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使用深度鸟枪法测序监测微生物群落以确保食品安全和质量。

Monitoring the microbiome for food safety and quality using deep shotgun sequencing.

作者信息

Beck Kristen L, Haiminen Niina, Chambliss David, Edlund Stefan, Kunitomi Mark, Huang B Carol, Kong Nguyet, Ganesan Balasubramanian, Baker Robert, Markwell Peter, Kawas Ban, Davis Matthew, Prill Robert J, Krishnareddy Harsha, Seabolt Ed, Marlowe Carl H, Pierre Sophie, Quintanar André, Parida Laxmi, Dubois Geraud, Kaufman James, Weimer Bart C

机构信息

Consortium for Sequencing the Food Supply Chain, San Jose, CA, USA.

IBM Almaden Research Center, San Jose, CA, USA.

出版信息

NPJ Sci Food. 2021 Feb 8;5(1):3. doi: 10.1038/s41538-020-00083-y.

DOI:10.1038/s41538-020-00083-y
PMID:33558514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7870667/
Abstract

In this work, we hypothesized that shifts in the food microbiome can be used as an indicator of unexpected contaminants or environmental changes. To test this hypothesis, we sequenced the total RNA of 31 high protein powder (HPP) samples of poultry meal pet food ingredients. We developed a microbiome analysis pipeline employing a key eukaryotic matrix filtering step that improved microbe detection specificity to >99.96% during in silico validation. The pipeline identified 119 microbial genera per HPP sample on average with 65 genera present in all samples. The most abundant of these were Bacteroides, Clostridium, Lactococcus, Aeromonas, and Citrobacter. We also observed shifts in the microbial community corresponding to ingredient composition differences. When comparing culture-based results for Salmonella with total RNA sequencing, we found that Salmonella growth did not correlate with multiple sequence analyses. We conclude that microbiome sequencing is useful to characterize complex food microbial communities, while additional work is required for predicting specific species' viability from total RNA sequencing.

摘要

在这项研究中,我们假设食品微生物组的变化可以用作意外污染物或环境变化的指标。为了验证这一假设,我们对31份禽肉粉宠物食品成分的高蛋白粉末(HPP)样本的总RNA进行了测序。我们开发了一种微生物组分析流程,该流程采用了关键的真核生物基质过滤步骤,在计算机模拟验证过程中将微生物检测特异性提高到了>99.96%。该流程平均每个HPP样本鉴定出119个微生物属,所有样本中共有65个属。其中最丰富的是拟杆菌属、梭菌属、乳球菌属、气单胞菌属和柠檬酸杆菌属。我们还观察到微生物群落的变化与成分组成差异相对应。当将基于培养的沙门氏菌结果与总RNA测序结果进行比较时,我们发现沙门氏菌的生长与多重序列分析不相关。我们得出结论,微生物组测序有助于表征复杂的食品微生物群落,而从总RNA测序预测特定物种的生存能力还需要进一步的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/d52e1b514af5/41538_2020_83_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/0965059e1f38/41538_2020_83_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/a910c288c829/41538_2020_83_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/64ad4d4eae23/41538_2020_83_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/a8db2b493412/41538_2020_83_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/880866cfb122/41538_2020_83_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/1f041a28091f/41538_2020_83_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/dc5831e7af6e/41538_2020_83_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/d52e1b514af5/41538_2020_83_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/0965059e1f38/41538_2020_83_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/a910c288c829/41538_2020_83_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/64ad4d4eae23/41538_2020_83_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/a8db2b493412/41538_2020_83_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/880866cfb122/41538_2020_83_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/1f041a28091f/41538_2020_83_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/dc5831e7af6e/41538_2020_83_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbe9/7870667/d52e1b514af5/41538_2020_83_Fig8_HTML.jpg

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