Genetic polymorphism of merozoite surface protein 1 and merozoite surface protein 2 in the Vietnam Plasmodium falciparum population

doi:10.21203/rs.3.rs-4864615/v1

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Genetic polymorphism of merozoite surface protein 1 and merozoite surface protein 2 in the Vietnam Plasmodium falciparum population

https://doi.org/10.21203/rs.3.rs-4864615/v1

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Background

Plasmodium falciparum merozoite surface proteins 1 (PfMSP1) and 2 (PfMSP2) are potential candidates for malaria vaccine development. However, the genetic diversity of these genes in the global P. falciparum population presents a significant challenge in developing an effective vaccine. Hence, understanding the genetic diversity and evolutionary trends in the global P. falciparum population is crucial.

Methods

This study analyzed the genetic variations and evolutionary changes of pfmsp1 and pfmsp2 in P. falciparum isolates from the Central Highland and South-Central regions of Vietnam. DNASTAR and MEGA7 programs were utilized for analyses. The polymorphic nature of global pfmsp1 and pfmsp2 was also investigated.

Results

A total of 337 sequences of pfmsp1 and 289 sequences of pfmsp2 were obtained. The pfmsp1 and pfmsp2 from Vietnam revealed a higher degree of genetic homogeneity compared to those from other malaria-endemic countries. Remarkably, the allele diversity patterns of Vietnam pfmsp1 and pfmsp2 differed significantly from those of neighboring countries in the Greater Mekong Subregion. Declines in allele diversity and polymorphic patterns of Vietnam pfmsp1 and pfmsp2 were observed.

Conclusions

The Vietnam P. falciparum population might be genetically isolated from the parasite populations in other neighboring GMS countries, likely due to geographical barriers and distinct evolutionary pressures. Furthermore, bottleneck effects or selective sweeps may have contributed to the genetic homogeneity of Vietnam pfmsp1 and pfmsp2.

Plasmodium falciparum

Merozoite surface proteins

Genetic diversity

Vietnam

Malaria, an acute febrile disease caused by infections with Plasmodium parasites, continues to be a significant global health challenge. According to the World Malaria Report 2023 from the World Health Organization (WHO), there were 249 million global malaria cases, making an increase of 5 million from the previous year, and an estimated 608,000 deaths were reported in 2022 [1]. Despite achievements in malaria control within the Greater Mekong Subregion (GMS) over recent decades, a surge in indigenous malaria cases from 90,082 to 170,527 was observed between 2021 and 2022. Specifically, the number of P. falciparum cases almost doubled during this period, with instances rising from 16,490 to 30,789 [1]. The rapid spread of antimalarial drug-resistant P. falciparum strains in the GMS poses a significant challenge to the region’s efforts to eliminate falciparum malaria [2, 3]. Although notable reductions in malaria morbidity and mortality have occurred in Vietnam over the last two decades [4], the disease remains endemic in the central and southern provinces, particularly in the Central Highland region where P. falciparum is the predominant species [5]. Understanding the genetic makeup and evolutionary trends of the P. falciparum population in certain endemic areas is crucial as it provides valuable insights to the epidemiological patterns and genetic characteristics of the parasites.

P. falciparum merozoite surface proteins (PfMSPs) are multigene family proteins that are expressed on the surfaces of merozoites and sporozoites of the parasite and play critical roles in the invasion of the parasite into host cells [6]. Over 10 species of PfMSPs have been identified in P. falciparum, among which PfMSP1 and PfMSP2 are the most intensively investigated due to their reliability as polymorphic markers. PfMSP1 is a transmembrane protein divided into 17 distinct blocks, with block II displaying the most significant polymorphic character [7, 8]. PfMSP1 is typically classified into three allelic variants, K1, MAD20, and RO33, based on the polymorphisms observed in block II [9, 10]. PfMSP2 consists of a central repeat region (CRR) flanked by conserved N-terminal and C-terminal regions and is classified into two distinct variants, 3D7 and FC27, depending on the sequence variations in the CRR [11, 12]. Due to these polymorphisms in pfmsp1 and pfmsp2, they are recognized as reliable polymorphic markers for studying genetic heterogenicity and evolutionary aspects of the P. falciparum population [13, 14].

Comprehensive studies analyzing the genetic nature of pfmsp genes in P. falciparum isolates from countries in the GMS conducted [15–19]. These studies indicated substantial genetic heterogeneities of pfmsp genes in the P. falciparum population in the GMS. The genetic characteristics of pfmsp genes in Vietnam P. falciparum have been partially characterized [20–22]. Similar to the pfmsp genes from other GMS countries, those in Vietnam P. falciparum also appear to exhibit considerable genetic diversity. However, these prior studies were limited by their reliance on simple typing instead of sequencing analysis and by being outdated, suggesting they may not accurately reflect the current genetic composition of the genes in Vietnam’s P. falciparum population. In this study, we explored the genetic diversities of pfmsp1 and pfmsp2 in Vietnam P. falciparum isolates collected in the Central Highland and South-Central regions of Vietnam between 2018 and 2022. We also comparatively analyzed the genetic differences among pfmsp1 and pfmsp2 populations from Vietnam and other malaria-endemic countries, including GMS countries.

Parasite samples and study area

A total of 382 blood samples were collected from P. falciparum-infected individuals residing in three provinces in the Central Highlands (Dak Lak, Dak Nong, and Gia Lai) and two provinces in the South-Central regions (Phu Yen and Khanh Hoa), Vietnam, during 2018–2022 (Fig. 1). P. falciparum infection was diagnosed by microscopic analysis of thin and thick blood smears. The dried blood filter (DBF) was prepared from each patient by finger-prick method and P. falciparum infection was verified by a species-specific polymerase chain reaction (PCR) targeting the 18S ribosomal RNA (rRNA) gene as reported previously [5, 23]. The study protocol was reviewed and approved by the Ethics Committee of the Ministry of Health, Institute of Malariology, Parasitology and Entomology Quy Nhon, Vietnam (IRB Approval numbers: 386/VSR-LSDT, 45/VSR-NCDT, and 637/VSR-NCDT).

Amplifications and sequence analyses of Vietnam pfmsp genes

Parasite DNA was isolated from each DBF using the QIAamp DNA Blood Kit (Qiagen, Hilden, Germany). Nested PCRs to amplify the pfmsp1 block II and pfmsp2 block III were performed using the primer sets and protocols described in previous studies [15, 17, 24]. Each PCR product was cloned into a T&A cloning vector (Real Biotech Corporation, Banqiao City, Taiwan) and transformed into Escherichia coli DH5α competent cells. The nucleotide sequences of the cloned gene were analyzed using the automated Sanger method with M13 forward and reverse primers. The nucleotide sequences of Vietnam pfmsp genes have been deposited in the GenBank with the accession numbers: pfmsp1 (OR425413–OR425789) and pfmsp2 (OR425790–OR426078).

Genetic diversity analysis

The nucleotide and inferred amino acid sequences of Vietnam pfmsp genes were analyzed using EditSeq and SeqMan in the DNASTAR package (DNASTAR, Madison, WI, USA). Sequences were analyzed based on the reference sequences: MAD20 (GenBank No.: X05624.2), K1 (GenBank No.: NC_004330.2), and RO33 (GenBank No.: M55001.1) for pfmsp1; 3D7 (GenBank No.: X53832) and FC27 (GenBank No.: J03828) for pfmsp2. The pfmsp sequences obtained in this study were also comparatively analyzed with the previously reported pfmsp sequences from Vietnam and other countries including the GMS countries (Supplemental File 1: Table S1).

Genetic diversity of Vietnam pfmsp1 block II

A total of 377 pfmsp1 block II sequences were successfully obtained from Vietnam P. falciparum, with MAD20 alleles being overwhelmingly predominant (375/377, 99.47%). Each of the K1 and RO33 alleles was identified only once, respectively (Fig. 2). Block II of the MAD20 alleles comprised various combinations and arrangements of seven distinct peptide repeat motifs (PRMs) of SGG, SVT, SVA, SKG, SSG, PVA, and TVA, yielding a total of 25 unique alleles of MAD20 (A1–A25). None of the allele shared the same PRM configuration with the reference sequence (X05624.2). The construction of each MAD20 allele varied, containing PRMs ranging from 1 to 14. The two alleles, A14 and A20, were the most prevalent, accounting for 180 and 139 sequences, respectively. Block II of the K1 allele also demonstrated genetic variation relative to the reference sequence (NC_004330.2) and contained only three PRMs: SAQ, SGT, and SGP. In contrast, block II of the RO33 allele was identical in sequence to the reference (M55001.1).

Genetic differences of pfmsp1 block II in the global population

The allelic diversity of Vietnam’s pfmsp1 block II was compared with those of other countries and previously reported Vietnam pfmsp1 (Fig. 3). The MAD20 alleles were predominant across all Vietnam pfmsp1 populations, a trend similarly observed in pfmsp1 populations of GMS countries, including Thailand and Myanmar, as well as Pacific countries such as the Philippines, PNG, and SI. Conversely, K1 alleles were primarily found in pfmsp1 populations from India, Africa, and South American countries. Notably, the RO33 allele was predominant in the Vanuatu pfmsp1 population. The global pfmsp1 population displayed significant genetic heterogeneity in MAD20 and K1 alleles, attributed to various compositions and arrangements of PRMs. For MAD20 alleles, 10 different PRMs including SGG, SVT, SVA, SKG, SSG, PVA, TVA, SGT, SGA, and SVG were identified globally (Fig. 4). These PRMs were unequally distributed, with SGG, SVT, and SVA universally present across all populations. Additionally, SKG and SSG appeared in Asia, the Pacific, and Africa, but were absent in South American populations. The five PRMs, namely PVA, TVA, SGT, SGA, and SVG, were uniquely identified in either Vietnam or Indian populations, with PVA and TVA being novel PRMs first detected in the Vietnam MAD20 alleles analyzed in this study. A similar variation in PRM distribution was found in global K1 alleles (Fig. 4). A total of 17 distinct PRMs were detected in global K1 alleles. Among these, SGT and SGP were consistently observed across all populations, while SAG was present in K1 alleles of all countries analyzed except Brazil. SGA occurred in some countries across Asia, Africa, and South America, but not in the Pacific region. The remaining 13 PRMs showed unique occurrence in specific countries such as India, Kenya, or Tanzania. These PRMs contributed to various combinations and arrangements within global MAD20 and K1 alleles, resulting in significant size variations and genetic heterogeneity of pfmsp1 by country (Fig. 5). Worldwide, MAD20 alleles varied immensely, containing 1 to 19 PRMs, with prevalent sizes ranging from 9 to 15 PRMs in the global MAD20 population. In comparison, global K1 alleles exhibited even greater size diversity due to different compositions of PRM compositions, ranging from 4 to 25. Each country displayed variability in the number of PRMs present, with pronounce size variations of PRMs in both MAD20 and K1 alleles notably in pfmsp1 from India and African countries.

Genetic diversity of Vietnam pfmsp2 block III

A total of 289 Vietnam pfmsp2 block III sequences were successfully obtained from the samples analyzed in this study. These sequences were categorized into 3D7 types. They displayed polymorphic characters, forming 7 distinct alleles (A1–A7) distinguished by sequence polymorphisms (Fig. 6). The A4 and A2 alleles were predominant, accounting for 52.2% (151/289) and 41.9% (121/289), respectively. In the E1 region, only four amino acid changes (T44E, N47K, P48T, and P49S) were observed, categorized into two groups of paired amino acid substitutions. Specifically, the T44E/P49S pair was present in 280 sequences (96.9%), while the N47K/P48T pair was found in 9 sequences (3.1%). Different numbers, types, and arrangements of PRMs were observed in the R1 region, contributing to the size polymorphisms of Vietnam pfmsp2 block III. GAGGSGSA, GGSGSA, and GAGASGSA served the fundamental units of PRMs. In the R2 region, all sequences exhibited poly-threonine (poly-T) signature characteristic of the 3D7 type. Alleles A1–A6 contained 8 threonines (T8), while A7 featured 14 threonines (T14). Compared to the 3D7 reference sequence, a notable characteristic in the E3 region of all Vietnam pfmsp2 was the insertion of 11 amino acids at position 156: PKGKGEVQKPN for A1–A6 alleles and PKGNGGVQEPN for the A7 allele. Additionally, an amino acid change of E154K was identified in the A7 allele.

Genetic differences of pfmsp2 block III in the global population

The distribution of alleles in the current Vietnam pfmsp2 was compared to pfmsp2 from Vietnam (1994 and 2017‒2019) and other countries including Myanmar, Thailand, India, PNG, and Gambia (Fig. 7). All populations exhibited the presence of both allelic types of 3D7 and FC27 in a substantial proportion except the current Vietnam and PNG. The previously reported Vietnam pfmsp2 (Vietnam 1994 and 2017‒2019) harbored both 3D7 and FC27, though they shared overlapping collection sites with the present study. Significant genetic diversity was observed in the global pfmsp2 block III. The regions of R1, R2, and E3 were the primary contributors to genetic diversity among and between pfmsp2 populations (Fig. 8). The R1 region exhibited exceptionally diverse polymorphisms, characterized by 16 different types of PRM with unequal arrangements and repetitions (Fig. 8A). Three Asian pfmsp2 populations, Myanmar (2013‒2015), Thailand, and India, possessed all PRM types. The PNG and Gambia populations also included 14 and 11 different PRM types, respectively. Notably, two Vietnam pfmsp2 populations exhibited distinct patterns. While the Vietnam pfmsp2 analyzed in this study displayed only 3 PRM types, Vietnam (1994) pfmsp2 comprised 10 different PRM types. In the R2 region, only two types of poly-T (T8 and T14) were identified in the Vietnam pfmsp2 population, whereas a variety of poly-T types were observed in the global population (Fig. 8B). The prevalence of poly-T types varied globally, with T8 and T14 being the dominant species. Intriguingly, T8 was markedly prevalent in the Vietnam pfmsp2 population. The E3 region of pfmsp2 also demonstrated substantial genetic diversity in the global population. A range of insertion types with diverse sequences was evident in the global pfmsp2 population (Fig. 8C). The PKGKGEVQKPN insertion appeared in all populations, albeit at varying frequencies by country. Additionally, pfmsp2 sequences lacking insertion were present in the global population, excluding PNG.

PfMSPs are key contenders in the development of vaccines against falciparum malaria; however, the extensive genetic diversity of these genes within the global P. falciparum population poses significant challenges to vaccine development. In our study, we examined the genetic polymorphisms of two pfmsp genes, pfmsp1 and pfmsp2, in P. falciparum isolates from Vietnam and compared their genetic diversities with those from other countries, including those in the GMS.

It has been previously suggested that pfmsp1 block II and pfmsp2 block III exhibit high levels of polymorphism [13, 14]. In contrast, our analysis revealed a marked genetic uniformity in the Vietnam pfmsp1 and pfmsp2 genes, with the dominant presence of MAD20 alleles in pfmsp1 and 3D7 alleles in pfmsp2. This uniformity sets the Vietnamese isolates apart from their counterparts in neighboring GMS countries like Myanmar and Thailand. Notably, when compared with earlier analyses of the Vietnam pfmsp1 and pfmsp2 populations (2017‒2019) [22], a significant reduction in allelic variation was noted in recent populations, despite their shared geographical origins. No mixed infections of pfmsp1 and pfmsp2 were identified in the P. falciparum population analyzed in this study. However, in our previous study on the genetic makeup analysis of Vietnam pfmsp1, mixed infections with different alleles were detected [5], albeit at low frequencies. This discrepancy may be attributed to the preferred amplification and cloning of the major alleles in mixed infection samples, if present. Nevertheless, our study revealed that Vietnam pfmsp1 and pfmsp2 exhibited a higher degree of genetic homogeneity compared to those from other malaria-endemic countries. PRMs are significant factors in inducing genetic complexity in Vietnam pfmsp1 and pfmsp2. Common PRMs identified in other global pfmsp1 and pfmsp2 populations were also found in Vietnam pfmsp1 and pfmsp2 as major PRMs. However, two novel PRMs (PVA, and TVA) that not been reported in global pfmsp1 were also discovered in Vietnam pfmsp1, though their prevalence was low. The most notable features in Vietnam pfmsp2 included the low diversity of PRM types in the R1 region and the exceedingly high frequency of a single type of insertion (PKGKGEVQKPN, 96.9%) in the E3 region. Compared to previous Vietnam sequences (1994) that exhibited more than five different insertion in the E3 region, only two types of insertion sequence (PKGKGEVQKPN and PKGNGGVQEPN) were identified in the Vietnam pfmsp2 analyzed in this study.

Differences in genetic diversity of other vaccine candidates between Vietnam and other GMS countries have previously been reported. The pattern of restricted genetic diversity in Vietnam’s P. falciparum is not confined solely to MSP family genes but also extends to other genes. In Vietnam P. falciparum, pfama1 and pfeba-175 demonstrated notably lower genetic diversity and a unique genetic profile compared to other GMS countries, such as Myanmar and Thailand [25, 26]. This phenomenon was not exclusive to P. falciparum genes. P. vivax circumsporozoite surface protein (pvcsp) of Vietnam also exhibited a distinct allelic pattern relative to pvcsp from other GMS countries [27]. The genetic distinctiveness of Vietnam’s Plasmodium populations compared to those of other GMS countries could be attributed to geographic feature. The Truong Son range, stretching across the north and south of western Vietnam, may act as a topographical barrier that impedes the transmission of parasites and mosquito vectors between western Vietnam and eastern Laos and Cambodia [26]. Furthermore, this barrier could also restrict the migratory patterns of the human population. The Plasmodium population in central Vietnam could be undergoing unique evolutionary changes, independent from those in the neighboring GMS countries. However, this study still presents limitations. The samples from GMS countries were collected at varying time points, which challenges the distinction of precise genetic variations in contemporary P. falciparum populations. To better understand the genetic dynamics of Plasmodium species in this region, comprehensive examinations with larger-scale samples and more systematic methodologies are required, especially in Laos and Cambodia, which border Vietnam.

The results of this study also indicated a decrease the sequence diversity of Vietnam’s pfmsp1 and pfmsp2 compared to earlier periods, potentially due to population bottlenecks in the parasite population. The recent decrease in malaria cases in this endemic region, attributed to sustained control efforts, may lead to a bottleneck effect, significantly reducing genetic polymorphism [28]. Conversely, the reduction in polymorphism at these sites could result from a selective sweep, where newly developed directional selection favors certain alleles over others [29].

Vietnam pfmsp1 and pfmsp2 exhibit less genetic diversity than those from other malaria-endemic countries, including the GMS countries. Vietnam P. falciparum population is likely genetically isolated from the parasite populations in other neighboring GMS countries, possibly due to geographical barriers and unique evolutionary pressures. The bottleneck effect or selective sweep may contribute to the genetic homogeneity of Vietnam pfmsp1 and pfmsp2, which warrants further investigation. This study provides a comprehensive understanding of the genetic characteristics and population structure of the Vietnam P. falciparum population, but a more comprehensive analysis of the genetic diversity and evolutionary aspects of the population is also necessary.

Declaration of Competing Interest

The authors declare that they have no competing interests.

Author contributions

Conceptualization: Võ TC, Huynh HQ, Na BK

Methodology: Võ TC, Lê HG, Kang JM, Nguyen TMT, Huynh HQ

Formal analysis: Võ TC, Lê HG, Kang JM, Huynh HQ, Na BK

Investigation: Huynh HQ, Na BK

Supervision: Huynh HQ, Na BK

Project administration; Na BK

Funding acquisition: Na BK

Validation: Huynh HQ, Na BK

Visualization: Võ TC, Na BK

Writing—original draft preparation: Võ TC, Na BK

Writing—review and editing: Lê HG, Kang JM, Nguyen TMT, Huynh HQ

Acknowledgements

This research was supported by a National Research Foundation of Korea (NRF) grants from

the Government of Korea (NRF-2023M3A9H506175721 and NRF-2024M3A9H5043141).

Ethics

The study protocol was approved by the Ministry of Health, Institute of Malariology, Parasitology and Entomology Quy Nhon, Vietnam (No.: 386/VSR-LSDT, 45/VSR-NCDT, and 637/VSR-NCDT

Conflicts of interest

The authors declare no conflict of interest.

Data Availability Statement

The data supporting the conclusions of this article are provided within the article. The original data in the present study are available from the corresponding authors upon request.

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Genetic polymorphism of merozoite surface protein 1 and merozoite surface protein 2 in the Vietnam Plasmodium falciparum population

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Abstract

Background

Methods

Results

Conclusions

Figures

Introduction

Materials and Methods

Parasite samples and study area

Genetic diversity analysis

Results

Discussion

Conclusion

Declarations

References

Additional Declarations

Supplementary Files

Status:

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