Publications by authors named "Byoung-Kuk Na"

, 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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Plasmodium vivax variant interspersed repeats (vir) refer to the key protein used for escaping the host immune system. Knowledge in the genetic variation of vir genes can be used for the development of vaccines or diagnostic methods. Therefore, we evaluated the genetic diversity of the vir genes of P.

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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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Rationale: Clinostomum complanatum is a laryngeal fluke whose hosts include birds and mammals.[1] In humans, infection occurs accidentally during the consumption of raw freshwater fish.[1,2].

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Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), encoded by the polymorphic var multigene family, is a highly polymorphic antigen that plays a crucial role in the pathology of malaria. The contribution of the genetic diversity of var toward the immune escape of P. falciparum has not yet been fully elucidated.

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Background The nucleocapsid protein (N protein) of SARS-CoV-2 is undeniably a potent target for the development of diagnostic tools due to its abundant expression and lower immune evasion pressure compared to spike (S) protein. Methods Blood samples of active COVID-19 infections (n=71) and post-COVID-19 (n=11) were collected from a tertiary care hospital in India; pre-COVID-19 (n=12) sera samples served as controls. Real-time reverse transcriptase-PCR (rRT-PCR) confirmed pooled sera samples (n=5) were used with PEPperCHIP® SARS-CoV-2 Proteome Microarray (PEPperPRINT GmbH, Germany) to screen immunodominant epitopes of SARS-CoV-2.

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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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  • Plasmodium vivax apical membrane antigen-1 (pvama-1) is a key target for malaria vaccine development, and understanding its genetic variation is essential for effective vaccine design.
  • A study analyzed blood samples from 84 malaria patients in Khyber Pakhtunkhwa, Pakistan, revealing 57 haplotypes of pvama-1, with notable prevalence of H-14 and H-5 haplotypes, and some geographical genetic distinctions.
  • The findings indicated population expansion and potential immune response modulation due to novel genetic variations, highlighting the importance of genetic assessment for vaccine strategies against malaria.
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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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Malaria continues to be one of the most crucial infectious burdens in endemic areas worldwide, as well as for travelers visiting malaria transmission regions. It has been reported that 8-aminoquinolines are effective against the Plasmodium species, particularly primaquine, for anti-hypnozoite therapy in P. vivax malaria.

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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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