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通过添加与转铁蛋白结合的铁增强小鼠脑膜炎奈瑟菌感染。

Enhancement of Neisseria meningitidis infection in mice by addition of iron bound to transferrin.

作者信息

Holbein B E

出版信息

Infect Immun. 1981 Oct;34(1):120-5. doi: 10.1128/iai.34.1.120-125.1981.

Abstract

Small quantities of iron bound specifically to human transferrin were found to stimulate infection with Neisseria meningitidis strain M1011 in mice. An intraperitoneal injection of 17.5 mg of transferrin carrying 22.7 micrograms of Fe resulted in 100% mortality from infection, as compared with no mortality for the controls which had received saline. Five milligrams of ferri-transferrin (FeTf), carrying 6.5 micrograms of Fe, stimulated and prolonged bacteremia in the mice. Thus, FeTf maintained infection, whereas infection was controlled due to iron limitation in control mice. Comparative studies with apotransferrin (iron-free) revealed that the enhancement of infection was due to the supply of iron. FeTf was also found to relieve an iron limitation of growth achieved by ethylenediaminedihydroxyphenylacetic acid (EDDA) in vitro. FeTf abolished the lag phase for growth of N. meningitidis in a defined medium. The results of this study suggest that human FeTf is an immediate source of iron to N. meningitidis both in vitro and in vivo. These findings support the hypothesis that the levels of iron in the circulating transferrin pool of mice determine the course of experimental N. meningitidis infection.

摘要

研究发现,少量与人类转铁蛋白特异性结合的铁可刺激小鼠感染脑膜炎奈瑟菌M1011菌株。腹腔注射17.5毫克携带22.7微克铁的转铁蛋白,感染导致的死亡率为100%,而接受生理盐水的对照组则无死亡情况。5毫克携带6.5微克铁的铁转铁蛋白(FeTf)可刺激并延长小鼠的菌血症。因此,FeTf维持了感染,而对照组小鼠因铁限制控制了感染。与脱铁转铁蛋白(无铁)的对比研究表明,感染增强是由于铁的供应。还发现FeTf可缓解体外乙二胺二羟基苯乙酸(EDDA)实现的铁生长限制。FeTf消除了脑膜炎奈瑟菌在特定培养基中生长的延迟期。本研究结果表明,人类FeTf在体外和体内都是脑膜炎奈瑟菌的直接铁源。这些发现支持了以下假设:小鼠循环转铁蛋白池中的铁水平决定了实验性脑膜炎奈瑟菌感染的进程。

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