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Featured researches published by Akif Uzman.


BMC Microbiology | 2007

Subtle genetic changes enhance virulence of methicillin resistant and sensitive Staphylococcus aureus

Sarah K. Highlander; Kristina G. Hulten; Xiang Qin; Huaiyang Jiang; Shailaja Yerrapragada; Edward O. Mason; Yue Shang; Tiffany M. Williams; Régine M Fortunov; Yamei Liu; Okezie Igboeli; Joseph F. Petrosino; Madhan R. Tirumalai; Akif Uzman; George E. Fox; Ana Maria Cardenas; Donna M. Muzny; Lisa Hemphill; Yan Ding; Shannon Dugan; Peter R Blyth; Christian Buhay; Huyen Dinh; Alicia Hawes; Michael Holder; Christie Kovar; Sandra L. Lee; Wen Liu; Lynne V. Nazareth; Qiaoyan Wang

BackgroundCommunity acquired (CA) methicillin-resistant Staphylococcus aureus (MRSA) increasingly causes disease worldwide. USA300 has emerged as the predominant clone causing superficial and invasive infections in children and adults in the USA. Epidemiological studies suggest that USA300 is more virulent than other CA-MRSA. The genetic determinants that render virulence and dominance to USA300 remain unclear.ResultsWe sequenced the genomes of two pediatric USA300 isolates: one CA-MRSA and one CA-methicillin susceptible (MSSA), isolated at Texas Childrens Hospital in Houston. DNA sequencing was performed by Sanger dideoxy whole genome shotgun (WGS) and 454 Life Sciences pyrosequencing strategies. The sequence of the USA300 MRSA strain was rigorously annotated. In USA300-MRSA 2658 chromosomal open reading frames were predicted and 3.1 and 27 kilobase (kb) plasmids were identified. USA300-MSSA contained a 20 kb plasmid with some homology to the 27 kb plasmid found in USA300-MRSA. Two regions found in US300-MRSA were absent in USA300-MSSA. One of these carried the arginine deiminase operon that appears to have been acquired from S. epidermidis. The USA300 sequence was aligned with other sequenced S. aureus genomes and regions unique to USA300 MRSA were identified.ConclusionUSA300-MRSA is highly similar to other MRSA strains based on whole genome alignments and gene content, indicating that the differences in pathogenesis are due to subtle changes rather than to large-scale acquisition of virulence factor genes. The USA300 Houston isolate differs from another sequenced USA300 strain isolate, derived from a patient in San Francisco, in plasmid content and a number of sequence polymorphisms. Such differences will provide new insights into the evolution of pathogens.


PLOS ONE | 2007

Paradoxical DNA Repair and Peroxide Resistance Gene Conservation in Bacillus pumilus SAFR-032

Jason Gioia; Shailaja Yerrapragada; Xiang Qin; Huaiyang Jiang; Okezie Igboeli; Donna M. Muzny; Shannon Dugan-Rocha; Yan Ding; Alicia Hawes; Wen Liu; Lesette Perez; Christie Kovar; Huyen Dinh; Sandra L. Lee; Lynne V. Nazareth; Peter R Blyth; Michael Holder; Christian Buhay; Madhan R. Tirumalai; Yamei Liu; Indrani Dasgupta; Lina Bokhetache; Masaya Fujita; Fathi Karouia; Prahathees Eswara Moorthy; Johnathan Siefert; Akif Uzman; Prince Buzumbo; Avani Verma; Hiba Zwiya

Background Bacillus spores are notoriously resistant to unfavorable conditions such as UV radiation, γ-radiation, H2O2, desiccation, chemical disinfection, or starvation. Bacillus pumilus SAFR-032 survives standard decontamination procedures of the Jet Propulsion Lab spacecraft assembly facility, and both spores and vegetative cells of this strain exhibit elevated resistance to UV radiation and H2O2 compared to other Bacillus species. Principal Findings The genome of B. pumilus SAFR-032 was sequenced and annotated. Lists of genes relevant to DNA repair and the oxidative stress response were generated and compared to B. subtilis and B. licheniformis. Differences in conservation of genes, gene order, and protein sequences are highlighted because they potentially explain the extreme resistance phenotype of B. pumilus. The B. pumilus genome includes genes not found in B. subtilis or B. licheniformis and conserved genes with sequence divergence, but paradoxically lacks several genes that function in UV or H2O2 resistance in other Bacillus species. Significance This study identifies several candidate genes for further research into UV and H2O2 resistance. These findings will help explain the resistance of B. pumilus and are applicable to understanding sterilization survival strategies of microbes.


Journal of Bacteriology | 2006

Chromosome Rearrangement and Diversification of Francisella tularensis Revealed by the Type B (OSU18) Genome Sequence

Joseph F. Petrosino; Qin Xiang; Sandor E. Karpathy; Huaiyang Jiang; Shailaja Yerrapragada; Yamei Liu; Jason Gioia; Lisa Hemphill; Arely Gonzalez; T. M. Raghavan; Akif Uzman; George E. Fox; Sarah K. Highlander; Mason V. Reichard; Rebecca J. Morton; Kenneth D. Clinkenbeard; George M. Weinstock

The gamma-proteobacterium Francisella tularensis is one of the most infectious human pathogens, and the highly virulent organism F. tularensis subsp. tularensis (type A) and less virulent organism F. tularensis subsp. holarctica (type B) are most commonly associated with significant disease in humans and animals. Here we report the complete genome sequence and annotation for a low-passage type B strain (OSU18) isolated from a dead beaver found near Red Rock, Okla., in 1978. A comparison of the F. tularensis subsp. holarctica sequence with that of F. tularensis subsp. tularensis strain Schu4 (P. Larsson et al., Nat. Genet. 37:153-159, 2005) highlighted genetic differences that may underlie different pathogenicity phenotypes and the evolutionary relationship between type A and type B strains. Despite extensive DNA sequence identity, the most significant difference between type A and type B isolates is the striking amount of genomic rearrangement that exists between the strains. All but two rearrangements can be attributed to homologous recombination occurring between two prominent insertion elements, ISFtu1 and ISFtu2. Numerous pseudogenes have been found in the genomes and are likely contributors to the difference in virulence between the strains. In contrast, no rearrangements have been observed between the OSU18 genome and the genome of the type B live vaccine strain (LVS), and only 448 polymorphisms have been found within non-transposase-coding sequences whose homologs are intact in OSU18. Nonconservative differences between the two strains likely include the LVS attenuating mutation(s).


Genome Announcements | 2015

Extreme Sensory Complexity Encoded in the 10-Megabase Draft Genome Sequence of the Chromatically Acclimating Cyanobacterium Tolypothrix sp. PCC 7601

Shaila Yerrapragada; Animesh Shukla; Kymberlie Hallsworth-Pepin; Kwangmin Choi; Aye Wollam; Sandra W. Clifton; Xiang Qin; Donna M. Muzny; Sriram Raghuraman; Haleh Ashki; Akif Uzman; Sarah K. Highlander; Bartlomiej G. Fryszczyn; George E. Fox; Madhan R. Tirumalai; Yamei Liu; Sun Kim; David M. Kehoe; George M. Weinstock

ABSTRACT Tolypothrix sp. PCC 7601 is a freshwater filamentous cyanobacterium with complex responses to environmental conditions. Here, we present its 9.96-Mbp draft genome sequence, containing 10,065 putative protein-coding sequences, including 305 predicted two-component system proteins and 27 putative phytochrome-class photoreceptors, the most such proteins in any sequenced genome.


Biochemistry and Molecular Biology Education | 2001

Molecular Cell Biology (4th edition): Harvey Lodish, Arnold Berk, S. Lawrence Zipursky, Paul Matsudaira, David Baltimore and James Darnell; Freeman & Co., New York, NY, 2000, 1084 pp., list price

Akif Uzman


Biochemistry and Molecular Biology Education | 2004

102.25, ISBN 0-7167-3136-3

Akif Uzman


Biochemistry and Molecular Biology Education | 2010

Essential cell biology (2nd ed.)

Akif Uzman


Biochemistry and Molecular Biology Education | 2007

Molecular Cell Biology, Sixth Edition

Akif Uzman


Biochemistry and Molecular Biology Education | 2010

The cell cycle: Principles of control (Primers in Biology series)

Akif Uzman


Biochemistry and Molecular Biology Education | 2003

Essential Cell Biology, Third Edition

Akif Uzman

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Yamei Liu

University of Houston

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Donna M. Muzny

Baylor College of Medicine

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Huaiyang Jiang

Baylor College of Medicine

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Alicia Hawes

Baylor College of Medicine

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Christian Buhay

Baylor College of Medicine

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Christie Kovar

Baylor College of Medicine

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