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Production of the hexitol D-mannitol by Cryptococcus neoformans in vitro and in rabbits with experimental meningitis.

机译:新型隐球菌在体外和实验性脑膜炎兔体内产生己糖醇D-甘露醇。

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We studied the ability of Cryptococcus neoformans to produce the hexitol D-mannitol in vitro and in rabbits with experimental meningitis. Twelve of twelve human isolates of C. neoformans produced D-mannitol in yeast nitrogen base plus 1% glucose and released D-mannitol into the medium. In a pilot study, pooled cerebrospinal fluid (CSF) from cortisone-treated rabbits given 3 x 10(7) C. neoformans H99 intracisternally contained more D-mannitol (identified by gas chromatography and enzymatically) than CSF from normal controls or cortisone-untreated rabbits with self-limited meningitis. In a second experiment, cortisone-treated rabbits given C. neoformans intracisternally had significantly higher CSF D-mannitol concentrations than controls given cortisone alone at 4, 6, and 8 days after infection. Moreover, log10 CSF D-mannitol correlated well with log10 CSF CFU (r = 0.81) and log10 CSF cryptococcal antigen titers (r = 0.78). Lastly, the initial volume of distribution and elimination half-life of D-mannitol given intracisternally to normal rabbits suggested that D-mannitol was distributed in total CSF and was removed by CSF bulk flow. Thus, C. neoformans produces D-mannitol in vitro and in vivo, and D-mannitol is a quantitative marker for experimental cryptococcal meningitis. D-Mannitol produced by C. neoformans may also contribute to brain edema and interfere with phagocyte killing by scavenging hydroxyl radicals.
机译:我们研究了新型隐球菌在体外和实验性脑膜炎兔体内产生己糖醇D-甘露醇的能力。十二个新形成梭状芽胞杆菌的人类分离株中的十二个在酵母氮基中加D-甘露醇加1%葡萄糖,然后将D-甘露醇释放到培养基中。在一项前瞻性研究中,来自可的松治疗的兔子的脑脊液(CSF)给予3 x 10(7)新生甲壳虫H99的脑池内含D-甘露醇(通过气相色谱法和酶法鉴定)比正常对照组或未经可的松治疗的CSF多。兔患有自限性脑膜炎。在第二个实验中,在感染后第4、6和8天,皮内注射内啡肽新孢子虫的可的松治疗兔子的CSF D-甘露醇浓度明显高于单独使用可的松的对照组。此外,log10 CSF D-甘露醇与log10 CSF CFU(r = 0.81)和log10 CSF隐球菌抗原滴度(r = 0.78)密切相关。最后,脑部内给予正常兔子的D-甘露醇的初始分布量和消除半衰期表明,D-甘露醇分布在总CSF中,并被CSF大量流动所清除。因此,新孢梭菌在体外和体内产生D-甘露醇,D-甘露醇是实验性隐球菌性脑膜炎的定量标记。新生梭菌产生的D-甘露醇也可能导致脑水肿,并通过清除羟基自由基来干扰吞噬细胞的杀伤。

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