Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-23T23:42:32.959Z Has data issue: false hasContentIssue false

Molecular characterization of a Toxocara variant from cats in Kuala Lumpur, Malaysia

Published online by Cambridge University Press:  01 August 1998

X. Q. ZHU
Affiliation:
Department of Veterinary Science, The University of Melbourne, 250 Princes Highway Werribee, Victoria 3030, Australia
D. E. JACOBS
Affiliation:
Department of Pathology and Infectious Diseases, The Royal Veterinary College, University of London, North Mymms, Hatfield AL9 7TA, UK
N. B. CHILTON
Affiliation:
Department of Veterinary Science, The University of Melbourne, 250 Princes Highway Werribee, Victoria 3030, Australia
R. A. SANI
Affiliation:
Faculty of Veterinary Medicine and Animal Science, Universiti Putra Malaysia, 43400, Serdang, Selangor DE, Malaysia
N. A. B. Y. CHENG
Affiliation:
Faculty of Veterinary Medicine and Animal Science, Universiti Putra Malaysia, 43400, Serdang, Selangor DE, Malaysia
R. B. GASSER
Affiliation:
Department of Veterinary Science, The University of Melbourne, 250 Princes Highway Werribee, Victoria 3030, Australia

Abstract

The ascaridoid nematode of cats from Kuala Lumpur, Malaysia, previously identified morphologically as Toxocara canis, was characterized using a molecular approach. The nuclear ribosomal DNA (rDNA) region spanning the first internal transcribed spacer (ITS-1), the 5·8S gene and the second internal transcribed spacer (ITS-2) was amplified and sequenced. The sequences for the parasite from Malaysian cats were compared with those for T. canis and T. cati. The sequence data showed that this taxon was genetically more similar to T. cati than to T. canis in the ITS-1, 5·8S and ITS-2. Differences in the ITS-1 and ITS-2 sequences between the taxa (9·4–26·1%) were markedly higher than variation between samples within T. canis and T. cati (0–2·9%). The sequence data demonstrate that the parasite from Malaysian cats is neither T. canis nor T. cati and indicate that it is a distinct species. Based on these data, PCR-linked restriction fragment length polymorphism (RFLP) and single-strand conformation polymorphism (SSCP) methods were employed for the unequivocal differentiation of the Toxocara variant from T. canis and T. cati. These methods should provide valuable tools for studying the life-cycle, transmission pattern(s) and zoonotic potential of this parasite.

Type
Research Article
Copyright
1998 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)