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

Other Titles
Genetic polymorphism and natural selection of circumsporozoite protein in Myanmar Plasmodium vivax
Authors
Vo, Tuan CuongLe, Huong GiangKang, Jung-MiMoe, MyaNaw, HaungMyint, Moe KyawLee, JinyoungSohn, Woon-MokKim, Tong-SooNa, Byoung-Kuk
Issue Date
Sep-2020
Publisher
BioMed Central
Keywords
Plasmodium vivax; Circumsporozoite protein; Genetic polymorphism; Natural selection; Myanmar
Citation
Malaria Journal, v.19, no.1
Indexed
SCIE
SCOPUS
Journal Title
Malaria Journal
Volume
19
Number
1
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/6190
DOI
10.1186/s12936-020-03366-7
ISSN
1475-2875
1475-2875
Abstract
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 incorporatingPlasmodium vivaxCSP (PvCSP) have demonstrated their effectiveness in preventing malaria, at least in part. However, genetic diversity ofpvcspin the natural population remains a major concern. Methods A total of 171 blood samples collected from patients infected withPlasmodium vivaxin Myanmar were analysed in this study. Thepvcspwas amplified by polymerase chain reaction, followed by cloning and sequencing. Polymorphic characteristics and natural selection ofpvcsppopulation in Myanmar were analysed using DNASTAR, MEGA6 and DnaSP programs. The polymorphic pattern and natural selection of publicly accessible globalpvcspsequences were also comparatively analysed. Results Myanmarpvcspsequences 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 ofpvcspdisplayed 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 globalpvcsppopulation. Meanwhile, the central repeat region (CRR) of Myanmar and globalpvcsp, 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 globalpvcsppopulation suggests a complex genetic profile ofpvcspin the global population. These results widen understanding of the genetic make-up ofpvcspin the globalP. vivaxpopulation and provide valuable information for the development of a vaccine based on PvCSP.
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