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Hajduk, J.

Publications and source records attributed to Hajduk, J..

3 recordsLinked to original sources

Maternal antibody-mediated elimination of a Puumala hantavirus outbreak in a bank vole colony

Bank voles (Myodes glareolus syn. Clethrionomys glareolus) are frequently used as an animal model in ecological and biomedical studies, and are important reservoir of viral and bacterial zoonotic pathogens, e.g. of Puumala hantavirus (PUUV). Here we describe an accidental PUUV outbreak in a large bank vole laboratory colony by incursion of infected wild-trapped bank voles, and a successful eradication of the virus. The eradication plan was based on results of previous studies, which showed that maternal antibodies (MatAb) protect the young from infection for up to 40 days after the weaning, four weeks longer than the estimated duration of maintaining infectivity of PUUV in the environment. After ensuring that most animals are infected, 620 pairs were mated on the same day. Only females that showed PUUV-specific antibodies and gave offspring within 26 days after the mating were retained. All individuals of the parental generation were euthanized before the last weaning. The weaned offspring was moved to individually ventilated cages (IVC) and repeatedly tested for the presence of PUUV-specific antibodies and RNA. A few infected and suspicious animals were euthanised. Then the animals were mated (in IVC) and after producing grand-offspring euthanised and tested for PUUV RNA in lungs. No PUUV RNA was detected, and no animals showed PUUV-specific antibodies in next generations. The successful clearance confirmed the protective efficiency of PUUV-specific MatAb. The procedure for clearance of PUUV in the bank vole colony may represent a blueprint for similar approaches in precious colonies of other rodents infected by similar pathogens. Author SummaryIn 2006 we started a unique long-term experiment on the bank vole, a common European rodent. Our goal was to study how animals can adapt to different challenges - a process called adaptive radiation. We established 16 vole lines: four control lines and others selected for specific behavioural and physiological traits. Over the years, this colony became an important model for studying evolution, physiology, and behaviour. Unfortunately, the colony became infected with Puumala hantavirus. The virus is mild for voles but can cause serious zoonotic illness in humans, without specific medical treatment available. At first, it seemed that the entire colony would have to be destroyed - a loss of thousands of animals and many years of research. However, we used a natural advantage: young voles born to infected mothers are temporarily protected by maternal antibodies. By carefully planning breeding, isolation, and testing, we created conditions where the virus lost its strength before the young lost their protection. This simple yet challenging approach worked - we saved the colony. Because many animals respond to viruses in a similar way, our method can help rescue other valuable research populations without complex procedures like embryo transfer or cross-fostering.

zoology↗

Software for semi-automatic analysis of microscopic images of adhesion structures and protein colocalization in cells

Background and ObjectiveAdhesion structures, such as focal and fibrillar adhesions, are protein complexes that mediate cell attachment to extracellular matrix via integrins. These structures participate in the mechanosensing process, transmitting forces from the cellular microenvironment to the cytoskeleton. The interaction between cells and their environment, along with the role of focal adhesion proteins, are areas of significant research interest. Accurate, quantitative analysis of adhesions structures in microscopic images is essential for advancing our understanding of the subject. However, the high variability and complexity of those structures in cells makes image analysis challenging, both in terms of subjectivity and time consumption. MethodsWe present a novel semi-automatic script for the detection of adhesion structures and analysis of their parameters, developed in MATLAB 2021a, to address the challenge of accurate image analysis of focal and fibrillar adhesions in cells. ResultsOur script offers a more time-efficient and less subjective alternative to manual analysis, while still allowing the user to retain control over the analytical process. It detects adhesion structures in confocal images and measures key parameters such as shape, orientation, and spatial distribution within cells, additionally providing visual label maps of the identified adhesion structures. The second add-on enables the calculation of correlation coefficients between two confocal microscopy image channels representing different stained cellular structures within the same cell, and generates visual colocalization maps, further enhancing the analysis of cellular architecture. ConclusionsThe presented open-source script offers a robust solution for the comprehensive, quantitative analysis of adhesion structures in microscopic images, based on user-defined analysis parameters. It is available online at https://github.com/patrycja-twardawa/FA-Colocalization.git.

bioinformatics↗

Talin1 adhesions' morphology is largely unaffected by polyacrylamide substrate stiffness

Cells sense the stiffness of their extracellular matrix (ECM) and adapt their behavior accordingly. We investigated how ECM stiffness affects the spatial organization of talin1, a key mechanosensitive focal adhesion protein. Using polyacrylamide (PA) hydrogels with tunable stiffnesses (0.2-188 kPa), we analyzed cell morphology, migration, talin1 distribution, colocalization with tensin3, and fibronectin deposition. Softer substrates enhanced filopodia activity and altered migration behavior. On softer ECMs, talin1 displayed a more even intracellular distribution, whereas on stiffer matrices it localized to the cell periphery. PA gels supported elongated talin1-based adhesions, whose morphology showed minimal variation across the 3-188 kPa stiffness range. Talin1-tensin3 colocalization was maintained regardless of stiffness, indicating a stable interaction. Notably, cells deposited more fibronectin on softer substrates. While talin1 adhesion morphology varied little with stiffness, cell migration behavior changed markedly. Combined with prior studies, our data suggests that ECM stiffness regulates talin1 primarily through conformational changes rather than macroscopic adhesion remodeling. These findings highlight talin1s central role in translating mechanical cues into dynamic cellular responses. Summary statementTalin1 forms elongated adhesions and robustly colocalizes with tensin3 across varying matrix stiffnesses, showing that their spatial organization is largely insensitive to mechanical cues.

cell biology↗