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Case Reports

Diagnosing Balamuthia mandrillaris amebic meningoencephalitis in a 64-year-old woman from the Southwest of China
Suhua Yao, Xiaoting Chen, Lian Qian, Shizheng Sun, Chunjing Zhao, Zongkai Bai, Zhaofang Chen, Youcong Wu
Parasites Hosts Dis 2023;61(2):183-193.
Published online May 23, 2023
DOI: https://doi.org/10.3347/PHD.23039
Balamuthia mandrillaris amebic encephalitis (BAE) can cause a fatal condition if diagnosis is delayed or effective treatment is lacking. Patients with BAE have been previously reported in 12 provinces of China, with skin lesions being the primary symptom and encephalitis developing after several years. However, a significantly lower number of cases has been reported in Southwest China. Here we report an aggressive BAE case of a 64-year-old woman farmer with a history of skin lesions on her left hand. She was admitted to our hospital due to symptoms of dizziness, headache, cough, vomiting, and gait instability. She was initially diagnosed with syphilitic meningoencephalitis and received a variety of empirical treatment that failed to improve her symptoms. Finally, she was diagnosed with BAE combined with amebic pneumonia using next-generation sequencing (NGS), qRT-PCR, sequence analysis, and imaging studies. She died approximately 3 weeks after the onset. This case highlights that the rapid development of encephalitis can be a prominent clinical manifestation of Balamuthia mandrillaris infection.

Citations

Citations to this article as recorded by  Crossref logo
  • The role of plasma metagenomic sequencing in identification of Balamuthia mandrillaris encephalitis
    Sarah Y. Edminster, Ryan W. Rebbe, Christopher Khatchadourian, Kyle M. Hurth, Anna J. Mathew, Julie Huss-Bawab, Mark S. Shiroishi, Devin Clark, Andrew P. Norgan, Susan M. Butler-Wu, Annie Hiniker
    Acta Neuropathologica Communications.2025;[Epub]     CrossRef
  • Balamuthia amoebic encephalitis directly causing intracranial infection: A case report
    Yuhan Liang, Yanhong Liu, Zelong Chen, Jiayi Sun, Xuemeng Zhang, Yulin Wang
    Radiology Case Reports.2025; 20(6): 2820.     CrossRef
  • Pulmonary infection due to Balamuthia mandrillaris in the southwestern United States: not all miliary disease is tuberculosis and coccidioidomycosis
    N. B. Price, H. Pariury, J. Papic, M. R. Anthony, W. Lainhart, K. W. Shehab, Carey-Ann D. Burnham
    ASM Case Reports.2025;[Epub]     CrossRef
  • Applications of the powerful next-generation sequencing tool for detecting parasitic infections: towards a smart laboratory platform
    Bahareh Basirpour, Rabeeh Tabaripour, Farzane Jafarian, Mahdi Fakhar, Hajar Ziaei Hezarjaribi, Shirzad Gholami
    Microbial Pathogenesis.2025; 206: 107746.     CrossRef
  • Next-Generation Sequencing for Diagnosis of Fatal Balamuthia Amoebic Encephalitis: A Case Report
    Yuanyuan Feng, Huiyu Feng, Xuegao Yu, Jing Zhao, Hongyan Zhou, Jiaoxing Li, Peisong Chen, Li Feng
    Diagnostics.2025; 15(20): 2590.     CrossRef
  • Dexamethasone/fructose/glycerol/sodium-chloride/mannitol

    Reactions Weekly.2023; 1970(1): 114.     CrossRef
  • 5,350 View
  • 188 Download
  • 3 Web of Science
  • Crossref
Primary Amebic Meningoencephalitis: A Case Report
Minhua Chen, Wei Ruan, Lingling Zhang, Bangchuan Hu, Xianghong Yang
Korean J Parasitol 2019;57(3):291-294.
Published online June 30, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.3.291
Primary amebic encephalitis (PAM) is a devastating central nervous system infection caused by Naegleria fowleri, a free-living amoeba, which can survive in soil and warm fresh water. Here, a 43-year-old healthy male was exposed to warm freshwater 5 days before the symptom onset. He rapidly developed severe cerebral edema before the diagnosis of PAM and was treated with intravenous conventional amphotericin B while died of terminal cerebral hernia finally. Comparing the patients with PAM who has similar clinical symptoms to those with other common types of meningoencephalitis, this infection is probably curable if treated early and aggressively. PAM should be considered in the differential diagnosis of purulent meningoencephalitis, especially in patients with recent freshwater-related activities during the hot season.

Citations

Citations to this article as recorded by  Crossref logo
  • Enlightening the promising role of nanoparticle-based treatments against Naegleria fowleri-induced primary amoebic meningoencephalitis: A brain-eating disease
    Sunita Jhulki, Biplab Bhowmik, Aparajita Pal
    Microbial Pathogenesis.2025; 199: 107234.     CrossRef
  • Naegleria fowleri Infections: Bridging Clinical Observations and Epidemiological Insights
    Carmen Rîpă, Roxana Gabriela Cobzaru, Miruna Raluca Rîpă, Alexandra Maștaleru, Andra Oancea, Carmen Marinela Cumpăt, Maria Magdalena Leon
    Journal of Clinical Medicine.2025; 14(2): 526.     CrossRef
  • Naegleria fowleri: An Amoeba That Eats your Brain
    Siddhi Suhas Shinde, Anuradha Prajapati, Sachin B. Narkhede, Shailesh Luhar
    Research Journal of Pharmaceutical Dosage Forms and Technology.2025; : 37.     CrossRef
  • Amoebicidal effect of chlorine dioxide gas against pathogenic Naegleria fowleri and Acanthamoeba polyphaga
    Hae-Jin Sohn, A-Young Park, Jeong-Heon Lee, Kyu-Hwa Yun, Kyoung-Ju Song, Jong-Hyun Kim, Ho-Joon Shin
    Parasitology Research.2024;[Epub]     CrossRef
  • A scoping review on epidemiology and pathogenesis of death due to primary amoebic meningoencephalitis
    Krishneswari Rajasekharan Nair Saraswathy
    International Journal Of Community Medicine And Public Health.2024; 12(1): 598.     CrossRef
  • Systematic Review of Brain-Eating Amoeba: A Decade Update
    Mohd ‘Ammar Ihsan Ahmad Zamzuri, Farah Nabila Abd Majid, Massitah Mihat, Siti Salwa Ibrahim, Muhammad Ismail, Suriyati Abd Aziz, Zuraida Mohamed, Lokman Rejali, Hazlina Yahaya, Zulhizzam Abdullah, Mohd Rohaizat Hassan, Rahmat Dapari, Abd Majid Mohd Isa
    International Journal of Environmental Research and Public Health.2023; 20(4): 3021.     CrossRef
  • Distribution and Current State of Molecular Genetic Characterization in Pathogenic Free-Living Amoebae
    Alejandro Otero-Ruiz, Leobardo Daniel Gonzalez-Zuñiga, Libia Zulema Rodriguez-Anaya, Luis Fernando Lares-Jiménez, Jose Reyes Gonzalez-Galaviz, Fernando Lares-Villa
    Pathogens.2022; 11(10): 1199.     CrossRef
  • Photolysis of sodium chloride and sodium hypochlorite by ultraviolet light inactivates the trophozoites and cysts of Acanthamoeba castellanii in the water matrix
    Beni J. M. Chaúque, Marilise B. Rott
    Journal of Water and Health.2021; 19(1): 190.     CrossRef
  • Drugs used for the treatment of cerebral and disseminated infections caused by free‐living amoebae
    Alexandre Taravaud, Zineb Fechtali‐Moute, Philippe M. Loiseau, Sébastien Pomel
    Clinical and Translational Science.2021; 14(3): 791.     CrossRef
  • Death From Primary Amebic Meningoencephalitis After Recreational Water Exposure During Recent Travel to India—Santa Clara County, California, 2020
    Glenn R Harris, Ellora N Karmarkar, Rebecca Quenelle, Lyndsey Chaille, Jai Madhok, Vivian Tien, Jyoti Gupta, Seema Jain, Maria Liu, Shantanu Roy, Supriya Narasimhan, Akiko Kimura, Jennifer R Cope, Ibne Karim M Ali
    Open Forum Infectious Diseases.2021;[Epub]     CrossRef
  • Various brain-eating amoebae: the protozoa, the pathogenesis, and the disease
    Hongze Zhang, Xunjia Cheng
    Frontiers of Medicine.2021; 15(6): 842.     CrossRef
  • Understanding the true burden of “Naegleria fowleri” (Vahlkampfiidae) in patients from Northern states of India: Source tracking and significance
    Ashutosh Panda, Bijay Ranjan Mirdha, Neha Rastogi, Samander Kasuhik
    European Journal of Protistology.2020; 76: 125726.     CrossRef
  • A Fatal Case of Primary Amoebic Meningoencephalitis (PAM) Complicated with Diabetes Insipidus (DI): A Case Report and Review of the Literature
    Muhammad Zain Mushtaq, Saad Bin Zafar Mahmood, Adil Aziz
    Case Reports in Infectious Diseases.2020; 2020: 1.     CrossRef
  • 7,629 View
  • 194 Download
  • 11 Web of Science
  • Crossref

Original Article

Neuronal Apoptosis: Pathological Basis of Behavioral Dysfunctions Induced by Angiostrongylus cantonensis in Rodents Model
Shiqi Luo, Lisi OuYang, Jie Wei, Feng Wu, Zhongdao Wu, Wanlong Lei, Dongjuan Yuan
Korean J Parasitol 2017;55(3):267-278.
Published online June 30, 2017
DOI: https://doi.org/10.3347/kjp.2017.55.3.267
Angiostrongylus cantonensis invades the central nervous system (CNS) of humans to induce eosinophilic meningitis and meningoencephalitis and leads to persistent headache, cognitive dysfunction, and ataxic gait. Infected mice (nonpermissive host), admittedly, suffer more serious pathological injuries than rats (permissive host). However, the pathological basis of these manifestations is incompletely elucidated. In this study, the behavioral test, histological and immunohistochemical techniques, and analysis of apoptotic gene expression, especially caspase-3, were conducted. The movement and motor coordination were investigated at week 2 post infection (PI) and week 3 PI in mice and rats, respectively. The cognitive impairs could be found in mice at week 2 PI but not in rats. The plaque-like lesion, perivascular cuffing of inflammatory cells, and dilated vessels within the cerebral cortex and hippocampus were more serious in mice than in rats at week 3 PI. Transcriptomic analysis showed activated extrinsic apoptotic pathway through increased expression of TNFR1 and caspase-8 in mice CNS. Immunohistochemical and double-labeling for NeuN and caspase-3 indicated the dramatically increased expression of caspase-3 in neuron of the cerebral cortex and hippocampus in mice but not in rats. Furthermore, western-blotting results showed high expression of cleaved caspase-3 proteins in mice but relatively low expression in rats. Thus, extrinsic apoptotic pathway participated in neuronal apoptosis might be the pathological basis of distinct behavioral dysfunctions in rodents with A. cantonensis infection. It provides the evidences of a primary molecular mechanism for the behavioral dysfunction and paves the ways to clinical diagnosis and therapy for A. cantonensis infection.

Citations

Citations to this article as recorded by  Crossref logo
  • Insights into the biology of the rat lungworm, Angiostrongylus cantonensis
    Chasen D. Griffin, Vanessa O. Ezenwa, Robert H. Cowie
    Parasites & Vectors.2025;[Epub]     CrossRef
  • Defective glycolysis in the cerebrum and cerebellum correlates with the pathology and neurological declines in mice with Angiostrongylus cantonensis infection
    Shih-Yi Peng, Ho Yin Pekkle Lam, Yu-Ting Huang
    Parasitology International.2024; 98: 102821.     CrossRef
  • Angiostrongylus cantonensis induces energy imbalance and dyskinesia in mice by reducing the expression of melanin-concentrating hormone
    Hui Huang, Zhongyuan Zhang, Mengdan Xing, Zihan Jin, Yue Hu, Minyu Zhou, Hang Wei, Yiwen Liang, Zhiyue Lv
    Parasites & Vectors.2024;[Epub]     CrossRef
  • IL-17A Mediates Demyelination by Activating A1 Astrocytes via SOCS3 During Angiostrongylus cantonensis Infection
    Zongpu Zhou, Tuo Lin, Zhen Liu, Qian Ding, Zhixuan Ma, Wanqi Li, Fukang Xie, Yue Lan, Ying Feng
    Frontiers in Immunology.2022;[Epub]     CrossRef
  • Mechanisms of the host immune response and helminth-induced pathology during Trichobilharzia regenti (Schistosomatidae) neuroinvasion in mice
    Tomáš Macháček, Roman Leontovyč, Barbora Šmídová, Martin Majer, Oldřich Vondráček, Iveta Vojtěchová, Tomáš Petrásek, Petr Horák, Elise O’Connell
    PLOS Pathogens.2022; 18(2): e1010302.     CrossRef
  • Improvements of cognitive functions in mice heavily infected by Angiostrongylus cantonensis after treatment with albendazole, dexamethasone, or co-therapy
    Kai-Yuan Jhan, Chien-Ju Cheng, Chih-Jen Chou, Shih-Ming Jung, Guan-Jhih Lai, Kuang-Yao Chen, Lian-Chen Wang
    Journal of Microbiology, Immunology and Infection.2022; 55(5): 935.     CrossRef
  • Necroptosis and Caspase-2-Mediated Apoptosis of Astrocytes and Neurons, but Not Microglia, of Rat Hippocampus and Parenchyma Caused by Angiostrongylus cantonensis Infection
    Hongli Zhou, Zhe Chen, Yanin Limpanont, Yue Hu, Yubin Ma, Ping Huang, Paron Dekumyoy, Minyu Zhou, Yixin Cheng, Zhiyue Lv
    Frontiers in Microbiology.2020;[Epub]     CrossRef
  • Severe CNS angiostrongyliasis in a young marine: a case report and literature review
    Liane McAuliffe, Shannon Fortin Ensign, Derek Larson, Mary Bavaro, Joseph Yetto, Michael Cathey, Mitsuru Mukaigawara, Masashi Narita, Kiyofumi Ohkusu, Timothy Quast, Charles Volk
    The Lancet Infectious Diseases.2019; 19(4): e132.     CrossRef
  • Regulatory effect of host miR-101b-3p on parasitism of nematode Angiostrongylus cantonensis via superoxide dismutase 3
    Dongjuan Yuan, Shiqi Luo, Lian Xu, Xingda Zeng, Zhongdao Wu
    Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms.2019; 1862(5): 557.     CrossRef
  • Trichostatin A, a Histone Deacetylase Inhibitor, Alleviates Eosinophilic Meningitis Induced by Angiostrongylus cantonensis Infection in Mice
    Yanhua Zhang, Hui Xie, Wenyan Tang, Xingda Zeng, Yu Lin, Lian Xu, Lihua Xiao, Jun Xu, Zhongdao Wu, Dongjuan Yuan
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • MicroRNA-125b mimic inhibits ischemia reperfusion-induced neuroinflammation and aberrant p53 apoptotic signalling activation through targeting TP53INP1
    Xiao-Qian Li, Qian Yu, Wen-Fei Tan, Zai-Li Zhang, Hong Ma
    Brain, Behavior, and Immunity.2018; 74: 154.     CrossRef
  • Apoptosis and necroptosis of mouse hippocampal and parenchymal astrocytes, microglia and neurons caused by Angiostrongylus cantonensis infection
    Zhang Mengying, Xu Yiyue, Pan Tong, Hu Yue, Yanin Limpanont, Huang Ping, Kamolnetr Okanurak, Wu Yanqi, Paron Dekumyoy, Zhou Hongli, Dorn Watthanakulpanich, Wu Zhongdao, Wang Zhi, Lv Zhiyue
    Parasites & Vectors.2017;[Epub]     CrossRef
  • 10,423 View
  • 151 Download
  • 13 Web of Science
  • Crossref

Brief Communication

Toxoplasmosis in a Pet Peach-Faced Lovebird(Agapornis roseicollis)
Madalyn K. Cooper, Jan ?lapeta, Shannon L. Donahoe, David N. Phalen
Korean J Parasitol 2015;53(6):749-753.
Published online December 31, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.6.749
Toxoplasma gondii atypical type II genotype was diagnosed in a pet peach-faced lovebird (Agapornis roseicollis) based on histopathology, immunohistochemistry, and multilocus DNA typing. The bird presented with severe neurological signs, and hematology was suggestive of chronic granulomatous disease. Gross post-mortem examination revealed cerebral hemorrhage, splenomegaly, hepatitis, and thickening of the right ventricular free wall. Histologic sections of the most significant lesions in the brain revealed intralesional protozoan organisms associated with malacia, spongiform changes, and a mild histiocytic response, indicative of diffuse, non-suppurative encephalitis. Immunohistochemistry confirmed the causative organisms to be T. gondii. DNA isolated from the brain was used to confirm the presence of T. gondii DNA. Multilocus genotyping based on SAG1, altSAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico markers demonstrated the presence of ToxoDB PCR-RFLP genotype #3 and B1 gene as atypical T. gondii type II. The atypical type II strain has been previously documented in Australian wildlife, indicating an environmental transmission route.

Citations

Citations to this article as recorded by  Crossref logo
  • Dolphins share Toxoplasma gondii Type II genotypes with terrestrial animals: Evidence of terrestrial T. gondii contamination in marine environments
    Yi-Jou Chen, Heather Fenton, Jane Hall, Karrie Rose, Victor M. Peddemors, Jan Šlapeta
    Veterinary Parasitology.2025; 335: 110439.     CrossRef
  • Global prevalence of Toxoplasma gondii in birds: A systematic review and meta-analysis
    Leila Zaki, Meysam Olfatifar, Fatemeh Ghaffarifar, Aida Vafae Eslahi, Amir KarimiPourSaryazdi, Ali Taghipour, Najla Hamidianfar, Milad Badri, Pikka Jokelainen
    Parasite Epidemiology and Control.2024; 25: e00350.     CrossRef
  • Successful Neoadjuvant Chemotherapy and Surgical Removal of a Nonmetastatic Testicular Round Cell Tumor in a Solomon Island Eclectus Parrot (Eclectus roratus solomonensis)
    Rachel Baden, Brian Speer, Michael Garner, Vanessa Hernández Urraca, Brenna Fitzgerald
    Journal of Avian Medicine and Surgery.2024;[Epub]     CrossRef
  • Epidemiology and isolation of viable Toxoplasma gondii strain from macropods
    Liulu Yang, Hongjie Ren, Niuping Zhu, Gaohui Mao, Junbao Li, Chunlei Su, Yibao Jiang, Yurong Yang
    Heliyon.2023; 9(3): e13960.     CrossRef
  • Epidemiologic significance of Toxoplasma gondii infections in turkeys, ducks, ratites and other wild birds: 2009–2020
    J. P. Dubey, F. H. A. Murata, C. K. Cerqueira-Cézar, O. C. H. Kwok, C. Su
    Parasitology.2021; 148(1): 1.     CrossRef
  • Comparison of genotypes of Toxoplasma gondii in domestic cats from Australia with latent infection or clinical toxoplasmosis
    Anthea Brennan, Shannon L. Donahoe, Julia A. Beatty, Katherine Belov, Scott Lindsay, Katherine A. Briscoe, Jan Šlapeta, Vanessa R. Barrs
    Veterinary Parasitology.2016; 228: 13.     CrossRef
  • 11,625 View
  • 113 Download
  • 8 Web of Science
  • Crossref

Case Reports

A Case of Ocular Angiostrongyliasis with Molecular Identification of the Species in Vietnam
Nguyen Van De, Le Van Duyet, Jong-Yil Chai
Korean J Parasitol 2015;53(6):713-717.
Published online December 31, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.6.713
A 23-year-old female residing in a village of Cao Bang Province, North Vietnam, visited the Hospital of Hanoi Medical University in July 2013. She felt dim eyes and a bulge-sticking pain in her left eye for some days before visiting the hospital. In the hospital, a clinical examination, an eye endoscopy, and an operation were carried out. A nematode specimen was collected from the eye of this patient. The body of this worm was thin and long and measured 22.0×0.3 mm. It was morphologically suggested as an immature female worm of Angiostrongylus cantonensis. By a molecular method using 18S rRNA gene, this nematode was confirmed as A. cantonensis. This is the first molecular study for identification of A. cantonensis in Vietnam.

Citations

Citations to this article as recorded by  Crossref logo
  • Insights into the genetic diversity of Angiostrongylus spp. causing human angiostrongyliasis and implications for molecular identification and diagnosis
    Abigail Hui En Chan, Chanisara Kaenkaew, Wallop Pakdee, Urusa Thaenkham
    Food and Waterborne Parasitology.2024; 35: e00230.     CrossRef
  • Identification and genetic characterization of Angiostrongylus cantonensis isolated from the human eye
    Abdulhakam Dumidae, Kanin Luangsawang, Aunchalee Thanwisai, Apichat Vitta
    Parasitology Research.2023; 122(9): 2217.     CrossRef
  • Two Ocular Angiostrongyliasis Cases in Thailand with Molecular Identification of Causative Parasite Species
    Patcharaporn Boonroumkaew, Thuss Sanguansak, Siriraksa Visaetsilpanonta, Oranuch Sanpool, Lakkhana Sadaow, Pewpan M. Intapan, Wanchai Maleewong
    The American Journal of Tropical Medicine and Hygiene.2020; 102(6): 1399.     CrossRef
  • The metagenomic next-generation sequencing in diagnosing central nervous system angiostrongyliasis: a case report
    Li Feng, Aiwu Zhang, Jiali Que, Hongyan Zhou, Haiyan Wang, Yuanlin Guan, Cunzhou Shen, Xunsha Sun, Rong Lai, Fuhua Peng, Huiyu Feng, Ling Chen
    BMC Infectious Diseases.2020;[Epub]     CrossRef
  • Angiostrongylus cantonensis Is an Important Cause of Eosinophilic Meningitis in Southern Vietnam
    Angela McBride, Tran Thi Hong Chau, Nguyen Thi Thu Hong, Nguyen Thi Hoang Mai, Nguyen To Anh, Tran Tan Thanh, Tran Thi Hue Van, Le Thi Xuan, Tran Phu Manh Sieu, Le Hong Thai, Ly Van Chuong, Dinh Xuan Sinh, Nguyen Duy Phong, Nguyen Hoan Phu, Jeremy Day, Ho
    Clinical Infectious Diseases.2017; 64(12): 1784.     CrossRef
  • Development of Lateral Flow Immunoassay for Antigen Detection in Human Angiostrongylus cantonensis Infection
    Mu-Xin Chen, Jia-Xu Chen, Shao-Hong Chen, Da-Na Huang, Lin Ai, Ren-Li Zhang
    The Korean Journal of Parasitology.2016; 54(3): 375.     CrossRef
  • Angiostrongylus cantonensis and A. malaysiensis Broadly Overlap in Thailand, Lao PDR, Cambodia and Myanmar: A Molecular Survey of Larvae in Land Snails
    Rutchanee Rodpai, Pewpan M. Intapan, Tongjit Thanchomnang, Oranuch Sanpool, Lakkhana Sadaow, Sakhone Laymanivong, Win Papa Aung, Issarapong Phosuk, Porntip Laummaunwai, Wanchai Maleewong, Donald James Colgan
    PLOS ONE.2016; 11(8): e0161128.     CrossRef
  • 10,522 View
  • 91 Download
  • 9 Web of Science
  • Crossref
Fatal Balamuthia Amebic Encephalitis in a Healthy Child: A Case Report with Review of Survival Cases
A. Krasaelap, S. Prechawit, J. Chansaenroj, P. Punyahotra, T. Puthanakit, K. Chomtho, S. Shuangshoti, J. Amornfa, Y. Poovorawan
Korean J Parasitol 2013;51(3):335-341.
Published online June 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.3.335

Balamuthia mandrillaris is one of the 4 amebas in fresh water and soil that cause diseases in humans. Granulomatous amebic encephalitis (GAE), caused by B. mandrillaris, is a rare but life-threatening condition. A 4-year-old, previously healthy, Thai girl presented with progressive headache and ataxia for over a month. Neuroimaging studies showed an infiltrative mass at the right cerebellar hemisphere mimicking a malignant cerebellar tumor. The pathological finding after total mass removal revealed severe necrotizing inflammation, with presence of scattered amebic trophozoites. Cerebrospinal fluid (CSF) obtained from lumbar puncture showed evidence of non-specific inflammation without identifiable organisms. A combination of pentamidine, sulfasalazine, fluconazole, and clarithromycin had been initiated promptly before PCR confirmed the diagnosis of Balamuthia amebic encephalitis (BAE). The patient showed initial improvement after the surgery and combined medical treatment, but gradually deteriorated and died of multiple organ failure within 46 days upon admission despite early diagnosis and treatment. In addition to the case, 10 survivors of BAE reported in the PubMed database were briefly reviewed in an attempt to identify the possible factors leading to survival of the patients diagnosed with this rare disease.

Citations

Citations to this article as recorded by  Crossref logo
  • The role of plasma metagenomic sequencing in identification of Balamuthia mandrillaris encephalitis
    Sarah Y. Edminster, Ryan W. Rebbe, Christopher Khatchadourian, Kyle M. Hurth, Anna J. Mathew, Julie Huss-Bawab, Mark S. Shiroishi, Devin Clark, Andrew P. Norgan, Susan M. Butler-Wu, Annie Hiniker
    Acta Neuropathologica Communications.2025;[Epub]     CrossRef
  • A Novel Balamuthia Lineage Causing Fatal Granulomatous Amoebic Encephalitis in an Immunocompetent Infant
    Zhongqiu Teng, Linlin Liu, Tianming Chen, Junrong Liang, Xingfeng Yao, Na Zhao, Fengmao Zhao, Hailang Sun, Lijuan Wang, Quan Wang, Gang Liu, Tian Qin
    International Journal of Infectious Diseases.2025; 161: 108063.     CrossRef
  • Drug susceptibility of a clinical isolate of Balamuthia mandrillaris , a pathogenic free-living amoeba
    Pratima Dubey, Porntida Kobpornchai, Nongnat Tongkrajang, Suwipa Chaiyaloom, Chenyang Lu, Christopher A. Rice, Kasem Kulkeaw, Audrey Odom John
    Antimicrobial Agents and Chemotherapy.2025;[Epub]     CrossRef
  • Balamuthia Amebic Encephalitis Cured and Discharged
    Benda Qin, Liyan Jia, Jian Chen, Wei Liu
    Journal of Craniofacial Surgery.2024; 35(6): e496.     CrossRef
  • Non-granulomatous meningoencephalitis with Balamuthia mandrillaris mimicking a tumor: First confirmed case from Pakistan
    Zanib Javed, Mustafa Mushtaq Hussain, Najia Ghanchi, Ahmed Gilani, S. Ather Enam
    Surgical Neurology International.2024; 15: 238.     CrossRef
  • Diagnosing Balamuthia mandrillaris amebic meningoencephalitis in a 64-year-old woman from the Southwest of China
    Suhua Yao, Xiaoting Chen, Lian Qian, Shizheng Sun, Chunjing Zhao, Zongkai Bai, Zhaofang Chen, Youcong Wu
    Parasites, Hosts and Diseases.2023; 61(2): 183.     CrossRef
  • Phenotypic assay for cytotoxicity assessment of Balamuthia mandrillaris against human neurospheroids
    Narisara Whangviboonkij, Worakamol Pengsart, Zhenzhong Chen, Seokgyu Han, Sungsu Park, Kasem Kulkeaw
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Diagnosis of Balamuthia mandrillaris Encephalitis by Thymine–Adenine Cloning Using Universal Eukaryotic Primers
    Ju Yeong Kim, Myung-Hee Yi, Myungjun Kim, Joon-Sup Yeom, Hyun Dong Yoo, Seong Min Kim, Tai-Soon Yong
    Annals of Laboratory Medicine.2022; 42(2): 196.     CrossRef
  • A patient with granulomatous amoebic encephalitis caused by Balamuthia mandrillaris survived with two excisions and medication
    Limei Peng, Quan Zhou, Yu Wu, Xiaoli Cao, Zili Lv, Minghua Su, Yachun Yu, Wen Huang
    BMC Infectious Diseases.2022;[Epub]     CrossRef
  • Cutaneous balamuthiasis: A clinicopathological study
    Patricia Alvarez, Carlos Torres-Cabala, Eduardo Gotuzzo, Francisco Bravo
    JAAD International.2022; 6: 51.     CrossRef
  • Encephalomyelitis Caused by Balamuthia mandrillaris in a Woman With Breast Cancer: A Case Report and Review of the Literature
    Juan Hu, Yiqi Zhang, Yongwei Yu, Huili Yu, Siruo Guo, Ding Shi, Jianqin He, Chi Hu, Jiqi Yang, Xueling Fang, Yonghong Xiao
    Frontiers in Immunology.2022;[Epub]     CrossRef
  • An Optical and Chemiluminescence Assay for Assessing the Cytotoxicity of Balamuthia mandrillaris against Human Neurospheroids
    Worakamol Pengsart, Kasem Kulkeaw
    Bioengineering.2022; 9(7): 330.     CrossRef
  • Distribution and Current State of Molecular Genetic Characterization in Pathogenic Free-Living Amoebae
    Alejandro Otero-Ruiz, Leobardo Daniel Gonzalez-Zuñiga, Libia Zulema Rodriguez-Anaya, Luis Fernando Lares-Jiménez, Jose Reyes Gonzalez-Galaviz, Fernando Lares-Villa
    Pathogens.2022; 11(10): 1199.     CrossRef
  • Diagnostic evaluation of fatal Balamuthia mandrillaris meningoencephalitis in a captive Bornean orangutan (Pongo pygmaeus) with identification of potential environmental source and evidence of chronic exposure
    Shawna J. Hawkins, Jason D. Struthers, Kristen Phair, Ibne Karim M. Ali, Shantanu Roy, Bonnie Mull, Gary West
    Primates.2021; 62(1): 51.     CrossRef
  • Current report on the prevalence of free-living amoebae (FLA) in natural hot springs: a systematic review
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A Fatal Case of Naegleria fowleri Meningoencephalitis in Taiwan
Mei-Yu Su, Ming-Shih Lee, Ling-Yuh Shyu, Wei-Chen Lin, Pei-Ching Hsiao, Chi-Ping Wang, Dar-Der Ji, Ke-Min Chen, Shih-Chan Lai
Korean J Parasitol 2013;51(2):203-206.
Published online April 25, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.2.203

After bathing at a hot spring resort, a 75-year-old man presented to the emergency department because of seizure-like attack with loss of conscious. This is the first case of primary amebic meningoencephalitis (PAM) caused by Naegleria fowleri in Taiwan. PAM was diagnosed based on detection of actively motile trophozoites in cerebrospinal fluid using a wet-mount smear and the Liu's stain. The amoebae were further confirmed by PCR and gene sequencing. In spite of administering amphotericin B treatment, the patient died 25 days later.

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  • Enlightening the promising role of nanoparticle-based treatments against Naegleria fowleri-induced primary amoebic meningoencephalitis: A brain-eating disease
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    Microbial Pathogenesis.2025; 199: 107234.     CrossRef
  • Naegleria fowleri Infections: Bridging Clinical Observations and Epidemiological Insights
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    Journal of Clinical Medicine.2025; 14(2): 526.     CrossRef
  • Pathogenic free-living amoebic encephalitis from 48 cases in China: A systematic review
    Xiang-Ting Chen, Qian Zhang, Si-Yuan Wen, Fei-Fei Chen, Chang-Qing Zhou
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    International Journal of Environmental Research and Public Health.2023; 20(4): 3021.     CrossRef
  • Understanding the true burden of “Naegleria fowleri” (Vahlkampfiidae) in patients from Northern states of India: Source tracking and significance
    Ashutosh Panda, Bijay Ranjan Mirdha, Neha Rastogi, Samander Kasuhik
    European Journal of Protistology.2020; 76: 125726.     CrossRef
  • Naegleria fowleri: diagnosis, treatment options and pathogenesis
    Mohammad Ridwane Mungroo, Naveed Ahmed Khan, Ruqaiyyah Siddiqui
    Expert Opinion on Orphan Drugs.2019; 7(2): 67.     CrossRef
  • Nested PCR assay for the rapid detection of Naegleria fowleri from swimming pools in Egypt
    W.M. Hikal, M.A. Dkhil
    Acta Ecologica Sinica.2018; 38(2): 102.     CrossRef
  • The therapeutic strategies against Naegleria fowleri
    Natália Karla Bellini, Thomás Michelena Santos, Marco Túlio Alves da Silva, Otavio Henrique Thiemann
    Experimental Parasitology.2018; 187: 1.     CrossRef
  • Effects of Culture Media On Naegleria fowleri Growth At Different Temperatures
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    Journal of Parasitology.2018; 104(5): 451.     CrossRef
  • Exotic Tourist Destinations and Transmission of Infections by Swimming Pools and Hot Springs—A Literature Review
    Athena Mavridou, Olga Pappa, Olga Papatzitze, Chrysa Dioli, Anastasia Maria Kefala, Panagiotis Drossos, Apostolos Beloukas
    International Journal of Environmental Research and Public Health.2018; 15(12): 2730.     CrossRef
  • Surviving Naegleria fowleri infections: A successful case report and novel therapeutic approach
    Travis W. Heggie, Thomas Küpper
    Travel Medicine and Infectious Disease.2017; 16: 49.     CrossRef
  • Review: Occurrence of the pathogenic amoeba Naegleria fowleri in groundwater
    Kelly R. Bright, Charles P. Gerba
    Hydrogeology Journal.2017; 25(4): 953.     CrossRef
  • Biology and pathogenesis of Naegleria fowleri
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    Acta Tropica.2016; 164: 375.     CrossRef
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    European Journal of Protistology.2015; 51(5): 401.     CrossRef
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Original Articles
Comparison of specific activity and cytopathic effects of purified 33 kDa serine proteinase from Acanthamoeba strains with different degree of virulence
Won-Tae Kim, Hyun-Hee Kong, Young-Ran Ha, Yeon-Chul Hong, Hae Jin Jeong, Hak Sun Yu, Dong-Il Chung
Korean J Parasitol 2006;44(4):321-330.
Published online December 20, 2006
DOI: https://doi.org/10.3347/kjp.2006.44.4.321

The pathogenic mechanism of granulomatous amebic encephalitis (GAE) and amebic keratitis (AK) by Acanthamoeba has yet to be clarified. Protease has been recognized to play an important role in the pathogenesis of GAE and AK. In the present study, we have compared specific activity and cytopathic effects (CPE) of purified 33 kDa serine proteinases from Acanthamoeba strains with different degree of virulence (A. healyi OC-3A, A. lugdunensis KA/E2, and A. castellanii Neff). Trophozoites of the 3 strains revealed different degrees of CPE on human corneal epithelial (HCE) cells. The effect was remarkably reduced by adding phenylmethylsulfonylfluoride (PMSF), a serine proteinase inhibitor. This result indicated that PMSF-susceptible proteinase is the main component causing cytopathy to HCE cells by Acanthamoeba. The purified 33 kDa serine proteinase showed strong activity toward HCE cells and extracellular matrix proteins. The purified proteinase from OC-3A, the most virulent strain, demonstrated the highest enzyme activity compared to KA/E2, an ocular isolate, and Neff, a soil isolate. Polyclonal antibodies against the purified 33 kDa serine proteinase inhibit almost completely the proteolytic activity of culture supernatant of Acanthamoeba. In line with these results, the 33 kDa serine proteinase is suggested to play an important role in pathogenesis and to be the main component of virulence factor of Acanthamoeba.

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  • Calcium ions in tap water may increase the adhesion ability of Acanthamoeba, potentially enhancing its cytopathic effects on corneal cells
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    Parasite.2025; 32: 71.     CrossRef
  • Proteases of Acanthamoeba
    Behroz Mahdavi Poor, Jalil Rashedi, Vahid Asgharzadeh, Amirali Mirmazhary, Nazila Gheitarani
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    Journal of Water and Health.2024; 22(12): 2289.     CrossRef
  • Identification of an Antimicrobial Protease from Acanthamoeba via a Novel Zymogram
    Alvaro de Obeso Fernández del Valle, Luis Javier Melgoza-Ramírez, María Fernanda Esqueda Hernández, Alfonso David Rios-Pérez, Sutherland K. Maciver
    Processes.2023; 11(9): 2620.     CrossRef
  • Acanthamoeba Mannose and Laminin Binding Proteins Variation across Species and Genotypes
    Daniele Corsaro
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    Rosnani Hanim Mohd Hussain, Mohamed Kamel Abdul Ghani, Naveed Ahmed Khan, Ruqaiyyah Siddiqui, Shafiq Aazmi, Hasseri Halim, Tengku Shahrul Anuar
    Pathogens.2022; 11(12): 1474.     CrossRef
  • Differential expression of Acanthamoeba castellanii proteins during amoebic keratitis in rats
    Ana Carolina Carvalho-Silva, Camila H. Coelho, Cecília Cirelli, Frederico Crepaldi, Isabela Aurora Rodrigues-Chagas, Cinthia Furst, Daniel Carvalho Pimenta, Juliano Simões de Toledo, Ana Paula Fernandes, Adriana Oliveira Costa
    Experimental Parasitology.2021; 221: 108060.     CrossRef
  • Peganum harmala Extract Has Antiamoebic Activity to Acanthamoeba triangularis Trophozoites and Changes Expression of Autophagy-Related Genes
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    Pathogens.2021; 10(7): 842.     CrossRef
  • Extracellular protease profile of Acanthamoeba after prolonged axenic culture and after interaction with MDCK cells
    Cecília Cirelli, Elaine Isabela Soares Mesquita, Isabela Aurora Rodrigues Chagas, Cinthia Furst, Cynara Oliveira Possamai, Jonatas Santos Abrahão, Ludmila Karen dos Santos Silva, Marina Felipe Grossi, Carlos Alberto Tagliati, Adriana Oliveira Costa
    Parasitology Research.2020; 119(2): 659.     CrossRef
  • Busting biofilms: free-living amoebae disrupt preformed methicillin-resistant Staphylococcus aureus (MRSA) and Mycobacterium bovis biofilms
    Kevin H. Martin, Grace I. Borlee, William H. Wheat, Mary Jackson, Bradley R. Borlee
    Microbiology .2020; 166(8): 695.     CrossRef
  • Anti-amoebic potential of azole scaffolds and nanoparticles against pathogenic Acanthamoeba
    Shweta Walvekar, Ayaz Anwar, Areeba Anwar, Nanthini Sridewi, Mohammad Khalid, Yoon Yen Yow, Naveed Ahmed Khan
    Acta Tropica.2020; 211: 105618.     CrossRef
  • Identification and biochemical characterisation of Acanthamoeba castellanii cysteine protease 3
    Zhixin Wang, Duo Wu, Hiroshi Tachibana, Meng Feng, Xun-jia Cheng
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Extracellular vesicles and vesicle-free secretome of the protozoa Acanthamoeba castellanii under homeostasis and nutritional stress and their damaging potential to host cells
    Diego de Souza Gonçalves, Marina da Silva Ferreira, Susie Coutinho Liedke, Kamilla Xavier Gomes, Gabriel Afonso de Oliveira, Pedro Ernesto Lopes Leão, Gabriele Vargas Cesar, Sergio H. Seabra, Juliana Reis Cortines, Arturo Casadevall, Leonardo Nimrichter,
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    Behroz Mahdavi Poor, Abdolhossein Dalimi, Fatemeh Ghafarifar, Fariba Khoshzaban, Jalal Abdolalizadeh
    Parasitology Research.2017; 116(12): 3373.     CrossRef
  • Characterisation and expression analysis of trophozoite and cyst proteins of Acanthamoeba spp. isolated from Acanthamoeba keratitis (AK) patient
    Himansu Sekhar Behera, Gita Satpathy
    Molecular and Biochemical Parasitology.2016; 205(1-2): 29.     CrossRef
  • Microbial collagenases: challenges and prospects in production and potential applications in food and nutrition
    Gaurav Kumar Pal, Suresh PV
    RSC Advances.2016; 6(40): 33763.     CrossRef
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    Bibiana Chávez‐Munguía, Lizbeth Salazar‐Villatoro, Maritza Omaña‐Molina, Martha Espinosa‐Cantellano, Elizabeth Ramírez‐Flores, Jacob Lorenzo‐Morales, Adolfo Martínez‐Palomo
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    Yu-Zhong Zhang, Li-Yuan Ran, Chun-Yang Li, Xiu-Lan Chen, F. E. Löffler
    Applied and Environmental Microbiology.2015; 81(18): 6098.     CrossRef
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    Journal of Biological Chemistry.2014; 289(9): 6041.     CrossRef
  • Structural and mechanistic insights into collagen degradation by a bacterial collagenolytic serine protease in the subtilisin family
    Li‐Yuan Ran, Hai‐Nan Su, Guo‐Yan Zhao, Xiang Gao, Ming‐Yang Zhou, Peng Wang, Hui‐Lin Zhao, Bin‐Bin Xie, Xi‐Ying Zhang, Xiu‐Lan Chen, Bai‐Cheng Zhou, Yu‐Zhong Zhang
    Molecular Microbiology.2013; 90(5): 997.     CrossRef
  • Pathological characteristics of the different stages of Acanthamoeba keratitis
    Yuzhao Sun, Jing Hong, Pei Zhang, Rongmei Peng, Gege Xiao
    Histopathology.2013; 63(6): 862.     CrossRef
  • Proteases fromEntamoebaspp. and Pathogenic Free-Living Amoebae as Virulence Factors
    Jesús Serrano-Luna, Carolina Piña-Vázquez, Magda Reyes-López, Guillermo Ortiz-Estrada, Mireya de la Garza
    Journal of Tropical Medicine.2013; 2013: 1.     CrossRef
  • Acanthamoeba interactions with the blood–brain barrier under dynamic fluid flow
    James Edwards-Smallbone, Richard J. Pleass, Naveed A. Khan, Robin J. Flynn
    Experimental Parasitology.2012; 132(3): 367.     CrossRef
  • Host-Parasite Interaction: Parasite-Derived and -Induced Proteases That Degrade Human Extracellular Matrix
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    Journal of Parasitology Research.2012; 2012: 1.     CrossRef
  • Serine protease activities in Leishmania (Leishmania) chagasi promastigotes
    Raquel Elisa da Silva-López, Tatiana Resende dos Santos, José Andrés Morgado-Díaz, Marcelo Neves Tanaka, Salvatore Giovanni de Simone
    Parasitology Research.2010; 107(5): 1151.     CrossRef
  • Pathogenesis of Acanthamoeba Keratitis
    Noorjahan Panjwani
    The Ocular Surface.2010; 8(2): 70.     CrossRef
  • Acanthamoeba culbertsoni Elicits Soluble Factors That Exert Anti-Microglial Cell Activity
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    Infection and Immunity.2010; 78(9): 4001.     CrossRef
  • Differential effects of α-helical and β-hairpin antimicrobial peptides against Acanthamoeba castellanii
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  • Elastase secretion in Acanthamoeba polyphaga
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    The Korean Journal of Parasitology.2007; 45(4): 283.     CrossRef
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Late season commercial mosquito trap and host seeking activity evaluation against mosquitoes in a malarious area of the Republic of Korea
Douglas A. Burkett, Won-Ja Lee, Kwan-Woo Lee, Heung-Chul Kim, Hee-Il Lee, Jong-Soo Lee, E-Hyun Shin, Robert A. Wirtz, Hae-Wol Cho, David M. Claborn, Russel E. Coleman, Wan Y Kim, Terry A. Klein
Korean J Parasitol 2002;40(1):45-54.
Published online March 31, 2002
DOI: https://doi.org/10.3347/kjp.2002.40.1.45

Field trials evaluating selected commercially available mosquito traps variously baited with light, carbon dioxide, and/or octenol were conducted from 18-27 September 2000 in a malarious area near Paekyeon-ri (Tongil-Chon ) and Camp Greaves in Paju County, Kyonggi Province, Republic of Korea. The host-seeking activity for common mosquito species, including the primary vector of Japanese encephalitis, Culex tritaeniorhynchus Giles, was determined using hourly aspirator collections from a human and propane lantern-baited Shannon trap during hours when temperatures exceeded 15℃. The total number of mosquitoes and number of each species captured during the test was compared using a block design. Significant differences were observed for the total number of mosquitoes collected, such that, the Mosquito MagnetTM with octenol > Shannon trap > ABC light trap with light and dry ice > Miniature Black Light trap (manufactured by John W. Hock) ≥ New Jersey Trap > ABC light trap with light only. Significant differences in numbers collected among traps were noted for several species including: Aedes vexans (Meigen), Anopheles lesteri Baisas and Hu, An. sinensis Weidemann, An. sineroides Yamada, An. yatsushiroensis Miyazaki, Culex pipiens pallens Coquillett L., Cx. orientalis Edwards and Cx. tritaeniorhynchus. Host-seeking activity for most common species showed a similar bimodal pattern. Results from these field trap evaluations can significantly enhance current vector and disease surveillance efforts especially for the primary vector of Japanese encephalitis, Cx. tritaeniorhynchus.

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    Heung-Chul Kim, Myung-Soon Kim, Kwang-Shik Choi, Do-Un Hwang, Jaree L. Johnson, Terry A. Klein
    Journal of Medical Entomology.2017; 54(1): 221.     CrossRef
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    Kyle L. O’Donnell, Mckenzie A. Bixby, Kelsey J. Morin, David S. Bradley, Jefferson A. Vaughan
    Journal of Medical Entomology.2017; 54(5): 1354.     CrossRef
  • A floral‐derived attractant for Aedes aegypti mosquitoes
    S. von Oppen, H. Masuh, S. Licastro, E. Zerba, P. Gonzalez‐Audino
    Entomologia Experimentalis et Applicata.2015; 155(3): 184.     CrossRef
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    Journal of the American Mosquito Control Association.2015; 31(3): 248.     CrossRef
  • Colonization and Maintenance ofAnopheles kleiniandAnopheles sinensisfrom the Republic of Korea
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    Journal of the American Mosquito Control Association.2014; 30(1): 1.     CrossRef
  • Estimating the Transmittable Prevalence of Infectious Diseases Using a Back-Calculation Approach
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    Communications for Statistical Applications and Methods.2014; 21(6): 487.     CrossRef
  • Distribution and Mosquito Hosts of Chaoyang Virus, a Newly Reported Flavivirus From the Republic of Korea, 2008–2011
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    Journal of Medical Entomology.2014; 51(2): 464.     CrossRef
  • Japanese Encephalitis Virus in Culicine Mosquitoes (Diptera: Culicidae) Collected at Daeseongdong, a Village in the Demilitarized Zone of the Republic of Korea
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