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1.
Sci Rep ; 6: 22908, 2016 Mar 11.
Article in English | MEDLINE | ID: mdl-26965911

ABSTRACT

Analysis of environmental DNA (eDNA) enables the detection of species of interest from water and soil samples, typically using species-specific PCR. Here, we describe a method to characterize the biodiversity of a given environment by amplifying eDNA using primer pairs targeting a wide range of taxa and high-throughput sequencing for species identification. We tested this approach on 91 water samples of 40 mL collected along the Cuyahoga River (Ohio, USA). We amplified eDNA using 12 primer pairs targeting mammals, fish, amphibians, birds, bryophytes, arthropods, copepods, plants and several microorganism taxa and sequenced all PCR products simultaneously by high-throughput sequencing. Overall, we identified DNA sequences from 15 species of fish, 17 species of mammals, 8 species of birds, 15 species of arthropods, one turtle and one salamander. Interestingly, in addition to aquatic and semi-aquatic animals, we identified DNA from terrestrial species that live near the Cuyahoga River. We also identified DNA from one Asian carp species invasive to the Great Lakes but that had not been previously reported in the Cuyahoga River. Our study shows that analysis of eDNA extracted from small water samples using wide-range PCR amplification combined with high-throughput sequencing can provide a broad perspective on biological diversity.


Subject(s)
Biodiversity , Classification , DNA/genetics , Metagenomics , Amphibians/classification , Amphibians/genetics , Animals , Birds/classification , Birds/genetics , Carps/classification , Carps/genetics , Computer Simulation , DNA/isolation & purification , Ecosystem , Environmental Monitoring , High-Throughput Nucleotide Sequencing , Mammals/classification , Mammals/genetics , Plants/classification , Rivers , Species Specificity
2.
Anim Biotechnol ; 26(1): 17-28, 2015.
Article in English | MEDLINE | ID: mdl-25153451

ABSTRACT

Next generation sequencing of mitochondrial DNA (mtDNA) facilitates studies into the metabolic characteristics of production animals and their relation to production traits. Sequence analysis of mtDNA from pure-bred swine with highly disparate production characteristics (Mangalica Blonde, Mangalica Swallow-bellied, Meishan, Turopolje, and Yorkshire) was initiated to evaluate the influence of mtDNA polymorphisms on mitochondrial function. Herein, we report the complete mtDNA sequences of five Sus scrofa breeds and evaluate their position within the phylogeny of domestic swine. Phenotypic traits of Yorkshire, Mangalica Blonde, and Swallow-belly swine are presented to demonstrate their metabolic characteristics. Our data support the division of European and Asian breeds noted previously and confirm European ancestry of Mangalica and Turopolje breeds. Furthermore, mtDNA differences between breeds suggest function-altering changes in proteins involved in oxidative phosphorylation such as ATP synthase 6 (MT-ATP6), cytochrome oxidase I (MT-CO1), cytochrome oxidase III (MT-CO3), and cytochrome b (MT-CYB), supporting the hypothesis that mtDNA polymorphisms contribute to differences in metabolic traits between swine breeds. Our sequence data form the basis for future research into the roles of mtDNA in determining production traits in domestic animals. Additionally, such studies should provide insight into how mtDNA haplotype influences the extreme adiposity observed in Mangalica breeds.


Subject(s)
DNA, Mitochondrial/genetics , Swine/genetics , Animals , Mitochondrial Proteins/chemistry , Mitochondrial Proteins/genetics , Molecular Sequence Data , Phenotype , Phylogeny , Sequence Analysis, DNA , Swine/classification
3.
Mitochondrion ; 11(1): 33-9, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20638486

ABSTRACT

Xenomitochondrial mice, harboring evolutionarily divergent Mus terricolor mitochondrial DNA (mtDNA) on a Mus musculus domesticus nuclear background (B6NTac(129S6)-mt(M. terricolor)/Capt; line D7), were subjected to molecular and phenotypic analyses. No overt in vivo phenotype was identified in contrast to in vitro xenomitochondrial cybrid studies. Microarray analyses revealed differentially expressed genes in xenomitochondrial mice, though none were directly involved in mitochondrial function. qRT-PCR revealed upregulation of mt-Co2 in xenomitochondrial mice. These results illustrate that cellular compensatory mechanisms for mild mitochondrial dysfunction alter mtDNA gene expression at a proteomic and/or translational level. Understanding these mechanisms will facilitate the development of therapeutics for mitochondrial disorders.


Subject(s)
DNA, Mitochondrial/genetics , Gene Expression Regulation , Hybridization, Genetic , Mitochondria/genetics , Mitochondrial Proteins/metabolism , Neurodegenerative Diseases/pathology , Animals , Cell Nucleus/genetics , Cell Nucleus/metabolism , Cells, Cultured , DNA, Mitochondrial/metabolism , Disease Models, Animal , Evolution, Molecular , Humans , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Mitochondria/metabolism , Mitochondria/pathology , Mitochondrial Proteins/genetics , Neurodegenerative Diseases/genetics , Oligonucleotide Array Sequence Analysis , Phenotype , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction
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