# Proteomic analyses of the regulatory mechanisms underlying Pochonia chlamydosporia infection in Parascaris equorum eggs

## TL;DR

This study explores how the fungus Pochonia chlamydosporia infects nematode eggs using proteomic analysis to understand its biological processes and potential for biocontrol.

## Contribution

The study reveals novel insights into the proteomic changes and regulatory mechanisms during P. chlamydosporia infection of nematode eggs.

## Key findings

- 4,293 differentially expressed proteins were identified, involved in energy metabolism, protein synthesis, and oxidative stress.
- Early infection involves enhanced metabolism and antioxidant capacity, while later stages focus on metabolic fine-tuning and DNA replication.
- Transporter-related proteins suggest roles in host recognition and invasion.

## Abstract

Pochonia chlamydosporia is an important egg-parasitic fungus with potential applications in the biological control of parasitic pests. However, the protein-response mechanisms during P. chlamydosporia infection of nematode eggs remain unclear. In this study, we employed four-dimensional data-independent acquisition (4D-DIA) proteomic sequencing to analyze the changes in the mycelial proteome of P. chlamydosporia at different infection stages.

In total, 4,293 differentially expressed proteins (DEPs) were identified, which were mainly involved in energy metabolism, protein synthesis and modification, oxidative stress, and other key biological processes. In the early stages of infestation, the fungus rapidly adapted to the host environment by enhancing metabolism and protein synthesis, initiating the infestation mechanism, and simultaneously enhancing its antioxidant capacity to cope with the host defense response. At later stages, it fine-tuned the metabolic pathways and enhanced DNA replication to maintain proliferation and continuously strengthened the antioxidant response to host oxidative stress. In addition, the number of proteins related to fungal transporter activity varied significantly after induction, indicating that a variety of transmembrane proteins may be involved in host recognition, adhesion, and formation of invasive structures.

This study provides critical insights into the molecular mechanisms underlying P. chlamydosporia parasitic activity and establishes a theoretical foundation for the development of novel biocontrol strategies for this fungus.