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Benefit from decline: The primary transcriptome of Alteromonas macleodii str. Te101 during Trichodesmium demise

  • Shengwei Hou
  • , Mario López-Pérez
  • , Ulrike Pfreundt
  • , Natalia Belkin
  • , Kurt Stüber
  • , Bruno Huettel
  • , Richard Reinhardt
  • , Ilana Berman-Frank
  • , Francisco Rodriguez-Valera
  • , Wolfgang R. Hess
  • University of Freiburg
  • Miguel Hernández University
  • Swiss Federal Institute of Technology Zurich
  • Max Planck-Genome-Centre Cologne

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

Interactions between co-existing microorganisms deeply affect the physiology of the involved organisms and, ultimately, the function of the ecosystem as a whole. Copiotrophic Alteromonas are marine gammaproteobacteria that thrive during the late stages of phytoplankton blooms in the marine environment and in laboratory co-cultures with cyanobacteria such as Trichodesmium. The response of this heterotroph to the sometimes rapid and transient changes in nutrient supply when the phototroph crashes is not well understood. Here, we isolated and sequenced the strain Alteromonas macleodii str. Te101 from a laboratory culture of Trichodesmium erythraeum IMS101, yielding a chromosome of 4.63 Mb and a single plasmid of 237 kb. Increasing salinities to ≥43 ppt inhibited the growth of Trichodesmium but stimulated growth of the associated Alteromonas. We characterized the transcriptomic responses of both microorganisms and identified the complement of active transcriptional start sites in Alteromonas at single-nucleotide resolution. In replicate cultures, a similar set of genes became activated in Alteromonas when growth rates of Trichodesmium declined and mortality was high. The parallel activation of fliA, rpoS and of flagellar assembly and growth-related genes indicated that Alteromonas might have increased cell motility, growth, and multiple biosynthetic activities. Genes with the highest expression in the data set were three small RNAs (Aln1a-c) that were identified as analogs of the small RNAs CsrB-C in E. coli or RsmX-Z in pathogenic bacteria. Together with the carbon storage protein A (CsrA) homolog Te101-05290, these RNAs likely control the expression of numerous genes in responding to changes in the environment.

Original languageEnglish
Pages (from-to)981-996
Number of pages16
JournalISME Journal
Volume12
Issue number4
DOIs
StatePublished - 1 Apr 2018

Bibliographical note

Publisher Copyright:
© 2017 International Society for Microbial Ecology.

Funding

Acknowledgements This work was supported by the EU project MaCuMBA (grant agreement no. 311975) to WRH and FRV and by the German Israeli Foundation grant no. 1133 to IB-F and WRH. Support of ML-P by a postdoctoral fellowship from the Valencian Consellería de Educació, Investigació, Cultura i Esport (APOSTD/2016/051) and of SH by the China Scholarship Council is gratefully acknowledged. We thank Viktoria Reimann for expert technical assistance and Dr. Rahul Kulkarni for sharing the source code of CSRA_TARGET. The authors are grateful for the constructive comments and suggestions from three anonymous reviewers.

FundersFunder number
German Israeli Foundation1133
Valencian Consellería de EducacióAPOSTD/2016/051
European Commission311975
China Scholarship Council

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 14 - Life Below Water
      SDG 14 Life Below Water

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