- Open Access
Genetic relatedness of Plasmodium falciparum isolates and the origin of allelic diversity at the merozoite surface protein-1 (MSP-1) locus in Brazil and Vietnam
© Hoffmann et al; licensee BioMed Central Ltd. 2003
- Received: 17 June 2003
- Accepted: 23 July 2003
- Published: 23 July 2003
Despite the extensive polymorphism at the merozoite surface protein-1 (MSP-1) locus of Plasmodium falciparum, that encodes a major repetitive malaria vaccine candidate antigen, identical and nearly identical alleles frequently occur in sympatric parasites. Here we used microsatellite haplotyping to estimate the genetic distance between isolates carrying identical and nearly identical MSP-1 alleles.
We analyzed 28 isolates from hypoendemic areas in north-western Brazil, collected between 1985 and 1998, and 23 isolates obtained in mesoendemic southern Vietnam in 1996. MSP-1 alleles were characterized by combining PCR typing with allele-specific primers and partial DNA sequencing. The following single-copy microsatellite markers were typed : Polyα, TA42 (only for Brazilian samples), TA81, TA1, TA87, TA109 (only for Brazilian samples), 2490, ARAII, PfG377, PfPK2, and TA60.
The low pair-wise average genetic distance between microsatellite haplotypes of isolates sharing identical MSP-1 alleles indicates that epidemic propagation of discrete parasite clones originated most identical MSP-1 alleles in parasite populations from Brazil and Vietnam. At least one epidemic clone propagating in Brazil remained relatively unchanged over more than one decade. Moreover, we found no evidence that rearrangements of MSP-1 repeats, putatively created by mitotic recombination events, generated new alleles within clonal lineages of parasites in either country.
Identical MSP-1 alleles originated from co-ancestry in both populations, whereas nearly identical MSP-1 alleles have probably appeared independently in unrelated parasite lineages.
- Genetic Relatedness
- Average Genetic Distance
- Brazilian Isolate
- Brazilian Sample
- Epidemic Clone
Despite its relatively recent expansion in human populations , Plasmodium falciparum displays extensive genetic variation in most surface antigens, affecting the development of effective immune responses . Understanding the patterns and mechanisms of DNA sequence variation in major P. falciparum surface antigens is important for predicting the efficacy of immunization strategies .
Despite the huge potential for variation at the MSP-1 locus, identical alleles often occur in areas of low and moderate malaria transmission [5, 7]. The epidemic propagation of a few discrete P. falciparum clones might explain these findings. This hypothesis is consistent with the epidemic structure (defined by Maynard Smith and colleagues  as the result of short-term expansions of highly successful clonal lineages in an otherwise panmictic population) that characterize most P. falciparum populations outside Africa, including those in Brazil  and Vietnam . Since identical MSP-1 alleles have been found in the same area in Brazil over more than one decade , some epidemic clones could have remained relatively unchanged over several generations. In addition, groups of nearly identical MSP-1 alleles, differing only in the number and arrangement of block 2 repeats, but identical elsewhere in the gene, are also prevalent in P. falciparum from Brazil and Vietnam . The hypothesis that nearly identical alleles have originated from each other by strand-slippage events within repeat arrays during the mitotic propagation of parasites  remains to be proved. Hypotheses regarding the origin of identical and nearly identical MSP-1 alleles were addressed here by microsatellite characterization of the overall genetic relatedness of parasites carrying known variants of this gene.
Parasite samples and MSP-1 typing
We analysed two sets of human blood samples with apparently single-clone P. falciparum infections, as judged by typing MSP-1 polymorphisms and single-copy DNA microsatellite markers. The first set comprised 28 isolates from hypoendemic areas in the towns of Porto Velho, Ariquemes and Guajará-Mirim, all in the state of Rondônia, north-western Brazil, collected in 1985, 1997 and 1998, while the second set comprised 23 isolates obtained in the mesoendemic town of Bao Loc, southern Vietnam, in January-December 1996. Blood samples were collected, after informed consent, at malaria treatment facilities, and all patients had symptomatic P. falciparum infections when enrolled. The average proportions of multiple-clone P. falciparum infections, as estimated by microsatellite typing, were 11.5% in Rondônia, Brazil , and 39.6% in Bao Loc, Vietnam . MSP-1 alleles had been previously characterized in these isolates by combining PCR typing with allele-specific primers and partial DNA sequencing (Figure 1A); each allele was defined as a unique combination of block 2 and 17 haplotypes and other polymorphisms across the molecule (Figure 1B) .
DNA microsatellite typing
The following single-copy microsatellite markers were typed (chromosome location in parentheses): Polyα (4), TA42 (only for Brazilian samples) (5), TA81 (5), TA1 (6), TA87 (6), TA109 (only for Brazilian samples) (6), 2490(10), ARAII (11), PfG377 (12), PfPK2 (12), and TA60 (13). We used no marker located on chromosome 9, where the MSP-1 locus is found, to avoid possible biases in overall distance estimates originated from hitchhiking due to selection on this locus. Microsatellite loci were PCR-amplified according to previously described protocols . Length variation of PCR products (a single PCR product was obtained for each locus in each isolate) was measured on either ABI377 (all Brazilian samples) or ABI3100 (all Vietnamese samples) automated DNA sequencers (Applied Biosystems). Part of these microsatellite data had been published elsewhere [9, 10].
The levels of genetic diversity at each microsatellite locus were estimated for both parasite samples by calculating the theoretical expected heterozygosity H as follows: , where n is the number of isolates sampled and p i is the frequency of each allele at a given locus . Estimates of overall pair-wise genetic distances between isolates from either country, obtained from microsatellite data (1 – proportion of alleles shared between haplotypes), were used to construct Fitch-Margoliash trees using the PHYLIP, version 3.5c, software package, distributed by its author (J. Felsenstein) at http://evolution.genetics.washington.edu. To test whether identical MSP-1 alleles within each country occurred predominantly in genetically related parasites, we first compared the overall genetic relatedness (based on pair-wise genetic distances defined as above) between isolates from each country sharing or not sharing MSP-1 alleles, by using two-sample randomization tests implemented in version 2.5 of the PopTools software (written by G. Hood and available at: http://www.cse.csiro.au/poptools). Monte-Carlo simulations (10,000 iterations) were used to estimate two-tailed P values. This approach was also used to test whether nearly identical MSP-1 alleles (defined as above) tended to occur in genetically related isolates. The second approach to examine the genetic relatedness of isolates sharing or not sharing identical MSP-1 alleles investigated the correlation between similarity matrices obtained with microsatellite data and MSP-1 typing data. We created two model matrices to describe the MSP-1 data set. In the first model matrix (hereafter Model I), values of 0 and 1 were assigned to pair-wise comparisons of isolates with identical and different MSP-1 alleles, respectively. In Model II, three levels of similarity were considered: values of 0, 0.5 and 1 were assigned to pair-wise comparisons of isolates with identical, nearly identical and different MSP-1 alleles, respectively. Mantel tests were used to assess the correlation between the microsatellite similarity matrix and each of the MSP-1 model matrices . Coefficients of determination (r2) were calculated and two-tailed P values were obtained by Monte Carlo simulation with 6,000 permutations performed with the PopTools software. Finally, we compared the overall genetic relatedness of isolates collected in Brazil in the same or different decades.
Distribution of MSP-1 alleles
Twenty-seven unique MSP-1 alleles were found, 10 in Brazil (alleles # 2, 3, 4, 5, 6, 7, 17, 28, 34 and 37) and 17 in Vietnam (alleles # 1, 8, 9, 10, 13, 15, 16, 18, 21, 23, 24, 27, 29, 31, 32, 33 and 38). Five MSP-1 alleles in Brazil and four in Vietnam were shared by two or more isolates, but no allele was shared by parasites from both countries (Figure 1B). Moreover, four groups of nearly identical MSP-1 alleles were found in parasites from the same country (one in Brazil and three in Vietnam). Alleles within each of these groups differed in the number and arrangement of tripeptide repeats in block 2, but were identical elsewhere in the MSP-1 gene .
Genetic relatedness of Brazilian isolates
Number of different alleles and expected heterozygozity at microsatellite loci in Plasmodium falciparum isolates from Brazil (n = 28) and Vietnam (n = 23).
No. of alleles
Poly - α
We next examined the overall genetic relatedness of Brazilian isolates with nearly identical MSP-1 alleles (alleles #3, #4 and #5), which differed only in the number of SGT repeats in their K1-type block 2 sequences (GenBank accession numbers: AF509630, AF509632-3 and AF509705) (Figure 1B). The average genetic distance of Brazilian isolates with nearly identical MSP-1 alleles (0.436; 5 pair-wise comparisons) was similar to that calculated for local isolates with different MSP-1 alleles (0.431; 323 pair-wise comparisons) (P = 0.810). The lack of evidence for co-ancestry of these isolates argues against the hypothesis that nearly identical MSP-1 alleles in Brazil were generated by mitotic recombination events in block 2 repeats within clonal lineages of parasites .
Figure 2 shows some temporal clustering of microsatellite haplotypes in Brazil. In fact, the average pair-wise genetic distance of isolates collected in the same decade (0.398; 218 pair-wise comparisons) was significantly lower (P = 0.010) than that estimated for isolates collected in different decades (0.438; 160 pair-wise comparisons). To test whether the date of sample collection confounded the previous analyses of genetic distance, we analysed separately 12 isolates collected in 1985 and 16 isolates collected in 1997–98. Isolates sharing identical MSP-1 alleles collected in 1985 (0.364; 9 pair-wise comparisons) and 1997–98 (0.282; 31 pair-wise comparisons) were again more closely related to each other than those with different MSP-1 alleles collected during the corresponding decade (0.405 [57 pair-wise comparisons] and 0.428 [89 pair-wise comparisons], respectively). Differences in genetic distance were significant for comparisons within 1997–98 (P < 0.0001) but not for those within 1985 (P = 0.441), probably due to the smaller sample size.
Genetic relatedness of Vietnamese isolates
We also examined the genetic relatedness within three groups of Vietnamese isolates with nearly identical MSP-1 alleles: (a) alleles #15 and #16, (b) alleles #21, #23 and #24, and (c) alleles #31, #32 and #33. Alleles within each group only differed in the number of SGG, SGA and SKG repeats in their MAD20-type block 2 sequences (GenBank accession numbers: AF509642, AF509645-7, AF509654, AF509670, AF509679, AF509686, AF509691-2 and AF509702) (Fig. 1B). No significant difference (P = 0.615) was found when the average genetic distance of Vietnamese isolates with nearly identical MSP-1 alleles (0.710; 13 pair-wise comparisons) was compared with that of isolates with quite different MSP-1 alleles (0.715, 231 pair-wise comparisons). This result supports the conclusion that nearly identical MSP-1 alleles in Vietnam have not been recently created by variation in block 2 repeats within clonal parasite lineages.
Matrix correlation analysis
The association between MSP-1 allele sharing and low overall genetic distance between isolates was further confirmed by the significant correlation (r2 = 0.082, P < 0.00001 for Brazil and r2 = 0.025, P = 0.014 for Vietnam) between the microsatellite-derived similarity matrices and Model I MSP-1 matrices. The magnitude of the coefficients of determination remained nearly unchanged when the microsatellite-derived similarity matrices were compared to Model II MSP-1 matrices (r2 = 0.079, P < 0.00001 for Brazil and r2 = 0.020, P = 0.025 for Vietnam), again indicating that pairs of isolates with nearly identical MSP-1 alleles could not be placed at intermediate levels of overall genetic distance, when compared with local isolates with either identical or different MSP-1 alleles.
The low overall genetic distance among microsatellite haplotypes of isolates sharing identical MSP-1 alleles supported the hypothesis that these identical alleles have originated from recent epidemic propagations of discrete parasite lineages within parasite populations from Brazil and Vietnam. Moreover, we found no evidence that isolates with nearly identical MSP-1 alleles (differing only in block 2 repeats) are genetically related. Although rearrangements in block 2 repeats may represent an important source of sequence variation in MSP-1 [2, 5], our results present no evidence for this process during the relatively short time frame for which clonal lineages were maintained within parasite populations in Brazil and Vietnam. One possible explanation for these negative findings is that, in areas of low to moderate levels of malaria transmission, selective pressure may be too weak to drive the emergence of new MSP-1 variants originated by putative mitotic recombination events during human infections, since most local P. falciparum-infected patients have not been able to develop effective variant-specific anti-parasite immunity.
This work was partially funded by grants from the UNDP/World Bank/World Health Organisation Special Programme for Research and Training in Tropical Diseases, the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). EHEH and MUF are supported by scholarships from FAPESP and CNPq, respectively. We thank Timothy J. C. Anderson and Shalini Nair (Southwest Foundation for Biomedical Research, San Antonio, TX, USA) for help in microsatellite analysis and critical reading of the manuscript, Fumihiko Kawamoto (Nagoya University School of Medicine, Nagoya, Japan) for providing parasite DNA samples from Vietnam, and the two anonymous reviewers for helpful comments and suggestions.
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