Cargando…

Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership

The mechanisms by which microbes interact in communities remain poorly understood. Here, we interrogated specific interactions between photoautotrophic and heterotrophic members of a model consortium to infer mechanisms that mediate metabolic coupling and acclimation to partnership. This binary cons...

Descripción completa

Detalles Bibliográficos
Autores principales: Bernstein, Hans C., McClure, Ryan S., Thiel, Vera, Sadler, Natalie C., Kim, Young-Mo, Chrisler, William B., Hill, Eric A., Bryant, Donald A., Romine, Margaret F., Jansson, Janet K., Fredrickson, Jim K., Beliaev, Alexander S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340862/
https://www.ncbi.nlm.nih.gov/pubmed/28289730
http://dx.doi.org/10.1128/mSystems.00181-16
_version_ 1782512885577023488
author Bernstein, Hans C.
McClure, Ryan S.
Thiel, Vera
Sadler, Natalie C.
Kim, Young-Mo
Chrisler, William B.
Hill, Eric A.
Bryant, Donald A.
Romine, Margaret F.
Jansson, Janet K.
Fredrickson, Jim K.
Beliaev, Alexander S.
author_facet Bernstein, Hans C.
McClure, Ryan S.
Thiel, Vera
Sadler, Natalie C.
Kim, Young-Mo
Chrisler, William B.
Hill, Eric A.
Bryant, Donald A.
Romine, Margaret F.
Jansson, Janet K.
Fredrickson, Jim K.
Beliaev, Alexander S.
author_sort Bernstein, Hans C.
collection PubMed
description The mechanisms by which microbes interact in communities remain poorly understood. Here, we interrogated specific interactions between photoautotrophic and heterotrophic members of a model consortium to infer mechanisms that mediate metabolic coupling and acclimation to partnership. This binary consortium was composed of a cyanobacterium, Thermosynechococcus elongatus BP-1, which supported growth of an obligate aerobic heterotroph, Meiothermus ruber strain A, by providing organic carbon, O(2), and reduced nitrogen. Species-resolved transcriptomic analyses were used in combination with growth and photosynthesis kinetics to infer interactions and the environmental context under which they occur. We found that the efficiency of biomass production and resistance to stress induced by high levels of dissolved O(2) increased, beyond axenic performance, as a result of heterotrophic partnership. Coordinated transcriptional responses transcending both species were observed and used to infer specific interactions resulting from the synthesis and exchange of resources. The cyanobacterium responded to heterotrophic partnership by altering expression of core genes involved with photosynthesis, carbon uptake/fixation, vitamin synthesis, and scavenging of reactive oxygen species (ROS). IMPORTANCE This study elucidates how a cyanobacterial primary producer acclimates to heterotrophic partnership by modulating the expression levels of key metabolic genes. Heterotrophic bacteria can indirectly regulate the physiology of the photoautotrophic primary producers, resulting in physiological changes identified here, such as increased intracellular ROS. Some of the interactions inferred from this model system represent putative principles of metabolic coupling in phototrophic-heterotrophic partnerships.
format Online
Article
Text
id pubmed-5340862
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-53408622017-03-13 Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership Bernstein, Hans C. McClure, Ryan S. Thiel, Vera Sadler, Natalie C. Kim, Young-Mo Chrisler, William B. Hill, Eric A. Bryant, Donald A. Romine, Margaret F. Jansson, Janet K. Fredrickson, Jim K. Beliaev, Alexander S. mSystems Research Article The mechanisms by which microbes interact in communities remain poorly understood. Here, we interrogated specific interactions between photoautotrophic and heterotrophic members of a model consortium to infer mechanisms that mediate metabolic coupling and acclimation to partnership. This binary consortium was composed of a cyanobacterium, Thermosynechococcus elongatus BP-1, which supported growth of an obligate aerobic heterotroph, Meiothermus ruber strain A, by providing organic carbon, O(2), and reduced nitrogen. Species-resolved transcriptomic analyses were used in combination with growth and photosynthesis kinetics to infer interactions and the environmental context under which they occur. We found that the efficiency of biomass production and resistance to stress induced by high levels of dissolved O(2) increased, beyond axenic performance, as a result of heterotrophic partnership. Coordinated transcriptional responses transcending both species were observed and used to infer specific interactions resulting from the synthesis and exchange of resources. The cyanobacterium responded to heterotrophic partnership by altering expression of core genes involved with photosynthesis, carbon uptake/fixation, vitamin synthesis, and scavenging of reactive oxygen species (ROS). IMPORTANCE This study elucidates how a cyanobacterial primary producer acclimates to heterotrophic partnership by modulating the expression levels of key metabolic genes. Heterotrophic bacteria can indirectly regulate the physiology of the photoautotrophic primary producers, resulting in physiological changes identified here, such as increased intracellular ROS. Some of the interactions inferred from this model system represent putative principles of metabolic coupling in phototrophic-heterotrophic partnerships. American Society for Microbiology 2017-03-07 /pmc/articles/PMC5340862/ /pubmed/28289730 http://dx.doi.org/10.1128/mSystems.00181-16 Text en Copyright © 2017 Bernstein et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Bernstein, Hans C.
McClure, Ryan S.
Thiel, Vera
Sadler, Natalie C.
Kim, Young-Mo
Chrisler, William B.
Hill, Eric A.
Bryant, Donald A.
Romine, Margaret F.
Jansson, Janet K.
Fredrickson, Jim K.
Beliaev, Alexander S.
Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title_full Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title_fullStr Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title_full_unstemmed Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title_short Indirect Interspecies Regulation: Transcriptional and Physiological Responses of a Cyanobacterium to Heterotrophic Partnership
title_sort indirect interspecies regulation: transcriptional and physiological responses of a cyanobacterium to heterotrophic partnership
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340862/
https://www.ncbi.nlm.nih.gov/pubmed/28289730
http://dx.doi.org/10.1128/mSystems.00181-16
work_keys_str_mv AT bernsteinhansc indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT mcclureryans indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT thielvera indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT sadlernataliec indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT kimyoungmo indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT chrislerwilliamb indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT hillerica indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT bryantdonalda indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT rominemargaretf indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT janssonjanetk indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT fredricksonjimk indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership
AT beliaevalexanders indirectinterspeciesregulationtranscriptionalandphysiologicalresponsesofacyanobacteriumtoheterotrophicpartnership