50 research outputs found

    Contemporary outbreaks of different avipoxviruses in Humboldt penguins of wild animal park Planckendael and in chickens of commercial poultry farms in Belgium

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    In the present study, the first outbreak of a penguinpox virus (PPV) in Humboldt penguins (Spheniscus humboldd) and four outbreaks of fowlpox virus (FPV) in layer chickens are reported. Clinically, cutaneous wart-like growths were observed around the eyes in four juvenile Humboldt penguins and cutaneous nodular lesions in the comb, wattles, around the eyes and other unfeathered skin parts of layer chickens. Histopathology (FPV and PPV), electron microscopy (PPV), virus isolation (FPV) and PCR amplification (FPV and PPV) confirmed that both isolates were avipoxviruses (APVs). According to the phylogenetic analysis of the partial P4b core protein gene, the Belgian Humboldt PPV clustered with sequences of free-range (domestic and synanthrope bird species) and wild bird species of the United States and Europe (99-100% homology), and all four Belgian FPV isolates clustered with FPV isolates of chickens, turkeys, canary and FPV attenuated live vaccines from all over the world (100% homology)

    Novel insights in the pathogenesis of infectious laryngotracheitis and bronchitis viruses in chickens

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    Infectious laryngotracheitis virus (ILTV) and infectious bronchitis virus (IBV) are two important avian respiratory viruses, which cause major economic losses in the worldwide commercial poultry. ILTV and IBV enter through respiratory and ocular routes. The ILTV and IBV invasion strategies at entry sites and subsequent pathogenesis mechanisms are poorly understood

    Productive replication of nephropathogenic infectious bronchitis virus in peripheral blood monocytic cells, a strategy for viral dissemination and kidney infection in chickens

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    In the present study, the replication kinetics of nephropathogenic (B1648) and respiratory (Massachusetts-M41) IBV strains were compared in vitro in respiratory mucosa explants and blood monocytes (KUL01(+) cells), and in vivo in chickens to understand why some IBV strains have a kidney tropism. B1648 was replicating somewhat better than M41 in the epithelium of the respiratory mucosa explants and used more KUL01(+) cells to penetrate the deeper layers of the respiratory tract. B1648 was productively replicating in KUL01(+) monocytic cells in contrast with M41. In B1648 inoculated animals, 10(2.7-6.8) viral RNA copies/100 mg were detected in tracheal secretions at 2, 4, 6, 8, 10 and 12 days post inoculation (dpi), 10(2.4-4.5) viral RNA copies/mL in plasma at 2, 4, 6, 8, 10 and 12 dpi and 10(1.8-4.4) viral RNA copies/10(6) mononuclear cells in blood at 2, 4, 6 and 8 dpi. In M41 inoculated animals, 10(2.6-7.0) viral RNA copies/100 mg were detected in tracheal secretions at 2, 4, 6, 8 and 10 dpi, but viral RNA was not demonstrated in plasma and mononuclear cells (except in one chicken at 6 dpi). Infectious virus was detected only in plasma and mononuclear cells of the B1648 group. At euthanasia (12 dpi), viral RNA and antigen positive cells were detected in lungs, liver, spleen and kidneys of only the B1648 group and in tracheas of both the B1648 and M41 group. In conclusion, only B1648 can easily disseminate to internal organs via a cell-free and - associated viremia with KUL01(+) cells as important carrier cells

    Barriers to Sustainable Waste Management in Mountain Tourism: Evidence from India

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    Goal 15 of the Sustainable Development Goals calls for efforts to protect fragile mountain ecosystems. Waste generated due to mountain tourism leads to environmental degradation, biodiversity loss, and poses a significant challenge to achieving this goal. Mountains which are characterized by uninhabitable terrain and remoteness, coupled with current tourism practices compound this challenge. The paper resolves this challenge by understanding barriers to sustainably manage waste using th Classical DEMATEL method. Based on data from 36 experts in India’s mountain tourism industry, barriers to sustainable management of non-biodegradable waste are analyzed. Results suggest that enforcement of regulations, waste collection infrastructure, and lack of transportation for waste transfer are the most prominent barriers that can be mitigated by collectively leveraging four tangible barriers: tourists’ motivation or achievement mentality, local government’s initiative, economic value of waste, and tourists’ lack of environmental awareness. Based on this, a policy intervention mandating certification standards for tourists is suggested before they embark on mountain tourism

    Effects of cigarette smoke condensate on proliferation and wound closure of bronchial epithelial cells in vitro: role of glutathione

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    BACKGROUND: Increased airway epithelial proliferation is frequently observed in smokers. To elucidate the molecular mechanisms leading to these epithelial changes, we studied the effect of cigarette smoke condensate (CSC) on cell proliferation, wound closure and mitogen activated protein kinase (MAPK) activation. We also studied whether modulation of intracellular glutathione/thiol levels could attenuate CSC-induced cell proliferation. METHODS: Cells of the bronchial epithelial cell line NCI-H292 and subcultures of primary bronchial epithelial cells were used for the present study. The effect of CSC on epithelial proliferation was assessed using 5-bromo-2-deoxyuridine (BrdU) incorporation. Modulation of epithelial wound repair was studied by analysis of closure of 3 mm circular scrape wounds during 72 hours of culture. Wound closure was calculated from digital images obtained at 24 h intervals. Activation of mitogen-activated protein kinases was assessed by Western blotting using phospho-specific antibodies. RESULTS: At low concentrations CSC increased proliferation of NCI-H292 cells, whereas high concentrations were inhibitory as a result of cytotoxicity. Low concentrations of CSC also increased epithelial wound closure of both NCI-H292 and PBEC, whereas at high concentrations closure was inhibited. At low, mitogenic concentrations, CSC caused persistent activation of ERK1/2, a MAPK involved in cell proliferation. Inhibition of cell proliferation by high concentrations of CSC was associated with activation of the pro-apoptotic MAP kinases p38 and JNK. Modulation of intracellular glutathione (GSH)/thiol levels using N-acetyl-L-cysteine, GSH or buthionine sulphoximine (BSO), demonstrated that both the stimulatory and the inhibitory effects of CSC were regulated in part by intracellular GSH levels. CONCLUSION: These results indicate that CSC may increase cell proliferation and wound closure dependent on the local concentration of cigarette smoke and the anti-oxidant status. These findings are consistent with increased epithelial proliferation in smokers, and may provide further insight in the development of lung cancer

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