Publications by authors named "Tuấn Cuờng Vo"

, a causative agent of quartan malaria, is prevalent across tropical and subtropical regions, but global cases have been usually very rare and sporadic. However, a significant outbreak of quartan malaria caused by occurred in Khanh Vinh District, Khanh Hoa Province, Vietnam in 2023 and the outbreak persists. In this report, we present the epidemiological and clinical characteristics of this unprecedented outbreak of quartan malaria in Vietnam.

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  • - The study investigates the genetic diversity of potential malaria vaccine targets, PfMSP1 and PfMSP2, in P. falciparum from Vietnam, highlighting the challenges posed by global genetic variation in vaccine development.
  • - Researchers found that P. falciparum in Vietnam showed higher genetic homogeneity in pfmsp1 and pfmsp2 compared to other countries, with unique allele diversity patterns differing significantly from its Greater Mekong Subregion neighbors.
  • - Results suggest that geographic isolation and specific evolutionary pressures may have led to the genetic characteristics seen in Vietnam's P. falciparum population, indicating potential factors like bottleneck effects influencing its genetic makeup.
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  • PvDBP is essential for the malaria parasite Plasmodium vivax to invade red blood cells by binding to a receptor called DARC, and its amino-terminal region II (PvDBPII) shows potential as a vaccine target.
  • A study of 118 P. vivax isolates from Pakistan identified 29 single nucleotide polymorphisms (SNPs), mainly in subdomains II and III of PvDBPII, with a notable 22 being nonsynonymous, indicating significant genetic variation.
  • Despite variation in amino acid changes between countries, both nucleotide diversity and patterns of natural selection in the Pakistan isolates align with those found globally, providing critical insights for developing effective vaccines against vivax malaria.
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  • * A study analyzed the genetic diversity of the pfama-1 gene in P. falciparum isolates from Khyber Pakhtunkhwa, Pakistan, revealing 58 amino acid changes, particularly in specific domains.
  • * The research found both familiar genetic variations and 13 new changes unique to the region, indicating that KP-Pakistan pfama-1 had a similar level of diversity as the global strains, with signs of natural selection and recombination.
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keratitis (AK) is a sight-threatening and difficult-to-treat ocular infection. The significant side effects of current AK treatments highlight the urgent need to develop a safe and effective AK medication. In this study, the amoebicidal activity of Pall.

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Myanmar aims to eliminate malaria by 2030. However, recent increase of malaria incidence is a great challenge to archive that goal. Increasing prevalence of Plasmodium vivax also hinders this endeavor.

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Naegleria fowleri invades the brain and causes a fatal primary amoebic meningoencephalitis (PAM). Despite its high mortality rate of approximately 97%, an effective therapeutic drug for PAM has not been developed. Approaches with miltefosine, amphotericin B, and other antimicrobials have been clinically attempted to treat PAM, but their therapeutic efficacy remains unclear.

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  • G6PD deficiency is a common X-linked hereditary disorder that can provide resistance to severe malaria but complicates treatment with the drug primaquine (PQ), which can cause harmful effects in patients with this deficiency.
  • A study conducted in Vietnam analyzed G6PD deficiency in 1721 individuals from malaria-endemic areas, revealing varied G6PD activity levels and no detectable phenotypic deficiency.
  • Genetic testing identified 26 individuals with specific G6PD mutations, indicating a low prevalence of G6PD deficiency (1.51%), highlighting the importance of screening for G6PD status prior to PQ treatment in high-risk areas.
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Background: Acanthamoeba is an opportunistic pathogen that can cause human infections such as granulomatous amebic encephalitis and acanthamoeba keratitis. However, no specific drug to treat the diseases has been developed. Therefore, the discovery or development of novel drugs for treating Acanthamoeba infections is urgently needed.

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Free-living amoebae (FLA) rarely cause human infections but can invoke fatal infections in the central nervous system (CNS). No consensus treatment has been established for FLA infections of the CNS, emphasizing the urgent need to discover or develop safe and effective drugs. Flavonoids, natural compounds from plants and plant-derived products, are known to have antiprotozoan activities against several pathogenic protozoa parasites.

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  • PfEBA-175 is crucial for P. falciparum's ability to invade red blood cells and is a key target for vaccine development, but its genetic diversity poses challenges for creating a universal vaccine.
  • The study found that the pfeba-175 region II in Vietnamese isolates had low genetic diversity, while the Myanmar isolates exhibited high genetic variation due to factors like point mutations and recombination.
  • Despite differing amino acid substitution patterns in various global populations, five significant mutations were identified universally, highlighting the importance of ongoing genetic monitoring to inform vaccine design.
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Extracellular vesicles (EVs) of protozoan parasites have diverse biological functions that are essential for parasite survival and host-parasite interactions. In this study, we characterized the functional properties of EVs from , a pathogenic amoeba that causes a fatal brain infection called primary amoebic meningoencephalitis (PAM). EVs (NfEVs) have been shown to be internalized by host cells such as C6 glial cells and BV-2 microglial cells without causing direct cell death, indicating their potential roles in modulating host cell functions.

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Background: Naegleria fowleri is a brain-eating amoeba causing a fatal brain infection called primary amoebic meningoencephalitis (PAM). Despite its high mortality over 95%, effective therapeutic drug for PAM has not been developed yet. Therefore, development of an effective and safe therapeutic drug for PAM is urgently needed.

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Acanthamoeba keratitis (AK) is an infectious ocular disease which is difficult to diagnose correctly and cure. Development of an effective and safe therapeutic drug for AK is needed. Our preliminary screening of more than 200 extracts from wild plants collected in Korea suggested the potential amoebicidal activity of (Cav.

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  • The study focuses on the circumsporozoite surface protein (PvCSP) of the malaria parasite, which is a key target for vaccine development, particularly for vivax malaria in Vietnam.
  • Researchers analyzed genetic variations and natural selection in parasite isolates from the Central Highlands of Vietnam, identifying VK210 and VK247 as the two major alleles, with VK247 being more common.
  • Findings revealed unique genetic patterns and low diversity in certain regions of the protein while highlighting divergent natural selection pressures compared to other populations, thus enhancing knowledge of parasite genetics in this endemic area.
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Emergence and spreading of antimalarial drug resistant malaria parasites are great hurdles to combating malaria. Although approaches to investigate antimalarial drug resistance status in Myanmar malaria parasites have been made, more expanded studies are necessary to understand the nationwide aspect of antimalarial drug resistance. In the present study, molecular epidemiological analysis for antimalarial drug resistance genes in and from the Mandalay region of Myanmar was performed.

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  • * Researchers discovered that the CsPmy from the parasite Clonorchis sinensis interacts with human complement protein C9, pinpointing the C-terminus as the specific binding region.
  • * The study highlighted that certain fragments of CsPmy can effectively block the polymerization of C9, suggesting that CsPmy plays a key role in helping the parasite evade the host's immune response by disrupting complement activation.
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is a ubiquitous protozoa parasite that can cause primary amoebic meningoencephalitis (PAM), a fatal brain infection in humans. Cathepsin Bs of (NfCBs) are multifamily enzymes. Although their pathogenic mechanism in PAM is not clearly understood yet, NfCBs have been proposed as pathogenic factors involved in the pathogenicity of amoeba.

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Background: Coccidiosis is a poultry disease that occurs worldwide and is caused by Eimeria species. The infection is associated with reduced feed efficiency, body weight gain, and egg production. This study aimed to investigate the current status of coccidiosis and anticoccidial resistance to anticoccidial drugs used as part of control strategies for this disease in Korean chicken farms.

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Cysteine proteases of malaria parasites have been recognized as potential targets in antimalarial drug development as they play pivotal roles in the biology of these parasites. However, strict regulation of their activities is also necessary to minimize or prevent deleterious damage to the parasite and the host. Previously, we have characterized falcipain family cysteine proteases of , named as malapains (MPs).

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  • The study focuses on the increasing resistance of a significant mosquito vector in Myanmar, which spreads various viral diseases.
  • The research specifically identifies mutations in the voltage-gated sodium channel (VGSC) that are linked to resistance against pyrethroid insecticides commonly used in mosquito control.
  • High frequencies of several key mutations were found in the mosquito population, indicating a serious level of resistance and emphasizing the need for improved vector control strategies in the region.
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Cysteine proteases belonging to the falcipain (FP) family play a pivotal role in the biology of malaria parasites and have been extensively investigated as potential antimalarial drug targets. Three paralogous FP-family cysteine proteases of , termed malapains 2-4 (MP2-4), were identified in PlasmoDB. The three MPs share similar structural properties with the FP-2/FP-3 subfamily enzymes and exhibit a close phylogenetic lineage with vivapains (VXs) and knowpains (KPs), FP orthologues of and .

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  • Apical membrane antigen-1 (PfAMA-1) is a key candidate for malaria vaccines, but genetic diversity in global strains poses challenges for developing effective vaccines.
  • In a study of 131 malaria isolates from Vietnam, researchers identified 37 distinct haplotypes with most genetic variations occurring in specific protein domains.
  • The Vietnamese isolates exhibited lower genetic diversity than those from other regions and showed signs of natural purifying selection, which could inform future vaccine design targeting PfAMA-1.
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  • Avian coccidiosis, caused by certain parasites, results in significant economic losses for the poultry industry, highlighting the need for effective vaccines.
  • Microneme protein 2 (MIC2) and surface antigen 1 (SAG1) are identified as promising vaccine candidates but their effectiveness is impacted by genetic diversity observed in field isolates.
  • A study on Korean isolates revealed low genetic diversity for both genes, but differences in nucleotide diversity and amino acid variations were noted when compared to isolates from other countries, emphasizing the need for broader genetic studies to ensure effective vaccine development.
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Despite a significant decline in the incidence of malaria in Myanmar recently, malaria is still an important public health concern in the country. Although is associated with the highest incidence of malaria in Myanmar, the proportion of cases has shown a gradual increase in recent years. The genetic diversity of merozoite surface protein-1 block 5-6 (- ICB 5-6) in the population of Myanmar was analyzed to obtain a comprehensive insight into its genetic heterogeneity and evolutionary history.

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