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宿主胃肠道动力学与大肠杆菌产生大肠杆菌素的频率。

Host gastro-intestinal dynamics and the frequency of colicin production by Escherichia coli.

作者信息

Barnes Belinda, Sidhu Harvinder, Gordon David M

机构信息

National Centre for Epidemiology and Population Health, Australian National University, Canberra, ACT 0200, Australia.

School of Physical, Environmental and Mathematical Sciences, University of New South Wales at ADFA, Canberra, ACT 2600, Australia.

出版信息

Microbiology (Reading). 2007 Sep;153(Pt 9):2823-2827. doi: 10.1099/mic.0.2007/007120-0.

Abstract

The production of antimicrobial compounds known as colicins has been shown to be an important mediator of competitive interactions among Escherichia coli genotypes. There is some understanding of the forces responsible for determining the frequency of colicin production in E. coli populations; however, this understanding cannot explain all of the observed variation. A survey of colicin production in E. coli isolated from native Australian mammals revealed that the frequency of colicin production in strains isolated from carnivores was significantly lower than the frequency of production in strains recovered from herbivores or omnivores. The intestine of Australian carnivores is tube-like and gut turnover rates are rapid compared with the turnover rates of the intestinal tracts of herbivores and omnivores, all of which possess a hindgut fermentation chamber. A mathematical model was developed in order to determine if variation in gut turnover rates could determine if a host was more likely to harbour a colicin-producing strain or a non-producer. The model predicted that a colicin producer was more likely to dominate in the gut of a host with lower gut turnover rates, and a non-producer to dominate in hosts with rapid gut turnover rates.

摘要

被称为大肠杆菌素的抗菌化合物的产生已被证明是大肠杆菌基因型之间竞争相互作用的重要介导因素。对于决定大肠杆菌群体中大肠杆菌素产生频率的因素已有一定了解;然而,这种了解并不能解释所有观察到的变异情况。一项对从澳大利亚本土哺乳动物分离出的大肠杆菌中大肠杆菌素产生情况的调查显示,从食肉动物分离出的菌株中大肠杆菌素产生频率显著低于从食草动物或杂食动物分离出的菌株中的产生频率。澳大利亚食肉动物的肠道呈管状,与具有后肠发酵腔的食草动物和杂食动物的肠道周转率相比,其肠道周转率较快。为了确定肠道周转率的差异是否能决定宿主更有可能携带产生大肠杆菌素的菌株还是不产生的菌株,开发了一个数学模型。该模型预测,在肠道周转率较低的宿主肠道中,产生大肠杆菌素的菌株更有可能占主导地位,而在肠道周转率较快的宿主中,不产生的菌株更有可能占主导地位。

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