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We report a new paper-based multiplex analytical device (mPAD) for simultaneous screening of three analytes (glutamate dehydrogenase, toxin A, and toxin B) known as biomarkers for Clostridioides difficile infection (CDI). To overcome the limitation of common rapid assays (e.g. lateral flow immunochromatographic and enzyme immunoassays) in terms of multiplexing, sensitivity, simplicity, and ease-of-use, the mPAD is constructed with a three dimensional (3D) configuration of paper components with a multi-channel design. Multiple fluidic paths developed with wax-patterned paper allow the simultaneous detection of glutamate dehydrogenase, toxin A, and toxin B without any cross-reactivity. The 3D fluidic network on the mPAD facilitates a self-operating test procedure for the mixing and addition of amplification reagents with a one-step sliding operation. The results of the multiplex CDI assay can be easily interpreted by the naked eye within 10 min, and are visually intensified over time resulting in up to 3-fold signal amplification. Our device exhibited remarkable analytical performances for the simultaneous detection of three CDI biomarkers, providing a sensitivity of 97%, specificity of 88%, accuracy of 95%, and limits of detection for glutamate dehydrogenase, toxin A, and toxin B of 0.16 ng mL, 0.09 ng mL, and 0.03 ng mL, respectively. These results indicate the high applicability and feasibility of mPAD for multiplex testing for CDI with the advantages of being simple, sensitive, inexpensive, user-friendly, and equipment-free.
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http://dx.doi.org/10.1016/j.bios.2020.112894 | DOI Listing |
Infect Dis Clin North Am
September 2025
Division of Gastroenterology & Hepatology, Department of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. Electronic address:
This article offers a clinically focused overview of Clostridioides difficile infection (CDI) diagnosis, emphasizing the need to test only symptomatic patients and to distinguish true infection from colonization. It reviews multistep diagnostic algorithms that pair glutamate dehydrogenase (GDH) testing or nucleic acid amplification tests (NAAT) with toxin assays to improve accuracy. The limitations of PCR-only approaches are discussed, with a strong emphasis on clinical correlation.
View Article and Find Full Text PDFBiochemistry
September 2025
Loyola University Chicago, Department of Chemistry and Biochemistry, 1068 W Sheridan Rd, Chicago, Illinois 60660, United States.
Dihydroorotate dehydrogenase 1B (DHOD1B) is one of several flavoproteins that utilize active half-sites. These enzymes have two flavin cofactors (FAD and FMN) that each interact with a specific reductant/oxidant substrate/product. Electrons gained at one-half-site must be transmitted to the other half-site and iron-sulfur centers between the flavin cofactors serve in this role.
View Article and Find Full Text PDFPlant J
September 2025
State Key Laboratory of Tree Genetics and Breeding, National Engineering Research Center of Tree Breeding and Ecological Restoration, Key Laboratory for Genetics and Breeding of Forest Trees and Ornamental Plants, Ministry of Education, College of Biological Sciences and Biotechnology, Beijing Fores
Floral thermogenesis in lotus (Nelumbo nucifera) is a highly energy-intensive process, requiring substantial metabolic reconfiguration and substrate input. However, the mechanisms coordinating energy substrate supply during this process remain unclear. Here, we integrated microscale proteomics, time-series transcriptomics, and mitochondrial feeding assays to elucidate the substrate provisioning strategies supporting thermogenesis in lotus receptacles.
View Article and Find Full Text PDFJ Biol Chem
September 2025
Department of Cell Physiology and Metabolism, University of Geneva Medical School, Geneva, Switzerland. Electronic address:
Upon glucose stimulation, metabolic pathways of pancreatic beta-cells promptly adapt metabolite levels inducing insulin secretion fine-tuned by mitochondrial glutamate dehydrogenase (GDH). Although well described in vitro, these responses cannot yet be captured in vivo due to the intrinsic nature of the islets scattered throughout the pancreas. Tested first in vitro, glutamate precursor glutamine enhanced glucose-stimulated insulin secretion without eliciting oxidative catabolism, as opposed to glucose.
View Article and Find Full Text PDFPlant Physiol Biochem
September 2025
College of Food Science and Pharmacy, Xinjiang Agricultural University, Urumqi, 830052, PR China. Electronic address:
The effect of ultrasound (US) treatment on storage quality and antioxidant capacity of fresh-cut broccoli was studied. Results indicated US treatment maintained a better appearance and retarded the increase of yellowing index, L∗, and microbial counts. Meanwhile, less reactive oxygen species accumulation including superoxide anion and hydrogen peroxide while higher antioxidant activities of superoxide dismutase, ascorbate peroxidase, catalase, and peroxidase were induced by US treatment.
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