# Antifungal Activity of Surfactin Against Cytospora chrysosperma

## TL;DR

This study shows how surfactin, a compound from Bacillus, inhibits the growth of the tree-infecting fungus Cytospora chrysosperma by disrupting its energy production and cell structure.

## Contribution

The study reveals that surfactin targets the tricarboxylic acid cycle in C. chrysosperma, a novel mechanism for its antifungal activity.

## Key findings

- Surfactin significantly inhibits C. chrysosperma with a half-maximal effective concentration of 0.787 mg/mL.
- Surfactin disrupts hyphal morphology and causes reactive oxygen species accumulation in C. chrysosperma.
- Transcriptome analysis shows surfactin interferes with the tricarboxylic acid cycle by binding to citrate synthase.

## Abstract

Cytospora chrysosperma is a common opportunistically parasitic fungus that mainly infects forest trees, severely restricting the development of the fruit and forest industry. Surfactin is a secondary metabolite produced by Bacillus species and exhibits antifungal activity; Although the core antifungal mechanism of surfactin against plant pathogens has been extensively studied, our study found that surfactin can target the tricarboxylic acid cycle of C. chrysosperma. This study aimed to investigate the potential mechanism underlying the inhibitory effect of surfactin on C. chrysosperma. The results showed that surfactin had a significant inhibitory effect on C. chrysosperma, with a half-maximal effective concentration of 0.787 ± 0.045 mg/mL and a minimum inhibitory concentration of 2 mg/mL. Morphological observations revealed that surfactin significantly disrupted the morphology and ultrastructure of C. chrysosperma hyphae. FDA/PI staining indicated that surfactin affected the cell membrane integrity of C. chrysosperma, while DCFH-DA fluorescent staining and antioxidant enzyme activity assays demonstrated the accumulation of reactive oxygen species in hyphal cells following surfactin treatment. Additionally, the reduction in adenosine triphosphate content, as well as the decreased activities of ATPase and succinate dehydrogenase, suggested that energy production might be inhibited. Finally, MDC staining showed the occurrence of autophagosomes in C. chrysosperma hyphae after surfactin treatment, which may lead to hyphal death. Transcriptome analysis revealed that surfactin impaired the normal biosynthesis of the C. chrysosperma cell membrane and interfered with the tricarboxylic acid cycle by binding to citrate synthase, resulting in intracellular energy metabolism disorders. This study provides new insights into the potential mechanism by which surfactin inhibits hyphal growth of C. chrysosperma.