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Mini Review

Research Progress on Leptotrombidium deliense
Yan Lv, Xian-Guo Guo, Dao-Chao Jin
Korean J Parasitol 2018;56(4):313-324.
Published online August 31, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.4.313
This article reviews Leptotrombidium deliense, including its discovery and nomenclature, morphological features and identification, life cycle, ecology, relationship with diseases, chromosomes and artificial cultivation. The first record of L. deliense was early in 1922 by Walch. Under the genus Leptotrombidium, there are many sibling species similar to L. deliense, which makes it difficult to differentiate L. deliense from another sibling chigger mites, for example, L. rubellum. The life cycle of the mite (L. deliense) includes 7 stages: egg, deutovum (or prelarva), larva, nymphochrysalis, nymph, imagochrysalis and adult. The mite has a wide geographical distribution with low host specificity, and it often appears in different regions and habitats and on many species of hosts. As a vector species of chigger mite, L. deliense is of great importance in transmitting scrub typhus (tsutsugamushi disease) in many parts of the world, especially in tropical regions of Southeast Asia. The seasonal fluctuation of the mite population varies in different geographical regions. The mite has been successfully cultured in the laboratory, facilitating research on its chromosomes, biochemistry and molecular biology.

Citations

Citations to this article as recorded by  Crossref logo
  • Distribution and Host Selection of the Chigger Mite Leptotrombidium rupestre, a Potential Vector of Scrub Typhus, in Southwest China
    Rong Yu, Xian‐Guo Guo, Yan Lv, Peng‐Wu Yin, Wen‐Yu Song, Pei‐Ying Peng, Ti‐Jun Qian, Rong Xiang, Yan‐Ling Chen, Bei Li
    Veterinary Medicine and Science.2025;[Epub]     CrossRef
  • Meteorological factors and normalized difference vegetation index drivers of scrub typhus incidence in Shandong Province based on a 16-year time-frequency analysis
    Zhisong Ni, Shufen Li, Rui Xi, Kemeng Liang, Sihao Song, Chuanlong Cheng, Hui Zuo, Liang Lu, Xiujun Li
    BMC Public Health.2025;[Epub]     CrossRef
  • History of scrub typhus in Indonesia
    Kartika Saraswati, J Kevin Baird, Stuart D Blacksell, Marlous L Grijsen, Nicholas P J Day
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2025; 119(4): 338.     CrossRef
  • A systemic immunoinformatics approach to design combinatorial multiepitope vaccine candidates against vector-borne bacterial infections exploiting the proteomes of the causative agent and vector for scrub typhus
    Swarna Shaw, Arka Bagchi, Debyani Ruj, Sudipta Paul Bhattacharya, Arunima Biswas, Arijit Bhattacharya
    The Microbe.2025; 7: 100324.     CrossRef
  • Epidemiological Trends and Environmental Influences on Scrub Typhus in South Korea from 2001 to 2023
    Chaewon Kim, Nam-Hyuk Cho
    Journal of Bacteriology and Virology.2025; 55(1): 42.     CrossRef
  • Predicting the potential distribution areas of Leptotrombidium rubellum under current and future climate change
    Qunzheng Mu, Fengfeng Li, Wenyu Li, Xiaoxia Wang, Mingyuan Tang, Kehan Chen, Yihao Jiang, Jingqi Liu, Shirong Zhang, Qiyong Liu, Chuan Wang
    Frontiers in Public Health.2025;[Epub]     CrossRef
  • Temperature effect on scrub typhus incidence in South Korea: the projection for climate change
    Donghee Seo, Yoon-Jung Choi, Yun-Chul Hong
    Postgraduate Medical Journal.2025;[Epub]     CrossRef
  • Seasonal dynamics and niches of three vector chigger species at a focus of scrub typhus in southwest China
    Yan Lv, Peng-Wu Yin, Xian-Guo Guo, Rong Fan, Cheng-Fu Zhao, Zhi-Wei Zhang, Ya-Fei Zhao, Lei Zhang
    Frontiers in Veterinary Science.2025;[Epub]     CrossRef
  • Infestation, community structure, seasonal fluctuation and climate-driven dynamics of mites on small mammals at a focus of scrub typhus in southwest China
    Peng-Wu Yin, Yan Lv, Xian-Guo Guo, Wen-Yu Song, Rong Fan, Cheng-Fu Zhao, Zhi-Wei Zhang, Ya-Fei Zhao, Wen-Ge Dong, Dao-Chao Jin
    Frontiers in Veterinary Science.2025;[Epub]     CrossRef
  • Scrub typhus in the era of climate change: exploring lagged and cumulative effects of meteorological factors in the Republic of Korea, 2001–2024, a nationwide time-series study
    Hye Young Lee, Jeong Ran Kwon, Yuna Kim
    Osong Public Health and Research Perspectives.2025; 16(5): 437.     CrossRef
  • Variation in Small Mammal Species Composition and the Occurrence of Parasitic Mites in Two Landscapes in a Scrub Typhus Endemic Region of Western Yunnan Province, China
    Yun‐Yan Luo, Jia‐Xiang Yin, Zong‐Ti Shao, Zeng‐Kan Liu, Shou‐Qin Yin, Jiang‐Li Lu, Jin‐Chun Li, Rong Wei, Alan Frederick Geater
    Ecology and Evolution.2025;[Epub]     CrossRef
  • Influence of meteorological factors on scrub typhus in Southeast China: a study across 100 districts in Jiangxi Province
    Yanwu Nie, Yisheng Zhou, Shu Yang, Xiaobo Liu, Yibing Fan, Qinhan Jiang, Yong Liu, Yangqing Liu, Daiwei Zhang, Yuanan Lu, Hui Li, Lei Wu
    Tropical Medicine and Health.2025;[Epub]     CrossRef
  • Environmental Conditions and Mite Vectors Shape the Spatiotemporal Patterns of Scrub Typhus in Guangdong Province, Mainland China
    Peiwei Fan, Tian Ma, Ze Meng, Fangyu Ding, Shuai Chen, Mengmeng Hao, Jiaqi Li, Jun Zhuo, Jiping Dong, Wenqi Xie, Qian Wang, Tingting Kang, Kai Sun, Genan Wu, Yongqing Bai, Canjun Zheng, Dong Jiang
    Tropical Medicine and Infectious Disease.2025; 10(11): 326.     CrossRef
  • Scrub typhus in Northeast India: epidemiology, clinical presentations, and diagnostic approaches
    Beyau M Konyak, Monika Soni, Shyamalima Saikia, Tochi Chang, Indrani Gogoi, Ibakmensi Khongstid, Chung-Ming Chang, Mohan Sharma, Ramendra Pati Pandey
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2024; 118(3): 206.     CrossRef
  • Spatiotemporal heterogeneity and long-term impact of meteorological, environmental, and socio-economic factors on scrub typhus in China from 2006 to 2018
    Jiaojiao Qian, Yifan Wu, Changqiang Zhu, Qiong Chen, Hongliang Chu, Licheng Liu, Chongcai Wang, Yizhe Luo, Na Yue, Wenhao Li, Xiaohong Yang, Jing Yi, Fuqiang Ye, Ji He, Yong Qi, Fei Lu, Chunhui Wang, Weilong Tan
    BMC Public Health.2024;[Epub]     CrossRef
  • Guillain–Barre syndrome following scrub typhus: a case report and literature review
    Shijun Hu, Zhichuan lin, Tao Liu, Shixiong Huang, Hui Liang
    BMC Neurology.2024;[Epub]     CrossRef
  • The impact of meteorological parameters on the scrub typhus incidence in Baoshan City, western Yunnan, China
    Yun-Yan Luo, Alan Frederick Geater, Jia-Xiang Yin
    Frontiers in Public Health.2024;[Epub]     CrossRef
  • Intraspecific sensilla dimorphism in Ascoschoengastia indica (Prostigmata, Trombiculidae)
    Shobiechah Aldillah Wulandhari, Vachirapong Charoennitiwat, Yudthana Samung, Piengchan Sonthayanon, Rawadee Kumlert, Serge Morand, Kittipong Chaisiri, Tanawat Chaiphongpachara, Jean-Pierre Dujardin, Suchada Sumruayphol
    Heliyon.2024; 10(14): e33908.     CrossRef
  • Rickettsial infections: prevalence and diagnosis of scrub typhus in India
    Vigneshwaran Ravishankar, Shridhar Narayanan, Radha Krishan Shandil
    Frontiers in Tropical Diseases.2024;[Epub]     CrossRef
  • Leptotrombidium deliense (Asian rodent chigger)
    Rohit Beniwal, Govindarajan Renu, Philip S. Paulraj
    Trends in Parasitology.2024; 40(12): 1199.     CrossRef
  • Infestation of Oriental House Rat (Rattus tanezumi) with Chigger Mites Varies along Environmental Gradients across Five Provincial Regions of Southwest China
    Yan-Ling Chen, Xian-Guo Guo, Fan Ding, Yan Lv, Peng-Wu Yin, Wen-Yu Song, Cheng-Fu Zhao, Zhi-Wei Zhang, Rong Fan, Pei-Ying Peng, Bei Li, Ting Chen, Dao-Chao Jin
    International Journal of Environmental Research and Public Health.2023; 20(3): 2203.     CrossRef
  • Impacts of meteorological factors on the risk of scrub typhus in China, from 2006 to 2020: A multicenter retrospective study
    Ling Han, Zhaobin Sun, Ziming Li, Yunfei Zhang, Shilu Tong, Tian Qin
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Potential distribution of Leptotrombidium scutellare in Yunnan and Sichuan Provinces, China, and its association with mite-borne disease transmission
    Wen-Yu Song, Yan Lv, Peng-Wu Yin, Yi-Yu Yang, Xian-Guo Guo
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Species diversity and related ecology of chiggers on small mammals in a unique geographical area of Yunnan Province, southwest China
    Yu Guo, Juan-Xiu Zhou, Xian-Guo Guo, Wen-Yu Song, Cheng-Fu Zhao, Zhi-Wei Zhang, Rong Fan, Ting Chen, Yan Lv, Peng-Wu Yin, Dao-Chao Jin
    Experimental and Applied Acarology.2023; 91(3): 439.     CrossRef
  • Mapping the distributions of blood-sucking mites and mite-borne agents in China: a modeling study
    Tao Wang, Fanfei Meng, Tianle Che, Jinjin Chen, Haiyang Zhang, Yang Ji, Zhengwei Fan, Guoping Zhao, Wenhui Zhang, Baogui Jiang, Qiang Xu, Chenlong Lv, Taoxing Shi, Shiman Ruan, Lanzheng Liu, Wei Liu, Yang Yang, Liqun Fang
    Infectious Diseases of Poverty.2022;[Epub]     CrossRef
  • The current and future risk of spread of Leptotrombidium deliense and Leptotrombidium scutellare in mainland China
    Tian Ma, Mengmeng Hao, Shuai Chen, Fangyu Ding
    Science of The Total Environment.2022; 843: 156986.     CrossRef
  • SFTSV infection in rodents and their ectoparasitic chiggers
    Xiao-Lan Gu, Wen-Qing Su, Chuan-Min Zhou, Li-Zhu Fang, Ke Zhu, Dong-Qiang Ma, Fa-Chun Jiang, Ze-Min Li, Dan Li, Shu-Hui Duan, Qiu-Ming Peng, Rui Wang, Yuan Jiang, Hui-Ju Han, Xue-Jie Yu, Masayuki Saijo
    PLOS Neglected Tropical Diseases.2022; 16(8): e0010698.     CrossRef
  • Orientia tsutsugamushi in Chiggers and Small Mammals in Laos
    Ivo Elliott, Rawadee Kumlert, Neeranuch Thangnimitchok, Stuart D. Blacksell, Ampai Tanganuchitcharnchai, Daniel H. Paris, Paul N. Newton, Serge Morand
    Vector-Borne and Zoonotic Diseases.2022; 22(10): 505.     CrossRef
  • Biology, Systematics, Microbiome, Pathogen Transmission and Control of Chiggers (Acari: Trombiculidae, Leeuwenhoekiidae) with Emphasis on the United States
    Kaiying Chen, R. Michael Roe, Loganathan Ponnusamy
    International Journal of Environmental Research and Public Health.2022; 19(22): 15147.     CrossRef
  • Infestation and seasonal fluctuation of chigger mites on the Southeast Asian house rat (Rattus brunneusculus) in southern Yunnan Province, China
    Yan Lv, Xianguo Guo, Daochao Jin, Wenyu Song, Peiying Peng, Hao Lin, Rong Fan, Chengfu Zhao, Zhiwei Zhang, Keyu Mao, Tijun Qian, Wenge Dong, Zhihua Yang
    International Journal for Parasitology: Parasites and Wildlife.2021; 14: 141.     CrossRef
  • Research Advances of Leptotrombidium scutellare in China
    Rong Xiang, Xian-Guo Guo
    The Korean Journal of Parasitology.2021; 59(1): 1.     CrossRef
  • Distribution and host selection of the chigger mite vector of scrub typhus,Leptotrombidium deliense, in southwest China
    Yan Lv, Xian-Guo Guo, Dao-Chao Jin, Rong Fan, Cheng-Fu Zhao, Zhang-Wei Zhang, Ke-Yu Mao, Wen-Yu Song, Wen-Ge Dong, Ti-Jun Qian, Zhi-Hua Yang
    International Journal of Acarology.2021; 47(3): 233.     CrossRef
  • Screening and genotyping of Orientia tsutsugamushi from field-collected on-host chiggers (Acari: Prostigmata) recovered from a positive scrub typhus locality in Kelantan, Malaysia
    F. C. L. Ernieenor, M. J. NorJaiza, A. Fadillah, J. Canedy, A. Mariana
    Experimental and Applied Acarology.2021; 84(1): 171.     CrossRef
  • High prevalence and low diversity of chigger infestation in small mammals found in Bangkok Metropolitan parks
    S. A. Wulandhari, Y. Paladsing, W. Saesim, V. Charoennitiwat, P. Sonthayanon, R. Kumlert, S. Morand, S. Sumruayphol, K. Chaisiri
    Medical and Veterinary Entomology.2021; 35(4): 534.     CrossRef
  • The epidemiology, diagnosis and management of scrub typhus disease in China
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    Human Vaccines & Immunotherapeutics.2021; 17(10): 3795.     CrossRef
  • A dataset of distribution and diversity of blood-sucking mites in China
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    Scientific Data.2021;[Epub]     CrossRef
  • Ecological and behavioural risk factors of scrub typhus in central Vietnam: a case-control study
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    Infectious Diseases of Poverty.2021;[Epub]     CrossRef
  • Infestation and Related Ecology of Chigger Mites on the Asian House Rat (Rattus tanezumi) in Yunnan Province, Southwest China
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    The Korean Journal of Parasitology.2021; 59(4): 377.     CrossRef
  • An annotated checklist of the eukaryotic parasites of humans, exclusive of fungi and algae
    Blaine A. Mathison, Sarah G. H. Sapp
    ZooKeys.2021; 1069: 1.     CrossRef
  • Spatiotemporal and demographic characteristics of scrub typhus in Southwest China, 2006–2017: An analysis of population‐based surveillance data
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    Transboundary and Emerging Diseases.2020; 67(4): 1585.     CrossRef
  • Mites, caterpillars and moths
    Rüdiger Panzer, Susanne Krebs
    JDDG: Journal der Deutschen Dermatologischen Gesellschaft.2020; 18(8): 867.     CrossRef
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    JDDG: Journal der Deutschen Dermatologischen Gesellschaft.2020; 18(8): 867.     CrossRef
  • Distribution and Ecological Drivers of Spotted Fever Group Rickettsia in Asia
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    EcoHealth.2019; 16(4): 611.     CrossRef
  • 13,857 View
  • 177 Download
  • 44 Web of Science
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Original Article

Life Cycle of Dermacentor everestianus Hirst, 1926 (Acari: Ixodidae) under Laboratory Conditions
Shang Jin, Tianhong Wang, Tuo Li, Ming Liu, Qingying Jia, Xiaolong Yang, Hui Wang, Zhijun Yu, Jingze Liu
Korean J Parasitol 2017;55(2):193-196.
Published online April 30, 2017
DOI: https://doi.org/10.3347/kjp.2017.55.2.193
This study investigated the development characteristics of Dermacentor everestianus under laboratory conditions. The time taken for D. everestianus to complete the whole life cycle was 110.2 days on average, and the average developmental durations of larvae and nymphs were 17.1 days and 29.5 days, respectively. The summation of the prefeeding, feeding, and preoviposition periods of females was 17.8 days, and the oviposition and egg incubation lasted for 18.1 days and 27.7 days, respectively. A highly positive correlation was observed between the weight of engorged female and the number of egg mass laid (r=0.947). The reproductive efficiency index and the reproductive fitness index were 7.1 and 6.1, respectively.

Citations

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  • Establishment of Pathogen-Free Rhipicephalus bursa Colonies Under Laboratory Conditions for the Vector Competence Studies
    Mehmet Can Ulucesme, Sezayi Ozubek, Munir Aktas
    Veterinary Sciences.2025; 12(1): 54.     CrossRef
  • The life cycle of Dermacentor nuttalli from the Qinghai-Tibetan Plateau under laboratory conditions and detection of spotted fever group Rickettsia spp.
    Hejia Ma, Jingkai Ai, Ming Kang, Jixu Li, Yali Sun
    Frontiers in Veterinary Science.2023;[Epub]     CrossRef
  • The life cycle and development characteristics of Dermacentor everestianus (Acari: Ixodidae) under field conditions in Qinghai–Tibet Plateau
    Tuo Li, Ming Liu, Tian-Tian Zhang, Yuan Li, Wen-Ying Wang, Meng-Meng Li, Zhi-Jun Yu, Jing-Ze Liu
    Experimental and Applied Acarology.2018; 76(4): 513.     CrossRef
  • 8,896 View
  • 123 Download
  • 6 Web of Science
  • Crossref

Articles from Symposium on Asian Taenia (October 2011, Osong, Korea)

State of the Art of Taenia solium as Compared to Taenia asiatica
Ana Flisser
Korean J Parasitol 2013;51(1):43-49.
Published online February 18, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.1.43

Three species of tapeworms infect humans in their adult stage (Taenia solium, Taenia saginata and Taenia asiatica). The 3 are flat, opaque white or yellowish, and exceptional long segmented parasites, measuring 1 to 12 m in their adult stage. In this review, the development of the knowledge regarding the first species, mainly focused on understanding how the larval stage or cysticercus is transmitted to humans, is described. The second species is a cosmopolitan parasite that only causes taeniosis and not cysticercosis; therefore, it will not be included. Information on the third species, which is presently being produced, since this species was recognized as such only at the end of the 20th century, will be discussed at the end of this review.

Citations

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  • Transcriptome of Taenia solium during in vitro cyst activation and initial growth into the tapeworm stage
    David Castaneda-Carpio, Renzo Gutierrez-Loli, Jose Maravi-Jaime, Segundo W. Del Aguila, Valeria Villar-Davila, Luz M. Moyano, Rafael Tapia-Limonchi, Stella M. Chenet, Cristina Guerra-Giraldez
    Scientific Data.2025;[Epub]     CrossRef
  • Seroprevalence and risk factors of porcine cysticercosis in Mpwapwa district, eastern-Central Tanzania
    Justine Daudi Maganira, Noel Mark Makwinya, Beda John Mwang'onde
    Parasite Epidemiology and Control.2025; 30: e00445.     CrossRef
  • Baseline Assessment of Taeniasis and Cysticercosis Infections in a High-Priority Region for Taenia solium Control in Colombia
    Carlos Franco-Muñoz, María Camila Jurado Guacaneme, Sonia Dayanni Castillo Ayala, Sofia Duque-Beltrán, Adriana Arévalo, Marcela Pilar Rojas Díaz, Julián Trujillo Trujillo, Luz Elena Borras Reyes, Luis Reinel Vásquez Arteaga, Julio César Giraldo Forero, Ma
    Pathogens.2025; 14(8): 755.     CrossRef
  • Novel Oral papaya-based preventive and therapeutic vaccine for controlling different zoonotic Taeniid parasites: Current advances
    Marisela Hernández, Anabel Ortiz Caltempa, Nelly Villalobos, María Celina Elisondo, Cynthia Guzmán, Juan A. Hernández-Aceves, Liliana Aguilar, Ivan Flores-Pérez, José Juan Martínez, Sahara D. Elguea Zarate, Maria Jesús Perteguer Prieto, Gabriela Meneses,
    Vaccine.2025; 66: 127818.     CrossRef
  • An inclusive approach to designing a multi-epitope chimeric vaccine for Taenia infections by integrating proteomics and reverse vaccinology
    Swati Sharma, Ujjawal Sharan, Rimanpreet Kaur, Anubha Chaudhary, Suraj S. Rawat, Anand K. Keshri, Naina Arora, Amit Prasad
    Frontiers in Tropical Diseases.2024;[Epub]     CrossRef
  • A Marked Decline in Taenia solium Taeniasis and Cysticercosis Infections in China: Possible Reasons from the Ecological Determinants Perspective
    Junqiang Li, Feifei Xu, Yuancai Chen, Md Robiul Karim, Yilin Wang, Kaihui Zhang, Xiaoying Li, Pitambar Dhakal, Rongjun Wang, Longxian Zhang
    Zoonoses.2023;[Epub]     CrossRef
  • An epidemiological survey of porcine cysticercosis in Rungwe District, Tanzania
    Tusane Alatupa Sanga, Justine Daudi Maganira, Winifrida Benedict Kidima
    Preventive Veterinary Medicine.2023; 213: 105866.     CrossRef
  • Molecular Identification and Appraisal of the Genetic Variation of Taenia saginata in Central Regions of Vietnam
    Giang Tran Thi, Ilenia Azzena, Fabio Scarpa, Piero Cossu, Cong Danh Le, Phuong Anh Ton Nu, Thi Minh Chau Ngo, Daria Sanna, Marco Casu
    Life.2022; 12(1): 70.     CrossRef
  • An Epidemiological Survey of Porcine Cysticercosis in Rungwe District, Tanzania
    Tusane Alatupa Sanga, Justine Daudi Maganira, Winifrida Benedict Kidima
    SSRN Electronic Journal .2022;[Epub]     CrossRef
  • Zoonotic Taenia infections with focus on cysticercosis due to Taenia solium in swine and humans
    Fela Mendlovic, Agnes Fleury, Ana Flisser
    Research in Veterinary Science.2021; 134: 69.     CrossRef
  • Current Diagnostic Criteria for Neurocysticercosis
    Carolina Guzman, Hector H Garcia
    Research and Reports in Tropical Medicine.2021; Volume 12: 197.     CrossRef
  • Challenges Encountered When Evaluating an Antibody-Detecting Point-of-Care Test for Taeniosis in an Endemic Community in Zambia: A Prospective Diagnostic Accuracy Study
    Chishimba Mubanga, Chiara Trevisan, Inge Van Damme, Veronika Schmidt, Isaac K. Phiri, Gideon Zulu, John Noh, Sukwan Handali, Richard Mambo, Mwelwa Chembensofu, Maxwell Masuku, Dries Reynders, Famke Jansen, Emmanuel Bottieau, Pascal Magnussen, Andrea S. Wi
    Diagnostics.2021; 11(11): 2039.     CrossRef
  • Diagnosis of Taenia solium infections based on “mail order” RNA-sequencing of single tapeworm egg isolates from stool samples
    Henrik Sadlowski, Veronika Schmidt, Jonathan Hiss, Johannes A. Kuehn, Christian G. Schneider, Gideon Zulu, Alex Hachangu, Chummy S. Sikasunge, Kabemba E. Mwape, Andrea S. Winkler, Markus Schuelke, Xiao-Nong Zhou
    PLOS Neglected Tropical Diseases.2021; 15(12): e0009787.     CrossRef
  • Taenia solium Cysticercosis and Its Impact in Neurological Disease
    Hector H. Garcia, Armando E. Gonzalez, Robert H. Gilman
    Clinical Microbiology Reviews.2020;[Epub]     CrossRef
  • Improving the specific diagnosis of trematode, cestode and nematode infections by a multiplex single-tube real-time PCR assay
    Samson S Y Wong, Rosana W S Poon, Kelvin K W To, Jasper F W Chan, Gang Lu, Fanfan Xing, Vincent C C Cheng, Kwok-Yung Yuen
    Journal of Clinical Pathology.2019; 72(7): 487.     CrossRef
  • Mapping the residual incidence of taeniasis and cysticercosis in Colombia, 2009–2013, using geographical information systems: Implications for public health and travel medicine
    Alfonso J. Rodríguez-Morales, María Camila Yepes-Echeverri, Wilmer F. Acevedo-Mendoza, Hamilton A. Marín-Rincón, Carlos Culquichicón, Esteban Parra-Valencia, Jaime A. Cardona-Ospina, Ana Flisser
    Travel Medicine and Infectious Disease.2018; 22: 51.     CrossRef
  • Identification and characterization of Taenia solium enolase as a plasminogen-binding protein
    Dolores A. Ayón-Núñez, Gladis Fragoso, Clara Espitia, Martín García-Varela, Xavier Soberón, Gabriela Rosas, Juan P. Laclette, Raúl J. Bobes
    Acta Tropica.2018; 182: 69.     CrossRef
  • Evaluation of activity of triclabendazole against Taenia solium metacestode in naturally infected pigs
    Ana Vargas-Calla, Luis A. Gomez-Puerta, Juan Calcina, Omar Gonzales-Viera, Cesar Gavidia, Maria T. Lopez-Urbina, Hector H. Garcia, Armando E. Gonzalez
    Asian Pacific Journal of Tropical Medicine.2016; 9(1): 23.     CrossRef
  • Multiplex real-time PCR monitoring of intestinal helminths in humans reveals widespread polyparasitism in Northern Samar, the Philippines
    Catherine A. Gordon, Donald P. McManus, Luz P. Acosta, Remigio M. Olveda, Gail M. Williams, Allen G. Ross, Darren J. Gray, Geoffrey N. Gobert
    International Journal for Parasitology.2015; 45(7): 477.     CrossRef
  • Epidemiology and genetic diversity of Taenia asiatica: a systematic review
    Anita Ale, Bjorn Victor, Nicolas Praet, Sarah Gabriël, Niko Speybroeck, Pierre Dorny, Brecht Devleesschauwer
    Parasites & Vectors.2014;[Epub]     CrossRef
  • Immunology ofTaenia soliumtaeniasis and human cysticercosis
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    Parasite Immunology.2014; 36(8): 388.     CrossRef
  • Rapid Molecular Identification of Human Taeniid Cestodes by Pyrosequencing Approach
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    PLoS ONE.2014; 9(6): e100611.     CrossRef
  • 27,224 View
  • 481 Download
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Original Article

Persistent infection with Strongyloides venezuelensis in the Mongolian gerbil (Meriones unguiculatus)
Byeong-Kirl Baek, In-Soo Whang, M. Khyrul Islam, Byeong-Soo Kim, Ibulaimu Kakoma
Korean J Parasitol 2002;40(4):181-186.
Published online December 30, 2002
DOI: https://doi.org/10.3347/kjp.2002.40.4.181

To examine the fate of Strongyloides venezuelensis, Mongolian gerbils (Meriones unguicalatus) were orally infected with 1,000 L3 larvae per animal. Altogether, 50 gerbils divided into 5 groups of 10 each were monitored for a period of 570 days to document the kinetics of faecal egg output, adults worm population, morphological development, fecundity, and hematological changes including peripheral blood eosinophilia. This study chronicled a life long parasitism of S. venezuelensis in the gerbil host, and showed that S. venezuelensis infection was quite stable throughout the course of infection and the worms maintained their normal development as evidenced by their body dimension. A progressive loss of body condition of the infected gerbils was observed as the level of infection advanced. However, no detectable pathological changes were observed in the gastrointestinal tract. The present findings indicate that an immunocompetent host, such as the Mongolian gerbil, can serve as a life long carrier model of S. venezuelensis if the worms are not expelled within 570 days after infection.

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  • Gastrointestinal effects of ivermectin treatment in rats infected with Strongyloides venezuelensis
    Jalvita C. Mendonça, Loyane A. Gama, Andrieli T. Hauschildt, Luciana A. Corá, Madileine F. Américo
    Acta Tropica.2019; 194: 69.     CrossRef
  • Strongyloides ratti and S. venezuelensis – rodent models of Strongyloides infection
    MARK VINEY, TAISEI KIKUCHI
    Parasitology.2017; 144(3): 285.     CrossRef
  • Parasitological and transcriptomic comparison of Strongyloides ratti infections in natural and in suboptimal permissive hosts
    Tegegn G. Jaleta, Christian Rödelsperger, Adrian Streit
    Experimental Parasitology.2017; 180: 112.     CrossRef
  • Callithrix penicillata as a nonhuman primate model for strongyloidiasis
    Alan Lane de Melo, Vitor Luís Tenório Mati, Wanderlany Amâncio Martins
    Primates.2012; 53(3): 303.     CrossRef
  • Role of angiogenic factors in acute experimental Strongyloides venezuelensis infection
    F. SHARIATI, J. L. PÉREZ-ARELLANO, J. LÓPEZ-ABÁN, A. M. EL BEHAIRY, A. MURO
    Parasite Immunology.2010; 32(6): 430.     CrossRef
  • Migration of Strongyloides venezuelensis in Rats after Oral Inoculation of Free-Living Infective Larvae
    Kiku MATSUDA, Byeong-Su KIM, In-Soo WHANG, Chae-Woong LIM, Byeong-Kirl BAEK
    Journal of Veterinary Medical Science.2003; 65(9): 971.     CrossRef
  • 7,677 View
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Mini Review

Tegumental ultrastructure of Echinoparyphium recurvatum according to developmental stages
Woon-Mok Sohn, Ho-Choon Woo, Sung-Jong Hong
Korean J Parasitol 2002;40(2):67-73.
Published online June 30, 2002
DOI: https://doi.org/10.3347/kjp.2002.40.2.67

The present study was performed to observe tegumental ultrastructure of Echinoparyphium recurvatum according to developmental stages. Worms (1, 3, 5 and 15-day old) were recovered from chicks experimentally infected with metacercariae from Radix auricularia coreana. One-day old worms were elongated and ventrally concave, and covered with peg-like tegumental spines except the adjacent areas of the head crown and excretory pore. Type I sensory papillae were distributed on the lip of the oral sucker, and grouped ciliated papillae were around the oral sucker. Peg-like tegumental spines were densely distributed on the anterior surface of the ventral sucker level. The ventral sucker had an aspinous tegument and no sensory papillae. Tegumental spines on the posterior surface of the ventral sucker level were sparsely distributed and disappeared posteriorly. In 3 and 5-day old worms, the tegument around the oral sucker was aspinose and wrinkled concentrically. The ventral sucker had a wrinkled tegument and many bulbous papillae. Type I sensory papillae were distributed between the bulbous papillae. Tegumental spines were spade-shaped with a terminal tip. A total of 45 collar spines including 4 end group ones on both ventral corners was alternately arranged in 2 rows. The 15-day old worms were very stout and their tegumental spines were tongue-shaped without a terminal tip. From the above results, it is confirmed that the surface ultrastructure of E. recurvatum was generally similar to that of other echinostomatid flukes. However, some features, i.e., morphological change of tegumental spines and appearence of sensory papillae on the ventral sucker according to development, and number, shape and arrangement of collar spines, were characteristic, which may be of taxonomic and bioecological significance.

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  • Morphological and molecular characterization of Acanthostomum species with Plesiomonas shigelloides coinfection: Immunological and histopathological appraisal in Bagrus bajad
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    Microbial Pathogenesis.2025; 200: 107365.     CrossRef
  • Ultrastructure of an opecoelid daughter sporocyst, Podocotyle sp. (Digenea: Opecoelidae): comparative analysis of the somatic tissues and new insights into the organization of the nervous system
    Sofia A. Denisova, Natalia N. Shunatova, Vladimir V. Lebedenkov, Sergei V. Shchenkov
    Canadian Journal of Zoology.2023; 101(7): 579.     CrossRef
  • New data on the nervous system ofCercaria parvicaudataStunkard & Shaw, 1931 (Trematoda: Renicolidae): revisiting old hypotheses
    S.A. Denisova, S.V. Shchenkov
    Journal of Helminthology.2020;[Epub]     CrossRef
  • The biology of Echinoparyphium (Trematoda, Echinostomatidae)
    Jane Huffman, Bernard Fried
    Acta Parasitologica.2012;[Epub]     CrossRef
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    Journal of Parasitology.2011; 97(6): 1049.     CrossRef
  • Scanning electron microscopy of adult Echinoparyphium recurvatum (Von Linstow, 1873) (Digenea: Echinostomatidae) from Britain
    A.M. McCarthy
    Journal of Helminthology.2011; 85(4): 453.     CrossRef
  • Identification of antigenic proteins from Echinostoma caproni (Trematoda) recognized by mouse immunoglobulins M, A and G using an immunoproteomic approach
    J. SOTILLO, L. VALERO, M. M. SÁNCHEZ DEL PINO, B. FRIED, J. G. ESTEBAN, A. MARCILLA, R. TOLEDO
    Parasite Immunology.2008; 30(5): 271.     CrossRef
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    Journal of Parasitology.2008; 94(3): 635.     CrossRef
  • Developmental and Functional Ultrastructure of Ornithodiplostomum ptychocheilus Diplostomula (Trematoda: Strigeoidea) during Invasion of the Brain of the Fish Intermediate Host, Pimephales promelas
    David Bruce Conn, Cameron P. Goater, Douglas Bray
    Journal of Parasitology.2008; 94(3): 635.     CrossRef
  • FIRST RECORD AND DESCRIPTION OF METACERCARIAE OF CURTUTERIA ARGUINAE N. SP. (DIGENEA: ECHINOSTOMATIDAE), PARASITE OF COCKLES CERASTODERMA EDULE (MOLLUSCA: BIVALVIA) IN ARCACHON BAY, FRANCE
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    Journal of Parasitology.2006; 92(3): 578.     CrossRef
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    Journal of Parasitology.2006; 92(2): 236.     CrossRef
  • Tegumental ultrastructure of the juvenile and adult Himasthla alincia (Digenea: Echinostomatidae)
    Eun-Taek Han, Kye-Young Han, Jong-Yil Chai
    The Korean Journal of Parasitology.2003; 41(1): 17.     CrossRef
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Original Article
Experimental induction of the two-host life cycle of Sarcocystis cruzi between dogs and Korean native calves
Sung-Hwan Wee, Sung-Shik Shin
Korean J Parasitol 2001;39(3):227-232.
Published online September 30, 2001
DOI: https://doi.org/10.3347/kjp.2001.39.3.227

Eight dogs were experimentally infected with Sarcocystis by oral inoculation of cardiac muscle from naturally infected cattle. The infected dogs commenced discharging of sporocysts in the feces after 10 to 12 days of inoculation, and continued until 20 and 35 days after inoculation. Three dogs were reinfected with cardiac muscle from the naturally infected cattle. Sporocysts reappeared in the feces on 12 to 13 days after reinfection. Sarcosystis sporocysts collected from the experimentally infected dogs were fed to each of the two 30-day-old Korean native calves. The infected calves remained clinically normal, except for the high fever (≥ 40℃) and decreased hematocrit values on day 30 to 40 post inoculation. Muscular cysts of Sarcocystis were found from infected calves on day 40 post inoculation. Proliferative forms of Sarcocystis were also observed in the muscle of infected calves. These results suggest that the Sarcocystis cruzi found in Korean native cattle has a 2-host life cycle with dogs as the definitive host and Korean native calves as the intermediate host.

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  • Sarcocystosis in Ruminants of Iran, as Neglected Food-Borne Disease: A Systematic Review and Meta-analysis
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    Acta Parasitologica.2020; 65(3): 555.     CrossRef
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    Heliyon.2020; 6(6): e04171.     CrossRef
  • Endoparasites in domestic animals surrounding an Atlantic Forest remnant, in São Paulo State, Brazil
    Anaiá da Paixão Sevá, Hilda Fátima de Jesus Pena, Alessandra Nava, Amanda Oliveira de Sousa, Luciane Holsback, Rodrigo Martins Soares
    Revista Brasileira de Parasitologia Veterinária.2018; 27(1): 12.     CrossRef
  • Detection and Identification of Sarcocystis cruzi (Protozoa: Apicomplexa) by Molecular and Ultrastructural Studies in Naturally Infected Korean Cattle (Bos taurus coreanae) from Daejeon, Korea
    Tong-Il Choi, Eui-Ju Hong, Si-Yun Ryu, Cheolho Sim, Joon-Seok Chae, Hyeon-Cheol Kim, Jinho Park, Kyoung-Seong Choi, Do-Hyeon Yu, Jae-Gyu Yoo, Bae-Keun Park
    The Korean Journal of Parasitology.2018; 56(2): 121.     CrossRef
  • Molecular Identification of Sarcocystis grueneri in Wild Korean Water Deer (Hydropotes inermis argyropus)
    Hye-won Kim, Hyeon-Cheol Kim, Si-Yun Ryu, Kyoung-Seong Choi, Do-Hyeon Yu, Jinho Park, Joon-Seok Chae, Bae-Keun Park
    The Korean Journal of Parasitology.2018; 56(2): 129.     CrossRef
  • Molecular differentiation of bovine sarcocysts
    Majedeh Akhlaghi, Mostafa Razavi, Arsalan Hosseini
    Parasitology Research.2016; 115(7): 2721.     CrossRef
  • Detection of sarcocystic infection in a wild rodent (Apodemus agrarius chejuensis) captured on Jeju island
    Tae-Hyoun Kim, Ju-Hee Han, Seo-Na Chang, Dong-Su Kim, Tamer Said Abdelkader, Seung-Hyeok Seok, Jong-Hwan Park, Hong-Shik Oh, Jong-Taek Kim, Byoung-Hee Lee, Jeong-Hwa Shin, Jung-Hyun Kim, Jong-Min Kim, Jae-Hak Park
    Laboratory Animal Research.2011; 27(4): 357.     CrossRef
  • Prevalence of thin-walled Sarcocystis cruzi and thick-walled Sarcocystis hirsuta or Sarcocystis hominis from cattle in Iran
    Hossein Nourani, Somayeh Matin, Abass Nouri, Hamidreza Azizi
    Tropical Animal Health and Production.2010; 42(6): 1225.     CrossRef
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