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Construction of a urease-negative mutant of Proteus mirabilis: analysis of virulence in a mouse model of ascending urinary tract infection.

机译:奇异变形杆菌尿素酶阴性突变体的构建:升尿路感染小鼠模型中的毒力分析。

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摘要

Proteus mirabilis, a urease-producing uropathogen, causes serious urinary tract infections in humans. To specifically evaluate the contribution of urease to virulence, a mutation was introduced into P. mirabilis HI4320 by homologous recombination. Virulence was assessed in the CBA mouse model of ascending urinary tract infection. Twenty mice each were challenged transurethrally with P. mirabilis HI4320 and its urease-negative derivative (1 x 10(9) to 2 x 10(9) CFU). At 48 h animals were sacrificed and the mean log10 CFU per milliliter of urine (parent, 6.23; mutant, 4.19; P = 0.0014) or per gram of bladder (parent, 6.29; mutant, 4.28; P = 0.0002), left kidney (parent, 4.11; mutant, 1.02; P = 0.00009), and right kidney (parent, 4.11; mutant, 2.43; P = 0.036) were all shown to be significantly different. These data demonstrate a role for urease as a critical virulence determinant for uropathogenic P. mirabilis.
机译:产生尿素酶的尿道病菌奇异变形杆菌引起人类严重的尿路感染。为了具体评估脲酶对毒力的贡献,通过同源重组将突变引入了奇异假单胞菌HI4320。在升尿路感染的CBA小鼠模型中评估了毒力。每只二十只小鼠经尿道尿道裂孔杆菌HI4320及其脲酶阴性衍生物(1 x 10(9)至2 x 10(9)CFU)攻击。在48 h处死动物,左肾(每毫升尿液(父母,6.23;突变体,4.19; P = 0.0014)或每克膀胱(父母,6.29;突变体,4.28; P = 0.0002)平均log10 CFU。亲本为4.11;突变为1.02; P = 0.00009)和右肾(父母为4.11;突变为2.43; P = 0.036)均表现出显着差异。这些数据证明脲酶作为尿毒症致病性体育假单胞菌的关键毒力决定因素的作用。

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