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Dive into the research topics where Nikhat Zafar is active.

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Featured researches published by Nikhat Zafar.


Proceedings of the National Academy of Sciences of the United States of America | 2003

The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000

C. Robin Buell; Vinita Joardar; Magdalen Lindeberg; Jeremy D. Selengut; Ian T. Paulsen; Michelle L. Gwinn; Robert J. Dodson; Robert T. DeBoy; A. Scott Durkin; James F. Kolonay; Ramana Madupu; Sean C. Daugherty; Lauren M. Brinkac; Maureen J. Beanan; Daniel H. Haft; William C. Nelson; Tanja Davidsen; Nikhat Zafar; Liwei Zhou; Jia Liu; Qiaoping Yuan; Hoda Khouri; Nadia Fedorova; Bao Tran; Daniel Russell; Kristi Berry; Teresa Utterback; Susan Van Aken; Tamara Feldblyum; Mark D'Ascenzo

We report the complete genome sequence of the model bacterial pathogen Pseudomonas syringae pathovar tomato DC3000 (DC3000), which is pathogenic on tomato and Arabidopsis thaliana. The DC3000 genome (6.5 megabases) contains a circular chromosome and two plasmids, which collectively encode 5,763 ORFs. We identified 298 established and putative virulence genes, including several clusters of genes encoding 31 confirmed and 19 predicted type III secretion system effector proteins. Many of the virulence genes were members of paralogous families and also were proximal to mobile elements, which collectively comprise 7% of the DC3000 genome. The bacterium possesses a large repertoire of transporters for the acquisition of nutrients, particularly sugars, as well as genes implicated in attachment to plant surfaces. Over 12% of the genes are dedicated to regulation, which may reflect the need for rapid adaptation to the diverse environments encountered during epiphytic growth and pathogenesis. Comparative analyses confirmed a high degree of similarity with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aeruginosa, yet revealed 1,159 genes unique to DC3000, of which 811 lack a known function.


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.


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.


Bioinformatics | 2005

Genome Properties: a system for the investigation of prokaryotic genetic content for microbiology, genome annotation and comparative genomics

Daniel H. Haft; Jeremy D. Selengut; Lauren M. Brinkac; Nikhat Zafar; Owen White

MOTIVATION The presence or absence of metabolic pathways and structures provide a context that makes protein annotation far more reliable. Compiling such information across microbial genomes improves the functional classification of proteins and provides a valuable resource for comparative genomics. RESULTS We have created a Genome Properties system to present key aspects of prokaryotic biology using standardized computational methods and controlled vocabularies. Properties reflect gene content, phenotype, phylogeny and computational analyses. The results of searches using hidden Markov models allow many properties to be deduced automatically, especially for families of proteins (equivalogs) conserved in function since their last common ancestor. Additional properties are derived from curation, published reports and other forms of evidence. Genome Properties system was applied to 156 complete prokaryotic genomes, and is easily mined to find differences between species, correlations between metabolic features and families of uncharacterized proteins, or relationships among properties. AVAILABILITY Genome Properties can be found at http://www.tigr.org/Genome_Properties SUPPLEMENTARY INFORMATION http://www.tigr.org/tigr-scripts/CMR2/genome_properties_references.spl.


Standards in Genomic Sciences | 2010

The JCVI standard operating procedure for annotating prokaryotic metagenomic shotgun sequencing data

David M. Tanenbaum; Johannes Goll; Sean Murphy; Prateek Kumar; Nikhat Zafar; Mathangi Thiagarajan; Ramana Madupu; Tanja Davidsen; Leonid Kagan; Saul Kravitz; Douglas B. Rusch; Shibu Yooseph

The JCVI metagenomics analysis pipeline provides for the efficient and consistent annotation of shotgun metagenomics sequencing data for sampling communities of prokaryotic organisms. The process can be equally applied to individual sequence reads from traditional Sanger capillary electrophoresis sequences, newer technologies such as 454 pyrosequencing, or sequence assemblies derived from one or more of these data types. It includes the analysis of both coding and non-coding genes, whether full-length or, as is often the case for shotgun metagenomics, fragmentary. The system is designed to provide the best-supported conservative functional annotation based on a combination of trusted homology-based scientific evidence and computational assertions and an annotation value hierarchy established through extensive manual curation. The functional annotation attributes assigned by this system include gene name, gene symbol, GO terms [1], EC numbers [2], and JCVI functional role categories [3].


Journal of Bacteriology | 2006

Comparative Genomic Evidence for a Close Relationship between the Dimorphic Prosthecate Bacteria Hyphomonas neptunium and Caulobacter crescentus

Jonathan H. Badger; Timothy R. Hoover; Yves V. Brun; Ronald M. Weiner; Michael T. Laub; Gladys Alexandre; Jan Mrázek; Qinghu Ren; Ian T. Paulsen; Karen E. Nelson; Hoda Khouri; Diana Radune; Julia Sosa; Robert J. Dodson; Steven A. Sullivan; M. J. Rosovitz; Ramana Madupu; Lauren M. Brinkac; A. Scott Durkin; Sean C. Daugherty; Sagar Kothari; Michelle G. Giglio; Liwei Zhou; Daniel H. Haft; Jeremy D. Selengut; Tanja Davidsen; Qi Yang; Nikhat Zafar; Naomi L. Ward

The dimorphic prosthecate bacteria (DPB) are alpha-proteobacteria that reproduce in an asymmetric manner rather than by binary fission and are of interest as simple models of development. Prior to this work, the only member of this group for which genome sequence was available was the model freshwater organism Caulobacter crescentus. Here we describe the genome sequence of Hyphomonas neptunium, a marine member of the DPB that differs from C. crescentus in that H. neptunium uses its stalk as a reproductive structure. Genome analysis indicates that this organism shares more genes with C. crescentus than it does with Silicibacter pomeroyi (a closer relative according to 16S rRNA phylogeny), that it relies upon a heterotrophic strategy utilizing a wide range of substrates, that its cell cycle is likely to be regulated in a similar manner to that of C. crescentus, and that the outer membrane complements of H. neptunium and C. crescentus are remarkably similar. H. neptunium swarmer cells are highly motile via a single polar flagellum. With the exception of cheY and cheR, genes required for chemotaxis were absent in the H. neptunium genome. Consistent with this observation, H. neptunium swarmer cells did not respond to any chemotactic stimuli that were tested, which suggests that H. neptunium motility is a random dispersal mechanism for swarmer cells rather than a stimulus-controlled navigation system for locating specific environments. In addition to providing insights into bacterial development, the H. neptunium genome will provide an important resource for the study of other interesting biological processes including chromosome segregation, polar growth, and cell aging.


BMC Genomics | 2012

Sequencing of mitochondrial genomes of nine Aspergillus and Penicillium species identifies mobile introns and accessory genes as main sources of genome size variability

Vinita Joardar; Natalie F Abrams; Jessica B. Hostetler; Paul J. Paukstelis; Suchitra Pakala; Suman B. Pakala; Nikhat Zafar; Olukemi O. Abolude; Gary A. Payne; Alex Andrianopoulos; David W. Denning; William C. Nierman

BackgroundThe genera Aspergillus and Penicillium include some of the most beneficial as well as the most harmful fungal species such as the penicillin-producer Penicillium chrysogenum and the human pathogen Aspergillus fumigatus, respectively. Their mitochondrial genomic sequences may hold vital clues into the mechanisms of their evolution, population genetics, and biology, yet only a handful of these genomes have been fully sequenced and annotated.ResultsHere we report the complete sequence and annotation of the mitochondrial genomes of six Aspergillus and three Penicillium species: A. fumigatus, A. clavatus, A. oryzae, A. flavus, Neosartorya fischeri (A. fischerianus), A. terreus, P. chrysogenum, P. marneffei, and Talaromyces stipitatus (P. stipitatum). The accompanying comparative analysis of these and related publicly available mitochondrial genomes reveals wide variation in size (25–36 Kb) among these closely related fungi. The sources of genome expansion include group I introns and accessory genes encoding putative homing endonucleases, DNA and RNA polymerases (presumed to be of plasmid origin) and hypothetical proteins. The two smallest sequenced genomes (A. terreus and P. chrysogenum) do not contain introns in protein-coding genes, whereas the largest genome (T. stipitatus), contains a total of eleven introns. All of the sequenced genomes have a group I intron in the large ribosomal subunit RNA gene, suggesting that this intron is fixed in these species. Subsequent analysis of several A. fumigatus strains showed low intraspecies variation. This study also includes a phylogenetic analysis based on 14 concatenated core mitochondrial proteins. The phylogenetic tree has a different topology from published multilocus trees, highlighting the challenges still facing the Aspergillus systematics.ConclusionsThe study expands the genomic resources available to fungal biologists by providing mitochondrial genomes with consistent annotations for future genetic, evolutionary and population studies. Despite the conservation of the core genes, the mitochondrial genomes of Aspergillus and Penicillium species examined here exhibit significant amount of interspecies variation. Most of this variation can be attributed to accessory genes and mobile introns, presumably acquired by horizontal gene transfer of mitochondrial plasmids and intron homing.


Fems Microbiology Letters | 2014

Mobile elements and mitochondrial genome expansion in the soil fungus and potato pathogen Rhizoctonia solani AG-3

Liliana Losada; Suman B. Pakala; Natalie D. Fedorova; Vinita Joardar; Svetlana A. Shabalina; Jessica B. Hostetler; Suchitra Pakala; Nikhat Zafar; Elizabeth Thomas; Marianela Rodriguez-Carres; Ralph A. Dean; Rytas Vilgalys; William C. Nierman; Marc A. Cubeta

The soil fungus Rhizoctonia solani is an economically important pathogen of agricultural and forestry crops. Here, we present the complete sequence and analysis of the mitochondrial genome of R. solani, field isolate Rhs1AP. The genome (235 849 bp) is the largest mitochondrial genome of a filamentous fungus sequenced to date and exhibits a rich accumulation of introns, novel repeat sequences, homing endonuclease genes, and hypothetical genes. Stable secondary structures exhibited by repeat sequences suggest that they comprise functional, possibly catalytic RNA elements. RNA-Seq expression profiling confirmed that the majority of homing endonuclease genes and hypothetical genes are transcriptionally active. Comparative analysis suggests that the mitochondrial genome of R. solani is an example of a dynamic history of expansion in filamentous fungi.


eLife | 2016

Structure of the germline genome of Tetrahymena thermophila and relationship to the massively rearranged somatic genome

Eileen P. Hamilton; Aurélie Kapusta; Piroska Huvos; Shelby Bidwell; Nikhat Zafar; Haibao Tang; Michalis Hadjithomas; Vivek Krishnakumar; Jonathan H. Badger; Elisabet Caler; Carsten Russ; Qiandong Zeng; Lin Fan; Joshua Z. Levin; Terrance Shea; Sarah K. Young; Ryan Hegarty; Riza Daza; Sharvari Gujja; Jennifer R. Wortman; Bruce W. Birren; Chad Nusbaum; Jainy Thomas; Clayton M. Carey; Ellen J. Pritham; Cédric Feschotte; Tomoko Noto; Kazufumi Mochizuki; Romeo Papazyan; Sean D. Taverna

The germline genome of the binucleated ciliate Tetrahymena thermophila undergoes programmed chromosome breakage and massive DNA elimination to generate the somatic genome. Here, we present a complete sequence assembly of the germline genome and analyze multiple features of its structure and its relationship to the somatic genome, shedding light on the mechanisms of genome rearrangement as well as the evolutionary history of this remarkable germline/soma differentiation. Our results strengthen the notion that a complex, dynamic, and ongoing interplay between mobile DNA elements and the host genome have shaped Tetrahymena chromosome structure, locally and globally. Non-standard outcomes of rearrangement events, including the generation of short-lived somatic chromosomes and excision of DNA interrupting protein-coding regions, may represent novel forms of developmental gene regulation. We also compare Tetrahymena’s germline/soma differentiation to that of other characterized ciliates, illustrating the wide diversity of adaptations that have occurred within this phylum. DOI: http://dx.doi.org/10.7554/eLife.19090.001


Genome Announcements | 2014

Draft Genome Sequence of the Plant-Pathogenic Soil Fungus Rhizoctonia solani Anastomosis Group 3 Strain Rhs1AP.

Marc A. Cubeta; Elizabeth Thomas; Ralph A. Dean; Suha Jabaji; S. M. Neate; Stellos M. Tavantzis; Takeshi Toda; Rytas Vilgalys; Narayanaswamy Bharathan; Natalie D. Fedorova-Abrams; Suman B. Pakala; Suchitra Pakala; Nikhat Zafar; Vinita Joardar; Liliana Losada; William C. Nierman

ABSTRACT The soil fungus Rhizoctonia solani is a pathogen of agricultural crops. Here, we report on the 51,705,945 bp draft consensus genome sequence of R. solani strain Rhs1AP. A comprehensive understanding of the heterokaryotic genome complexity and organization of R. solani may provide insight into the plant disease ecology and adaptive behavior of the fungus.

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Daniel H. Haft

J. Craig Venter Institute

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Ramana Madupu

J. Craig Venter Institute

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Tanja Davidsen

J. Craig Venter Institute

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Hoda Khouri

J. Craig Venter Institute

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William C. Nelson

Pacific Northwest National Laboratory

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