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IONESCU DannyORCID_LOGO

  • MIBI, Technical University of Berlin, Berlin, Germany
  • Bacteria and archaea, Bioinformatics, Evolutionary genomics, Functional genomics, Metagenomics
  • recommender, manager, administrator

Recommendation:  1

Reviews:  0

Areas of expertise
My research encompasses many areas of microbial ecology in aquatic environments. This includes limnic, marine, and extreme environments. I am interested in linking the organismal response to the environments from single cells up to entire communities. In particular, I am interested in polyploid giant bacteria trying to understand how they coordinate and fine-tune their response given the hundreds and thousands of chromosomes that are often not identical.

Recommendation:  1

05 May 2021
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A primer and discussion on DNA-based microbiome data and related bioinformatics analyses

A hitchhiker’s guide to DNA-based microbiome analysis

Recommended by based on reviews by Nicolas Pollet, Rafael Cuadrat and 1 anonymous reviewer

In the last two decades, microbial research in its different fields has been increasingly focusing on microbiome studies. These are defined as studies of complete assemblages of microorganisms in given environments and have been benefiting from increases in sequencing length, quality, and yield, coupled with ever-dropping prices per sequenced nucleotide. Alongside localized microbiome studies, several global collaborative efforts have emerged, including the Human Microbiome Project [1], the Earth Microbiome Project [2], the Extreme Microbiome Project, and MetaSUB [3].

Coupled with the development of sequencing technologies and the ever-increasing amount of data output, multiple standalone or online bioinformatic tools have been designed to analyze these data. Often these tools have been focusing on either of two main tasks: 1) Community analysis, providing information on the organisms present in the microbiome, or 2) Functionality, in the case of shotgun metagenomic data, providing information on the metabolic potential of the microbiome. Bridging between the two types of data, often extracted from the same dataset, is typically a daunting task that has been addressed by a handful of tools only.

The extent of tools and approaches to analyze microbiome data is great and may be overwhelming to researchers new to microbiome or bioinformatic studies. In their paper “A primer and discussion on DNA-based microbiome data and related bioinformatics analyses”, Douglas and Langille [4] guide us through the different sequencing approaches useful for microbiome studies. alongside their advantages and caveats and a selection of tools to analyze these data, coupled with examples from their own field of research.

Standing out in their primer-style review is the emphasis on the coupling between taxonomic/phylogenetic identification of the organisms and their functionality. This type of analysis, though highly important to understand the role of different microorganisms in an environment as well as to identify potential functional redundancy, is often not conducted. For this, the authors identify two approaches. The first, using shotgun metagenomics, has higher chances of attributing a function to the correct taxon. The second, using amplicon sequencing of marker genes, allows for a deeper coverage of the microbiome at a lower cost, and extrapolates the amplicon data to close relatives with a sequenced genome. As clearly stated, this approach makes the leap between taxonomy and functionality and has been shown to be erroneous in cases where the core genome of the bacterial genus or family does not encompass the functional diversity of the different included species. This practice was already common before the genomic era, but its accuracy is improving thanks to the increasing availability of sequenced reference genomes from cultures, environmentally picked single cells or metagenome-assembled genome.

In addition to their description of standalone tools useful for linking taxonomy and functionality, one should mention the existence of online tools that may appeal to researchers who do not have access to adequate bioinformatics infrastructure. Among these are the Integrated Microbial Genomes and Microbiomes (IMG) from the Joint Genome Institute [5], KBase [6] and MG-RAST [7].

A second important point arising from this review is the need for standardization in microbiome data analyses and the complexity of achieving this. As Douglas and Langille [4] state, this has been previously addressed, highlighting the variability in results obtained with different tools. It is often the case that papers describing new bioinformatic tools display their superiority relative to existing alternatives, potentially misleading newcomers to the field that the newest tool is the best and only one to be used. This is often not the case, and while benchmarking against well-defined datasets serves as a powerful testing tool, “real-life” samples are often not comparable. Thus, as done here, future primer-like reviews should highlight possible cross-field caveats, encouraging researchers to employ and test several approaches and validate their results whenever possible.

In summary, Douglas and Langille [4] offer both the novice and experienced researcher a detailed guide along the paths of microbiome data analysis, accompanied by informative background information, suggested tools with which analyses can be started, and an insightful view on where the field should be heading.

References

[1]  Turnbaugh PJ, Ley RE, Hamady M, Fraser-Liggett CM, Knight R, Gordon JI (2007) The Human Microbiome Project. Nature, 449, 804–810. https://doi.org/10.1038/nature06244

[2]  Gilbert JA, Jansson JK, Knight R (2014) The Earth Microbiome project: successes and aspirations. BMC Biology, 12, 69. https://doi.org/10.1186/s12915-014-0069-1

[3]  Mason C, Afshinnekoo E, Ahsannudin S, Ghedin E, Read T, Fraser C, Dudley J, Hernandez M, Bowler C, Stolovitzky G, Chernonetz A, Gray A, Darling A, Burke C, Łabaj PP, Graf A, Noushmehr H, Moraes  s., Dias-Neto E, Ugalde J, Guo Y, Zhou Y, Xie Z, Zheng D, Zhou H, Shi L, Zhu S, Tang A, Ivanković T, Siam R, Rascovan N, Richard H, Lafontaine I, Baron C, Nedunuri N, Prithiviraj B, Hyat S, Mehr S, Banihashemi K, Segata N, Suzuki H, Alpuche Aranda CM, Martinez J, Christopher Dada A, Osuolale O, Oguntoyinbo F, Dybwad M, Oliveira M, Fernandes A, Oliveira M, Fernandes A, Chatziefthimiou AD, Chaker S, Alexeev D, Chuvelev D, Kurilshikov A, Schuster S, Siwo GH, Jang S, Seo SC, Hwang SH, Ossowski S, Bezdan D, Udekwu K, Udekwu K, Lungjdahl PO, Nikolayeva O, Sezerman U, Kelly F, Metrustry S, Elhaik E, Gonnet G, Schriml L, Mongodin E, Huttenhower C, Gilbert J, Hernandez M, Vayndorf E, Blaser M, Schadt E, Eisen J, Beitel C, Hirschberg D, Schriml L, Mongodin E, The MetaSUB International Consortium (2016) The Metagenomics and Metadesign of the Subways and Urban Biomes (MetaSUB) International Consortium inaugural meeting report. Microbiome, 4, 24. https://doi.org/10.1186/s40168-016-0168-z

[4]  Douglas GM, Langille MGI (2021) A primer and discussion on DNA-based microbiome data and related bioinformatics analyses. OSF Preprints, ver. 4 peer-reviewed and recommended by Peer Community In Genomics. https://doi.org/10.31219/osf.io/3dybg

[5]  Chen I-MA, Markowitz VM, Chu K, Palaniappan K, Szeto E, Pillay M, Ratner A, Huang J, Andersen E, Huntemann M, Varghese N, Hadjithomas M, Tennessen K, Nielsen T, Ivanova NN, Kyrpides NC (2017) IMG/M: integrated genome and metagenome comparative data analysis system. Nucleic Acids Research, 45, D507–D516. https://doi.org/10.1093/nar/gkw929

[6]  Arkin AP, Cottingham RW, Henry CS, Harris NL, Stevens RL, Maslov S, Dehal P, Ware D, Perez F, Canon S, Sneddon MW, Henderson ML, Riehl WJ, Murphy-Olson D, Chan SY, Kamimura RT, Kumari S, Drake MM, Brettin TS, Glass EM, Chivian D, Gunter D, Weston DJ, Allen BH, Baumohl J, Best AA, Bowen B, Brenner SE, Bun CC, Chandonia J-M, Chia J-M, Colasanti R, Conrad N, Davis JJ, Davison BH, DeJongh M, Devoid S, Dietrich E, Dubchak I, Edirisinghe JN, Fang G, Faria JP, Frybarger PM, Gerlach W, Gerstein M, Greiner A, Gurtowski J, Haun HL, He F, Jain R, Joachimiak MP, Keegan KP, Kondo S, Kumar V, Land ML, Meyer F, Mills M, Novichkov PS, Oh T, Olsen GJ, Olson R, Parrello B, Pasternak S, Pearson E, Poon SS, Price GA, Ramakrishnan S, Ranjan P, Ronald PC, Schatz MC, Seaver SMD, Shukla M, Sutormin RA, Syed MH, Thomason J, Tintle NL, Wang D, Xia F, Yoo H, Yoo S, Yu D (2018) KBase: The United States Department of Energy Systems Biology Knowledgebase. Nature Biotechnology, 36, 566–569. https://doi.org/10.1038/nbt.4163

[7]  Wilke A, Bischof J, Gerlach W, Glass E, Harrison T, Keegan KP, Paczian T, Trimble WL, Bagchi S, Grama A, Chaterji S, Meyer F (2016) The MG-RAST metagenomics database and portal in 2015. Nucleic Acids Research, 44, D590–D594. https://doi.org/10.1093/nar/gkv1322

avatar

IONESCU DannyORCID_LOGO

  • MIBI, Technical University of Berlin, Berlin, Germany
  • Bacteria and archaea, Bioinformatics, Evolutionary genomics, Functional genomics, Metagenomics
  • recommender, manager, administrator

Recommendation:  1

Reviews:  0

Areas of expertise
My research encompasses many areas of microbial ecology in aquatic environments. This includes limnic, marine, and extreme environments. I am interested in linking the organismal response to the environments from single cells up to entire communities. In particular, I am interested in polyploid giant bacteria trying to understand how they coordinate and fine-tune their response given the hundreds and thousands of chromosomes that are often not identical.