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Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein

BACKGROUND: Proteins secreted from the rhoptry in Plasmodium merozoites are associated with the formation of tight junctions and parasitophorous vacuoles during invasion of erythrocytes and are sorted within the rhoptry neck or bulb. Very little information has been obtained to date about Plasmodium...

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Autores principales: Cheng, Yang, Li, Jian, Ito, Daisuke, Kong, Deok-Hoon, Ha, Kwon-Soo, Lu, Feng, Wang, Bo, Sattabongkot, Jetsumon, Lim, Chae Seung, Tsuboi, Takafumi, Han, Eun-Taek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435652/
https://www.ncbi.nlm.nih.gov/pubmed/25925592
http://dx.doi.org/10.1186/s12936-015-0698-z
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author Cheng, Yang
Li, Jian
Ito, Daisuke
Kong, Deok-Hoon
Ha, Kwon-Soo
Lu, Feng
Wang, Bo
Sattabongkot, Jetsumon
Lim, Chae Seung
Tsuboi, Takafumi
Han, Eun-Taek
author_facet Cheng, Yang
Li, Jian
Ito, Daisuke
Kong, Deok-Hoon
Ha, Kwon-Soo
Lu, Feng
Wang, Bo
Sattabongkot, Jetsumon
Lim, Chae Seung
Tsuboi, Takafumi
Han, Eun-Taek
author_sort Cheng, Yang
collection PubMed
description BACKGROUND: Proteins secreted from the rhoptry in Plasmodium merozoites are associated with the formation of tight junctions and parasitophorous vacuoles during invasion of erythrocytes and are sorted within the rhoptry neck or bulb. Very little information has been obtained to date about Plasmodium vivax rhoptry-associated leucine (Leu) zipper-like protein 1 (PvRALP1; PVX_096245), a putative rhoptry protein. PvRALP1 contains a signal peptide, a glycine (Gly)/glutamate (Glu)-rich domain, and a Leu-rich domain, all of which are conserved in other Plasmodium species. METHODS: Recombinant PvRALP1s were expressed as full-length protein without the signal peptide (PvRALP1-Ecto) and as truncated protein consisting of the Gly/Glu- and Leu-rich domains (PvRALP1-Tr) using the wheat germ cell-free expression system. The immunoreactivity to these two fragments of recombinant PvRALP1 protein in serum samples from P. vivax-infected patients and immunized mice, including analysis of immunoglobulin G (IgG) subclasses, was evaluated by enzyme-linked immunosorbent assay or protein microarray technology. The subcellular localization of PvRALP1 in blood stage parasites was also determined. RESULTS: Recombinant PvRALP1-Ecto and PvRALP1-Tr proteins were successfully expressed, and in serum samples from P. vivax patients from the Republic of Korea, the observed immunoreactivities to these proteins had 58.9% and 55.4% sensitivity and 95.0% and 92.5% specificity, respectively. The response to PvRALP1 in humans was predominantly cytophilic antibodies (IgG1 and IgG3), but a balanced Th1/Th2 response was observed in mice. Unexpectedly, there was no significant inverse correlation between levels of parasitaemia and levels of antibody against either PvRALP1-Ecto (R(2) = 0.11) or PvRALP1-Tr (R(2) = 0.14) antigens. PvRALP1 was localized in the rhoptry neck of merozoites, and this was the first demonstration of the localization of this protein in P. vivax. CONCLUSIONS: This study analysed the antigenicity and immunogenicity of PvRALP1 and suggested that PvRALP1 may be immunogenic in humans during parasite infection and might play an important role during invasion of P. vivax parasites.
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spelling pubmed-44356522015-05-19 Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein Cheng, Yang Li, Jian Ito, Daisuke Kong, Deok-Hoon Ha, Kwon-Soo Lu, Feng Wang, Bo Sattabongkot, Jetsumon Lim, Chae Seung Tsuboi, Takafumi Han, Eun-Taek Malar J Research BACKGROUND: Proteins secreted from the rhoptry in Plasmodium merozoites are associated with the formation of tight junctions and parasitophorous vacuoles during invasion of erythrocytes and are sorted within the rhoptry neck or bulb. Very little information has been obtained to date about Plasmodium vivax rhoptry-associated leucine (Leu) zipper-like protein 1 (PvRALP1; PVX_096245), a putative rhoptry protein. PvRALP1 contains a signal peptide, a glycine (Gly)/glutamate (Glu)-rich domain, and a Leu-rich domain, all of which are conserved in other Plasmodium species. METHODS: Recombinant PvRALP1s were expressed as full-length protein without the signal peptide (PvRALP1-Ecto) and as truncated protein consisting of the Gly/Glu- and Leu-rich domains (PvRALP1-Tr) using the wheat germ cell-free expression system. The immunoreactivity to these two fragments of recombinant PvRALP1 protein in serum samples from P. vivax-infected patients and immunized mice, including analysis of immunoglobulin G (IgG) subclasses, was evaluated by enzyme-linked immunosorbent assay or protein microarray technology. The subcellular localization of PvRALP1 in blood stage parasites was also determined. RESULTS: Recombinant PvRALP1-Ecto and PvRALP1-Tr proteins were successfully expressed, and in serum samples from P. vivax patients from the Republic of Korea, the observed immunoreactivities to these proteins had 58.9% and 55.4% sensitivity and 95.0% and 92.5% specificity, respectively. The response to PvRALP1 in humans was predominantly cytophilic antibodies (IgG1 and IgG3), but a balanced Th1/Th2 response was observed in mice. Unexpectedly, there was no significant inverse correlation between levels of parasitaemia and levels of antibody against either PvRALP1-Ecto (R(2) = 0.11) or PvRALP1-Tr (R(2) = 0.14) antigens. PvRALP1 was localized in the rhoptry neck of merozoites, and this was the first demonstration of the localization of this protein in P. vivax. CONCLUSIONS: This study analysed the antigenicity and immunogenicity of PvRALP1 and suggested that PvRALP1 may be immunogenic in humans during parasite infection and might play an important role during invasion of P. vivax parasites. BioMed Central 2015-04-29 /pmc/articles/PMC4435652/ /pubmed/25925592 http://dx.doi.org/10.1186/s12936-015-0698-z Text en © Cheng et al.; licensee BioMed Central. 2015 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
Cheng, Yang
Li, Jian
Ito, Daisuke
Kong, Deok-Hoon
Ha, Kwon-Soo
Lu, Feng
Wang, Bo
Sattabongkot, Jetsumon
Lim, Chae Seung
Tsuboi, Takafumi
Han, Eun-Taek
Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title_full Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title_fullStr Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title_full_unstemmed Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title_short Antigenicity and immunogenicity of PvRALP1, a novel Plasmodium vivax rhoptry neck protein
title_sort antigenicity and immunogenicity of pvralp1, a novel plasmodium vivax rhoptry neck protein
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435652/
https://www.ncbi.nlm.nih.gov/pubmed/25925592
http://dx.doi.org/10.1186/s12936-015-0698-z
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