Genetic diversity of Plasmodium vivax populations from the China-Myanmar border identified by genotyping merozoite surface protein markers.

Genotyping Merozoite surface protein Mixed-strain infection Multiplicity of infection Plasmodium vivax Population differentiation

Journal

Tropical medicine and health
ISSN: 1348-8945
Titre abrégé: Trop Med Health
Pays: Japan
ID NLM: 101215093

Informations de publication

Date de publication:
11 Jan 2023
Historique:
received: 23 09 2022
accepted: 20 12 2022
entrez: 11 1 2023
pubmed: 12 1 2023
medline: 12 1 2023
Statut: epublish

Résumé

Parasite diversity and population structure influence malaria control measures. Malaria transmission at international borders affects indigenous residents and migrants, defying management efforts and resulting in malaria re-introduction. Here we aimed to determine the extent and distribution of genetic variations in Plasmodium vivax populations and the complexity of infections along the China-Myanmar border. We collected clinical P. vivax samples from local and migrant malaria patients from Laiza and Myitsone, Kachin State, Myanmar, respectively. We characterized the polymorphisms in two P. vivax merozoite surface protein markers, Pvmsp-3α and Pvmsp-3β, by PCR-restriction fragment length polymorphism (PCR-RFLP) analysis. We sought to determine whether these genetic markers could differentiate these two neighboring parasite populations. PCR revealed three major size variants for Pvmsp-3α and four for Pvmsp-3β among the 370 and 378 samples, respectively. PCR-RFLP resolved 26 fragment-size alleles by digesting Pvmsp-3α with Alu I and Hha I and 28 alleles by digesting Pvmsp-3β with Pst I. PCR-RFLP analysis of Pvmsp-3α found that infections in migrant laborers from Myitsone bore more alleles than did infections in residents of Laiza, while such difference was not evident from genotyping Pvmsp-3β. Infections originating from these two places contained distinct but overlapping subpopulations of P. vivax. Infections from Myitsone had a higher multiplicity of infection as judged by the size of the Pvmsp-3α amplicons and alleles after Alu I/Hha I digestion. Migrant laborers from Myitsone and indigenous residents from Laiza harbored overlapping but genetically distinct P. vivax parasite populations. The results suggested a more diverse P. vivax population in Myitsone than in the border town of Laiza. PCR-RFLP of Pvmsp-3α offers a convenient method to determine the complexity of P. vivax infections and differentiate parasite populations.

Sections du résumé

BACKGROUND BACKGROUND
Parasite diversity and population structure influence malaria control measures. Malaria transmission at international borders affects indigenous residents and migrants, defying management efforts and resulting in malaria re-introduction. Here we aimed to determine the extent and distribution of genetic variations in Plasmodium vivax populations and the complexity of infections along the China-Myanmar border.
METHODS METHODS
We collected clinical P. vivax samples from local and migrant malaria patients from Laiza and Myitsone, Kachin State, Myanmar, respectively. We characterized the polymorphisms in two P. vivax merozoite surface protein markers, Pvmsp-3α and Pvmsp-3β, by PCR-restriction fragment length polymorphism (PCR-RFLP) analysis. We sought to determine whether these genetic markers could differentiate these two neighboring parasite populations.
RESULTS RESULTS
PCR revealed three major size variants for Pvmsp-3α and four for Pvmsp-3β among the 370 and 378 samples, respectively. PCR-RFLP resolved 26 fragment-size alleles by digesting Pvmsp-3α with Alu I and Hha I and 28 alleles by digesting Pvmsp-3β with Pst I. PCR-RFLP analysis of Pvmsp-3α found that infections in migrant laborers from Myitsone bore more alleles than did infections in residents of Laiza, while such difference was not evident from genotyping Pvmsp-3β. Infections originating from these two places contained distinct but overlapping subpopulations of P. vivax. Infections from Myitsone had a higher multiplicity of infection as judged by the size of the Pvmsp-3α amplicons and alleles after Alu I/Hha I digestion.
CONCLUSIONS CONCLUSIONS
Migrant laborers from Myitsone and indigenous residents from Laiza harbored overlapping but genetically distinct P. vivax parasite populations. The results suggested a more diverse P. vivax population in Myitsone than in the border town of Laiza. PCR-RFLP of Pvmsp-3α offers a convenient method to determine the complexity of P. vivax infections and differentiate parasite populations.

Identifiants

pubmed: 36631913
doi: 10.1186/s41182-022-00492-7
pii: 10.1186/s41182-022-00492-7
pmc: PMC9832627
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2

Subventions

Organisme : NINR NIH HHS
ID : U19AI089672
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI089672
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Xun Wang (X)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Yao Bai (Y)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Zheng Xiang (Z)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Weilin Zeng (W)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Yanrui Wu (Y)

Department of Cell Biology and Genetics, Kunming Medical University, Kunming, China.

Hui Zhao (H)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Wei Zhao (W)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Xi Chen (X)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Mengxi Duan (M)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Xiaosong Li (X)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Wenya Zhu (W)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Kemin Sun (K)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Yiman Wu (Y)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Yanmei Zhang (Y)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China.

Xiaomei Li (X)

Faculty of Public Health, Kunming Medical University, Kunming, Yunnan Province, China.

Benjamin M Rosenthal (BM)

Animal Parasitic Disease Laboratory, Agricultural Research Service, US Department of Agriculture, Beltsville, MD, USA.

Liwang Cui (L)

Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL, 33612, USA. liwangci@usf.edu.

Zhaoqing Yang (Z)

Department of Pathogen Biology and Immunology, Kunming Medical University, Kunming, 650500, Yunnan, China. zhaoqingy92@hotmail.com.

Classifications MeSH