No evidence that horn trimming affects white rhinoceros horn use during comfort behaviour and resource access

Rhino species use their horns in social interactions but also when accessing resources, rubbing and in interspecific defence. The current poaching crisis has seen southern white rhinos (Ceratotherium simum simum) increasingly dehorned as a conservation management practise, but few studies have evaluated whether the procedure has any behavioural effects. This study sought to document and describe horn-contingent behaviours during resource access, wallowing and rubbing in freeranging white rhinos and establish whether dehorning, also known as horn trimming, impacts on their frequency or function. Data were collected through camera trapping and field observations at two sites in South Africa. The results provide no evidence that dehorning disrupts digging behaviours during mineral consumption or wallowing and suggests that dehorning is unlikely to have a strong biological impact on resource access. Furthermore, the frequency of horn-rubbing behaviours did not appear to be influenced by levels of horn growth. This suggests the procedure has a limited impact on these aspects of the species’ ecology and provides support that dehorning can be employed as a management tool to reduce poaching in freeranging populations of white rhino.

Development and evaluation of indirect enzyme-linked immunosorbent assays for the determination of immune response to multiple clostridial antigens in vaccinated captive bred southern white rhinoceros (Ceratotherium simum simum)

Background An overall increase in poaching of white rhinoceros results in captive breeding becoming a significant component of white rhinoceros conservation. However, this type of conservation comes with its own difficulties. When wildlife is captured, transported and/or confined to a boma environment, they are more predisposed to diseases caused by bacterial organisms such as spore forming Clostridium spp. A southern white rhinoceros (Ceratotherium simum simum) population on a captive bred farm was suspected to be affected by Clostridium infections. These endangered animals were apparently exposed to Clostridium spp., in the conservation area previously used for cattle farming. The rhinoceros population on the breeding operation property was vaccinated with a multi-component clostridial vaccine registered for use in cattle. Multiple indirect enzyme-linked immunosorbent assays (iELISAs) were developed in order to evaluate the serum antibody titres of these vaccinated animals. In evaluating vaccine efficacy, the gold standard mouse neutralization test (MNT) was not available and therefore iELISAs were developed for the detection of serum antibodies to C. perfringens type A (alpha toxin), C. chauvoei (whole cell), C. novyi (alpha toxin), C. septicum (alpha toxin) and C. sordellii (lethal toxin) in the white rhinoceros population using international reference sera of equine origin. Antibody titres against each clostridial antigen was evaluated in the vaccinated white rhinoceros population (n = 75). Analytical specificity showed slight cross-reactions for C. chauvoei and C. perfringens type A with the other antigens. Individual assay cut-off values were calculated with 95% confidence. Coefficient of variance (CV) values for both the international reference sera and in-house control sera across all the antigens were well below 16%, indicating good assay repeatability. This convenient and fast assay is suitable for monitoring humoral immune responses to clostridial antigens in vaccinated white rhinoceroses. Results Checkerboard titrations indicated optimal antigen and antibody concentrations to be used for each respective iELISA developed. Each titration set of the respective international reference and in-house control sera showed good repeatability with low standard deviations and coefficient of variance values calculated between repeats for each antigen. Individual assays proved repeatable and showed good analytical sensitivity and specificity. Conclusions The developed iELISAs are able to evaluate antibody profiles of phospholipase C, C. chauvoei whole cells, TcnA, ATX, TcsL in white rhinoceros serum using international reference sera.