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Amplicon-Based Next Generation Sequencing for Rapid Identification of

机译:基于扩增子的下一代测序用于快速识别

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摘要

Background: Next generation sequencing (NGS) technology has been used for a wide range of epidemiological and surveillance studies. Here, we used amplicon-based NGS to species identify Rickettsia and their arthropod hosts from entomological surveillance. Methods: During 2015–2016, we screened 1825 samples of rodents and ectoparasites collected from rodents and domestic mammals (dog, cat, and cattle) across Thailand for Rickettsia. The citrate synthase gene was amplified to identify Rickettsia to species, while the Cytochrome Oxidase subunit I (COI) and subunit II (COII) genes were used as target genes for ectoparasite identification. All target gene amplicons were pooled for library preparation and sequenced with Illumina MiSeq platform. Result: The highest percentage of Rickettsia DNA was observed in fleas collected from domestic animals (56%) predominantly dogs. Only a few samples of ticks from domestic animals, rodent fleas, and rodent tissue were positive for Rickettisia DNA. NGS based characterization of Rickettsia by host identified Rickettsia asembonensis as the most common bacteria in positive fleas collected from dogs (83.2%) while “Candidatus Rickettsia senegalensis” was detected in only 16.8% of Rickettsia positive dog fleas. Sequence analysis of COI and COII revealed that almost all fleas collected from dogs were Ctenocephalides felis orientis. Other Rickettsia species were detected by NGS including Rickettsia heilongjiangensis from two Haemaphysalis hystricis ticks, and Rickettsia typhi in two rodent tissue samples. Conclusion: This study demonstrates the utility of NGS for high-throughput sequencing in the species characterization/identification of bacteria and ectoparasite for entomological surveillance of rickettsiae. A high percentage of C. f. orientis are positive for R. asembonensis. In addition, our findings indicate there is a risk of tick-borne Spotted Fever Group rickettsiosis, and flea-borne murine typhus transmission in Tak and Phangnga provinces of Thailand.
机译:背景:下一代测序(NGS)技术已被用于广泛的流行病学和监测研究。在这里,我们使用基于扩增子的NGS鉴定Rickettia及其节肢动物的主持人免受昆虫学监测。方法:2015 - 2016年期间,我们筛选了1825年啮齿动物和植物遗传癖的样本和从啮齿动物和家庭哺乳动物(狗,猫和牛)的敌意,用于Rickettia。扩增柠檬酸酯合酶基因以鉴定Rickettia至物种,而细胞色素氧化酶亚基I(COI)和亚基II(COII)基因被用作异位酸盐酯鉴定的靶基因。将所有靶基因扩增子合并用于库制备并用Illumina Miseq平台测序。结果:从家畜(56%)中,在从家畜(56%)中收集的蜗皮中,rickettsia DNA的最高百分比。只有一些来自家畜,啮齿动物跳蚤和啮齿动物组织的蜱虫样品对于RickettiaIa DNA呈阳性。基于宿主的Rickettia的NGS鉴定了Rickettia患者作为从狗收集的积极跳蚤(83.2%)的最常见的细菌,而“CandidatusRickettsia senegalensis”只在16.8%的Rickettsia阳性狗跳蚤中检测到。 COI和COII的序列分析显示,几乎所有从狗收集的跳蚤都是Ctenocephalides Felis Orientis。其他Rickettsia物种被NGS检测到,包括来自两种Haemaphysalis Hystricis蜱的Rickettsia黑龙江,在两个啮齿动物组织样品中的Rickettsia Typhi。结论:本研究证明了NGS在细菌的特征/鉴定中进行高通量测序的效用,用于Rictometsiae的昆虫学监测。高百分比的C.f。 Orientis对R. embonensis是阳性的。此外,我们的研究结果表明,蜱传染发烧群Rickettios病的风险,德国邦和邦邦省的跳蚤鼠耳塞传播。

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