Analyze Diet
Parasitology research1991; 77(2); 177-179; doi: 10.1007/BF00935433

Enrichment of Babesia caballi-infected erythrocytes from microaerophilous stationary-phase cultures using Percoll gradients.

Abstract: A rapid and simple method for concentrating leucocyte-free Babesia caballi-infected erythrocytes from in vitro cultures is described. Infected erythrocytes amounted to at least 95% of all red cells obtained.
Publication Date: 1991-01-01 PubMed ID: 2027885DOI: 10.1007/BF00935433Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research paper discusses a fast and easy method developed for collecting Babesia caballi-infected red blood cells (erythrocytes) in an environment that mimics the parasite’s natural growth conditions.

Background of Research

  • The research is primarily based on Babesia caballi, parasites that infect red blood cells in numerous mammalian species, particularly causing disease in horses.
  • These parasites live and multiply in the host animal’s red blood cells, causing the destruction of these cells and severe, sometimes fatal, illness.
  • Understanding the behavior of these parasites in red blood cells is crucial for developing effective treatments or preventive measures.
  • The concentration of the infected red blood cells in a controlled environment aids researchers in understanding the interaction between the host cells and the parasite.

The Method

  • In this paper, the researchers describe a method to concentrate infected red blood cells from in vitro cultures.
  • The technique involves culturing the parasites in a microaerophilous stationary-phase culture. This culture condition mimics the parasite’s natural environment inside the host.
  • The researchers employ Percoll gradients, a solution used to separate cells based on their density, to obtain a higher concentration of infected cells.
  • With this method, they reported that at least 95% of the erythrocytes obtained were infected with Babesia caballi.

Significance of the Research

  • This simple and quick method allows for the enrichment and isolation of infected red blood cells, facilitating detailed studies on the parasite’s behavior.
  • The research provides a promising tool for investigating the interaction between Babesia caballi and their host cells, potentially offering crucial insights for the intervention or prevention of related diseases.
  • Lastly, the information gained from this method can be used to develop effective treatments and prevention strategies for infections caused by the Babesia caballi parasites in horses and possibly in other mammals.

Cite This Article

APA
Bhushan C, Müller I, Friedhoff KT. (1991). Enrichment of Babesia caballi-infected erythrocytes from microaerophilous stationary-phase cultures using Percoll gradients. Parasitol Res, 77(2), 177-179. https://doi.org/10.1007/BF00935433

Publication

ISSN: 0932-0113
NlmUniqueID: 8703571
Country: Germany
Language: English
Volume: 77
Issue: 2
Pages: 177-179

Researcher Affiliations

Bhushan, C
  • Institut für Parasitologie, Hannover, Federal Republic of Germany.
Müller, I
    Friedhoff, K T

      MeSH Terms

      • Animals
      • Babesia / physiology
      • Babesiosis / blood
      • Cell Separation
      • Centrifugation, Density Gradient
      • Erythrocytes / parasitology
      • Horse Diseases / blood
      • Horses

      References

      This article includes 8 references
      1. Kramer KJ, Kan SC, Siddiqui WA. Concentration of Plasmodium falciparum-infected erythrocytes by density gradient centrifugation in Percoll.. J Parasitol 1982 Apr;68(2):336-7.
        pubmed: 6281409
      2. Levy MG, Ristic M. Babesia bovis: continuous cultivation in a microaerophilous stationary phase culture.. Science 1980 Mar 14;207(4436):1218-20.
        pubmed: 7355284doi: 10.1126/science.7355284google scholar: lookup
      3. Pertoft H, Rubin K, Kjellén L, Laurent TC, Klingeborn B. The viability of cells grown or centrifuged in a new density gradient medium, Percoll(TM).. Exp Cell Res 1977 Dec;110(2):449-57.
        pubmed: 201479doi: 10.1016/0014-4827(77)90311-1google scholar: lookup
      4. Andrysiak PM, Collins WE, Campbell GH. Concentration of Plasmodium ovale- and Plasmodium vivax-infected erythrocytes from nonhuman primate blood using Percoll gradients.. Am J Trop Med Hyg 1986 Mar;35(2):251-4.
        pubmed: 3006527doi: 10.4269/ajtmh.1986.35.251google scholar: lookup
      5. Mahoney DF. Bovine babesiosis: preparation and assessment of complement fixing antigens.. Exp Parasitol 1967 Apr;20(2):232-41.
        pubmed: 4962449doi: 10.1016/0014-4894(67)90043-4google scholar: lookup
      6. WATKINS RG. A concentration and staining technique for diagnosing equine piroplasmosis.. J Am Vet Med Assoc 1962 Dec 1;141:1330-2.
        pubmed: 13999174
      7. Vega CA, Buening GM, Rodriguez SD, Carson CA. Concentration and enzyme content of in vitro-cultured Babesia bigemina-infected erythrocytes.. J Protozool 1986 Nov;33(4):514-8.
      8. Richards WH, Williams SG. The removal of leucocytes from malaria infected blood.. Ann Trop Med Parasitol 1973 Jun;67(2):249-50.
        pubmed: 4578939doi: 10.1080/00034983.1973.11686885google scholar: lookup

      Citations

      This article has been cited 3 times.
      1. Zhao J, Liu Z, Yao B, Ma L. Studies on the in vitro cultivation of Babesia from buffaloes.. Trop Anim Health Prod 1997 Nov;29(4 Suppl):37S-39S.
        doi: 10.1007/BF02632915pubmed: 9512743google scholar: lookup
      2. Hauschild S, Shayan P, Schein E. Characterization and comparison of merozoite antigens of different Babesia canis isolates by serological and immunological investigations.. Parasitol Res 1995;81(8):638-42.
        doi: 10.1007/BF00931839pubmed: 8570577google scholar: lookup
      3. Böse R, Peymann B, Barbosa IP. Identification of diagnostic antigens for South American Babesia caballi infections.. Int J Parasitol 1994 Apr;24(2):255-8.
        doi: 10.1016/0020-7519(94)90034-5pubmed: 8026903google scholar: lookup