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使用 gnd 作为靶基因进行非培养分析,以评估大肠杆菌的多样性和群落结构。

Culture independent analysis using gnd as a target gene to assess Escherichia coli diversity and community structure.

机构信息

AgResearch Limited, Hopkirk Research Institute, Palmerston North, New Zealand.

mEpiLab, Hopkirk Research Institute, Massey University, Palmerston North, New Zealand.

出版信息

Sci Rep. 2017 Apr 12;7(1):841. doi: 10.1038/s41598-017-00890-6.

Abstract

Current culture methods to investigate changes in Escherichia coli community structure are often slow and laborious. Genes such as gnd (6-phosphogluconate dehydrogenase) have a highly variable nucleotide sequence and may provide a target for E. coli microbiome analysis using culture-independent methods. Metabarcoded PCR primers were used to generate separate libraries from calf faecal samples for high throughput sequencing. Although a total of 348 separate gnd sequence types (gSTs) were identified, 188 were likely to be due to sequencing errors. Of the remaining 160 gSTs, 92 did not match those in a database of 319 separate gnd sequences. 'Animal' was the main determinant of E. coli diversity with limited impact of sample type or DNA extraction method on intra-host E. coli community variation from faeces and recto-anal mucosal swab samples. This culture-independent study has addressed the difficulties of quantifying bacterial intra-species diversity and revealed that, whilst individual animals may harbour >50 separate E. coli strains, communities are dominated by <10 strains alongside a large pool of subdominant strains present at low abundances. This method will be useful for characterising the diversity and population structure of E. coli in experimental studies designed to assess the impact of interventions on the gut microbiome.

摘要

目前,研究大肠杆菌群落结构变化的传统培养方法往往既缓慢又费力。gnd(6-磷酸葡萄糖酸脱氢酶)等基因具有高度多变的核苷酸序列,可能成为使用非培养方法进行大肠杆菌微生物组分析的目标。代谢条码 PCR 引物用于从小牛粪便样本中生成单独的文库,以便进行高通量测序。虽然总共鉴定出了 348 种不同的 gnd 序列类型(gST),但其中 188 种可能是由于测序错误造成的。在剩下的 160 种 gST 中,有 92 种与数据库中 319 种不同的 gnd 序列不匹配。“动物”是大肠杆菌多样性的主要决定因素,样本类型或 DNA 提取方法对粪便和直肠黏膜拭子样本中宿主内大肠杆菌群落变异的影响有限。这项非培养研究解决了量化细菌种内多样性的困难,表明尽管单个动物可能携带超过 50 种不同的大肠杆菌菌株,但群落主要由不到 10 种菌株主导,同时还有大量低丰度的次要菌株。这种方法将有助于描述实验研究中大肠杆菌的多样性和种群结构,旨在评估干预措施对肠道微生物组的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886d/5429811/e19c9c988f22/41598_2017_890_Fig1_HTML.jpg

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