A University of Maine study researching polymicrobial infections found that Pseudomonas aeruginosa actually teams up with the antifungal Fluconazole to fight Candida albicans infections.
Polymicrobial infections—diseases caused by a combination of bacteria, viruses, fungi and parasites—are challenging to treat because scientists don’t fully understand how pathogens interact during infection and how these interactions impact the drugs used to treat them, UMaine researchers say.
In their study published in the journal Infection and Immunity, researchers looked at two pathogens that often occur at similar sites, particularly in cystic fibrosis and mechanically ventilated patients: Candida albicans and Pseudomonas aeruginosa.
Candida albicans is the fourth most common hospital-acquired pathogen, and is particularly difficult to treat. It is targeted by a number of antifungal agents, but some only slow it rather than kill it outright. Meanwhile, P. aeruginosa infects 90% of all adult cystic fibrosis patients. Combined, Candida albicans and P. aeruginosa cause more serious disease in cystic fibrosis and ventilated patients.
The researchers investigated the effectiveness of an antifungal drug, fluconazole, in the test tube and during infection of the zebrafish with both pathogens. Fluconazole is known to slow fungal growth, but Candida albicans can become tolerant to the drug and not only survive, but also develop tolerance that leads to failed therapy and, potentially, death.
What the study found was promising. The results showed that P. aeruginosa works with fluconazole to eliminate drug tolerance and clear the Candida albicans infection in the culture and the zebrafish.
“Polymicrobial infections are challenging to treat not only because of the lack of understanding of how invading microorganisms interact but also because we don’t know how these interactions affect treatment efficacy. Our work demonstrates that polymicrobial interactions can indeed affect treatment efficacy and, most importantly, it highlights the importance of nutrient availability in the environment—such as iron in our study—and how it modulates treatment efficacy,” says Siham Hattab, lead author of the study who conducted the research as part of her PhD in the Department of Molecular and Biomolecular Sciences.
What’s more, the bacteria also enhance the drug’s ability against a second pathogenic Candida species that tends to be more resistant to the drug.
The increased effectiveness of the drug suggests to the researchers that there is still much more to learn about how current drugs work when targeting these dangerous and complex polymicrobial infections.
“We are really excited to have revealed that sometimes drugs against fungal infection can work even better in a more ‘real-world’ situation than in the test tube. There is still a lot to learn about how pathogens interact during infection, and it will be interesting to see how the bacteria manage to work with the drugs to target Candida albicans,” says Robert Wheeler, associate professor of microbiology and senior author of the study.