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No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures

To survive within complex environmental niches, including the human host, bacteria have evolved intricate interspecies communities driven by competition for limited nutrients, cooperation via complementary metabolic proficiencies, and establishment of homeostatic relationships with the host immune s...

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Detalles Bibliográficos
Autores principales: Jalali, Fatemeh, Ellett, Felix, Balani, Pooja, Duncan, Margaret J., Dewhirst, Floyd E., Borisy, Gary G., Irimia, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882712/
https://www.ncbi.nlm.nih.gov/pubmed/33544453
http://dx.doi.org/10.1002/mbo3.1137
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author Jalali, Fatemeh
Ellett, Felix
Balani, Pooja
Duncan, Margaret J.
Dewhirst, Floyd E.
Borisy, Gary G.
Irimia, Daniel
author_facet Jalali, Fatemeh
Ellett, Felix
Balani, Pooja
Duncan, Margaret J.
Dewhirst, Floyd E.
Borisy, Gary G.
Irimia, Daniel
author_sort Jalali, Fatemeh
collection PubMed
description To survive within complex environmental niches, including the human host, bacteria have evolved intricate interspecies communities driven by competition for limited nutrients, cooperation via complementary metabolic proficiencies, and establishment of homeostatic relationships with the host immune system. The study of such complex, interdependent relationships is often hampered by the challenges of culturing many bacterial strains in research settings and the limited set of tools available for studying the dynamic behavior of multiple bacterial species at the microscale. Here, we utilize a microfluidic‐based co‐culture system and time‐lapse imaging to characterize dynamic interactions between Streptococcus species, Staphylococcus aureus, and Actinomyces species. Co‐culture of Streptococcus cristatus or S. salivarius in nanoliter compartments with Actinomyces graevenitzii revealed localized exclusion of Streptococcus and Staphylococcus from media immediately surrounding A. graevenitzii microcolonies. This community structure did not occur with S. mitis or S. oralis strains or in co‐cultures containing other Actinomycetaceae species such as S. odontolyticus or A. naeslundii. Moreover, fewer neutrophils were attracted to compartments containing both A. graevenitzii and Staphylococcus aureus than to an equal number of either species alone, suggesting a possible survival benefit together during immune responses.
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spelling pubmed-78827122021-02-19 No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures Jalali, Fatemeh Ellett, Felix Balani, Pooja Duncan, Margaret J. Dewhirst, Floyd E. Borisy, Gary G. Irimia, Daniel Microbiologyopen Original Articles To survive within complex environmental niches, including the human host, bacteria have evolved intricate interspecies communities driven by competition for limited nutrients, cooperation via complementary metabolic proficiencies, and establishment of homeostatic relationships with the host immune system. The study of such complex, interdependent relationships is often hampered by the challenges of culturing many bacterial strains in research settings and the limited set of tools available for studying the dynamic behavior of multiple bacterial species at the microscale. Here, we utilize a microfluidic‐based co‐culture system and time‐lapse imaging to characterize dynamic interactions between Streptococcus species, Staphylococcus aureus, and Actinomyces species. Co‐culture of Streptococcus cristatus or S. salivarius in nanoliter compartments with Actinomyces graevenitzii revealed localized exclusion of Streptococcus and Staphylococcus from media immediately surrounding A. graevenitzii microcolonies. This community structure did not occur with S. mitis or S. oralis strains or in co‐cultures containing other Actinomycetaceae species such as S. odontolyticus or A. naeslundii. Moreover, fewer neutrophils were attracted to compartments containing both A. graevenitzii and Staphylococcus aureus than to an equal number of either species alone, suggesting a possible survival benefit together during immune responses. John Wiley and Sons Inc. 2021-02-05 /pmc/articles/PMC7882712/ /pubmed/33544453 http://dx.doi.org/10.1002/mbo3.1137 Text en © 2020 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Jalali, Fatemeh
Ellett, Felix
Balani, Pooja
Duncan, Margaret J.
Dewhirst, Floyd E.
Borisy, Gary G.
Irimia, Daniel
No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title_full No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title_fullStr No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title_full_unstemmed No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title_short No man's land: Species‐specific formation of exclusion zones bordering Actinomyces graevenitzii microcolonies in nanoliter cultures
title_sort no man's land: species‐specific formation of exclusion zones bordering actinomyces graevenitzii microcolonies in nanoliter cultures
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882712/
https://www.ncbi.nlm.nih.gov/pubmed/33544453
http://dx.doi.org/10.1002/mbo3.1137
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