PCR tools for the verification of the specific identity of ascaridoid nematodes from dogs and cats

• Published in: Molecular and cellular probes Vol. 21; no. 5; pp. 349 - 354
• Main Authors: Li, M.W., Lin, R.Q., Chen, H.H., Sani, R.A., Song, H.Q., Zhu, X.Q.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.10.2007
• Subjects: Animals; Cat; Cats; DNA, Ribosomal Spacer - analysis; DNA, Ribosomal Spacer - genetics; Dog; Dogs; Internal transcribed spacers (ITS); Polymerase chain reaction (PCR); Polymerase Chain Reaction - methods; Toxascaris leonina; Toxocara - genetics; Toxocara - isolation & purification; Toxocara canis; Toxocara cati; Toxocara malaysiensis; Toxocara canis; Internal transcribed spacers (ITS); Toxocara cati; Polymerase chain reaction (PCR); Cat; Toxascaris leonina; Dog; Toxocara malaysiensis
• ISSN: 0890-8508; 1096-1194
• DOI: 10.1016/j.mcp.2007.04.004

Based on the sequences of the internal transcribed spacers (ITS-1 and ITS-2) of nuclear ribosomal DNA (rDNA) of Toxocara canis, Toxocara cati, Toxocara malaysiensis and Toxascaris leonina, specific forward primers were designed in the ITS-1 or ITS-2 for each of the four ascaridoid species of dogs and cats. These primers were used individually together with a conserved primer in the large subunit of rDNA to amplify partial ITS-1 and/or ITS-2 of rDNA from 107 DNA samples from ascaridoids from dogs and cats in China, Australia, Malaysia, England and the Netherlands. This approach allowed their specific identification, with no amplicons being amplified from heterogeneous DNA samples, and sequencing confirmed the identity of the sequences amplified. The minimum amounts of DNA detectable using the PCR assays were 0.13–0.54 ng. These PCR assays should provide useful tools for the diagnosis and molecular epidemiological investigations of toxocariasis in humans and animals.