Freestone P P, Lyte M, Neal C P, Maggs A F, Haigh R D, Williams P H
Department of Microbiology & Immunology, University of Leicester, Leicester LE1 9HN, United Kingdom.
J Bacteriol. 2000 Nov;182(21):6091-8. doi: 10.1128/JB.182.21.6091-6098.2000.
Norepinephrine stimulates the growth of a range of bacterial species in nutritionally poor SAPI minimal salts medium containing 30% serum. Addition of size-fractionated serum components to SAPI medium indicated that transferrin was required for norepinephrine stimulation of growth of Escherichia coli. Since bacteriostasis by serum is primarily due to the iron-withholding capacity of transferrin, we considered the possibility that norepinephrine can overcome this effect by supplying transferrin-bound iron for growth. Incubation with concentrations of norepinephrine that stimulated bacterial growth in serum-SAPI medium resulted in loss of bound iron from iron-saturated transferrin, as indicated by the appearance of monoferric and apo- isoforms upon electrophoresis in denaturing gels. Norepinephrine also caused the loss of iron from lactoferrin. The pharmacologically inactive metabolite norepinephrine 3-O-sulfate, by contrast, did not result in iron loss from transferrin or lactoferrin and did not stimulate bacterial growth in serum-SAPI medium. Norepinephrine formed stable complexes with transferrin, lactoferrin, and serum albumin. Norepinephrine-transferrin and norepinephrine-lactoferrin complexes, but not norepinephrine-apotransferrin or norepinephrine-albumin complexes, stimulated bacterial growth in serum-SAPI medium in the absence of additional norepinephrine. Norepinephrine-stimulated growth in medium containing (55)Fe complexed with transferrin or lactoferrin resulted in uptake of radioactivity by bacterial cells. Moreover, norepinephrine-stimulated growth in medium containing [(3)H]norepinephrine indicated concomitant uptake of norepinephrine. In each case, addition of excess iron did not affect growth but significantly reduced levels of radioactivity ((55)Fe or (3)H) associated with bacterial cells. A role for catecholamine-mediated iron supply in the pathophysiology of infectious diseases is proposed.
去甲肾上腺素可刺激一系列细菌在含30%血清的营养匮乏的SAPI最低盐培养基中生长。向SAPI培养基中添加经大小分级的血清成分表明,转铁蛋白是去甲肾上腺素刺激大肠杆菌生长所必需的。由于血清的抑菌作用主要归因于转铁蛋白的铁扣留能力,我们考虑了去甲肾上腺素可通过提供与转铁蛋白结合的铁来促进生长从而克服这种作用的可能性。在血清-SAPI培养基中,用能刺激细菌生长的去甲肾上腺素浓度进行孵育,结果导致铁饱和转铁蛋白中结合铁的丢失,这在变性凝胶电泳上单铁和脱辅基异构体的出现得以表明。去甲肾上腺素还导致乳铁蛋白中铁的丢失。相比之下,药理活性无的代谢物去甲肾上腺素3-O-硫酸盐不会导致转铁蛋白或乳铁蛋白中铁的丢失,也不会刺激血清-SAPI培养基中的细菌生长。去甲肾上腺素与转铁蛋白、乳铁蛋白和血清白蛋白形成稳定的复合物。在没有额外去甲肾上腺素的情况下,去甲肾上腺素-转铁蛋白和去甲肾上腺素-乳铁蛋白复合物而非去甲肾上腺素-脱铁转铁蛋白或去甲肾上腺素-白蛋白复合物可刺激血清-SAPI培养基中的细菌生长。在含有与转铁蛋白或乳铁蛋白络合的(55)Fe的培养基中,去甲肾上腺素刺激的生长导致细菌细胞摄取放射性物质。此外,在含有[(3)H]去甲肾上腺素的培养基中,去甲肾上腺素刺激的生长表明同时摄取了去甲肾上腺素。在每种情况下,添加过量铁不会影响生长,但会显著降低与细菌细胞相关的放射性((55)Fe或(3)H)水平。本文提出了儿茶酚胺介导的铁供应在传染病病理生理学中的作用。