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Parasitology research2002; 88(5); 460-462; doi: 10.1007/s00436-002-0609-4

Culture, isolation and propagation of Babesia caballi from naturally infected horses.

Abstract: Thirteen blood samples of horses from South Africa, five of which were seropositive for Babesia caballi and eight for both B. caballi and Theileria equi, were subjected to in vitro culture to identify carrier animals. None of the animals had a detectable parasitaemia on Giemsa-stained blood smears before culture initiation. Cultures were initiated in L-cysteine-enriched medium, either in an oxygen-reduced gas mixture or in a 5% CO2-in-air atmosphere. All five animals seropositive for B. caballi were identified as carrier animals using an oxygen-reduced atmosphere, whereas only four samples became culture positive under normal atmospheric conditions. Among the eight samples seropositive for both B. caballi and T. equi, two were identified as carriers for both. The remaining six samples were identified as carrying only T. equi.
Publication Date: 2002-06-07 PubMed ID: 12049465DOI: 10.1007/s00436-002-0609-4Google Scholar: Lookup
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Summary

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The research is focused on successfully isolating and cultivating Babesia caballi from horses in South Africa, discovered by conducting in vitro cultures on blood samples from horses which show no apparent symptoms of being infected.

Research Context and Methodology

  • Babesia caballi is a type of parasite known to infect horses. It is carried by ticks and causes babesiosis or ‘Piroplasmosis’, a serious, sometimes fatal disease of horses. This research study aimed at identifying horses that are carriers of B. caballi without showing any health symptoms or detectable parasitaemia (presence of parasites in the blood), as these carrier animals play a crucial role in the epidemiology of the disease.
  • Thirteen blood samples were gathered from horses in South Africa. Five of these samples were known to be seropositive towards B. caballi (presence of specific antibodies in the blood against the organism), and eight were seropositive for both B. caballi and another parasite, Theileria equi.
  • These samples were subjected to in vitro culture – a process wherein organisms are grown outside their natural environment, in a controlled setting. This helped researchers identify any carrier animals in the sample population.
  • The cultures were started using a medium enriched with L-cysteine, an amino acid, under two different atmospheres: an oxygen-reduced gas mixture or a 5% CO2-in-air atmosphere.

Findings

  • Among the five animals with B. caballi seropositivity, all were identified as carriers when the cultures were initiated under an oxygen-reduced atmosphere. When the cultures were initiated under normal atmospheric conditions, only four became culture positive.
  • Within the eight samples that were seropositive for both B. caballi and T. equi, two were found to be carriers of both parasites. The remaining six samples were found to be carrying only T. equi.
  • The experiment highlighted the significance of atmospheric conditions in the successful culture of B. caballi.

Implications

  • The findings of this study on the culture, isolation, and propagation of B. caballi may have applications in diagnosing and controlling the spread of equine babesiosis in areas where the disease is prevalent.
  • Identifying and understanding carriers of B. caballi (that do not show any symptoms) is crucial in managing and combating Babesia infection at an epidemiological level.
  • The study further underscores the importance of environmental conditions (such as atmosphere) during in vitro culture of parasites for efficient results.

Cite This Article

APA
Zweygarth E, Lopez-Rebollar LM, Nurton J, Guthrie AJ. (2002). Culture, isolation and propagation of Babesia caballi from naturally infected horses. Parasitol Res, 88(5), 460-462. https://doi.org/10.1007/s00436-002-0609-4

Publication

ISSN: 0932-0113
NlmUniqueID: 8703571
Country: Germany
Language: English
Volume: 88
Issue: 5
Pages: 460-462

Researcher Affiliations

Zweygarth, Erich
  • Onderstepoort Veterinary Institute, Parasitology Division, South Africa. erich@moon.ovi.ac.za
Lopez-Rebollar, Laura M
    Nurton, Jane
      Guthrie, Alan J

        MeSH Terms

        • Animals
        • Antibodies, Protozoan / blood
        • Babesia / growth & development
        • Babesia / isolation & purification
        • Babesiosis / parasitology
        • Babesiosis / veterinary
        • Carrier State / parasitology
        • Culture Media
        • Horse Diseases / parasitology
        • Horses / parasitology
        • Oxygen / pharmacology
        • Parasitology / methods

        Citations

        This article has been cited 7 times.
        1. Tirosh-Levy S, Gottlieb Y, Fry LM, Knowles DP, Steinman A. Twenty Years of Equine Piroplasmosis Research: Global Distribution, Molecular Diagnosis, and Phylogeny. Pathogens 2020 Nov 8;9(11).
          doi: 10.3390/pathogens9110926pubmed: 33171698google scholar: lookup
        2. Montes-Cortés MG, Fernández-García JL, Martínez-Estéllez MÁH. Genetic Variation of the β-tubulin Gene of Babesia caballi Strains. J Arthropod Borne Dis 2017 Sep;11(3):344-353.
          pubmed: 29322051
        3. Malekifard F, Tavassoli M, Yakhchali M, Darvishzadeh R. Detection of Theileria equi and Babesia caballi using microscopic and molecular methods in horses in suburb of Urmia, Iran. Vet Res Forum 2014 Spring;5(2):129-33.
          pubmed: 25568706
        4. Zweygarth E, Josemans AI. L-cysteine replaces microaerophilous culture conditions for the in vitro initiation of Theileria equi. Parasitol Res 2014 Jan;113(1):433-5.
          doi: 10.1007/s00436-013-3672-0pubmed: 24257973google scholar: lookup
        5. Jaffer O, Abdishakur F, Hakimuddin F, Riya A, Wernery U, Schuster RK. A comparative study of serological tests and PCR for the diagnosis of equine piroplasmosis. Parasitol Res 2010 Feb;106(3):709-13.
          doi: 10.1007/s00436-009-1669-5pubmed: 19894063google scholar: lookup
        6. Alhassan A, Govind Y, Tam NT, Thekisoe OM, Yokoyama N, Inoue N, Igarashi I. Comparative evaluation of the sensitivity of LAMP, PCR and in vitro culture methods for the diagnosis of equine piroplasmosis. Parasitol Res 2007 Apr;100(5):1165-8.
          doi: 10.1007/s00436-006-0430-6pubmed: 17216488google scholar: lookup
        7. Axt CW, Springer A, Strube C, Jung C, Naucke TJ, Müller E, Schäfer I. Molecular and Serological Detection of Vector-Borne Pathogens Responsible for Equine Piroplasmosis in Europe between 2008 and 2021. Microorganisms 2024 Apr 17;12(4).