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Zhumanov, K.

Publications and source records attributed to Zhumanov, K..

2 recordsLinked to original sources

Deep Learning-enabled Sperm Morphology Analysis of Bovine Sperm for label-free Imaging Flow Cytometry

Data analysis of sperm morphology is critical for evaluating bull fertility, yet it is often performed using light microscopy and staining techniques in a highly subjective and manual manner. In this study, we introduce a scalable, high-resolution approach combining label-free Imaging Flow Cytometry (IFC) with deep learning for automated classification of bovine sperm morphology. We analyzed 436,374 single-cell images obtained from three prominent bull breeds in Kazakhstan - Kazakh Whitehead, Auliekol, and Simmental from fresh and cryopreserved sperm - providing a uniquely large and diverse dataset. The dataset was used for training and evaluation of deep learning models, among which the convolutional neural network (CNN) MobileNetV4 yielded superior results, achieving 92.3% accuracy and a 0.91 F1-score after training with a Layer-wise Pretraining and Fine-Tuning (LP-FT) strategy. The model classified spermatozoa into eight distinct morphological categories. The CNN-based pipeline ensured consistent, observer-independent classification across all samples. Testing across different conditions and breeds resulted in a 5-10% drop in generalization performance, highlighting the impact of domain-specific biases and underscoring the need for larger, standardized datasets. The proportion of morphologically abnormal spermatozoa varied between seasons and after cryopreservation. This study highlights the advantages of integrating IFC and artificial intelligence (AI) algorithms for robust, high-throughput, and objective label- free spermatozoa morphology assessment in fresh and cryopreserved sperm, offering a promising tool for improving fertility diagnostics and breeding strategies in veterinary practice.

systems biology↗

Brucella proline racemase protein A targets Tpl2 to promote IL-10 secretion for establishment of chronic infection

IL-10, an anti-inflammatory cytokine, plays a crucial role in limiting immune responses to pathogens, preventing host damage. However, the mechanisms underlying Brucella-mediated IL- 10 production remain incompletely understood. In this study, we demonstrate that the proline racemase protein A (PrpA) of Brucella melitensis M5-90 induces macrophages to secrete IL-10 by activating the Tpl2-ERK signaling pathway, thereby promoting chronic infection. Moreover, Tpl2 deletion impairs macrophage bactericidal ability, accompanied by reduced TNF- and IL-1{beta} but unaffected IL-10 levels. Additionally, Trp309, Glu103, and Glu129 of PrpA participate in interaction with Tpl2, but these residues do not influence PrpA-mediated IL-10 production in macrophages. PrpA deletion enhances IFN-{gamma} levels, specific anti-Brucella IgG, and CD4+ and CD8+ T cell numbers in mice. Furthermore, the Brucella melitensis M5-90 prpA mutant provides higher protection than the parental strain against virulent Brucella melitensis M28 infection in mice. Our findings suggest that Brucella PrpA promotes IL-10 secretion by macrophages through Tpl2 activation for bacterial survival and persistent infection, making the Brucella melitensis M5-90 prpA mutant a promising vaccine for enhanced protection. Author SummaryIL-10, an anti-inflammatory cytokine, is exploited by Brucella for survival. We identified Brucella PrpA as a potent IL-10 inducer, activating the Tpl2-ERK signaling pathway. Tpl2 deletion increased Brucella survival in macrophages, accompanied by reduced TNF- and IL-1{beta} but unaffected IL-10 secretion. Residues (Trp309, Glu103, and Glu129) of PrpA were crucial for interaction with Tpl2, yet did not impact PrpA-mediated IL-10 production. The B. melitensis M5-90 prpA mutant induced higher anti-Brucella IgG, IFN-{gamma}, and CD4+ and CD8+ T cell numbers in mice, providing better protection than B. melitensis M5-90. These findings unveil PrpAs role in IL-10 production and highlight the potential of the B. melitensis M5-90 prpA mutant as a promising vaccine for further evaluation.

microbiology↗