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Dive into the research topics where Steven A. Sullivan is active.

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Featured researches published by Steven A. Sullivan.


Nature | 2008

Comparative genomics of the neglected human malaria parasite Plasmodium vivax.

Jane M. Carlton; John H. Adams; Joana C. Silva; Shelby Bidwell; Hernan Lorenzi; Elisabet Caler; Jonathan Crabtree; Samuel V. Angiuoli; Emilio F. Merino; Paolo Amedeo; Qin Cheng; Richard M. R. Coulson; Brendan S. Crabb; Hernando A. del Portillo; Kobby Essien; Tamara V. Feldblyum; Carmen Fernandez-Becerra; Paul R. Gilson; Amy H. Gueye; Xiang Guo; Simon Kang’a; Taco W. A. Kooij; Michael L. J. Korsinczky; Esmeralda V. S. Meyer; Vish Nene; Ian T. Paulsen; Owen White; Stuart A. Ralph; Qinghu Ren; Tobias Sargeant

The human malaria parasite Plasmodium vivax is responsible for 25–40% of the ∼515 million annual cases of malaria worldwide. Although seldom fatal, the parasite elicits severe and incapacitating clinical symptoms and often causes relapses months after a primary infection has cleared. Despite its importance as a major human pathogen, P. vivax is little studied because it cannot be propagated continuously in the laboratory except in non-human primates. We sequenced the genome of P. vivax to shed light on its distinctive biological features, and as a means to drive development of new drugs and vaccines. Here we describe the synteny and isochore structure of P. vivax chromosomes, and show that the parasite resembles other malaria parasites in gene content and metabolic potential, but possesses novel gene families and potential alternative invasion pathways not recognized previously. Completion of the P. vivax genome provides the scientific community with a valuable resource that can be used to advance investigation into this neglected species.


PLOS Biology | 2005

Major structural differences and novel potential virulence mechanisms from the genomes of multiple campylobacter species.

Derrick E. Fouts; Emmanuel F. Mongodin; Robert E. Mandrell; William G. Miller; David A. Rasko; Jacques Ravel; Lauren M. Brinkac; Robert T. DeBoy; Craig T. Parker; Sean C. Daugherty; Robert J. Dodson; A. Scott Durkin; Ramana Madupu; Steven A. Sullivan; Jyoti Shetty; Mobolanle A Ayodeji; Alla Shvartsbeyn; Michael C. Schatz; Jonathan H. Badger; Claire M. Fraser; Karen E. Nelson

Sequencing and comparative genome analysis of four strains of Campylobacter including C. lari RM2100, C. upsaliensis RM3195, and C. coli RM2228 has revealed major structural differences that are associated with the insertion of phage- and plasmid-like genomic islands, as well as major variations in the lipooligosaccharide complex. Poly G tracts are longer, are greater in number, and show greater variability in C. upsaliensis than in the other species. Many genes involved in host colonization, including racR/S, cadF, cdt, ciaB, and flagellin genes, are conserved across the species, but variations that appear to be species specific are evident for a lipooligosaccharide locus, a capsular (extracellular) polysaccharide locus, and a novel Campylobacter putative licABCD virulence locus. The strains also vary in their metabolic profiles, as well as their resistance profiles to a range of antibiotics. It is evident that the newly identified hypothetical and conserved hypothetical proteins, as well as uncharacterized two-component regulatory systems and membrane proteins, may hold additional significant information on the major differences in virulence among the species, as well as the specificity of the strains for particular hosts.


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.


Nature | 2004

Genome sequence of Silicibacter pomeroyi reveals adaptations to the marine environment

Mary Ann Moran; Alison Buchan; José M. González; John F. Heidelberg; William B. Whitman; Ronald P. Kiene; James R. Henriksen; Gary M. King; Robert Belas; Clay Fuqua; Lauren M. Brinkac; Matthew S. Lewis; Shivani Johri; Bruce Weaver; Grace Pai; Jonathan A. Eisen; Elisha Rahe; Wade M. Sheldon; Wenying Ye; Todd R. Miller; Jane M. Carlton; David A. Rasko; Ian T. Paulsen; Qinghu Ren; Sean C. Daugherty; Robert T. DeBoy; Robert J. Dodson; A. Scott Durkin; Ramana Madupu; William C. Nelson

Since the recognition of prokaryotes as essential components of the oceanic food web, bacterioplankton have been acknowledged as catalysts of most major biogeochemical processes in the sea. Studying heterotrophic bacterioplankton has been challenging, however, as most major clades have never been cultured or have only been grown to low densities in sea water. Here we describe the genome sequence of Silicibacter pomeroyi, a member of the marine Roseobacter clade (Fig. 1), the relatives of which comprise ∼10–20% of coastal and oceanic mixed-layer bacterioplankton. This first genome sequence from any major heterotrophic clade consists of a chromosome (4,109,442 base pairs) and megaplasmid (491,611 base pairs). Genome analysis indicates that this organism relies upon a lithoheterotrophic strategy that uses inorganic compounds (carbon monoxide and sulphide) to supplement heterotrophy. Silicibacter pomeroyi also has genes advantageous for associations with plankton and suspended particles, including genes for uptake of algal-derived compounds, use of metabolites from reducing microzones, rapid growth and cell-density-dependent regulation. This bacterium has a physiology distinct from that of marine oligotrophs, adding a new strategy to the recognized repertoire for coping with a nutrient-poor ocean.


Proceedings of the National Academy of Sciences of the United States of America | 2006

Evolution of sensory complexity recorded in a myxobacterial genome.

Barry S. Goldman; William C. Nierman; Dale Kaiser; S. C. Slater; Anthony S. Durkin; Jonathan A. Eisen; Catherine M. Ronning; W. B. Barbazuk; M. Blanchard; C. Field; C. Halling; G. Hinkle; O. Iartchuk; H. S. Kim; Chris Mackenzie; Ramana Madupu; N. Miller; Alla Shvartsbeyn; Steven A. Sullivan; M. Vaudin; R. Wiegand; Heidi B. Kaplan

Myxobacteria are single-celled, but social, eubacterial predators. Upon starvation they build multicellular fruiting bodies using a developmental program that progressively changes the pattern of cell movement and the repertoire of genes expressed. Development terminates with spore differentiation and is coordinated by both diffusible and cell-bound signals. The growth and development of Myxococcus xanthus is regulated by the integration of multiple signals from outside the cells with physiological signals from within. A collection of M. xanthus cells behaves, in many respects, like a multicellular organism. For these reasons M. xanthus offers unparalleled access to a regulatory network that controls development and that organizes cell movement on surfaces. The genome of M. xanthus is large (9.14 Mb), considerably larger than the other sequenced δ-proteobacteria. We suggest that gene duplication and divergence were major contributors to genomic expansion from its progenitor. More than 1,500 duplications specific to the myxobacterial lineage were identified, representing >15% of the total genes. Genes were not duplicated at random; rather, genes for cell–cell signaling, small molecule sensing, and integrative transcription control were amplified selectively. Families of genes encoding the production of secondary metabolites are overrepresented in the genome but may have been received by horizontal gene transfer and are likely to be important for predation.


Journal of Bacteriology | 2005

Whole-Genome Sequence Analysis of Pseudomonas syringae pv. phaseolicola 1448A Reveals Divergence among Pathovars in Genes Involved in Virulence and Transposition

Vinita Joardar; Magdalen Lindeberg; Robert W. Jackson; Jeremy D. Selengut; Robert J. Dodson; Lauren M. Brinkac; Sean C. Daugherty; Robert T. DeBoy; A. Scott Durkin; Michelle G. Giglio; Ramana Madupu; William C. Nelson; M. J. Rosovitz; Steven A. Sullivan; Jonathan Crabtree; Todd Creasy; Tanja Davidsen; Daniel H. Haft; Nikhat Zafar; Liwei Zhou; Rebecca A. Halpin; Tara Holley; Hoda Khouri; Tamara Feldblyum; Owen White; Claire M. Fraser; Arun K. Chatterjee; Sam Cartinhour; David J. Schneider; John W. Mansfield

Pseudomonas syringae pv. phaseolicola, a gram-negative bacterial plant pathogen, is the causal agent of halo blight of bean. In this study, we report on the genome sequence of P. syringae pv. phaseolicola isolate 1448A, which encodes 5,353 open reading frames (ORFs) on one circular chromosome (5,928,787 bp) and two plasmids (131,950 bp and 51,711 bp). Comparative analyses with a phylogenetically divergent pathovar, P. syringae pv. tomato DC3000, revealed a strong degree of conservation at the gene and genome levels. In total, 4,133 ORFs were identified as putative orthologs in these two pathovars using a reciprocal best-hit method, with 3,941 ORFs present in conserved, syntenic blocks. Although these two pathovars are highly similar at the physiological level, they have distinct host ranges; 1448A causes disease in beans, and DC3000 is pathogenic on tomato and Arabidopsis. Examination of the complement of ORFs encoding virulence, fitness, and survival factors revealed a substantial, but not complete, overlap between these two pathovars. Another distinguishing feature between the two pathovars is their distinctive sets of transposable elements. With access to a fifth complete pseudomonad genome sequence, we were able to identify 3,567 ORFs that likely comprise the core Pseudomonas genome and 365 ORFs that are P. syringae specific.


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.


Proceedings of the National Academy of Sciences of the United States of America | 2010

Identification of protective and broadly conserved vaccine antigens from the genome of extraintestinal pathogenic Escherichia coli

Danilo Gomes Moriel; Isabella Bertoldi; Angela Spagnuolo; Sara Marchi; Roberto Rosini; Barbara Nesta; Ilaria Pastorello; Vanja A. Mariani Corea; Giulia Torricelli; Elena Cartocci; Silvana Savino; Maria Scarselli; Ulrich Dobrindt; Jörg Hacker; Hervé Tettelin; Luke J. Tallon; Steven A. Sullivan; Lothar H. Wieler; Christa Ewers; Derek Pickard; Gordon Dougan; Maria Rita Fontana; Rino Rappuoli; Mariagrazia Pizza; Laura Serino

Extraintestinal pathogenic Escherichia coli (ExPEC) are a common cause of disease in both mammals and birds. A vaccine to prevent such infections would be desirable given the increasing antibiotic resistance of these bacteria. We have determined the genome sequence of ExPEC IHE3034 (ST95) isolated from a case of neonatal meningitis and compared this to available genome sequences of other ExPEC strains and a few nonpathogenic E. coli. We found 19 genomic islands present in the genome of IHE3034, which are absent in the nonpathogenic E. coli isolates. By using subtractive reverse vaccinology we identified 230 antigens present in ExPEC but absent (or present with low similarity) in nonpathogenic strains. Nine antigens were protective in a mouse challenge model. Some of them were also present in other pathogenic non-ExPEC strains, suggesting that a broadly protective E. coli vaccine may be possible. The gene encoding the most protective antigen was detected in most of the E. coli isolates, highly conserved in sequence and found to be exported by a type II secretion system which seems to be nonfunctional in nonpathogenic strains.


Nucleic Acids Research | 2009

GiardiaDB and TrichDB: integrated genomic resources for the eukaryotic protist pathogens Giardia lamblia and Trichomonas vaginalis

Cristina Aurrecoechea; John Brestelli; Brian P. Brunk; Jane M. Carlton; Jennifer Dommer; Steve Fischer; Bindu Gajria; Xin Gao; Alan R. Gingle; Gregory R. Grant; Omar S. Harb; Mark Heiges; Frank Innamorato; John Iodice; Jessica C. Kissinger; Eileen Kraemer; Wei Li; John A. Miller; Hilary G. Morrison; Vishal Nayak; Cary Pennington; Deborah F. Pinney; David S. Roos; Chris Ross; Christian J. Stoeckert; Steven A. Sullivan; Charles Treatman; Haiming Wang

GiardiaDB (http://GiardiaDB.org) and TrichDB (http://TrichDB.org) house the genome databases for Giardia lamblia and Trichomonas vaginalis, respectively, and represent the latest additions to the EuPathDB (http://EuPathDB.org) family of functional genomic databases. GiardiaDB and TrichDB employ the same framework as other EuPathDB sites (CryptoDB, PlasmoDB and ToxoDB), supporting fully integrated and searchable databases. Genomic-scale data available via these resources may be queried based on BLAST searches, annotation keywords and gene ID searches, GO terms, sequence motifs and other protein characteristics. Functional queries may also be formulated, based on transcript and protein expression data from a variety of platforms. Phylogenetic relationships may also be interrogated. The ability to combine the results from independent queries, and to store queries and query results for future use facilitates complex, genome-wide mining of functional genomic data.


Journal of Bacteriology | 2011

Two New Complete Genome Sequences Offer Insight into Host and Tissue Specificity of Plant Pathogenic Xanthomonas spp.

Adam J. Bogdanove; Ralf Koebnik; Hong Lu; Ayako Furutani; Samuel V. Angiuoli; Prabhu B. Patil; Marie-Anne Van Sluys; Robert P. Ryan; Damien Meyer; Sang-Wook Han; Gudlur Aparna; Misha Rajaram; Arthur L. Delcher; Adam M. Phillippy; Daniela Puiu; Michael C. Schatz; Martin Shumway; Daniel D. Sommer; Cole Trapnell; Faiza Benahmed; George Dimitrov; Ramana Madupu; Diana Radune; Steven A. Sullivan; Gopaljee Jha; Hiromichi Ishihara; Sang Won Lee; Alok K. Pandey; Vikas Sharma; Malinee Sriariyanun

Xanthomonas is a large genus of bacteria that collectively cause disease on more than 300 plant species. The broad host range of the genus contrasts with stringent host and tissue specificity for individual species and pathovars. Whole-genome sequences of Xanthomonas campestris pv. raphani strain 756C and X. oryzae pv. oryzicola strain BLS256, pathogens that infect the mesophyll tissue of the leading models for plant biology, Arabidopsis thaliana and rice, respectively, were determined and provided insight into the genetic determinants of host and tissue specificity. Comparisons were made with genomes of closely related strains that infect the vascular tissue of the same hosts and across a larger collection of complete Xanthomonas genomes. The results suggest a model in which complex sets of adaptations at the level of gene content account for host specificity and subtler adaptations at the level of amino acid or noncoding regulatory nucleotide sequence determine tissue specificity.

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Ramana Madupu

J. Craig Venter Institute

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William C. Nelson

Pacific Northwest National Laboratory

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Daniel H. Haft

J. Craig Venter Institute

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Hoda Khouri

George Washington University

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Robert T. DeBoy

J. Craig Venter Institute

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A. Scott Durkin

J. Craig Venter Institute

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