EDITORIAL
Many microorganisms can persist in a reversible state of reduced metabolic activity called dormancy. Dormancy allows microbes to survive unfavorable conditions, disperse and immigrate widely, broaden community diversity, extend lifespan, and preserve genetic information for future generations. Yet, there remain critical and fundamental unknowns about dormancy and its implications for microbial systems biology.
Persister cells and antimicrobial, metal, or other abiotic or biotic control of microbial activity switching.
Viable but non-cultivable phenotypes, their drivers, and their consequences for cellular systems, community ecology, or population fitness.
New methods for discriminating activity states among microbial cells, including laboratory and computational/bioinformatic tools.
Assessment of microbial activity (e.g., using SIP, BONCAT, flow cytometry, and 16S rRNA ratios) and to inform understanding of patterns of biodiversity, ecology, or evolution.
Phylogenetic insights into the distributions and diversification of dormancy strategies.
Implications of microbial dormancy for microbe-microbe or microbe-host interactions (including competition, synergisms, symbioses, or microbiome outcomes).
Dormancy-driven alterations in cellular, population, or microbiome primary or secondary metabolism, metabolic networks, or regulation.
Development of theory, conceptual frameworks, or mathematical models for understanding dormancy or activity state switching or predicting dormant states.
Discovery of new biological signatures of dormant states.
Articles belonging to the special collection will be published as they are accepted, and we especially welcome the application of multidisciplinary and innovative approaches to understanding the drivers and consequences of dormancy in microbial systems.
This special collection is catalyzed in parallel to the
University of California San Diego , La Jolla , California , USA
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