Archaea joins the battle! Finding a new way to fight bacteria

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Photo by Michael Schiffer on Unsplash
Photo by Michael Schiffer on Unsplash

A class of micro-organisms generally neglected by research could provide new ways to fight bacteria as antibiotic resistance grows, according to international research. Archaea are one of the three domains of life alongside bacteria and eukaryotes (animals and plants). Many species of archaea live among bacteria, and the researchers predicted that they must have ways of fighting those bacteria to survive. They studied the genomes of over 3700 archaea species, looking for proteins that can impact a specific molecule that helps protect bacteria. The researchers say 5% of the archaea species had those proteins, which were able to kill bacteria in the lab. They say it's early days, but it's likely archaea have many untapped strategies to kill bacteria that could one day be harnessed for antibacterials.

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From: PLOS

Archaea can kill bacteria with new antibacterials

A first look into the molecular defenses of archaea highlights the importance of surveying diverse microbes to discover new types of antimicrobials

As bacteria become increasingly resistant to antibiotics and other antibacterials, there is a growing need for alternatives. In a study published on August 14th in the open-access journal PLOS Biology, Tobias Warnecke and colleagues from the University of Oxford and the MRC Laboratory of Medical Sciences, United Kingdom, identified untapped antimicrobials produced by archaea, single-celled organisms that make up one of the three domains of life (the other two being bacteria and eukaryotes, the group that includes us).

Microbes are in constant competition for space and resources and have developed various chemical weapons to fend off other microbial species. All of our antibiotics originally came from these defense systems, though historically, researchers have only investigated the arsenals of bacteria and fungi. There are over 20,000 species of archaea, and these cells often live surrounded by even more numerous bacterial species. The researchers predicted that to survive, the archaeal cells must have ways to compete with the bacteria, representing an unexplored trove of antimicrobials.

The researchers surveyed the genomes of over 3,700 species of archaea, looking for genes encoding proteins that could possibly be wielded against bacteria. They focused specifically on proteins that can cut the molecule peptidoglycan, an essential part of the cell walls of bacteria. The large majority of archaea don’t have peptidoglycan, so these proteins would only be necessary for microbial warfare.

These proteins were present among 5% of the archaeal species surveyed, with some species having multiple types. In the lab, the researchers tested the efficacy of some of the proteins and found that they successfully killed bacteria. They also studied the proteins’ structures, which indicated many were deployed outside of the cell, and some archaea even had components for an injection system that might directly deliver the deadly proteins to competing bacteria.

Much still remains to be discovered on how these molecular weapons may be used in the wild. The peptidoglycan-cutting proteins also represent only one type of antibacterial among many others that may be present among diverse species of archaea.

Warnecke notes, “Archaea are their own Domain of Life, different from bacteria, and different from eukaryotes (humans, plants, flies, etc.). We know very little about their social lives, including how they interact with their ubiquitous brethren - bacteria.”

Warnecke adds, “Our work sheds new light on the social lives or archaea and has implications for how we understand microbial communities. It also suggests that archaea might be a large, untapped reservoir for discovering novel antimicrobials in the future.”

Romain Strock, first author, adds, “Archaea are often depicted as either lone extremophiles or syntrophic partners. Our research depicts another, darker side to their social life.”

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PLOS Biology
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Organisation/s: Medical Research Council Laboratory of Medical Sciences, UK
Funder: This work was funded by core funding from the Medical Research Council (https:// www.ukri.org/councils/mrc/, grant number: MC-A658-5TY40) to TW. VWCS is supported by an MRC CDA (MR/X007421/1) and AH by a Wellcome Trust CDA (227755/Z/23/Z). The funders played no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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