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1.
Mol Biol Rep ; 49(11): 11177-11186, 2022 Nov.
Article in English | MEDLINE | ID: mdl-36097126

ABSTRACT

BACKGROUND: Populations exhibit signatures of local adaptive traits due to spatial and environmental heterogeneity resulting in microevolution. The blue sheep is widely distributed across the high Asian mountains and are the snow leopard's principal prey species. These mountains differ in their evolutionary history due to differential glaciation and deglaciation periods, orography, and rainfall patterns, and such factors causes diversification in species. METHODS AND RESULTS: Therefore, we assess the phylogeographic status of blue sheep using the mitochondrial cytochrome b gene (220 bp) across the Indian Himalayan region (IHR) and its relationship with other populations. Of the observed five haplotypes, two and three were from the western Himalayas (WH) and eastern Himalayas (EH) respectively. One of the haplotypes from WH was shared with the population of Pamir plateau, suggesting historical maternal connectivity between these areas. The phylogenetic analyses split the blue sheep into two paraphyletic clades, and western and eastern populations of IHR were within the Pamir and Tibetan plateau clades, respectively. We observed a relatively higher mean sequence divergence in the EH population than in the WH. CONCLUSION: We propose five 'Evolutionary Significant Units' across the blue sheep distribution range based on observed variation in the species' ecological requirements, orography, climatic conditions, and maternal lineages, viz.; Western Himalaya-Pamir plateau (WHPP); Eastern Himalaya-Tibetan plateau (EHTP); Qilian mountains; Helan mountains and Hengduan mountains population. Despite the small sample size, population divergence was observed across the IHR, therefore, we suggest a transboundary, collaborative study on comparative morphology, anatomy, ecology, behaviour, and population genetics using harmonized different genetic markers for identifying the overall taxonomic status of the blue sheep across its range for planning effective conservation strategies.


Subject(s)
Cytochromes b , Genetics, Population , Mitochondria , Animals , Cytochromes b/genetics , Haplotypes/genetics , Phylogeny , Phylogeography , Sheep/genetics , Mitochondria/metabolism
2.
Forensic Sci Int ; 332: 111172, 2022 Mar.
Article in English | MEDLINE | ID: mdl-35091157

ABSTRACT

Antlers are unique characteristic of males of family Cervidae. It fully regenerates each year in relation to their sexual cycles. It is primarily used as weapons in intra-specific fighting or possibly as organs displaying strength. These are formed by the calcification, beneath the velvet of the fast growing pre-osseous tissue known as velvet antlers. Continuous dividing velvet antlers replace dead antlers every year through shedding. Antlers are composed primarily of minerals, protein, carbohydrates and fatty acids. Calcium and phosphorus, primarily present as hydroxyapatite [Ca5(PO4)3OH] (Chapman 1975). In India there are nine species of deer viz. Kashmir stag (Cervus elaphus), mouse deer (Tragulus meminna), musk deer (Moschus moschiferus), swamp deer (Rucervus duvaucelii), thamin (Rucervus eldii), barking deer (Muntiacus muntjak), chital (Axis axis), hog deer (Axis porcinus) and sambar (Rusa unicolor). Mouse deer and musk deer possess only canines and antler is absent in both the deer species. Previously, the export of shed antlers and peacock feathers was allowed in India. Although, antlers are not very extensive in illegal wildlife trade but artifacts of antlers and they are used for traditional medicines for treatment of various diseases in different countries. The problem of illegal trade of antlers is mainly due to the mis-declaration of its quantity. Mostly antlers of chital, sambar and swamp deer are widely traded. Visualizing the current status of some of the deer species, trade of antler in India has been recently banned. Therefore, to provide legal protection to deer and other related species accordingly brow-antlered deer (Rucervus elidii), hog deer (Axis procinus), and swamp deer (R. duvaucelii) are included in Schedule I, whereas barking deer (Muntiacus muntjak), chital (Axis axis), and sambar (R. unicolor) were in schedule III of Wildlife (Protection) Act, 1972. To strengthen the legal measures and to protect deer species, identification of antlers in complete, pieces or pulverized form is very important. Very few scientific studies deal with identification of antlers belonging to different species. Thus, present study is aimed to identify species from antlers using species specific signature using elemental analysis. Morphological features of antlers in artiodactyls often used as a diagnostic tool to identify species. Although, morphometry is very good technique to identify antlers but as malformation in antlers is common also antlers are seized either in complete form or in small pieces or powder form, therefore, identification through morphometry becomes difficult for deformed antlers or pieces. In such cases, elemental analysis is helpful. Elemental composition of antlers of different species helps in inter-species distinction. This study will help managers, scientists and enforcement agencies to identify species from parts and products of antler.

3.
Sci Rep ; 11(1): 14164, 2021 07 08.
Article in English | MEDLINE | ID: mdl-34238947

ABSTRACT

Big cats (Genus: Panthera) are among the most threatened mammal groups of the world, owing to hunting, habitat loss, and illegal transnational trade. Conservation genetic studies and effective curbs on poaching are important for the conservation of these charismatic apex predators. A limited number of microsatellite markers exists for Panthera species and researchers often cross-amplify domestic cat microsatellites to study these species. We conducted data mining of seven Panthera genome sequences to discover microsatellites for conservation genetic studies of four threatened big cat species. A total of 32 polymorphic microsatellite loci were identified in silico and tested with 152 big cats, and were found polymorphic in most of the tested species. We propose a set of 12 novel microsatellite markers for use in conservation genetics and wildlife forensic investigations of big cat species. Cumulatively, these markers have a high discriminatory power of one in a million for unrelated individuals and one in a thousand for siblings. Similar PCR conditions of these markers increase the prospects of achieving efficient multiplex PCR assays. This study is a pioneering attempt to synthesise genome wide microsatellite markers for big cats.


Subject(s)
Conservation of Natural Resources , Genome , Microsatellite Repeats/genetics , Panthera/genetics , Surveys and Questionnaires , Animals , Base Sequence , Genetic Markers , Polymorphism, Genetic , Probability
4.
Mol Biol Rep ; 48(6): 5151-5160, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34213708

ABSTRACT

The Indian antelope or blackbuck (Antilope cervicapra) is endemic to the Indian subcontinent, inhabiting scrublands and dry grasslands. Most of the blackbuck populations are small, isolated, and threatened by habitat fragmentation and degradation. Management of such disjunct populations requires genetic characterization, which is critical for assessing hazards of stochastic events and inbreeding. Addressing the scarcity of such information on the blackbuck, we describe a novel panel of microsatellite markers that could be used to monitor blackbuck demography and population genetic parameters using non-invasive faecal sampling. We screened microsatellites (n = 40) that had been reported to amplify in bovid and cervid species using faecal samples of the blackbuck collected from Kaimoor Wildlife Sanctuary, Uttar Pradesh, India and its vicinities. We selected 12 markers for amplification using faecal DNA extracts (n = 140) in three multiplex reactions. We observed a mean amplification success rate of 72.4% across loci (92.1-25.7%) with high allele diversity (mean number of alleles/locus = 8.67 ± 1.03). Mean genotyping error rates across the markers were low to moderate (allelic drop-out rate = 0.09; false allele rate = 0.11). The proportions of first- and second-order relatives in the study population were 0.69% and 6.21%, respectively. Based on amplification success, genotyping error rates and the probability of identity (PID), we suggest (i) a panel of five microsatellite markers (cumulative PID = 1.24 × 10-5) for individual identification and population monitoring and (ii) seven additional markers for conservation genetics studies. This study provides essential tools capable of augmenting blackbuck conservation strategies at the landscape level, integral to protecting the scrubland-grassland ecosystem.


Subject(s)
Antelopes/genetics , Microsatellite Repeats/genetics , Population Surveillance/methods , Animals , Conservation of Natural Resources/methods , Ecosystem , Feces , Genetics, Population/methods , India , Nucleic Acid Amplification Techniques/methods
5.
PLoS One ; 15(4): e0231621, 2020.
Article in English | MEDLINE | ID: mdl-32298359

ABSTRACT

Of the sub-species of Holarctic wolf, the Woolly wolf (Canis lupus chanco) is uniquely adapted to atmospheric hypoxia and widely distributed across the Himalaya, Qinghai Tibetan Plateau (QTP) and Mongolia. Taxonomic ambiguity still exists for this sub-species because of complex evolutionary history anduse of limited wild samples across its range in Himalaya. We document for the first time population genetic structure and taxonomic affinity of the wolves across western and eastern Himalayan regions from samples collected from the wild (n = 19) using mitochondrial control region (225bp). We found two haplotypes in our data, one widely distributed in the Himalaya that was shared with QTP and the other confined to Himachal Pradesh and Uttarakhand in the western Himalaya, India. After combining our data withpublished sequences (n = 83), we observed 15 haplotypes. Some of these were shared among different locations from India to QTP and a few were private to geographic locations. A phylogenetic tree indicated that Woolly wolves from India, Nepal, QTP and Mongolia are basal to other wolves with shallow divergence (K2P; 0.000-0.044) and high bootstrap values. Demographic analyses based on mismatch distribution and Bayesian skyline plots (BSP) suggested a stable population over a long time (~million years) with signs of recent declines. Regional dominance of private haplotypes across its distribution range may indicate allopatric divergence. This may be due to differences in habitat characteristics, availability of different wild prey species and differential deglaciation within the range of the Woolly wolf during historic time. Presence of basal and shallow divergence within-clade along with unique ecological requirements and adaptation to hypoxia, the Woolly wolf of Himalaya, QTP, and Mongolian regions may be considered as a distinct an Evolutionary Significant Unit (ESU). Identifying management units (MUs) is needed within its distribution range using harmonized multiple genetic data for effective conservation planning.


Subject(s)
Phylogeny , Wolves/genetics , Animals , Asia , Bayes Theorem , Cytochromes b/genetics , DNA, Mitochondrial/genetics , Ecosystem , Genetics, Population , Haplotypes , Wolves/classification
6.
Mol Biol Rep ; 46(6): 6187-6195, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31486977

ABSTRACT

Indian antelope or Blackbuck (Antilope cervicapra) is one of the widely distributed endemic species in India among wild bovids and a majority of preferred habitats are in human-dominated landscapes. Poaching threats and habitat degradation are major factors for the decline in Blackbuck population from its distribution range. Till date, there is no detailed study using molecular techniques in India on Blackbuck, except a few studies entailing phylogenetic scenario based on inadequate sampling and DNA sequences restricted over limited geographic areas. In view of this, the present study is aimed to screen the Blackbuck samples from a large part of its distribution range and to investigate the genetic diversity as well as to identify the forensically informative nucleotide sequences (FINS) for species identification. We relied on multi-genes approach using three genes of mtDNA genome viz. Cytochrome Oxidase I, Cytochrome b and 16S rRNA and identified the FINS in the Blackbuck population along with conspecific sequences divergence and genetic diversity indices. In all three genes, we observed 8 to 17 haplotypes with the intra-species sequence divergence of 0.004-0.016. Inter-species sequence divergence with the other closely related species of the Blackbuck was 0.0225-0.033. We report the presence of FINS across three genes from 12 to 18 and found more informative nucleotide sites using Cytochrome Oxidase I genes compared to Cytochrome b and 16S rRNA gene. We did not observe the presence of geographic-specific FINS amongst Blackbuck population that can be used to assign individuals to geographic origin. Besides, in the phylogenetic tree, samples from different locations did not cluster into geographic-specific clade and exhibited mixed homology for these sequences. We suggest exploring the feasibility of using nuclear markers for population assignment.


Subject(s)
Antelopes/genetics , Genetic Variation , Genome, Mitochondrial , Genomics , Animals , Antelopes/classification , Base Composition , Evolution, Molecular , Genes, Mitochondrial , Genetics, Population , Genomics/methods , India , Phylogeny
7.
Zool Stud ; 58: e19, 2019.
Article in English | MEDLINE | ID: mdl-31966320

ABSTRACT

Sex identification of individuals is an important task in wildlife forensics as well as in conservation biology. It helps scientists understand population sex ratios with respect to maintaining genetic diversity, managing inbreeding depression and preventing the demographic consequences of sex-biased poaching. The literature on the use of mammalian molecular sex markers indicates that the success of accurate sex identification is variable across species. Very little is known about the effectiveness of such markers on the mammals of South and Southeast Asia. Therefore, we selected and tested three sets of universal primers for low-cost gel-based sex identification of mammals. We amplified different sets of markers-SRY (157 bp) and 12S rRNA (384 bp); Y-53-SRY (225 bp) and ZFX/ZFY (P1/P2; 445); SRY (157 bp) and 12S rRNA (151 bp)-to be used with different types (tissue, hair and skin) of samples from 20 mammalian species. All three sets of primers amplified the sex-specific fragment in a range of samples from hair to tissue. With an increasing number of field studies using non-invasively collected samples, this proposed low-cost gel- based method of molecular sexing may be applied in various aspects of the ecology and biology of South and Southeast Asian mammals, their conservation and forensics. We suggest that at least two sets of primers be used for any biological samples to avoid ambiguity.

8.
Anim Biotechnol ; 30(3): 193-201, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30522381

ABSTRACT

Musk deer are of high conservation priority owing to poaching pressure because of its musk pod. Representation of musk deer status using genetics is poorly documented in India, and it is not confirmed as to how many species of musk deer are present. We characterize for the first time, the genetic diversity of musk deer from Uttarakhand using Cytochrome Oxidase sub-unit (COI) gene (486 bp) and compared with the data available for other species. Results revealed the presence of six haplotypes in the Uttarakhand population amongst 17 sequences. Of these, 12 sequences shared the single haplotype. The intra-species sequences divergence was 0.003-0.017, whereas divergence with other species of musk deer was 0.071-0.081. Bayesian phylogenetic tree revealed that samples from Uttarakhand formed a separate clade with respect to other species of musk deer, whereas three species distributed in China clustered in the same clade and showed low sequences divergence, i.e., 0.002-0.061. Because of different ecomorph reported, we suggest using the barcoding based approach for inter and intra-species distinction and delineating species boundaries across the range for effective conservation. Besides, systematic classification, DNA barcoding would also help in dealing wildlife offence cases for disposal of the legal report in court.


Subject(s)
Electron Transport Complex IV/genetics , Genetic Variation , Ruminants/genetics , Animals , Bayes Theorem , Endangered Species , Geography , Haplotypes , India , Phylogeny , Ruminants/classification
9.
Mitochondrial DNA B Resour ; 3(1): 245-249, 2018 Feb 15.
Article in English | MEDLINE | ID: mdl-33474132

ABSTRACT

Genetic analysis is an important tool in understanding population structure, genetic diversity, and phylogenetics of endangered species likely to be affected by microevolution and anthropogenic factors. Western Ghats landscape is one of the identified biodiversity hotspots in India, and micro-evolutionary processes are observed in this landscape due to the presence of the gaps in the mountain ranges. Nilgiri tahr is endemic to and distributed in this landscape while very little is known about genetic characteristics, population structure and impact of these gaps on the species. In the present study, two different populations of Nilgiri tahr from the north (NPG) and south (SPG) of Palghat gap (PG) were studied using the cytochrome b gene (Cyt b; 310 bp) of mtDNA genome in the Western Ghats, India. Two variable sites were observed in the Cyt b fragment while the mean pairwise genetic distance between these two populations was 0.007. All the samples phylogenetically clustered in either north or south of PG. The presence of shallow divergence indicates the presence of suitable habitat in past which may have facilitated movement between NPG and SPG. A subsequent change in Paleo-climatic conditions and gradual formation of PG may have resulted in population diversification during the Pleistocene. Besides, Forensically Informative Nucleotide Sequence (FINS) observed would help in geo-assigning any individual from NPG or SPG to understand the likely influences on population demography due to poaching.

10.
Mitochondrial DNA B Resour ; 3(2): 640-644, 2018 May 24.
Article in English | MEDLINE | ID: mdl-33474269

ABSTRACT

Pangolins are the world`s most trafficked mammalian species classified under family Manidae and face severe threat of extinction, largely due to the illicit trade of its parts and products, especially scales, in international markets. Pangolin scales are believed to be used in Traditional Chinese Medicines (TCM) and meat is used as delicacies in restaurants. Of the eight extant species of pangolin, morphological discrimination is easy but the situation becomes precarious once the scales and meat samples are seized and it is difficult to identify species based on morphology in such cases. However, wildlife DNA forensics has played an instrumental role in the identification of species from such type of materials. The present study investigated that three mitochondrial genes (Cyt b, 16S rRNA, and 12S rRNA) clearly showed the variation among seven extant pangolin species (Manis culionensis; possibly extinct), whereas, maximum variation was obtained in cytochrome b when compared to another two mitochondrial genes. The present study revealed that obtained SNPs based on short sequence length (Intervals) within the three mitochondrial genes will be helpful to design the short molecular marker and species-specific probe that is used in wildlife forensic for identifying pangolin species from the degraded sample. We also advocate using more than one molecular marker for species discrimination so as to minimize any false identification of the mammal's species reported in the trade. Furthermore, data generated from the study would help in strengthening the DNA database of Indian pangolin species.

11.
PLoS One ; 12(4): e0174371, 2017.
Article in English | MEDLINE | ID: mdl-28445499

ABSTRACT

Despite massive global conservation strategies, tiger populations continued to decline until recently, mainly due to habitat loss, human-animal conflicts, and poaching. These factors are known to affect the genetic characteristics of tiger populations and decrease local effective population sizes. The Terai Arc Landscape (TAL) at the foothills of the Himalaya is one of the 42 source sites of tigers around the globe. Therefore, information on how landscape features and anthropogenic factors affect the fine-scale spatial genetic structure and variation of tigers in TAL is needed to develop proper management strategies for achieving long-term conservation goals. We document, for the first time, the genetic characteristics of this tiger population by genotyping 71 tiger samples using 13 microsatellite markers from the western region of TAL (WTAL) of 1800 km2. Specifically, we aimed to estimate the genetic variability, population structure, and gene flow. The microsatellite markers indicated that the levels of allelic diversity (MNA = 6.6) and genetic variation (Ho = 0.50, HE = 0.64) were slightly lower than those reported previously in other Bengal tiger populations. We observed moderate gene flow and significant genetic differentiation (FST= 0.060) and identified the presence of cryptic genetic structure using Bayesian and non-Bayesian approaches. There was low and significantly asymmetric migration between the two main subpopulations of the Rajaji Tiger Reserve and the Corbett Tiger Reserve in WTAL. Sibship relationships indicated that the functionality of the corridor between these subpopulations may be retained if the quality of the habitat does not deteriorate. However, we found that gene flow is not adequate in view of changing land use matrices. We discuss the need to maintain connectivity by implementing the measures that have been suggested previously to minimize the level of human disturbance, including relocation of villages and industries, prevention of encroachment, and banning sand and boulder mining in the corridors.


Subject(s)
Genetics, Population , Tigers/genetics , Alleles , Animals , Bayes Theorem , Conservation of Natural Resources , Ecosystem , Gene Flow , Genetic Variation , Genotype , Humans , India , Microsatellite Repeats/genetics
12.
Mitochondrial DNA A DNA Mapp Seq Anal ; 28(6): 965-970, 2017 11.
Article in English | MEDLINE | ID: mdl-27782757

ABSTRACT

Swamp deer (Rucervus duvaucelii) is an endemic, Scheduled I species under the Wildlife (Protection) Act 1972, India. According to variations in antler size, it has been classified into three subspecies, namely Western (R. duvaucelii duvaucelii), Central (R. duvaucelii branderi), and Eastern (R. duvaucelii ranjitsinhii). For planning effective ex situ and in situ conservation of a wide-ranging species in different bioclimatic regions and in wildlife forensic, the use of genetic characterization in defining morpho/ecotypes has been suggested because of the geographic clines and reproductive isolation. In spite of these morphotypes, very little is known about the genetic characteristics of the three subspecies, hence no strict subspecies-based breeding plan for retaining the evolutionary characteristics in captive populations for subsequent re-introduction is available except for a few studies. We describe the genetic characteristics of these three subspecies using cytochrome b of the mtDNA genome (400 bp). The DNA sequence data indicated 11 variable sites within the three subspecies. Two paraphyletic clades, namely the Central India and Western-Eastern populations were found, whereas the Western and Eastern populations are monophyletic with a bootstrap value of 69% within the clade. We suggest the need of sorting these three subspecies using different molecular mtDNA markers in zoos for captive breeding purposes so as to retain the genetic diversity of the separate geographic clines and to use a subspecies-specific fixed-state nucleotide to assess the extent of poaching to avoid any population demography stochastically in India.


Subject(s)
Deer/genetics , Genetic Variation , Phylogeny , Animals , Animals, Wild , Cytochromes b/genetics , Deer/metabolism , Genes, Mitochondrial , India , Sequence Analysis, DNA , Wetlands
13.
Forensic Sci Int ; 266: 226-233, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27322503

ABSTRACT

The illegal trade in wildlife is a serious threat to the existence of wild animals throughout the world. The short supply and high demand for wildlife articles have caused an influx of many different forms of fake wildlife articles into this trade. The task of identifying the materials used in making such articles poses challenges in wildlife forensics as different approaches are required for species identification. Claws constitute 3.8% of the illegal animal parts (n=2899) received at the Wildlife Institute of India (WII) for species identification. We describe the identification of seized suspected tiger claws (n=18) using a combined approach of morphometric and DNA-based analysis. The differential keratin density, determined using X-ray radiographs, indicated that none of the 18 claws were of any large cat but were fake. We determined three claw measurements, viz. ac (from the external coronary dermo-epidermal interface to the epidermis of the skin fold connecting the palmar flanges of the coronary horn), bc (from the claw tip to the epidermis of the skin fold connecting the palmar flanges of the coronary horn) and the ratio bc/ac, for all the seized (n=18), tiger (n=23) and leopard (n=49) claws. Univariate and multivariate statistical analyses were performed using SPSS. A scatter plot generated using canonical discriminant function analysis revealed that of the 18 seized claws, 14 claws formed a cluster separate from the clusters of the tiger and leopard claws, whereas the remaining four claws were within the leopard cluster. Because a discrepancy was observed between the X-ray images and the measurements of these four claws, one of the claw that clustered with the leopard claws was chosen randomly and DNA analysis carried out using the cyt b (137bp) and 16S rRNA (410bp) genes. A BLAST search and comparison with the reference database at WII indicated that the keratin material of the claw was derived from Bos taurus (cattle). This is a pioneering discovery, and we suggest that a hierarchical combination of techniques be used for identifying claws involved in wildlife offences, i.e. that an X-ray, morphometric and DNA-based analysis be carried out, to ascertain whether the claws are of tigers or leopards. To identify species in the illegal wildlife trade morphometric and genetic reference database should be developed. Morphological features as well as DNA profiles need to be used for better implementation of the Wildlife (Protection) Act, 1972 of India and other laws/treaties in South-east Asia.


Subject(s)
Forensic Sciences/methods , Hoof and Claw/chemistry , Animals , Animals, Wild , Cattle , Commerce/standards , Conservation of Natural Resources , Cytochromes b/genetics , DNA/analysis , India , RNA, Ribosomal, 16S/genetics , Species Specificity , Tigers
14.
Springerplus ; 3: 462, 2014.
Article in English | MEDLINE | ID: mdl-25187884

ABSTRACT

Tropical evergreen forests in northeast India are a biological hot spot for conservation of flora and fauna. Little is known, however, about tiger abundance, which is a flagship species for tropical evergreen forests. Our objective was to document the capture rate and population density of tigers based on spatial explicit capture-recapture (SECR) approaches using camera trap data in an intensive study area (ISA) of 158 km(2) in Pakke Tiger Reserve (PTR) during March to May 2006. The Reserve lies in the foothills of the Eastern Himalayan Mountains, northeast India. We monitored 38 camera traps in ISA for 70 days and documented 10 photo-captures of tigers (5 left and 5 right flanks) with an average trap success rate of 1.3 captures/100 trap days. The overall capture probability was 0.05. The tiger density estimated using a SECR model was 0.97 ± 0.23 individuals/100 km(2). This is the first systematic sampling study in tropical semi evergreen forests of India, and information on capture rate and population density of tigers provides baseline data from which to determining changes in the future to assist conservation.

15.
Springerplus ; 3: 4, 2014 Jan 03.
Article in English | MEDLINE | ID: mdl-24455462

ABSTRACT

In India, six landscapes and source populations that are important for long-term conservation of Bengal tigers (Panthera tigris tigris) have been identified. Except for a few studies, nothing is known regarding the genetic structure and extent of gene flow among most of the tiger populations across India as the majority of them are small, fragmented and isolated. Thus, individual-based relationships are required to understand the species ecology and biology for planning effective conservation and genetics-based individual identification has been widely used. But this needs screening and describing characteristics of microsatellite loci from DNA from good-quality sources so that the required number of loci can be selected and the genotyping error rate minimized. In the studies so far conducted on the Bengal tiger, a very small number of loci (n = 35) have been tested with high-quality source of DNA, and information on locus-specific characteristics is lacking. The use of such characteristics has been strongly recommended in the literature to minimize the error rate and by the International Society for Forensic Genetics (ISFG) for forensic purposes. Therefore, we describe for the first time locus-specific genetic and genotyping profile characteristics, crucial for population genetic studies, using high-quality source of DNA of the Bengal tiger. We screened 39 heterologous microsatellite loci (Sumatran tiger, domestic cat, Asiatic lion and snow leopard) in captive individuals (n = 8), of which 21 loci are being reported for the first time in the Bengal tiger, providing an additional choice for selection. The mean relatedness coefficient (R = -0.143) indicates that the selected tigers were unrelated. Thirty-four loci were polymorphic, with the number of alleles ranging from 2 to 7 per locus, and the remaining five loci were monomorphic. Based on the PIC values (> 0.500), and other characteristics, we suggest that 16 loci (3 to 7 alleles) be used for genetic and forensic study purposes. The probabilities of matching genotypes of unrelated individuals (3.692 × 10(-19)) and siblings (4.003 × 10(-6)) are within the values needed for undertaking studies in population genetics, relatedness, sociobiology and forensics.

16.
PLoS One ; 10(4): e0118846, 2014.
Article in English | MEDLINE | ID: mdl-25919139

ABSTRACT

The Sundarbans tiger inhabits a unique mangrove habitat and are morphologically distinct from the recognized tiger subspecies in terms of skull morphometrics and body size. Thus, there is an urgent need to assess their ecological and genetic distinctiveness and determine if Sundarbans tigers should be defined and managed as separate conservation unit. We utilized nine microsatellites and 3 kb from four mitochondrial DNA (mtDNA) genes to estimate genetic variability, population structure, demographic parameters and visualize historic and contemporary connectivity among tiger populations from Sundarbans and mainland India. We also evaluated the traits that determine exchangeability or adaptive differences among tiger populations. Data from both markers suggest that Sundarbans tiger is not a separate tiger subspecies and should be regarded as Bengal tiger (P. t. tigris) subspecies. Maximum likelihood phylogenetic analyses of the mtDNA data revealed reciprocal monophyly. Genetic differentiation was found stronger for mtDNA than nuclear DNA. Microsatellite markers indicated low genetic variation in Sundarbans tigers (He= 0.58) as compared to other mainland populations, such as northern and Peninsular (Hebetween 0.67- 0.70). Molecular data supports migration between mainland and Sundarbans populations until very recent times. We attribute this reduction in gene flow to accelerated fragmentation and habitat alteration in the landscape over the past few centuries. Demographic analyses suggest that Sundarbans tigers have diverged recently from peninsular tiger population within last 2000 years. Sundarbans tigers are the most divergent group of Bengal tigers, and ecologically non-exchangeable with other tiger populations, and thus should be managed as a separate "evolutionarily significant unit" (ESU) following the adaptive evolutionary conservation (AEC) concept.


Subject(s)
Conservation of Natural Resources , Tigers/genetics , Adaptation, Biological , Animals , DNA, Mitochondrial/analysis , Evolution, Molecular , Gene Flow , Genetic Variation , India , Microsatellite Repeats , Phylogeny , Phylogeography , Population Dynamics , Tigers/classification , Tigers/physiology
17.
Immunogenetics ; 62(10): 667-79, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20821315

ABSTRACT

Bengal tigers are highly endangered and knowledge on adaptive genetic variation can be essential for efficient conservation and management. Here we present the first assessment of allelic variation in major histocompatibility complex (MHC) class I and MHC class II DRB genes for wild and captive tigers from India. We amplified, cloned, and sequenced alpha-1 and alpha-2 domain of MHC class I and beta-1 domain of MHC class II DRB genes in 16 tiger specimens of different geographic origin. We detected high variability in peptide-binding sites, presumably resulting from positive selection. Tigers exhibit a low number of MHC DRB alleles, similar to other endangered big cats. Our initial assessment-admittedly with limited geographic coverage and sample size-did not reveal significant differences between captive and wild tigers with regard to MHC variability. In addition, we successfully amplified MHC DRB alleles from scat samples. Our characterization of tiger MHC alleles forms a basis for further in-depth analyses of MHC variability in this illustrative threatened mammal.


Subject(s)
Animals, Zoo/genetics , Genes, MHC Class II , Genes, MHC Class I , Tigers/genetics , Alleles , Amino Acid Sequence , Amino Acid Substitution , Animals , Animals, Wild , Animals, Zoo/immunology , DNA/isolation & purification , Endangered Species , Feces/chemistry , Felidae/genetics , Genetic Variation , India , Molecular Sequence Data , Phylogeny , Polymorphism, Genetic , Sequence Alignment , Sequence Homology , Tigers/immunology
18.
Forensic Sci Int ; 162(1-3): 144-51, 2006 Oct 16.
Article in English | MEDLINE | ID: mdl-16891073

ABSTRACT

There is a need to characterize Asian elephant ivory and compare with African ivory for controlling illegal trade and implementation of national and international laws. In this paper, we characterize ivory of Asian and African elephants using Schreger angle measurements, elemental analysis {X-ray fluorescence (XRF), inductively coupled plasma-atomic emission spectroscopy (ICP-AES), and inductively coupled plasma-mass spectroscopy (ICP-MS)} and isotopic analysis. We recorded Schreger angle characteristics of elephant ivory at three different zones in ivory samples of African (n=12) and Asian (n=28) elephants. The Schreger angle ranged from 32 degrees to 145 degrees and 30 degrees to 153 degrees in Asian and African ivory, respectively. Elemental analysis (for Asian and African ivory) by XRF, ICP-AES and ICP-MS provided preliminary data. We attempted to ascertain source of origin of Asian elephant ivory similarly as in African ivory based on isotopes of carbon, nitrogen and strontium. We determined isotopic ratios of carbon (n=31) and nitrogen (n=31) corresponding to diet and rainfall, respectively. Reference ivory samples from five areas within India were analyzed using collagen and powder sample and the latter was found more suitable for forensic analysis. During our preliminary analysis, the range of delta13C values (-13.6+/-0.15 per thousand and -25.6+/-0.15 per thousand) and delta15N values (10.2+/-0.15 per thousand and 3.5+/-0.15 per thousand) were noted.


Subject(s)
Carbon Isotopes/analysis , Conservation of Natural Resources , Dentin/chemistry , Nitrogen Isotopes/analysis , Trace Elements/analysis , Africa , Animals , Asia , Crime , Elephants , Forensic Medicine , Spectrometry, X-Ray Emission , Spectrophotometry, Atomic
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