von Koenig C H, Tacken A, Finger H
Institute for Hygiene and Laboratory Medicine, Municipal Hospital, Krefeld, Federal Republic of Germany.
J Clin Microbiol. 1988 Dec;26(12):2558-60. doi: 10.1128/jcm.26.12.2558-2560.1988.
The use of Stainer-Scholte broth supplemented with (2,6-O-dimethyl)beta-cyclodextrin (heptakis) for the isolation of Bordetella pertussis from clinical specimens was evaluated with 3,632 nasal swabs from children and adults with suspected whooping cough or from their family contacts. The liquid enrichment medium was subcultured on charcoal agar with 10% defibrinated horse blood. Charcoal agar and soft charcoal agar served as the standard procedure to detect B. pertussis. We isolated 772 strains of B. pertussis (21%). Charcoal agar alone detected 87% of all strains (n = 668), soft charcoal agar grew 78% (n = 602), and 637 strains (83%) were isolated when Stainer-Scholte broth with heptakis was used. We detected 590 isolates with all three media. Whereas 65 strains grew only on charcoal agar, 27 strains were detected by soft charcoal agar. Supplemented Stainer-Scholte broth allowed the isolation of an additional 77 strains which did not primarily grow on charcoal media (P less than 0.05). Our data indicate that Stainer-Scholte medium supplemented with heptakis can be effectively used as an enrichment medium for detection of B. pertussis in clinical specimens.
使用添加了(2,6 - O - 二甲基)β - 环糊精(七聚体)的施泰纳 - 斯科尔特肉汤从临床标本中分离百日咳博德特氏菌,对3632份来自疑似百日咳儿童和成人或其家庭接触者的鼻拭子进行了评估。将液体增菌培养基接种于含10%去纤维马血的活性炭琼脂上进行传代培养。活性炭琼脂和软活性炭琼脂用作检测百日咳博德特氏菌的标准方法。我们分离出772株百日咳博德特氏菌(21%)。仅活性炭琼脂检测出所有菌株的87%(n = 668),软活性炭琼脂培养出78%(n = 602),使用含七聚体的施泰纳 - 斯科尔特肉汤时分离出637株(83%)。我们用这三种培养基共检测出590株分离株。其中65株仅在活性炭琼脂上生长,27株由软活性炭琼脂检测出。添加了七聚体的施泰纳 - 斯科尔特肉汤还能分离出另外77株最初不能在活性炭培养基上生长的菌株(P < 0.05)。我们的数据表明,添加了七聚体的施泰纳 - 斯科尔特培养基可有效用作临床标本中百日咳博德特氏菌检测的增菌培养基。