Molecular Identification ofIntermediate Hosts by Nested PCR Using Internal Transcribed Spacer 1 (ITS1).

Abstract

Recently, the heteroxenous eyeworm,has gained attention due to its prevalence in the declining game bird, Northern bobwhite (), but the intermediate hosts of many nematodes remain unknown. However, identifying the intermediate host ofwith traditional techniques would be difficult and time-consuming, especially considering there are more than 80 potential orthopteran hosts just in Texas. To screen a large number of samples quickly and effectively, primers for nested PCR (nPCR) were developed using the internal transcribed spacer 1 (ITS1) region. Then the nPCR was used to identify which of the 35 species collected from the Order Orthoptera were potential intermediate hosts of. With this technique, 18 potential intermediate hosts were identified. Later, we collected live specimens of species that tested positive to confirm the presence of larvae, but larvae were not found in the live specimens, nor in the extra tissue of the species that had tested positive forDNA. Despite this, this study demonstrated that nPCR is more sensitive than traditional techniques and can be a valuable tool in determining the intermediate hosts of parasites.