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DNA-based culture-independent analysis detects the presence of group a streptococcus in throat samples from healthy adults in Japan

机译:基于DNA的文化独立分析检测日本健康成年人的喉咙样本中是否存在链球菌

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Background Group A Streptococcus (GAS; Streptococcus pyogenes ) causes a range of mild to severe infections in humans. It can also colonize healthy persons asymptomatically. Therefore, it is important to study GAS carriage in healthy populations, as carriage of it might lead to subsequent disease manifestation, clonal spread in the community, and/or diversification of the organism. Throat swab culture is the gold standard method for GAS detection. Advanced culture-independent methods provide rapid and efficient detection of microorganisms directly from clinical samples. We investigated the presence of GAS in throat swab samples from healthy adults in Japan using culture-dependent and culture-independent methods. Results Two throat swab samples were collected from 148 healthy volunteers. One was cultured on selective medium, while total DNA extracted from the other was polymerase chain reaction (PCR) amplified with two GAS-specific primer pairs: one was a newly designed 16S rRNA-specific primer pair, the other a previously described V-Na+-ATPase primer pair. Although only 5 (3.4?%) of the 148 samples were GAS-positive by the culture-dependent method, 146 (98.6?%) were positive for the presence of GAS DNA by the culture-independent method. To obtain serotype information by emm typing, we performed nested PCR using newly designed emm primers. We detected the four different emm types in 25 (16.9?%) samples, and these differed from the common emm types associated with GAS associated diseases in Japan. The different emm types detected in the healthy volunteers indicate that the presence of unique emm types might be associated with GAS carriage. Conclusions Our results suggest that culture-independent methods should be considered for profiling GAS in the healthy hosts, with a view to obtaining better understanding of these organisms. The GAS-specific primers (16S rRNA and V-Na+-ATPase) used in this study can be used to estimate the maximum potential GAS carriage in people.
机译:背景技术A组链球菌(GAS;化脓性链球菌)在人类中引起一系列轻度至重度感染。它也可以无症状地定殖于健康人。因此,在健康人群中研究GAS携带非常重要,因为其携带可能会导致随后的疾病表现,社区中的克隆传播和/或生物多样性。咽拭子培养是GAS检测的金标准方法。先进的与培养无关的方法可直接从临床样品中快速有效地检测微生物。我们使用依赖于文化和不依赖于文化的方法调查了日本健康成年人的咽拭子样本中GAS的存在。结果从148名健康志愿者中采集了2份咽拭子样本。一个在选择性培养基上培养,而从另一个中提取的总DNA用两个GAS特异性引物对进行聚合酶链反应(PCR)扩增:一个是新设计的16S rRNA特异性引物对,另一个是先前描述的V-Na + -ATPase引物对。尽管通过培养依赖性方法在148个样品中只有5个(3.4%)为GAS阳性,但通过非培养依赖性方法则有146个样品(98.6%)为GAS DNA阳性。为了通过emm分型获得血清型信息,我们使用新设计的emm引物进行了巢式PCR。我们在25个样本(16.9%)中检测到四种不同的emm类型,这些类型不同于日本与GAS相关疾病相关的常见emm类型。在健康志愿者中检测到的不同emm类型表明,独特的emm类型可能与GAS运输有关。结论我们的结果表明,应考虑在健康宿主中对GAS进行谱分析时应采用与培养无关的方法,以期更好地了解这些生物。本研究中使用的GAS特异引物(16S rRNA和V-Na + -ATPase)可用于估计人们潜在的最大GAS携带量。

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