3 results match your criteria: "University of Washingtongrid.34477.33 School of Medicine[Affiliation]"
J Bacteriol
December 2022
Department of Microbiology, University of Washingtongrid.34477.33 School of Medicine, Seattle, Washington, USA.
Many bacterial species use the secondary messenger, c-di-GMP, to promote the production of biofilm matrix components. In Pseudomonas aeruginosa, c-di-GMP production is stimulated upon initial surface contact and generally remains high throughout biofilm growth. Transcription of several gene clusters, including the Sia signal transduction system, are induced in response to high cellular levels of c-di-GMP.
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October 2022
Department of Laboratory Medicine and Pathology, University of Washingtongrid.34477.33 School of Medicine, Seattle, Washington, USA.
Within-host evolution produces genetic diversity in bacterial strains that cause chronic human infections. However, the lack of facile methods to measure bacterial allelic variation in clinical samples has limited understanding of intrastrain diversity's effects on disease. Here, we report a new method termed genome capture sequencing (GenCap-Seq) in which users inexpensively make hybridization probes from genomic DNA or PCR amplicons to selectively enrich and sequence targeted bacterial DNA from clinical samples containing abundant human or nontarget bacterial DNA.
View Article and Find Full Text PDFInfect Immun
January 2022
Department of Laboratory Medicine and Pathology, University of Washingtongrid.34477.33 School of Medicine, Seattle, Washington, USA.
A variety of eubacteria, plants, and protozoa can modify membrane lipids by cyclopropanation, which is reported to modulate membrane permeability and fluidity. The ability to cyclopropanate membrane lipids has been associated with resistance to oxidative stress in Mycobacterium tuberculosis, organic solvent stress in Escherichia coli, and acid stress in E. coli and Salmonella.
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