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      Genetic diversity of Plasmodium falciparum populations in three malaria transmission settings in Madagascar

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          Abstract

          Background

          Assessment of the genetic diversity of Plasmodium falciparum parasites from various malaria transmission settings could help to define tailored local strategies for malaria control and elimination. Such assessments are currently scarce in Madagascar. The study presented here aimed to bridge this gap by investigating the genetic diversity of P. falciparum populations in three epidemiological strata (Equatorial, Tropical and Fringes) in Madagascar.

          Methods

          Two-hundred and sixty-six P. falciparum isolates were obtained from patients with uncomplicated malaria enrolled in clinical drug efficacy studies conducted at health centres in Tsaratanana (Equatorial stratum), Antanimbary (Tropical stratum) and Anjoma Ramartina (Fringes) in 2013 and 2016. Parasite DNA was extracted from blood samples collected before anti-malarial treatment. Plasmodium species were identified by nested PCR targeting the 18 S rRNA gene. The genetic profiles of P. falciparum parasites were defined by allele-specific nested PCR on the polymorphic regions of the msp- 1 and msp- 2 genes.

          Results

          Fifty-eight alleles were detected in the P. falciparum samples tested: 18 alleles for msp-1 and 40 for msp-2. K1 (62.9%, 139/221) and FC27 (69.5%, 114/164) were the principal msp-1 and msp-2 allele families detected, although the proportions of the msp-1 and msp-2 alleles varied significantly between sites. Polyclonal infections were more frequent at sites in the Equatorial stratum (69.8%) than at sites in the Tropical stratum (60.5%) or Fringes (58.1%). Population genetics analyses showed that genetic diversity was similar between sites and that parasite flow within sites was limited.

          Conclusions

          This study provides recent information about the genetic diversity of P. falciparum populations in three transmission strata in Madagascar, and valuable baseline data for further evaluation of the impact of the control measures implemented in Madagascar.

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          Most cited references46

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          Estimation of average heterozygosity and genetic distance from a small number of individuals.

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          The magnitudes of the systematic biases involved in sample heterozygosity and sample genetic distances are evaluated, and formulae for obtaining unbiased estimates of average heterozygosity and genetic distance are developed. It is also shown that the number of individuals to be used for estimating average heterozygosity can be very small if a large number of loci are studied and the average heterozygosity is low. The number of individuals to be used for estimating genetic distance can also be very small if the genetic distance is large and the average heterozygosity of the two species compared is low.
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            THE INTERPRETATION OF POPULATION STRUCTURE BY F-STATISTICS WITH SPECIAL REGARD TO SYSTEMS OF MATING

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              High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction

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                Author and article information

                Contributors
                ral.fano@yahoo.fr
                aratsimbasoa@gmail.com
                Journal
                Malar J
                Malar J
                Malaria Journal
                BioMed Central (London )
                1475-2875
                27 May 2021
                27 May 2021
                2021
                : 20
                : 239
                Affiliations
                [1 ]National Malaria Control Programme of Madagascar, Androhibe, Antananarivo, Madagascar
                [2 ]GRID grid.440419.c, ISNI 0000 0001 2165 5629, Faculty of Sciences, , University of Antananarivo, ; Antananarivo, Madagascar
                [3 ]Centre National d’Application de Recherches Pharmaceutiques, Analamahitsy, Antananarivo, Madagascar
                [4 ]GRID grid.428999.7, ISNI 0000 0001 2353 6535, Malaria Genetics and Resistance Unit and INSERM U1201, , Institut Pasteur Paris, ; Paris, France
                [5 ]Faculty of Medicine, University of Fianarantsoa, Fianarantsoa, Madagascar
                Author information
                http://orcid.org/0000-0002-4755-4241
                Article
                3776
                10.1186/s12936-021-03776-1
                8161981
                34044837
                12ff7c28-385a-4950-b728-ad23f2d2c0e0
                © The Author(s) 2021

                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.

                History
                : 28 January 2021
                : 17 May 2021
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Infectious disease & Microbiology
                plasmodium falciparum,malaria,genetic diversity,msp-1,msp-2 gene,madagascar

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