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小鼠中的致死性B型流感嗜血杆菌感染。

Lethal Haemophilus influenzae type b infection in mice.

作者信息

Marks M I, Ziegler E J, Douglas H, Corbeil L B

出版信息

Infection. 1982 Sep-Oct;10(5):261-6. doi: 10.1007/BF01640870.

Abstract

Previous animal models of invasive Haemophilus influenzae type b (HITB) infection are characterized by a low mortality rate. We produced a highly lethal infection in CF1 mice using mouse passage, mucin, and hemoglobin to enhance infectivity. Infection by the intraperitoneal route was followed by progressive peritonitis and bacteremia with subsequent HITB infection of the brain and meninges, and death. Death occurred between eight and 72 hours after infection and was associated with 10(6) to 10(9) HITB per ml of blood and with 10(2) to 10(5) HITB per g of brain. Mucin-hemoglobin did not augment HITB growth, but impaired macrophage adherence to glass in vitro, without decreasing cellular viability. In vivo, mucin-hemoglobin decreased the rate of disappearance of 51Cr-labelled HITB from the blood by impairment of hepatic clearance. This technically simple and inexpensive model is useful for the study of HITB infections in which bacterial multiplication, invasion and host lethality are desired features.

摘要

先前的侵袭性b型流感嗜血杆菌(HITB)感染动物模型的特点是死亡率低。我们使用小鼠传代、粘蛋白和血红蛋白来增强感染性,在CF1小鼠中制造了一种高致死性感染。通过腹腔途径感染后,会出现进行性腹膜炎和菌血症,随后HITB感染大脑和脑膜,并导致死亡。死亡发生在感染后8至72小时之间,每毫升血液中有10(6)至10(9)个HITB,每克大脑中有10(2)至10(5)个HITB。粘蛋白-血红蛋白并没有促进HITB的生长,但在体外损害了巨噬细胞对玻璃的粘附,而不降低细胞活力。在体内,粘蛋白-血红蛋白通过损害肝脏清除功能降低了51Cr标记的HITB从血液中消失的速率。这个技术简单且成本低廉的模型对于研究HITB感染很有用,在这种感染中,细菌繁殖、侵袭和宿主致死性是期望的特征。

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