The first and second internal transcribed spacer sequences of 28 morphologi
cally-defined species of horse strongyle were characterized, and specific o
ligonucleotide primers were designed for some species based on the nucleoti
de differences. Utilizing these primers, a PCR approach was developed for t
he specific amplification of ribosomal DNA of Strongylus vulgaris, Cyathost
omum catinatum, Cylicocyclus nassatus, Cylicostephanus longibursatus or Cyl
icostephanus goldi. The method allowed the species-specific amplification o
f parasite DNA derived from faecal samples and/or copro-cultures, demonstra
ting the potential of thr approach for the diagnosis of equine strongyloido
sis. The establishment of this PCR assay also has implications for studying
the biology and epidemiology of equine strongyles and anthelmintic resista
nce using faecal egg count reduction tests.