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首页> 外文期刊>Diagnostic cytopathology >Gardnerella vaginalis and Lactobacillus sp in liquid-based cervical samples in healthy and disturbed vaginal flora using cultivation-independent methods.
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Gardnerella vaginalis and Lactobacillus sp in liquid-based cervical samples in healthy and disturbed vaginal flora using cultivation-independent methods.

机译:使用与培养无关的方法,在健康和受干扰的阴道菌群中,以液体为基础的宫颈样本中的阴道加德纳菌和乳酸杆菌sp。

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摘要

Our objective was to determine the morphotype of the adherent bacteria in liquid-based cytology (LBC) in smears with healthy and disturbed vaginal flora. And to use PCR technology on the same fixed cell sample to establish DNA patterns of the 16S RNA genes of the bacteria in the sample. Thirty samples were randomly selected from a large group of cervical cell samples suspended in a commercial coagulant fixative "(BoonFix)." PCR was used to amplify DNA of five bacterial species: Lactobacillus acidophilus, Lactobacillus crispatus, Lactobacillus jensenii, Gardnerella vaginalis, and Mycoplasma hominis. The LBC slides were then analyzed by light microscopy to estimate bacterial adhesion. DNA of lactobacilli was detected in all cell samples. Seventeen smears showed colonization with Gardnerella vaginalis (range 2.6 x 10(2)-3.0 x 10(5) bacteria/mul BoonFix sample). Two cases were identified as dysbacteriotic with high DNA values for Gardnerella vaginalis and low values for Lactobacillus crispatus. The sample with the highest concentration for Gardnerella vaginalis showed an unequivocal Gardnerella infection. This study indicates that the adherence pattern of a disturbed flora in liquid-based cervical samples can be identified unequivocally, and that these samples are suitable for quantitative PCR analysis. This cultivation independent method reveals a strong inverse relationship between Gardnerella vaginalis and Lactobacillus crispatus in dysbacteriosis and unequivocal Gardnerella infection. Diagn. Cytopathol. 2008;36:277-284. (c) 2008 Wiley-Liss, Inc.
机译:我们的目的是在健康和受干扰的阴道菌群涂片中确定液基细胞学(LBC)中粘附细菌的形态。并使用PCR技术在同一固定细胞样品上建立样品中细菌的16S RNA基因的DNA模式。从悬浮在市售凝血固定剂“(BoonFix)”中的一大批宫颈细胞样品中随机选择30个样品。 PCR被用于扩增五个细菌种类的DNA:嗜酸乳杆菌,crispatus乳杆菌,詹森乳杆菌,阴道加德纳菌和人支原体。然后通过光学显微镜分析LBC载玻片以估计细菌粘附。在所有细胞样品中都检测到了乳酸杆菌的DNA。十七次涂片显示阴道加德纳菌定植(范围为2.6 x 10(2)-3.0 x 10(5)细菌/ mul BoonFix样品)。确认有2例是细菌感染性细菌病,阴道加德纳菌的DNA值较高,而薄脆乳杆菌的DNA值较低。阴道加德纳菌浓度最高的样品显示出明确的加德纳菌感染。这项研究表明,可以清楚地确定液体基宫颈样品中受干扰菌群的粘附模式,并且这些样品适用于定量PCR分析。这种独立于栽培的方法揭示了阴道加德纳菌与曲霉乳杆菌在菌群失调和明确加德纳菌感染中有很强的逆向关系。诊断细胞病。 2008; 36:277-284。 (c)2008 Wiley-Liss,Inc.

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