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Dive into the research topics where Martin Wu is active.

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Featured researches published by Martin Wu.


Nature | 2009

A phylogeny-driven genomic encyclopaedia of Bacteria and Archaea.

Dongying Wu; Philip Hugenholtz; Konstantinos Mavromatis; Rüdiger Pukall; Eileen Dalin; Natalia Ivanova; Victor Kunin; Lynne Goodwin; Martin Wu; Brian J. Tindall; Sean D. Hooper; Amrita Pati; Athanasios Lykidis; Stefan Spring; Iain Anderson; Patrik D’haeseleer; Adam Zemla; Alla Lapidus; Matt Nolan; Alex Copeland; Cliff Han; Feng Chen; Jan-Fang Cheng; Susan Lucas; Cheryl A. Kerfeld; Elke Lang; Sabine Gronow; Patrick Chain; David Bruce; Edward M. Rubin

Sequencing of bacterial and archaeal genomes has revolutionized our understanding of the many roles played by microorganisms. There are now nearly 1,000 completed bacterial and archaeal genomes available, most of which were chosen for sequencing on the basis of their physiology. As a result, the perspective provided by the currently available genomes is limited by a highly biased phylogenetic distribution. To explore the value added by choosing microbial genomes for sequencing on the basis of their evolutionary relationships, we have sequenced and analysed the genomes of 56 culturable species of Bacteria and Archaea selected to maximize phylogenetic coverage. Analysis of these genomes demonstrated pronounced benefits (compared to an equivalent set of genomes randomly selected from the existing database) in diverse areas including the reconstruction of phylogenetic history, the discovery of new protein families and biological properties, and the prediction of functions for known genes from other organisms. Our results strongly support the need for systematic ‘phylogenomic’ efforts to compile a phylogeny-driven ‘Genomic Encyclopedia of Bacteria and Archaea’ in order to derive maximum knowledge from existing microbial genome data as well as from genome sequences to come.


Nature | 2003

The genome sequence of Bacillus anthracis Ames and comparison to closely related bacteria

Timothy D. Read; Scott N. Peterson; Nicolas J. Tourasse; Les W. Baillie; Ian T. Paulsen; Karen E. Nelson; Hervé Tettelin; Derrick E. Fouts; Jonathan A. Eisen; Steven R. Gill; E. Holtzapple; Ole Andreas Økstad; Erlendur Helgason; Jennifer Rilstone; Martin Wu; James F. Kolonay; Maureen J. Beanan; Robert J. Dodson; Lauren M. Brinkac; Michelle L. Gwinn; Robert T. DeBoy; Ramana Madpu; Sean C. Daugherty; A. Scott Durkin; Daniel H. Haft; William C. Nelson; Jeremy Peterson; Mihai Pop; Hoda Khouri; Diana Radune

Bacillus anthracis is an endospore-forming bacterium that causes inhalational anthrax. Key virulence genes are found on plasmids (extra-chromosomal, circular, double-stranded DNA molecules) pXO1 (ref. 2) and pXO2 (ref. 3). To identify additional genes that might contribute to virulence, we analysed the complete sequence of the chromosome of B. anthracis Ames (about 5.23 megabases). We found several chromosomally encoded proteins that may contribute to pathogenicity—including haemolysins, phospholipases and iron acquisition functions—and identified numerous surface proteins that might be important targets for vaccines and drugs. Almost all these putative chromosomal virulence and surface proteins have homologues in Bacillus cereus, highlighting the similarity of B. anthracis to near-neighbours that are not associated with anthrax. By performing a comparative genome hybridization of 19 B. cereus and Bacillus thuringiensis strains against a B. anthracis DNA microarray, we confirmed the general similarity of chromosomal genes among this group of close relatives. However, we found that the gene sequences of pXO1 and pXO2 were more variable between strains, suggesting plasmid mobility in the group. The complete sequence of B. anthracis is a step towards a better understanding of anthrax pathogenesis.


Applied and Environmental Microbiology | 2009

Three Genomes from the Phylum Acidobacteria Provide Insight into the Lifestyles of These Microorganisms in Soils

Naomi L. Ward; Jean F. Challacombe; Peter H. Janssen; Bernard Henrissat; Pedro M. Coutinho; Martin Wu; Gary Xie; Daniel H. Haft; Michelle Sait; Jonathan H. Badger; Ravi D. Barabote; Brent Bradley; Thomas Brettin; Lauren M. Brinkac; David Bruce; Todd Creasy; Sean C. Daugherty; Tanja Davidsen; Robert T. DeBoy; J. Chris Detter; Robert J. Dodson; A. Scott Durkin; Anuradha Ganapathy; Michelle Gwinn-Giglio; Cliff Han; Hoda Khouri; Hajnalka Kiss; Sagar Kothari; Ramana Madupu; Karen E. Nelson

ABSTRACT The complete genomes of three strains from the phylum Acidobacteria were compared. Phylogenetic analysis placed them as a unique phylum. They share genomic traits with members of the Proteobacteria, the Cyanobacteria, and the Fungi. The three strains appear to be versatile heterotrophs. Genomic and culture traits indicate the use of carbon sources that span simple sugars to more complex substrates such as hemicellulose, cellulose, and chitin. The genomes encode low-specificity major facilitator superfamily transporters and high-affinity ABC transporters for sugars, suggesting that they are best suited to low-nutrient conditions. They appear capable of nitrate and nitrite reduction but not N2 fixation or denitrification. The genomes contained numerous genes that encode siderophore receptors, but no evidence of siderophore production was found, suggesting that they may obtain iron via interaction with other microorganisms. The presence of cellulose synthesis genes and a large class of novel high-molecular-weight excreted proteins suggests potential traits for desiccation resistance, biofilm formation, and/or contribution to soil structure. Polyketide synthase and macrolide glycosylation genes suggest the production of novel antimicrobial compounds. Genes that encode a variety of novel proteins were also identified. The abundance of acidobacteria in soils worldwide and the breadth of potential carbon use by the sequenced strains suggest significant and previously unrecognized contributions to the terrestrial carbon cycle. Combining our genomic evidence with available culture traits, we postulate that cells of these isolates are long-lived, divide slowly, exhibit slow metabolic rates under low-nutrient conditions, and are well equipped to tolerate fluctuations in soil hydration.


Genome Biology | 2008

A simple, fast, and accurate method of phylogenomic inference.

Martin Wu; Jonathan A. Eisen

The explosive growth of genomic data provides an opportunity to make increased use of protein markers for phylogenetic inference. We have developed an automated pipeline for phylogenomic analysis (AMPHORA) that overcomes the existing bottlenecks limiting large-scale protein phylogenetic inference. We demonstrated its high throughput capabilities and high quality results by constructing a genome tree of 578 bacterial species and by assigning phylotypes to 18,607 protein markers identified in metagenomic data collected from the Sargasso Sea.


Proceedings of the National Academy of Sciences of the United States of America | 2002

The complete genome sequence of Chlorobium tepidum TLS, a photosynthetic, anaerobic, green-sulfur bacterium

Jonathan A. Eisen; Karen E. Nelson; Ian T. Paulsen; John F. Heidelberg; Martin Wu; Robert J. Dodson; Robert T. DeBoy; Michelle L. Gwinn; William C. Nelson; Daniel H. Haft; Erin Hickey; Jeremy Peterson; A. Scott Durkin; James L. Kolonay; Fan Yang; Ingeborg Holt; Lowell Umayam; Tanya Mason; Michael Brenner; Terrance Shea; Debbie S. Parksey; William C. Nierman; Tamara Feldblyum; Cheryl L. Hansen; M. Brook Craven; Diana Radune; Jessica Vamathevan; Hoda Khouri; Owen White; Tanja M. Gruber

The complete genome of the green-sulfur eubacterium Chlorobium tepidum TLS was determined to be a single circular chromosome of 2,154,946 bp. This represents the first genome sequence from the phylum Chlorobia, whose members perform anoxygenic photosynthesis by the reductive tricarboxylic acid cycle. Genome comparisons have identified genes in C. tepidum that are highly conserved among photosynthetic species. Many of these have no assigned function and may play novel roles in photosynthesis or photobiology. Phylogenomic analysis reveals likely duplications of genes involved in biosynthetic pathways for photosynthesis and the metabolism of sulfur and nitrogen as well as strong similarities between metabolic processes in C. tepidum and many Archaeal species.


Journal of Bacteriology | 2006

Genome Sequence of Aeromonas hydrophila ATCC 7966T: Jack of All Trades

Rekha Seshadri; Sam W. Joseph; Ashok K. Chopra; Jian Sha; Jonathan G. Shaw; Joerg Graf; Daniel H. Haft; Martin Wu; Qinghu Ren; M. J. Rosovitz; Ramana Madupu; Luke J. Tallon; Mary Kim; Shaohua Jin; Hue Vuong; O. Colin Stine; Afsar Ali; Amy J. Horneman; John F. Heidelberg

The complete genome of Aeromonas hydrophila ATCC 7966(T) was sequenced. Aeromonas, a ubiquitous waterborne bacterium, has been placed by the Environmental Protection Agency on the Contaminant Candidate List because of its potential to cause human disease. The 4.7-Mb genome of this emerging pathogen shows a physiologically adroit organism with broad metabolic capabilities and considerable virulence potential. A large array of virulence genes, including some identified in clinical isolates of Aeromonas spp. or Vibrio spp., may confer upon this organism the ability to infect a wide range of hosts. However, two recognized virulence markers, a type III secretion system and a lateral flagellum, that are reported in other A. hydrophila strains are not identified in the sequenced isolate, ATCC 7966(T). Given the ubiquity and free-living lifestyle of this organism, there is relatively little evidence of fluidity in terms of mobile elements in the genome of this particular strain. Notable aspects of the metabolic repertoire of A. hydrophila include dissimilatory sulfate reduction and resistance mechanisms (such as thiopurine reductase, arsenate reductase, and phosphonate degradation enzymes) against toxic compounds encountered in polluted waters. These enzymes may have bioremediative as well as industrial potential. Thus, the A. hydrophila genome sequence provides valuable insights into its ability to flourish in both aquatic and host environments.


PLOS Biology | 2004

Genomic Insights into Methanotrophy: The Complete Genome Sequence of Methylococcus capsulatus (Bath)

Naomi L. Ward; Øivind Larsen; James Sakwa; Live J. Bruseth; Hoda Khouri; A. Scott Durkin; George Dimitrov; Lingxia Jiang; David Scanlan; Katherine H. Kang; Matthew Lewis; Karen E. Nelson; Barbara A. Methé; Martin Wu; John F. Heidelberg; Ian T. Paulsen; Derrick E. Fouts; Jacques Ravel; Hervé Tettelin; Qinghu Ren; Timothy D. Read; Robert T. DeBoy; Rekha Seshadri; Harald B. Jensen; Nils-Kåre Birkeland; William C. Nelson; Robert J. Dodson; Svenn Helge Grindhaug; Ingeborg Holt; Ingvar Eidhammer

Methanotrophs are ubiquitous bacteria that can use the greenhouse gas methane as a sole carbon and energy source for growth, thus playing major roles in global carbon cycles, and in particular, substantially reducing emissions of biologically generated methane to the atmosphere. Despite their importance, and in contrast to organisms that play roles in other major parts of the carbon cycle such as photosynthesis, no genome-level studies have been published on the biology of methanotrophs. We report the first complete genome sequence to our knowledge from an obligate methanotroph, Methylococcus capsulatus (Bath), obtained by the shotgun sequencing approach. Analysis revealed a 3.3-Mb genome highly specialized for a methanotrophic lifestyle, including redundant pathways predicted to be involved in methanotrophy and duplicated genes for essential enzymes such as the methane monooxygenases. We used phylogenomic analysis, gene order information, and comparative analysis with the partially sequenced methylotroph Methylobacterium extorquens to detect genes of unknown function likely to be involved in methanotrophy and methylotrophy. Genome analysis suggests the ability of M. capsulatus to scavenge copper (including a previously unreported nonribosomal peptide synthetase) and to use copper in regulation of methanotrophy, but the exact regulatory mechanisms remain unclear. One of the most surprising outcomes of the project is evidence suggesting the existence of previously unsuspected metabolic flexibility in M. capsulatus, including an ability to grow on sugars, oxidize chemolithotrophic hydrogen and sulfur, and live under reduced oxygen tension, all of which have implications for methanotroph ecology. The availability of the complete genome of M. capsulatus (Bath) deepens our understanding of methanotroph biology and its relationship to global carbon cycles. We have gained evidence for greater metabolic flexibility than was previously known, and for genetic components that may have biotechnological potential.


PLOS Genetics | 2005

Life in Hot Carbon Monoxide: The Complete Genome Sequence of Carboxydothermus hydrogenoformans Z-2901

Martin Wu; Qinghu Ren; A. Scott Durkin; Sean C. Daugherty; Lauren M. Brinkac; Robert J. Dodson; Ramana Madupu; Steven A. Sullivan; James F. Kolonay; William C. Nelson; Luke J. Tallon; Kristine M Jones; Luke E. Ulrich; Juan M. González; Igor B. Zhulin; Frank T. Robb; Jonathan A. Eisen

We report here the sequencing and analysis of the genome of the thermophilic bacterium Carboxydothermus hydrogenoformans Z-2901. This species is a model for studies of hydrogenogens, which are diverse bacteria and archaea that grow anaerobically utilizing carbon monoxide (CO) as their sole carbon source and water as an electron acceptor, producing carbon dioxide and hydrogen as waste products. Organisms that make use of CO do so through carbon monoxide dehydrogenase complexes. Remarkably, analysis of the genome of C. hydrogenoformans reveals the presence of at least five highly differentiated anaerobic carbon monoxide dehydrogenase complexes, which may in part explain how this species is able to grow so much more rapidly on CO than many other species. Analysis of the genome also has provided many general insights into the metabolism of this organism which should make it easier to use it as a source of biologically produced hydrogen gas. One surprising finding is the presence of many genes previously found only in sporulating species in the Firmicutes Phylum. Although this species is also a Firmicutes, it was not known to sporulate previously. Here we show that it does sporulate and because it is missing many of the genes involved in sporulation in other species, this organism may serve as a “minimal” model for sporulation studies. In addition, using phylogenetic profile analysis, we have identified many uncharacterized gene families found in all known sporulating Firmicutes, but not in any non-sporulating bacteria, including a sigma factor not known to be involved in sporulation previously.


PLOS Biology | 2012

Rapid Evolution of Enormous, Multichromosomal Genomes in Flowering Plant Mitochondria with Exceptionally High Mutation Rates

Daniel B. Sloan; Andrew J. Alverson; John P. Chuckalovcak; Martin Wu; David E. McCauley; Jeffrey D. Palmer; Douglas R. Taylor

A pair of species within the genus Silene have evolved the largest known mitochondrial genomes, coinciding with extreme changes in mutation rate, recombination activity, and genome structure.


PLOS Computational Biology | 2012

Incorporating 16S Gene Copy Number Information Improves Estimates of Microbial Diversity and Abundance

Steven W. Kembel; Martin Wu; Jonathan A. Eisen; Jessica L. Green

The abundance of different SSU rRNA (“16S”) gene sequences in environmental samples is widely used in studies of microbial ecology as a measure of microbial community structure and diversity. However, the genomic copy number of the 16S gene varies greatly – from one in many species to up to 15 in some bacteria and to hundreds in some microbial eukaryotes. As a result of this variation the relative abundance of 16S genes in environmental samples can be attributed both to variation in the relative abundance of different organisms, and to variation in genomic 16S copy number among those organisms. Despite this fact, many studies assume that the abundance of 16S gene sequences is a surrogate measure of the relative abundance of the organisms containing those sequences. Here we present a method that uses data on sequences and genomic copy number of 16S genes along with phylogenetic placement and ancestral state estimation to estimate organismal abundances from environmental DNA sequence data. We use theory and simulations to demonstrate that 16S genomic copy number can be accurately estimated from the short reads typically obtained from high-throughput environmental sequencing of the 16S gene, and that organismal abundances in microbial communities are more strongly correlated with estimated abundances obtained from our method than with gene abundances. We re-analyze several published empirical data sets and demonstrate that the use of gene abundance versus estimated organismal abundance can lead to different inferences about community diversity and structure and the identity of the dominant taxa in microbial communities. Our approach will allow microbial ecologists to make more accurate inferences about microbial diversity and abundance based on 16S sequence data.

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Lowell S. Young

California Pacific Medical Center

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William C. Nelson

Pacific Northwest National Laboratory

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Ramana Madupu

J. Craig Venter Institute

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Zhang Wang

University of Virginia

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Daniel H. Haft

J. Craig Venter Institute

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