Understanding how microbes adapt to a novel environment is essential to our understanding of how microbes respond during acute infection or long-term disease. Specifically, the genetic architecture underlying the constraints on producing and maintaining molecular variation within bacterial genomes directly influences the population's potential for adaptation and eventual evolutionary fate. Upon colonization, competition for resources within populations drives adaptation, which can result in cooperation, innovation, or interference among individuals within the population. Previous studies have shown that microbial subpopulation structure can be established as a potential adaptive outcome in heterogeneous environments, but have yet to investigate the long-term stability of this structure and the genetic framework that allows subpopulation structure to be maintained. To bridge this gap of knowledge I propose to: (i) conduct genetic and environmental manipulations of Escherichia coli K-12 MG1655 in order to determine the importance of biofilm formation for establishment of subpopulation structure, (ii) isolate individual clones from E. coli populations experiencing different degrees of starvation to identify how nutrient limitation affects the stability of subpopulation structure, and (iii) analyze spent media from these clones to define the different nutrient utilization strategies within and among populations. In addition to the populations created for the specific purpose of this study, sampling will also occur from 320 long-term E. coli populations which will have been maintained up to 6 years and over 17,000 generations at the conclusion of this fellowship, generating a well of opportunity for future research questions through which I aspire to establish a career as an independent investigator.

Public Health Relevance

Understanding how genetic variation is introduced and maintained in microbial populations is important not only for studies of evolutionary biology, but also for the treatment and control of human disease. When cultured in a heterogeneous environment, such as the environment inside a human host, bacteria are observed to evolve complex subpopulation structure resulting in niche and habitat specificity. By determining potential sources for the underlying genetic support of subpopulation structure, novel treatment strategies can be developed for the management of chronic and acute bacterial infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM123703-03
Application #
9561900
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Hoodbhoy, Tanya
Project Start
2017-08-28
Project End
2019-08-27
Budget Start
2018-08-28
Budget End
2019-08-27
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Arizona State University-Tempe Campus
Department
Type
Organized Research Units
DUNS #
943360412
City
Tempe
State
AZ
Country
United States
Zip Code
85287
Behringer, Megan G; Choi, Brian I; Miller, Samuel F et al. (2018) Escherichia coli cultures maintain stable subpopulation structure during long-term evolution. Proc Natl Acad Sci U S A 115:E4642-E4650
McCully, Alexandra L; Behringer, Megan G; Gliessman, Jennifer R et al. (2018) An Escherichia coli Nitrogen Starvation Response Is Important for Mutualistic Coexistence with Rhodopseudomonas palustris. Appl Environ Microbiol 84: