Taguchi F, Saito-Taki T, Okuda S, Kikuno R
Department of Microbiology, Kitasato University School of Hygienic Sciences, Japan.
Nihon Saikingaku Zasshi. 1992 Nov;47(6):759-65. doi: 10.3412/jsb.47.759.
We have developed a new selective medium, tentatively named MR(SA)2, for rapid identification of methicillin-resistant Staphylococcus aureus (MRSA) from clinical specimens. MR(SA)2 medium contained modified Müller-Hinton agar supplemented with 75 g of NaCl, 10 g of mannit, 20 mg of bromcresol purple, 20 g of egg-yolk, 4 mg of oxacillin, and 12.5 mg of ceftisoxime per 1,000 ml. There were no differences between the growth of MRSA strains on this medium at 30 C and that of 37 C. This medium can detect the egg-yolk reaction instead of the coagulase reaction. By single streaking of a test material on the surfaces of MR(SA)2 agar, MRSAs can easily be distinguished from methicillin-resistant coagulase-negative staphylococci (MR-CNS), other bacteria and fungi from their colony morphologies in a quantitative manner. A few MRSA strains would not form colonies on this medium because of their susceptibilities to ceftisoxime, but this may not inpede its use, since most MRSA strains isolated from clinical materials showed resistance to ceftisoxime. From the above results, the MR(SA)2 medium may be suitable for rapid detection of MRSA and MR-CNS.
我们开发了一种新的选择性培养基,暂定名为MR(SA)2,用于从临床标本中快速鉴定耐甲氧西林金黄色葡萄球菌(MRSA)。MR(SA)2培养基含有改良的Müller-Hinton琼脂,每1000毫升补充75克氯化钠、10克甘露醇、20毫克溴甲酚紫、20克蛋黄、4毫克苯唑西林和12.5毫克头孢西丁。MRSA菌株在该培养基上30℃时的生长与37℃时的生长没有差异。该培养基可以检测蛋黄反应而非凝固酶反应。通过将测试材料单划线接种在MR(SA)2琼脂表面,可根据菌落形态以定量方式轻松区分MRSA与耐甲氧西林凝固酶阴性葡萄球菌(MR-CNS)、其他细菌和真菌。少数MRSA菌株由于对头孢西丁敏感,在该培养基上不会形成菌落,但这可能不妨碍其使用,因为从临床材料中分离出的大多数MRSA菌株对头孢西丁耐药。根据上述结果,MR(SA)2培养基可能适用于快速检测MRSA和MR-CNS。