Identification of novel prophage regions in Xenorhabdus nematophila genome and gene expression analysis during phage-like particle induction

PeerJ. 2022 Feb 15:10:e12956. doi: 10.7717/peerj.12956. eCollection 2022.

Abstract

Background: Entomopathogenic Xenorhabdus bacteria are endosymbionts of Steinernema nematodes and together they form an insecticidal mutualistic association that infects a wide range of insect species. Xenorhabdus produce an arsenal of toxins and secondary metabolites that kill the insect host. In addition, they can induce the production of diverse phage particles. A few studies have focused on one integrated phage responsible for producing a phage tail-like bacteriocin, associated with an antimicrobial activity against other Xenorhabdus species. However, very little is known about the diversity of prophage regions in Xenorhabdus species.

Methods: In the present study, we identified several prophage regions in the genome of Xenorhabdus nematophila AN6/1. We performed a preliminary study on the relative expression of genes in these prophage regions. We also investigated some genes (not contained in prophage region) known to be involved in SOS bacterial response (recA and lexA) associated with mitomycin C and UV exposure.

Results: We described two integrated prophage regions (designated Xnp3 and Xnp4) not previously described in the genome of Xenorhabdus nematophila AN6/1. The Xnp3 prophage region appears very similar to complete Mu-like bacteriophage. These prophages regions are not unique to X. nematophila species, although they appear less conserved among Xenorhabdus species when compared to the previously described p1 prophage region. Our results showed that mitomycin C exposure induced an up-regulation of recA and lexA suggesting activation of SOS response. In addition, mitomycin C and UV exposure seems to lead to up-regulation of genes in three of the four integrated prophages regions.

Keywords: Diversity; Gene expression; Induction; Mitomycin; Phage-like particle; Prophages; UV; Xenorhabdus nematophila.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteriophages* / genetics
  • Gene Expression Profiling
  • Insecta / genetics
  • Mitomycin / pharmacology
  • Prophages / genetics
  • Xenorhabdus* / genetics

Substances

  • Mitomycin

Grants and funding

This work was supported with start-up funds provided by the College of Agriculture and Life Sciences, University of Arizona to SPS. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.