In JoVE (1)
Articles by Aoi Hiroyasu in JoVE
Extraktion von Hemocytes aus Drosophila Melanogaster Larven für mikrobielle Infektionen und Analyse Aoi Hiroyasu1, David C. DeWitt2, Alan G. Goodman1 1School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, 2Integrative Physiology and Neuroscience, College of Veterinary Medicine, Washington State University Diese Methode zeigt, wie Erreger Invasion in Insektenzellen mit dreidimensionalen (3D) Modellen zu visualisieren. Hemocytes von Drosophila Larven infiziert wurden mit viralen oder bakteriellen Erregern, Ex Vivo oder in Vivo. Infizierte Hemocytes wurden dann fixiert und für die Bildgebung mit einem confocal Mikroskop und anschließende zelluläre 3D-Rekonstruktion befleckt.
Other articles by Aoi Hiroyasu on PubMed
Invertebrate Iridescent Virus 6, a DNA Virus, Stimulates a Mammalian Innate Immune Response Through RIG-I-Like Receptors PloS One. | Pubmed ID: 27824940 Insects are not only major vectors of mammalian viruses, but are also host to insect-restricted viruses that can potentially be transmitted to mammals. While mammalian innate immune responses to arboviruses are well studied, less is known about how mammalian cells respond to viruses that are restricted to infect only invertebrates. Here we demonstrate that IIV-6, a DNA virus of the family Iridoviridae, is able to induce a type I interferon-dependent antiviral immune response in mammalian cells. Although IIV-6 is a DNA virus, we demonstrate that the immune response activated during IIV-6 infection is mediated by the RIG-I-like receptor (RLR) pathway, and not the canonical DNA sensing pathway via cGAS/STING. We further show that RNA polymerase III is required for maximal IFN-β secretion, suggesting that viral DNA is transcribed by this enzyme into an RNA species capable of activating the RLR pathway. Finally, we demonstrate that the RLR-driven mammalian innate immune response to IIV-6 is functionally capable of protecting cells from subsequent infection with the arboviruses Vesicular Stomatitis virus and Kunjin virus. These results represent a novel example of an invertebrate DNA virus activating a canonically RNA sensing pathway in the mammalian innate immune response, which reduces viral load of ensuing arboviral infection.
Host and Bacterial Factors Control Susceptibility of Drosophila Melanogaster to Coxiella Burnetii Infection Infection and Immunity. | Pubmed ID: 28438980 is the causative agent of Q fever, a zoonotic disease that threatens both human and animal health. Due to the paucity of experimental animal models, little is known about how host factors interface with bacterial components and affect pathogenesis. Here, we used , in conjunction with the biosafety level 2 (BSL2) Nine Mile phase II (NMII) clone 4 strain of , as a model to investigate host and bacterial components implicated in infection. We demonstrate that adult flies are susceptible to NMII infection and that this bacterial strain, which activates the immune deficiency (IMD) pathway, is able to replicate and cause mortality in the animals. We show that in the absence of Eiger, the only known tumor necrosis factor (TNF) superfamily homolog in , -infected flies exhibit reduced mortality from infection. We also demonstrate that the type 4 secretion system (T4SS) is critical for the formation of the -containing vacuole and establishment of infection in Altogether, our data reveal that the TNF homolog Eiger and the T4SS are implicated in the pathogenesis of in flies. The /NMII model mimics relevant aspects of the infection in mammals, such as a critical role of host TNF and the bacterial T4SS in pathogenesis. Our work also demonstrates the usefulness of this BSL2 model to investigate both host and components implicated in infection.