首页> 外文期刊>Journal of Clinical Microbiology >Comparison of NNA Agar Culture and Selective Broth Culture for Detection of Group B Streptococcal Colonization in Women
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Comparison of NNA Agar Culture and Selective Broth Culture for Detection of Group B Streptococcal Colonization in Women

机译:NNA琼脂培养物和选择性肉汤培养物检测妇女B组链球菌定植的比较

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In 1996, the Centers for Disease Control and Prevention recommended the use of a selective broth culture for the improved detection of genital tract or anorectal carriage of group B streptococci (GBS) in pregnant women. In order to verify this recommendation in our laboratory, we compared the sensitivity of Todd-Hewitt medium with gentamicin and nalidixic acid (SBM) with our current method of direct plating on blood agar medium containing neomycin and nalidixic acid (NNA). Five hundred consecutive cervicovaginal and anorectal specimens submitted for GBS culture were included in the study. Swabs were plated onto NNA and the swabs were immersed in SBM, followed by overnight incubation at 35°C. On the following day, the NNA plates were examined for colonies typical of GBS and the organisms were identified by the CAMP test or by latex agglutination. SBM cultures were subcultured onto blood agar and CNA agar plates, and the plates were reincubated for 24 h. Negative specimens from either medium were incubated for an additional 24 h and were examined again before finalization of the results. GBS were recovered from 78 specimens by both methods; from SBM only for 17 specimens (sensitivity, 86%) and from NNA only for 16 specimens (sensitivity, 85%). A moderate to heavy growth of Enterococcus faecalis was observed on plates containing NNA-positive, SBM-negative specimens. Competitive growth studies suggested that E. faecalis suppressed the growth potential of GBS in SBM. Our study suggests that direct plating on NNA, as a single method, is equivalent in sensitivity to SBM for the recovery of GBS, and the results are often available 24 h sooner. However, it appears that both direct plating and selective broth amplification techniques are required for the maximum level of identification of colonization with GBS in pregnant women.
机译:1996年,疾病控制与预防中心建议使用选择性肉汤培养物,以改善孕妇B组链球菌(GBS)的生殖道或肛门直肠运输的检测。为了在我们的实验室中验证该建议,我们将Todd-Hewitt培养基与庆大霉素和萘啶酸(SBM)的敏感性与我们目前直接电镀在含有新霉素和萘啶酸(NNA)的血液琼脂培养基上的方法进行了比较。该研究包括连续提交用于GBS培养的500例宫颈阴道和肛门直肠标本。将拭子铺在NNA上,并将拭子浸入SBM中,然后在35℃下孵育过夜。第二天,检查NNA平板的典型GBS菌落,并通过CAMP试验或乳胶凝集法鉴定出该微生物。将SBM培养物继代培养到血琼脂和CNA琼脂平板上,并将平板再孵育24小时。将来自两种培养基的阴性标本再孵育24小时,并在结果最终确定之前再次进行检查。两种方法均可从78个标本中回收GBS。 SBM仅适用于17个样本(灵敏度86%)和NNA仅适用于16个样本(灵敏度85%)。在含有NNA阳性,SBM阴性标本的平板上观察到粪肠球菌的中度至重度生长。竞争性增长研究表明, E。粪便抑制了GBS在SBM中的生长潜力。我们的研究表明,直接电镀在NNA上,作为单一方法,对于SGB恢复GBS的敏感性与SBM相当,并且通常可在24小时之前获得结果。然而,似乎最大程度地鉴定孕妇中GBS的定植水平需要直接铺板和选择性肉汤扩增技术。

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