Stevenson T H, Lucia L M, Acuff G R
Department of Animal Science, Texas A&M University, College Station, Texas 77843, USA.
Appl Environ Microbiol. 2000 Feb;66(2):723-7. doi: 10.1128/AEM.66.2.723-727.2000.
Helicobacter pylori has been isolated from the human stomach with media containing only minimal selective agents. However, current research on the transmission and sources of infection requires more selective media due to the higher numbers of contaminants in environmental, oral, and fecal samples. The objective of this study was to develop and evaluate detection techniques that are sufficiently selective to isolate H. pylori from potential animal and food sources. Since H. pylori survives in the acidic environment of the stomach, low pH with added urea was studied as a potential selective combination. H. pylori grew fairly well on H. pylori Special Peptone plating medium supplemented with 10 mM urea at pH 4. 5, but this pH did not sufficiently inhibit the growth of contaminants. Various antibiotic combinations were then compared, and a combination consisting of 10 mg of vancomycin per liter, 5 mg of amphotericin B per liter, 10 mg of cefsulodin per liter, 62,000 IU of polymyxin B sulfate per liter, 40 mg of trimethoprim per liter, and 20 mg of sulfamethoxazole per liter proved to be highly selective but still allowed robust colonies of H. pylori to grow. This medium was highly selective for recovering H. pylori from cattle and beef samples, and it is possible that it could be used to enhance the recovery of this bacterium from human and environmental samples, which may be contaminated with large numbers of competing microorganisms.
幽门螺杆菌已从人类胃部被分离出来,所用培养基仅含有极少的选择性试剂。然而,由于环境、口腔和粪便样本中污染物数量较多,当前关于感染传播和来源的研究需要更具选择性的培养基。本研究的目的是开发和评估具有足够选择性的检测技术,以便从潜在的动物和食物来源中分离出幽门螺杆菌。由于幽门螺杆菌能在胃部的酸性环境中存活,因此研究了添加尿素的低pH值作为一种潜在的选择性组合。幽门螺杆菌在补充了10 mM尿素、pH值为4.5的幽门螺杆菌专用蛋白胨平板培养基上生长良好,但该pH值不足以抑制污染物的生长。随后比较了各种抗生素组合,结果表明每升含10毫克万古霉素、5毫克两性霉素B、10毫克头孢磺啶、62000国际单位硫酸多粘菌素B、40毫克甲氧苄啶和20毫克磺胺甲恶唑的组合具有高度选择性,但仍能使幽门螺杆菌的健壮菌落生长。这种培养基对从牛和牛肉样本中回收幽门螺杆菌具有高度选择性,并且有可能用于提高从人类和环境样本中回收这种细菌的效率,因为这些样本可能被大量竞争性微生物污染。