Trypanosoma evansi: molecular homogeneity as inferred by phenetical analysis of ribosomal internal transcribed spacers DNA of an eclectic parasite.
Abstract: The protozoan Trypanosoma evansi is described as presenting high morphological and genetic similarities among the isolates despite its biological heterogeneity and wide geographical distribution. PCR amplification of the internal transcribed spacers of the ribosomal gene in combination with the coding region of the 5.8S ribosomal subunit further submitted to restriction enzymes digestion were carried out in DNAs extracted from 41 T. evansi strains isolated from horses, dogs, coatis and capybaras from two distinct regions of the Brazilian Pantanal. We also used one T. evansi isolate from Africa, one from Asia and one isolate of T. b. brucei from Africa. Analysis of the RFLP profiles yielded a unique "riboprinting" that does not vary intraspecifically. These results provide insights on the ribosomal gene organization of T. evansi and showed that ITS analysis by RFLP show high genetic similarity of this locus among isolates of this protozoan parasite.
Publication Date: 2007-10-12 PubMed ID: 18158150DOI: 10.1016/j.exppara.2007.10.003Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research explores the genetic similarity and molecular homogeneity of the parasitic protozoan, Trypanosoma evansi, across different geographical regions and hosts, using sophisticated DNA methodologies like PCR amplification and analysis of restriction fragment length polymorphism (RFLP).
Objective and Methods Used
- The primary objective of this study was to investigate the variety or homogeneity among different strains of the parasite T. evansi on a molecular level.
- The researchers used various strains isolated from different host species (dogs, horses, coatis, capybaras) from two distinct regions of the Brazilian Pantanal, as well as one isolate each from Africa and Asia, and a strain of T. b. brucei from Africa.
- DNA was extracted from these strains and a technique called PCR (Polymerase Chain Reaction) was used to amplify the ribosomal genes. More specifically, the internal transcribed spacers of the ribosomal gene and the coding region for the 5.8S ribosomal subunit were focused on.
- The amplified DNA was further subjected to restriction enzymes digestion. These enzymes cut the DNA strand into specific sites, creating a set of unique fragments for each DNA sequence.
- The resulting fragments (or restriction fragment length polymorphisms – RFLP) were then analysed to generate a unique “riboprint” for each strain.
Findings and Interpretation
- The study shows that, despite the biological diversity and wide geographic distribution of the T. evansi parasite, there is a high level of genetic similarity among its isolates.
- All analysed strains produced an identical “riboprint” for the sections of the ribosomal gene studied, indicating a high level of genetic homogeneity. The implication here is that the internal genetic mechanisms of T. evansi are highly conserved, irrespective of the host animal or the parasite’s region of origin.
- The results provide new insights into the organizational structure of the ribosomal genes of T. evansi and confirm the stability of these genomic regions in this parasite.
- Such genetic stability can be an important factor in the adaptability and survival of the parasite across different hosts and environments.
- The study also displays the usefulness of methods like PCR and RFLP in studying genetic homogeneity or variability in parasitic organisms, and the potential implications such knowledge may have on parasite control and treatment strategies.
Cite This Article
APA
de Oliveira Lima AN, da Silva Santos S, Herrera HM, Gama C, Cupolillo E, Jansen AM, Fernandes O.
(2007).
Trypanosoma evansi: molecular homogeneity as inferred by phenetical analysis of ribosomal internal transcribed spacers DNA of an eclectic parasite.
Exp Parasitol, 118(3), 402-407.
https://doi.org/10.1016/j.exppara.2007.10.003 Publication
Researcher Affiliations
- Laboratory of Tripanosomatid Biology, Oswaldo Cruz Institute, FIOCRUZ, Av. Brasil 4365, CEP. 21040-360, Rio de Janeiro/RJ, Brazil.
MeSH Terms
- Animals
- Brazil
- Camelus
- Cattle
- China
- DNA, Protozoan / chemistry
- DNA, Ribosomal Spacer / chemistry
- Dogs
- Ethiopia
- Horses
- Phylogeny
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Procyonidae
- Rodentia
- Sheep
- Trypanosoma / classification
- Trypanosoma / genetics
- Trypanosoma brucei brucei / classification
- Trypanosoma brucei brucei / genetics
- Uganda
Citations
This article has been cited 4 times.- Dantas-Torres F, Otranto D. Dogs, cats, parasites, and humans in Brazil: opening the black box.. Parasit Vectors 2014 Jan 14;7:22.
- Desquesnes M, Holzmuller P, Lai DH, Dargantes A, Lun ZR, Jittaplapong S. Trypanosoma evansi and surra: a review and perspectives on origin, history, distribution, taxonomy, morphology, hosts, and pathogenic effects.. Biomed Res Int 2013;2013:194176.
- Pourjafar M, Badiei K, Sharifiyazdi H, Chalmeh A, Naghib M, Babazadeh M, Mootabi Alavi A, Hosseini Joshani-Zadeh N. Genetic characterization and phylogenetic analysis of Trypanosoma evansi in Iranian dromedary camels.. Parasitol Res 2013 Feb;112(2):899-903.
- Salim B, de Meeûs T, Bakheit MA, Kamau J, Nakamura I, Sugimoto C. Population genetics of Trypanosoma evansi from camel in the Sudan.. PLoS Negl Trop Dis 2011 Jun;5(6):e1196.
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