Murdoch University Research Repository

Welcome to the Murdoch University Research Repository

The Murdoch University Research Repository is an open access digital collection of research
created by Murdoch University staff, researchers and postgraduate students.

Learn more

Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia

Dawood, K.E., Morgan, J.A.T., Busfield, F., Srivastava, M., Fletcher, T.I., Sambono, J., Jackson, L.A., Venus, B., Philbey, A.W. and Lew-Tabor, A.E. (2013) Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia. International Journal for Parasitology: Parasites and Wildlife, 2 . pp. 54-61.

PDF - Published Version
Download (1MB)
Free to read:
*No subscription required


Laboratory confirmation methods are important in bovine cysticerosis diagnosis as other pathologies can result in morphologically similar lesions resulting in false identifications. We developed a probe-based real-time PCR assay to identify Taenia saginata in suspect cysts encountered at meat inspection and compared its use with the traditional method of identification, histology, as well as a published nested PCR. The assay simultaneously detects T. saginata DNA and a bovine internal control using the cytochrome c oxidase subunit 1 gene of each species and shows specificity against parasites causing lesions morphologically similar to those of T. saginata. The assay was sufficiently sensitive to detect 1 fg (Ct 35.09 ± 0.95) of target DNA using serially-diluted plasmid DNA in reactions spiked with bovine DNA as well as in all viable and caseated positive control cysts. A loss in PCR sensitivity was observed with increasing cyst degeneration as seen in other molecular methods. In comparison to histology, the assay offered greater sensitivity and accuracy with 10/19 (53%) T. saginata positives detected by real-time PCR and none by histology. When the results were compared with the reference PCR, the assay was less sensitive but offered advantages of faster turnaround times and reduced contamination risk. Estimates of the assay's repeatability and reproducibility showed the assay is highly reliable with reliability coefficients greater than 0.94.

Item Type: Journal Article
Murdoch Affiliation(s): Centre for Comparative Genomics
Publisher: Elsevier Limited
Copyright: © 2013. Published by Elsevier B.V.
Item Control Page Item Control Page


Downloads per month over past year