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Bacteriophage trigger antiviral immunity and prevent clearance of bacterial infection

机译:噬菌体触发抗病毒免疫力并防止细菌感染清除

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摘要

Bacteriophage are abundant at sites of bacterial infection, but their effects on mammalian hosts are unclear. We have identified pathogenic roles for filamentous Pf bacteriophage produced by Pseudomonas aeruginosa (Pa) in suppression of immunity against bacterial infection. Pf promote Pa wound infection in mice and are associated with chronic human Pa wound infections. Murine and human leukocytes endocytose Pf, and internalization of this single-stranded DNA virus results in phage RNA production. This triggers Toll-like receptor 3 (TLR3)- and TIR domain-containing adapter-inducing interferon-beta (TRIF)-dependent type I interferon production, inhibition of tumor necrosis factor (TNF), and the suppression of phagocytosis. Conversely, immunization of mice against Pf prevents Pa wound infection. Thus, Pf triggers maladaptive innate viral pattern-recognition responses, which impair bacterial clearance. Vaccination against phage virions represents a potential strategy to prevent bacterial infection.
机译:噬菌体在细菌感染部位丰富,但对哺乳动物宿主的作用尚不清楚。我们已经确定了由铜绿假单胞菌(Pa)产生的丝状Pf噬菌体在抑制针对细菌感染的免疫中的致病作用。 Pf促进小鼠Pa伤口感染,并与慢性人类Pa伤口感染相关。鼠和人白细胞内吞Pf,并且这种单链DNA病毒的内在化导致噬菌体RNA的产生。这会触发Toll样受体3(TLR3)和TIR域包含的衔接子诱导干扰素-β(TRIF)依赖性I型干扰素产生,抑制肿瘤坏死因子(TNF),并抑制吞噬作用。相反,对Pf免疫小鼠可预防Pa伤口感染。因此,Pf会触发适应不良的先天病毒模式识别反应,从而损害细菌清除率。针对噬菌体病毒粒子的疫苗接种是预防细菌感染的一种潜在策略。

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  • 来源
    《Science》 |2019年第6434期|1416-1416|共1页
  • 作者单位

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Stanford Univ, Stanford Immunol, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Palo Alto Vet Inst Res, Palo Alto, CA USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Stanford Univ, Stanford Immunol, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Mayo Clin, Div Infect Dis, Coll Med, Rochester, MN USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Stanford Univ, Stanford Immunol, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Stanford Univ, Stanford Immunol, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA|Baylor Coll Med, Dept Surg, Div Pediat Surg, Houston, TX 77030 USA;

    Baylor Coll Med, Dept Surg, Div Pediat Surg, Houston, TX 77030 USA;

    Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA USA;

    Univ Montana, Div Biol Sci, Missoula, MT 59812 USA;

    Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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