» Articles » PMID: 26052318

Antagonistic Interactions Are Sufficient to Explain Self-assemblage of Bacterial Communities in a Homogeneous Environment: a Computational Modeling Approach

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2015 Jun 9
PMID 26052318
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Most of the studies in Ecology have been devoted to analyzing the effects the environment has on individuals, populations, and communities, thus neglecting the effects of biotic interactions on the system dynamics. In the present work we study the structure of bacterial communities in the oligotrophic shallow water system of Churince, Cuatro Cienegas, Mexico. Since the physicochemical conditions of this water system are homogeneous and quite stable in time, it is an excellent candidate to study how biotic factors influence the structure of bacterial communities. In a previous study, the binary antagonistic interactions of 78 bacterial strains, isolated from Churince, were experimentally determined. We employ these data to develop a computer algorithm to simulate growth experiments in a cellular grid representing the pond. Remarkably, in our model, the dynamics of all the simulated bacterial populations is determined solely by antagonistic interactions. Our results indicate that all bacterial strains (even those that are antagonized by many other bacteria) survive in the long term, and that the underlying mechanism is the formation of bacterial community patches. Patches corresponding to less antagonistic and highly susceptible strains are consistently isolated from the highly-antagonistic bacterial colonies by patches of neutral strains. These results concur with the observed features of the bacterial community structure previously reported. Finally, we study how our findings depend on factors like initial population size, differential population growth rates, homogeneous population death rates, and enhanced bacterial diffusion.

Citing Articles

Higher-order interactions and emergent properties of microbial communities: The power of synthetic ecology.

Gallardo-Navarro O, Aguilar-Salinas B, Rocha J, Olmedo-Alvarez G Heliyon. 2024; 10(14):e33896.

PMID: 39130413 PMC: 11315108. DOI: 10.1016/j.heliyon.2024.e33896.


A three-species synthetic community model whose rapid response to antagonism allows the study of higher-order dynamics and emergent properties in minutes.

Aguilar-Salinas B, Olmedo-Alvarez G Front Microbiol. 2023; 14:1057883.

PMID: 37333661 PMC: 10272403. DOI: 10.3389/fmicb.2023.1057883.


Extracellular DNAses Facilitate Antagonism and Coexistence in Bacterial Competitor-Sensing Interference Competition.

Ogawa A, Gole C, Bermudez M, Habarugira O, Joslin G, McCain T Appl Environ Microbiol. 2022; 88(23):e0143722.

PMID: 36374088 PMC: 9746292. DOI: 10.1128/aem.01437-22.


Experimental Analysis of Interactions Among Saprotrophic Fungi from A Phosphorous-Poor Desert Oasis in the Chihuahuan Desert.

Marini-Macouzet C, Munoz L, Gonzalez-Rubio A, Eguiarte L, Souza V, Velez P Mycobiology. 2020; 48(5):410-417.

PMID: 33177920 PMC: 7580559. DOI: 10.1080/12298093.2020.1788271.


Three-Way Interactions in an Artificial Community of Bacterial Strains Directly Isolated From the Environment and Their Effect on the System Population Dynamics.

Gallardo-Navarro O, Santillan M Front Microbiol. 2019; 10:2555.

PMID: 31798544 PMC: 6865335. DOI: 10.3389/fmicb.2019.02555.


References
1.
Sole R, Montoya J . Complexity and fragility in ecological networks. Proc Biol Sci. 2001; 268(1480):2039-45. PMC: 1088846. DOI: 10.1098/rspb.2001.1767. View

2.
Escalante A, Eguiarte L, Espinosa-Asuar L, Forney L, Noguez A, Souza Saldivar V . Diversity of aquatic prokaryotic communities in the Cuatro Cienegas basin. FEMS Microbiol Ecol. 2008; 65(1):50-60. DOI: 10.1111/j.1574-6941.2008.00496.x. View

3.
Aguirre-von-Wobeser E, Soberon-Chavez G, Eguiarte L, Ponce-Soto G, Vazquez-Rosas-Landa M, Souza V . Two-role model of an interaction network of free-living γ-proteobacteria from an oligotrophic environment. Environ Microbiol. 2013; 16(5):1366-77. DOI: 10.1111/1462-2920.12305. View

4.
Kerr B, Riley M, Feldman M, Bohannan B . Local dispersal promotes biodiversity in a real-life game of rock-paper-scissors. Nature. 2002; 418(6894):171-4. DOI: 10.1038/nature00823. View

5.
Servais P, Billen G, Rego J . Rate of bacterial mortality in aquatic environments. Appl Environ Microbiol. 1985; 49(6):1448-54. PMC: 241745. DOI: 10.1128/aem.49.6.1448-1454.1985. View