Studying the genetic variability of endangered species is becoming increasingly necessary for species conservation and monitoring. But, endangered species are difficult to observe and sample, and typically harbour very limited genetic diversity.
This is a Bornean elephant in the wild.
Credit: Rudi Delvaux/DGFC
Until now, the process of finding genetic markers was time consuming and quite expensive. These obstacles make the collection of genetic data from endangered animals a difficult task to fulfill.
A research team led by Lounès Chikhi (http://www.igc.gulbenkian.pt/research/unit/88), group leader at the Instituto Gulbenkian de Ciência (IGC) and CNRS researcher (http://www.edb.ups-tlse.fr/Chikhi-Lounes.html) (in Toulouse, France), has now contributed to change the odds when looking for diversity.
Taking advantage of cutting edge DNA sequencing methodology and the collaborations with the Sabah Wildlife Department in Malaysia, Rachel O'Neill's laboratory (http://www.mcb.uconn.edu/fac.php?name=oneillrj) (University of Connecticut) and a private company (Floragenex, http://www.floragenex.com/), they were able to identify the genetic markers for the Bornean elephant, an endangered species, using blood from very few animals.
The results showed that Bornean elephants have very low genetic variability that can impact on their survival to a threatened habitat, but that variable genetic markers can still be identified. The study now published in the journal PLOS ONE*, besides contributing to the conservation of the Bornean elephant, opens new avenues for the conservation of other endangered species.
The Bornean elephant is a unique subspecies of the Asian elephant, with a quite distinct morphology and behavior. They are generally smaller than other elephants, with straight tusks and a long tail. Currently, there are around 2000 individuals, located only in the North of Borneo. It remains unknown how this population of elephants evolved to become so different and why its distribution is so restricted.
Despite being one of the highest priority populations for Asian elephant conservation, until now there were limited genetic tools available to study its genetic variability and none that had been specifically designed for this species. Now, in the work conducted by Reeta Sharma, a Post-Doctoral fellow in Lounès Chikhi's group, for the first time DNA sequences that characterize the genome of the Bornean elephants, called genetic markers, were identified. The research team used two different DNA sequencing technologies that are fast and increasingly cheaper. This kind of technology has been used for common laboratory species such as mice and fruit-flies, but they are only now starting to be used on endangered and "non-model" species.
Until now, in order to determine whether the species still harboured sufficient genetic diversity it was necessary to look through huge regions of the genome, using classical genetics methodologies, or use markers developed for other species, with varying levels of success. This approach can become unsustainable for the endangered species, whose numbers have gone bellow a certain size for long time. The only study that previously had tried to analyse Bornean elephants, using genetic markers developed for other Asian elephants had found nearly no genetic diversity. The work now developed demonstrates that if the methodology can be applied to the Bornean elephant, it should be possible to find the needles we need, and not get stuck with the hay, i.e., to find variable genetic markers in many other species.
The DNA analysis done resulted from blood samples collected only from seven Bornean elephants from the Lok Kawi Wildlife Park (Sabah, Malaysia) and from Chendra, the star elephant of Oregon zoo (Portland, USA). But, the research team is confident that these DNA sequencing methods can be used to type genetically other biological samples, such as hair or faeces, easier to obtain from wild animals, even though blood or tissue samples are still necessary to identify the markers during the first steps.
Reeta Sharma, first author of this work, says: 'The methodology applied to identify the genetic markers for the Bornean elephant can be used in the future for studies on the genetic variability of other species or populations facing the risk of extinction.'
The Bornean elephants live in an environment where natural habitats disappear quickly, due to oil palm plantations and populations get isolated from each other. Having access to variable genetic markers will be crucial to identify populations that are isolated and genetically depauperate, and monitor them in the future.
The origin of these elephants in Borneo raises controversy that has been long discussed. The only study done on the basis of genetic data concluded that they had been present in Borneo for more than 300,000 years. This theory does not satisfy all researchers as there is lack of elephant fossils in Borneo to support it. Another theory is that the sultan of Java sent Javan elephants as a gift to the sultan of Sulu, who would have introduced them to Borneo.Lounes Chikhi suggests: 'The new genetic markers that we found may also allow us to unravel the mystery of the origin of these elephants in Borneo, and perhaps reconstruct part of their demographic history. This is very exciting '.
This research was carried out at the IGC in collaboration with the Laboratoire Evolution et Diversité Biologique in Toulouse, and with the School of Biosciences, Cardiff University (UK), the Sabah Wildlife Department (Malaysia), the Danau Girang Field Centre (Malaysia), the Center for Applied Genetics and Technology, University of Connecticut (USA) and Floragenex, Inc. (USA). Research was funded mainly by Fundação para a Ciência e a Tecnologia (FCT), Portugal, and Laboratoire d'Excellence (LABEX), France.
* Sharma R, Goossens B, Kun-Rodrigues C, Teixeira T, Othman N, Boone JQ, Jue NK, Obergfell C, O'Neill RJ and Chikhi L (2012) Two Different High Throughput Sequencing Approaches Identify Thousands of De Novo Genomic Markers for the Genetically Depleted Bornean Elephant. PLoS ONE 7(11): e49533. doi:10.1371/journal.pone.0049533
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