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Screening genome-wide sets of mutants for fitness defects provides a simple but powerful approach for exploring gene function, mapping genetic networks and probing mechanisms of drug action. For yeast and other microorganisms with global mutant collections, genetic or chemical-genetic interactions can be effectively quantified by growing an ordered array of strains on agar plates as individual colonies, and then scoring the colony size changes in response to a genetic or environmental perturbation. To do so, requires efficient tools for the extraction and analysis of quantitative data. Here, we describe SGAtools (http://sgatools.ccbr.utoronto.ca), a web-based analysis system for designer genetic screens. SGAtools outlines a series of guided steps that allow the user to quantify colony sizes from images of agar plates, correct for systematic biases in the observations and calculate a fitness score relative to a control experiment. The data can also be visualized online to explore the colony sizes on individual plates, view the distribution of resulting scores, highlight genes with the strongest signal and perform Gene Ontology enrichment analysis.
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http://dx.doi.org/10.1093/nar/gkt400 | DOI Listing |
Vet Dermatol
September 2025
Department of Veterinary Clinical Sciences, College of Veterinary Medicine, Iowa State University, Ames, Iowa, USA.
Background: The antibacterial efficacy of chlorhexidine shampoo is directly affected by formulation and bathing factors.
Hypothesis/objective: To evaluate the in vitro antibacterial efficacy of chlorhexidine-containing shampoos at various dilutions and to compare their lathering ability.
Animals: No animals were utilised in this study.
Front Microbiol
August 2025
Evolutionary Ecology and Genetics, Zoological Institute, Kiel University, Kiel, Germany.
Introduction: Antimicrobial resistance (AMR) is a critical global health issue caused by antibiotic overuse, leading to the rise of multi-resistant pathogens such as in bacteria of the ESKAPE group. Alternative or combination therapies, including bacteriophages and plaque-forming predatory bacteria, are being explored in response. , a Gram-negative bacterial predator belonging to the and like organisms (BALOs), can kill other Gram-negative bacteria after the periplasmic invasion, including multidrug-resistant pathogens.
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August 2025
Veterinary Epidemiology Unit, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Cleaning and disinfection (C&D) procedures are essential components of farm biosecurity, aiming to reduce microbial load and eliminate the pathogenic microorganisms in livestock farms facilities. This review examines the various methods used to assess the effectiveness of both cleaning and disinfection, exploring their strengths, limitations, and optimal-use scenarios. For cleaning evaluation, common methods include basic visual inspections, ultraviolet (UV) fluorescence, adenosine triphosphate (ATP) bioluminescence, rapid protein tests (RPT), redox potential, and microbiological swabbing.
View Article and Find Full Text PDFInfect Drug Resist
August 2025
School of Medicine, Huzhou University, Huzhou, 313000, China.
Background: Milk powder is a key food source, especially for infants and vulnerable groups. However, Bacillus contamination during production, storage, or handling can cause spoilage, quality issues, or health risks. This study identified and isolated from commercially available Chinese milk powder.
View Article and Find Full Text PDFJ Med Microbiol
September 2025
Microbiology, Mater Pathology, Mater Hospital Brisbane, South Brisbane, QLD 4101, Australia.
Blood cultures are an important test for the diagnosis of sepsis, and the time to an accurate result can allow for optimized antibiotic therapy. The 'choc drop' is a commonly performed, reliable and cheap rapid identification method, using a drop of positive blood culture broth incubated for a short period (2-4 h) before performing matrix-assisted laser desorption/ionization time-of-flight MS on any early growth/microbiological veil present. Due to the short incubation time (~2 h), agar plates may not reach the target temperature for optimal bacterial growth, leading to reduced accuracy of identification.
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