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PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis
BACKGROUND: Adhesin proteins are used by Plasmodium parasites to bind and invade target cells. Hence, characterising molecules that participate in reticulocyte interaction is key to understanding the molecular basis of Plasmodium vivax invasion. This study focused on predicting functionally restrict...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438544/ https://www.ncbi.nlm.nih.gov/pubmed/28526096 http://dx.doi.org/10.1186/s13071-017-2183-8 |
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author | Baquero, Luis A. Moreno-Pérez, Darwin A. Garzón-Ospina, Diego Forero-Rodríguez, Johanna Ortiz-Suárez, Heidy D. Patarroyo, Manuel A. |
author_facet | Baquero, Luis A. Moreno-Pérez, Darwin A. Garzón-Ospina, Diego Forero-Rodríguez, Johanna Ortiz-Suárez, Heidy D. Patarroyo, Manuel A. |
author_sort | Baquero, Luis A. |
collection | PubMed |
description | BACKGROUND: Adhesin proteins are used by Plasmodium parasites to bind and invade target cells. Hence, characterising molecules that participate in reticulocyte interaction is key to understanding the molecular basis of Plasmodium vivax invasion. This study focused on predicting functionally restricted regions of the P. vivax GPI-anchored micronemal antigen (PvGAMA) and characterising their reticulocyte binding activity. RESULTS: The pvgama gene was initially found in P. vivax VCG-I strain schizonts. According to the genetic diversity analysis, PvGAMA displayed a size polymorphism very common for antigenic P. vivax proteins. Two regions along the antigen sequence were highly conserved among species, having a negative natural selection signal. Interestingly, these regions revealed a functional role regarding preferential target cell adhesion. CONCLUSIONS: To our knowledge, this study describes PvGAMA reticulocyte binding properties for the first time. Conserved functional regions were predicted according to natural selection analysis and their binding ability was confirmed. These findings support the notion that PvGAMA may have an important role in P. vivax merozoite adhesion to its target cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-017-2183-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5438544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54385442017-05-22 PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis Baquero, Luis A. Moreno-Pérez, Darwin A. Garzón-Ospina, Diego Forero-Rodríguez, Johanna Ortiz-Suárez, Heidy D. Patarroyo, Manuel A. Parasit Vectors Research BACKGROUND: Adhesin proteins are used by Plasmodium parasites to bind and invade target cells. Hence, characterising molecules that participate in reticulocyte interaction is key to understanding the molecular basis of Plasmodium vivax invasion. This study focused on predicting functionally restricted regions of the P. vivax GPI-anchored micronemal antigen (PvGAMA) and characterising their reticulocyte binding activity. RESULTS: The pvgama gene was initially found in P. vivax VCG-I strain schizonts. According to the genetic diversity analysis, PvGAMA displayed a size polymorphism very common for antigenic P. vivax proteins. Two regions along the antigen sequence were highly conserved among species, having a negative natural selection signal. Interestingly, these regions revealed a functional role regarding preferential target cell adhesion. CONCLUSIONS: To our knowledge, this study describes PvGAMA reticulocyte binding properties for the first time. Conserved functional regions were predicted according to natural selection analysis and their binding ability was confirmed. These findings support the notion that PvGAMA may have an important role in P. vivax merozoite adhesion to its target cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-017-2183-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-19 /pmc/articles/PMC5438544/ /pubmed/28526096 http://dx.doi.org/10.1186/s13071-017-2183-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Baquero, Luis A. Moreno-Pérez, Darwin A. Garzón-Ospina, Diego Forero-Rodríguez, Johanna Ortiz-Suárez, Heidy D. Patarroyo, Manuel A. PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title | PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title_full | PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title_fullStr | PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title_full_unstemmed | PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title_short | PvGAMA reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
title_sort | pvgama reticulocyte binding activity: predicting conserved functional regions by natural selection analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438544/ https://www.ncbi.nlm.nih.gov/pubmed/28526096 http://dx.doi.org/10.1186/s13071-017-2183-8 |
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