9 results match your criteria: "University of Edinburghgrid.4305.2[Affiliation]"

Species A rotavirus (RVA) vaccines based on live attenuated viruses are used worldwide in humans. The recent establishment of a reverse genetics system for rotoviruses (RVs) has opened the possibility of engineering chimeric viruses expressing heterologous peptides from other viral or microbial species in order to develop polyvalent vaccines. We tested the feasibility of this concept by two approaches.

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Reviewing the genetics underlying the arms race between bacteria and bacteriophages can offer an interesting insight into the development of bacterial resistance and phage co-evolution. This study shows how the natural development of resistances to the K1F bacteriophage, a phage which targets the K1 capsule of pathogenic Escherichia coli, can come about through insertion sequences (IS). Of the K1F resistant mutants isolated, two were of particular interest.

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Highly Sensitive Lineage Discrimination of SARS-CoV-2 Variants through Allele-Specific Probe PCR.

J Clin Microbiol

April 2022

Peter Medawar Building for Pathogen Research, Nuffield Department of Medicine, University of Oxfordgrid.4991.5, Oxford, United Kingdom.

Article Synopsis
  • Tools to detect SARS-CoV-2 variants are crucial for public health and the development of vaccines and therapies.
  • A new allele-specific probe PCR (ASP-PCR) method was created to efficiently identify virus variants, especially in samples with low viral loads or poor RNA quality.
  • ASP-PCR demonstrated higher accuracy than next-generation sequencing (NGS) in certain conditions and yielded nearly identical results to NGS, making it a strong complementary method for screening SARS-CoV-2.
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The single-celled parasite Trypanosoma brucei is transmitted by hematophagous tsetse flies. Life cycle progression from mammalian bloodstream form to tsetse midgut form and, subsequently, infective salivary gland form depends on complex developmental steps and migration within different fly tissues. As the parasite colonizes the glucose-poor insect midgut, ATP production is thought to depend on activation of mitochondrial amino acid catabolism via oxidative phosphorylation (OXPHOS).

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Kinetoplastid parasites cause diverse neglected diseases in humans and livestock, with an urgent need for new treatments. The survival of kinetoplastids depends on their uniquely structured mitochondrial genome (kDNA), the eponymous kinetoplast. Here, we report the development of a high-content screen for pharmacologically induced kDNA loss, based on specific staining of parasites and automated image analysis.

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Article Synopsis
  • Tick-borne encephalitis virus (TBEV) causes severe brain inflammation, primarily in northern Asia and Europe, and can lead to chronic illness or death; climate change is expanding its reach.
  • Interferon-induced transmembrane proteins (IFITMs), particularly IFITM3, are crucial for inhibiting TBEV infection and preventing cell death caused by the virus, with studies employing CRISPR-Cas9 methods confirming their protective roles.
  • Despite their protective effects, TBEV may partially evade IFITM suppression during high-density infections by spreading directly between cells, highlighting the need for further research into antiviral strategies and innate immune responses.
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Preexisting immune responses toward adenoviral vectors limit the use of a vector based on particular serotypes and its clinical applicability for gene therapy and/or vaccination. Therefore, there is a significant interest in vectorizing novel adenoviral types that have low seroprevalence in the human population. Here, we describe the discovery and vectorization of a chimeric human adenovirus, which we call HAdV-20-42-42.

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Evolutionary and Functional Analysis of Coagulase Positivity among the Staphylococci.

mSphere

August 2021

The Roslin Institute and Edinburgh Infectious Diseases, University of Edinburghgrid.4305.2, Easter Bush, Midlothian, Scotland, United Kingdom.

The bacterial genus Staphylococcus comprises a large group of pathogenic and nonpathogenic species associated with an array of host species. Staphylococci are differentiated into coagulase-positive or coagulase-negative groups based on the capacity to promote clotting of plasma, a phenotype historically associated with the ability to cause disease. However, the genetic basis of this important diagnostic and pathogenic trait across the genus has not been examined to date.

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