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1.
Environ Sci Technol ; 47(14): 8005-14, 2013 Jul 16.
Article in English | MEDLINE | ID: mdl-23758687

ABSTRACT

Silver nanoparticles cause toxicity in exposed organisms and are an environmental health concern. The mechanisms of silver nanoparticle toxicity, however, remain unclear. We examined the effects of exposure to silver in nano-, bulk-, and ionic forms on zebrafish embryos (Danio rerio) using a Next Generation Sequencing approach in an Illumina platform (High-Throughput SuperSAGE). Significant alterations in gene expression were found for all treatments and many of the gene pathways affected, most notably those associated with oxidative phosphorylation and protein synthesis, overlapped strongly between the three treatments indicating similar mechanisms of toxicity for the three forms of silver studied. Changes in oxidative phosphorylation indicated a down-regulation of this pathway at 24 h of exposure, but with a recovery at 48 h. This finding was consistent with a dose-dependent decrease in oxygen consumption at 24 h, but not at 48 h, following exposure to silver ions. Overall, our data provide support for the hypothesis that the toxicity caused by silver nanoparticles is principally associated with bioavailable silver ions in exposed zebrafish embryos. These findings are important in the evaluation of the risk that silver particles may pose to exposed vertebrate organisms.


Subject(s)
Metal Nanoparticles/toxicity , Silver/chemistry , Zebrafish/embryology , Animals
2.
Nucleic Acids Res ; 39(5): e26, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21131275

ABSTRACT

Microarray and next-generation sequencing techniques which allow whole genome analysis of chromatin structure and sequence-specific protein binding are revolutionizing our view of chromosome architecture and function. However, many current methods in this field rely on biochemical purification of highly specific fractions of DNA prepared from chromatin digested with either micrococcal nuclease or DNaseI and are restricted in the parameters they can measure. Here, we show that a broad size-range of genomic DNA species, produced by partial micrococcal nuclease digestion of chromatin, can be sequenced using paired-end mode next-generation technology. The paired sequence reads, rather than DNA molecules, can then be size-selected and mapped as particle classes to the target genome. Using budding yeast as a model, we show that this approach reveals position and structural information for a spectrum of nuclease resistant complexes ranging from transcription factor-bound DNA elements up to mono- and poly-nucleosomes. We illustrate the utility of this approach in visualizing the MNase digestion landscape of protein-coding gene transcriptional start sites, and demonstrate a comparative analysis which probes the function of the chromatin-remodelling transcription factor Cbf1p.


Subject(s)
Nucleosomes/chemistry , Sequence Analysis, DNA/methods , Basic Helix-Loop-Helix Leucine Zipper Transcription Factors/analysis , Chromatin/chemistry , Chromatin Assembly and Disassembly , DNA-Binding Proteins/analysis , High-Throughput Nucleotide Sequencing , Micrococcal Nuclease , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae Proteins/analysis , Transcription Initiation Site
3.
FEMS Microbiol Lett ; 309(2): 136-43, 2010 Aug 01.
Article in English | MEDLINE | ID: mdl-20584081

ABSTRACT

Clinical isolates of Photorhabdus asymbiotica have been recovered from patients in both the United States of America and Australia, and the full sequence of P. asymbiotica ATCC43949 from the United States has been reported recently. In contrast to other bacteria in the genus that only infect insects, P. asymbiotica strains are able to infect both insects and humans. Using a combination of Solexa (Illumina) and 454 Life Sciences (Roche) sequence data in different assembly pipelines, we report on a draft genome sequence of a strain of P. asymbiotica recovered from a patient from Kingscliff, Australia. The best assembly yielded an N50 scaffold size of 288 627 base pairs (bp) with >88.6% of the predicted genome covered by scaffolds over 100 000 bp. One of the central differences found between this Australian isolate and the US isolate is the presence of an additional plasmid, pPAA3. This plasmid is similar to pCRY from Yersinia pestis, the causative agent of bubonic plague, and the presence of pPAA3 may account for the increased virulence of Australian isolates both against tissue culture cells and infected patients. The genome of the Kingscliff strain also contains several genomic differences from the US isolate, whose potential significance in virulence against both humans and insects is discussed.


Subject(s)
Enterobacteriaceae Infections/microbiology , Genome, Bacterial , Photorhabdus/genetics , Plasmids/genetics , Virulence Factors/genetics , Australia , Humans , Photorhabdus/isolation & purification , Photorhabdus/metabolism , Physical Chromosome Mapping , Plasmids/metabolism , Sequence Analysis, DNA , Virulence Factors/metabolism
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