Publications by authors named "Reboud J"

Milk is commonly screened both for indicators of animal disease and health, but also for foodborne hazards. Included in these analyses is the detection of , that can produce an enterotoxin, causing staphylococcal food poisoning (SFP), which often leads to sudden onset of significant gastrointestinal symptoms in humans. Epidemiological data on SFP are limited, particularly in low- and middle-income countries.

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  • Smartphone colorimetry is being utilized in clinical settings, but issues like environmental biases and manufacturer variability limit its effectiveness.
  • This study systematically identifies imaging interferences in conventional smartphone cameras and introduces a new method for accurate sample quantification, enabling real-time imaging.
  • The research demonstrates the clinical use of smartphones for diagnosing conditions like cyanosis and monitoring oxygen levels, accounting for individual differences in skin tone to improve accuracy in healthcare diagnostics.
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Oximetry is used to quantify the presence of oxygen in soft tissues. It can be expressed as, for example, tissue oxygen saturation (StO), arterial oxygen saturation (SaO) and pulsatile oxygen saturation (SpO), among others. Non-invasive medical devices are used to estimate (SaO).

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Foot-and-mouth disease (FMD) is a highly contagious viral disease of cloven-hoofed animals responsible for economic losses that amount to >$20 billion annually. Rapid recognition of FMD cases provides vital information to guide control programmes. A range of point-of-need amplification technologies have been developed which allow sensitive detection of the causative virus (FMDV) in the field at locations remote from laboratories.

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Introduction: Diagnosis is a key step towards the provision of medical intervention and saving lives. However, in low- and middle-income countries, diagnostic services are mainly centralized in large cities and are costly. Point of care (POC) diagnostic technologies have been developed to fill the diagnostic gap for remote areas.

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Background: In countries where malaria is endemic, the use of rapid diagnostic tests(RDTs) has become routine, especially in rural settings. Such regions are characterised by often having other co-endemic infectious diseases, at high levels of prevalence.

Aim: To illustrate the potential added-value of "sentinel" screening for patients presenting for a routine diagnostic test for malaria, at healthcare facilities in Uganda.

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  • The study focuses on improving immunotherapy outcomes for cancer patients by analyzing both genetic and phenotypic diversity in individual cells, potentially leading to better-targeted treatments.
  • Researchers developed a nanoplatform that captures circulating tumor cells (CTCs) from blood samples and uses advanced technology to measure gene expression and analyze cell behavior in real-time.
  • This platform successfully generated a predictive index for identifying patients likely to benefit from immune checkpoint inhibitors, showing higher accuracy compared to existing clinical methods based on data from 80 lung cancer patients.
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  • Neisseria meningitidis is a serious bacterial pathogen causing meningitis and meningococcemia, with traditional diagnosis being slow due to time-consuming culture methods.
  • The study combined LAMP (a rapid DNA amplification technique) with CRISPR/Cas12a (a precise gene editing tool) to create a fast and reliable diagnostic test for N. meningitidis.
  • The results indicated that the LAMP-CRISPR/Cas method had high sensitivity (91%) and specificity (99%) for detecting the bacterium in clinical samples, outperforming traditional PCR techniques.
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Despite its importance, the functional heterogeneity surrounding the dynamics of interactions between mycobacterium tuberculosis and human immune cells in determining host immune strength and tuberculosis (TB) outcomes, remains far from understood. This work now describes the development of a new technological platform to elucidate the immune function differences in individuals with TB, integrating single-cell RNA sequencing and cell surface antibody sequencing to provide both genomic and phenotypic information from the same samples. Single-cell analysis of 23 990 peripheral blood mononuclear cells from a new cohort of primary TB patients and healthy controls enables to not only show four distinct immune phenotypes (TB, myeloid, and natural killer (NK) cells), but also determine the dynamic changes in cell population abundance, gene expression, developmental trajectory, transcriptomic regulation, and cell-cell signaling.

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Haemonchus contortus is a parasitic haematophagous nematode that primarily affects small ruminants and causes significant economic loss to the global livestock industry. Treatment of haemonchosis typically relies on broad-spectrum anthelmintics, resistance to which is an important cause of treatment failure. Resistance to levamisole remains less widespread than to other major anthelmintic classes, prompting the need for more effective and accurate surveillance to maintain its efficacy.

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  • Enterotoxins from Staphylococcus aureus are a leading cause of food poisoning, causing serious gastrointestinal issues and hospitalizations.
  • A systematic review of 128 studies on enterotoxins in raw ruminant milk showed an increase in research from 1980 to 2021, predominantly from Europe and South America, with a focus on cattle with mastitis.
  • The review identified a significant gap in data reporting quality, making it difficult to accurately assess the prevalence and distribution of enterotoxigenic S. aureus in raw milk.
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Although polydimethylsiloxane (PDMS) is a versatile and easy-to-use material for microfluidics, its inherent hydrophobicity often necessitates specific hydrophilic treatment to fabricate microchip architectures for generating double emulsions. These additional processing steps frequently lead to increased complexity, potentially creating barriers to the wider use of promising microfluidic techniques. Here we describe an alignment-free spatial hydrophilic PDMS patterning technique to produce devices for the creation of double emulsions using combinations of PDMS and PDMS/surfactant bilayers.

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The recent COVID-19 outbreak highlighted the need for lab-on-chip diagnostic technology fit for real-life deployment in the field. Existing bottlenecks in multistep analytical microsystem integration and upscalable, standardized fabrication techniques delayed the large-scale deployment of lab-on-chip solutions during the outbreak, throughout a global diagnostic test shortage. This study presents a technology that has the potential to address these issues by redeploying and repurposing the ubiquitous printed circuit board (PCB) technology and manufacturing infrastructure.

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  • The study explores the role of microRNA-155 (miR-155) in rheumatoid arthritis (RA), specifically how its increased expression may hinder monocyte polarization into anti-inflammatory macrophages.
  • Researchers tested the therapeutic effects of antagomiR-155-5p, a molecule designed to inhibit miR-155, using PEGylated liposomes in two mouse models of RA.
  • Results showed that injecting these liposomes reduced arthritis symptoms and improved the differentiation of bone marrow monocytes into anti-inflammatory macrophages, indicating a potential treatment strategy for RA in humans.
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Phage-inducible chromosomal islands (PICIs) are a family of phage satellites that hijack phage components to facilitate their mobility and spread. Recently, these genetic constructs are repurposed as antibacterial drones, enabling a new toolbox for unorthodox applications in biotechnology. To illustrate a new suite of functions, the authors have developed a user-friendly diagnostic system, based upon PICI transduction to selectively enrich bacteria, allowing the detection and sequential recovery of Escherichia coli and Staphylococcus aureus.

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The detection of changes in nucleic acid sequences at specific sites remains a critical challenge in epigenetics, diagnostics and therapeutics. To date, such assays often require extensive time, expertise and infrastructure for their implementation, limiting their application in clinical settings. Here we demonstrate a generalizable method, named Specific Terminal Mediated Polymerase Chain Reaction (STEM-PCR) for the detection of DNA modifications at specific sites, in a similar way as DNA sequencing techniques, but using simple and widely accessible PCR-based workflows.

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Despite its strong growth in many parts of the world, mobile health access is still limited in low- and middle-income countries. Among the many factors restricting implementation are the lack of information security, insufficient evidence base, low sensitization, and user acceptance. Limited evidence has been obtained on current practices, perceptions, and user acceptability in such settings.

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The current COVID-19 pandemic has shown us that the pulse oximeter is a key medical device for monitoring blood-oxygen levels non-invasively in patients with chronic or acute illness. It has also emphasised limitations in accuracy for individuals with darker skin pigmentation, calling for new methods to provide better measurements. The aim of our study is to identify the impact of skin pigmentation on pulse oximeter measurements.

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Accelerating the design of nucleic acid amplification methods remains a critical challenge in the development of molecular tools to identify biomarkers to diagnose both infectious and non-communicable diseases. Many of the principles that underpin these mechanisms are often complex and can require iterative optimisation. Here we focus on creating a generalisable isothermal nucleic acid amplification methodology, describing the systematic implementation of abstraction-based models for the algorithmic design and application of assays.

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Viral evolution impacts diagnostic test performance through the emergence of variants with sequences affecting the efficiency of primer binding. Such variants that evade detection by nucleic acid-based tests are subject to selective pressure, enabling them to spread more efficiently. Here, we report a variant-tolerant diagnostic test for SARS-CoV-2 using a loop-mediated isothermal nucleic acid-based amplification (LAMP) assay containing high-fidelity DNA polymerase and a high-fidelity DNA polymerase-medicated probe (HFman probe).

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The early diagnosis of active hepatitis C virus (HCV) infection remains a significant barrier to the treatment of the disease and to preventing the associated significant morbidity and mortality seen, worldwide. Current testing is delayed due to the high cost, long turnaround times and high expertise needed in centralised diagnostic laboratories. Here we demonstrate a user-friendly, low-cost pan-genotypic assay, based upon reverse transcriptase loop mediated isothermal amplification (RT-LAMP).

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In infectious disease diagnosis, results need to be rapidly communicated to doctors once testing has been completed, in order for care pathways to be implemented. This is a challenge when testing in remote low-resource rural communities, in which such diseases often create the largest burden. Here we report a smartphone-based end-to-end platform for multiplexed DNA malaria diagnosis.

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Human immunodeficiency virus (HIV) continues to be a major burden on public health globally with on-going increases in the number of new infections each year. Rapid and sensitive point-of-care tests allow timely interventions and are essential to control the spread of the disease. However the highly variable nature of the virus, resulting in the evolution of many subtypes and inter-subtype recombinants, poses important challenges for its diagnosis.

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The emergence of lipid membranes and embedded proteins was essential for the evolution of cells. Translocon complexes mediate cotranslational recruitment and membrane insertion of nascent proteins, but they already contain membrane-integral proteins. Therefore, a simpler mechanism must exist, enabling spontaneous membrane integration while preventing aggregation of unchaperoned protein in the aqueous phase.

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