4.6 Review

Advances in experimental and computational methodologies for the study of microbial-surface interactions at different omics levels

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.1006946

Keywords

biofilms; genomics; transcriptomics; metabolomics; proteomics; omics data integration; systems biology

Categories

Funding

  1. European Union [BU058P20]
  2. Junta de Castilla y Leon-FEDER
  3. [952379]

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The study of microbial cells interacting with natural and synthetic interfaces has been enriched by the development of advanced omics technologies, allowing for the isolation and analysis of nucleic acids, proteins, and metabolites from complex samples. This review discusses the challenges in analyzing microbial cells at genomic, transcriptomic, proteomic, and metabolomic levels, and describes both experimental and computational approaches to address them. The integration of multi omics datasets is presented as a means to achieve a systems level understanding of these complex interactions.
The study of the biological response of microbial cells interacting with natural and synthetic interfaces has acquired a new dimension with the development and constant progress of advanced omics technologies. New methods allow the isolation and analysis of nucleic acids, proteins and metabolites from complex samples, of interest in diverse research areas, such as materials sciences, biomedical sciences, forensic sciences, biotechnology and archeology, among others. The study of the bacterial recognition and response to surface contact or the diagnosis and evolution of ancient pathogens contained in archeological tissues require, in many cases, the availability of specialized methods and tools. The current review describes advances in in vitro and in silico approaches to tackle existing challenges (e.g., low-quality sample, low amount, presence of inhibitors, chelators, etc.) in the isolation of high-quality samples and in the analysis of microbial cells at genomic, transcriptomic, proteomic and metabolomic levels, when present in complex interfaces. From the experimental point of view, tailored manual and automatized methodologies, commercial and in-house developed protocols, are described. The computational level focuses on the discussion of novel tools and approaches designed to solve associated issues, such as sample contamination, low quality reads, low coverage, etc. Finally, approaches to obtain a systems level understanding of these complex interactions by integrating multi omics datasets are presented.

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