Poultry semen preservation is crucial for sustaining genetic diversity, improving production efficiency, and facilitating various breeding initiatives. This review underscores the importance and challenges associated with different preservation techniques. We investigate effective techniques for semen collection and evaluation, focusing on vital parameters such as volume, concentration, motility, and morphology. Preservation strategies are categorized into short-term approaches, such as dilution with extenders, and mid-to-long-term strategies, like freezing and the use of cryoprotectants. Additionally, we explore several factors affecting semen quality, including male age and genetics, seasonal impacts, and stress during handling. Assessing the quality of preserved semen is critical, particularly regarding post-thaw motility. The applications of these preservation techniques in artificial insemination, genetic enhancement, the conservation of endangered breeds, and biobanking are highlighted. This review identifies critical research opportunities, including the development of improved cryoprotectants, refining freezing protocols, comprehending the mechanisms of semen damage, and innovating novel preservation technologies. Addressing these challenges will enhance poultry semen preservation and contribute to sustainable poultry farming.

The only cells in an organism that could do any other sort of cell until 2006 (except sperm or egg) were known as embryonic stem cells, ESC

Chicken coccidiosis, a severe intestinal parasitic disease caused by Eimeria protozoa, causes substantial annual economic losses to the global poultry industry. This study focused on investigating the role of tumor necrosis factor receptor (TNFR)-associated factor 6 (TRAF6) in modulating chicken innate immune responses against Eimeria tenella (E. tenella) infections. Here, we show that TRAF6 is sensitive to the process of E. tenella infection, and cecal tissue responds to the early infection of E. tenella by up-regulating the expression of TRAF6. Specifically, TRAF6 overexpression enhances E. tenella-induced activation of the NF-κB pathway (a core innate immune signaling cascade), thereby promoting host inflammatory cytokines production and cell apoptosis, while TRAF6 knockdown mitigates these pathological effects. Mechanistically, TRAF6-mediated regulation of NF-κB pathway activation and inflammatory responses during E. tenella infection can be specifically targeted by key microRNAs (miRNA), gga-miR-7b, in chickens. Taken together, this study identifies that TRAF6 plays an important regulatory role in innate immune response against E. tenella infection, providing novel insights into host–parasite interactions and potential targets for coccidiosis control.

The growing global demand for ethical, resource-efficient protein sources has renewed serious interest in cultured meat as a viable alternative to conventional livestock production. Two revolutionary biotechnological systems, induced pluripotent stem cell (iPSC) reprogramming and CRISPR-Cas9-mediated genome editing, when combined, offer unparalleled accuracy and scalability for the biofabrication of avian flesh. In this review, we present a comprehensive pipeline that involves the ectopic expression of Yamanaka factors (Oct4, Sox2, Klf4, and c-Myc) to reprogram primary somatic cells derived from Gallus gallus into induced pluripotent stem cells (iPSCs). This process is subsequently followed by targeted genome editing to enhance myogenic potential, growth efficiency, nutritional composition, and disease resistance. iPSCs are cultivated in a xeno-free bioreactor following genome editing, and subsequently directed to develop into myoblasts and mature myotubes. Three-dimensional tissue biofabrication is realized by combining biomaterial scaffolds and perfusion bioreactor systems, structuring an authentic muscle tissue matrix. These engineering platforms enable precise control over microenvironmental parameters, including oxygenation and nutrient perfusion. The resulting biofabricated poultry product is compositionally optimized, free of antibiotic residues, and exhibits a significantly reduced environmental footprint than poultry that is grown in the traditional way. This all-in-one solution solves important problems in food security, animal welfare, land use efficiency, and greenhouse gas emissions while also setting up a scalable biomanufacturing framework for making proteins for the next generation.

The preservation of rooster semen quality during short-term liquid storage remains a challenge in poultry reproductive biotechnology because sperm cells rapidly lose functional competence under ambient conditions. This deterioration is largely associated with oxidative stress and lipid peroxidation of sperm membranes, which are particularly vulnerable in avian species due to their high polyunsaturated fatty acid content and limited cytoplasmic antioxidant defenses. Selenium is an essential trace element involved in cellular antioxidant protection through its incorporation into several selenoproteins that regulate redox balance and protect cellular structures from oxidative injury. The present study evaluated the effects of selenium methionine supplementation on rooster semen quality during liquid storage at 25 °C. Semen was diluted using a standard poultry semen extender composed of sodium glutamate, glucose, potassium acetate, magnesium acetate, and potassium citrate. Selenium methionine was incorporated into the semen extender at concentrations of 0.5%, 1%, and 2% (w/v) at the time of semen dilution prior to storage. Semen quality was assessed at 0, 4, 8, 12, and 24 h of storage. Functional parameters, including total sperm motility, sperm viability, and dead sperm percentage, together with kinematic variables (VSL, VCL, VAP, ALH, LIN, and STR), were analyzed using computer-assisted sperm analysis (CASA). Structural integrity was evaluated through acrosome and plasma membrane integrity tests, while sperm physiological status and apoptotic progression were assessed using Annexin V-FITC/propidium iodide flow cytometry. Significant effects of storage time, selenium methionine concentration, and their interaction were observed for multiple semen quality parameters (p < 0.05). Among the tested concentrations, supplementation with 0.5% selenium methionine consistently produced the most favorable results, maintaining higher sperm motility, viability, and membrane integrity while reducing dead sperm percentage and apoptotic progression during storage, with protective effects particularly evident at 8, 12, and 24 h compared with the control and higher concentrations. Polynomial contrast analysis indicated predominantly non-linear dose–response relationships, with quadratic and cubic components providing the best model fit (R² = 0.90–0.99; p < 0.0001), suggesting a hormetic antioxidant effect. Overall, these findings indicate that selenium methionine supplementation in semen extender improves the stability of rooster semen during short-term liquid storage at ambient temperature, with 0.5% showing the most consistent protective effects among the concentrations evaluated.