Literature DB >> 33478576

Whole microbial community viability is not quantitatively reflected by propidium monoazide sequencing approach.

Ya Wang1,2, Yan Yan1,2, Kelsey N Thompson1,2, Sena Bae1,2, Emma K Accorsi1, Yancong Zhang1,2, Jiaxian Shen3, Hera Vlamakis2, Erica M Hartmann3, Curtis Huttenhower4,5,6.   

Abstract

BACKGROUND: High-throughput sequencing provides a powerful window into the structural and functional profiling of microbial communities, but it is unable to characterize only the viable portion of microbial communities at scale. There is as yet not one best solution to this problem. Previous studies have established viability assessments using propidium monoazide (PMA) treatment coupled with downstream molecular profiling (e.g., qPCR or sequencing). While these studies have met with moderate success, most of them focused on the resulting "viable" communities without systematic evaluations of the technique. Here, we present our work to rigorously benchmark "PMA-seq" (PMA treatment followed by 16S rRNA gene amplicon sequencing) for viability assessment in synthetic and realistic microbial communities.
RESULTS: PMA-seq was able to successfully reconstruct simple synthetic communities comprising viable/heat-killed Escherichia coli and Streptococcus sanguinis. However, in realistically complex communities (computer screens, computer mice, soil, and human saliva) with E. coli spike-in controls, PMA-seq did not accurately quantify viability (even relative to variability in amplicon sequencing), with its performance largely affected by community properties such as initial biomass, sample types, and compositional diversity. We then applied this technique to environmental swabs from the Boston subway system. Several taxa differed significantly after PMA treatment, while not all microorganisms responded consistently. To elucidate the "PMA-responsive" microbes, we compared our results with previous PMA-based studies and found that PMA responsiveness varied widely when microbes were sourced from different ecosystems but were reproducible within similar environments across studies.
CONCLUSIONS: This study provides a comprehensive evaluation of PMA-seq exploring its quantitative potential in synthetic and complex microbial communities, where the technique was effective for semi-quantitative purposes in simple synthetic communities but provided only qualitative assessments in realistically complex community samples. Video abstract.

Entities:  

Keywords:  16S rRNA-sequencing; Built environment communities; Propidium monoazide

Mesh:

Substances:

Year:  2021        PMID: 33478576      PMCID: PMC7819323          DOI: 10.1186/s40168-020-00961-3

Source DB:  PubMed          Journal:  Microbiome        ISSN: 2049-2618            Impact factor:   14.650


  49 in total

1.  Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set.

Authors:  Mangala A Nadkarni; F Elizabeth Martin; Nicholas A Jacques; Neil Hunter
Journal:  Microbiology       Date:  2002-01       Impact factor: 2.777

2.  Search and clustering orders of magnitude faster than BLAST.

Authors:  Robert C Edgar
Journal:  Bioinformatics       Date:  2010-08-12       Impact factor: 6.937

3.  Comparison of propidium monoazide with ethidium monoazide for differentiation of live vs. dead bacteria by selective removal of DNA from dead cells.

Authors:  Andreas Nocker; Ching-Ying Cheung; Anne K Camper
Journal:  J Microbiol Methods       Date:  2006-06-05       Impact factor: 2.363

4.  Relic DNA is abundant in soil and obscures estimates of soil microbial diversity.

Authors:  Paul Carini; Patrick J Marsden; Jonathan W Leff; Emily E Morgan; Michael S Strickland; Noah Fierer
Journal:  Nat Microbiol       Date:  2016-12-19       Impact factor: 17.745

5.  The Environmental Exposures and Inner- and Intercity Traffic Flows of the Metro System May Contribute to the Skin Microbiome and Resistome.

Authors:  Kang Kang; Yueqiong Ni; Jun Li; Lejla Imamovic; Chinmoy Sarkar; Marie Danielle Kobler; Yoshitaro Heshiki; Tingting Zheng; Sarika Kumari; Jane Ching Yan Wong; Anand Archna; Cheong Wai Martin Wong; Caroline Dingle; Seth Denizen; David Michael Baker; Morten Otto Alexander Sommer; Christopher John Webster; Gianni Panagiotou
Journal:  Cell Rep       Date:  2018-07-31       Impact factor: 9.423

6.  Evaluation of viability-qPCR detection system on viable and dead Salmonella serovar Enteritidis.

Authors:  Elodie Barbau-Piednoir; Jacques Mahillon; Julie Pillyser; Wim Coucke; Nancy H Roosens; Nadine Botteldoorn
Journal:  J Microbiol Methods       Date:  2014-06-11       Impact factor: 2.363

7.  Using propidium monoazide to distinguish between viable and nonviable bacteria, MS2 and murine norovirus.

Authors:  S Y Kim; G Ko
Journal:  Lett Appl Microbiol       Date:  2012-07-20       Impact factor: 2.858

8.  Human and Extracellular DNA Depletion for Metagenomic Analysis of Complex Clinical Infection Samples Yields Optimized Viable Microbiome Profiles.

Authors:  Maria T Nelson; Christopher E Pope; Robyn L Marsh; Daniel J Wolter; Eli J Weiss; Kyle R Hager; Anh T Vo; Mitchell J Brittnacher; Matthew C Radey; Hillary S Hayden; Alexander Eng; Samuel I Miller; Elhanan Borenstein; Lucas R Hoffman
Journal:  Cell Rep       Date:  2019-02-19       Impact factor: 9.423

Review 9.  The roles of the outdoors and occupants in contributing to a potential pan-microbiome of the built environment: a review.

Authors:  Marcus H Y Leung; Patrick K H Lee
Journal:  Microbiome       Date:  2016-05-24       Impact factor: 14.650

10.  Improving saliva shotgun metagenomics by chemical host DNA depletion.

Authors:  Clarisse A Marotz; Jon G Sanders; Cristal Zuniga; Livia S Zaramela; Rob Knight; Karsten Zengler
Journal:  Microbiome       Date:  2018-02-27       Impact factor: 14.650

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2.  The sanitary indoor environment-a potential source for intact human-associated anaerobes.

Authors:  Manuela-Raluca Pausan; Marcus Blohs; Alexander Mahnert; Christine Moissl-Eichinger
Journal:  NPJ Biofilms Microbiomes       Date:  2022-06-01       Impact factor: 8.462

3.  Toward Accurate and Robust Environmental Surveillance Using Metagenomics.

Authors:  Jiaxian Shen; Alexander G McFarland; Vincent B Young; Mary K Hayden; Erica M Hartmann
Journal:  Front Genet       Date:  2021-03-05       Impact factor: 4.599

4.  An Assay Combining Droplet Digital PCR With Propidium Monoazide Treatment for the Accurate Detection of Live Cells of Vibrio vulnificus in Plasma Samples.

Authors:  Ling Hu; Yidong Fu; Shun Zhang; Zhilei Pan; Jiang Xia; Peng Zhu; Jing Guo
Journal:  Front Microbiol       Date:  2022-07-15       Impact factor: 6.064

  4 in total

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