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从田鼠中提取的细菌的宏基因组评估。

Metagenomic Evaluation of Bacteria from Voles.

机构信息

1 Centre for Military Medicine , Helsinki, Finland .

2 Department of Virology, University of Helsinki , Helsinki, Finland .

出版信息

Vector Borne Zoonotic Dis. 2017 Feb;17(2):123-133. doi: 10.1089/vbz.2016.1969. Epub 2016 Nov 17.

Abstract

Voles (Arvicolinae, Rodentia) are known carriers of zoonotic bacteria such as Bartonella spp. and Francisella tularensis. However, apart from F. tularensis, the bacterial microbiome of voles has not previously been determined in Finland and rarely elsewhere. Therefore, we studied liver samples from 61 voles using 16S ribosomal RNA gene PCR analysis, followed by Sanger sequencing. Twenty-three of these samples were also studied with tag-encoded pyrosequencing. The samples originated from 21 field voles (Microtus agrestis), 37 tundra voles (Microtus oeconomus), and 3 bank voles (Myodes glareolus). With the more conventional 16S rDNA PCR analysis, 90 (33%) of the recovered 269 sequence types could be identified to genus level, including Bartonella, Francisella, Mycoplasma, Anaplasma, and Acinetobacter in 31, 15, 9, 9, and 9 sequences, respectively. Seventy-five (28%) matched best with sequences of uncultured bacteria, of which 40/75 could be classified to the order Clostridiales and, more specifically, to families Lachnospiraceae and Ruminococcaceae. Pyrosequencing from 23 samples revealed comparable and similar results: clinically relevant bacterial families such as Mycoplasmataceae, Bartonellaceae, Anaplasmataceae, and Francisellaceae were recognized. These analyses revealed significant bacterial diversity in vole livers, consisting of distinct and constant sequence patterns reflecting bacteria found in the intestinal gut, but including some known zoonotic pathogens as well. The molecular bacterial sequence types determined with the two different techniques shared major similarities and verified remarkable congruency between the methods.

摘要

田鼠(Arvicolinae,啮齿目)已知是携带兽疫细菌的载体,如巴尔通体属和土拉弗朗西斯菌。然而,除了土拉弗朗西斯菌,芬兰以前从未确定过田鼠的细菌微生物组,在其他地方也很少有研究。因此,我们使用 16S 核糖体 RNA 基因 PCR 分析研究了 61 只田鼠的肝脏样本,随后进行了 Sanger 测序。其中 23 个样本还进行了标签编码焦磷酸测序。这些样本来自 21 只草原田鼠(Microtus agrestis)、37 只冻原田鼠(Microtus oeconomus)和 3 只鼷鼠(Myodes glareolus)。通过更传统的 16S rDNA PCR 分析,在回收的 269 个序列类型中,有 90 个(33%)可鉴定到属水平,其中 31 个、15 个、9 个、9 个和 9 个序列分别为巴尔通体属、土拉弗朗西斯菌、支原体、无形体属和不动杆菌属。75 个(28%)与未培养细菌的序列最匹配,其中 40/75 可归类为梭菌目,更具体地说,为毛螺菌科和真杆菌科。23 个样本的焦磷酸测序显示出可比且相似的结果:识别出临床相关的细菌家族,如支原体科、巴尔通体科、无形体科和弗朗西斯菌科。这些分析显示,田鼠肝脏中的细菌多样性显著,包括肠道中发现的不同且恒定的序列模式,但也包括一些已知的人畜共患病病原体。这两种不同技术确定的分子细菌序列类型具有主要相似性,两种方法之间具有显著的一致性。

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