E. Eszterbauer et al., Identification of fish-parasitic Myxobolus (Myxosporea) species using a combined PCR-RFLP method, DIS AQU ORG, 44(1), 2001, pp. 35-39
Polymerase chain reaction (PCR) with primers specific for the family Myxobo
lidae was used to amplify a part of the 18S ribosomal RNA gene of Myxobolus
species. The length of the amplified fragments was approximately 1600 base
pairs. Six Myxobolus species identified on the basis of morphological feat
ures were compared using a combined PCR-RFLP method. The cleavage patterns
generated by 2 frequent cutter restriction enzymes (HinfI and MspI) were su
itable for the differentiation of the examined Myxobolus species.