V. Snabel et al., Estimating the genetic divergence and identification of three Trichinella species by isoenzyme analysis, PARASITE, 8(2), 2001, pp. S30-S33
Citations number
16
Categorie Soggetti
Biology
Journal title
PARASITE-JOURNAL DE LA SOCIETE FRANCAISE DE PARASITOLOGIE
Isoenzyme-based approach was applied to compare Trichinella spiralis, T. br
itovi and T. pseudospiralis species. Among 13 enzyme systems examined, este
rase (EST), malic enzyme (ME) and phosphoglucomutase (PGM) have been found
as fully diagnostic, with no common allele in species studied. Adenosine de
aminase (ADA), adenylate kinase (AK), hexokinase (HK), peptidase leucyl-ala
nine (PEP-C) and fructose-bis-phosphatase (FBP) have been capable of distin
guishing 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 mul of extracts). Based on allozyme data,
T. pseudospiralis has been found as the most distinct species within the g
roup of taxa. Only a subtle genetic variability was recorded for T. pseudos
piralis in which solely phosphoglucomutase exhibited variant patterns. In a
ddition to the study of reference isolates, T. spiralis from lowland fox in
Eastern Slovakia has been evidenced by use of genetic markers. This findin
g has proved that T. britovi is not the exclusive species parasitizing in t
he sylvatic ecosystem of the Slovak region.