Reduction in Plasmodium falciparum Pfk13 and pfg377 allele diversity through time in southern Vietnam.

Artemisinin resistance Gametocyte K13-propeller gene Plasmodium falciparum Vietnam pfg377 gene

Journal

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

Informations de publication

Date de publication:
01 Mar 2022
Historique:
received: 29 11 2021
accepted: 20 02 2022
entrez: 2 3 2022
pubmed: 3 3 2022
medline: 3 3 2022
Statut: epublish

Résumé

Plasmodium falciparum has acquired resistance to artemisinin in Southeast Asia, with mutations in the P. falciparum Kelch-13 (Pfk13) gene associated with the resistance phenotype. The widespread use of Artemisinin-based combination therapy (ACT)s in Southeast Asia has led to the selection and spread of parasites carrying mutations in Pfk13. We characterised the allele diversity of Pfk13 and pfg377, an artemisinin-resistance neutral polymorphic gene, in parasite DNA extracted human blood from in southern Vietnam in 2003, 2012, 2015 and 2018. This study was conducted in Bu Gia Map commune, Binh Phuoc province, Vietnam, from May 2018 to January 2019. Twenty-four samples from 2018 to 2019, 30 from 2003, 24 from 2012 and 32 from 2015 were analysed. Malaria-infected human blood was collected by finger-prick and used for molecular analysis. A nested-PCR targeting the small subunit ribosomal RNA gene was used for Plasmodium species identification, followed by amplification and nucleotide sequencing of Pfk13 and region 3 of pfg377. Archived blood samples collected in the same region in 2012 and 2015 were also analysed as above for comparison. The genetic diversity of Pfk13 and pfg377 was lower in 2018-2019 compared to 2012 and 2015. The number of distinct Pfk13 mutants decreased from three in 2012 and 2015, P553L, V568G and C580Y, to one, C580Y in 2018-2019. In 2018-2019, the frequency of C580Y mutant strains was 71% (17/24 isolates). All samples were wild type in 2003. In 2012 and 2015, there were single-strain infections as well as co-infections with two mutant strains or with mutant and wild strains, whereas there were no co-infections in 2018. pfg377 allele diversity decreased from five alleles in 2012 to two alleles in 2018-2019. The genetic diversity of P. falciparum was reduced at the two genetic loci surveyed in this study, Pfk13 and pfg377. In the case of the former gene, we observed an increase in the prevalence of parasites carrying the C580Y gene, known to confer reduced susceptibility to ACTs. The reduction in the diversity of pfg377 may be linked to the clonal expansion of parasite strains carrying the C580Y mutation, leading to an overall reduction in parasite genetic diversity across the population.

Sections du résumé

BACKGROUND BACKGROUND
Plasmodium falciparum has acquired resistance to artemisinin in Southeast Asia, with mutations in the P. falciparum Kelch-13 (Pfk13) gene associated with the resistance phenotype. The widespread use of Artemisinin-based combination therapy (ACT)s in Southeast Asia has led to the selection and spread of parasites carrying mutations in Pfk13. We characterised the allele diversity of Pfk13 and pfg377, an artemisinin-resistance neutral polymorphic gene, in parasite DNA extracted human blood from in southern Vietnam in 2003, 2012, 2015 and 2018.
METHOD METHODS
This study was conducted in Bu Gia Map commune, Binh Phuoc province, Vietnam, from May 2018 to January 2019. Twenty-four samples from 2018 to 2019, 30 from 2003, 24 from 2012 and 32 from 2015 were analysed. Malaria-infected human blood was collected by finger-prick and used for molecular analysis. A nested-PCR targeting the small subunit ribosomal RNA gene was used for Plasmodium species identification, followed by amplification and nucleotide sequencing of Pfk13 and region 3 of pfg377. Archived blood samples collected in the same region in 2012 and 2015 were also analysed as above for comparison.
RESULTS RESULTS
The genetic diversity of Pfk13 and pfg377 was lower in 2018-2019 compared to 2012 and 2015. The number of distinct Pfk13 mutants decreased from three in 2012 and 2015, P553L, V568G and C580Y, to one, C580Y in 2018-2019. In 2018-2019, the frequency of C580Y mutant strains was 71% (17/24 isolates). All samples were wild type in 2003. In 2012 and 2015, there were single-strain infections as well as co-infections with two mutant strains or with mutant and wild strains, whereas there were no co-infections in 2018. pfg377 allele diversity decreased from five alleles in 2012 to two alleles in 2018-2019.
CONCLUSION CONCLUSIONS
The genetic diversity of P. falciparum was reduced at the two genetic loci surveyed in this study, Pfk13 and pfg377. In the case of the former gene, we observed an increase in the prevalence of parasites carrying the C580Y gene, known to confer reduced susceptibility to ACTs. The reduction in the diversity of pfg377 may be linked to the clonal expansion of parasite strains carrying the C580Y mutation, leading to an overall reduction in parasite genetic diversity across the population.

Identifiants

pubmed: 35232492
doi: 10.1186/s41182-022-00409-4
pii: 10.1186/s41182-022-00409-4
pmc: PMC8887123
doi:

Types de publication

Journal Article

Langues

eng

Pagination

19

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 26360029
Organisme : Japan Society for the Promotion of Science
ID : 17H04513
Organisme : Japan Society for the Promotion of Science
ID : 20H04411

Informations de copyright

© 2022. The Author(s).

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Auteurs

Nguyen Quang Thieu (NQ)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Vu Duc Chinh (VD)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Truong Van Hanh (T)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Nguyen Van Dung (N)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Hidekazu Takagi (H)

Department of Microbiology and Immunology, Aichi Medical University School of Medicine, Aichi, Japan.

Takeshi Annoura (T)

Department of Parasitology, National Institute of Infectious Diseases, Tokyo, Japan.

Satoru Kawai (S)

Laboratory of Tropical Medicine and Parasitology, Dokkyo Medical University, Tochigi, Japan.

Gaku Masuda (G)

Department of International Affairs and Tropical Medicine, Tokyo Women's Medical University, Tokyo, Japan.
School of Tropical Medicine and Global Health, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan.

Nguyen Van Tuan (N)

Faculty of Medical Engineering, Phenikaa University, Hanoi, Vietnam.

Vu Viet Hung (VV)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Shusuke Nakazawa (S)

Department of Protozoology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.

Richard Culleton (R)

Department of Protozoology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Division of Molecular Parasitology, Proteo-Science Centre, Ehime University, Ehime, Japan.

Nguyen Thi Huong Binh (NTH)

National Institute of Malariology, Parasitology and Entomology, Hanoi, Vietnam.

Yoshimasa Maeno (Y)

School of Tropical Medicine and Global Health, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan. yoshimaeno@gmail.com.
Department of Virology and Parasitology, Fujita Health University School of Medicine, Aichi, Japan. yoshimaeno@gmail.com.

Classifications MeSH