Study reveals ‘bug wars’ that take place in cystic fibrosis

by eLife

Scientists have revealed how common respiratory bugs that cause serious infections in people with cystic fibrosis interact together, according to a new study in eLife.

The results provide insights into how bacterial pathogens wrestle each other for territory that could open avenues for new antibacterial treatments.

Studies of microbes from mouths, intestines, chronic wounds and chronic respiratory infections show that interactions between bacteria in these communities influence survival of the bugs and progression of disease. For example, infection with two bacterial species called Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa) in the airways of cystic fibrosis patients is linked to decreased lung function and a shorter lifespan.

“One strategy to improve outcomes for people with cystic fibrosis carrying multiple infections is to block harmful interspecies interactions before they begin,” explains lead author Dominique Limoli, Assistant Professor of Microbiology and Immunology at the University of Iowa, US. “We designed a system to visualise the early interactions between two microbes that cause infections in people with cystic fibrosis to follow their behaviour over time.”

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Limoli and her team used a co-culture system to grow both microbes together and then studied them using time-lapse microscopy to create videos of the bacteria’s movements. They found that, on their own, P. aeruginosa cells multiply and form groups that appear like ‘rafts’ under a microscope. By contrast, when grown along with S. aureus, the P. aeruginosa cells move as single cells and accelerate their movement in the direction of the S. aureus colony. Studying the cells in more detail revealed that once the single P. aeruginosa cells reach the S. aureus cells, they enter the colony and dismantle it.

The researchers proposed that P. aeruginosa behaves in this way because S. aureus produces substances into the environment that trigger the change in movement of P. aeruginosa. To prove this, they took the liquid that S. aureus had been growing in and placed it in the bottom of a petri dish, before using it to grow P. aeruginosa. In this environment, P. aeruginosa was much more mobile—moving across a greater surface area than on the normal petri dish.

When grown along with S. aureus bacteria, P. aeruginosa cells move as single cells and increase their movements significantly. Credit: Limoli et al. (CC BY 4.0)
So, does this hold true for other types of bacteria? Of three pathogens commonly found in patients with cystic fibrosis, the team found one that enhanced the movement of P. aeruginosa. However, when they looked at a broader group of bacteria, including Salmonella, Escherichia coli and Bacillus subtilis, they found a significant increase in the movement of P. aeruginosa in the presence of these communities.

“By acquiring a fundamental understanding of how bacteria sense and respond to life with each other, we move closer to learning how to rationally manipulate these behaviors during infection and in the environment,” says Limoli. “For cystic fibrosis patients, this may mean preventing P. aeruginosa and S. aureus physical interactions. In other instances, we might bring together bacterial species that synergise to produce a beneficial compound.”

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