Raghda R. Qadir , Hamin J. Mohammed , Samir M. Hamad , Yousef Mirzaei , Mukhtar H. Ahmed
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引用次数: 0
Abstract
Background
Coccidiosis is a significant parasitic disease affecting poultry, resulting in substantial economic losses due to its impact on growth, increased mortality, and compromised bird health.
Aim
This study aimed to evaluate the in vitro anticoccidial effects of a novel green-synthesised ZnO-Ag-CuO nanocomposite, using Thymus vulgaris extract.
Methods
The nanocomposite was synthesised through an eco-friendly method employing T. vulgaris as a stabilising and reducing agent. Characterisation was performed using UV-Vis spectroscopy, FTIR, XRD, SEM, and EDX, confirming its high crystallinity, nanoscale size, and the successful integration of ZnO, Ag, and CuO phases. Anticoccidial activity was assessed via a sporulation inhibition assay against Eimeria spp. Oocysts isolated from broiler chickens.
Results
The nanocomposite significantly reduced oocyst sporulation and increased the proportion of damaged and unpopulated oocysts in a dose-dependent manner (0.1–1 mg/mL) (p < 0.0001). ZnO–Ag–CuO NCs showed a dose-dependent anticoccidial effect, reducing sporulated oocysts to 56.41 %, 33.63 % and 22.9 % at 0.1, 0.5 and 1.0 mg/mL (control 88.62 %; p < 0.0001). Unsporulated oocysts increased to 15.9–62.22 % (control 13.33 %), while damaged oocysts reached up to 14.82 % (control 0 %).
Conclusion
The green-synthesised ZnO-Ag-CuO nanocomposite demonstrated strong in vitro anticoccidial activity; however, further studies are needed to evaluate the nanocomposite’s potential toxicity, formulation, stability under biological conditions, safety before practical applications and potential environmental impact within a One Health framework.
Future plans
In vivo studies are recommended to validate the efficacy and safety of these approaches for large-scale applications.
期刊介绍:
The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are:
• the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances
• intermediary metabolism and bioenergetics
• drug target characterization and the mode of action of antiparasitic drugs
• molecular and biochemical aspects of membrane structure and function
• host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules.
• analysis of genes and genome structure, function and expression
• analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance.
• parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules
• parasite programmed cell death, development, and cell division at the molecular level.