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首页> 外文期刊>MBio >A Perfect Storm: Increased Colonization and Failure of Vaccination Leads to Severe Secondary Bacterial Infection in Influenza Virus-Infected Obese Mice
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A Perfect Storm: Increased Colonization and Failure of Vaccination Leads to Severe Secondary Bacterial Infection in Influenza Virus-Infected Obese Mice

机译:一场完美的风暴:殖民化和疫苗接种失败导致流感病毒感染的肥胖小鼠严重继发细菌感染。

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ABSTRACT Obesity is a risk factor for developing severe disease following influenza virus infection; however, the comorbidity of obesity and secondary bacterial infection, a serious complication of influenza virus infections, is unknown. To fill this gap in knowledge, lean and obese C57BL/6 mice were infected with a nonlethal dose of influenza virus followed by a nonlethal dose of Streptococcus pneumoniae . Strikingly, not only did significantly enhanced death occur in obese coinfected mice compared to lean controls, but also high mortality was seen irrespective of influenza virus strain, bacterial strain, or timing of coinfection. This result was unexpected, given that most influenza virus strains, especially seasonal human A and B viruses, are nonlethal in this model. Both viral and bacterial titers were increased in the upper respiratory tract and lungs of obese animals as early as days 1 and 2 post-bacterial infection, leading to a significant decrease in lung function. This increased bacterial load correlated with extensive cellular damage and upregulation of platelet-activating factor receptor, a host receptor central to pneumococcal invasion. Importantly, while vaccination of obese mice against either influenza virus or pneumococcus failed to confer protection, antibiotic treatment was able to resolve secondary bacterial infection-associated mortality. Overall, secondary bacterial pneumonia could be a widespread, unaddressed public health problem in an increasingly obese population. IMPORTANCE Worldwide obesity rates have continued to increase. Obesity is associated with increased severity of influenza virus infection; however, very little is known about respiratory coinfections in this expanding, high-risk population. Our studies utilized a coinfection model to show that obesity increases mortality from secondary bacterial infection following influenza virus challenge through a “perfect storm” of host factors that lead to excessive viral and bacterial outgrowth. In addition, we found that vaccination of obese mice against either virus or bacteria failed to confer protection against coinfection, but antibiotic treatment did alleviate mortality. Combined, these results represent an understudied and imminent public health concern in a weighty portion of the global population.
机译:摘要肥胖是流感病毒感染后发展为严重疾病的危险因素。然而,肥胖和继发性细菌感染的合并症,即流感病毒感染的严重并发症,是未知的。为了填补这一知识空白,用非致死剂量的流感病毒,然后非致死剂量的肺炎链球菌感染瘦和肥胖的C57BL / 6小鼠。令人惊讶的是,与瘦对照组相比,肥胖的并发感染小鼠不仅死亡显着增加,而且无论流感病毒株,细菌株或并发感染的时间如何,死亡率都很高。鉴于大多数流感病毒株,尤其是季节性人类A和B病毒在该模型中均非致命性,因此这一结果是出乎意料的。最早在细菌感染后的第1天和第2天,肥胖动物的上呼吸道和肺中的病毒和细菌滴度都增加,导致肺功能显着下降。这种增加的细菌负荷与广泛的细胞损伤和血小板活化因子受体(肺炎球菌入侵的中心受体)的上调有关。重要的是,尽管对肥胖小鼠的流感病毒或肺炎球菌疫苗接种未能提供保护,但抗生素治疗能够解决继发于细菌感染的死亡率。总体而言,在日益肥胖的人群中,继发性细菌性肺炎可能是广泛的,尚未解决的公共卫生问题。重要全球肥胖率持续上升。肥胖与流感病毒感染的严重程度增加有关;然而,在这个不断扩大的高风险人群中,人们对呼吸道合并感染的了解很少。我们的研究使用了共感染模型,表明肥胖通过“完美风暴”等宿主因素导致流感和病毒的过度繁殖而增加了流感病毒攻击后继发细菌感染的死亡率。此外,我们发现,针对病毒或细菌的肥胖小鼠接种疫苗无法赋予抗合并感染的保护,但是抗生素治疗确实可以降低死亡率。综合起来,这些结果表明,在全球人口的很大一部分中,人们对公共卫生的关注尚未得到充分研究。

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