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Oct 07
Phylogenetic approaches to microbial community classification.
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Phylogenetic approaches to microbial community classification.
Microbiome. 2015;3(1):47
Authors: Ning J, Beiko RG
Abstract
BACKGROUND: The microbiota from different body sites are dominated by different major groups of microbes, but the variations within a body site such as the mouth can be more subtle. Accurate predictive models can serve as useful tools for distinguishing sub-sites and understanding key organisms and their roles and can highlight deviations from expected distributions of microbes. Good classification depends on choosing the right combination of classifier, feature representation, and learning model. Machine-learning procedures have been used in the past for supervised classification, but increased attention to feature representation and selection may produce better models and predictions.
RESULTS: We focused our attention on the classification of nine oral sites and dental plaque in particular, using data collected from the Human Microbiome Project. A key focus of our representations was the use of phylogenetic information, both as the basis for custom kernels and as a way to represent sets of microbes to the classifier. We also used the PICRUSt software, which draws on phylogenetic relationships to predict molecular functions and to generate additional features for the classifier. Custom kernels based on the UniFrac measure of community dissimilarity did not improve performance. However, feature representation was vital to classification accuracy, with microbial clade and function representations providing useful information to the classifier; combining the two types of features did not yield increased prediction accuracy. Many of the best-performing clades and functions had clear associations with oral microflora.
CONCLUSIONS: The classification of oral microbiota remains a challenging problem; our best accuracy on the plaque dataset was approximately 81 %. Perfect accuracy may be unattainable due to the close proximity of the sites and intra-individual variation. However, further exploration of the space of both classifiers and feature representations is likely to increase the accuracy of predictive models.
PMID: 26437943 [PubMed – in process]
Oct 07
Microbial Malaise: How Can We Classify the Microbiome?
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Microbial Malaise: How Can We Classify the Microbiome?
Trends Microbiol. 2015 Sep 19;
Authors: Beiko RG
Abstract
The names and lineages of microorganisms are critical to our understa…
Oct 07
Archaea.
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Archaea.
Curr Biol. 2015 Oct 5;25(19):R851-5
Authors: Eme L, Doolittle WF
Abstract
A headline on the front page of the New York Times for November 3, 1977, read “Scientists Discover …
Oct 07
Endosymbiosis and Eukaryotic Cell Evolution.
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Endosymbiosis and Eukaryotic Cell Evolution.
Curr Biol. 2015 Oct 5;25(19):R911-21
Authors: Archibald JM
Abstract
Understanding the evolution of eukaryotic cellular complexity is one of the grand challenges of modern biology. It has now been firmly established that mitochondria and plastids, the classical membrane-bound organelles of eukaryotic cells, evolved from bacteria by endosymbiosis. In the case of mitochondria, evidence points very clearly to an endosymbiont of α-proteobacterial ancestry. The precise nature of the host cell that partnered with this endosymbiont is, however, very much an open question. And while the host for the cyanobacterial progenitor of the plastid was undoubtedly a fully-fledged eukaryote, how – and how often – plastids moved from one eukaryote to another during algal diversification is vigorously debated. In this article I frame modern views on endosymbiotic theory in a historical context, highlighting the transformative role DNA sequencing played in solving early problems in eukaryotic cell evolution, and posing key unanswered questions emerging from the age of comparative genomics.
PMID: 26439354 [PubMed – in process]
Oct 01
Seasonal Preservation Success of the Marine Dinoflagellate Coral Symbiont, Symbiodinium sp.
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Seasonal Preservation Success of the Marine Dinoflagellate Coral Symbiont, Symbiodinium sp.
PLoS One. 2015;10(9):e0136358
Authors: Hagedorn M, Carter VL
Abstract
Coral reefs are som…
Sep 30
The Semantics of the Modular Architecture of Protein Structures.
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The Semantics of the Modular Architecture of Protein Structures.
Curr Protein Pept Sci. 2015 Sep 22;
Authors: Hleap JS, Blouin C
Abstract
Protein structures can be conceptualized as …
Sep 25
Identification of microRNAs in the Toxigenic Dinoflagellate Alexandrium catenella by High-Throughput Illumina Sequencing and Bioinformatic Analysis.
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Identification of microRNAs in the Toxigenic Dinoflagellate Alexandrium catenella by High-Throughput Illumina Sequencing and Bioinformatic Analysis.
PLoS One. 2015;10(9):e0138709
Authors: Geng H, S…
Sep 22
Projection scenarios of body mass index (2013-2030) for Public Health Planning in Quebec.
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Projection scenarios of body mass index (2013-2030) for Public Health Planning in Quebec.
BMC Public Health. 2014;14:996
Authors: Lo E, Hamel D, Jen Y, Lamontagne P, Martel S, Steensma C, Blouin C…
Sep 22
Phylogenomics Reveals Convergent Evolution of Lifestyles in Close Relatives of Animals and Fungi.
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Phylogenomics Reveals Convergent Evolution of Lifestyles in Close Relatives of Animals and Fungi.
Curr Biol. 2015 Sep 9;
Authors: Torruella G, de Mendoza A, Grau-Bové X, Antó M, Chaplin MA, Del Campo J, Eme L, Pérez-Cordón G, Whipps CM, Nichols KM, Paley R, Roger AJ, Sitjà-Bobadilla A, Donachie S, Ruiz-Trillo I
Abstract
The Opisthokonta are a eukaryotic supergroup divided in two main lineages: animals and related protistan taxa, and fungi and their allies [1, 2]. There is a great diversity of lifestyles and morphologies among unicellular opisthokonts, from free-living phagotrophic flagellated bacterivores and filopodiated amoebas to cell-walled osmotrophic parasites and saprotrophs. However, these characteristics do not group into monophyletic assemblages, suggesting rampant convergent evolution within Opisthokonta. To test this hypothesis, we assembled a new phylogenomic dataset via sequencing 12 new strains of protists. Phylogenetic relationships among opisthokonts revealed independent origins of filopodiated amoebas in two lineages, one related to fungi and the other to animals. Moreover, we observed that specialized osmotrophic lifestyles evolved independently in fungi and protistan relatives of animals, indicating convergent evolution. We therefore analyzed the evolution of two key fungal characters in Opisthokonta, the flagellum and chitin synthases. Comparative analyses of the flagellar toolkit showed a previously unnoticed flagellar apparatus in two close relatives of animals, the filasterean Ministeria vibrans and Corallochytrium limacisporum. This implies that at least four different opisthokont lineages secondarily underwent flagellar simplification. Analysis of the evolutionary history of chitin synthases revealed significant expansions in both animals and fungi, and also in the Ichthyosporea and C. limacisporum, a group of cell-walled animal relatives. This indicates that the last opisthokont common ancestor had a complex toolkit of chitin synthases that was differentially retained in extant lineages. Thus, our data provide evidence for convergent evolution of specialized lifestyles in close relatives of animals and fungi from a generalist ancestor.
PMID: 26365255 [PubMed – as supplied by publisher]
Sep 02
The genome of Aiptasia, a sea anemone model for coral symbiosis.
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The genome of Aiptasia, a sea anemone model for coral symbiosis.
Proc Natl Acad Sci U S A. 2015 Aug 31;
Authors: Baumgarten S, Simakov O, Esherick LY, Liew YJ, Lehnert EM, Michell CT, Li Y, Hambleto…
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