Abstract
The black-backed jackal has proven difficult to study in the wild due to its elusive behaviour. As a rabies vector and predator of livestock, understanding dispersal patterns and population structure is of importance when considering the management of this species in South Africa's rural areas. We have characterised a suite of six cross-species microsatellite markers suitable for this purpose and present a method to isolate suitable quantities of host DNA from faeces in order to undertake endpoint PCR. Allelic dropout and null allele frequencies were shown to be negligible for all loci. No evidence of selection could be detected at any of the loci examined. The genotype frequencies of the total sampled population were tested for concordance with Hardy-einberg equilibrium. No significant deficit of heterozygote individuals was detected globally when tested by locus and marker set. An excess of heterozygosity was recorded at three loci within a single study site. The total inbreeding coefficient FST was calculated at 3% across the sampled population. The average DNA copy number recovered from faecal deposits was quantified using a qPCR-TacMan reporter probe method. The results of this study indicate that the quantity of DNA recovered from faeces was sufficient to undertake endpoint PCR.
Original language | English |
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Pages (from-to) | 1-21 |
Number of pages | 21 |
Journal | Cogent Biology |
Issue number | 1 |
DOIs | |
Publication status | Published - 1 Nov 2015 |
Bibliographical note
© 2015 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.Keywords
- microsatellite
- black-backed jackal
- qPCR
- faeces
- non-invasive genetic sampling
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Andrew Overall
- School of Applied Sciences - Senior Lecturer
- Ecology, Conservation and Society Research Excellence Group
Person: Academic