Scientists from Skoltech and research centers in Sweden and Switzerland presented results that help better understand the mechanism of interaction between bacteria and phages — viruses that infect bacterial cells. The discovery can be an important step on the way to develop new ways for fighting infections. The study is published in the Cell Reports journal.
Disease-causing microorganisms become more resistant to antibiotics. Researchers across the world keep searching for new mechanisms to combat pathogenic bacteria — one of them is phage therapy. Bacteriophages are natural “predators” and enemies of bacteria with a high infection specificity. They are harmless to the human organism, have a natural origin, and can be found wherever there is life and bacteria. Phages had been studied more than 100 years ago, but when antibiotics were discovered, the research interest declined.
“Our laboratory at Skoltech pursues research into the new systems of bacterial immunity. In recent years, bioinformatics has allowed predictions of a plethora of novel antivirus systems and a new field emerged — microbial immunology. Molecular mechanisms for most of those systems have not been uncovered yet, so one of the ways to learn how microbial immunity works is to find out how viruses managed to overcome the defense. The interaction between viruses and bacteria can be described as an arms race: when bacteria acquire a new defense strategy, it exerts great pressure on the opposing side — phages. In turn, phages that somehow acquire resistance to the bacterial immunity should emerge. It initiates a new stage of bacterial adaptation, and such intense competition leads to a wide variety of antiviral systems,” says Head of the Laboratory of Metagenome Analysis and a study co-author Artem Isaev.
Image 1. Laboratory experiments. Credit: Aleksandr Andriianov, a PhD student at Skoltech and the leading author of the study
The authors studied the BREX (short for BacteRiophage EXclusion) immunity system, a protective mechanism of bacteria against phages, and showed that bacteriophage T3 can infect the BREX culture only when the special enzyme is expressed — the SAM lyase, which destroys S-adenosyl-methionine, an important cell metabolite.
“SAM is used as a donor of methyl groups, which can regulate the expression of genes. In the case of the BREX system, a methyl group also serves as a label, which allows bacteria to distinguish between their own DNA and the non-methylated DNA of the virus. Unexpectedly, the methylation function of BREX was not severely affected, while the BREX protection was completely disrupted by the SAMase expression. We can assume that SAM is also a cofactor necessary for inhibition of the virus infection by the BREX system,” clarifies Artem Isaev.
Image 2. Structure of the T3 SAMase-E. coli synthase. Credit: Artem Isaev
According to the researchers, many countries are developing bacteriophage banks and support projects allowing the use of phages for therapeutic purposes. Modification of virus particles might allow the construction of modular bacteriophages effective against a specific pathogenic microorganism detected in the body of a particular patient.
“We still do not know much about the repertoire of anti-defense proteins encoded by phages, while these proteins are largely responsible for the success of bacterial cells’ infection in the natural environment, considering a huge variety of immune systems present in bacteria (including pathogenic species). Our research contributes to the establishment of the interaction network between viral anti-defense proteins and bacterial immunity systems. It has to be considered at the next stage of the phage therapy development when we will approach the creation of phages capable of killing specific pathogenic bacteria,” adds Artem Isaev.
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