Publications by authors named "Won Il Kim"

Porcine reproductive and respiratory syndrome virus (PRRSV) causes significant economic losses in the global swine industry due to its high genetic diversity and different virulence levels, which complicate disease management and vaccine development. This study evaluated longitudinal changes in the immune cell composition of bronchoalveolar lavage fluid and the clinical outcomes across PRRSV strains with varying virulence, using techniques including single-cell transcriptomics. In highly virulent infection, faster viral replication results in an earlier peak lung-damage time point, marked by significant interstitial pneumonia, a significant decrease in macrophages, and an influx of lymphocytes.

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  • Caseous lymphadenitis (CLA) is a bacterial disease affecting ruminants that has seen a rise in cases in South Korea since 2014, prompting the development of a new vaccine.
  • Researchers created the first inactivated CLA vaccine in South Korea and tested its effectiveness through trials on mice, guinea pigs, and Korean Native Black Goats (KNBGs), finding no clinical symptoms in vaccinated KNBGs and significant levels of CLA-specific IgG.
  • The vaccine is designed to prevent infection from a variety of CLA strains, with the potential to protect livestock and support the growth of the domestic KNBG industry in South Korea.
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  • Porcine respiratory coronavirus (PRCV) is prevalent in Korean pig farms, with a farm-level seroprevalence of 68.6%, indicating ongoing circulation of the virus since its identification in 1997.
  • In samples from seropositive farms, PRCV RNA was detected in 28.3% of oral fluid samples, while no TGEV RNA was found, highlighting the focus on PRCV.
  • Genetic analysis of Korean PRCV strains revealed high homology among them and suggested a European origin due to a significant amino acid deletion, indicating that Korean PRCVs have evolved independently from American strains.
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All pigs in the Republic of Korea are given the foot-and-mouth disease virus (FMDV) vaccine intramuscularly (IM) as part of the country's vaccination policy. However, the IM administration of the FMDV vaccine to pig results in residual vaccine components in the muscle and undesirable changes in muscle and soft tissues, causing economic losses in swine production. In this study, we evaluated whether intradermal (ID) vaccination could be proposed as an alternative to IM administration.

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  • - The study reports the first detection of novel swine orthopneumovirus (SOV) infections in South Korea, with a 4.4% detection rate in oral fluid samples from pigs across four provinces.
  • - Two complete genome sequences and one glycoprotein gene sequence of the SOV strains from South Korea show significant genetic similarity (98.2% and 95.4%) to previously identified SOV strains from the USA and China.
  • - A genetic analysis classifies the Korean SOV strains into a distinct group (G2) compared to other orthopneumoviruses, contributing to a better understanding of the virus's genetic diversity and distribution in global pig populations.
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For rapid and reliable detection of porcine epidemic diarrhea virus (PEDV) from pig clinical samples, a multiplex, real-time, reverse transcription loop-mediated isothermal amplification (mqRT-LAMP) was developed using two sets of primers and assimilating probes specific to the PEDV N gene and the gene, which was used as an endogenous internal positive control (EIPC) to avoid false-negative results. The assay specifically amplified both target genes of PEDV and EIPC in a single reaction without any interference but did not amplify other porcine viral nucleic acids. The limit of detection was 10 copies/μL, 100-fold lower than that of a reverse transcription-polymerase chain reaction (RT-PCR) and equivalent to that of quantitative/real-time RT-PCR (qRT-PCR).

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Introduction: The antiviral activity of different mutagens against single-stranded RNA viruses is well documented; however, their activity on the replication of double-stranded RNA viruses remains unexplored. This study aims to investigate the effect of different antivirals on the replication of a chicken embryo fibroblast-adapted Infectious Bursal Disease virus, FVSKG2. This study further explores the antiviral mechanism utilized by the most effective anti-IBDV agent.

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Porcine reproductive and respiratory syndrome virus (PRRSV) infection severely affects the swine industry each year. Although the host mechanisms against PRRSV infection have been identified in key target tissues through whole transcriptome sequencing, specific molecular regulators have not been elucidated. Long non-coding RNA (lncRNA) expression is highly specific and could thus be used to effectively identify PRRSV-specific candidates.

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Background: The porcine epidemic diarrhea virus (PEDV) represents a major health issue for piglets worldwide and does significant damage to the pork industry. Thus, new therapeutic approaches are urgently needed to manage PEDV infections. Due to the current lack of a reliable remedy, this present study aims to identify novel compounds that inhibit the 3CL protease of the virus involved in replication and pathogenesis.

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Recently, intercalation pseudocapacitance has received significant interest as an abnormal charge storage mechanism owing to the battery-like intercalation energy storage into the bulk electrodes and the fast charge storage kinetics of electrochemical capacitors. However, intercalation pseudocapacitance of molybdenum-based polyoxometalates (POMs) for high-performance Zn ion battery (ZIB) cathodes is yet to be exploited. Herein, we demonstrate the fast and reversible intercalation pseudocapacitance of vanadium-substituted Keggin-type molybdenum-based POMs (XPMoV), where H of HPMoV is replaced by X cations (X = Li, Na, K, or Rb).

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  • Peripheral blood mononuclear cells (PBMCs) are typically used to study immune responses, but isolating them is time-consuming and requires a lot of blood, while whole blood assays (WBA) offer a quicker and more efficient alternative.
  • This study aimed to create a WBA for evaluating immune responses in pigs, using diluted whole blood and specific stimuli to assess T-cell activity and cytokine production.
  • Results showed that the best dilution for assessing immune responses was 1/8, with increased production of key immune markers like IFN-γ and TNF-α when blood was stimulated with certain substances and viruses, suggesting WBAs are a practical method for immune evaluation.
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Porcine reproductive and respiratory syndrome (PRRS) is a disease that has inflicted economic losses in the swine industry. The causative agent, porcine reproductive and respiratory syndrome virus (PRRSV), is known to have a high genetic diversity which leads to heterogeneous pathogenicity. To date, the impact of PRRS outbreaks on swine production and the economy of the swine industry in South Korea has been rarely reported.

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The COVID-19 pandemic was caused by the zoonotic SARS-CoV-2. A variety of animals involved in human life worldwide have been investigated for infection. As the degree of infection increased, extensive monitoring in animals became necessary to determine the degree of infection in animals.

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  • Porcine respirovirus 1 (PRV1) is a new respiratory virus affecting pigs, first identified in Hong Kong in 2009, and has now been found in several countries, including Korea.
  • In Korea, PRV1 was detected in pigs across 16 farms in seven provinces, with a high prevalence rate of 71.4% in oral fluid samples, indicating widespread infection.
  • Genetic analysis revealed that the Korean PRV1 strains belong to European lineage 1 and are closely related to strains from other countries, although the origin of the virus remains unclear due to limited sequence data.
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Porcine circovirus type 2 (PCV2) is an economically important swine pathogen that causes porcine circovirus-associated diseases (PCVADs). The objective of this study was to evaluate the use of specific pathogen-free Yucatan miniature pigs (YMPs) as an experimental model for PCV2d challenge and vaccine assessment because PCV2-negative pigs are extremely rare in conventional swine herds in Korea. In the first experiment, every three pigs were subjected to PCV2d field isolate or mock challenge.

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  • PRRSV (Porcine reproductive and respiratory syndrome virus) significantly impacts the global swine industry due to its high genetic and pathogenic variability, divided into European (PRRSV1) and North American (PRRSV2) strains.
  • This study employed a new method, SISPA-NGS, for whole-genome sequencing of Korean PRRSV strains, enabling detailed genetic characterization and phylogenetic analysis.
  • Results identified distinct lineages among Korean PRRSV strains, revealed conserved genetic patterns, and indicated natural recombination events, enhancing understanding of the virus's evolution and variants in the region.
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  • The study investigates the prevalence of classical porcine parvovirus (PPV1) and newer strains (PPV2-PPV7) in pig populations in Korea, analyzing various biological samples collected between 2018 and 2020.
  • Findings indicate that these viruses are widespread, with the highest detection rates in lung samples, particularly in fattening pigs, suggesting a chronic infection cycle.
  • The presence of PPVs was notably higher in samples co-infected with porcine circovirus type 2 (PCV2) and porcine reproductive and respiratory virus (PRRSV), highlighting the potential interactions between these pathogens and the need for further research into their combined effects.
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Immortalized cell lines are valuable resources to expand the molecular characterization of major histocompatibility complex genes and their presented antigens. We generated a panel of immortalized cell lines by transfecting human telomerase reverse transcriptase () into primary fibroblast cells prepared from ear, fetal, and lung tissues of 10 pigs from five breeds and successfully cultured them for 30-45 passages. The cell growth characteristic of the immortalized fibroblasts was similar to that of primary fibroblast, which was unable to form colonies on soft agar.

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To date, few studies related to the evaluation of the pathogenicity of different PRRSV isolates using a reproductive model have been undertaken, and the main focus has remained on respiratory models using young pigs. This study aimed to evaluate the pathogenicity of two PRRSV-1 isolates (D40 and CBNU0495) and two PRRSV-2 isolates (K07-2273 and K08-1054) in a reproductive model. Pregnant sows were experimentally infected with PRRSV at gestational day 93 or used as an uninfected negative control.

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This study aimed to determine the prevalence of several pathovirotypes and evaluate the association of haemolysis with the virotypes of pathogenic isolated from post-weaning piglets in South Korea from 2015 to 2019. We isolated 890 and tested for O-serogroups, virulence genes, haemolysis, and multilocus sequence typing. The predominant virotypes were STb:EAST1:AIDA-I, F18b:Stx2e:AIDA-I, F18:STa:STb:Stx2e, and eae:Paa in enterotoxigenic (ETEC), Shiga toxin-producing (STEC), ETEC/STEC, and enteropathogenic (EPEC), respectively.

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Despite the routine use of porcine reproductive and respiratory syndrome (PRRS)-modified live vaccines, serious concerns are currently being raised due to their quick reversion to virulence and limited cross-protection against divergent PRRS virus (PRRSV) strains circulating in the field. Therefore, a PRRS chimeric vaccine (JB1) was produced using a DNA-launched infectious clone by replacing open reading frames (ORFs) 3-6 with those from a mixture of two genetically different PRRSV2 strains (K07-2273 and K08-1054) and ORF1a with that from a mutation-resistant PRRSV strain (RVRp22) exhibiting an attenuated phenotype. To evaluate the safety and cross-protective efficacy of JB1 in a reproductive model, eight PRRS-negative pregnant sows were purchased and divided into four groups.

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  • A new virus called porcine circovirus 4 (PCV4) has been discovered in China and Korea, creating a need for effective detection methods in field samples.
  • Researchers developed a loop-mediated isothermal amplification (LAMP) assay that provides quick and visible results for detecting PCV4 within 40 minutes.
  • This LAMP method is highly sensitive, detecting less than 50 DNA copies, and outperforms traditional methods, making it an ideal option for diagnosing PCV4 in clinical settings, even in labs with limited resources.
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Vaccines against porcine circovirus type 2 (PCV2) and Mycoplasma hyopneumoniae (Mhp) are routinely used by intramuscular injection. However, since intramuscular vaccination causes stress and increases the risk of cross-contamination among pigs, research on intradermal vaccination is currently being actively conducted. This study was designed to evaluate the efficacy of intradermally administered inactivated vaccines against PCV2 and Mhp in pigs.

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We aimed to comprehensively understand the functional mechanisms of immunity, especially of the CD8 subsets of gamma delta (γδ) T cells, using an RNA-sequencing analysis. Herein, γδ T cells were obtained from bronchial lymph node tissues of 38-day-old (after weaning 10-day: D10) and 56-day-old (after weaning 28-day: D28) weaned pigs and sorted into CD8 and CD8 groups. Differentially expressed genes (DEGs) were identified based on the CD8 groups at D10 and D28 time points.

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Porcine reproductive and respiratory syndrome virus (PRRSV) is the most important pathogen in the Korean swine industry. Despite efforts including improved biosecurity and vaccination protocols, the virus continues to circulate and evolve. Based on phylogenetic analysis of open reading frame 5 (ORF5), Korean PRRSVs are known to form not only globally circulating lineages but also country-specific lineages (Lin Kor A, B, and C).

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