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Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax

BACKGROUND: Circumsporozoite surface protein (CSP) of malaria parasites has been recognized as one of the leading vaccine candidates. Clinical trials of vaccines for vivax malaria incorporating Plasmodium vivax CSP (PvCSP) have demonstrated their effectiveness in preventing malaria, at least in part...

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Autores principales: Võ, Tuấn Cường, Lê, Hương Giang, Kang, Jung-Mi, Moe, Mya, Naw, Haung, Myint, Moe Kyaw, Lee, Jinyoung, Sohn, Woon-Mok, Kim, Tong-Soo, Na, Byoung-Kuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650223/
https://www.ncbi.nlm.nih.gov/pubmed/32883283
http://dx.doi.org/10.1186/s12936-020-03366-7
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author Võ, Tuấn Cường
Lê, Hương Giang
Kang, Jung-Mi
Moe, Mya
Naw, Haung
Myint, Moe Kyaw
Lee, Jinyoung
Sohn, Woon-Mok
Kim, Tong-Soo
Na, Byoung-Kuk
author_facet Võ, Tuấn Cường
Lê, Hương Giang
Kang, Jung-Mi
Moe, Mya
Naw, Haung
Myint, Moe Kyaw
Lee, Jinyoung
Sohn, Woon-Mok
Kim, Tong-Soo
Na, Byoung-Kuk
author_sort Võ, Tuấn Cường
collection PubMed
description BACKGROUND: Circumsporozoite surface protein (CSP) of malaria parasites has been recognized as one of the leading vaccine candidates. Clinical trials of vaccines for vivax malaria incorporating Plasmodium vivax CSP (PvCSP) have demonstrated their effectiveness in preventing malaria, at least in part. However, genetic diversity of pvcsp in the natural population remains a major concern. METHODS: A total of 171 blood samples collected from patients infected with Plasmodium vivax in Myanmar were analysed in this study. The pvcsp was amplified by polymerase chain reaction, followed by cloning and sequencing. Polymorphic characteristics and natural selection of pvcsp population in Myanmar were analysed using DNASTAR, MEGA6 and DnaSP programs. The polymorphic pattern and natural selection of publicly accessible global pvcsp sequences were also comparatively analysed. RESULTS: Myanmar pvcsp sequences were divided into two subtypes VK210 and VK247 comprising 143 and 28 sequences, respectively. The VK210 subtypes showed higher levels of genetic diversity and polymorphism than the VK247 subtypes. The N-terminal non-repeat region of pvcsp displayed limited genetic variations in the global population. Different patterns of octapeptide insertion (ANKKAEDA in VK210 and ANKKAGDA in VK247) and tetrapeptide repeat motif (GGNA) were identified in the C-terminal region of global pvcsp population. Meanwhile, the central repeat region (CRR) of Myanmar and global pvcsp, both in VK210 and VK247 variants, was highly polymorphic. The high level of genetic diversity in the CRR has been attributed to the different numbers, types and combinations of peptide repeat motifs (PRMs). Interestingly, 27 and 5 novel PRMs were found in Myanmar VK210 and VK247 variants, respectively. CONCLUSION: Comparative analysis of the global pvcsp population suggests a complex genetic profile of pvcsp in the global population. These results widen understanding of the genetic make-up of pvcsp in the global P. vivax population and provide valuable information for the development of a vaccine based on PvCSP.
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spelling pubmed-76502232020-11-09 Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax Võ, Tuấn Cường Lê, Hương Giang Kang, Jung-Mi Moe, Mya Naw, Haung Myint, Moe Kyaw Lee, Jinyoung Sohn, Woon-Mok Kim, Tong-Soo Na, Byoung-Kuk Malar J Research BACKGROUND: Circumsporozoite surface protein (CSP) of malaria parasites has been recognized as one of the leading vaccine candidates. Clinical trials of vaccines for vivax malaria incorporating Plasmodium vivax CSP (PvCSP) have demonstrated their effectiveness in preventing malaria, at least in part. However, genetic diversity of pvcsp in the natural population remains a major concern. METHODS: A total of 171 blood samples collected from patients infected with Plasmodium vivax in Myanmar were analysed in this study. The pvcsp was amplified by polymerase chain reaction, followed by cloning and sequencing. Polymorphic characteristics and natural selection of pvcsp population in Myanmar were analysed using DNASTAR, MEGA6 and DnaSP programs. The polymorphic pattern and natural selection of publicly accessible global pvcsp sequences were also comparatively analysed. RESULTS: Myanmar pvcsp sequences were divided into two subtypes VK210 and VK247 comprising 143 and 28 sequences, respectively. The VK210 subtypes showed higher levels of genetic diversity and polymorphism than the VK247 subtypes. The N-terminal non-repeat region of pvcsp displayed limited genetic variations in the global population. Different patterns of octapeptide insertion (ANKKAEDA in VK210 and ANKKAGDA in VK247) and tetrapeptide repeat motif (GGNA) were identified in the C-terminal region of global pvcsp population. Meanwhile, the central repeat region (CRR) of Myanmar and global pvcsp, both in VK210 and VK247 variants, was highly polymorphic. The high level of genetic diversity in the CRR has been attributed to the different numbers, types and combinations of peptide repeat motifs (PRMs). Interestingly, 27 and 5 novel PRMs were found in Myanmar VK210 and VK247 variants, respectively. CONCLUSION: Comparative analysis of the global pvcsp population suggests a complex genetic profile of pvcsp in the global population. These results widen understanding of the genetic make-up of pvcsp in the global P. vivax population and provide valuable information for the development of a vaccine based on PvCSP. BioMed Central 2020-09-04 /pmc/articles/PMC7650223/ /pubmed/32883283 http://dx.doi.org/10.1186/s12936-020-03366-7 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
Võ, Tuấn Cường
Lê, Hương Giang
Kang, Jung-Mi
Moe, Mya
Naw, Haung
Myint, Moe Kyaw
Lee, Jinyoung
Sohn, Woon-Mok
Kim, Tong-Soo
Na, Byoung-Kuk
Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title_full Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title_fullStr Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title_full_unstemmed Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title_short Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
title_sort genetic polymorphism and natural selection of circumsporozoite protein in myanmar plasmodium vivax
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650223/
https://www.ncbi.nlm.nih.gov/pubmed/32883283
http://dx.doi.org/10.1186/s12936-020-03366-7
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