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"Bo Young Jeon"

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"Bo Young Jeon"

Original Articles
Genetic diversity and phylogeographic structure of Anopheles kochi, Anopheles maculatus, and Anopheles vagus: ITS2-based analysis of highland transboundary populations in the Menoreh Hills, Java, Indonesia
Derico Hitipeuw, Raisha Nuranindita, Martini Martini, Arif Suryo Prasetyo, Jin-Hee Han, Hojong Jun, Bo Young Jeon, Triwibowo Ambar Garjito, Rohmadi Rohmadi, Fauzi Muh
Parasites Hosts Dis 2025;63(3):228-242.
Published online August 20, 2025
DOI: https://doi.org/10.3347/PHD.25026
Baseline genetic characterization of malaria vector populations provides critical data for evidence-based surveillance in persistent transmission foci. This pilot study generated preliminary genetic baseline data for Anopheles populations in the Menoreh Hills border region between Central Java and Yogyakarta provinces, Indonesia, addressing a key geographic gap in regional vector research. Adult female mosquitoes were collected from 3 houses with reported malaria cases in Ngadirejo Village using standardized entomological methods, including human landing, animal landing, and resting collections. Specimens were morphologically identified and molecularly characterized via ITS2 gene sequencing. Phylogenetic analyses were assessed using maximum likelihood methods, and genetic diversity indices were calculated to examine population structure. A total of 62 specimens representing 3 species were collected exclusively through animal landing collections: Anopheles vagus (48 specimens, 77.4%), Anopheles maculatus (9 specimens, 14.5%), and Anopheles kochi (5 specimens, 8.1%). An. kochi exhibited high haplotype diversity (Hd=0.709) with low nucleotide diversity (π=0.004), while An. maculatus showed lower haplotype diversity (Hd=0.480) and higher nucleotide diversity (π=0.026). Phylogenetic analysis revealed Purworejo specimens clustered with regional populations: An. kochi grouped within Clade I with Indonesian isolates; An. maculatus distributed across multiple clades; An. vagus formed a cohesive unit with other Indonesian populations. The exclusive success of animal landing collections in the Menoreh Hills highlands provides key methodological insights. This study offers essential baseline reference data, validates cost-effective genetic surveillance approaches, and supports future large-scale population connectivity studies across the Menoreh Hills malaria transmission complex.
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Prevalence of chigger mites and Orientia tsutsugamushi strains in northern regions of Gangwon-do, Korea
Soojin Kim, In Yong Lee, Sezim Monoldorova, Jiro Kim, Jang Hoon Seo, Tai-Soon Yong, Bo Young Jeon
Parasites Hosts Dis 2023;61(3):263-271.
Published online August 21, 2023
DOI: https://doi.org/10.3347/PHD.22148
The present study aimed to survey the prevalence of chigger mites and Orientia tsutsugamushi (O. tsutsugamushi) infection in the northern regions of Gangwon-do, Korea. From early February to early June 2015, a total of 17,050 chiggers were collected from striped field mice, Apodemus agrarius, in Cheorwon-gun, Hwacheon-gun, Yanggu-gun, and Goseong-gun, which are well-known endemic areas of scrub typhus in Korea. The chiggers were analyzed using molecular genomic methods, as previously described. Among the 7,964 identified chiggers, the predominant species was Leptotrombidium pallidum (76.9%), followed by L. zetum (16.4%), L. orientale (4.3%), L. palpale (0.3%), L. tectum (0.2%), and Neotrombicula tamiyai (1.8%). The chigger index (CI) was highest in Hwacheon (115.58), followed by Cheorwon (97.02), Yanggu (76.88), and Goseong (54.68). Out of the 79 O. tsutsugamushi-positive chigger pools, 67 (84.8%) were identified as the Boryong strain, 10 (12.7%) as the Youngworl strain, and only 2 were the Jecheon strain. Based on the high infestation of chiggers in striped field rodents and the high rate of O. tsutsugamushi infection in chigger mites, Hwacheon-gun and Cheorwon-gun are presumed to be high-risk areas for scrub typhus. Furthermore, L. pallidum, a major vector of scrub typhus, and the dominant O. tsutsugamushi serotype, the Boryong strain, were found in the northern regions of Gangwon-do, Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Geographic distribution of Orientia tsutsugamushi strains on chigger mites in the Republic of Korea (2021–2023)
    Hyeon Seung Lee, Byung-Eon Noh, Hyunwoo Kim, Heeil Lee
    Parasites & Vectors.2025;[Epub]     CrossRef
  • Surveillance of Vector‐Borne Zoonotic Diseases in South Korea: Uncovering Novel Pathogen Carriers Among Rodents and Mites Nationwide
    Beoul Kim, You-Jeong Lee, Hee Il Lee, Dongmi Kwak, Min-Goo Seo, Nan-hua Chen
    Transboundary and Emerging Diseases.2024;[Epub]     CrossRef
  • 2022년 쯔쯔가무시증 매개 털진드기 감시 현황
    세훈 조, 태규 김, 현우 김, 정원 주, 희일 이
    Public Health Weekly Report.2023; 16(46): 1563.     CrossRef
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  • 119 Download
  • 2 Web of Science
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Cytokine Production in Cholangiocarcinoma Cells in Response to Clonorchis sinensis Excretory-Secretory Products and Their Putative Protein Components
Jhang Ho Pak, Ji-Yun Lee, Bo Young Jeon, Fuhong Dai, Won Gi Yoo, Sung-Jong Hong
Korean J Parasitol 2019;57(4):379-387.
Published online August 31, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.4.379
Clonorchis sinensis is a carcinogenic human liver fluke that promotes hepatic inflammatory environments via direct contact or through their excretory-secretory products (ESPs), subsequently leading to cholangitis, periductal fibrosis, liver cirrhosis, and even cholangiocarcinoma (CCA). This study was conducted to examine the host inflammatory responses to C. sinensis ESPs and their putative protein components selected from C. sinensis expressed sequenced tag (EST) pool databases, including TGF-β receptor interacting protein 1(CsTRIP1), legumain (CsLeg), and growth factor binding protein 2 (CsGrb2). Treatment of CCA cells (HuCCT1) with the ESPs or bacterial recombinant C. sinensis proteins differentially promoted the secretion of proinflammatory cytokines (IL-1β, IL-6, and TNF-α) as well as anti-inflammatory cytokines (IL-10, TGF-β1, and TGF-β2) in a time-dependent manner. In particular, recombinant C. sinensis protein treatment resulted in increase (at maximum) of ~7-fold in TGF-β1, ~30-fold in TGF-β2, and ~3-fold in TNF-α compared with the increase produced by ESPs, indicating that CsTrip1, CsLeg, and CsGrb2 function as strong inducers for secretion of these cytokines in host cells. These results suggest that C. sinensis ESPs contribute to the immunopathological response in host cells, leading to clonorchiasis-associated hepatobiliary abnormalities of greater severity.

Citations

Citations to this article as recorded by  Crossref logo
  • Immunogenomics of cholangiocarcinoma
    Virag Gehl, Colm J. O’Rourke, Jesper B. Andersen
    Hepatology.2025; 82(2): 522.     CrossRef
  • Clonorchis sinensis-driven hepatocarcinogenesis via E2F1-CD24 transcriptional axis: mechanistic and therapeutic implications
    Wen-Min Lu, Jin Yan, Zhao-Ji Liu, Yong Wu, Qian-Ru Cui, Ji Feng, Yu Chen, Guang-Zhi Zhu, Tao Peng, Jing Zhou, Guo-Dong Lu
    Parasites & Vectors.2025;[Epub]     CrossRef
  • The crosstalk between cholangiocytes and hepatic stellate cells promotes the progression of epithelial-mesenchymal transition and periductal fibrosis during Clonorchis sinensis infection
    Junyeong Yi, Ji Hoon Jeong, Jihee Won, Seok Chung, Jhang Ho Pak
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Clonorchis sinensisinfection induces pathological changes in feline bile duct epithelium and alters biliary microbiota composition
    Feng Li, Yanli Zhang, Chunfu Li, Fenqi Li, Baojiang Gan, Hong Yu, Jian Li, Xinyu Feng, Wei Hu
    Parasite.2024; 31: 53.     CrossRef
  • Up-regulation of MDSCs accumulation and Th2 biased response to co-stimulation of CsESP from Clonorchis sinensis and HBeAg in vitro
    Qiannan Liu, Nian Wang, Hengchang Sun, Huimin Dong, Xuerong Li, Xinbing Yu, Yan Huang
    Acta Tropica.2024; 260: 107405.     CrossRef
  • The expression of sICAM-1 influenced by Clonorchis sinensis co-infection in CHB patients
    J. Qiu, M. Shang, W. Li, H. Zhang, Y. Liao, H. Dong
    Journal of Helminthology.2024;[Epub]     CrossRef
  • Genus Bithynia: morphological classification to molecular identification
    Guoyang Huang, Xiaohong Peng
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Clonorchis sinensis granulin promotes malignant transformation of human intrahepatic biliary epithelial cells through interaction with M2 macrophages via regulation of STAT3  phosphorylation and the MEK/ERK pathway
    Qing He, Xiaowen Pan, Yingxuan Yin, Anyuan Xu, Xueqing Yi, Yinjuan Wu, Xuerong Li
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Recombinant protein EBI3 attenuates Clonorchis sinensis-induced liver fibrosis by inhibiting hepatic stellate cell activation in mice
    Lei Zhao, Jia Li, Gang Mo, Deping Cao, Chun Li, Guoyang Huang, Liping Jiang, Gen Chen, Hongbing Yao, Xiaohong Peng
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Cancerogenic parasites in veterinary medicine: a narrative literature review
    Niccolò Fonti, Francesca Parisi, Francesca Mancianti, Giulia Freer, Alessandro Poli
    Infectious Agents and Cancer.2023;[Epub]     CrossRef
  • Molecular Mechanisms of Clonorchis sinensis-Host Interactions and Implications for Vaccine Development
    Stephane Koda, Xing-Quan Zhu, Kui-Yang Zheng, Chao Yan
    Frontiers in Cell and Developmental Biology.2022;[Epub]     CrossRef
  • Roles of microRNAs and Long Non-Coding RNAs Encoded by Parasitic Helminths in Human Carcinogenesis
    Ana Gabriela Leija-Montoya, Javier González-Ramírez, Gustavo Martínez-Coronilla, María Esther Mejía-León, Mario Isiordia-Espinoza, Fausto Sánchez-Muñoz, Elda Georgina Chávez-Cortez, Viviana Pitones-Rubio, Nicolas Serafín-Higuera
    International Journal of Molecular Sciences.2022; 23(15): 8173.     CrossRef
  • The role of helminths in the development of non-communicable diseases
    Yifan Wu, Megan Duffey, Saira Elizabeth Alex, Charlie Suarez-Reyes, Eva H. Clark, Jill E. Weatherhead
    Frontiers in Immunology.2022;[Epub]     CrossRef
  • Spirocerca lupi Proteomics and Its Role in Cancer Development: An Overview of Spirocercosis-Induced Sarcomas and Revision of Helminth-Induced Carcinomas
    Catalina Porras-Silesky, María José Mejías-Alpízar, Javier Mora, Gad Baneth, Alicia Rojas
    Pathogens.2021; 10(2): 124.     CrossRef
  • The Dark Side of the Force: When the Immune System Is the Fuel of Tumor Onset
    Elisabeth Digifico, Silvia Balinzo, Cristina Belgiovine
    International Journal of Molecular Sciences.2021; 22(3): 1224.     CrossRef
  • Tumor-associated macrophages in cholangiocarcinoma: complex interplay and potential therapeutic target
    Menghua Zhou, Chaoqun Wang, Shounan Lu, Yanan Xu, Zihao Li, Hongchi Jiang, Yong Ma
    EBioMedicine.2021; 67: 103375.     CrossRef
  • Omega-Class Glutathione Transferases of Carcinogenic Liver Fluke, Clonorchis sinensis, Modulate Apoptosis and Differentiation of Host Cholangiocytes
    Chun-Seob Ahn, Jeong-Geun Kim, Insug Kang, Yoon Kong
    Antioxidants.2021; 10(7): 1017.     CrossRef
  • Clonorchis sinensis and clonorchiasis
    Byoung-Kuk Na, Jhang Ho Pak, Sung-Jong Hong
    Acta Tropica.2020; 203: 105309.     CrossRef
  • CD19+CD1dhiCD5hi B Cells Can Downregulate Malaria ITV Protection by IL-10 Secretion
    Hongli Guan, Jiacong Peng, Liping Jiang, Gang Mo, Xiang Li, Xiaohong Peng
    Frontiers in Public Health.2020;[Epub]     CrossRef
  • Dopaminergic antagonists inhibit bile chemotaxis of adult Clonorchis sinensis and its egg production
    Fuhong Dai, Jin-Ho Song, Yeon Pyo Hong, Xuelian Bai, Woon-Mok Sohn, Sung-Jong Hong, jong-Yil Chai
    PLOS Neglected Tropical Diseases.2020; 14(3): e0008220.     CrossRef
  • Identification and Analysis of the Tegument Protein and Excretory-Secretory Products of the Carcinogenic Liver Fluke Clonorchis sinensis
    Yunliang Shi, Kai Yu, Anli Liang, Yan Huang, Fangqi Ou, Haiyan Wei, Xiaoling Wan, Yichao Yang, Weiyu Zhang, Zhihua Jiang
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Bile Ductal Transcriptome Identifies Key Pathways and Hub Genes in Clonorchis sinensis-Infected Sprague-Dawley Rats
    Won Gi Yoo, Jung-Mi Kang, Huong Giang Lê, Jhang Ho Pak, Sung-Jong Hong, Woon-Mok Sohn, Byoung-Kuk Na
    The Korean Journal of Parasitology.2020; 58(5): 513.     CrossRef
  • 7,615 View
  • 142 Download
  • 23 Web of Science
  • Crossref