Abstract

Metabolic cross-feeding plays vital roles in promoting ecological diversity. While some microbes depend on exchanges of essential nutrients for growth, the forces driving the extensive cross-feeding needed to support the coexistence of free-living microbes are poorly understood. Here we characterize bacterial physiology under self-acidification and establish that extensive excretion of key metabolites following growth arrest provides a collaborative, inter-species mechanism of stress resistance. This collaboration occurs not only between species isolated from the same community, but also between unrelated species with complementary (glycolytic vs. gluconeogenic) modes of metabolism. Cultures of such communities progress through distinct phases of growth-dilution cycles, comprising of exponential growth, acidification-triggered growth arrest, collaborative deacidification, and growth recovery, with each phase involving different combinations of physiological states of individual species. Our findings challenge the steady-state view of ecosystems commonly portrayed in ecological models, offering an alternative dynamical view based on growth advantages of complementary species in different phases.

Microbes can cooperate and share resources via metabolic cross-feeding. Here, the authors show that excretion of key metabolites following acid stress provides a collaborative, inter-species mechanism of stress resistance.

Details

Title
Stress-induced metabolic exchanges between complementary bacterial types underly a dynamic mechanism of inter-species stress resistance
Author
Amarnath, Kapil 1   VIAFID ORCID Logo  ; Narla, Avaneesh V. 1 ; Pontrelli, Sammy 2   VIAFID ORCID Logo  ; Dong, Jiajia 3   VIAFID ORCID Logo  ; Reddan, Jack 4   VIAFID ORCID Logo  ; Taylor, Brian R. 1   VIAFID ORCID Logo  ; Caglar, Tolga 1 ; Schwartzman, Julia 5   VIAFID ORCID Logo  ; Sauer, Uwe 2   VIAFID ORCID Logo  ; Cordero, Otto X. 5   VIAFID ORCID Logo  ; Hwa, Terence 6   VIAFID ORCID Logo 

 U.C. San Diego, Department of Physics, La Jolla, USA (GRID:grid.516081.b) (ISNI:0000 0000 9217 9714) 
 ETH Zürich, Institute of Molecular and Systems Biology, Zürich, Switzerland (GRID:grid.5801.c) (ISNI:0000 0001 2156 2780) 
 U.C. San Diego, Department of Physics, La Jolla, USA (GRID:grid.516081.b) (ISNI:0000 0000 9217 9714); Bucknell University, Department of Physics and Astronomy, Lewisburg, USA (GRID:grid.253363.2) (ISNI:0000 0001 2297 9828) 
 U.C. San Diego, Division of Biological Sciences, La Jolla, USA (GRID:grid.516081.b) (ISNI:0000 0000 9217 9714) 
 MIT, Department of Civil and Environmental Engineering, Cambridge, USA (GRID:grid.116068.8) (ISNI:0000 0001 2341 2786) 
 U.C. San Diego, Department of Physics, La Jolla, USA (GRID:grid.516081.b) (ISNI:0000 0000 9217 9714); U.C. San Diego, Division of Biological Sciences, La Jolla, USA (GRID:grid.516081.b) (ISNI:0000 0000 9217 9714) 
Pages
3165
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2821255689
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.