Ly Anh, Henderson James, Lu Annie, Culham Doreen E, Wood Janet M
Department of Microbiology, University of Guelph, Guelph, Ontario, Canada N1G 2W1.
J Bacteriol. 2004 Jan;186(2):296-306. doi: 10.1128/JB.186.2.296-306.2004.
Multiple transporters mediate osmoregulatory solute accumulation in Escherichia coli K-12. The larger genomes of naturally occurring strains such as pyelonephritis isolates CFT073 and HU734 may encode additional osmoregulatory systems. CFT073 is more osmotolerant than HU734 in the absence of organic osmoprotectants, yet both strains grew in high osmolality medium at low K(+) (micromolar concentrations) and retained locus trkH, which encodes an osmoregulatory K(+) transporter. Both lacked the trkH homologue trkG. Transporters ProP and ProU account for all glycine-betaine uptake activity in E. coli K-12 and CFT073, but not in HU734, yet elimination of ProP and ProU impairs the growth of HU734, but not CFT073, in high osmolality human urine. No known osmoprotectant stimulated the growth of CFT073 in high osmolality minimal medium, but putative transporters YhjE, YiaMNO, and YehWXYZ may mediate uptake of additional osmoprotectants. Gene betU was isolated from HU734 by functional complementation and shown to encode a betaine uptake system that belongs to the betaine-choline-carnitine transporter family. The incidence of trkG and betU within the ECOR collection, representatives of the E. coli pathotypes (PATH), and additional strains associated with urinary tract infection (UTI) were determined. Gene trkG was present in 66% of the ECOR collection but only in 16% of the PATH and UTI collections. Gene betU was more frequently detected in ECOR groups B2 and D (50% of isolates) than in groups A, B1, and E (20%), but it was similar in overall incidence in the ECOR collection and in the combined UTI and PATH collections (32 and 34%, respectively). Genes trkG and betU may have been acquired by lateral gene transfer, since trkG is part of the rac prophage and betU is flanked by putative insertion sequences. Thus, BetU and TrkG contribute, with other systems, to the osmoregulatory capacity of the species E. coli, but they are not characteristic of a particular phylogenetic group or pathotype.
多种转运蛋白介导大肠杆菌K-12中的渗透调节溶质积累。肾盂肾炎分离株CFT073和HU734等天然菌株的较大基因组可能编码额外的渗透调节系统。在没有有机渗透保护剂的情况下,CFT073比HU734更耐渗透,但两种菌株都能在低钾(微摩尔浓度)的高渗培养基中生长,并且保留了编码渗透调节钾转运蛋白的trkH基因座。两者都缺乏trkH同源物trkG。转运蛋白ProP和ProU介导了大肠杆菌K-12和CFT073中所有的甘氨酸甜菜碱摄取活性,但在HU734中并非如此,然而,去除ProP和ProU会损害HU734在高渗人尿中的生长,但不会损害CFT073。在高渗基本培养基中,没有已知的渗透保护剂能刺激CFT073的生长,但推测的转运蛋白YhjE、YiaMNO和YehWXYZ可能介导其他渗透保护剂的摄取。通过功能互补从HU734中分离出betU基因,结果表明它编码一种属于甜菜碱-胆碱-肉碱转运蛋白家族的甜菜碱摄取系统。测定了trkG和betU基因在大肠杆菌参考菌株(ECOR)集合、大肠杆菌致病型(PATH)代表菌株以及与尿路感染(UTI)相关的其他菌株中的发生率。trkG基因存在于66%的ECOR集合菌株中,但仅存在于16%的PATH和UTI集合菌株中。betU基因在ECOR的B2和D组(50%的分离株)中比在A、B1和E组(20%)中更频繁地被检测到,但它在ECOR集合以及UTI和PATH集合的合并菌株中的总体发生率相似(分别为32%和34%)。trkG和betU基因可能是通过横向基因转移获得的,因为trkG是rac原噬菌体的一部分,betU基因两侧是推测的插入序列。因此,BetU和TrkG与其他系统一起,对大肠杆菌的渗透调节能力有贡献,但它们并非特定系统发育组或致病型的特征。