» Articles » PMID: 35575545

Complex Ecotype Dynamics Evolve in Response to Fluctuating Resources

Overview
Journal mBio
Specialty Microbiology
Date 2022 May 16
PMID 35575545
Authors
Affiliations
Soon will be listed here.
Abstract

Ecotypic diversification and its associated cooperative behaviors are frequently observed in natural microbial populations whose access to resources is often sporadic. However, the extent to which fluctuations in resource availability influence the emergence of cooperative ecotypes is not fully understood. To determine how exposure to repeated resource limitation affects the establishment and long-term maintenance of ecotypes in a structured environment, we followed 32 populations of Escherichia coli evolving to either 1-day or 10-day feast/famine cycles for 900 days. Population-level analysis revealed that compared to populations evolving to 1-day cycles, 10-day populations evolved increased biofilm density, higher parallelism in mutational targets, and increased mutation rates. As previous investigations of evolution in structured environments have identified biofilm formation as the earliest observable phenotype associated with diversification of ecotypes, we revived cultures midway through the evolutionary process and conducted additional genomic, transcriptional, and phenotypic analyses of clones isolated from these evolving populations. We found not only that 10-day feast/famine cycles support multiple ecotypes but also that these ecotypes exhibit cooperative behavior. Consistent with the black queen hypothesis, or evolution of cooperation by gene loss, transcriptomic evidence suggests the evolution of bidirectional cross-feeding behaviors based on essential resources. These results provide insight into how analogous cooperative relationships may emerge in natural microbial communities. Despite regular feast and famine conditions representing an environmental pressure that is commonly encountered by microbial communities, the evolutionary outcomes of repeated cycles of feast and famine have been less studied. By experimentally evolving initially isogenic Escherichia coli populations to 10-day feast/famine cycles, we observed rapid diversification into ecotypes with evidence of bidirectional cross-feeding on costly resources and frequency-dependent fitness. Although unidirectional cross-feeding has been repeatedly observed to evolve in laboratory culture, most investigations of bidirectional cooperative behaviors in microbial populations have been conducted in engineered communities. This work demonstrates the evolution of black queen relationships in a microbial population originating from a single ancestor, providing a model for investigation of the eco-evolutionary processes leading to mutualistic cooperation.

Citing Articles

Evolution of pH-sensitive transcription termination in during adaptation to repeated long-term starvation.

Worthan S, McCarthy R, Delaleau M, Stikeleather R, Bratton B, Boudvillain M Proc Natl Acad Sci U S A. 2024; 121(39):e2405546121.

PMID: 39298488 PMC: 11441560. DOI: 10.1073/pnas.2405546121.


Genome and transcriptomic analysis of the adaptation of to environmental stresses.

Jiao J, Lv X, Shen C, Morigen M Comput Struct Biotechnol J. 2024; 23():2132-2140.

PMID: 38817967 PMC: 11137339. DOI: 10.1016/j.csbj.2024.05.033.


Evolution of pH-sensitive transcription termination during adaptation to repeated long-term starvation.

Worthan S, McCarthy R, Delaleau M, Stikeleather R, Bratton B, Boudvillain M bioRxiv. 2024; .

PMID: 38464051 PMC: 10925284. DOI: 10.1101/2024.03.01.582989.


Trade-offs, trade-ups, and high mutational parallelism underlie microbial adaptation during extreme cycles of feast and famine.

Behringer M, Ho W, Miller S, Worthan S, Cen Z, Stikeleather R Curr Biol. 2024; 34(7):1403-1413.e5.

PMID: 38460514 PMC: 11066936. DOI: 10.1016/j.cub.2024.02.040.


Bacterial adenine cross-feeding stems from a purine salvage bottleneck.

Chuang Y, Haas N, Pepin R, Behringer M, Oda Y, LaSarre B ISME J. 2024; 18(1).

PMID: 38452196 PMC: 10976475. DOI: 10.1093/ismejo/wrae034.


References
1.
Morris J, Lenski R, Zinser E . The Black Queen Hypothesis: evolution of dependencies through adaptive gene loss. mBio. 2012; 3(2). PMC: 3315703. DOI: 10.1128/mBio.00036-12. View

2.
Mitri S, Clarke E, Foster K . Resource limitation drives spatial organization in microbial groups. ISME J. 2015; 10(6):1471-82. PMC: 5029182. DOI: 10.1038/ismej.2015.208. View

3.
Harcombe W . Novel cooperation experimentally evolved between species. Evolution. 2010; 64(7):2166-72. DOI: 10.1111/j.1558-5646.2010.00959.x. View

4.
Mao E, Lane L, Lee J, Miller J . Proliferation of mutators in A cell population. J Bacteriol. 1997; 179(2):417-22. PMC: 178711. DOI: 10.1128/jb.179.2.417-422.1997. View

5.
Deatherage D, Barrick J . Identification of mutations in laboratory-evolved microbes from next-generation sequencing data using breseq. Methods Mol Biol. 2014; 1151:165-88. PMC: 4239701. DOI: 10.1007/978-1-4939-0554-6_12. View