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1.
mSphere ; 2(5)2017.
Article in English | MEDLINE | ID: mdl-28959737

ABSTRACT

Tacaribe virus (TCRV) is a mammalian arenavirus that was first isolated from artibeus bats in the 1950s. Subsequent experimental infection of Jamaican fruit bats (Artibeus jamaicensis) caused a disease similar to that of naturally infected bats. Although substantial attention has focused on bats as reservoir hosts of viruses that cause human disease, little is known about the interactions between bats and their pathogens. We performed a transcriptome-wide study to illuminate the response of Jamaican fruit bats experimentally infected with TCRV. Differential gene expression analysis of multiple tissues revealed global and organ-specific responses associated with innate antiviral responses, including interferon alpha/beta and Toll-like receptor signaling, activation of complement cascades, and cytokine signaling, among others. Genes encoding proteins involved in adaptive immune responses, such as gamma interferon signaling and costimulation of T cells by the CD28 family, were also altered in response to TCRV infection. Immunoglobulin gene expression was also elevated in the spleens of infected bats, including IgG, IgA, and IgE isotypes. These results indicate an active innate and adaptive immune response to TCRV infection occurred but did not prevent fatal disease. This de novo assembly provides a high-throughput data set of the Jamaican fruit bat and its host response to TCRV infection, which remains a valuable tool to understand the molecular signatures involved in antiviral responses in bats. IMPORTANCE As reservoir hosts of viruses associated with human disease, little is known about the interactions between bats and viruses. Using Jamaican fruit bats infected with Tacaribe virus (TCRV) as a model, we characterized the gene expression responses to infection in different tissues and identified pathways involved with the response to infection. This report is the most detailed gene discovery work in the species to date and the first to describe immune gene expression responses in bats during a pathogenic viral infection.

2.
J Res Natl Bur Stand (1977) ; 90(3): 255-257, 1985.
Article in English | MEDLINE | ID: mdl-34566152

ABSTRACT

This short note describes an apparatus that has been designed and constructed to allow assessment of the extent of chemical decomposition of fluids and fluid mixtures under high temperature, high pressure conditions. The apparatus is used to screen fluid systems prior to PVT (pressure-volume-temperature) or VLE (vapor-liquid equilibrium) experiments under severe conditions. For a predetermined residence time, the fluids are maintained at the temperature and pressure at which the PVT or VLE experiment will be conducted. The residence time in the reactor is comparable to the expected residence time in the PVT or VLE apparatus. Samples of fluid are withdrawn directly at regular intervals for analysis by gas chromatography, or collected In a sampling vessel for more extensive analysis.

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