SNP discovery and characterisation in White Rhino (Ceratotherium simum) with application to parentage assignment

Abstract The white rhino is one of the great success stories of modern wildlife conservation, growing from as few as 50-100 animals in the 1880s, to approximately 20,000 white rhinoceros remaining today. However, illegal trade in conservational rhinoceros horns is adding constant pressure on remaining populations. Captive management of ex situ populations of endangered species using molecular methods can contribute to improving the management of the species. Here we compare for the first time the utility of 33 Single Nucleotide Polymorphisms (SNPs) and nine microsatellites (MS) in isolation and in combination for assigning parentage in captive White Rhinoceros. We found that a combined dataset of SNPs and microsatellites was most informative with the highest confidence level. This study thus provided us with a useful set of SNP and MS markers for parentage and relatedness testing. Further assessment of the utility of these markers over multiple (> three) generations and the incorporation of a larger variety of relationships among individuals (e.g. half-siblings or cousins) is strongly suggested

DNA extraction protocol for animal blood samples using the EZNA blood mini kit.

The E.Z.N.A. Blood DNA Mini Kit provides an easy and rapid method for the isolationof genomic DNA for consistent PCR and Southern analysis. Up to 250 μL fresh,frozen, or anticoagulated whole blood can be readily processed at one time. TheE.Z.N.A. Blood DNA Mini Kit can also be used for the preparation of genomic DNAfrom buffy coat, serum, plasma, saliva, buccal swabs, and other body fluids. TheE.Z.N.A. Blood DNA Kit allows for single or multiple simultaneous processing ofmultiple samples. There is no need for phenol/chloroform extractions, and timeconsuming steps are eliminated (e.g. precipitation using isopropanol or ethanol).Purified DNA obtained with the E.Z.N.A. Blood DNA Kit is ready for applications suchas PCR, restriction digestion, and Southern blotting

Lack of diversity at innate immunity Toll-like receptor genes in the Critically Endangered White winged Flufftail (Sarothrura ayresi)

The White-winged Flufftail (Sarothrura ayresi) population is listed as globally Critically Endangered. White-winged Flufftails are only known to occur, with any regularity, in the high-altitude wetlands of South Africa and Ethiopia. Threats to the species include the limited number of suitable breeding sites in Ethiopia and severe habitat degradation and loss both in Ethiopia and South Africa. Toll-like receptors (TLRs) are increasingly being studied in a variety of taxa as a broader approach to determine functional genetic diversity. In this study, we confirm low genetic diversity in the innate immune regions of the White-winged Flufftail similar to that observed in other bird species that have undergone population bottlenecks. Low TLR diversity in White-winged Flufftail indicates that this species is more likely to be threatened by changes to the environment that would potentially expose the species to new diseases. Thus, conservation efforts should be directed towards maintaining pristine habitat for White-winged Flufftail in its current distribution range. To date, no studies on immunogenetic variation in White-winged Flufftail have been conducted and to our knowledge, this is the first study of TLR genetic diversity in a critically endangered species

Complete mitochondrial genomes of the African clawless (Aonyx capensis) and spotted necked (Hydrictis maculicollis) otter: structure, annotation, and interspecies variation

Otters are flagship species for pristine habitats and their southernmost distribution in Africa includes two species; Aonyx capensis and Hydrictis maculicollis. Here, we present novel full mitochondrial genomes of these otter species. The comparable mitogenomes consist of 36 genes including 13 protein-coding genes, 2 ribosomal RNAs, and 22 tRNAs including a hypervariable region. Only 19 out of the 36 genes showed some level of variation between species with the smallest being trnV (68 bp difference) and the biggest being nad5 (1830 bp difference). Such variations may provide guidance in selecting gene regions during marker development for phylogenetic assessments