Publications by authors named "Werling D"

Article Synopsis
  • Macrophage cellular metabolism during tuberculosis (TB) infection is important because of the changes caused by different species, specifically their effects on macrophage bioenergetics.
  • Recent research indicates that TB infection leads to a shift in macrophage metabolism towards aerobic glycolysis, similar to the pro-inflammatory response seen with LPS in M1 macrophages, but there are notable differences in metabolic profiles between mice and humans.
  • This study compared the metabolic responses of bovine and human macrophages to TLR ligands, finding that while both species showed similar respiratory profiles, human macrophages had a unique reaction to PPD, enhancing both basal respiration and glycolysis, which could explain varying inflammatory responses in zoonotic diseases.
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  • * A pilot study used Reduced Representation Bisulfite Sequencing to compare methylation patterns in healthy calves versus those with BRD, and healthy calves versus adult dairy cows, revealing significant differences in gene methylation.
  • * Findings showed that BRD-affected calves had 964 differentially methylated genes related to immune responses and vascular regulation, highlighting the need for further research to improve breeding for disease resistance and longevity in cattle.
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  • Whole-genome sequencing (WGS) of Korean autism families reveals that autistic females have a higher genetic burden than males, indicating a higher liability threshold for females compared to males across different ancestries.
  • The study analyzes data from a large sample of Korean individuals and compares it with European ancestry cohorts, finding that sex differences in genetic burden and autism symptoms vary significantly.
  • Results show that while females carry more damaging genetic variants, male siblings of autistic females display more severe social communication issues, highlighting the complexity of autism's genetic factors and the influence of sex on autistic traits.
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Coccidiosis, caused by parasites, significantly impacts poultry farm economics and animal welfare. Beyond its direct impact on health, infection disrupts enteric microbial populations leading to dysbiosis and increases vulnerability to secondary diseases such as necrotic enteritis, caused by . The impact of infection or anticoccidial vaccination on host gastrointestinal phenotypes and enteric microbiota remains understudied.

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Variants in cis-regulatory elements link the noncoding genome to human pathology; however, detailed analytic tools for understanding the association between cell-level brain pathology and noncoding variants are lacking. CWAS-Plus, adapted from a Python package for category-wide association testing (CWAS), enhances noncoding variant analysis by integrating both whole-genome sequencing (WGS) and user-provided functional data. With simplified parameter settings and an efficient multiple testing correction method, CWAS-Plus conducts the CWAS workflow 50 times faster than CWAS, making it more accessible and user-friendly for researchers.

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Background: Sex-differential biology may contribute to the consistently male-biased prevalence of autism spectrum disorder (ASD). Gene expression differences between males and females in the brain can indicate possible molecular and cellular mechanisms involved, although transcriptomic sex differences during human prenatal cortical development have been incompletely characterized, primarily due to small sample sizes.

Methods: We performed a meta-analysis of sex-differential expression and co-expression network analysis in 2 independent bulk RNA sequencing datasets generated from cortex of 273 prenatal donors without known neuropsychiatric disorders.

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Article Synopsis
  • The research explores the link between noncoding genome variants and brain diseases, emphasizing a lack of tools to analyze these connections effectively.
  • A new tool called CWAS-Plus has been developed to enhance the analysis of noncoding variants using whole-genome sequencing and functional data, providing quicker and more efficient results.
  • CWAS-Plus successfully identified significant noncoding variant associations in autism and Alzheimer's disease, showcasing its effectiveness for large-scale genomic studies.
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Many questions are raised, and challenges faced in the new era of (intranasal) bovine respiratory disease complex vaccination. An increase in vaccination rate is expected, due to its positive impact on cattle health, reduction of antimicrobial use and economic factors. However, engagement of farmers and veterinarians with regard to vaccination is often affected by limitations, resulting in the development of barriers to vaccination, but also opportunities to overcome these.

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The global poultry industry has experienced dramatic growth in recent decades, increasing the significance of pathogens of chickens. Protozoan parasites of the genus Eimeria can cause the disease coccidiosis, compromising animal health and welfare, and incurring significant annual costs. Seven Eimeria species have long been recognised to infect chickens, supplemented by three new candidate species first reported from Australia in 2007/8.

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  • FMRP deficiency causes fragile X syndrome (FXS), affecting prenatal brain development in humans and macaques.
  • FMRP is crucial for regulating essential genes, and its deficiency leads to mitochondrial dysfunctions and hyperexcitability in neurons derived from FXS patients.
  • Targeting mitochondrial dysfunction may offer a potential treatment strategy to mitigate the developmental issues associated with FMRP deficiency.
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Differentiating between canine inflammatory bowel disease (IBD) and intestinal T-cell lymphoma by histopathological examination of endoscopically-derived intestinal biopsies can be challenging and involves an invasive procedure requiring specialized equipment and training. A rapid, non-invasive method of diagnosis, such as blood or faecal analysis for a conserved and stable biomarker, would be a useful adjunct or replacement. Studies on dogs and humans with various types of lymphoma have shown altered microRNA (miRNA) expression patterns in blood, faeces and tissues indicating their potential use as biomarkers of disease.

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Innate immune receptors that form complexes with secondary receptors, activating multiple signalling pathways, modulate cellular activation and play essential roles in regulating homeostasis and immunity. We have previously identified a variety of bovine C-type lectin-like receptors that possess similar functionality than their human orthologues. Mincle (), a heavily glycosylated monomer, is involved in the recognition of the mycobacterial component Cord factor (trehalose 6,6'-dimycolate).

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The interfascicular matrix (IFM; also known as the endotenon) is critical to the mechanical adaptations and response to load in energy-storing tendons, such as the human Achilles and equine superficial digital flexor tendon (SDFT). We hypothesized that the IFM is a tendon progenitor cell niche housing an exclusive cell subpopulation. Immunolabelling of equine superficial digital flexor tendon was used to identify the interfascicular matrix niche, localising expression patterns of CD31 (endothelial cells), Desmin (smooth muscle cells and pericytes), CD146 (interfascicular matrix cells) and LAMA4 (interfascicular matrix basement membrane marker).

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Since its discovery, bovine theileriosis has caused major socioeconomic losses in sub-Saharan Africa. Acaricide resistance of the intermediate host, paucity of therapeutics, and lack of sufficiently cross-protective vaccines increase the risk of parasite spread due to global warming. Here, we highlight three important areas that require investigation to develop next-generation vaccines.

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The risk and severity of clinical infection with as a causative pathogen for bovine mastitis is influenced by the hosts' phenotypic and genotypic variables. We used RNA-Seq analysis of circulating leukocytes to investigate global transcriptomic profiles and genetic variants from Holstein cows with naturally occurring cases of clinical mastitis, diagnosed using clinical symptoms and milk microbiology. Healthy lactation-matched cows served as controls (CONT, = 6).

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Tuberculosis has severe impacts on both humans and animals. Understanding the genetic basis of survival of both Mycobacterium tuberculosis, the human-adapted species, and Mycobacterium bovis, the animal-adapted species, is crucial to deciphering the biology of both pathogens. There are several studies that identify the genes required for survival of M.

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Cheap, easy-to-produce oral vaccines are needed for control of coccidiosis in chickens to reduce the impact of this disease on welfare and economic performance. yeast expressing three antigens were developed and delivered as heat-killed, freeze-dried whole yeast oral vaccines to chickens in four separate studies. After vaccination, replication was reduced following low dose challenge (250 oocysts) in Hy-Line Brown layer chickens (p<0.

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Members of the complex (MTBC) show distinct host adaptations, preferences and phenotypes despite being >99% identical at the nucleic acid level. Previous studies have explored gene expression changes between the members, however few studies have probed differences in gene essentiality. To better understand the functional impacts of the nucleic acid differences between and , we used the Mycomar T7 phagemid delivery system to generate whole genome transposon libraries in laboratory strains of both species and compared the essentiality status of genes during growth under identical conditions.

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Article Synopsis
  • * Whole genome sequencing of Brown Swiss cattle revealed important candidate genes, particularly TLR2, which plays a role in recognizing these pathogens and has different single nucleotide polymorphisms (SNPs) between breeds.
  • * The study shows that the SNP H326Q enhances the immune response to mycobacterial antigens in Brown Swiss cattle, suggesting that genetic differences in TLR2 impact susceptibility to infections among cattle breeds.
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  • Local genetic correlation measures the genetic similarity of complex traits in specific genomic areas, but estimating it accurately is difficult due to overlapping genetic factors and study samples.
  • The paper introduces a new method called SUPERGNOVA, which uses summary statistics from genome-wide association studies to better estimate local genetic correlations.
  • SUPERGNOVA proves to be more effective than existing methods, revealing insights like the intricate genetic relationship between autism spectrum disorder and cognitive performance through two different genetic influences.
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Classical swine fever (CSF) is a highly contagious disease caused by the classical swine fever virus (CSFV). The live attenuated C-strain vaccine is highly efficacious, initiating protection within several days of delivery. The vaccine strain is detected in the tonsil early after inoculation, yet little is known of the role that tonsillar immune cells might play in initiating protection.

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Background: Genetic variants in the voltage-gated sodium channels SCN1A, SCN2A, SCN3A, and SCN8A are leading causes of epilepsy, developmental delay, and autism spectrum disorder. The mRNA splicing patterns of all four genes vary across development in the rodent brain, including mutually exclusive copies of the fifth protein-coding exon detected in the neonate (5N) and adult (5A). A second pair of mutually exclusive exons is reported in SCN8A only (18N and 18A).

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