# Genomic and functional dissection of natural transformation-related genes in Piscirickettsia salmonis

## TL;DR

This study explores how natural transformation-related genes in Piscirickettsia salmonis affect its survival and infection, revealing their roles vary by gene and strain.

## Contribution

The paper introduces a versatile genetic platform for functional studies in P. salmonis, enabling deeper understanding of its biology.

## Key findings

- CRISPRi repression of comL/bamD showed its essentiality in one strain and critical role during infection in another.
- Repression of comM and comFB reduced cytopathogenicity and delayed damage in P. salmonis strains.
- Heterologous expression of comEC impaired viability, suggesting a fitness burden in P. salmonis.

## Abstract

Piscirickettsia salmonis, the etiological agent of piscirickettsiosis, represents the main health challenge for Chilean salmon farming and an emerging threat to global salmonid production. Inspection of all P. salmonis genomes available shows that the comEC gene, encoding the DNA uptake channel required for natural transformation (NT) in competent bacteria, is interrupted by various transposable elements, whereas other NT determinants (comEA, comFB, comM, comL/bamD, and dprA) remain intact and highly conserved. Using P. salmonis Psal-103 (EM-genogroup) and Psal-104b (LF-genogroup) as representatives of the two most prevalent genogroups in Chile, we combined comparative genomics, gene expression analysis, heterologous expression of comEC using homologs from naturally competent bacteria, and CRISPRi-mediated knockdown of the remaining NT-related genes to examine their functionality. According to our results, expression of comEC with homologs from Legionella pneumophila and Vibrio cholerae impaired P. salmonis viability in axenic culture, indicating a fitness burden. CRISPRi-mediated repression of comL/bamD revealed its essentiality in Psal-104b and a critical role during infection of the SHK-1 cell line in Psal-103. Repression of comM tended to reduce cytopathogenicity in both strains, while repression of comFB was associated with a modest delay in cytopathic damage in Psal-104b. Repression of recA and comEA caused moderate reductions in cytopathic activity in Psal-103. By contrast, dprA showed no detectable phenotypes. Together, our results indicate that despite the irreversible interruption of comEC, P. salmonis has retained NT-related genes that contribute to fitness in a gene- and genogroup-specific manner, providing a framework to investigate how determinants of horizontal gene transfer function beyond DNA uptake.

Despite its major impact on salmon aquaculture, Piscirickettsia salmonis remains poorly characterized at the functional level, largely due to long-standing limitations in genetic tractability. Here, we implement and combine multiple genetic approaches, including CRISPR interference, site-specific chromosomal integration, and heterologous gene expression, to functionally interrogate natural transformation (NT)-related genes in this pathogen. Using representative strains from the two most prevalent Chilean genogroups, we show that conserved NT-associated genes contribute to bacterial physiology and infection in a genogroup-dependent manner. Moreover, and beyond the specific biological findings, this work establishes a versatile genetic platform for functional studies in P. salmonis, expanding the experimental toolbox available to study this pathogen and supporting future efforts aimed at understanding its biology and the development of novel biotechnological approaches.