13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Temporal changes in genetic diversity of msp- 1, msp- 2, and msp- 3 in Plasmodium falciparum isolates from Grande Comore Island after introduction of ACT

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Malaria is still one of the serious public health problems in Grande Comore Island, although the number of annual cases has been greatly reduced in recent years. A better understanding of malaria parasite population diversity and transmission dynamics is critical for assessing the effectiveness of malaria control measures. The objective of this study is to investigate temporal changes in genetic diversity of Plasmodium falciparum populations and multiplicity of infection (MOI) in Grande Comore 10 years after introduction of ACT.

          Methods

          A total of 232 P. falciparum clinical isolates were collected from the Grande Comore Island during two sampling periods (118 for 2006‒2007 group, and 114 for 2013‒2016 group). Parasite isolates were characterized for genetic diversity and complexity of infection by genotyping polymorphic regions in merozoite surface protein gene 1 ( msp- 1), msp- 2, and msp- 3 using nested PCR and DNA sequencing.

          Results

          Three msp- 1 alleles (K1, MAD20, and RO33), two msp- 2 alleles (FC27 and 3D7), and two msp- 3 alleles (K1 and 3D7) were detected in parasites of both sampling periods. The RO33 allele of msp- 1 (84.8%), 3D7 allele of msp- 2 (90.8%), and K1 allele of msp- 3 (66.7%) were the predominant allelic types in isolates from 2006–2007 group. In contrast, the RO33 allele of msp- 1 (63.4%), FC27 allele of msp- 2 (91.1%), and 3D7 allele of msp- 3 (53.5%) were the most prevalent among isolates from the 2013–2016 group. Compared with the 2006‒2007 group, polyclonal infection rates of msp- 1 (from 76.7 to 29.1%, P < 0.01) and msp- 2 (from 62.4 to 28.3%, P < 0.01) allelic types were significantly decreased in those from 2013‒2016 group. Similarly, the MOIs for both msp- 1 and msp- 2 were higher in P. falciparum isolates in the 2006 2007 group than those in 2013 2016 group (MOI = 3.11 vs 1.63 for msp- 1; MOI = 2.75 vs 1.35 for msp- 2). DNA sequencing analyses also revealed reduced numbers of distinct sequence variants in the three genes from 2006‒2007 to 2013‒2016: msp- 1, from 32 to 23 (about 28% decline); msp- 2 from 29 to 21 (about 28% decline), and msp- 3 from 11 to 3 (about 72% decline).

          Conclusions

          The present data showed dramatic reduction in genetic diversity and MOI among Grande Comore P. falciparum populations over the course of the study, suggesting a trend of decreasing malaria transmission intensity and genetic diversity in Grande Comore Island. These data provide valuable information for surveillance of P. falciparum infection and for assessing the appropriateness of the current malarial control strategies in the endemic area.

          Related collections

          Most cited references52

          • Record: found
          • Abstract: found
          • Article: not found

          Microsatellite markers reveal a spectrum of population structures in the malaria parasite Plasmodium falciparum.

          Multilocus genotyping of microbial pathogens has revealed a range of population structures, with some bacteria showing extensive recombination and others showing almost complete clonality. The population structure of the protozoan parasite Plasmodium falciparum has been harder to evaluate, since most studies have used a limited number of antigen-encoding loci that are known to be under strong selection. We describe length variation at 12 microsatellite loci in 465 infections collected from 9 locations worldwide. These data reveal dramatic differences in parasite population structure in different locations. Strong linkage disequilibrium (LD) was observed in six of nine populations. Significant LD occurred in all locations with prevalence <1% and in only two of five of the populations from regions with higher transmission intensities. Where present, LD results largely from the presence of identical multilocus genotypes within populations, suggesting high levels of self-fertilization in populations with low levels of transmission. We also observed dramatic variation in diversity and geographical differentiation in different regions. Mean heterozygosities in South American countries (0.3-0.4) were less than half those observed in African locations (0. 76-0.8), with intermediate heterozygosities in the Southeast Asia/Pacific samples (0.51-0.65). Furthermore, variation was distributed among locations in South America (F:(ST) = 0.364) and within locations in Africa (F:(ST) = 0.007). The intraspecific patterns of diversity and genetic differentiation observed in P. falciparum are strikingly similar to those seen in interspecific comparisons of plants and animals with differing levels of outcrossing, suggesting that similar processes may be involved. The differences observed may also reflect the recent colonization of non-African populations from an African source, and the relative influences of epidemiology and population history are difficult to disentangle. These data reveal a range of population structures within a single pathogen species and suggest intimate links between patterns of epidemiology and genetic structure in this organism.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            A recombinant blood-stage malaria vaccine reduces Plasmodium falciparum density and exerts selective pressure on parasite populations in a phase 1-2b trial in Papua New Guinea.

            The malaria vaccine Combination B comprises recombinant Plasmodium falciparum ring-infected erythrocyte surface antigen and 2 merozoite surface proteins (MSP1 and MSP2) formulated in oil-based adjuvant. A phase 1-2b double-blind, randomized, placebo-controlled trial in 120 children (5-9 years old) in Papua New Guinea demonstrated a 62% (95% confidence limits: 13%, 84%) reduction in parasite density in children not pretreated with sulfadoxine-pyrimethamine. Vaccinees had a lower prevalence of parasites carrying the MSP2-3D7 allelic form (corresponding to that in the vaccine) and a higher incidence of morbid episodes associated with FC27-type parasites. These results demonstrate functional activity of Combination B against P. falciparum in individuals with previous malaria exposure. The specific effects on parasites with particular msp2 genotypes suggest that the MSP2 component, at least in part, accounted for the activity. The vaccine-induced selection pressure exerted on the parasites and its consequences for morbidity strongly argue for developing vaccines comprising conserved antigens and/or multiple components covering all important allelic types.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Genetic diversity among Plasmodium falciparum field isolates in Pakistan measured with PCR genotyping of the merozoite surface protein 1 and 2

              Background The genetic diversity of Plasmodium falciparum has been extensively studied in various parts of the world. However, limited data are available from Pakistan. This study aimed to establish molecular characterization of P. falciparum field isolates in Pakistan measured with two highly polymorphic genetic markers, i.e. the merozoite surface protein 1 (msp-1)and 2 (msp-2). Methods Between October 2005 and October 2007, 244 blood samples from patients with symptomatic blood-slide confirmed P. falciparum mono-infections attending the Aga Khan University Hospital, Karachi, or its collection units located in Sindh and Baluchistan provinces, Pakistan were collected. The genetic diversity of P. falciparum was analysed by length polymorphism following gel electrophoresis of DNA products from nested polymerase chain reactions (PCR) targeting block 2 of msp-1 and block 3 of msp-2, including their respective allelic families KI, MAD 20, RO33, and FC27, 3D7/IC. Results A total of 238/244 (98%) patients had a positive PCR outcome in at least one genetic marker; the remaining six were excluded from analysis. A majority of patients had monoclonal infections. Only 56/231 (24%) and 51/236 (22%) carried multiple P. falciparum genotypes in msp-1 and msp-2, respectively. The estimated total number of genotypes was 25 msp-1 (12 KI; 8 MAD20; 5 RO33) and 33 msp-2 (14 FC27; 19 3D7/IC). Conclusions This is the first report on molecular characterization of P. falciparum field isolates in Pakistan with regards to multiplicity of infection. The genetic diversity and allelic distribution found in this study is similar to previous reports from India and Southeast Asian countries with low malaria endemicity.
                Bookmark

                Author and article information

                Contributors
                songjpgz@sina.com
                dcs19811202@hotmail.com
                Journal
                Malar J
                Malar. J
                Malaria Journal
                BioMed Central (London )
                1475-2875
                20 February 2018
                20 February 2018
                2018
                : 17
                : 83
                Affiliations
                [1 ]ISNI 0000 0000 8848 7685, GRID grid.411866.c, Institute of Tropical Medicine, , Guangzhou University of Chinese Medicine, ; Guangzhou, 510006 Guangdong People’s Republic of China
                [2 ]ISNI 0000 0000 8848 7685, GRID grid.411866.c, Science and Technology Park, , Guangzhou University of Chinese Medicine, ; Guangzhou, 510445 Guangdong People’s Republic of China
                [3 ]ISNI 0000 0004 1790 3548, GRID grid.258164.c, School of Stomatology, , Jinan University, ; Guangzhou, 510632 Guangdong People’s Republic of China
                [4 ]Artepharm, Co., Ltd, Guangzhou, 510405 Guangdong People’s Republic of China
                [5 ]ISNI 0000 0001 2164 9667, GRID grid.419681.3, Laboratory of Malaria and Vector Research, , National Institute of Allergy and Infectious Diseases, National Institutes of Health, ; Bethesda, MD 20892 USA
                [6 ]National Malaria Control Programme, BP 500, Moroni, Comoros
                [7 ]Ministry of Health Comoros, BP 403, Moroni, Comoros
                Article
                2227
                10.1186/s12936-018-2227-3
                5819244
                29458365
                52b31d25-31b6-4012-bf8e-c8b3ff7d3206
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

                History
                : 10 October 2017
                : 8 February 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 81702020
                Award ID: 81403295
                Award Recipient :
                Funded by: Guangdong Provincial Natural Science Foundation
                Award ID: 2015A030310107
                Award Recipient :
                Funded by: Guangdong Provincial Medicine Science Foundation
                Award ID: A2016315
                Award Recipient :
                Funded by: Guangdong Provincial Science Technology Program
                Award ID: 2014B050502013
                Award ID: 2015B020234003
                Award Recipient :
                Funded by: State Administration of Traditional Chinese Medicine Project
                Award ID: GJZX2016003
                Award Recipient :
                Funded by: YangFan Innovative and Entrepreneurial Research Team Project
                Award ID: 2014YT02S008
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Infectious disease & Microbiology
                malaria population,grande comore,genetic diversity,multiplicity of infection,pcr,dna sequencing

                Comments

                Comment on this article