Misfolded proteins serve as 'inherited memory' of toxic insults

 28-Aug-2018

The E. coli bacterium was used to test the effects of protein aggregates as a protection against toxic stresses.

https://youtu.be/dNdQhxd0Eoc

Protein aggregates have a bad reputation in conditions such as Alzheimer's disease and Parkinson's disease, but in bacteria, inheritance of aggregates by daughter cells may help protect against the same toxic stresses that triggered them in parental cells, according to a new study publishing 28 August in the open access journal PLOS Biology, by Sander Govers, Abram Aertsen, and colleagues at KU Leuven, Belgium. The aggregates thus serve as a kind of inherited memory, protecting offspring against the challenges experienced by their ancestors.

Protein misfolding is a risk for any cell, and is especially common when the cell is exposed to heat, oxidative stress, or other insults. Misfolded proteins that are not immediately disposed of often clump together to form long-lived aggregates. Such aggregates are seen in neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease, where they are thought to contribute to the neurodegenerative process. Aggregates also form in bacteria such as Escherichia coli, found in the gut, and have been thought to be damaging to these cells as well. But some evidence suggests aggregates may also play a protective role, at least in eukaryotic cells, leading the authors to ask whether they might confer some benefit in prokaryotic cells. 

To test this, they induced aggregates in E. coli by exposing the cells to heat, antibiotics, or peroxide. When a given bacterial cell subsequently divided, the aggregate it contained was segregated into only one of the two daughter cells. After multiple generations, cells were again exposed to aggregate-inducing stressors. Those sibling cells containing inherited aggregates displayed improved survival and faster recovery than those without them. The same survival benefit could be induced by expression of an inert aggregation-prone protein, suggesting it was the presence of an aggregate, rather than its composition, that improved survival. The authors found that cells with aggregates inherited more of the proteins that protect against stresses, even before exposure to those stresses, which they suggest accounts for the increase in survival.

"Our findings indicate the potential of protein aggregates to improve cellular robustness, in contrast to the prevailing view that they are inevitably detrimental to cellular health," said Aertsen. "Moreover, because protein aggregates can persist and be inherited for many generations as a functional physical relic of an ancestral insult, they can serve as long-term epigenetic memory in prokaryotes."

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Peer-reviewed / Experimental Study / Cells

In your coverage please use this URL to provide access to the freely available article in PLOS Biology:  http://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.2003853

Citation: Govers SK, Mortier J, Adam A, Aertsen A (2018) Protein aggregates encode epigenetic memory of stressful encounters in individual Escherichia coli cells. PLoS Biol 16(8): e2003853. https://doi.org/10.1371/journal.pbio.2003853

Image Caption: The E. coli bacterium was used to test the effects of protein aggregates as a protection against toxic stresses.

Image Credit: NIAID, Flickr, CC-BY.

Funding: Flemish Agency for Innovation by Science and Technology (IWT-Vlaanderen). Doctoral fellowship received by SKG. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Research Foundation - Flanders (FWO-Vlaanderen). Doctoral fellowship received by JM. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Research Foundation - Flanders (FWO-Vlaanderen) (grant number G058011N). Project grant. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. KU Leuven Research Fund (grant number IDO/10/012; DBOF/12/035; DBOF/14/049). Project grants. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

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https://www.eurekalert.org/pub_releases/2018-08/p-mps082318.php