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Camel piroplasmosis is a tick-borne disease (TBD) caused by hemoprotozoan parasites. Hereby, we describe a cross-sectional study aiming at identifying spp.-infecting camels in Egypt using a multipronged molecular diagnostic approach. A total of 531 blood samples from camels () were collected from slaughterhouses at different governorates in Egypt for analysis during the period from June 2018 to May 2019. spp. was identified using microscopical examination and several different and sequential polymerase chain reaction (PCR) assays targeting the 18S rRNA genes. The overall prevalence of spp. in microscopical and molecular analyses in the samples was 11% (58/531) and 38% (203/531), respectively. Further discriminative multiplex PCR analysis targeting the 18S rRNA gene applied on all spp.-positive samples allowed the detection of (41%) (5.4%) (0.5%), and (4%). Additionally, the blast analysis of nested (n) PCR, targeting the V4 region, amplicon sequences resulted in the identification of (22%), sp. (9%), and sp. (3%). Overall, the results of this study confirmed the high prevalence of TBDs caused by several types of piroplasm hemoparasites in camel and suggests the need for future interventions aimed at improving the control of these potentially debilitating diseases that may be t-hreatening important economic resources and food security in Egypt.
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http://dx.doi.org/10.3389/fvets.2023.1178511 | DOI Listing |
RSC Adv
August 2025
Departamento de Química Módulo 13, Universidad Autónoma de Madrid, Campus de Excelencia UAM-CSIC Cantoblanco 28049 Madrid Spain.
[This corrects the article DOI: 10.1039/D4RA09076D.].
View Article and Find Full Text PDFBiomed Pharmacother
August 2025
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Zagazig University, Zagazig 44519, Egypt. Electronic address:
Globally and within Egypt, obesity fuels a growing health crisis, demanding novel therapeutic approaches rooted in systems medicine. This framework promotes the classification of diseases based on causal molecular mechanisms and use multi-target interventions to achieve synergistic effects within these pathways. Our previous research identified a dysregulated interaction among fatty acid synthase (FASN), arginase (ARG), and endothelial nitric oxide synthase (eNOS) as a potential mechanistic driver of obesity and its sequelae.
View Article and Find Full Text PDF3 Biotech
June 2025
Departamento de Química, Módulo 13, Universidad Autónoma de Madrid, Campus de Excelencia UAM-CSIC Cantoblanco, 28049 Madrid, Spain.
In this study, we measured the inhibitory potential of six coumarins against aldose reductase using both computational and experimental approaches. Molecular docking, molecular dynamics simulations, and MM/PBSA binding free energy calculations identified auraptene, marmesin, and isopimpinellin as the most promising inhibitors, with binding affinities of ΔG = -34.88, -29.
View Article and Find Full Text PDFRSC Adv
January 2025
Departamento de Química, Módulo 13, Universidad Autónoma de Madrid, Campus de Excelencia UAM-CSIC Cantoblanco 28049 Madrid Spain.
Squalene epoxidase (SQLE) is a crucial enzyme in the sterol biosynthesis pathway and a promising target for therapeutic intervention in hypercholesterolemia and fungal infections. This study evaluates the inhibitory potential of six flavonoids namely silibinin, baicalin, naringenin, chrysin, apigenin-7-O-glucoside, and isorhamnetin against SQLE using an integrative approach combining and experimental methods. Molecular docking revealed that apigenin-7-O-glucoside, silibinin, and baicalin displayed the highest binding affinities (-10.
View Article and Find Full Text PDFPharmaceuticals (Basel)
January 2025
Department of Clinical Pharmacology, Faculty of Medicine, Ain Shams University, Cairo 11566, Egypt.
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