Search Results (418)

Cryptosporidium spp. are common protist pathogens, and the growing popularity of pet rodents raises concerns about their potential role in zoonotic parasites transmission. However, epidemiological data on Cryptosporidium spp. in pet rodents in Yunnan Province is scarce. To examine the occurrence of Cryptosporidium spp. in pet rodents in Yunnan, we collected 762 fecal samples from four rodent species across four cities. Nested PCR and DNA sequencing were used to characterize the species and subtypes of Cryptosporidium. The occurrence of Cryptosporidium spp. in guinea pigs (Cavia porcellus), Siberian dwarf hamsters (Phodopus sungorus), Syrian hamsters (Mesocricetus auratus) and fancy rats (Rattus norvegicus domestica) was 18.7% (80/426), 17.3% (36/207), 12.5% (15/120), 0% (0/9), respectively, with an overall rate of 17.2% (131/762). According to regions, the positivity rate of Cryptosporidium spp. in Zhaotong city, Kunming city, Yuxi city and Qujing city was 21.0%, 17.9%, 16.8% and 10.5%, respectively. In terms of sampling location, the occurrence of Cryptosporidium spp. in pet markets, farms and shops was 19.5%, 18.6% and 0%, respectively. Sequence analysis of the small subunit ribosomal RNA (SSU rRNA) gene identified six Cryptosporidium species/genotypes: Cryptosporidium homai (n = 52), Cryptosporidium wrairi (n = 30), Cryptosporidium sp. hamster genotype (n = 25), Cryptosporidium andersoni (n = 20), Cryptosporidium parvum (n = 5), and Cryptosporidium muris (n = 1). Further subtyping of C. andersoni isolates using multilocus sequence typing (MLST) revealed a single subtype, with all isolates identified as A3A4A2A2. All five C. parvum isolates were identified as subtype IIdA15G1 based on the gp60 gene. Our findings demonstrated the presence of the zoonotic C. parvum IIdA15G1 subtype in pet rodents, suggesting that these animals, particularly hamsters, may serve as reservoirs for human-pathogenic Cryptosporidium species. These results underscore the need for improved biosecurity and husbandry practices in the pet rodent trade to mitigate public health risks. Full article

N-Lactoyl-phenylalanine (Lac-Phe), identified in 2022 as an exercise-inducible signaling metabolite, is formed by carnosine dipeptidase 2 via conjugation of lactate and phenylalanine. Its circulating levels rise sharply after intense exercise in mice, humans, and racehorses, reflecting increased glycolytic flux. Beyond exercise, Lac-Phe also rises with feeding and metformin, positioning it as a potential integrator of energy intake, expenditure, and metabolic homeostasis. Centrally, Lac-Phe may contribute to appetite suppression by inhibiting hypothalamic orexigenic agouti-related protein neurons, primarily observed in obese rodent models, while sparing anorexigenic pro-opiomelanocortin neurons, thereby reducing food intake, promoting weight loss, and improving glucose tolerance in obese models without altering energy expenditure. Peripherally, it drives anti-inflammatory M2 macrophage polarization, ameliorating colitis and aiding recovery after spinal cord injury via NF-κB suppression and reactive oxygen species reduction. As a biomarker, Lac-Phe may offer advantages over lactate in reflecting mitochondrial dysfunction in conditions such as MELAS, sepsis, and NADH-reductive stress; however, these observations derive mainly from small-scale or exploratory studies and require prospective validation. Recent studies from 2024 to 2025 further reveal its partial and context-dependent role in mediating metformin’s effects, intensity- and sex-dependent responses, renal clearance via SLC17A1/3 transporters, and links to exercise-induced redox adaptations. The first human phase I trial (NCT06743009), launched in 2025, is assessing the metabolic effects of Lac-Phe in obesity. This Perspective summarizes Lac-Phe biosynthesis, physiological mechanisms, including its emerging but largely correlative connections to redox homeostasis, and therapeutic promise, underscoring its potential relevance for exercise-mimicking strategies in metabolic, inflammatory, and redox-related disorders. Full article

This review examines how forest microrefugia (fine-scale thermal and moisture shelters formed by canopy complexity, deadwood, topography, and snow) protect small mammals from climate extremes in European forests. It synthesizes evidence on the physiological and behavioral sensitivity of rodents and shrews to near-ground abiotic environmental conditions and highlights methods for measuring and modeling microclimatic factors using LiDAR and sensor networks. These findings are integrated into a framework that links structural retention, coarse woody debris, and canopy heterogeneity to microclimate resilience. Despite global advances in microclimate research and the development of new research methods and equipment, empirical data from European forests remain scarce, particularly regarding operative temperature, humidity, and vapor pressure deficit near the ground and within subnivean habitats. By bridging the fields of microclimate physics, small mammal ecology, and silvicultural design, the review identifies the mechanisms and metrics recommended to sustain functional refugia. The synthesis identifies knowledge gaps, standardizes microclimate metrics, and outlines required forest management practices, revitalizing research and inspiring new approaches to small mammal ecology. Full article

Bladder cancer (BCa) is the second most common cancer of the genitourinary tract globally. It has limited treatment options, high recurrence rate, and acquires resistance to platinum-based therapy. Therefore, identifying novel therapeutic targets is urgently needed. Analysis of the TCGA data revealed that the enzyme galactokinase-1 (GALK1) is overexpressed (p < 0.0001) in bladder tumors compared to normal tissue. Our data also confirmed GALK1 protein upregulation in multiple human BCa cell lines and rodent bladder tumors. However, the precise role of GALK1 in BCa progression and effects of its specific inhibitor remain unexamined. In this study, we demonstrate that GALK1 gene silencing using shRNA resulted in a significant reduction in BCa cell proliferation, migration, and invasion. Pharmacological inhibition of GALK1 using small molecule Cpd36 resulted in anticancer efficacy against BCa. Cpd36 inhibited proliferation, migration, and invasion of BCa cells. Further, Cpd36 induced G1 phase cell cycle arrest, apoptosis, mitochondrial membrane depolarization, and ROS production in the BCa cells. Mechanistically, Cpd36-induced reduction in cell proliferation was associated with a decrease in expression of GALK1, PCNA proteins. Inhibition of metastatic potential was accompanied by decreased migration, invasion, and MMP-9 expression. Cell cycle arrest was associated with decrease in Cyclin D1 and increased expression of p21 and p27. Induction of apoptosis was linked with increased expression of cleaved caspase-3 and cleaved PARP, while downregulating p-AKT. Additionally, Cpd36 in combination with cisplatin or gemcitabine showed a strong synergistic effect on BCa cells. Taken together, our findings suggest that GALK1 plays a significant role in BCa cell survival and validates its inhibitors as promising therapeutic options for managing this disease. Full article

Chapare virus (CHAPV) is an Arenaviridae family member and causative agent of Chapare hemorrhagic fever (CHHF). Endemic to Bolivia, CHAPV was found to be the cause of several outbreaks of CHHF in Bolivia in 2003 and 2019 with high case-fatality rates and instances of human-to-human transmission. The pathogenesis of CHAPV infection is poorly understood, and no vaccines or antivirals are available, in part due to a dearth of available animal models. Mice lacking signal transducer and activator of transcription 1 (STAT1^-/-) have been shown to succumb to infection by related arenaviruses, including Machupo virus, and were investigated for their susceptibility to CHAPV infection. Challenge with CHAPV resulted in partial lethality in STAT1^-/- mice with a biphasic disease course characterized by initial viral load and pathology in the spleen and liver followed by inflammation and high viral titers in the brain and spinal cord that immediately preceded mortality. Adaptation in the brains of STAT1^-/- mice resulted in a fully lethal mouse-adapted CHAPV variant, with a similar biphasic disease course, but virus in tissues was detected more proximal to challenge. The result of this study is a lethal small-animal rodent model for CHAPV that recapitulates many aspects of human CHAPV disease. Full article

Background/Objectives: Habitat degradation and fragmentation reduce population size, genetic diversity, and connectivity, increasing extinction risk in small and isolated populations. Coastal wetlands of northwestern Peru have undergone extensive anthropogenic modification, yet the genetic and ecological status of resident carnivore populations remains poorly documented. This study aimed to assess genetic diversity, relatedness, demographic signals, and diet composition of a Pampas cat (Leopardus garleppi) population inhabiting the Mangroves San Pedro de Vice (MSPV), a Ramsar-listed coastal wetland. Methods: We combined noninvasive fecal genotyping using eight nuclear microsatellite loci with vertebrate DNA metabarcoding. Scat samples were collected across three field seasons (2019–2021). Individual identification, genetic diversity metrics, genetic mark–recapture estimation of census size (Nc), effective population size (Ne), bottleneck tests, and relatedness analyses were performed to evaluate population status and kin structure. Dietary composition was characterized using metabarcoding and assessed for sex-specific differences. Results: Sixty-eight scats yielded multilocus genotypes for nine individuals (six males, three females). Genetic analyses revealed moderate diversity (mean allelic richness = 3.47; observed heterozygosity = 0.69; expected heterozygosity = 0.58) and evidence consistent with a recent genetic bottleneck. Genetic mark–recapture analyses estimated a small census size (Nc = 9; 95% CI: 7.0–9.0), while the effective population size was markedly low (Ne = 2.4; 95% CI: 1.5–7.4), yielding an Ne/Nc ratio of ~0.27. Multiple first-order kin dyads were detected, indicating strong local kin structure and limited external recruitment. Metabarcoding identified eight vertebrate prey species, with diet dominated by the native rodent Aegialomys xanthaeolus. No significant sex-specific differences in diet composition were detected. Conclusions: The MSPV Pampas cat population represents a small, kin-structured range-edge population showing signatures consistent with recent genetic erosion and restricted connectivity. These patterns align with isolation in a degraded coastal wetland landscape, highlighting the importance of habitat protection, prey resource conservation, and restoration of functional connectivity to support long-term population persistence. Full article

Despite the growing interest in brain structural plasticity and the substantial body of knowledge that has accumulated over recent decades, some issues remain poorly defined, leading to confusion in the interpretation of results. In addition to stem cell-driven neurogenesis in adult neurogenic niches (adult neurogenesis), neuronal precursors in a state of arrested maturation have also been described, representing a form of neurogenesis without division based on so-called “immature” or late-maturing neurons. These processes occur in different brain regions yet share certain molecular markers and temporal windows. Recent advances in comparative neuroplasticity have further complicated our understanding. Studies reveal a reduction in adult neurogenesis in the olfactory bulb and hippocampus of large-brained, gyrencephalic mammals compared with small-brained species such as rodents. Conversely, a higher prevalence of immature neurons has been reported in the neocortex and amygdala of larger-brained mammals. It is becoming evident that evolutionary trade-offs took place in distinct plastic processes, resulting in the predominance of certain forms in particular species, while others coexist and share overlapping markers. Regardless of the approach employed (neuroanatomical, immunocytochemical, phylogenetic, or transcriptional), current evidence indicates substantial heterogeneity in cell types with different origins and fates across diverse mammalian species. These patterns appear to be sculpted by evolutionary pressures yet unified by shared transient maturational states. Full article

The common vole is one of the mammalian pests causing more agricultural damage in Europe. Since the late 1970s, this species has invaded the Duero valley in NW Spain, colonizing ca. 5 million ha of agricultural areas of the valley in about 20 years. Once settled in agricultural landscapes, the species experienced cyclic population outbreaks causing crop damages. The major vole population outbreak of 2006–2007 was managed by the Regional Government (Junta de Castilla y León, JCYL) mainly through large-scale application of anticoagulant rodenticides (ARs) and widespread destruction of field margins, natural vegetation patches, and crop stubbles by burning. These actions caused serious damage to regional agrarian biodiversity, including small game species. The coordinated action of scientific institutions and environmental NGOs, with the support of the main Spanish hunting association at a critical time, led to a progressive shift in pest management strategies during subsequent outbreaks, promoting the adoption of biological control and other management techniques causing less environmental damage. Finally, JCYL implemented an IPM program mainly based on biological control, good farming practices, and habitat management. This program has been increasingly adopted in recent years, leading to a marked reduction in chemical control and the complete elimination of burning as a tool of management. Over this period, the scientific knowledge of the species’ ecology has expanded substantially, providing key insights for the development and refinement of IPM strategies. Here, we synthesize this body of knowledge and provide additional recommendations to further improve the current IPM program, which may serve as a model for rodent pest management in other regions worldwide. Full article

Intranasal drug delivery represents a transformative “backdoor” to the brain, bypassing the blood–brain barrier (BBB) that bars 98% of small molecules and nearly all large biopharmaceuticals. By harnessing the unique anatomy of the olfactory and trigeminal nerves, therapeutics can travel directly from the nasal cavity to the central nervous system, achieving therapeutic concentrations without the systemic toxicity of traditional routes. Clinical and preclinical evidence highlight the efficacy of intranasal insulin (INI) in treating Alzheimer’s disease (AD) and delirium, with studies showing significant improvements in cognitive scores and reduced hospital stays (7.9 vs. 12.9 days; p = 0.014). Additionally, other peptides can be administered intranasally like oxytocin, neuropeptide Y, and novel metabolic modulators for neuroprotection and affective disorders (AD, autism, Down syndrome). Despite these promises, critical translational gaps remain, including anatomical differences between macrosmatic rodents and microsmatic humans, and significant sex-based dosing dimorphism. The ease of intranasal administration introduces profound bioethical dilemmas regarding neuroenhancement, authenticity, and informed consent in vulnerable populations. The current literature concludes that realizing the full potential of nose-to-brain (N2B) therapy requires a commitment to precision medicine, utilizing specialized delivery devices and objective biomarkers to ensure safe and equitable clinical application. Full article

Rapid vascularization is essential for bone regeneration in oral and maxillofacial surgery. This systematic review synthesised in vivo evidence on 3D-printed composite scaffolds in rodent critical-size calvarial defects quantified by Microfil perfusion and micro-CT. “Composite” was defined as an organic–inorganic construct within the printed scaffold (not a single-phase scaffold with a surface coating). PubMed, MEDLINE, and Web of Science Core Collection were searched for studies published from January 2014 to December 2025. Eligible studies compared composite scaffolds with non-composite (single-phase) scaffolds and/or empty controls and reported vascular outcomes (vessel number, vascularized area) together with bone outcomes (new bone area, bone volume fraction [BV/TV], and bone mineral density). Ten studies met the inclusion criteria. In outcome-specific exploratory analyses, composite scaffolds were associated with higher new bone area than comparators (p = 0.031). Functional modifications were associated with higher vascularized area (p = 0.025) and higher new bone area (p = 0.038), while dual-factor modifications showed the largest gain in new bone area (p = 0.002). Pore sizes ≥ 400 μm were associated with higher BV/TV (p = 0.029). Heterogeneity in designs, follow-up, and reporting, together with small sample sizes, precluded meta-analysis. Composite scaffolds appear promising, but standardised methodologies and improved reporting are needed to define optimal design features and support translation. Full article

This study examines risky decision-making in a free-ranging population of Balinese long-tailed macaques (Macaca fascicularis fascicularis), addressing gaps in research that have largely focused on captive primates and have rarely considered individual differences by age and sex. Thirty-three macaques of different age–sex classes were tested using a choice task contrasting a guaranteed small reward with a probabilistic larger reward. At the group level, macaques showed no preference for safe or risky options. However, substantial individual variation emerged: some individuals were risk-prone, others risk-averse, and many indifferent. Notably, age and sex interacted in shaping risk preferences. Among males, adults and juveniles were more risk-prone than younger adults, whereas among females, adults were more risk-prone than juveniles. Juveniles also displayed outcome-dependent flexibility, choosing the risky option more often after a previous successful risky choice, consistent with a win–stay strategy. Like in rodents, this pattern may reflect adaptive learning during developmental transitions. Importantly, the observed behavioral differences were not due to misunderstanding of the task, as macaques reliably chose the larger option when outcomes were visible. This pronounced individual variability in primate risk preferences underscore the importance of considering demographic factors when characterizing species-typical risk preferences. Full article

Precise quantification of fine motor behaviour is essential for understanding neural circuit function and for evaluating therapeutic interventions in neurological disorders. While markerless pose estimation frameworks such as DeepLabCut (DLC) have transformed behavioural phenotyping, the choice of convolutional neural network (CNN) backbone has a critical impact on tracking performance, particularly in tasks involving small distal joints and frequent occlusions. In this study, we present the first systematic comparison of nine CNN architectures implemented in DLC for lateral-view analysis of skilled reaching movements in the Montoya Staircase test, a gold-standard assay for forelimb dexterity in rodent models of stroke and neurodegenerative disease. Using a dataset comprising both control and primary motor cortex (M1)–lesioned mice, we evaluated model performance across six key dimensions: spatial accuracy (RMSE, PCK@5 px), mean average precision (mAP), robustness to occlusions, inference speed, and GPU memory usage. Our results demonstrate that multi-scale DLCRNet architectures substantially outperform conventional backbones. DLCRNet_ms5 achieved the highest overall accuracy, while DLCRNet_stride16_ms5 provided the most favourable balance between precision and computational efficiency. These findings provide practical methodological guidance for neuroscience laboratories and highlight the importance of CNN architecture selection for the reliable quantification of fine motor behaviour in preclinical research. Full article

Cystinosis is a rare autosomal recessive lysosomal storage disorder that is caused by mutations in the CTNS gene. The hallmark of this disease is the accumulation of cystine within lysosomes, which functions as a pivotal diagnostic and monitoring biomarker. Cysteamine therapy has been demonstrated to reduce lysosomal cystine and improve outcomes; however, it does not fully halt progression, particularly renal decline. Consequently, preclinical research relies on diverse in vitro and in vivo models to explore mechanisms and test new treatments. Accurate intracellular cystine quantification is vital for clinical and research purposes. Conventional granulocyte cystine measurement, the prevailing standard, is technically intricate and necessitates volumes of samples, which presents challenges for rodent models. Advancements in analytical chemistry, such as the use of liquid chromatography with tandem mass spectrometry (LC-MS/MS), have enhanced the sensitivity of analytical methods. However, the development of optimized methods for analyzing small volumes of biological samples remains a limitation. This study presents a novel micro-quantification protocol for measuring cystine in a minimal volume of whole blood from rodent models. This protocol enhances the sensitivity, reproducibility, and feasibility of longitudinal studies. Addressing this methodological gap is imperative for accelerating translational research and supporting the development of improved therapies for cystinosis. Full article

Infestations of small terrestrial mammals (e.g., rodents and lagomorphs) on the Qinghai–Tibet Plateau pose formidable challenges, which are exacerbated by the region’s vast expanse and extreme environmental conditions. Conventional chemical treatments have proven unsustainable and environmentally detrimental, highlighting the urgent need for innovative solutions. We introduce the Grassland Guidance Trap System (GGTS), an innovative control method specifically designed for ecologically sensitive plateau regions experiencing severe small terrestrial mammal infestations. In this study, we systematically investigated the capturing mechanisms of the GGTS and its sustained control effect during large–scale enclosed field deployment. The results demonstrate that the guide net achieves a 2.62–fold increase in the number of plateau pikas (Ochotona curzoniae) captured through targeted behavioral guidance; field–based behavioral trials confirm that the guide net significantly elevates plateau pikas’ observation area entries and observation area duration in adjacent areas. The open–field test demonstrated that the movement distance and activity time of plateau pikas in the corner area of the device were both significantly higher than those in the central area. In addition, rigorous 600–day field tests across 400 hm² confirmed the system’s exceptional efficacy, reducing plateau pika density by 46.38% within 100 m and 20.45% at 500 m. Notably, its effectiveness improved over time, highlighting its potential as a scalable, sustainable management solution. This research not only establishes the GGTS as a viable solution for plateau pika control but also represents a significant advancement in ecological plateau pika management, fostering long–term ecological balance on the Qinghai–Tibet Plateau. Full article

Background: Africa is a continent with diverse climates, landscapes, rainfall patterns, and vegetation types, all of which significantly influence its mammalian fauna, particularly small mammals. Rodents, which are highly diverse across the continent, serve as reservoirs for various zoonotic pathogens. Frequent human–rodent interactions heighten the risk of zoonotic disease transmission, posing a serious public health concern. Methods: This study conducted a comprehensive review of rodent control methods and their effectiveness in mitigating zoonotic diseases in Africa. Literature searches were performed using PubMed, Web of Science, ResearchGate, and Google Scholar. Additionally, one study was manually identified from the reference lists of the retrieved papers. Results: Thirteen relevant studies were identified, including seven field-based studies, five model evaluations, and one review. The distribution of studies varied by country, with the highest numbers conducted in Guinea (n = 3) and Nigeria (n = 3), followed by Sierra Leone (n = 2), Uganda (n = 2), Morocco (n = 1), Tanzania (n = 1), and Madagascar (n = 1). Two primary rodent control methods, kill traps and rodenticides, were used, targeting multimammate rats (Mastomys natalensis) and black/roof rats (Rattus rattus), the species most frequently encountered in human settings. Conclusion: Most studies examined short-term rodent management strategies, which proved insufficient in significantly reducing zoonotic disease prevalence. These findings highlight the need for Africa to adopt more sustainable, ecologically based rodent control approaches to effectively curb zoonotic risks in the long term. Full article