Abstract

Human and animal health is globally affected by a variety of parasitic helminths. The impact of co-infections and development of anthelmintic resistance requires improved diagnostic tools, especially for parasitic nematodes e.g., to identify resistant species or attribute pathological effects to individual species or particular species combinations. In horses, co-infection with cyathostomins is rather a rule than an exception with typically 5 to 15 species (out of more than 40 described) per individual host. In cyathostomins, reliable morphological species differentiation is currently limited to adults and requires highly specialized expertize while precise morphological identification of eggs and early stage larvae is impossible. The situation is further complicated by a questionable validity of some cyathostomins while others might actually represent cryptic species complexes. Several molecular methods using different target sequences were established to overcome these limitations. For adult worms, PCR followed by sequencing of mitochondrial genes or external or internal ribosomal RNA spacers is suitable to genetically confirm morphological identifications. The most commonly used method to differentiate eggs or larvae is the reverse-line-blot hybridization assay. However, both methods suffer from the fact that target sequences are not available for many species or even that GenBank® entries are unreliable regarding the cyathostomin species. Recent advances in proteomic tools for identification of metazoans including insects and nematodes of the genus Trichinella will be evaluated for suitability to diagnose cyathostomins. Future research should focus on the comparative analysis of morphological, molecular and proteomic data from the same cyathostomin specimen to optimize tools for species-specific identification.

Highlights

  • Parasitic helminths globally affect human and animal health and can be of zoonotic relevance (e.g., Ascaris spp.)

  • The most important intestinal nematodes belong to the family Strongylidae and are comprised of two subfamilies: The Strongylinae encompassing 14 species in 5 genera (Strongylus, Oesophagodontus, Triodontophorus, Bidentostomum, and Craterostomum), and the Cyathostominae encompassing currently 50 valid species in 14 genera

  • 100% prevalence in equids (Lyons et al, 1999), (ii) numerous reports of anthelmintic resistance and (iii) their pathogenicity which becomes manifest in cases of sometimes fatal larval cyathostominosis (Love et al, 1999)

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Summary

INTRODUCTION

Parasitic helminths globally affect human and animal health and can be of zoonotic relevance (e.g., Ascaris spp.). Cyathostomins are a threat to equine welfare and scientific efforts to address this problem are frequently undertaken, research is impaired by the lack of sufficient identification methods (Lichtenfels, 2008). Morphological identification of adult strongyles relies on careful examination of faint characters at the anterior end of the adult nematodes or of the reproductive system. These traits include the size and shape of buccal capsules, internal and external leaf crowns and its extra-chitinous support as illustrated in Figure 1 to point out that differences are very faint. The morphological features include qualitative and quantitative traits such as the number, arrangement and shape of intestinal/midgut cells, the length of the intestine and the length of the sheath tail

MOLECULAR METHODS
SEROLOGICAL METHODS
PROTEOMICS METHOD
PROTEMICS METHOD
CONCLUSION
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