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Phenotypic Diversity Caused by Differential RpoS Activity among Environmental Escherichia coli Isolates

机译:环境大肠杆菌分离物之间RpoS活性差异引起的表型多样性

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Enteric bacteria deposited into the environment by animal hosts are subject to diverse selective pressures. These pressures may act on phenotypic differences in bacterial populations and select adaptive mutations for survival in stress. As a model to study phenotypic diversity in environmental bacteria, we examined mutations of the stress response sigma factor, RpoS, in environmental Escherichia coli isolates. A total of 2,040 isolates from urban beaches and nearby fecal pollution sources on Lake Ontario (Canada) were screened for RpoS function by examining growth on succinate and catalase activity, two RpoS-dependent phenotypes. The rpoS sequence was determined for 45 isolates, including all candidate RpoS mutants, and of these, six isolates were confirmed as mutants with the complete loss of RpoS function. Similarly to laboratory strains, the RpoS expression of these environmental isolates was stationary phase dependent. However, the expression of RpoS regulon members KatE and AppA had differing levels of expression in several environmental isolates compared to those in laboratory strains. Furthermore, after plating rpoS ~(+) isolates on succinate, RpoS mutants could be readily selected from environmental E. coli . Naturally isolated and succinate-selected RpoS mutants had lower generation times on poor carbon sources and lower stress resistance than their rpoS ~(+) isogenic parental strains. These results show that RpoS mutants are present in the environment (with a frequency of 0.003 among isolates) and that, similarly to laboratory and pathogenic strains, growth on poor carbon sources selects for rpoS mutations in environmental E. coli . RpoS selection may be an important determinant of phenotypic diversification and, hence, the survival of E. coli in the environment.
机译:动物宿主沉积到环境中的肠细菌要承受多种选择压力。这些压力可能作用于细菌种群的表型差异,并为应激中的生存选择适应性突变。作为研究环境细菌表型多样性的模型,我们检查了环境大肠杆菌分离株中应激反应西格玛因子RpoS的突变。通过检查琥珀酸和过氧化氢酶活性的增长(两种依赖RpoS的表型),从安大略湖(加拿大)的城市海滩和附近粪便污染源中分离出总共2040株菌株,以检测RpoS的功能。确定了45个分离株的rpoS序列,包括所有候选RpoS突变体,其中6个分离株被确认为具有RpoS功能完全丧失的突变体。与实验室菌株相似,这些环境分离株的RpoS表达与固定相有关。但是,与实验室菌株相比,RpoS调控子成员KatE和AppA在几种环境分离物中的表达水平不同。此外,将rpoS〜(+)分离物涂在琥珀酸盐上后,RpoS突变体可以很容易地从环境大肠杆菌中选择。与rpoS〜(+)等基因亲本菌株相比,天然分离的琥珀酸选择的RpoS突变体在较差的碳源上具有较短的生成时间,并且具有较低的抗逆性。这些结果表明,RpoS突变体存在于环境中(分离株之间的频率为0.003),并且与实验室和致病菌株相似,在不良碳源上的生长会在环境大肠杆菌中选择rpoS突变。 RpoS的选择可能是表型多样化的重要决定因素,因此可能是环境中大肠杆菌生存的重要决定因素。

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