Genetic polymorphism of merozoite surface protein-3 in Myanmar Plasmodium falciparum field isolates.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
19 May 2020
Historique:
received: 03 04 2020
accepted: 08 05 2020
entrez: 21 5 2020
pubmed: 21 5 2020
medline: 6 1 2021
Statut: epublish

Résumé

Plasmodium falciparum merozoite surface protein-3 (PfMSP-3) is a target of naturally acquired immunity against P. falciparum infection and is a promising vaccine candidate because of its critical role in the erythrocyte invasion of the parasite. Understanding the genetic diversity of pfmsp-3 is important for recognizing genetic nature and evolutionary aspect of the gene in the natural P. falciparum population and for designing an effective vaccine based on the antigen. Blood samples collected from P. falciparum-infected patients in Naung Cho and Pyin Oo Lwin, Myanmar, in 2015 were used in this study. The pfmsp-3 was amplified by polymerase chain reaction, cloned, and sequenced. Genetic polymorphism and natural selection of Myanmar pfmsp-3 were analysed using the programs DNASTAR, MEGA6, and DnaSP 5.10.00. Genetic diversity and natural selection of the global pfmsp-3 were also comparatively analysed. Myanmar pfmsp-3 displayed 2 different alleles, 3D7 and K1. The 3D7 allelic type was predominant in the population, but genetic polymorphism was less diverse than for the K1 allelic type. Polymorphic characters in both allelic types were caused by amino acid substitutions, insertions, and deletions. Amino acid substitutions were mainly occurred at the alanine heptad repeat domains, whereas most insertions and deletions were found at the glutamate rich domain. Overall patterns of amino acid polymorphisms detected in Myanmar pfmsp-3 were similar in the global pfmsp-3 population, but novel amino acid changes were observed in Myanmar pfmsp-3 with low frequencies. Complicated patterns of natural selection and recombination events were predicted in the global pfmsp-3, which may act as major driving forces to maintain and generate genetic diversity of the global pfmsp-3 population. Global pfmsp-3 revealed genetic polymorphisms, suggesting that the functional and structural consequences of the polymorphisms should be considered in designing a vaccine based on PfMSP-3. Further examination of genetic diversity of pfmsp-3 in the global P. falciparum population is necessary to gain in-depth insight for the population structure and evolutionary aspect of global pfmsp-3.

Sections du résumé

BACKGROUND BACKGROUND
Plasmodium falciparum merozoite surface protein-3 (PfMSP-3) is a target of naturally acquired immunity against P. falciparum infection and is a promising vaccine candidate because of its critical role in the erythrocyte invasion of the parasite. Understanding the genetic diversity of pfmsp-3 is important for recognizing genetic nature and evolutionary aspect of the gene in the natural P. falciparum population and for designing an effective vaccine based on the antigen.
METHODS METHODS
Blood samples collected from P. falciparum-infected patients in Naung Cho and Pyin Oo Lwin, Myanmar, in 2015 were used in this study. The pfmsp-3 was amplified by polymerase chain reaction, cloned, and sequenced. Genetic polymorphism and natural selection of Myanmar pfmsp-3 were analysed using the programs DNASTAR, MEGA6, and DnaSP 5.10.00. Genetic diversity and natural selection of the global pfmsp-3 were also comparatively analysed.
RESULTS RESULTS
Myanmar pfmsp-3 displayed 2 different alleles, 3D7 and K1. The 3D7 allelic type was predominant in the population, but genetic polymorphism was less diverse than for the K1 allelic type. Polymorphic characters in both allelic types were caused by amino acid substitutions, insertions, and deletions. Amino acid substitutions were mainly occurred at the alanine heptad repeat domains, whereas most insertions and deletions were found at the glutamate rich domain. Overall patterns of amino acid polymorphisms detected in Myanmar pfmsp-3 were similar in the global pfmsp-3 population, but novel amino acid changes were observed in Myanmar pfmsp-3 with low frequencies. Complicated patterns of natural selection and recombination events were predicted in the global pfmsp-3, which may act as major driving forces to maintain and generate genetic diversity of the global pfmsp-3 population.
CONCLUSION CONCLUSIONS
Global pfmsp-3 revealed genetic polymorphisms, suggesting that the functional and structural consequences of the polymorphisms should be considered in designing a vaccine based on PfMSP-3. Further examination of genetic diversity of pfmsp-3 in the global P. falciparum population is necessary to gain in-depth insight for the population structure and evolutionary aspect of global pfmsp-3.

Identifiants

pubmed: 32429986
doi: 10.1186/s12936-020-03256-y
pii: 10.1186/s12936-020-03256-y
pmc: PMC7235555
doi:

Substances chimiques

Antigens, Protozoan 0
Protozoan Proteins 0
merozoite surface protein 3, Plasmodium 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

184

Subventions

Organisme : National Research Foundation
ID : 2018M3A9H5055614
Organisme : National Research Foundation
ID : NRF-2019K1A3A9A01000005

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Auteurs

Hương Giang Lê (HG)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea.

Thị Lam Thái (TL)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea.

Jung-Mi Kang (JM)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea.

Jinyoung Lee (J)

Department of Tropical Medicine, Inha University College of Medicine, Incheon, 22212, Republic of Korea.

Mya Moe (M)

Department of Medical Research Pyin Oo Lwin Branch, Pyin Oo Lwin, Myanmar.

Tuấn Cường Võ (TC)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea.

Haung Naw (H)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea.

Moe Kyaw Myint (MK)

Department of Medical Research Pyin Oo Lwin Branch, Pyin Oo Lwin, Myanmar.

Zaw Than Htun (ZT)

Department of Medical Research Pyin Oo Lwin Branch, Pyin Oo Lwin, Myanmar.

Tong-Soo Kim (TS)

Department of Tropical Medicine, Inha University College of Medicine, Incheon, 22212, Republic of Korea.

Ho-Joon Shin (HJ)

Department of Microbiology, Ajou University School of Medicine, Suwon, 16499, Republic of Korea.

Byoung-Kuk Na (BK)

Department of Parasitology and Tropical Medicine, Gyeongsang National University College of Medicine, Jinju, 52727, Republic of Korea. bkna@gnu.ac.kr.
BK21Plus Team for Anti-aging Biotechnology and Industry, Department of Convergence Medical Science, Gyeongsang National University, Jinju, 52727, Republic of Korea. bkna@gnu.ac.kr.

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