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Estimating the genetic divergence and identification of threetrichinellaspecies by isoenzyme analysis
- Source :
- Parasite, Vol 8, Pp S30-S33 (2001), University of Copenhagen
- Publication Year :
- 2001
- Publisher :
- EDP Sciences, 2001.
-
Abstract
- Isoenzyme-based approach was applied to compare Trichinella spiralis, T. britovi and T. pseudospiralis species. Among 13 enzyme systems examined, esterase (EST), malic enzyme (ME) and phosphoglucomutase (PGM) have been found as fully diagnostic, with no common allele in species studied. Adenosine deaminase (ADA), adenylate kinase (AK), hexokinase (HK), peptidase leucyl-alanine (PEP-C) and fructose-bis-phosphatase (FBP) have been capable of distinguishing the two species from resulting profiles. In addition, ADA, AK and PGM displayed the enzyme expression in the lowest amounts of muscle larvae in systems tested (100 larvae/100 microliters of extracts). Based on allozyme data, T. pseudospiralis has been found as the most distinct species within the group of taxa. Only a subtle genetic variability was recorded for T. pseudospiralis in which solely phosphoglucomutase exhibited variant patterns. In addition to the study of reference isolates, T. spiralis from lowland fox in Eastern Slovakia has been evidenced by use of genetic markers. This finding has proved that T. britovi is not the exclusive species parasitizing in the sylvatic ecosystem of the Slovak region.
- Subjects :
- Swine
diagnosis
Trichinella
Veterinary (miscellaneous)
Carnivora
Trichinella spiralis
Foxes
lcsh:Infectious and parasitic diseases
Trichinella britovi
Genetic variation
Animals
lcsh:RC109-216
Genetic variability
Phylogeny
Genetics
isoenzymes
biology
fungi
Genetic Variation
biology.organism_classification
Genetic divergence
isoelectrofocusing
Infectious Diseases
Genetic marker
Insect Science
Immunology
Raccoons
Animal Science and Zoology
Parasitology
Phosphoglucomutase
Subjects
Details
- ISSN :
- 17761042 and 1252607X
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Parasite
- Accession number :
- edsair.doi.dedup.....01f13e1b62ecf14ac53a23b7c0362404