Differential Profiles of Gut Microbiota and Metabolites Associated with Host Shift of Plutella xylostella

Int J Mol Sci. 2020 Aug 30;21(17):6283. doi: 10.3390/ijms21176283.

Abstract

Evolutionary and ecological forces are important factors that shape gut microbial profiles in hosts, which can help insects adapt to different environments through modulating their metabolites. However, little is known about how gut microbes and metabolites are altered when lepidopteran pest species switch hosts. In the present study, using 16S-rDNA sequencing and mass spectrometry-based metabolomics, we analyzed the gut microbiota and metabolites of three populations of Plutella xylostella: one feeding on radish (PxR) and two feeding on peas (PxP; with PxP-1 and PxP-17 being the first and 17th generations after host shift from radish to peas, respectively). We found that the diversity of gut microbes in PxP-17 was significantly lower than those in PxR and PxP-1, which indicates a distinct change in gut microbiota after host shift. Kyoto Encyclopedia of Genes and Genomes analysis revealed that the functions of energy metabolism, signal transduction, and xenobiotics biodegradation and metabolism were increased in PxP-17, suggesting their potential roles in host adaptation. Metabolic profiling showed a significant difference in the abundance of gut metabolites between PxR and PxP-17, and significant correlations of gut bacteria with gut metabolites. These findings shed light on the interaction among plants, herbivores, and symbionts, and advance our understanding of host adaptation associated with gut bacteria and metabolic activities in P. xylostella.

Keywords: diamondback moth; host expansion; insect–microbe interaction; insect–plant interaction; inter-omic; metabolome.

MeSH terms

  • Animals
  • Bacteria / classification*
  • Bacteria / metabolism
  • Gastrointestinal Microbiome*
  • Gastrointestinal Tract / metabolism*
  • Gastrointestinal Tract / microbiology
  • Host-Pathogen Interactions*
  • Larva / metabolism*
  • Larva / microbiology
  • Metabolome*
  • Moths
  • Phylogeny
  • Raphanus / microbiology*