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Association of Bacillus anthracis Capsule with Lethal Toxin during Experimental Infection

机译:炭疽芽孢杆菌胶囊与实验性感染期间致死毒素的关联

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摘要

Bacillus anthracis lethal toxin (LT) was characterized in plasma from infected African Green monkeys, rabbits, and guinea pigs. In all cases, during the terminal phase of infection only the protease-activated 63-kDa form of protective antigen (PA63) and the residual 20-kDa fragment (PA20) were detected in the plasma. No uncut PA with a molecular mass of 83 kDa was detected in plasma from toxemic animals during the terminal stage of infection. PA63 was largely associated with lethal factor (LF), forming LT. Characterization of LT by Western blotting, capture enzyme-linked immunosorbent assay, and size exclusion chromatography revealed that the antiphagocytic poly-γ-d-glutamic acid (γ-DPGA) capsule released from B. anthracis bacilli was associated with LT in animal blood in variable amounts. While the nature of this in vivo association is not understood, we were able to determine that a portion of these LT/γ-DPGA complexes retained LF protease activity. Our findings suggest that the in vivo LT complexes differ from in vitro-produced LT and that including γ-DPGA when examining the effects of LT on specific immune cells in vitro may reveal novel and important roles for γ-DPGA in anthrax pathogenesis.
机译:炭疽芽孢杆菌致死毒素(LT)的特征在于感染的非洲绿猴,兔子和豚鼠的血浆中。在所有情况下,在感染的末期,血浆中仅检测到蛋白酶激活的63 kDa形式的保护性抗原(PA63)和残留的20 kDa片段(PA20)。在感染的末期,在毒物动物的血浆中未检测到分子量为83 kDa的未切割PA。 PA63与致死因子(LF)密切相关,形成LT。通过Western印迹,捕获酶联免疫吸附试验和尺寸排阻色谱法对LT进行表征,结果表明,从炭疽杆菌释放的抗吞噬聚γ-d-谷氨酸(γ-DPGA)胶囊与动物血液中的LT有关。可变数量。虽然尚不了解这种体内结合的性质,但我们能够确定这些LT /γ-DPGA复合物的一部分保留了LF蛋白酶的活性。我们的发现表明,体内LT复合物不同于体外产生的LT,并且当检查LT对体外特定免疫细胞的作用时,包括γ-DPGA可能揭示了γ-DPGA在炭疽病发病机理中的新的重要作用。

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