Notermans S, Heuvelman K J, Wernars K
Laboratory of Water and Food Microbiology, National Institute of Public Health and Environmental Hygiene, Bilthoven, The Netherlands.
Appl Environ Microbiol. 1988 Feb;54(2):531-3. doi: 10.1128/aem.54.2.531-533.1988.
DNA-DNA colony hybridization experiments with three different synthetic probes were carried out with 210 strains of Staphylococcus aureus. The synthetic probes encoded the amino acids 15 to 29 (probe 1), 179 to 192 (probe 2), and 207 to 219 (probe 3) of staphylococcal enterotoxin B (SEB). The amino acid sequences of these parts of SEB are identical to those of SEC1. All 21 SEB-producing strains tested reacted with each of the three probes. Of the 69 SEC-producing strains, 21 reacted with probe 1, none reacted with probe 2, and all 69 reacted with probe 3. With other strains no hybridization signals were obtained. The results presented here show that with a single synthetic DNA probe (probe 3) both SEB- and SEC-producing strains are detectable.
使用三种不同的合成探针,对210株金黄色葡萄球菌进行了DNA - DNA菌落杂交实验。这些合成探针编码葡萄球菌肠毒素B(SEB)的第15至29位氨基酸(探针1)、第179至192位氨基酸(探针2)和第207至219位氨基酸(探针3)。SEB这些部分的氨基酸序列与SEC1的相同。所有测试的21株产SEB菌株都与这三种探针中的每一种发生反应。在69株产SEC菌株中,21株与探针1反应,无菌株与探针2反应,所有69株都与探针3反应。对于其他菌株,未获得杂交信号。此处呈现的结果表明,使用单个合成DNA探针(探针3)就可以检测出产SEB和产SEC的菌株。