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首页> 外文期刊>BMC Veterinary Research >Illumina MiSeq 16S amplicon sequence analysis of bovine respiratory disease associated bacteria in lung and mediastinal lymph node tissue
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Illumina MiSeq 16S amplicon sequence analysis of bovine respiratory disease associated bacteria in lung and mediastinal lymph node tissue

机译:牛和纵隔淋巴结组织中牛呼吸系统疾病相关细菌的Illumina MiSeq 16S扩增子序列分析

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Background Bovine respiratory disease (BRD) is caused by growth of single or multiple species of pathogenic bacteria in lung tissue following stress and/or viral infection. Next generation sequencing of 16S ribosomal RNA gene PCR amplicons (NGS 16S amplicon analysis) is a powerful culture-independent open reference method that has recently been used to increase understanding of BRD-associated bacteria in the upper respiratory tract of BRD cattle. However, it has not yet been used to examine the microbiome of the bovine lower respiratory tract. The objective of this study was to use NGS 16S amplicon analysis to identify bacteria in post-mortem lung and lymph node tissue samples harvested from fatal BRD cases and clinically healthy animals. Cranial lobe and corresponding mediastinal lymph node post-mortem tissue samples were collected from calves diagnosed as BRD cases by veterinary laboratory pathologists and from clinically healthy calves. NGS 16S amplicon libraries, targeting the V3-V4 region of the bacterial 16S rRNA gene were prepared and sequenced on an Illumina MiSeq. Quantitative insights into microbial ecology (QIIME) was used to determine operational taxonomic units (OTUs) which corresponded to the 16S rRNA gene sequences. Results Leptotrichiaceae, Mycoplasma, Pasteurellaceae , and Fusobacterium were the most abundant OTUs identified in the lungs and lymph nodes of the calves which died from BRD. Leptotrichiaceae, Fusobacterium , Mycoplasma, Trueperella and Bacteroides had greater relative abundances in post-mortem lung samples collected from fatal cases of BRD in dairy calves, compared with clinically healthy calves without lung lesions. Leptotrichiaceae, Mycoplasma and Pasteurellaceae showed higher relative abundances in post-mortem lymph node samples collected from fatal cases of BRD in dairy calves, compared with clinically healthy calves without lung lesions. Two Leptotrichiaceae sequence contigs were subsequently assembled from bacterial DNA-enriched shotgun sequences. Conclusions The microbiomes of the cranial lung lobe and mediastinal lymph node from calves which died from BRD and from clinically healthy H-F calves have been characterised. Contigs corresponding to the abundant Leptotrichiaceae OTU were sequenced and found not to be identical to any known bacterial genus. This suggests that we have identified a novel bacterial species associated with BRD.
机译:背景技术牛呼吸道疾病(BRD)是由压力和/或病毒感染后肺组织中单一或多种病原细菌的生长引起的。 16S核糖体RNA基因PCR扩增子的下一代测序(NGS 16S扩增子分析)是一种与培养无关的强大开放参考方法,最近已用于增强对BRD牛上呼吸道与BRD相关细菌的了解。但是,它尚未用于检查牛下呼吸道的微生物组。这项研究的目的是使用NGS 16S扩增子分析来鉴定从致命BRD病例和临床健康动物身上采集的死后肺和淋巴结组织样本中的细菌。从兽医实验室病理学家诊断为BRD病例的小牛和临床健康的小牛中收集颅脑叶和相应的纵隔淋巴结死后组织样本。制备了靶向细菌16S rRNA基因V3-V4区的NGS 16S扩增子文库,并在Illumina MiSeq上测序。使用微生物生态学(QIIME)的定量见解来确定对应于16S rRNA基因序列的操作分类单位(OTU)。结果钩端螺旋体科,支原体,巴斯德杆菌科和梭菌是在BRD死亡小牛的肺和淋巴结中发现的最丰富的OTU。与无肺部病变的临床健康小牛相比,从乳牛小牛致命性BRD病例收集的死后肺样本中,钩端毛菌科,梭菌,支原体,真小球藻和拟杆菌具有更高的相对丰度。与没有肺部病变的临床健康小牛相比,从乳牛小牛的BRD致命病例中收集的死后淋巴结样本中,钩毛菌科,支原体和巴斯德杆菌科显示出较高的相对丰度。随后从细菌DNA富集的shot弹枪序列中组装了两个钩端螺旋体科重叠群。结论已鉴定出死于BRD的犊牛和临床健康的H-F犊牛的颅肺叶和纵隔淋巴结的微生物群。对与丰富的钩端螺旋体科OTU相对应的重叠群进行测序,发现与任何已知细菌属都不相同。这表明我们已经鉴定出一种与BRD相关的新型细菌。

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