Skip to main navigation Skip to main content
  • KSPTM
  • E-Submission

PHD : Parasites, Hosts and Diseases

OPEN ACCESS
ABOUT
BROWSE ARTICLES
FOR CONTRIBUTORS

Page Path

11
results for

"18S rRNA"

Article category

Keywords

Publication year

Authors

Funded articles

"18S rRNA"

Brief Communications

Standard- and large-sized eggs of Trichuris trichiura in the feces of schoolchildren in the Yangon Region, Myanmar: Morphological and molecular analyses
Seungwan Ryoo, Bong-Kwang Jung, Sooji Hong, Hyejoo Shin, Hyemi Song, Hyun-Seung Kim, Jin-Youp Ryu, Woon-Mok Sohn, Sung-Jong Hong, Thi Thi Htoon, Htay Htay Tin, Jong-Yil Chai
Parasites Hosts Dis 2023;61(3):317-324.
Published online August 21, 2023
DOI: https://doi.org/10.3347/PHD.23059
Standard- and large-sized eggs of Trichuris trichiura were found in the feces of schoolchildren in Yangon, Myanmar during epidemiological surveys and mass deworming with albendazole in 2017-2019. The standard-sized eggs were identified as those of T. trichiura, but it was necessary to exclude the possibility of the large-sized eggs belonging to Trichuris vulpis, a dog whipworm. We conducted morphological and molecular studies to determine the species of the 2 types of Trichuris eggs. Individual eggs of both sizes were isolated from Kato-Katz fecal smears (n=20) and mechanically destroyed using a 23G injection needle. Nuclear DNA was extracted, and the 18S rRNA region was sequenced in 15 standard-sized eggs and 15 large-sized eggs. The average size of standard-sized eggs (T. trichiura) was 55.2×26.1 μm (range: 51.7-57.6×21.3-28.0 μm; n=97), whereas the size of large-sized eggs was 69.3×32.0 μm (range: 65.1-76.4×30.1-34.5 μm; n=20), slightly smaller than the known size of T. vulpis. Regarding standard-sized eggs, the 18S rRNA nucleotide sequences exhibited 100% homology with T. trichiura deposited in GenBank and 88.6-90.5% homology with T. vulpis. Regarding large-sized eggs, the nucleotide sequences showed 99.8-100% homology with T. trichiura in GenBank and 89.6-90.7% homology with T. vulpis. Both standard- and large-sized eggs of Trichuris spp. found in Myanmar schoolchildren during 2017-2019 were morphologically and molecularly confirmed to belong to T. trichiura. The conversion of eggs from smaller to large sizes might be due to anthelmintic treatments with albendazole.

Citations

Citations to this article as recorded by  Crossref logo
  • Paleoparasitology research on ancient helminth eggs and larvae in the Republic of Korea
    Jong-Yil Chai, Min Seo, Dong Hoon Shin
    Parasites, Hosts and Diseases.2023; 61(4): 345.     CrossRef
  • 8,925 View
  • 101 Download
  • 2 Web of Science
  • Crossref
Molecular Detection and Genetic Diversity of Blastocystis in Korean Dogs
Sangsu Suh, Haeseung Lee, Min-Goo Seo, Kyoo-Tae Kim, Kyung-Yeon Eo, Young-Sam Kwon, Sang-Joon Park, Oh-Deog Kwon, Tae-Hwan Kim, Dongmi Kwak
Korean J Parasitol 2022;60(4):289-293.
Published online August 24, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.4.289
Blastocystis is a genus of unicellular heterokont parasites belonging to a group of organisms known as Stramenopiles, which includes algae, diatoms, and water molds. Blastocystis includes several species that habitat in the gastrointestinal tracts of organisms as diverse as humans, farm animals, birds, rodents, reptiles, amphibians, fish, and cockroaches. It is important to public health and distributed globally, but its prevalence in dogs in Korea has not been reported to date. Here, we collected 787 canine fecal samples and assessed Blastocystis infection by age, sex, region, season, and diarrhea symptoms. We determined Blastocystis subtypes using phylogenetic analyses based on 18S rRNA gene sequences. We identified, 10 Blastocystis positive samples (1.3%). A higher proportion of infected dogs was asymptomatic; however, infection rates did not significantly differ according to region, age, sex, and season. Phylogenetic analysis showed that the Blastocystis sp. identified belonged to 4 subtypes (STs), ST1, ST5, ST10, and ST14, thus revealed the genetic diversity of Blastocystis sp. in dogs Korean. This is first report on the presence of Blastocystis sp. in dogs Korean. This study revealed a lower infection rate than expected and differed from previous studies in STs. Further studies are warranted to observe the national infection status of Blastocystis in dogs and the genetic characteristics of this genus.

Citations

Citations to this article as recorded by  Crossref logo
  • Prevalence and molecular characterization of intestinal parasites in shelter dogs from South Korea
    You-Jeong Lee, Beoul Kim, Gyeonghyeon Lee, Yong-Myung Kang, Dongmi Kwak, Min-Goo Seo
    Research in Veterinary Science.2025; 188: 105620.     CrossRef
  • High prevalence of Blastocystis sp. in farmed sika deer (Cervus nippon) in Northern China
    Zhen-Qiu Gao, Yang Gao, Hong-Di Zhuang, Guang-Rong Bao, Jing Liu, Jian-Ming Li, Nian-Yu Xue, Hong-Wei Cao, Shuo Liu
    Frontiers in Veterinary Science.2025;[Epub]     CrossRef
  • Molecular analysis of Rickettsia spp. and related tick-borne pathogens detected in dogs in Korea
    Kyoo-Tae Kim, Min-Goo Seo
    Acta Tropica.2023; 243: 106934.     CrossRef
  • First identification of Blastocystis sp. subtypes in Rex rabbits in China
    Miaomiao Zhang, Junchen Zhang, Jingjing Sun, Shuying Zhu, Huiyan Xu, Xiaoying Li, Longxain Zhang, Junqiang Li
    Parasitology Research.2023; 122(5): 1079.     CrossRef
  • 3,759 View
  • 147 Download
  • 5 Web of Science
  • Crossref
Molecular Detection and Subtyping of Blastocystis in Korean Pigs
Seunghyun Paik, Byeong Yeal Jung, Haeseung Lee, Mi-Hye Hwang, Jee Eun Han, Man Hee Rhee, Tae-Hwan Kim, Oh-Deog Kwon, Dongmi Kwak
Korean J Parasitol 2019;57(5):525-529.
Published online October 31, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.5.525
Blastocystis is one of the most commonly detected genera of protozoan parasites in the human intestines as well as the intestines of many other species such as pigs in several geographical regions worldwide. However, no studies have examined Blastocystis in pigs in Korea. In this study, PCR and nucleotide sequencing were performed to evaluate the genetic diversity and zoonotic potential of Blastocystis using pig fecal samples. We obtained 646 stool samples from groups of piglets, weaners, growers, finishers, and sows in Korea. A total of 390 Blastocystis-positive samples were identified, and the infection rate was 60.4%. The infection rates were significantly related to age and region. The 4 subtypes (STs) of Blastocystis confirmed by phylogenetic analysis were ST1, ST2, ST3, and ST5, indicating the high genetic diversity of Blastocystis in Korean pigs. ST5 was highly distributed in Korean pigs among detected STs in this study. Some sequences were closely related to those of Blastocystis isolated from humans. This is the first study of Blastocystis in pigs in Korea. Based on the results, Blastocystis is prevalent in Korean pigs. Although a small number of samples were obtained in some areas, the clinical development of Blastocystis infection in pigs and potential for human transmission should be further examined.

Citations

Citations to this article as recorded by  Crossref logo
  • Epidemiology of Blastocystis in farm animals: A review
    Jinnat Rehena, Anas Bin Harun, Md Robiul Karim
    Veterinary Parasitology.2025; 334: 110382.     CrossRef
  • First molecular detection and subtyping of Blastocystis in pigs raised by hilly ethnic communities in Bangladesh: a zoonotic concern
    Jinnat Rehena, Anas Bin Harun, Abdullah Al Bayazid, Md. Farhan Hasan, Tania Sultana, Ainun Nahar, Joynti Saha, Mokammel Hossain Tito, Shuvo Singha, S. H. M. Faruk Siddiki, M. Nazmul Hoque, Md Robiul Karim
    Veterinary Research Communications.2025;[Epub]     CrossRef
  • Molecular Prevalence of Blastocystis sp. from Patients with Diarrhea in the Republic of Korea
    Ji-Young Kwon, Jong-Hoon Choi, Hee-Il Lee, Jung-Won Ju, Myoung-Ro Lee
    Microorganisms.2024; 12(3): 523.     CrossRef
  • Molecular Identification and Genotyping of Cryptosporidium spp. and Blastocystis sp. in Cattle in Representative Areas of Shanxi Province, North China
    Yao Liang, Ya-Ya Liu, Jin-Jin Mei, Wen-Bin Zheng, Qing Liu, Wen-Wei Gao, Xing-Quan Zhu, Shi-Chen Xie
    Animals.2023; 13(18): 2929.     CrossRef
  • Subtype analysis and prevalence of mixed subtype infection of Blastocystis in farmed pigs from Chiba Prefecture, Japan
    Aya Masuda, Yukino Matsuda, Tetsuya Horikita, Jun Matsumoto
    Parasitology International.2022; 87: 102490.     CrossRef
  • Distribution of Gastrointestinal Parasitic Infection in Domestic Pigs in the Republic of Korea: Nationwide Survey from 2020-2021
    Subin Lee, Badriah Alkathiri, Dongmi Kwak, Sang-Myeong Lee, Wan-Kyu Lee, Jae-Won Byun, Seung-Hun Lee
    The Korean Journal of Parasitology.2022; 60(3): 207.     CrossRef
  • Molecular Detection and Genetic Diversity of Blastocystis in Korean Dogs
    Sangsu Suh, Haeseung Lee, Min-Goo Seo, Kyoo-Tae Kim, Kyung-Yeon Eo, Young-Sam Kwon, Sang-Joon Park, Oh-Deog Kwon, Tae-Hwan Kim, Dongmi Kwak
    The Korean Journal of Parasitology.2022; 60(4): 289.     CrossRef
  • Prevalencia de Dientamoeba fragilis y otros protozoarios intestinales en porcinos de una granja en la región Andina de Colombia
    K. J. Suarez, M. J. García García, E. Y. Restrepo Restrepo, L. F. Campo Campo, A. L. Galván–Diaz Galván–Diaz
    Revista de la Facultad de Medicina Veterinaria y de Zootecnia.2022;[Epub]     CrossRef
  • Blastocystis in domesticated and wild mammals and birds
    Josephine S.Y. Hublin, Jenny G. Maloney, Monica Santin
    Research in Veterinary Science.2021; 135: 260.     CrossRef
  • Molecular detection and subtype distribution of Blastocystis in farmed pigs in southern China
    Yang Zou, Wen-Bin Yang, Feng-Cai Zou, Rui-Qing Lin, Xing-Quan Zhu, Jun-Ling Hou
    Microbial Pathogenesis.2021; 151: 104751.     CrossRef
  • The Presence of Blastocystis in Tibetan Antelope (Pantholops hodgsonii)
    Hong-Li Geng, Yu-Zhe Sun, Jing Jiang, He-Ting Sun, Yuan-Guo Li, Si-Yuan Qin, Zhen-Jun Wang, Tao Ma, Jun-Hui Zhu, Nian-Yu Xue, Hong-Bo Ni
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Global prevalence, subtypes distribution, zoonotic potential, and associated risk factors of Blastocystis sp. in domestic pigs (Sus domesticus) and wild boars (Sus scrofa): A systematic review and meta-analysis
    Ali Asghari, Alireza Sadrebazzaz, Laya Shamsi, Morteza Shams
    Microbial Pathogenesis.2021; 160: 105183.     CrossRef
  • Molecular prevalence and subtype distribution ofBlastocystissp. in Asia and in Australia
    Sara Nemati, Mohammad Reza Zali, Paul Johnson, Hamed Mirjalali, Panagiotis Karanis
    Journal of Water and Health.2021; 19(5): 687.     CrossRef
  • Prevalence and Subtype Distribution of Blastocystis sp. in Diarrheic Pigs in Southern China
    Pei Wang, Sen Li, Yang Zou, Zhao-Wei Hong, Ping Wang, Xing-Quan Zhu, De-Ping Song, Xiao-Qing Chen
    Pathogens.2021; 10(9): 1189.     CrossRef
  • The Coexistence of Blastocystis spp. in Humans, Animals and Environmental Sources from 2010–2021 in Asia
    Adedolapo Aminat Rauff-Adedotun, Farah Haziqah Meor Termizi, Nurshafarina Shaari, Ii Li Lee
    Biology.2021; 10(10): 990.     CrossRef
  • Molecular Detection and Subtyping of Human Blastocystis and the Clinical Implications: Comparisons between Diarrheal and Non-diarrheal Groups in Korean Populations
    Moon-Ju Kim, Eun Jeong Won, Soo Hyun Kim, Jong Hee Shin, Jong-Yil Chai
    The Korean Journal of Parasitology.2020; 58(3): 321.     CrossRef
  • First Report of Blastocystis Infection in Pigs from Large Farms in Xinjiang, China
    Rongjun Wang, Ying Zhang, Yuxi Jiang, Jinming Xing, Dayong Tao, Meng Qi
    Journal of Eukaryotic Microbiology.2020; 67(6): 642.     CrossRef
  • First Report on the Occurrence and Subtypes of Blastocystis in Pigs in Poland Using Sequence-Tagged-Site PCR and Barcode Region Sequencing
    Monika Rudzińska, Beata Kowalewska, Beata Szostakowska, Maciej Grzybek, Katarzyna Sikorska, Agnieszka Świątalska
    Pathogens.2020; 9(7): 595.     CrossRef
  • Genetic Diversity and Zoonotic Potential of Blastocystis in Korean Water Deer, Hydropotes inermis argyropus
    Kyoo-Tae Kim, Gyeonguk Noh, Haeseung Lee, Seon-Hee Kim, Hyesung Jeong, Yongkwan Kim, Weon-Hwa Jheong, Jae-Ku Oem, Tae-Hwan Kim, Oh-Deog Kwon, Dongmi Kwak
    Pathogens.2020; 9(11): 955.     CrossRef
  • 7,578 View
  • 137 Download
  • 18 Web of Science
  • Crossref

Original Articles

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
Korean J Parasitol 2018;56(2):129-134.
Published online April 30, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.2.129
The cysts of Sarcocystis grueneri were detected and characterized from the cardiac muscles of the Korean water deer (Hydropotes inermis argyropus). Of the 38 heart muscle samples examined by light microscopy, 10 were found infected with the cysts of Sarcocystis sp. The cysts appeared oval to spherical shape and measured 110-380 μm in length and 90-170 μm in width. A phylogenetic tree of the 18S rRNA sequences (1.5 kb) revealed a close relationship of the infected cysts to genus Sarcocystis. The 18S rRNA sequence of the infected cysts showed 100% identity to S. grueneri and 97% to S. capracanis. Here, we first report the S. grueneri infections in the Korean water deer.

Citations

Citations to this article as recorded by  Crossref logo
  • Fasciola hepatica infection in Korean water deer (Hydropotes inermis argyropus)
    Na-Hyeon Kim, Min-Gyeong Seo, Bumseok Kim, Yu Jeong Jeon, In Jung Jung, Il-Hwa Hong
    Parasites, Hosts and Diseases.2025; 63(3): 243.     CrossRef
  • High prevalence of Sarcocystis spp. in the Eurasian wolf (Canis lupus lupus): Third-generation sequencing resolves mixed infections
    Sinah Lückner, Gastón Moré, Iris Marti, Caroline F. Frey, Javier E. Fernandez, Chahrazed Belhout, Walter Basso
    International Journal for Parasitology: Parasites and Wildlife.2025; 28: 101140.     CrossRef
  • Metastatic Osteosarcoma of the Distal Femur in a Korean Water Deer (Hydropotes inermis argyropus)
    Min-Gyeong Seo, Inhey Hong, Bumseok Kim, Jong-Hyun Kim, Changgeun Kang, Il-Hwa Hong
    Journal of Wildlife Diseases.2024;[Epub]     CrossRef
  • First Report of Sarcocystis pilosa from a Red Fox (Vulpes vulpes) Released for the Re-Introduction Project in South Korea
    Yeonghoon Jo, Sook Jin Lee, Mohammed Mebarek Bia, Seongjun Choe, Dong-Hyuk Jeong
    Animals.2023; 14(1): 89.     CrossRef
  • 8,239 View
  • 125 Download
  • 4 Web of Science
  • 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
Korean J Parasitol 2018;56(2):121-127.
Published online April 30, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.2.121
To survey the prevalence of Sarcocystis infections, 210 heart samples were collected from Korean native cattle (Bos taurus coreanae) at an abattoir in Daejeon Metropolitan City, Republic of Korea. Sarcocysts were detected form 31 specimens (14.8%) and identified as Sarcocystis cruzi via transmission electron microscopy. The wall of S. cruzi has flattened protrusions that did not contain fibrils or microfilaments. The protrusions arose irregularly from the base, contained a fine granular substance, lacked internal microfilaments, and measured approximately 0.21-1.25 μm in length and 0.05-0.07 μm in width. Sequence analysis revealed 99.5% homology to S. cruzi. This is the first report on the prevalence of S. cruzi in native cattle from the Republic of Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Sarcocystis species: molecular identification and seroprevalence in water buffaloes (Bubalus bubalis)
    Nagwa I. Toaleb, Raafat M. Shaapan, Haitham Elaadli, Kadria N. Abdel Megeed, Dina Aboelsoued
    BMC Veterinary Research.2025;[Epub]     CrossRef
  • Infection survey, molecular, pathogenicity, and morphological characteristics of Sarcocystis species naturally infected water buffaloes (Bubalus bubalis) in Egypt
    Lamiaa K. Elsharkawy, Safaa M. Barghash, Basma M. Abou El-Nour, Wafaa Labib, Al-Shaimaa M. Sadek
    BMC Veterinary Research.2024;[Epub]     CrossRef
  • Molecular Identification, Pathogenesis, and Life Cycle of Sarcocystis cruzi from Cattle (Bos taurus) in New Valley Governorate, Egypt
    Mohammed B. M. El-Mahdi, Soheir A. Rabie, Reda M. El-S. Hassanine, Amal A. Hassan, Obaida F. Abo Elhussien, Mamdooh Ghoneum, Mohamed S. A. El-Gerbed, Eric Agola Lelo
    Journal of Parasitology Research.2023; 2023: 1.     CrossRef
  • Molecular Epidemiology, Species Distribution, and Zoonotic Importance of the Neglected Meat-Borne Pathogen Sarcocystis spp. in Cattle (Bos taurus): A Global Systematic Review and Meta-analysis
    Morteza Shams, Laya Shamsi, Ali Asghari, Mohammad Hossein Motazedian, Behnam Mohammadi-Ghalehbin, Mostafa Omidian, Naser Nazari, Alireza Sadrebazzaz
    Acta Parasitologica.2022; 67(3): 1055.     CrossRef
  • Infection survey and morphological characteristics of Sarcocystis spp. in naturally infected Tibetan sheep from Qinghai in northwestern China
    Yali Sun, Jinling Ju, Xiaoxue Su, Caiying Xie, Ying Li, Ming Kang
    Parasitology International.2021; 80: 102219.     CrossRef
  • Meat-borne parasites in the Arab world: a review in a One Health perspective
    Sameh Abuseir
    Parasitology Research.2021; 120(12): 4153.     CrossRef
  • Opportunistic parasitic infections in patients with human immunodeficiency virus/acquired immunodeficiency syndrome: A review
    D. A. Laksemi, L. T. Suwanti, M. Mufasirin, K. Suastika, M. Sudarmaja
    Veterinary World.2020; 13(4): 716.     CrossRef
  • Morphological and Molecular Characterization of Toxocara apodemi (Nematoda: Ascarididae) from Striped Field Mice, Apodemus agrarius, in Korea
    Hyeon Cheol Kim, Eui Ju Hong, Si Yun Ryu, Jinho Park, Jeong Gon Cho, Do Hyeon Yu, Joon Seok Chae, Kyoung Seong Choi, Bae Keun Park
    The Korean Journal of Parasitology.2020; 58(4): 403.     CrossRef
  • Prevalence and molecular analysis of Sarcocystis infections in cattle in Northwest Iran and the first global report of S. gigantea in cattle
    Nazila Sarafraz, Adel Spotin, Ali Haniloo, Asghar Fazaeli
    Comparative Immunology, Microbiology and Infectious Diseases.2020; 73: 101566.     CrossRef
  • Molecular identification of four Sarcocystis species in cattle from Lithuania, including S. hominis, and development of a rapid molecular detection method
    Petras Prakas, Živilė Strazdaitė-Žielienė, Vytautas Januškevičius, Francesco Chiesa, Agnė Baranauskaitė, Eglė Rudaitytė-Lukošienė, Elena Servienė, Saulius Petkevičius, Dalius Butkauskas
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Ultrastructural and Molecular Identification of the sarcocysts of Sarcocystis tenella and Sarcocystis arieticanis Infecting Domestic Sheep (Ovis aries) from Egypt
    Ahmed El-Morsey, Walied Abdo, Khaled Sultan, Nagwa M. Elhawary, Attia Abdallah AbouZaid
    Acta Parasitologica.2019; 64(3): 501.     CrossRef
  • Sarcocystis spp. in Romanian Slaughtered Cattle: Molecular Characterization and Epidemiological Significance of the Findings
    Kálmán Imre, Gheorghe Dărăbuș, Emil Tîrziu, Sorin Morariu, Mirela Imre, Judit Plutzer, Marius V. Boldea, Adriana Morar
    BioMed Research International.2019; 2019: 1.     CrossRef
  • 9,609 View
  • 143 Download
  • 13 Web of Science
  • Crossref

Brief Communications

Detection and Molecular Characterization of Cryptosporidium spp. from Wild Rodents and Insectivores in South Korea
Juha Song, C-Yoon Kim, Seo-Na Chang, Tamer Said Abdelkader, Juhee Han, Tae-Hyun Kim, Hanseul Oh, Ji Min Lee, Dong-Su Kim, Jong-Taek Kim, Hong-Shik Oh, Moonsuk Hur, Jae-Hwa Suh, Jae-Hak Park
Korean J Parasitol 2015;53(6):737-743.
Published online December 31, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.6.737
In order to examine the prevalence of Cryptosporidium infection in wild rodents and insectivores of South Korea and to assess their potential role as a source of human cryptosporidiosis, a total of 199 wild rodents and insectivore specimens were collected from 10 regions of South Korea and screened for Cryptosporidium infection over a period of 2 years (2012-2013). A nested-PCR amplification of Cryptosporidium oocyst wall protein (COWP) gene fragment revealed an overall prevalence of 34.2% (68/199). The sequence analysis of 18S rRNA gene locus of Cryptosporidium was performed from the fecal and cecum samples that tested positive by COWP amplification PCR. As a result, we identified 4 species/genotypes; chipmunk genotype I, cervine genotype I, C. muris, and a new genotype which is closely related to the bear genotype. The new genotype isolated from 12 Apodemus agrarius and 2 Apodemus chejuensis was not previously identified as known species or genotype, and therefore, it is supposed to be a novel genotype. In addition, the host spectrum of Cryptosporidium was extended to A. agrarius and Crosidura lasiura, which had not been reported before. In this study, we found that the Korean wild rodents and insectivores were infected with various Cryptosporidium spp. with large intra-genotypic variationa, indicating that they may function as potential reservoirs transmitting zoonotic Cryptosporidium to livestock and humans.

Citations

Citations to this article as recorded by  Crossref logo
  • Prevalence and novel genetic characteristics of Cryptosporidium spp. in wild rodents in the northern foothills of the Dabie Mountains, southeast Henan Province, China
    Mengyao Yang, Yin Fu, Pitambar Dhakal, Zi Yan, Jiashu Lang, Chaofeng Ma, Yuhong Jiang, Congzhou Wang, Longxian Zhang, Lihua Xiao,
    PLOS Neglected Tropical Diseases.2025; 19(5): e0013117.     CrossRef
  • Critters and contamination: Zoonotic protozoans in urban rodents and water quality
    Siobhon Egan, Amanda D. Barbosa, Yaoyu Feng, Lihua Xiao, Una Ryan
    Water Research.2024; 251: 121165.     CrossRef
  • Detection and Molecular Characterization of Giardia and Cryptosporidium spp. Circulating in Wild Small Mammals from Portugal
    Laura Lux, Rainer G. Ulrich, Sérgio Santos-Silva, João Queirós, Christian Imholt, Christian Klotz, Joana Paupério, Ricardo Pita, Hélia Vale-Gonçalves, Paulo Célio Alves, João R. Mesquita
    Animals.2023; 13(3): 515.     CrossRef
  • Outbreak of severe diarrhea due to zoonotic Cryptosporidium parvum and C. xiaoi in goat kids in Chungcheongbuk-do, Korea
    Ah-Young Kim, Badriah Alkathiri, Subin Lee, Kyung-Duk Min, Soochong Kim, Sang-Myeong Lee, Wan-Kyu Lee, Dongmi Kwak, Seung-Hun Lee
    Parasitology Research.2023; 122(9): 2045.     CrossRef
  • Cryptosporidium mortiferum n. sp. (Apicomplexa: Cryptosporidiidae), the species causing lethal cryptosporidiosis in Eurasian red squirrels (Sciurus vulgaris)
    Lenka Tůmová, Jana Ježková, Jitka Prediger, Nikola Holubová, Bohumil Sak, Roman Konečný, Dana Květoňová, Lenka Hlásková, Michael Rost, John McEvoy, Lihua Xiao, Monica Santín, Martin Kváč
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Public health and ecological significance of rodents in Cryptosporidium infections
    Kaihui Zhang, Yin Fu, Junqiang Li, Longxian Zhang
    One Health.2022; 14: 100364.     CrossRef
  • Cryptosporidium rattin. sp. (Apicomplexa: Cryptosporidiidae) and genetic diversity ofCryptosporidiumspp. in brown rats (Rattus norvegicus) in the Czech Republic
    Jana Ježková, Jitka Prediger, Nikola Holubová, Bohumil Sak, Roman Konečný, Yaoyu Feng, Lihua Xiao, Michael Rost, John McEvoy, Martin Kváč
    Parasitology.2021; 148(1): 84.     CrossRef
  • The Role of Peridomestic Rodents as Reservoirs for Zoonotic Foodborne Pathogens
    Nusrat A. Jahan, Laramie L. Lindsey, Peter A. Larsen
    Vector-Borne and Zoonotic Diseases.2021; 21(3): 133.     CrossRef
  • Biodiversity of the Coccidia (Apicomplexa: Conoidasida) in vertebrates: what we know, what we do not know, and what needs to be done
    Donald W. Duszynski
    Folia Parasitologica.2021;[Epub]     CrossRef
  • Genetic characterizations of Cryptosporidium spp. from pet rodents indicate high zoonotic potential of pathogens from chinchillas
    Jia Chen, Weijian Wang, Yu Lin, Lianbei Sun, Na Li, Yaqiong Guo, Martin Kvac, Una Ryan, Yaoyu Feng, Lihua Xiao
    One Health.2021; 13: 100269.     CrossRef
  • Zoonotic Cryptosporidium spp. in Wild Rodents and Shrews
    Rauni Kivistö, Sofia Kämäräinen, Otso Huitu, Jukka Niemimaa, Heikki Henttonen
    Microorganisms.2021; 9(11): 2242.     CrossRef
  • Taxonomy and molecular epidemiology of Cryptosporidium and Giardia – a 50 year perspective (1971–2021)
    Una M. Ryan, Yaoyu Feng, Ronald Fayer, Lihua Xiao
    International Journal for Parasitology.2021; 51(13-14): 1099.     CrossRef
  • Molecular Detection of Cryptosporidium spp. and Enterocytozoon bieneusi Infection in Wild Rodents From Six Provinces in China
    Hong-Bo Ni, Yu-Zhe Sun, Si-Yuan Qin, Yan-Chun Wang, Quan Zhao, Zheng-Yao Sun, Miao Zhang, Ding Yang, Zhi-Hui Feng, Zheng-Hao Guan, Hong-Yu Qiu, Hao-Xian Wang, Nian-Yu Xue, He-Ting Sun
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Serosurvey and molecular detection of the main zoonotic parasites carried by commensal Rattus norvegicus population in Tehran, Iran
    Taher Azimi, Mohammad Reza Pourmand, Fatemeh Fallah, Abdollah Karimi, Roxana Mansour-Ghanaie, Seyedeh Mahsan Hoseini-Alfatemi, Mehdi Shirdoust, Leila Azimi
    Tropical Medicine and Health.2020;[Epub]     CrossRef
  • Diversity of Cryptosporidium spp. in wild rodents from the Canary Islands, Spain
    Katherine García-Livia, Aarón Martín-Alonso, Pilar Foronda
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Diversity of Cryptosporidium spp. in Apodemus spp. in Europe
    Šárka Čondlová, Michaela Horčičková, Nikola Havrdová, Bohumil Sak, Lenka Hlásková, Agnieszka Perec-Matysiak, Marta Kicia, John McEvoy, Martin Kváč
    European Journal of Protistology.2019; 69: 1.     CrossRef
  • Cryptosporidium apodemi sp. n. and Cryptosporidium ditrichi sp. n. (Apicomplexa: Cryptosporidiidae) in Apodemus spp.
    Šárka Čondlová, Michaela Horčičková, Bohumil Sak, Dana Květoňová, Lenka Hlásková, Roman Konečný, Michal Stanko, John McEvoy, Martin Kváč
    European Journal of Protistology.2018; 63: 1.     CrossRef
  • Molecular characterizations of Cryptosporidium spp. and Enterocytozoon bieneusi in brown rats (Rattus norvegicus) from Heilongjiang Province, China
    Wei Zhao, Jianguang Wang, Guangxu Ren, Ziyin Yang, Fengkun Yang, Weizhe Zhang, Yingchu Xu, Aiqin Liu, Hong Ling
    Parasites & Vectors.2018;[Epub]     CrossRef
  • Subtype analysis of zoonotic pathogen Cryptosporidium skunk genotype
    Wenchao Yan, Kerri Alderisio, Dawn M. Roellig, Kristin Elwin, Rachel M. Chalmers, Fengkun Yang, Yuanfei Wang, Yaoyu Feng, Lihua Xiao
    Infection, Genetics and Evolution.2017; 55: 20.     CrossRef
  • Native and introduced squirrels in Italy host different Cryptosporidium spp.
    Jitka Prediger, Michaela Horčičková, Lada Hofmannová, Bohumil Sak, Nicola Ferrari, Maria Vittoria Mazzamuto, Claudia Romeo, Lucas A. Wauters, John McEvoy, Martin Kváč
    European Journal of Protistology.2017; 61: 64.     CrossRef
  • Cryptosporidium homai n. sp. (Apicomplexa: Cryptosporidiiae) from the guinea pig (Cavia porcellus)
    Alireza Zahedi, Zoey Durmic, Alexander W. Gofton, Susan Kueh, Jill Austen, Malcolm Lawson, Lauren Callahan, John Jardine, Una Ryan
    Veterinary Parasitology.2017; 245: 92.     CrossRef
  • 10,594 View
  • 134 Download
  • 21 Web of Science
  • Crossref
Ancient Mitochondrial DNA Analyses of Ascaris Eggs Discovered in Coprolites from Joseon Tomb
Chang Seok Oh, Min Seo, Jong Ha Hong, Jong-Yil Chai, Seung Whan Oh, Jun Bum Park, Dong Hoon Shin
Korean J Parasitol 2015;53(2):237-242.
Published online April 22, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.2.237
Analysis of ancient DNA (aDNA) extracted from Ascaris is very important for understanding the phylogenetic lineage of the parasite species. When aDNAs obtained from a Joseon tomb (SN2-19-1) coprolite in which Ascaris eggs were identified were amplified with primers for cytochrome b (cyt b) and 18S small subunit ribosomal RNA (18S rRNA) gene, the outcome exhibited Ascaris specific amplicon bands. By cloning, sequencing, and analysis of the amplified DNA, we obtained information valuable for comprehending genetic lineage of Ascaris prevalent among pre-modern Joseon peoples.

Citations

Citations to this article as recorded by  Crossref logo
  • Paleoparasitology research on ancient helminth eggs and larvae in the Republic of Korea
    Jong-Yil Chai, Min Seo, Dong Hoon Shin
    Parasites, Hosts and Diseases.2023; 61(4): 345.     CrossRef
  • Historic and Prehistoric Epidemics: An Overview of Sources Available for the Study of Ancient Pathogens
    Antoinette C. van der Kuyl
    Epidemiologia.2022; 3(4): 443.     CrossRef
  • Mummification in Korea and China: Mawangdui, Song, Ming and Joseon Dynasty Mummies
    Dong Hoon Shin, Raffaella Bianucci, Hisashi Fujita, Jong Ha Hong
    BioMed Research International.2018; 2018: 1.     CrossRef
  • Estimation of parasite infection prevalence of Joseon people by paleoparasitological data updates from the ancient feces of pre-modern Korean mummies
    MIN SEO, CHANG SEOK OH, JONG HA HONG, JONG-YIL CHAI, SOON CHUL CHA, YURI BANG, IN GUK CHA, YANG GUN WI, JUNG MIN PARK, DONG HOON SHIN
    Anthropological Science.2017; 125(1): 9.     CrossRef
  • A Case of Ectopic Paragonimiasis in a 17th Century Korean Mummy
    D. H. Shin, Y.-S. Kim, D. S. Yoo, M. J. Kim, C. S. Oh, J. H. Hong, E. Lee, J. Y. Chai, M. Seo
    Journal of Parasitology.2017; 103(4): 399.     CrossRef
  • Paleogenetic study on the 17th century Korean mummy with atherosclerotic cardiovascular disease
    Dong Hoon Shin, Chang Seok Oh, Jong Ha Hong, Yusu Kim, Soong Deok Lee, Eunju Lee, David Caramelli
    PLOS ONE.2017; 12(8): e0183098.     CrossRef
  • Ancient Ascaris DNA Sequences of Cytochrome B, Cytochrome C Oxidase Subunit 1, NADH Dehydrogenase Subunit 1, and Internal Transcribed Spacer 1 Genes from Korean Joseon Mummy Feces
    Jong Ha Hong, Chang Seok Oh, Min Seo, Jong-Yil Chai, Dong Hoon Shin
    Journal of Parasitology.2017; 103(6): 795.     CrossRef
  • 11,898 View
  • 129 Download
  • 7 Web of Science
  • Crossref
Original Articles
Genetic Characterization of Clinical Acanthamoeba Isolates from Japan using Nuclear and Mitochondrial Small Subunit Ribosomal RNA
Md Moshiur Rahman, Kenji Yagita, Akira Kobayashi, Yosaburo Oikawa, Amjad I.A. Hussein, Takahiro Matsumura, Masaharu Tokoro
Korean J Parasitol 2013;51(4):401-411.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.401

Because of an increased number of Acanthamoeba keratitis (AK) along with associated disease burdens, medical professionals have become more aware of this pathogen in recent years. In this study, by analyzing both the nuclear 18S small subunit ribosomal RNA (18S rRNA) and mitochondrial 16S rRNA gene loci, 27 clinical Acanthamoeba strains that caused AK in Japan were classified into 3 genotypes, T3 (3 strains), T4 (23 strains), and T5 (one strain). Most haplotypes were identical to the reference haplotypes reported from all over the world, and thus no specificity of the haplotype distribution in Japan was found. The T4 sub-genotype analysis using the 16S rRNA gene locus also revealed a clear sub-conformation within the T4 cluster, and lead to the recognition of a new sub-genotype T4i, in addition to the previously reported sub-genotypes T4a-T4h. Furthermore, 9 out of 23 strains in the T4 genotype were identified to a specific haplotype (AF479533), which seems to be a causal haplotype of AK. While heterozygous nuclear haplotypes were observed from 2 strains, the mitochondrial haplotypes were homozygous as T4 genotype in the both strains, and suggested a possibility of nuclear hybridization (mating reproduction) between different strains in Acanthamoeba. The nuclear 18S rRNA gene and mitochondrial 16S rRNA gene loci of Acanthamoeba spp. possess different unique characteristics usable for the genotyping analyses, and those specific features could contribute to the establishment of molecular taxonomy for the species complex of Acanthamoeba.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular Evidence for Greater Diversity Within Acanthamoeba
    Daniele Corsaro
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Molecular Typing of Acanthamoeba Using Mitochondrial rDNA Spacers
    Daniele Corsaro
    Microorganisms.2025; 13(10): 2285.     CrossRef
  • Sub-Genotyping of Acanthamoeba T4 Complex: Experience from North India
    Kirti Megha, Megha Sharma, Amit Gupta, Rakesh Sehgal, Sumeeta Khurana
    Parasitologia.2023; 3(1): 69.     CrossRef
  • Molecular evidence for a new lineage within the Acanthamoeba T4 genotype
    Daniele Corsaro, Danielle Venditti
    Parasitology Research.2023; 122(6): 1445.     CrossRef
  • Identification and genotyping of Acanthamoeba spp. in the water resources of western Iran
    Azadeh Karimi, Farnaz Kheirandish, Amirreza Javadi Mamaghani, Niloofar Taghipour, Syedeh Fatemeh Mousavi, Ali Aghajani, Nozhat Zebardast, Majid Faraji, Shirzad Fallahi
    Parasite Epidemiology and Control.2023; 22: e00308.     CrossRef
  • The Risk Factors and Clinical Features of Acanthamoeba Keratitis: First Time Detection of Acanthamoeba T5 Genotype from Keratitis Patients in Turkey
    Derya Dirim Erdogan, Mehmet Aykur, Nur Selvi Gunel, Melis Palamar, Ozlem Barut Selver, Buket Ozel, Ayse Yagci, Cumhur Gunduz, Hande Dagci
    Acta Parasitologica.2022; 67(3): 1384.     CrossRef
  • Exploring LSU and ITS rDNA Sequences for Acanthamoeba Identification and Phylogeny
    Daniele Corsaro
    Microorganisms.2022; 10(9): 1776.     CrossRef
  • Genotype distribution of Acanthamoeba in keratitis: a systematic review
    Maria Luisa Nunes Diehl, Júlia Paes, Marilise Brittes Rott
    Parasitology Research.2021; 120(9): 3051.     CrossRef
  • Molecular identification and phylogenetic analysis of free-living amoeba (Naegleria and Acanthamoeba) from treated and untreated drinking water
    Omid Ahmadi, Yousef Sharifi, Nazgol Khosravinia, Elham Moghaddas, Mohammad Akhoundi, Reza Fotouhi-Ardakani, Jaber Asadi, Amir Hossein Mohamadzade, Ghodratolah Salehi Sangani, Hamed Mirjalali, Mehdi Zarean
    Gene Reports.2021; 25: 101328.     CrossRef
  • Isolates from ancient permafrost help to elucidate species boundaries in Acanthamoeba castellanii complex (Amoebozoa: Discosea)
    Stas Malavin, Lyubov Shmakova
    European Journal of Protistology.2020; 73: 125671.     CrossRef
  • Update on Acanthamoeba phylogeny
    Daniele Corsaro
    Parasitology Research.2020; 119(10): 3327.     CrossRef
  • Lower prevalence of Entamoeba species in children with vertically transmitted HIV infection in Western Kenya
    Elizabeth Jemaiyo Matey, Masaharu Tokoro, Takehiro Nagamoto, Tetsushi Mizuno, Matilda Chelimo Saina, Xiuqiong Bi, Jane A. Oyombra, Paul Okumu, Benard Kibet Langat, Willie Kipkemboi Sang, Elijah Maritim Songok, Hiroshi Ichimura
    AIDS.2016; 30(5): 803.     CrossRef
  • Positive correlation of HIV infection with Giardia intestinalis assemblage B but not with assemblage A in asymptomatic Kenyan children
    Elizabeth J. Matey, Masaharu Tokoro, Tetsushi Mizuno, Takahiro Matsumura, Takehiro Nagamoto, Xiuqiong Bi, Jane A. Oyombra, Willie K. Sang, Elijah M. Songok, Hiroshi Ichimura
    AIDS.2016; 30(15): 2385.     CrossRef
  • Isolation and Genotyping of Acanthamoeba spp. as Neglected Parasites in North of Iran
    Azar Shokri, Shahabeddin Sarvi, Ahmad Daryani, Mehdi Sharif
    The Korean Journal of Parasitology.2016; 54(4): 447.     CrossRef
  • Presence of potential pathogenic genotypes of free-living amoebae isolated from sandboxes in children's playgrounds
    Marcin Cholewinski, Piotr Solarczyk, Monika Derda, Agnieszka Wojtkowiak-Giera, Edward Hadas
    Folia Parasitologica.2015;[Epub]     CrossRef
  • Morphological Features andIn VitroCytopathic Effect ofAcanthamoeba griffiniTrophozoites Isolated from a Clinical Case
    Arturo González-Robles, Lizbeth Salazar-Villatoro, Maritza Omaña-Molina, Maria Reyes-Batlle, Carmen M. Martín-Navarro, Jacob Lorenzo-Morales
    Journal of Parasitology Research.2014; 2014: 1.     CrossRef
  • 11,586 View
  • 116 Download
  • Crossref
Molecular Identification and Real-time Quantitative PCR (qPCR) for Rapid Detection of Thelohanellus kitauei, a Myxozoan Parasite Causing Intestinal Giant Cystic Disease in the Israel Carp
Jung Soo Seo, Eun Ji Jeon, Moo Sang Kim, Sung Ho Woo, Jin Do Kim, Sung Hee Jung, Myoung Ae Park, Bo Young Jee, Jin Woo Kim, Yi-Cheong Kim, Eun Hye Lee
Korean J Parasitol 2012;50(2):103-111.
Published online May 24, 2012
DOI: https://doi.org/10.3347/kjp.2012.50.2.103

Intestinal giant-cystic disease (IGCD) of the Israel carp (Cyprinus carpio nudus) has been recognized as one of the most serious diseases afflicting inland farmed fish in the Republic of Korea, and Thelohanellus kitauei has been identified as the causative agent of the disease. Until now, studies concerning IGCD caused by T. kitauei in the Israel carp have been limited to morphological and histopathological examinations. However, these types of diagnostic examinations are relatively time-consuming, and the infection frequently cannot be detected in its early stages. In this study, we cloned the full-length 18S rRNA gene of T. kitauei isolated from diseased Israel carps, and carried out molecular identification by comparing the sequence with those of other myxosporeans. Moreover, conventional PCR and real-time quantitative PCR (qPCR) using oligonucleotide primers for the amplification of 18S rRNA gene fragment were established for further use as methods for rapid diagnosis of IGCD. Our results demonstrated that both the conventional PCR and real-time quantitative PCR systems applied herein are effective for rapid detection of T. kitauei spores in fish tissues and environmental water.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular phylogenetics reveals a species complex pattern of closely related members of genus Thelohanellus (Cnidaria: Myxosporea) from the Indian subcontinent
    Harpreet Kaur, Aditya Gupta, Rajni Attri
    Microbial Pathogenesis.2021; 150: 104690.     CrossRef
  • Potential Application of PCR Based Molecular Methods in Fish Pathogen Identification: A Review
    Md. Ali Arman Ador, Md. Shameul Haque, Sulav Indra Paul, Jui Chakma, Rakib Ehsan, Ashikur Rahman
    Aquaculture Studies.2021;[Epub]     CrossRef
  • A new species Myxodavisia jejuensis n. sp. (Myxosporea: Sinuolineidae) isolated from cultured olive flounder Paralichthys olivaceus in South Korea
    Sang Phil Shin, Chang Nam Jin, Han Chang Sohn, Hiroshi Yokoyama, Jehee Lee
    Parasitology Research.2019; 118(11): 3105.     CrossRef
  • Development of PCR method for detecting Kudoa iwatai (Myxozoa: Multivalvulida) from rock bream Oplegnathus fasciatus
    Chan-Hyeok Jeon, Jeung-Wan Do, U-Hwa Nam, Wi-Sik Kim, Jeong-Ho Kim
    Parasitology Research.2017; 116(2): 789.     CrossRef
  • Molecular identification of a new myxozoan, Myxobolus dermiscalis n. sp. (Myxosporea) infecting scales of Labeo rohita Hamilton in Harike Wetland, Punjab (India)
    Harpreet Kaur, Rajni Attri, Jyoti Joshi
    International Journal for Parasitology: Parasites and Wildlife.2016; 5(2): 139.     CrossRef
  • The life cycle of Thelohanellus kitauei (Myxozoa: Myxosporea) infecting common carp (Cyprinus carpio) involves aurantiactinomyxon in Branchiura sowerbyi
    Dandan Zhao, Muhammad Hafiz Borkhanuddin, Weimin Wang, Yang Liu, Gábor Cech, Yanhua Zhai, Csaba Székely
    Parasitology Research.2016; 115(11): 4317.     CrossRef
  • Genetic relatedness provides support for a species complex of myxosporeans infecting the Indian major carp, Labeo rohita
    Harpreet Kaur, Aditya Gupta
    Animal Biology.2015; 65(3-4): 337.     CrossRef
  • Morphology and Phylogeny of Thelohanellus marginatus n. sp. (Myxozoa: Myxosporea), a Parasite Infecting the Gills of the Fish Hypophthalmus marginatus (Teleostei: Pimelodidae) in the Amazon River
    Sónia Rocha, Graça Casal, Michele Velasco, Ângela Alves, Edilson Matos, Saleh Al‐Quraishy, Carlos Azevedo
    Journal of Eukaryotic Microbiology.2014; 61(6): 586.     CrossRef
  • The phylogenetic study on Thelohanellus species (Myxosporea) in relation to host specificity and infection site tropism
    Sang Phil Shin, Van Giap Nguyen, Jae Mook Jeong, Jin Woo Jun, Ji Hyung Kim, Jee Eun Han, Gun Wook Baeck, Se Chang Park
    Molecular Phylogenetics and Evolution.2014; 72: 31.     CrossRef
  • New phylogenomic and comparative analyses provide corroborating evidence that Myxozoa is Cnidaria
    Jin-Mei Feng, Jie Xiong, Jin-Yong Zhang, Ya-Lin Yang, Bin Yao, Zhi-Gang Zhou, Wei Miao
    Molecular Phylogenetics and Evolution.2014; 81: 10.     CrossRef
  • Discrimination and simultaneous detection of two myxozoan parasites belonging to genus Thelohanellus by multiplex polymerase chain reaction
    Sung Ho Woo, Jung Soo Seo, Eun Hye Lee
    Veterinary Parasitology.2014; 203(1-2): 212.     CrossRef
  • Understanding myxozoan infection dynamics in the sea: Seasonality and transmission of Ceratomyxa puntazzi
    Gema Alama-Bermejo, Radek Šíma, Juan A. Raga, Astrid S. Holzer
    International Journal for Parasitology.2013; 43(9): 771.     CrossRef
  • 11,456 View
  • 80 Download
  • Crossref
Natural occurrence of Mycobacterium as an endosymbiont of Acanthamoeba isolated from a contact lens storage case
Hak Sun Yu, Hae Jin Jeong, Yeon-Chul Hong, Seong-Yong Seol, Dong-Il Chung, Hyun-Hee Kong
Korean J Parasitol 2007;45(1):11-18.
Published online March 20, 2007
DOI: https://doi.org/10.3347/kjp.2007.45.1.11

Recent in vitro studies have revealed that a certain Mycobacterium can survive and multiply within free-living amoebae. It is believed that protozoans function as host cells for the intracellular replication and evasion of Mycobacterium spp. under harmful conditions. In this study, we describe the isolation and characterization of a bacterium naturally observed within an amoeba isolate acquired from a contact lens storage case. The bacterium multiplied within Acanthamoeba, but exerted no cytopathic effects on the amoeba during a 6-year amoebic culture. Trasnmission electron microscopy showed that the bacteria were randomly distributed within the cytoplasm of trophozoites and cysts of Acanthamoeba. On the basis of the results of 18S rRNA gene analysis, the amoeba was identified as A. lugdunensis. A 16S rRNA gene analysis placed this bacterium within the genus Mycobacterium. The bacterium evidenced positive reactivity for acid-fast and fluorescent acid-fast stains. The bacterium was capable of growth on the Middlebrook 7H11-Mycobacterium-specific agar. The identification and characterization of bacterial endosymbionts of free-living protozoa bears significant implications for our understanding of the ecology and the identification of other atypical mycobacterial pathogens.

Citations

Citations to this article as recorded by  Crossref logo
  • A Comparative Genomic Approach to Determine the Virulence Factors and Horizontal Gene Transfer Events of Clinical Acanthamoeba Isolates
    Xiaobin Gu, Xiuhai Lu, Shudan Lin, Xinrui Shi, Yue Shen, Qingsong Lu, Yiying Yang, Jing Yang, Jiabei Cai, Chunyan Fu, Yongliang Lou, Meiqin Zheng, Tim Downing, Kirti Megha
    Microbiology Spectrum.2022;[Epub]     CrossRef
  • A Systematic Review of Intracellular Microorganisms within Acanthamoeba to Understand Potential Impact for Infection
    Binod Rayamajhee, Dinesh Subedi, Hari Kumar Peguda, Mark Duncan Willcox, Fiona L. Henriquez, Nicole Carnt
    Pathogens.2021; 10(2): 225.     CrossRef
  • Detection of Free-Living Amoebae and Their Intracellular Bacteria in Borehole Water before and after a Ceramic Pot Filter Point-of-Use Intervention in Rural Communities in South Africa
    Clarissa van der Loo, Catheleen Bartie, Tobias George Barnard, Natasha Potgieter
    International Journal of Environmental Research and Public Health.2021; 18(8): 3912.     CrossRef
  • The key factors contributing to the risk, diagnosis and treatment of non-tuberculous mycobacterial opportunistic infections
    Anna Grzegorzewicz, Mariola Paściak
    Postępy Higieny i Medycyny Doświadczalnej.2021; 75(1): 696.     CrossRef
  • Co-Existence of Free-Living Amoebae and Potential Human Pathogenic Bacteria Isolated from Rural Household Water Storage Containers
    Natasha Potgieter, Clarissa van der Loo, Tobias George Barnard
    Biology.2021; 10(12): 1228.     CrossRef
  • The core microbiome of sessile ciliate Stentor coeruleus is not shaped by the environment
    Olivia Lanzoni, Andrey Plotnikov, Yuri Khlopko, Giulio Munz, Giulio Petroni, Alexey Potekhin
    Scientific Reports.2019;[Epub]     CrossRef
  • Repertoire of free-living protozoa in contact lens solutions
    Ibtissem Bouchoucha, Aurore Aziz, Louis Hoffart, Michel Drancourt
    BMC Ophthalmology.2016;[Epub]     CrossRef
  • Current and Past Strategies for Bacterial Culture in Clinical Microbiology
    Jean-Christophe Lagier, Sophie Edouard, Isabelle Pagnier, Oleg Mediannikov, Michel Drancourt, Didier Raoult
    Clinical Microbiology Reviews.2015; 28(1): 208.     CrossRef
  • Looking in amoebae as a source of mycobacteria
    M. Drancourt
    Microbial Pathogenesis.2014; 77: 119.     CrossRef
  • Molecular characterization and ultrastructure of a new amoeba endoparasite belonging to the Stenotrophomonas maltophilia complex
    Daniele Corsaro, Karl-Dieter Müller, Rolf Michel
    Experimental Parasitology.2013; 133(4): 383.     CrossRef
  • Identification of Free-Living Amoebae and Amoeba-Associated Bacteria from Reservoirs and Water Treatment Plants by Molecular Techniques
    Alicia Garcia, Pilar Goñi, Joanna Cieloszyk, Maria Teresa Fernandez, Laura Calvo-Beguería, Encarnacion Rubio, Maria Francisca Fillat, Maria Luisa Peleato, Antonio Clavel
    Environmental Science & Technology.2013; 47(7): 3132.     CrossRef
  • Cooccurrence of Free-Living Amoebae and Nontuberculous Mycobacteria in Hospital Water Networks, and Preferential Growth of Mycobacterium avium in Acanthamoeba lenticulata
    Alida R. Ovrutsky, Edward D. Chan, Marinka Kartalija, Xiyuan Bai, Mary Jackson, Sara Gibbs, Joseph O. Falkinham, Michael D. Iseman, Paul R. Reynolds, Gerald McDonnell, Vincent Thomas
    Applied and Environmental Microbiology.2013; 79(10): 3185.     CrossRef
  • Detection of Bacterial Endosymbionts in Clinical Acanthamoeba Isolates
    Alfonso Iovieno, Dolena R. Ledee, Darlene Miller, Eduardo C. Alfonso
    Ophthalmology.2010; 117(3): 445.     CrossRef
  • Biodiversity of amoebae and amoeba-associated bacteria in water treatment plants
    Daniele Corsaro, Gemma Saucedo Pages, Vicente Catalan, Jean-François Loret, Gilbert Greub
    International Journal of Hygiene and Environmental Health.2010; 213(3): 158.     CrossRef
  • Free-living amoebae and their intracellular pathogenic microorganisms: risks for water quality
    Vincent Thomas, Gerald McDonnell, Stephen P. Denyer, Jean-Yves Maillard
    FEMS Microbiology Reviews.2010; 34(3): 231.     CrossRef
  • Free-living amoebae, a training field for macrophage resistance of mycobacteria
    I.B. Salah, E. Ghigo, M. Drancourt
    Clinical Microbiology and Infection.2009; 15(10): 894.     CrossRef
  • Endosymbionts of Acanthamoeba Isolated from Domestic Tap Water in Korea
    Seon Hee Choi, Min Kyoung Cho, Soon Cheol Ahn, Ji Eun Lee, Jong Soo Lee, Dong-Hee Kim, Ying-Hua Xuan, Yeon Chul Hong, Hyun Hee Kong, Dong Il Chung, Hak Sun Yu
    The Korean Journal of Parasitology.2009; 47(4): 337.     CrossRef
  • Survival of amoebae on building materials
    T. Yli-Pirilä, J. Kusnetsov, M.-R. Hirvonen, M. Seuri, A. Nevalainen
    Indoor Air.2009; 19(2): 113.     CrossRef
  • Occurrence of Free-Living Amoebae in Communities of Low and High Endemicity for Buruli Ulcer in Southern Benin
    Miriam Eddyani, Johan F. De Jonckheere, Lies Durnez, Patrick Suykerbuyk, Herwig Leirs, Françoise Portaels
    Applied and Environmental Microbiology.2008; 74(21): 6547.     CrossRef
  • Relationship between mycobacteria and amoebae: ecological and epidemiological concerns
    V. Thomas, G. McDonnell
    Letters in Applied Microbiology.2007; 45(4): 349.     CrossRef
  • 10,874 View
  • 97 Download
  • Crossref
PCR Detection and Molecular Characterization of Pentatrichomonas hominis from Feces of Dogs with Diarrhea in the Republic of Korea
Kim, Yun Ah , Kim, Hye Youn , Cho, Shin Hyeong , Cheun, Hyeong Il , Yu, Jae Ran , Lee, Sang Eun
Korean J Parasitol 2010;48(1):9-13.
DOI: https://doi.org/10.3347/kjp.2010.48.1.9
Pentatrichomonas hominis is considered a commensal protozoan in the large intestine of a number of mammalian hosts, such as cats, dogs, and non-human primates. The resulting infections, which can induce diarrhea, have been attributed to opportunistic overgrowth of P. hominis. This study was performed to confirm the P. hominis infection and its molecular characterization from the feces of puppies with diarrhea. Fecal samples were obtained from 14 German shepherd puppies with diarrhea over 1 week (7 females and 7 males, 2-9 months of age) residing on a dog farm in August 2007. Species-specific PCR assay identified P. hominis 18S rRNA genes in 3 of the 14 puppies (1 female and 2 males; 1 aged 2 months and 2 aged 9 months). This phylogenetic analysis established that P. hominis belonged to the 1st clade, which is comprised of Bos taurus and Felines.

Citations

Citations to this article as recorded by  Crossref logo
  • Development of a single-cell cloning technique for isolation of Pentatrichomonas hominis: a promising tool for diagnosing Trichomonas spp. infections in the pig breeding industry
    Yibin Zhu, Haiming Cai, Shenquan Liao, Juan Li, Siyun Fang, Hanqin Shen, Dingai Wang, Zhuanqiang Yan, Minna Lv, Xuhui Lin, Junjing Hu, Yongle Song, Xiangjie Chen, Lijun Yin, Jianfei Zhang, Nanshan Qi, Mingfei Sun
    Parasites & Vectors.2025;[Epub]     CrossRef
  • Prevalence of Pentatrichomonas hominis infection in wild rodents
    Yan Tang, Hai-Tao Wang, Jing-Hao Li, Qing-Yu Hou, Si-Yuan Qin, He Ma, Ya Qin, Quan Zhao, Hany M. Elsheikha, Shuo Liu
    BMC Veterinary Research.2025;[Epub]     CrossRef
  • Genetic diversity of Trichomonads from Milu deer (Elaphurus davidianus) in China
    Yilei Zhang, Zhouchun Li, Xinglong Song, Guodong Xiao, Lingru He, Jiade Bai, Zhenyu Zhong, Lijie Tian, Yan Chang, Zhuang Li, Qingyun Guo, Congshan Yang, Qingxun Zhang
    Parasite.2025; 32: 23.     CrossRef
  • Epidemiology of Pentatrichomonas Hominis in Farmed Mink and Raccoon Dogs Across Five Provinces in China
    Na Lu, Hai-Tao Wang, Qing-Yu Hou, Ya Qin, Xue-Min Li, Xing Yang, Jing Jiang, Shuo Liu
    Foodborne Pathogens and Disease.2025;[Epub]     CrossRef
  • Molecular Identification and Survey of Tetratrichomonas buttreyi and Pentatrichomonas hominis in Cattle in Shanxi Province, North China
    Yu-Xuan Wang, Tao Jia, Zi-Rui Wang, Jin-Long Wang, Ze-Dong Zhang, Ze-Xuan Wu, Wen-Wei Gao, Xing-Quan Zhu, Qing Liu
    Animals.2025; 15(13): 1899.     CrossRef
  • Development of a novel one-tube LAMP-CRISPR/Cas12b technique for detecting Pentatrichomonas hominis
    Qing-Xin Fan, Jin-Long Wang, Yao Liang, Yu-Xuan Wang, Han-Dan Xiao, Xing-Quan Zhu, Qing Liu
    Microchemical Journal.2025; 215: 114488.     CrossRef
  • Genetic diversity, prevalence and risk factors of trichomonads from captive non-human primates in China
    Yilei Zhang, Yangfan Li, Jiawei Mi, Jiawen Zhang, Guodong Xiao, Siqi Xiong, Yew Hwong, Shibin Feng, Congshan Yang
    Acta Tropica.2025; 270: 107816.     CrossRef
  • Prevalence of Pentatrichomonas hominis in foxes and raccoon dogs and changes in the gut microbiota of infected female foxes in the Hebei and Henan Provinces in China
    Pengtao Song, Yunan Guo, Shoujun Zuo, Liangliang Li, Fang Liu, Tao Zhang, Hongyu Dai, Haiju Dong
    Parasitology Research.2024;[Epub]     CrossRef
  • Fatal coinfection of blastocystosis and intestinal trichomoniasis in a rhesus macaque (Macaca mulatta)
    Varun Kumar Sarkar, Ujjwal Kumar De, Pooja Solanki, Harshit Saxena, Shivansh Mehra, Devendra Prasad Pateer, Sudhir Kumar Prajapati
    Journal of Parasitic Diseases.2024; 48(2): 400.     CrossRef
  • Molecular Identification and Survey of Trichomonad Species in Pigs in Shanxi Province, North China
    Zi-Rui Wang, Qing-Xin Fan, Jin-Long Wang, Shuo Zhang, Yu-Xuan Wang, Ze-Dong Zhang, Wen-Wei Gao, Xing-Quan Zhu, Qing Liu
    Veterinary Sciences.2024; 11(5): 203.     CrossRef
  • Morphological and molecular characterization of parabasilids isolated from ex situ nonhuman primates and their keepers at different institutions in Brazil
    Lais Verdan Dib, Alynne da Silva Barbosa, Lais Lisboa Correa, Breno da Silva Torres, Alcides Pissinatti, Silvia Bahadian Moreira, Rodrigo Hidalgo Friciello Teixeira, André Luíz Mota da Costa, José Augusto Pereira Carneiro Muniz, Amauri Michel Junglos, Zel
    International Journal for Parasitology: Parasites and Wildlife.2024; 24: 100946.     CrossRef
  • Molecular-phylogenetic investigation of trichomonads in dogs and cats reveals a novel Tritrichomonas species
    Barbara Tuska-Szalay, Julia Gilbert, Nóra Takács, Sándor A. Boldogh, József Fáy, Ágnes Sterczer, Roland Psáder, Jenő Kontschán, Ádám Izsó, Sándor Hornok
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Prevalence of Intestinal Parasites in Dogs and Cats from the Kvarner Region in Croatia
    Siniša Faraguna, Ivan Vlahek, Kristina Tea Miočić, Tibor Andreanszky, Marko Pećin
    Acta Veterinaria.2023; 73(1): 41.     CrossRef
  • Development of an LFD-RPA Assay for Rapid Detection of Pentatrichomonas hominis Infection in Dogs
    Yao Rong, Xichen Zhang, Xuejiao Chen, Jianhua Li, Pengtao Gong, Xiaocen Wang, Xin Li, Xu Zhang, Taotao Yue, Hongbo Zhang, Xiaofei Zhou, Nan Zhang
    Current Issues in Molecular Biology.2023; 45(11): 9252.     CrossRef
  • Prevalence and molecular characterization of Pentatrichomonas hominis in Siberian tigers (Panthera tigris altaica) in northeast China
    Hongbo ZHANG, Nan ZHANG, Pengtao GONG, Shuqin CHENG, Xiaocen WANG, Xin LI, Zhijun HOU, Chang LIU, Tianqi BI, Bobo WANG, Yidan CHENG, Jianhua LI, Xichen ZHANG
    Integrative Zoology.2022; 17(4): 543.     CrossRef
  • Identification of Pentatrichomonas hominis in preputial washes of bulls in Brazil
    Otávia Reis e Silva, Laura Ribeiro, Vera Lucia Teixeira de Jesus, Douglas McIntosh, Lara Nogueira Silenciato, Joaquim Esquerdo Ferreira, Marco Roberto Bourg de Mello
    Revista Brasileira de Parasitologia Veterinária.2022;[Epub]     CrossRef
  • Molecular identification of Pentatrichomonas hominis in animals in central and western Thailand
    Aongart Mahittikorn, Ruenruetai Udonsom, Khuanchai Koompapong, Rachatawan Chiabchalard, Chantira Sutthikornchai, Preeyaporn Monatrakul Sreepian, Hirotake Mori, Supaluk Popruk
    BMC Veterinary Research.2021;[Epub]     CrossRef
  • Prevalence of Tetratrichomonas buttreyi and Pentatrichomonas hominis in yellow cattle, dairy cattle, and water buffalo in China
    Wen-Chao Li, Jia-min Huang, Zhui Fang, Qi Ren, Li Tang, Zhen-zhen Kan, Xin-chao Liu, You-fang Gu
    Parasitology Research.2020; 119(2): 637.     CrossRef
  • Prevalence of Tritrichomonas foetus infection in cats in Bangkok metropolitan area and in vitro drug sensitivity testing
    Alisara Leelanupat, Ketsarin Kamyingkird, Wissanuwat Chimnoi, Burin Nimsuphan
    Veterinary Parasitology: Regional Studies and Reports.2020; 21: 100440.     CrossRef
  • A case of “misplaced” Tritrichomonas foetus infection in a dog in Northern Italy
    Roberta Franchi, Walter Bertazzolo, Michele Marino, Barbara De Marco
    Veterinary Parasitology: Regional Studies and Reports.2020; 22: 100451.     CrossRef
  • Protozoan genital invasions caused by the representatives of trichomonas and giardia
    Pavlo V. Fedorych, Gennadiy I. Mavrov, Tetiana V. Osinska, Yuliia V. Shcherbakova
    Wiadomości Lekarskie.2020; 73(2): 380.     CrossRef
  • Molecular prevalence of trichomonad species from pet shop puppies and kittens in Japan
    Naoyuki Itoh, Yuko Iijima, Isao Ogura, Natsumi Yonekura, Satoshi Kameshima, Yuya Kimura
    Revista Brasileira de Parasitologia Veterinária.2020;[Epub]     CrossRef
  • High prevalence of Pentatrichomonas hominis infection in gastrointestinal cancer patients
    Nan Zhang, Hongbo Zhang, Yanhui Yu, Pengtao Gong, Jianhua Li, Ziyi Li, Ting Li, Zhanjie Cong, Chunying Tian, Xiaofeng Liu, Xiuyan Yu, Xichen Zhang
    Parasites & Vectors.2019;[Epub]     CrossRef
  • Pentatrichomonas hominis infection in two domestic cats with chronic diarrhea
    Bethânia Ferreira Bastos, Beatriz Brener, Mariana Alves de Figueiredo, Daniela Leles, Flavya Mendes-de-Almeida
    Journal of Feline Medicine and Surgery Open Reports.2018;[Epub]     CrossRef
  • Prevalence of Pentatrichomonas hominis infections in six farmed wildlife species in Jilin, China
    Xianhe Li, Jianhua Li, Xichen Zhang, Zhengtao Yang, Ju Yang, Pengtao Gong
    Veterinary Parasitology.2017; 244: 160.     CrossRef
  • Pentatrichomonas hominis: prevalence and molecular characterization in humans, dogs, and monkeys in Northern China
    Wen-Chao Li, Meng Ying, Peng-Tao Gong, Jian-Hua Li, Ju Yang, He Li, Xi-Chen Zhang
    Parasitology Research.2016; 115(2): 569.     CrossRef
  • Prevalence and Molecular Characterization of Intestinal Trichomonads in Pet Dogs in East China
    Wen-Chao Li, Kai Wang, Wei Zhang, Jingjing Wu, You-Fang Gu, Xi-Chen Zhang
    The Korean Journal of Parasitology.2016; 54(6): 703.     CrossRef
  • Detection of Pentatrichomonas hominis in dogs using real-time PCR
    M. Michalczyk, R. Sokół, P. Socha
    Polish Journal of Veterinary Sciences.2015; 18(4): 775.     CrossRef
  • Molecular and morphologic identification of Pentatrichomonas hominis in swine
    Weizhi Li, Wei Li, Pengtao Gong, Ying Meng, Wenchao Li, Chengcai Zhang, Shijie Li, Ju Yang, He Li, Xichen Zhang, Jianhua Li
    Veterinary Parasitology.2014; 202(3-4): 241.     CrossRef
  • Pentatrichomonas hominis: first isolation from the feces of a dog with diarrhea in China
    Wen-Chao Li, Peng-Tao Gong, Meng Ying, Jian-Hua Li, Ju Yang, He Li, Zheng-Tao Yang, Guo-Cai Zhang, Xi-Chen Zhang
    Parasitology Research.2014; 113(5): 1795.     CrossRef
  • Molecular characterization of trichomonads isolated from animal hosts in the Philippines
    Kris Genelyn B. Dimasuay, Windell L. Rivera
    Veterinary Parasitology.2013; 196(3-4): 289.     CrossRef
  • New Hosts ofSimplicimonas similisandTrichomitus batrachorumIdentified by 18S Ribosomal RNA Gene Sequences
    Kris Genelyn B. Dimasuay, Orlie John Y. Lavilla, Windell L. Rivera
    Journal of Parasitology Research.2013; 2013: 1.     CrossRef
  • PCR amplification and DNA sequence analysis of parasitic intestinal protozoa in specimens stained with Chlorazol Black E
    Norihito Morimoto, Masataka Korenaga, Yoshie Nishida, Hiroaki Takeuchi, Yoshitaka Kumon, Tetsuro Sugiura
    Acta Parasitologica.2013;[Epub]     CrossRef
  • Prevalence, risk factors of infection and molecular characterization of trichomonads in puppies from French breeding kennels
    Aurélien Grellet, BrunoPolack, Alexandre Feugier, Corine Boucraut-Baralon, Dominique Grandjean, Laurine Vandewynckel, Amandine Cian, Dionigia Meloni, Eric Viscogliosi
    Veterinary Parasitology.2013; 197(3-4): 418.     CrossRef
  • Species identification of trichomonads and associated coinfections in dogs with diarrhea and suspected trichomonosis
    M.K. Tolbert, C.M. Leutenegger, R. Lobetti, J. Birrell, J.L. Gookin
    Veterinary Parasitology.2012; 187(1-2): 319.     CrossRef
  • Identification of putative miRNAs from the deep-branching unicellular flagellates
    Po-Jung Huang, Wei-Chen Lin, Shih-Chieh Chen, Yong-Han Lin, Chin-Hung Sun, Ping-Chiang Lyu, Petrus Tang
    Genomics.2012; 99(2): 101.     CrossRef
  • Molecular identification of Pentatrichomonas hominis in two patients with gastrointestinal symptoms
    Dionigia Meloni, Cléa Mantini, Julien Goustille, Guillaume Desoubeaux, Zoha Maakaroun-Vermesse, Jacques Chandenier, Nausicaa Gantois, Christophe Duboucher, Pier Luigi Fiori, Eduardo Dei-Cas, Thanh Hai Duong, Eric Viscogliosi
    Journal of Clinical Pathology.2011; 64(10): 933.     CrossRef
  • Update on the Diagnosis and Management of Tritrichomonas foetus Infections in Cats
    Kristin Manning
    Topics in Companion Animal Medicine.2010; 25(3): 145.     CrossRef
  • 12,105 View
  • 116 Download
  • Crossref