Mutation drives bacterial adaptation to immune response

A team of Roslin Institute scientists have uncovered a genetic mutation that helps a common bacteria affecting humans and animals to survive against immune defences and antibiotics

Researchers have developed a model to study how Staphylococcus aureus, a major pathogen associated with human and animal diseases, adapts to antibiotics and immune responses.

The research team designed a framework to repeatedly expose different strains of bacteria to immune cells, known as macrophages, which resulted in changes in bacterial characteristics over time.

The study identified mutations in the bacteria that enhanced several survival traits, such as growth within immune cells and resisting common antibiotics.

However, this advantage was conditional and was lost when the bacteria were grown in nutrient-rich conditions outside the macrophage environment.

Using this experimental model in future research could enable scientists to better understand interactions between bacterial pathogens and immune cells, the team says.

Physical adaptation

The physical change, or phenotype, that promoted bacterial survival within immune cells was identified to be a new type of small colony variant (SCV).

These variants are associated with a transition to a more persistent and less virulent form of the pathogen, often linked with chronic infections such as osteomyelitis and lung infections in cystic fibrosis patients.

This new SCV adaptation also caused the bacteria to become more resilient against antibiotics such as vancomycin.

New interventions

The proposed model to repeatedly expose grow bacteria with macrophages can shed light on the conditional nature of bacterial adaptation to specific niches.

Furthermore, understanding bacterial adaptation to evade the immune system could provide insights into potential treatment strategies for infectious diseases in humans and animals.

This research was published in mBio in article entitled "Experimental evolution of Staphylococcus aureus in macrophages: dissection of a conditional adaptive trait promoting intracellular survival". It was carried out in collaboration with colleagues in the Florey Institute and The University of Sheffield. The work was supported by funding to Professor Ross Fitzgerald from Wellcome Trust, the Medical Research Council, and the BBSRC.

 

 

Our study uncovers a novel adaptation strategy by S. aureus in response to immune challenges, highlighting the remarkable ingenuity of pathogens in evading host defences. Our findings demonstrate the power of experimental models to unravel the complex mechanisms underlying bacterial adaptation during infection

We've identified this novel fitness trait that highlights the potential of our model for identifying adaptive traits that emerge during infection. Understanding the key interactions between bacteria and the immune system can pave the way to new interventions and treatments for infections