Publications by authors named "Takayuki Kuraishi"

Article Synopsis
  • The study investigates how HIV infection affects the skin microbiome, particularly in Cameroonian individuals, highlighting potential changes in skin health.
  • Findings indicate that HIV-infected individuals exhibited higher alpha-diversity but significantly altered beta-diversity in their skin microbiome compared to healthy individuals.
  • The research suggests that specific skin microbes were affected by HIV, pointing to early changes that may influence skin diseases, even independent of CD4 T cell counts, paving the way for new treatments for skin-related microbial disorders.
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Commensal microbes in animals have a profound impact on tissue homeostasis, stress resistance, and ageing. We previously showed in Drosophila melanogaster that Acetobacter persici is a member of the gut microbiota that promotes ageing and shortens fly lifespan. However, the molecular mechanism by which this specific bacterial species changes lifespan and physiology remains unclear.

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Allopathic medicines play a key role in the prevention and treatment of diseases. However, long-term consumption of these medicines may cause serious undesirable effects that harm human health. Plant-based medicines have emerged as alternatives to allopathic medicines because of their rare side effects.

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The commensal microbes of the skin have a significant impact on dermal physiology and pathophysiology. Racial and geographical differences in the skin microbiome are suggested and may play a role in the sensitivity to dermatological disorders, including infectious diseases. However, little is known about the skin microbiome profiles of people living in Central Africa, where severe tropical infectious diseases impose a burden on the inhabitants.

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The nuclear factor-kappa B (NF-κB) pathway is an evolutionarily conserved signaling pathway that plays a central role in immune responses and inflammation. Here, we show that NF-κB signaling is activated via a pathway in parallel with the Toll receptor by receptor-type guanylate cyclase, Gyc76C. Gyc76C produces cyclic guanosine monophosphate (cGMP) and modulates NF-κB signaling through the downstream Tollreceptor components dMyd88, Pelle, Tube, and Dif/Dorsal (NF-κB).

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Article Synopsis
  • An early inflammatory response during the development of Drosophila impacts long-term health, increasing adult starvation resistance but decreasing lifespan.
  • Activation of the immune pathway in larvae causes noticeable effects, with lifespan shortening linked to Imd activation in the gut while starvation resistance relates to neuronal changes.
  • The study highlights how early immune responses lead to lasting changes in gut microbiota, resulting in chronic inflammation and a reduced lifespan in adult flies.
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Excessive melanin formation has been linked to various skin disorders such as hyperpigmentation and skin cancer. Tyrosinase is the most prominent target for inhibitors of melanin production. In this study, we investigated whether arbutin and its prodrug, arbutin undecylenic acid ester, might inhibit phenoloxidase (PO), a tyrosinase-like enzyme.

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Stem cells fuel the development and maintenance of tissues. Many studies have addressed how local signals from neighboring niche cells regulate stem cell identity and their proliferative potential. However, the regulation of stem cells by tissue-extrinsic signals in response to environmental cues remains poorly understood.

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is a highly pathogenic bacterium that infects insects. It is also used as a suitable model pathogen to analyze innate immunity. virulence is largely derived from Monalysin, a β-barrel pore-forming toxin that damages tissues, inducing necrotic cell death.

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A synthetic biology method based on heterologous biosynthesis coupled with genome mining is a promising approach for increasing the opportunities to rationally access natural product with novel structures and biological activities through total biosynthesis and combinatorial biosynthesis. Here, we demonstrate the advantage of the synthetic biology method to explore biological activity-related chemical space through the comprehensive heterologous biosynthesis of fungal decalin-containing diterpenoid pyrones (DDPs). Genome mining reveals putative DDP biosynthetic gene clusters distributed in five fungal genera.

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Innate immunity is an evolutionarily conserved host defense system against infections. The fruit fly relies solely on innate immunity for infection defense, and the conservation of innate immunity makes an ideal model for understanding the principles of innate immunity, which comprises both humoral and cellular responses. The mechanisms underlying the coordination of humoral and cellular responses, however, has remained unclear.

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Characterization of microbial communities in the skin in healthy individuals and diseased patients holds valuable information for understanding pathogenesis of skin diseases and as a source for developing novel therapies. Notably, resources regarding skin microbiome are limited in developing countries where skin disorders from infectious diseases are extremely common. A simple method for sample collection and processing for skin microbiome studies in such countries is crucial.

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Central nervous system (CNS)-related disorders, including neurodegenerative diseases, are common but difficult to treat. As effective medical interventions are limited, those diseases will likely continue adversely affecting people's health. There is evidence that the hyperactivation of innate immunity is a hallmark of most neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and polyglutamine diseases.

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In the past decades, much has been learned about the protective signatures of innate immune responses during the course of infections. However, it is now evident that induction of immune effectors also commonly occurs in the absence of pathogenic cues. Such an event, termed sterile inflammation, has been linked to several debilitating acute and chronic host conditions.

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The Drosophila Toll pathway is involved in embryonic development, innate immunity, and cell-cell interactions. However, compared to the mammalian Toll-like receptor innate immune pathway, its intracellular signaling mechanisms are not fully understood. We have previously performed a series of ex vivo genome-wide RNAi screenings to identify genes required for the activation of the Toll pathway.

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Article Synopsis
  • The Drosophila Toll-1 receptor plays a key role in embryonic development, immunity, and tissue maintenance, with Spätzle being the only known ligand until now.
  • This research identifies Spz5, another protein from the Spz family, as a ligand for the Toll-1 receptor, demonstrating that it does not require Furin protease processing for its functionality.
  • The study also reveals that the ligand activity in larval extracts mainly comes from Spz5 and highlights a genetic interaction between spz and spz5, suggesting that Toll-1 is a multi-ligand receptor, akin to mammalian Toll-like receptors.
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In this study, fruit fly of the genus Drosophila is utilized as a suitable model animal to investigate the molecular mechanisms of innate immunity. To combat orally transmitted pathogenic Gram-negative bacteria, the Drosophila gut is armed with the peritrophic matrix, which is a physical barrier composed of chitin and glycoproteins: the Duox system that produces reactive oxygen species (ROS), which in turn sterilize infected microbes, and the IMD pathway that regulates the expression of antimicrobial peptides (AMPs), which in turn control ROS-resistant pathogens. However, little is known about the defense mechanisms against Gram-positive bacteria in the fly gut.

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The molecular mechanisms underlying the phagocytosis of apoptotic cells need to be elucidated in more detail because of its role in immune and inflammatory intractable diseases. We herein developed an experimental method to investigate phagocytosis quantitatively using the fruit fly Drosophila, in which the gene network controlling engulfment reactions is evolutionally conserved from mammals. In order to accurately detect and count engulfing and un-engulfing phagocytes using whole animals, Drosophila embryos were homogenized to obtain dispersed cells including phagocytes and apoptotic cells.

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adults have been utilized as a genetically tractable model organism to decipher the molecular mechanisms of humoral innate immune responses. In an effort to promote the utility of larvae as an additional model system, in this study, we describe a novel aspect of an induction mechanism for innate immunity in these larvae. By using a fine tungsten needle created for manipulating semi-conductor devices, larvae were subjected to septic injury.

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Article Synopsis
  • - The metazoan gut is vital for digestion and nutrient absorption, as well as acting as a barrier against pathogens and harmful particles, with its functions partially regulated by the nervous system.
  • - In a study using Drosophila, researchers inhibited specific neurons and discovered that a specific genetic line (NP3253) is vulnerable to bacterial infections due to gut structure issues.
  • - The research suggests that neural control is essential for maintaining gut barrier function and opens up possibilities for further genetic studies on the complex brain-gut interaction in adult Drosophila.
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Article Synopsis
  • The Drosophila Toll pathway is crucial for the insect's immune response to Gram-positive bacteria and fungi, and this study aims to discover new components of this pathway.
  • Researchers conducted genome-wide RNA interference screens, identifying the E3 ubiquitin ligase Sherpa as essential for activating Toll signaling in Drosophila.
  • Mutant flies lacking sherpa showed reduced production of antimicrobial peptides and greater vulnerability to bacterial infections, while Sherpa was found to play a role in the ubiquitylation of dMyd88 and its localization within immune signaling complexes.
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Damage-associated molecular patterns (DAMPs), so-called "danger signals," play important roles in host defense and pathophysiology in mammals and insects. In Drosophila, the Toll pathway confers damage responses during bacterial infection and improper cell-fate control. However, the intrinsic ligands and signaling mechanisms that potentiate innate immune responses remain unknown.

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The NF-κB pathway is a phylogenetically conserved signaling pathway with a central role in inflammatory and immune responses. Here we demonstrate that a cochaperone protein, Droj2/DNAJA3, is involved in the activation of canonical NF-κB signaling in flies and in human cultured cells. Overexpression of Droj2 induced the expression of an antimicrobial peptide in Drosophila.

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The intestinal tract is the main organ involved in host nutritional homeostasis. Intestinal function in both vertebrates and invertebrates is partly controlled by enteric neurons that innervate the gut. Though anatomical and functional aspects of enteric neurons are relatively less characterized in Drosophila than in large insects, analyses of the role of the enteric neurons in flies have remarkably progressed in the last few years.

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