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首页> 外文期刊>Journal of the American College of Nutrition >Antioxidants and viral infections: host immune response and viral pathogenicity.
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Antioxidants and viral infections: host immune response and viral pathogenicity.

机译:抗氧化剂和病毒感染:宿主的免疫反应和病毒致病性。

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摘要

Malnutrition has long been associated with increased susceptibility to infectious disease. The increase in severity from and susceptibility to infectious disease in malnourished hosts is thought to be the result of an impaired immune response. For example, malnutrition could influence the immune response by inducing a less effective ability to manage the challenge of an infectious disease. Work in our laboratory has demonstrated that not only is the host affected by the nutritional deficiency, but the invading pathogen is as well. Using a deficiency in selenium (Se) as a model system, mice deficient in Se were more susceptible to infection with coxsackievirus, as well as with influenza virus. Se-deficient mice develop myocarditis when infected with a normally benign strain of coxsackievirus. They also develop severe pneumonitis when infected with a mild strain of influenza virus. The immune system was altered in the Se-deficient animals, as was the viral pathogen itself. Sequencing of viral isolates recovered from Se-deficient mice demonstrated mutations in the viral genome of both coxsackievirus and influenza virus. These changes in the viral genome are associated with the increased pathogenesis of the virus. The antioxidant selenoenzyme, glutathione peroxidase-1, was found to be critically important, as glutathione peroxidase knockout mice developed myocarditis, similar to the Se-deficient mice, when infected with the benign strain of myocarditis. This work points to the importance of host nutrition in not only optimizing the host immune response, but also in preventing viral mutations which could increase the viral pathogenicity.
机译:营养不良长期以来与传染病易感性增加有关。营养不良的宿主中传染病的严重程度和对传染病的易感性增加被认为是免疫反应受损的结果。例如,营养不良可能通过诱导处理传染病挑战的能力降低而影响免疫反应。我们实验室的工作表明,宿主不仅受到营养缺乏的影响,而且入侵的病原体也受到影响。使用硒(Se)缺乏作为模型系统,硒缺乏的小鼠更容易感染柯萨奇病毒和流感病毒。缺乏硒的小鼠感染了正常的柯萨奇病毒柯萨奇病毒株后会患上心肌炎。当感染轻度流感病毒株时,它们也会发展为严重的肺炎。硒缺乏动物的免疫系统发生了变化,病毒病原体本身也发生了变化。从缺硒小鼠中回收的病毒分离株的测序表明柯萨奇病毒和流感病毒的病毒基因组均发生突变。病毒基因组中的这些变化与病毒的发病机理增加有关。发现抗氧化剂硒酶谷胱甘肽过氧化物酶-1至关重要,因为当被良性心肌炎株感染时,谷胱甘肽过氧化物酶基因敲除小鼠发展成心肌炎,类似于Se缺乏症小鼠。这项工作指出宿主营养的重要性不仅在于优化宿主免疫反应,还在于预防可能增加病毒致病性的病毒突变。

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