Results of the RLB and modified <i>cox</i> III qPCR assays for selected samples and clones.

*<p>Indicates a non-species specific melting peak located between the peaks for the species indicated in brackets.</p>**<p>Did not cluster with any of the other sequences and its identity could not be established.</p

Origin and no. of samples analysed by the modified <i>cox</i> III qPCR assay.

*<p>SA – South Africa.</p>**<p>Cattle.</p

Phylogenetic relationships of the <i>cox</i> III gene sequence variants of <i>Theileria</i> spp.

<p>The figure shows sequences identified in this study (black) with <i>Theileria</i> control sequences (bold) and published <i>Theileria</i> spp. (italics). Bootstrap values indicate the degree of support for each cluster. The tree was outgroup rooted using the <i>cox</i> III gene sequence of <i>T. annulata</i>.</p

Occurrence of <i>Theileria</i> species infections in buffalo and cattle samples from South Africa and Mozambique.

<p>(a) As determined by the RLB and <i>cox</i> III qPCR assays (n = 224). The number of samples with non-species specific melting temperatures on the <i>cox</i> III qPCR assay (*) and those that hybridized only with the <i>Theileria</i>/<i>Babesia</i> genus-specific probes using the RLB assay (**) are shown. (b) Comparison of the RLB, 18S qPCR and <i>cox</i> III qPCR assays for detection of <i>T. parva</i> (n = 206).</p

Alignment of the probe area of the <i>cox</i> III gene sequences.

<p>The modified anchor (light blue shading) and sensor (yellow shading) probe sequences are indicated. <i>cox</i> III sequences were obtained from clones from control samples (blue text) and clones from selected African buffalo samples. Differences are based on the <i>cox</i> III sequence of <i>T. mutans</i> (ZAM/C9142.2). The identified <i>cox</i> III sequence variants are indicated.</p