is a significant cause of morbidity and mortality in koalas and a major contributor to population decline. Due to its crucial role in vaccine development and use as a strain typing tool, multiple studies have investigated the prevalence and diversity of the outer membrane protein A (MOMP), encoded by A. This prior work has shown that A genotypes vary across geographical regions, with multiple genotypes identified across Eastern Australia. Despite these earlier studies, our understanding of the diversity and distribution of MOMP remains incomplete. Here, we aimed to assess the geographical distribution, diversity, and temporal stability of the A across wild koalas infected with in north-eastern Australia. Full-length A sequences were generated from 226 samples collected from 173 unique animals from multiple koala populations over a 4-year time span. A genotypes F and G were the most common and were identified across all geographical regions. Genotype A was the next most common but mostly restricted to the South Brisbane region. In addition to two novel genotypes, rare genotypes, including livestock-associated types E58 and L1, and koala-associated H and I were sporadically identified. Comparison with historical A genotypes showed that the distribution of genotypes has remained stable over the past decade, suggesting limited selective pressure despite ongoing vaccination trials and management programmes. The stability of genotypes coupled with the identification of novel and livestock-associated genotypes underscores the importance of continued surveillance to inform future vaccine development and conservation strategies for koalas.
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http://dx.doi.org/10.1002/ece3.70973 | DOI Listing |
Genetic factors contribute to the development of metabolic syndrome and subsequent arterial hypertension (AH). The study of the T786C polymorphism of the endothelial nitric oxide synthase (eNOS) gene in arterial hypertension is important as its correlation with adipokine imbalance is a novelty area to find associations between hypertension development, obesity, and heredity. The purpose of the current study was to investigate serum adipokines levels, depending on the T786C polymorphism of the eNOS in patients with arterial hypertension.
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Institute of Forest Sciences (ICIFOR-INIA), Consejo Superior de Investigaciones Cientificas, 28040 Madrid, Spain.
Stone pine (Pinus pinea L.) is an emblematic tree species within the Mediterranean basin, with high ecological and economic relevance due to the production of edible nuts. Breeding programmes to improve pine nut production started decades ago in Southern Europe but have been hindered by the near absence of polymorphisms in the species genome and the lack of suitable genomic tools.
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January 2025
Institute of Virology and Immunology, Mittelhäusern, Switzerland.
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February 2025
Department of Medical Genetics and Genomic Medicine, School of Medical Sciences, Universidade Estadual de Campinas, São Paulo, Brazil.
Heterozygous variants in the Early B cell factor 3 (EBF3) have been reported in individuals presenting with hypotonia, ataxia and delayed development syndrome (HADDS) (MIM#617330). However, individuals with pathogenic variants in EBF3 show phenotypic heterogeneity and very few variants in the C-terminal domain have been described. We report on a heterozygous de-novo variant in the EBF3 gene in an individual with neurodevelopmental delay and behavioural problems.
View Article and Find Full Text PDFOxygen plays a critical role in early neural development in brains, particularly before establishment of complete vasculature; however, it has seldom been investigated due to technical limitations. This study uses an in vitro human cerebral organoid model with multiomic analysis, integrating advanced microscopies and single-cell RNA sequencing, to monitor tissue oxygen tension during neural development. Results reveal a key period between weeks 4 and 6 with elevated intra-organoid oxygen tension, altered energy homeostasis, and rapid neurogenesis within the organoids.
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