It was previously thought that only mutations in a fungi’s DNA would result in antifungal drug resistance. Current diagnostic techniques rely on sequencing all of a fungi’s DNA to find such mutations.
Drug resistance
Scientists from the University of Edinburgh have discovered that fungi can develop drug resistance without changes to their DNA – their genetic code.
The new research, published in Nature, finds that resistance can emerge in fungi without genetic changes. Instead the fungi exhibit epigenetic changes – alterations that do not affect their DNA – suggesting that many causes and cases of antifungal resistance could have been previously missed.
Fungal diseases
Each year fungal diseases affect billions of people globally, causing an estimated 1.6 million deaths.
Infections resistant to treatment are a growing problem, particularly in patients with weakened immune systems such as those with HIV. Few effective antifungal drugs exist.
Overuse of agricultural fungicides is also leading to increasing resistance in soil borne fungi. Fungal disease results in the loss of up to a third of the world’s food crops annually.
Caffeine treatment
A team of scientists from the University of Edinburgh’s Wellcome Centre for Cell Biology studied the emergence of resistance in a yeast, Schizosaccharomyces pombe, by treating it with caffeine to mimic the activity of antifungal drugs.
The team discovered that the resulting resistant yeast had alterations in special chemical tags that affect how their DNA is organized. Some genes became packed into structures known as heterochromatin, which silences or inactivates underlying genes, causing resistance as a result of this epigenetic change.
New treatments
This discovery could pave the way for new therapies to treat resistant infections by modifying existing epigenetic drugs or developing new drugs that interfere with fungal heterochromatin.
Improved fungicides to treat food crops could limit agricultural losses and also reduce the number of resistant fungal strains in the environment that continue to fuel increased infections in humans.