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Identification of uncultured bacteria from abscesses of exotic pet animals using broad-range nested 16S rRNA polymerase chain reaction and Sanger sequencing

机译:使用宽范围巢16S rRNA聚合酶链反应和Sanger测序鉴定来自异国宠物动物的脓肿脓肿细菌的鉴定

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Background: The Sanger sequencing technique has been questioned and challenged by advanced high-throughput sequencing approaches. Sanger sequencing seems to be an obsolete technology. However, there are still research problems that could be answered using the Sanger sequencing technology. Fastidious obligate anaerobic bacteria are mostly associated with abscesses in animals. These bacteria are difficult to isolate from abscesses and are frequently excluded due to the bias of conventional bacterial culturing. Aim: This study demonstrated the usefulness of a broad-range polymerase chain reaction (PCR) with Sanger sequencing to identify the majority population of bacteria in abscesses from exotic pet animals. Materials and Methods: This study performed a pilot investigation of abscesses from 20 clinical cases (17 rabbits, 2 hedgehogs, and 1 sugar glider) using standard culture methods for both aerobes and anaerobes and broad-range nested PCR targeting the 16S rRNA gene followed by the Sanger sequencing technique. Results: The standard culture and PCR techniques detected bacteria in 9 and 17 of 20 samples, respectively. From the 17 sequencings of the 16S rRNA, 10 PCR products were found to be closely related with obligate anaerobes including Bacteroides spp., Fusobacterium spp., Prevotella spp. Phylogenetic analysis using the rpoB gene revealed that the species for the Bacteroides was thetaiotaomicron and for the Fusobacterium was varium and nucleatum . However, the amplification of the rpoB gene for the Prevotella spp. was unsuccessful. Correlations between the standard culture and PCR techniques were found in 9 (6 positive and 3 negative samples) of 20 samples. Eleven samples were discordant between the standard culture and PCR techniques which were composed of eight samples negative by culture but positive by PCR and three samples had different bacteria by the culture and PCR techniques. Conclusion: According to this study, broad-range PCR combined with Sanger sequencing might be useful for the detection of dominant anaerobic bacteria in abscesses that were overlooked based on conventional bacterial culture.
机译:背景:Sanger测序技术受到高级高通量测序方法的质疑和挑战。 Sanger测序似乎是过时的技术。但是,仍有研究问题可以使用Sanger测序技术回答。严厉的迫使厌氧细菌大多与动物脓肿有关。这些细菌难以与脓肿分离,并且由于常规细菌培养的偏差而经常被排除。目的:本研究表明,宽范围的聚合酶链式反应(PCR)与Sanger测序的有用性,以鉴定异国情调的宠物动物的脓肿中的大多数细菌。材料和方法:本研究采用了使用标准培养方法的20例临床病例(17只兔子,2个刺猬和1个糖滑翔机)进行了试验调查,所述标准培养方法对于Aerobes和Anaerobes以及靶向16S rRNA基因的广泛巢式PCR,然后是Sanger测序技术。结果:标准培养和PCR技术分别检测到20个样品的9和17个样品中的细菌。从16S rRNA的17个顺序中,发现10个PCR产物与强烈的厌氧物(包括Bacteroides),Fusobacterium,Fluotella SPP。使用RPOB基因的系统发育分析显示,拟杆菌的物种是THETAIOSOOMICRON,并且对于血管杆菌是毒性和核心的。但是,扩增vPoB基因的FRVotella SPP。是不成功的。在20个样品的9(6个阳性和3个阴性样本)中发现了标准培养和PCR技术之间的相关性。在标准培养和PCR技术之间不风化,由培养的八个样品组成,但PCR和三个样品的阳性由培养物和PCR技术具有不同的细菌。结论:根据该研究,宽范围的PCR与Sanger测序相结合,可用于检测基于常规细菌培养的脓肿中脓肿的显性厌氧菌细菌。

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