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

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...

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Autores principales: Kristen L. Beck, Niina Haiminen, David Chambliss, Stefan Edlund, Mark Kunitomi, B. Carol Huang, Nguyet Kong, Balasubramanian Ganesan, Robert Baker, Peter Markwell, Ban Kawas, Matthew Davis, Robert J. Prill, Harsha Krishnareddy, Ed Seabolt, Carl H. Marlowe, Sophie Pierre, André Quintanar, Laxmi Parida, Geraud Dubois, James Kaufman, Bart C. Weimer
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/2c00c0d566954b1792fdf043d8b9114f
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spelling oai:doaj.org-article:2c00c0d566954b1792fdf043d8b9114f2021-12-02T14:11:00ZMonitoring the microbiome for food safety and quality using deep shotgun sequencing10.1038/s41538-020-00083-y2396-8370https://doaj.org/article/2c00c0d566954b1792fdf043d8b9114f2021-02-01T00:00:00Zhttps://doi.org/10.1038/s41538-020-00083-yhttps://doaj.org/toc/2396-8370Abstract 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.Kristen L. BeckNiina HaiminenDavid ChamblissStefan EdlundMark KunitomiB. Carol HuangNguyet KongBalasubramanian GanesanRobert BakerPeter MarkwellBan KawasMatthew DavisRobert J. PrillHarsha KrishnareddyEd SeaboltCarl H. MarloweSophie PierreAndré QuintanarLaxmi ParidaGeraud DuboisJames KaufmanBart C. WeimerNature PortfolioarticleNutrition. Foods and food supplyTX341-641Food processing and manufactureTP368-456ENnpj Science of Food, Vol 5, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Nutrition. Foods and food supply
TX341-641
Food processing and manufacture
TP368-456
spellingShingle Nutrition. Foods and food supply
TX341-641
Food processing and manufacture
TP368-456
Kristen L. Beck
Niina Haiminen
David Chambliss
Stefan Edlund
Mark Kunitomi
B. Carol Huang
Nguyet Kong
Balasubramanian Ganesan
Robert Baker
Peter Markwell
Ban Kawas
Matthew Davis
Robert J. Prill
Harsha Krishnareddy
Ed Seabolt
Carl H. Marlowe
Sophie Pierre
André Quintanar
Laxmi Parida
Geraud Dubois
James Kaufman
Bart C. Weimer
Monitoring the microbiome for food safety and quality using deep shotgun sequencing
description 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.
format article
author Kristen L. Beck
Niina Haiminen
David Chambliss
Stefan Edlund
Mark Kunitomi
B. Carol Huang
Nguyet Kong
Balasubramanian Ganesan
Robert Baker
Peter Markwell
Ban Kawas
Matthew Davis
Robert J. Prill
Harsha Krishnareddy
Ed Seabolt
Carl H. Marlowe
Sophie Pierre
André Quintanar
Laxmi Parida
Geraud Dubois
James Kaufman
Bart C. Weimer
author_facet Kristen L. Beck
Niina Haiminen
David Chambliss
Stefan Edlund
Mark Kunitomi
B. Carol Huang
Nguyet Kong
Balasubramanian Ganesan
Robert Baker
Peter Markwell
Ban Kawas
Matthew Davis
Robert J. Prill
Harsha Krishnareddy
Ed Seabolt
Carl H. Marlowe
Sophie Pierre
André Quintanar
Laxmi Parida
Geraud Dubois
James Kaufman
Bart C. Weimer
author_sort Kristen L. Beck
title Monitoring the microbiome for food safety and quality using deep shotgun sequencing
title_short Monitoring the microbiome for food safety and quality using deep shotgun sequencing
title_full Monitoring the microbiome for food safety and quality using deep shotgun sequencing
title_fullStr Monitoring the microbiome for food safety and quality using deep shotgun sequencing
title_full_unstemmed Monitoring the microbiome for food safety and quality using deep shotgun sequencing
title_sort monitoring the microbiome for food safety and quality using deep shotgun sequencing
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/2c00c0d566954b1792fdf043d8b9114f
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