Bacteriophages: The 'good viruses' that fight bacteria | Health - Hindustan Times

Bacteriophages: The 'good viruses' that fight bacteria

By | Posted by Krishna Priya Pallavi, Delhi
Jul 20, 2023 11:16 AM IST

With antibiotic resistance rising, scientists think bacteriophages — which hunt and kill bacteria — could cure bacterial infections.

For such tiny agents, viruses have taken a huge toll on humanity. Outbreaks of viral diseases, such as smallpox, influenza, HIV, and COVID-19 have killed billions and fundamentally shaped societies throughout human history. But not all viruses are killers. As with bacteria, "good" or "friendly" viruses can also be beneficial for health. Scientists now talk of a virome — all the different types of viruses we host in our bodies which contribute to health, much like the bacterial microbiome.

Bacteriophages are antibacterial viruses that could help fight antibacterial resistant forms of infectious diseases. (DW/Ake Puttisarn/Zoonar/picture alliance)
Bacteriophages are antibacterial viruses that could help fight antibacterial resistant forms of infectious diseases. (DW/Ake Puttisarn/Zoonar/picture alliance)

This virome is huge. You have 380 trillion virus particles living (or existing) in or on your body right now — 10 times more than the number of bacteria. These viruses lurk in our lungs and blood, live on our skin and linger inside the microbes in our guts.

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They're not all bad, however: There are viruses that kill cancer cells and help break down tumors, others that train our immune system and help them fight pathogens, and even some that control gene expression in pregnancy.

Bacteriophages: Anti-bacterial guard dogs

The vast majority of viruses inside us are bacteriophages — viruses that kill bacteria in our microbiomes. Bacteriophages, also known as phages, are harmless to human cells as they do not recognize them as their bacterial prey.

They work by hunting down bacteria and attaching themselves to the surface of a bacterial cell, before injecting viral DNA material into the cell.

The viral DNA then replicates inside the bacteria, sometimes by borrowing the DNA replication hardware of the bacteria. (Also Read | Post traumatic stress disorder: How Yoga and physiotherapy can help in PTSD)

Once enough new viruses have been created inside the bacterial cell, the cell then bursts to release the new viral particles.

All this takes just 30 minutes, meaning one virus can become many in a couple of hours.

Phage therapy: A short history

The ability of phages to take down bacteria had scientists pondering whether they could be used to treat bacterial infections in the early 20th century, but when antibiotics like penicillin came along, that research faded away.

But antibiotic-resistant strains of bacteria are now on the rise, with experts saying antibiotic resistance is one of the greatest medical challenges facing global communities.

As a result, scientists are racing to find new forms of antibiotic agents, putting phages back on the menu as agents to fight bacterial infections.

"The advantages of phages lie in their effectiveness against every multi-resistant pathogen," said Mathias Pletz, Director of the Institute for Infectious Medicine and Hospital Hygiene at Jena University Hospital.

Pletz added that phages are extremely precise in their elimination of bacterial strains — so much so that you don't disturb the gut microbiome, as is the case with antibiotics.

In theory, then, phages could be a huge boon in our fight against antibacterial resistance. But what does the evidence really say?

Phages were a Soviet medicine

Phages didn't fade out of use everywhere. Due to the scarcity of antibiotics in Soviet-era Russia, phages were used to treat bacterial infections, and their use has continued in countries like Georgia, Ukraine and Russia for decades.

Georgia is a hot spot for phage tourism, with patients from all over the world going there to be treated with phages. It's from these clinics that some scientists say we have good evidence that phages can work against infections that are resistant to conventional antibacterial agents.

Georgia has developed into one of the global centers of phage therapy, hosting one of the largest therapeutic collections of bacteriophages in the world.

But countries like Belgium and the US are beginning to use phages for exceptional cases in specialized therapy centers as well.

Germany is beginning to take an interest in phage therapies, too. A research report published on July 18 urged policymakers to ensure phages are better explored and used, not just for human medicine but also for foodborne infections and crop protection.

Is there a place for phages in medicine?

Could phages be the answer to the problems of antibacterial resistance? Perhaps, say experts. But they also caution that there are disadvantages to phage therapies that need to be addressed before they are approved for widespread use.

"A central problem is that there is no standardization of therapy. Phage therapy must be precisely tailored to the bacteria that cause an infection in a patient," said Gerd Fätkenheuer, an infectious disease expert at University Hospital Cologne, Germany.

Fätkenheuer said infections can be caused by bacteria with various properties, so you need a cocktail of different phages as a therapy, and that mix of phages has to be available very quickly before the infection gets out of hand.

And bacteria do also develop resistance to phage therapies.

But phage therapies have good safety records. Pletz said humans ingest billions of phages every day with our food without any relevant side effects. That means our bodies should be able to tolerate phage therapies very well.

The German research report recommends the next steps should include large-scale research and clinical projects to nail down effective phage therapies for different types of infections.

For now, bacteriophages are unlikely to replace antibiotics. But scientists are optimistic they could be used in combination to make antibiotics more effective, especially against resistant strains of bacteria.

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