GENERAL COMMENTARY article

Front. Microbiol., 11 April 2017

Sec. Evolutionary and Genomic Microbiology

Volume 8 - 2017 | https://doi.org/10.3389/fmicb.2017.00620

Commentary: A bacterial global regulator forms a prion

  • Faculty of Veterinary Medicine, University of Teramo Teramo, Italy

The recently reported identification, within the transcription terminator Rho of Clostridium botulinum (Cb-Rho), of a prion-like domain functionally similar to that of a yeast prion-forming protein, along with the amyloidogenicity conferred by it on Cb-Rho, represent findings of extraordinary scientific relevance (Yuan and Hochschild, 2017). In this respect, another recent study has shown that lactic acid, a common bacterial metabolite, is a powerful inducer in yeast cells of [GAR+], a prion-like genetic element allowing the simultaneous metabolism of glucose and other carbon sources (Garcia et al., 2016). Still noteworthy, while synthetic mammalian prions were successfully generated in Escherichia coli bacteria (Legname et al., 2004, 2005), the amyloid-ß peptide—a protein crucially involved in Alzheimer's disease pathogenesis—has been recently reported to bind and trap bacterial pathogens inside the brain, thereby behaving like a natural antibiotic (Kumar et al., 2016). Furthermore, the normal host's cellular prion protein (PrPC) has been also shown to play a pivotal role in Brucella abortus infection of murine macrophages, with no evidence of bacterial colonization nor replication in cells from PrPC-deficient mice (Aguzzi and Hardt, 2003; Watarai et al., 2003).

Although no doubts seem to exist that, based upon the results of the elegant work (Yuan and Hochschild, 2017) which is being addressed by the present commentary, Cb-Rho acts like a prion-like element of inheritance in bacteria, I do not feel entirely confident about the Authors' conclusion, “suggesting that the emergence of prions predates the evolutionary split between eukaryotes and bacteria” (Yuan and Hochschild, 2017). As a matter of fact, although this would appear to be absolutely plausible from a biological standpoint, prior evidence of similar, or related prion-like domains in Rho or Rho-like proteins from other Clostridium genus members should be obtained to justify the Authors' statement. In this respect, Clostridium (C.) baratii, C. butyricum, and C. tetani, which are phylogenetically related to C. botulinum (Collins and East, 1998), could represent valuable “first choices” for “comparative” investigations of this kind. Finally, the prion-driven, putative evolutionary links between bacterial and eukaryotic cells could gain additional insights from the study of mitochondria, ubiquitous cytoplasmic organelles derived from an alphaproteobacterial endosymbiont, which were acquired in the course of eukaryogenesis (Poole and Gribaldo, 2014).

Statements

Author contributions

After having carefully read the recent Science article by Drs. Yuan and Hochschild, upon which this manuscript is commenting, the Author (GD) has autonomously and independently written the present Commentary.

Conflict of interest

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

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    AguzziA.HardtW.-D. (2003). Dangerous liaisons between a microbe and the prion protein. J. Exp. Med.198, 14. 10.1084/jem.20030732

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    CollinsM. D.EastA. K. (1998). Phylogeny and taxonomy of the food-borne pathogen Clostridium botulinum and its neurotoxins. J. Appl. Microbiol.84, 517. 10.1046/j.1365-2672.1997.00313.x

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    GarciaD. M.DietrichD.ClardyJ.JaroszD. F. (2016). A common bacterial metabolite elicits prion-based bypass of glucose repression. Elife5:e17978. 10.7554/eLife.17978

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    KumarD. K.ChoiS. H.WashicoskyK. J.EimerW. A.TuckerS.GhofraniJ.et al. (2016). Amyloid-β peptide protects against microbial infection in mouse and worm models of Alzheimer's disease. Sci. Transl. Med.8:340ra72. 10.1126/scitranslmed.aaf1059

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    LegnameG.BaskakovI. V.NguyenH. O.RiesnerD.CohenF. E.DeArmondS. J.et al. (2004). Synthetic mammalian prions. Science305, 673676. 10.1126/science.1100195

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    LegnameG.NguyenH. O.BaskakovI. V.CohenF. E.DearmondS. J.PrusinerS. B. (2005). Strain-specified characteristics of mouse synthetic prions. Proc. Natl. Acad. Sci. U.S.A.102, 21682173. 10.1073/pnas.0409079102

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    PooleA. M.GribaldoS. (2014). Eukaryotic origins: How and when was the mitochondrion acquired?Cold Spring Harb. Perspect. Biol.6:a015990. 10.1101/cshperspect.a015990

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    WataraiM.KimS.ErdenebaatarJ.MakinoS.HoriuchiM.ShirahataT.et al. (2003). Cellular prion protein promotes Brucella infection into macrophages. J. Exp. Med.198, 517. 10.1084/jem.20021980

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    YuanA. H.HochschildA. (2017). A bacterial global regulator forms a prion. Science355, 198201. 10.1126/science.aai7776

Summary

Keywords

Clostridium botulinum, prions, amyloid, bacterial inheritance, bacteria, yeasts, prokaryotes, eukaryotes

Citation

Di Guardo G (2017) Commentary: A bacterial global regulator forms a prion. Front. Microbiol. 8:620. doi: 10.3389/fmicb.2017.00620

Received

22 January 2017

Accepted

27 March 2017

Published

11 April 2017

Volume

8 - 2017

Edited by

Frank T. Robb, University of Maryland, Baltimore, USA

Reviewed by

Santosh Kumar C. M., National Centre for Cell Science, India

Updates

Copyright

*Correspondence: Giovanni Di Guardo

This article was submitted to Evolutionary and Genomic Microbiology, a section of the journal Frontiers in Microbiology

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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