takafumi Han, Eun-Taek |
author_sort | Cheng, Yang |
collection | PubMed |
description | In Plasmodium, the membrane of intracellular parasites is initially formed during invasion as an invagination of the red blood cell surface, which forms a barrier between the parasite and infected red blood cells in asexual blood stage parasites. The membrane proteins of intracellular parasites of Plasmodium species have been identified such as early-transcribed membrane proteins (ETRAMPs) and exported proteins (EXPs). However, there is little or no information regarding the intracellular parasite membrane in Plasmodium vivax. In the present study, recombinant PvETRAMP11.2 (PVX_003565) and PvEXP1 (PVX_091700) were expressed and evaluated antigenicity tests using sera from P. vivax-infected patients. A large proportion of infected individuals presented with IgG antibody responses against PvETRAMP11.2 (76.8%) and PvEXP1 (69.6%). Both of the recombinant proteins elicited high antibody titers capable of recognizing parasites of vivax malaria patients. PvETRAMP11.2 partially co-localized with PvEXP1 on the intracellular membranes of immature schizont. Moreover, they were also detected at the apical organelles of newly formed merozoites of mature schizont. We first proposed that these proteins might be synthesized in the preceding schizont stage, localized on the parasite membranes and apical organelles of infected erythrocytes, and induced high IgG antibody responses in patients. |
format | Online Article Text |
id | pubmed-4444142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44441422015-06-16 Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 Cheng, Yang Lu, Feng Lee, Seong-Kyun Kong, Deok-Hoon Ha, Kwon-Soo Wang, Bo Sattabongkot, Jetsumon Tsuboi, Takafumi Han, Eun-Taek PLoS One Research Article In Plasmodium, the membrane of intracellular parasites is initially formed during invasion as an invagination of the red blood cell surface, which forms a barrier between the parasite and infected red blood cells in asexual blood stage parasites. The membrane proteins of intracellular parasites of Plasmodium species have been identified such as early-transcribed membrane proteins (ETRAMPs) and exported proteins (EXPs). However, there is little or no information regarding the intracellular parasite membrane in Plasmodium vivax. In the present study, recombinant PvETRAMP11.2 (PVX_003565) and PvEXP1 (PVX_091700) were expressed and evaluated antigenicity tests using sera from P. vivax-infected patients. A large proportion of infected individuals presented with IgG antibody responses against PvETRAMP11.2 (76.8%) and PvEXP1 (69.6%). Both of the recombinant proteins elicited high antibody titers capable of recognizing parasites of vivax malaria patients. PvETRAMP11.2 partially co-localized with PvEXP1 on the intracellular membranes of immature schizont. Moreover, they were also detected at the apical organelles of newly formed merozoites of mature schizont. We first proposed that these proteins might be synthesized in the preceding schizont stage, localized on the parasite membranes and apical organelles of infected erythrocytes, and induced high IgG antibody responses in patients. Public Library of Science 2015-05-26 /pmc/articles/PMC4444142/ /pubmed/26011536 http://dx.doi.org/10.1371/journal.pone.0127500 Text en © 2015 Cheng 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 Cheng, Yang Lu, Feng Lee, Seong-Kyun Kong, Deok-Hoon Ha, Kwon-Soo Wang, Bo Sattabongkot, Jetsumon Tsuboi, Takafumi Han, Eun-Taek Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title | Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title_full | Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title_fullStr | Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title_full_unstemmed | Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title_short | Characterization of Plasmodium vivax Early Transcribed Membrane Protein 11.2 and Exported Protein 1 |
title_sort | characterization of plasmodium vivax early transcribed membrane protein 11.2 and exported protein 1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444142/ https://www.ncbi.nlm.nih.gov/pubmed/26011536 http://dx.doi.org/10.1371/journal.pone.0127500 |
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