四环素耐药决定因素的遗传迁移和分布。

Ciba Foundation symposium Pub Date : 1997-01-01
M C Roberts
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引用次数: 0

摘要

自1953年以来,在人类、动物、食物和环境中发现了越来越多的四环素耐药细菌。四环素耐药通常是由于获得新的基因,主要是由于四环素的能量依赖性外排或核糖体免受其作用的保护。革兰氏阴性外排基因通常与共轭质粒有关,而革兰氏阳性外排基因通常在小的可移动质粒或染色体上发现。核糖体保护基因通常与对染色体有偏好的共轭转座子相关。最近,在分枝杆菌属、诺卡菌属、链霉菌属和密螺旋体属中发现了四环素耐药基因。Tet M决定因子编码一种核糖体保护蛋白,这种蛋白存在于革兰氏阳性、革兰氏阴性、无细胞壁、需氧、厌氧、致病性、机会性和正常菌群中。这种混杂的性质可能与它在共轭转座子上的位置以及它跨越细菌中发现的大多数生化和物理障碍的能力有关。Tet B外排决定因子不同于其他外排基因产物,因为它对四环素、多西环素和二甲胺四环素具有耐药性,并且在所有革兰氏阴性外排决定因子中具有最广泛的宿主范围。我们假设细菌的移动性和环境可能有助于影响特定tet基因的最终宿主范围。如果我们要扭转致病菌对抗生素越来越耐药的趋势,我们就需要改变抗生素在人类和动物健康以及食品生产中的使用方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic mobility and distribution of tetracycline resistance determinants.

Since 1953, tetracycline-resistant bacteria have been found increasingly in humans, animals, food and the environment. Tetracycline resistance is normally due to the acquisition of new genes and is primarily due to either energy-dependent efflux of tetracycline or protection of the ribosomes from its action. Gram-negative efflux genes are frequently associated with conjugative plasmids, whereas Gram-positive efflux genes are often found on small mobilizable plasmids or in the chromosome. The ribosomal protection genes are generally associated with conjugative transposons which have a preference for the chromosome. Recently, tetracycline resistance genes have been found in the genera Mycobacterium, Nocardia, Streptomyces and Treponema. The Tet M determinant codes for a ribosomal protection protein which can be found in Gram-positive, Gram-negative, cell-wall-free, aerobic, anaerobic, pathogenic, opportunistic and normal flora species. This promiscuous nature may be correlated with its location on a conjugative transposon and its ability to cross most biochemical and physical barriers found in bacteria. The Tet B efflux determinant is unlike other efflux gene products because it confers resistance to tetracycline, doxycycline and minocycline and has the widest host range of all Gram-negative efflux determinants. We have hypothesized that mobility and the environment of the bacteria may help influence the ultimate host range of specific tet genes. If we are to reverse the trend towards increasingly antibiotic-resistant pathogenic bacteria, we will need to change how antibiotics are used in both human and animal health as well as food production.

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