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Easy Breezy Species ID for the Forensic Lab Using a method that works for even the most challenging samples. Terry Melton, PhD President and Laboratory Director Mitotyping Technologies State College, PA www.mitotyping.com. 12S mtDNA species testing.
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Easy Breezy Species IDfor the Forensic LabUsing a method that works for even the most challenging samples Terry Melton, PhD President and Laboratory Director Mitotyping Technologies State College, PA www.mitotyping.com
12S mtDNA species testing • Prior to 2004, 8% of our casework hairs failed to amplify with human specific primers* • 2 possible explanations: • Human hair with no detectable (degraded) mtDNA • Hair is of non-human origin May be important and useful information for investigation… *Journal of Forensic Sciences: 691 Casework Hairs, 50:73-80
For example: • (Actual case): 26 year old homicide of young boy… • Evidence was collected at the time of the crime, but mitochondrial DNA analysis was not available until the late 1990s. • Several crime scene hairs gave partial to full human mtDNA profiles that will be useful in examining crime theories and testing suspects. • Two crime scene hairs gave no results… • Availability of species testing will keep investigators from worrying if human hairs were just too degraded. • With 12S testing, species testing revealed one hair was from a raccoon and one hair was from a pig.
DOG HUMAN HUMAN CAT HUMAN DEER Believe it or not: • Microscopic examination (although we recommend it on every hair submission) is becoming less common prior to submission of hairs • Even if carried out, not all examiners are successful in recognizing a non-human hair
Highly conserved regionstraditionally used for species testing • 16S rRNA Mitochondrial DNA • 12S rRNA Mitochondrial DNA • Cytochrome b Mitochondrial DNA • Original protocols used restriction endonucleases, later sequencing
Forensic application requires: • Ease of use • Specificity (at least to rule out human source) • Applicability to degraded samples • In our lab, most likely to be forensically relevant when larger animals (vertebrates->bones) and mammals (hair) are involved…
12s = Species Determination D-Loop = Forensic Analysis
From: Kitano T et al, International Journal of Legal Medicine DOI 10:1007/s00414-006-0133-7 (June 2007: Two universal primer sets for species identification among vertebrates) Primer selection attributed to Kocher et al. 1989, PNAS 86:6196
Q + - Protocol applied to extraction product • PCR using primers that amplify ~100bp from the 12S ribosomal gene • PCR product gel • Sequence PCR product using same primers • Import sequence into NCBI BLASTn tool and search for homologous sequences (www.ncbi.nlm.nih.gov/BLAST)
Testing strategy for hairs Amplify with regular human primer set ~250bp to capture intact DNA If no human-specific product Amplify with human mini-primer set ~80-100bp to capture degraded DNA If no human-specific product Amplify with 12S primers to determine species
Case results using 12S species testing Non-human species obtained from casework hairs: • Dog • Cat • Goat • Rat • Pig • Raccoon
Case background • Beauty supply retail store contacts Mitotyping regarding their wigs and hair extensions • Received tip that their supplier is selling them non-human hair and claiming that it is 100% human • Wanted us to determine whether their hair products are human or non-human
12S testing results • A result was obtained using the 12S primers on the hair DNA extract • The 12S sequence was searched in GenBank using BLASTn • The resulting species was…….
“Bos grunniens” ???????
Learning something new • Yak hair has all the properties of human hair • Yak hair is often used in wigs, hair weaves, and hair extensions (especially Santa Claus costumes) • 100% human hair is often diluted with yak hair to lower the cost
Will this method work on fish, birds, and other species? • Scenario: Object in a restaurant-prepared salad…(an actual case): • Is it a human fingertip, or calamari? • We have to question if 12S will work for every situation. • Fortunately (!) the sample was human skin…
Other species? • Examination of the first 1000 closest sequences to a variety of GenBank Blastn Search sequences shows an immense variety of possible species (including non-mammalian species) • As always, match possibilities are limited by the contents of the database • Nucleotide database search yielded the following: • Total sequences for search “12S ribosomal” = 34,809 • Total sequences for search “12S + vertebrata” = 23,717 • Total sequences for search “12S + mammalia” = 7,619 • Most mammals are in GenBank, and the most common North American mammals certainly are
Consequences of using 12S • Availability of 12S testing on hairs has reduced failure rate of hair testing from 7.2% to 4.5% (e.g, 95.5% of hairs give a profile). • The assay is suitable for the most degraded samples, with an amplicon size equal to that of the standard “mini-primer” sets used for ancient DNA. • Until hair microscopy (a forensic skill that we recommend be enhanced with training and experience) improves and increases, this assay will be a helpful adjunct for mitochondrial DNA analysis.
Canine Hairs as Evidence • 2002: David Westerfield on trial for murder of 7 year old Danielle VanDam. • Dog hairs from suspect’s motor home, quilt, and dryer lint matched Danielle’s dog. • Frequency of the mtDNA type in question was about 9% • First trial in the US to admit canine mtDNA • Westerfield was convicted on all counts
High potential utility • www.denverda.org lists 31 significant cases where non-human DNA played a role in conviction • 18 of these cases involved dog DNA, including hair, blood, feces, and saliva • Prior limitation was lack of a validated mitochondrial DNA database to provide a statistical context
Canine D-loop (non-coding region) • Two hypervariable regions connected by a region consisting of 10bp tandem repeats “HV1”:15431-15782 “HV2”: 15739-16092 Repeat region: 16130-16430 “HV3”:16451-00014
Protocols are unchanged from human mtDNA analysis • Hair extraction method uses glass grinder, 2 hour proteinase K incubation, and phenol-chloroform-isoamyl alcohol (PCIA)
PCR and sequencing • Amplification and sequencing of three fragments results in 1,004 bp of sequence data and a profile of ~953 bp • Protocols differ from human mtDNA only with respect to the primers used • Resulting sequence is compared to a “dog reference sequence” from Kim et al. 1998 that is also in GenBank
Material Modification Experiments • Development of a “positive control animal” • Species specificity: • HV1 primers amplify cat and human but amplicon size is different from dog • HV2 primers amplify cat but amplicon size is different • HV3 primers do not amplify cat or human • Results indicate that all PCR products should be sequenced and compared with Genbank
Material Modification Experiments • Reproducibility: a total of 18 dogs and wolves were sampled • Probative evidence types and sensitivity: guard hairs and undercoat hairs all performed well at different sizes • Mixtures: hairs with saliva from a second dog were sufficiently cleaned to get the hair type only
First Project • For a private client: can one distinguish dogs and wolves via control region sequencing? • Non-forensic, investigational, allowed us to combine implementation of new methods and material modification experiments
Blind Testing • Four bindles of hair were received • We were told only that they were collected from dogs or wolves • Hair appearance was not informative at least at the macroscopic level • Hairs were profiled using standard hair methods and primers designed for dogs and other canines from published literature • Results were compared with the published literature on mtDNA variation in dogs and wolves
Results • Full mitochondrial DNA sequences were obtained from all four samples • Two of the samples had identical profiles • The other two were different • Profiles were searched in GenBank
All results were correct; W4 is product of domestic dog mother and wolf father
Providing a forensic context for a canine mtDNA match • Requires a database to estimate the frequency of a particular type • Database must be searchable with user-friendly interface • Current model for this software and database is “MitoSearch”, provided by the FBI for human mitochondrial DNA cases. • “MitoSearch” is used in every human case where there is a failure to exclude (match)
Sampling Statistics Case where type previously observed: Case where type never observed: 95% Upper Bound 95% Confidence Interval Where p=frequency n=size of database α=significance level (0.01 or 0.05)
FidoSearchTM • Mitotyping Technologies is developing a software package to search the canine profiles already available in GenBank • There are 2800 canine mtDNA profiles in GenBank, representing about 2400 domestic dogs (C. familiaris) as well as wolves, dingos, coyotes, extinct species (specimens from museums) • We have downloaded the 2800 sequences and are creating a user-friendly interface that will be resident on our website (www.mitotyping.com)
Dog Diversity • Dogs are not nearly as diverse with respect to their mitochondrial DNA as humans • There are only 10 major haplogroups, and only 4 of those are found in Europe • Therefore, the ability to provide a powerful forensic statistic is reduced… “Only 78% of dogs can be excluded as the donor of this particular mtDNA profile”…for example
Diversity of canine mtDNA • Savolainen et al: • 1576 dogs and 40 wolves: 582 bp for CR • 169 dogs and 8 wolves: whole genome • Dog mtDNA haplotypes are distributed across the wolf diversity, in 6 phylogenetic clades • Dogs across the Old World share a common homogeneous mtDNA genepool, but diversity follows a gradient from high values in southeastern Asia to low in Europe • 100% of dogs have a haplotype belonging to the main phylogenetic groups
Genetic Diversity • East Asia: 735 dogs have 121 haplotypes • West(Europe/SW Asia/Africa/India): 585 dogs have 68 haplotypes • Europe: 336 dogs have 39 haplotypes Comparatively: in any human population, the proportion of haplotypes to individuals is 2/3, meaning that out of 900 individuals, there would be 600 different haplotypes
Conclusions: • Dogs originated in Southeastern Asia from multiple wolf founders • Using mtDNA mutation rate to estimate time to most recent common ancestor give a date range of 5,400-16,300 years ago • At that time, there existed at least 51 different mtDNA lineages leading to today’s dogs (most likely hundreds) • Domestication of wolves most likely resulted from close contact with increasingly sedentary hunter-gatherers or early rice farmers… • Question: was the wolf a food source as opposed to hunting helper/guard/or companion?
“Well, well—another blonde hair…conducting a little more “research” with that Jane Goodall tramp?”
Animal DNA Forensics • Animal-on-animal crimes • Animal cruelty cases • Animal on human crimes (bear attack) • Suspect/victim pets leave transfer evidence such as urine, feces, and hair • CITES: importing endangered species illegally, protecting endangered populations, museum specimens • Hunting violations, poaching
Not just mtDNA, also nuDNA • Most famous case? 1997… • Snowball the cat, from PEI, Canada, has her own Wikipedia entry • White hairs were recovered from a jacket found in the grave of murdered Shirley Duguay • STR analysis showed Snowball, the cat of Duguay’s estranged husband, was the donor of the hairs • First known usage of animal DNA in a crime • Article published in Nature indicated significance
Endangered Species and Forensics NY museum to bank endangered species DNA DNA registry for whales DNA test confirms tiger meat for sale at Chinese farm DNA shows what species of sharks were illegally finned Frankfurt zoo stores frozen stem cells from Aye-Aye
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