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Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis
BACKGROUND: Plasmodium falciparum circumsporozoite protein (PfCSP) is a potential malaria vaccine candidate, but various polymorphisms of the pfcsp gene among global P. falciparum population become the major barrier to the effectiveness of vaccines. This study aimed to investigate the genetic polymo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359586/ https://www.ncbi.nlm.nih.gov/pubmed/32660484 http://dx.doi.org/10.1186/s12936-020-03315-4 |
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author | Huang, Hui-Ying Liang, Xue-Yan Lin, Li-Yun Chen, Jiang-Tao Ehapo, Carlos Salas Eyi, Urbano Monsuy Li, Jian Jiang, Ting-Ting Zheng, Yu-Zhong Zha, Guang-Cai Xie, Dong-De He, Jin-Quan Chen, Wei-Zhong Liu, Xiang-Zhi Mo, Huan-Tong Chen, Xin-Yao Lin, Min |
author_facet | Huang, Hui-Ying Liang, Xue-Yan Lin, Li-Yun Chen, Jiang-Tao Ehapo, Carlos Salas Eyi, Urbano Monsuy Li, Jian Jiang, Ting-Ting Zheng, Yu-Zhong Zha, Guang-Cai Xie, Dong-De He, Jin-Quan Chen, Wei-Zhong Liu, Xiang-Zhi Mo, Huan-Tong Chen, Xin-Yao Lin, Min |
author_sort | Huang, Hui-Ying |
collection | PubMed |
description | BACKGROUND: Plasmodium falciparum circumsporozoite protein (PfCSP) is a potential malaria vaccine candidate, but various polymorphisms of the pfcsp gene among global P. falciparum population become the major barrier to the effectiveness of vaccines. This study aimed to investigate the genetic polymorphisms and natural selection of pfcsp in Bioko and the comparison among global P. falciparum population. METHODS: From January 2011 to December 2018, 148 blood samples were collected from P. falciparum infected Bioko patients and 96 monoclonal sequences of them were successfully acquired and analysed with 2200 global pfcsp sequences mined from MalariaGEN Pf3k Database and NCBI. RESULTS: In Bioko, the N-terminus of pfcsp showed limited genetic variations and the numbers of repetitive sequences (NANP/NVDP) were mainly found as 40 (35%) and 41 (34%) in central region. Most polymorphic characters were found in Th2R/Th3R region, where natural selection (p > 0.05) and recombination occurred. The overall pattern of Bioko pfcsp gene had no obvious deviation from African mainland pfcsp (Fst = 0.00878, p < 0.05). The comparative analysis of Bioko and global pfcsp displayed the various mutation patterns and obvious geographic differentiation among populations from four continents (p < 0.05). The global pfcsp C-terminal sequences were clustered into 138 different haplotypes (H_1 to H_138). Only 3.35% of sequences matched 3D7 strain haplotype (H_1). CONCLUSIONS: The genetic polymorphism phenomena of pfcsp were found universal in Bioko and global isolates and the majority mutations located at T cell epitopes. Global genetic polymorphism and geographical characteristics were recommended to be considered for future improvement of malaria vaccine design. |
format | Online Article Text |
id | pubmed-7359586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73595862020-07-17 Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis Huang, Hui-Ying Liang, Xue-Yan Lin, Li-Yun Chen, Jiang-Tao Ehapo, Carlos Salas Eyi, Urbano Monsuy Li, Jian Jiang, Ting-Ting Zheng, Yu-Zhong Zha, Guang-Cai Xie, Dong-De He, Jin-Quan Chen, Wei-Zhong Liu, Xiang-Zhi Mo, Huan-Tong Chen, Xin-Yao Lin, Min Malar J Research BACKGROUND: Plasmodium falciparum circumsporozoite protein (PfCSP) is a potential malaria vaccine candidate, but various polymorphisms of the pfcsp gene among global P. falciparum population become the major barrier to the effectiveness of vaccines. This study aimed to investigate the genetic polymorphisms and natural selection of pfcsp in Bioko and the comparison among global P. falciparum population. METHODS: From January 2011 to December 2018, 148 blood samples were collected from P. falciparum infected Bioko patients and 96 monoclonal sequences of them were successfully acquired and analysed with 2200 global pfcsp sequences mined from MalariaGEN Pf3k Database and NCBI. RESULTS: In Bioko, the N-terminus of pfcsp showed limited genetic variations and the numbers of repetitive sequences (NANP/NVDP) were mainly found as 40 (35%) and 41 (34%) in central region. Most polymorphic characters were found in Th2R/Th3R region, where natural selection (p > 0.05) and recombination occurred. The overall pattern of Bioko pfcsp gene had no obvious deviation from African mainland pfcsp (Fst = 0.00878, p < 0.05). The comparative analysis of Bioko and global pfcsp displayed the various mutation patterns and obvious geographic differentiation among populations from four continents (p < 0.05). The global pfcsp C-terminal sequences were clustered into 138 different haplotypes (H_1 to H_138). Only 3.35% of sequences matched 3D7 strain haplotype (H_1). CONCLUSIONS: The genetic polymorphism phenomena of pfcsp were found universal in Bioko and global isolates and the majority mutations located at T cell epitopes. Global genetic polymorphism and geographical characteristics were recommended to be considered for future improvement of malaria vaccine design. BioMed Central 2020-07-13 /pmc/articles/PMC7359586/ /pubmed/32660484 http://dx.doi.org/10.1186/s12936-020-03315-4 Text en © The Author(s) 2020 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 Huang, Hui-Ying Liang, Xue-Yan Lin, Li-Yun Chen, Jiang-Tao Ehapo, Carlos Salas Eyi, Urbano Monsuy Li, Jian Jiang, Ting-Ting Zheng, Yu-Zhong Zha, Guang-Cai Xie, Dong-De He, Jin-Quan Chen, Wei-Zhong Liu, Xiang-Zhi Mo, Huan-Tong Chen, Xin-Yao Lin, Min Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title | Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title_full | Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title_fullStr | Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title_full_unstemmed | Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title_short | Genetic polymorphism of Plasmodium falciparum circumsporozoite protein on Bioko Island, Equatorial Guinea and global comparative analysis |
title_sort | genetic polymorphism of plasmodium falciparum circumsporozoite protein on bioko island, equatorial guinea and global comparative analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359586/ https://www.ncbi.nlm.nih.gov/pubmed/32660484 http://dx.doi.org/10.1186/s12936-020-03315-4 |
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