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首页> 外文期刊>Influenza and other respiratory viruses. >Obese mice have increased morbidity and mortality compared to non-obese mice during infection with the 2009 pandemic H1N1 influenza virus
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Obese mice have increased morbidity and mortality compared to non-obese mice during infection with the 2009 pandemic H1N1 influenza virus

机译:与2009年大流行H1N1流感病毒感染期间的非肥胖小鼠相比,肥胖小鼠的发病率和死亡率增加

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Please cite this paper as: Easterbrook et al. (2011) Obese mice have increased morbidity and mortality compared to non-obese mice during infection with the 2009 pandemic H1N1 influenza virus. Influenza and Other Respiratory Viruses 5(6), 418–425.Background Obesity has been identified as an independent risk factor for severe or fatal infection with 2009 pandemic H1N1 influenza (2009 pH1N1), but was not previously recognized for previous pandemic or seasonal influenza infections.Objectives Our aim was to evaluate the role of obesity as an independent risk factor for severity of infection with 2009 pH1N1, seasonal H1N1, or a pathogenic H1N1 influenza virus.Methods Diet-induced obese (DIO) and their non-obese, age-matched control counterparts were inoculated with a 2009 pH1N1, A/California/04/2009 (CA/09), current seasonal H1N1, A/NY/312/2001 (NY312), or highly pathogenic 1918-like H1N1, A/Iowa/Swine/1931 (Sw31), virus.Results Following inoculation with CA/09, DIO mice had higher mortality (80%) than control mice (0%) and lost more weight during infection. No effect of obesity on morbidity and mortality was observed during NY312 or Sw31 infection. Influenza antigen distribution in the alveolar regions of the lungs was more pronounced in DIO than control mice during CA/09 infection at 3 days post-inoculation (dpi), despite similar virus titers. During CA/09 infection, localized interferon-β and proinflammatory cytokine protein responses in the lungs were significantly lower in DIO than control mice. Conversely, serum cytokine concentrations were elevated in DIO, but not control mice following infection with CA/09. The effect of obesity on differential immune responses was abrogated during NY312 or Sw31 infection.Conclusions Together, these data support epidemiologic reports that obesity may be a risk factor for severe 2009 pandemic H1N1 influenza infection, but the role of obesity in seasonal or highly virulent pandemic influenza infection remains unclear.
机译:请将此论文引用为:Easterbrook等。 (2011)与2009年大流行H1N1流感病毒感染期间的非肥胖小鼠相比,肥胖小鼠的发病率和死亡率增加。流感和其他呼吸道病毒5(6),418–425。背景肥胖症已被确定为2009年H1N1大流行性流感(2009 pH1N1)严重或致命感染的独立危险因素,但以前并未被确认为先前的大流行或季节性流感目的我们的目的是评估肥胖作为2009年pH1N1,季节性H1N1或致病性H1N1流感病毒感染严重程度的独立危险因素的作用。方法饮食诱发的肥胖(DIO)及其非肥胖,年龄匹配的对照接种了2009 pH1N1,A /加利福尼亚04/2009(CA / 09),当前季节性H1N1,A / NY / 312/2001(NY312)或高致病性的1918样H1N1,A /爱荷华州结果/ Swine / 1931(Sw31),病毒。结果接种CA / 09后,DIO小鼠的死亡率(80%)比对照小鼠(0%)高,并且在感染过程中体重减轻。在NY312或Sw31感染期间,未观察到肥胖对发病率和死亡率的影响。尽管病毒滴度相似,但在接种后3天(dpi)的CA / 09感染期间,DIO中的肺泡抗原分布在DIO中比对照小鼠更为明显。在CA / 09感染期间,DIO中肺中的局部干扰素-β和促炎性细胞因子蛋白应答显着低于对照组小鼠。相反,在感染了CA / 09的DIO中,血清细胞因子浓度升高,而对照组则没有。结论在NY312或Sw31感染期间,肥胖对差异性免疫反应的影响被消除。流感感染仍不清楚。

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