The first molecular detection of equine piroplasmosis in Vietnam and genetic characterization of three co-circulating genotypes of Theileria equi.
Abstract: Equine piroplasmosis, caused by , and , significantly impacts on the veterinary and economic aspects of the global horse industry. However, many countries, including Vietnam, have not yet conducted epidemiological surveys to determine the prevalence of these haemoparasites. This study aimed to detect and/or infections in horses and to identify their genotypes. Blood samples were collected from 154 apparently healthy horses in eight districts of Hanoi, Thai Nguyen, and Son La provinces located in the northern part of the country. Twenty-four horses (15.58%, 95%CI: 10.70–22.14%) were found to be infected with across six districts. was not detected. No significant association was found between gender, host age, and the number of infected horses. Phylogenetic analysis of the 18S rRNA sequences from the positive DNA samples revealed genotypes A, C, and E. These results confirm the presence of equine theileriosis in northern Vietnam, highlighting the need for nationwide studies of equine piroplasmosis involving larger sample sizes. The online version contains supplementary material available at 10.1007/s00436-026-08630-4.
Publication Date: 2026-02-05 PubMed ID: 41644779PubMed Central: PMC12876454DOI: 10.1007/s00436-026-08630-4Google Scholar: Lookup
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- Journal Article
Summary
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Overview
- This study reports the first molecular evidence of equine piroplasmosis caused by Theileria equi in horses from northern Vietnam.
- It also identifies three distinct genetic types (genotypes A, C, and E) of the parasite circulating in this region.
Background
- Equine piroplasmosis is a disease affecting horses globally, caused mainly by two types of blood parasites: Babesia caballi and Theileria equi.
- The disease negatively impacts horse health and imposes significant economic costs on the horse industry.
- Despite its importance, some countries, such as Vietnam, had no prior comprehensive surveys to detect or study these parasites in their equine populations.
Study Objective
- The main aim was to detect infections of Babesia caballi and/or Theileria equi in horses in northern Vietnam and to genetically characterize the parasite genotypes present.
Methodology
- Blood samples were collected from 154 apparently healthy horses across eight districts in three northern Vietnamese provinces: Hanoi, Thai Nguyen, and Son La.
- Molecular techniques, specifically PCR targeting the 18S rRNA gene, were used to detect the presence of the parasites’ DNA.
- Genetic sequencing and phylogenetic analysis of positive samples were performed to identify different genotypes of Theileria equi present in the horse population.
Key Findings
- Out of 154 horses sampled, 24 (15.58%) tested positive for Theileria equi.
- The parasite was found in horses from six of the eight districts tested, indicating widespread presence.
- Babesia caballi was not detected in any of the samples.
- There was no statistically significant relationship between the horses’ gender or age and their infection status, suggesting that infection risk is generally consistent across these factors.
Genetic Characterization
- Phylogenetic analysis of the 18S rRNA gene sequences identified three genotypes of Theileria equi: A, C, and E.
- This shows that multiple genetic variants of the parasite are co-circulating in northern Vietnam.
- Understanding genotype distribution is important for disease control and epidemiological tracking.
Implications and Recommendations
- This study confirms for the first time that equine piroplasmosis caused by Theileria equi is present in Vietnam, particularly in the north.
- The findings highlight the need for more extensive, nationwide epidemiological surveys to assess the true prevalence and distribution of this disease.
- Such data can help inform veterinary strategies, control measures, and economic assessments related to equine health management in Vietnam.
- The identification of multiple genotypes indicates potential complexity in disease dynamics, which should be considered in diagnostic and intervention planning.
Additional Resources
- The article provides supplementary materials online for further details, supporting transparency and enabling follow-up research.
- The DOI link given helps access the full publication for those interested in more technical specifics or data.
Cite This Article
APA
Dao TTH, Szűts T, Duong NN, Troung DTQ, Solymosi N, Takács N, Hornok S, Farkas R.
(2026).
The first molecular detection of equine piroplasmosis in Vietnam and genetic characterization of three co-circulating genotypes of Theileria equi.
Parasitol Res, 125(1), 14.
https://doi.org/10.1007/s00436-026-08630-4 Publication
Researcher Affiliations
- Department of Parasitology, National Institute of Veterinary Research, Hanoi, Vietnam.
- Department of Zoology, University of Veterinary Medicine Budapest, Budapest, Hungary.
- Department of Parasitology, National Institute of Veterinary Research, Hanoi, Vietnam.
- Department of Parasitology, National Institute of Veterinary Research, Hanoi, Vietnam.
- Centre for Bioinformatics, University of Veterinary Medicine Budapest, Budapest, Hungary.
- Department of Parasitology and Zoology, University of Veterinary Medicine Budapest, Budapest, Hungary.
- HUN-REN-UVMB Climate Change: New Blood-sucking Parasites and Vector-borne Pathogens Research Group, Budapest, Hungary.
- Department of Parasitology and Zoology, University of Veterinary Medicine Budapest, Budapest, Hungary.
- HUN-REN-UVMB Climate Change: New Blood-sucking Parasites and Vector-borne Pathogens Research Group, Budapest, Hungary.
- Department of Parasitology and Zoology, University of Veterinary Medicine Budapest, Budapest, Hungary. farkas.robert@univet.hu.
Conflict of Interest Statement
Declarations. Ethical approval: The protocol used in this study followed the QCVN 01–83:2011/BNN&PTNT ( https://cucthuy.gov.vn/en/tieu-chuan-quy-chuan/-/standards/detail/77582 ) and approved by the Proposal Committee of Ministry of Science and Technology, Vietnam (No. 02/2022/HD-NDT). Competing interests: The authors declare no competing interests.
References
This article includes 47 references
- Agresti A. Categorical data analysis. Second edition. New York: Wiley. Pages 91–101.
- Allsopp MT, Lewis BD, Penzhorn BL. Molecular evidence for transplacental transmission of from carrier mares to their apparently healthy foals. Vet Parasitol 148:130–136.
- Bhoora R, Franssen L. Sequence heterogeneity in the 18S rRNA gene within and from horses in South Africa. Vet Parasitol 159:112–120.
- Brüning A. Equine piroplasmosis an update on diagnosis, treatment and prevention. Br Vet J 152:139–151.
- Casati S, Sager H. Presence of potentially pathogenic sp. for human in in Switzerland. Ann Agric Environ Med 13:65–70.
- Chauvin A, Moreau E. Babesia and its hosts: adaptation to long-lasting interactions as a way to achieve efficient transmission. Vet Res 40(2):37.
- Chen K, Hu Z. Development of a duplex real-time PCR assay for simultaneous detection and differentiation of and . Transbound Emerg Dis 69:e1338–1349.
- Chhabra S, Ranjan R. Transplacental transmission of () from carrier mares to foals. J Parasit Dis 36:31–33.
- R Core Team. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria.
- Criscuolo A, Gribaldo S. Bmge (block mapping and gathering with entropy): a new software for selection of phylogenetic informative regions from multiple sequence alignments. BMC Evol Biol 10(1):210.
- De Waal DT. Equine piroplasmosis: a review. Br Vet J 148(1):6–14.
- Githaka N, Konnai S. Identification and sequence characterization of novel genotypes from the waterbuck () in a -endemic area in Kenya. Vet Parasitol 202(3–4):180–193.
- Guindon S, Dufayard JF. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 59(3):307–321.
- Hornok S, Takács N. DNA of , and in stable flies (). Parasit Vectors 13:186.
- Hornok S, Farkas R. A morpho-phylogenetic update on ixodid ticks infesting cattle and buffalos in Vietnam, with three new species to the fauna and a checklist of all species indigenous to the country. Parasit Vectors 17:319.
- Kalantari M, Sharifiyazdi H. in the horses of Iran: molecular detection, genetic diversity, and hematological findings. Vet Parasitol Reg Stud Rep 36:100792.
- Kamyingkird K, Yangtara S. Seroprevalence of and in horses and mules from Northern Thailand. J Protozool Res 17:11–17.
- Katoh K, Toh H. Recent developments in the MAFFT multiple sequence alignment program. Brief Bioinform 9(4):286–298.
- Khaing Y, Htun LL. Microscopic examination of haemoparasites and the first molecular detection of in horses in Myanmar. Parasitol Res 124:42.
- Knowles DP, Kappmeyer LS. Discovery of a novel species, n. sp., infective to equids, highlights exceptional genomic diversity within the genus : implications for apicomplexan parasite surveillance. Int J Parasitol 48:679–690.
- Kumar S, Sudan V. () genotype A among Indian equine population. Vet Parasitol Reg Stud Rep 19:100367.
- Laveran M. Contribution a l’etude de . CR Soc Biol 53:385–388.
- Lefort V, Longueville JE, Gascuel O. SMS: smart model selection in PhyML. Mol Biol Evol 34(9):2422–2424.
- Lemoine F, Correia D. NGPhylogeny. Fr: new generation phylogenetic services for non-specialists. Nucleic Acids Res 47(W1):W260–265.
- Letunic I, Bork P. Interactive tree of life (iTOL) v6: recent updates to the phylogenetic tree display and annotation tool. Nucleic Acids Res 52(W1):78–82.
- Manna G, Cersini A, Nardini R. Genetic diversity of and infecting horses of Central-Southern Italy and preliminary results of its correlation with clinical and serological status. Ticks Tick-borne Dis 9:1212–1220.
- Mendoza FJ, Pérez-Écija A. New insights in the diagnosis and treatment of equine piroplasmosis: pitfalls, idiosyncrasies, and myths. Front Vet Sci 11:1459989.
- Moretti A, Mangili V, Salvatori R. Prevalence and diagnosis of Babesia and Theileria infections in horses in Italy: a preliminary study. Vet J 184:346–350.
- Munkhjargal T, Sivakumar T. Prevalence and genetic diversity of equine piroplasms in Tov province, Mongolia. Infect Genet Evol 16:178–185.
- Ngoc DP, Ha TDT. The current status and predicted climate-driven range expansion of in northern Vietnam. Acta Trop 268:107732.
- Nugraha AB, Cahyaningsih U. Serological and molecular prevalence of equine piroplasmosis in Western Java, Indonesia. Vet Parasitol Reg Stud Rep 14:1–6.
- Onyiche TGE, Suganuma K. A review on equine piroplasmosis: epidemiology, vector ecology, risk factors, host immunity, diagnosis and control. Int J Environ Res Public Health 16:1736.
- Otgonsuren D, Amgalanbaatar T, Narantsatsral S. Epidemiology and genetic diversity of and in Mongolian horses. Infect Genet Evol 119:105571.
- Qablan MA, Sloboda M. Quest for the piroplasms in camels: identification of and in Jordanian dromedaries by PCR. Vet Parasitol 186:456–460.
- Rothschild CM. Equine piroplasmosis. J Equine Vet Sci 33:497–508.
- Ruegg SR, Torgerson P. Age-dependent dynamics of and infections in southwest Mongolia based on IFAT and/or PCR prevalence data from domestic horses and ticks. Parasitology 134:939–947.
- Salim B, Alanazi AD. Potential role of dogs as sentinels and reservoirs for piroplasms infecting equine and cattle in Riyadh City, Saudi Arabia. Acta Trop 193:7883.
- Schein H. Equine piroplasmosis in South Annam, French Indo-China. Bull Soc Exot Pathol 10:871–873.
- Scoles GA, Ueti MW. Vector ecology of equine piroplasmosis. Annu Rev Entomol 60:561–580.
- Steinman A, Zimmerman T. Demographic and environmental risk factors for infection by in 590 horses in Israel. Vet Parasitol 187:558–562.
- Tamzali Y. Equine piroplasmosis: an updated review. Equine Vet Educ 25:590–598.
- Tirosh-Levy S, Gottlieb Y. Twenty years of equine piroplasmosis research: global distribution, molecular diagnosis, and phylogeny. Pathogens 9(11):926.
- Tirosh-Levy S, Mazuz ML, Savitsky I. A serological and molecular prevalence of in apparently healthy horses in Israel. Pathogens 10:445.
- Wang J, Liua J. The first molecular detection and genetic diversity of and in horses of Gansu province, China. Ticks Tick Born Dis 10:528–532.
- Wise LN, Kappmeyer LS. Review of equine piroplasmosis. J Vet Intern Med 27:1334–1346.
- Ybañez AP, Ybañez RHD. Serological and molecular detection of and in Philippine horses. Ticks Tick-borne Dis 9:1125–1128.
- Zhao S, Wang H. First report of genetic diversity and risk factor analysis of equine piroplasm infection in equids in Jilin, China. Parasit Vectors 13:459.
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