Species markers for equine strongyles detected in intergenic rDNA by PCR-RFLP

Abstract

Five species of equine strongyle belonging to the subfamily Strongylinae ( Strongylus edentatus, S. equinus, S. vulgaris, Oesophagodontus robustusand Triodontophorus serratus) and 11 species belonging to the subfamily Cyathostominae ( Poteriostomum imparidentatum, P. ratzii, Cylicocyclus insignis, Cc. leptostomus, Cc. nassatus, Cylicostephanus calicatus, Cs. longibursatus, Cs. goldi, Cyathostomum catinatum, Cy. labiatumand Cy. pateratum) were characterized using a polymerase chain reaction-linked restriction fragment length polymorphism technique (PCR-RFLP). Internal transcribed spacer ribosomal DNA was amplified from genomic DNA by polymerase chain reaction (PCR) using conserved primers, digested separately with six restriction endonucleases ( AluI, BfaI, CfoI, HaeIII, VspI and XbaI) and the fragments separated by agarose gel electrophoresis. The PCR products of the three Strongylusspecies were approx. 90–100 bp smaller in size compared with those of the other 13 species. The PCR-RFLP analysis of the rDNA region spanning the first and second internal transcribed spacers plus the 5·8S rDNA gene (ITS+) produced characteristic patterns for each of the 16 species examined, and no variation in RFLP patterns was detected within the species Cy. catinatum, where multiple isolates were analysed. The study demonstrates that the internal transcribed spacer sequences provide genetic markers for the species identification of a range of equine strongyles. These markers will be of use for the identification of egg and larval stages, where morphological characters alone are unreliable. The results also indicate that the spacer sequences will be of use to study the systematics of equine strongyles.