Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/19653
Appears in Collections:Biological and Environmental Sciences Journal Articles
Peer Review Status: Refereed
Title: Effects of storage type and time on DNA amplification success in tropical ungulate faeces
Authors: Soto-Calderon, Ivan D
Ntie, Stephan
Mickala, Patrick
Maisels, Fiona
Wickings, E Jean
Anthony, Nicola M
Contact Email: boo.maisels@stir.ac.uk
Keywords: faeces
microsatellite
mitochondrial DNA
quantitative PCR
storage
ungulate
Issue Date: Mar-2009
Publisher: Wiley-Blackwell
Citation: Soto-Calderon ID, Ntie S, Mickala P, Maisels F, Wickings EJ & Anthony NM (2009) Effects of storage type and time on DNA amplification success in tropical ungulate faeces, Molecular Ecology Resources, 9 (2), pp. 471-479.
Abstract: The present study compares the effect of three storage media (silica, RNAlater®, ethanol) and time to extraction (1 week, 1 month and 3 months) on mitochondrial and nuclear marker amplification success in faecal DNA extracts from a sympatric community of small to medium-sized Central African forest ungulates (genera Cephalophus, Tragelaphus, Hyemoschus). The effect of storage type and time on nuclear DNA concentrations, genotyping errors and percentage recovery of consensus genotypes was also examined. Regardless of storage method, mitochondrial and nuclear amplification success was high in DNA extracted within the first week after collection. Over longer storage periods, RNAlater yielded better amplification success rates in the mitochondrial assay. However, samples stored on silica showed (i) highest nuclear DNA concentrations, (ii) best microsatellite genotyping success, (iii) lowest genotyping errors, and (iv) greatest percentage recovery of the consensus genotype. The quantity of nuclear DNA was generally a good predictor of microsatellite performance with 83% amplification success or greater achieved with sample DNA concentrations of ≥ 50 pg/µL. If faecal DNA samples are to be used for nuclear microsatellite analyses, we recommend silica as the best storage method. However, for maximum mitochondrial amplification success, RNAlater appears to be the best storage medium. In contrast, ethanol appeared inferior to the other two methods examined here and should not be used to store tropical ungulate faeces. Regardless of storage method, samples should be extracted as soon as possible after collection to ensure optimal recovery of DNA.
Type: Journal Article
URI: http://hdl.handle.net/1893/19653
DOI Link: http://dx.doi.org/10.1111/j.1755-0998.2008.02462.x
Rights: The publisher does not allow this work to be made publicly available in this Repository. Please use the Request a Copy feature at the foot of the Repository record to request a copy directly from the author. You can only request a copy if you wish to use this work for your own research or private study.
Affiliation: University of New Orleans
University of New Orleans
Universite des Sciences et Techniques de Masuku, Gabon
Wildlife Conservation Society (Africa Program)
Centre International de Recherches Médicales de Franceville
University of New Orleans

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