4.7 Article

Identification of essential genes involved in metabolism-based resistance mechanism to fenoxaprop-P-ethyl in Polypogon fugax

Journal

PEST MANAGEMENT SCIENCE
Volume 78, Issue 3, Pages 1164-1175

Publisher

JOHN WILEY & SONS LTD
DOI: 10.1002/ps.6733

Keywords

acetyl-CoA carboxylase (ACCase); grass weed; metabolic resistance; isoform-sequencing (Iso-Seq); RNA-sequencing (RNA-Seq); real-time quantitative PCR (RT-qPCR)

Funding

  1. National Natural Science Foundation of China [32102237]
  2. Anhui Provincial Natural Science Foundation [2108085QC115]
  3. Talent Research Project of Anhui Agricultural University [rc342004]

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The study confirmed the metabolic resistance of fenoxaprop-P-ethyl in the Asia minor bluegrass population AHHY. Transcriptomic analysis identified 28 detoxifying enzyme genes that were consistently up-regulated in resistant plants, including P450s, glutathione-S-transferase, UDP-glucosyltransferase, and ATP-binding cassette transporters. The enhanced rates of herbicide metabolism in P. fugax were likely driven by these herbicide metabolism-related genes, providing valuable gene resources for understanding resistance mechanisms in this weed species.
BACKGROUND Metabolic resistance is a worldwide concern for weed control but has not yet been well-characterized at the genetic level. Previously, we have identified an Asia minor bluegrass (Polypogon fugax Nees ex Steud.) population AHHY exhibiting cytochrome P450 (P450)-involved metabolic resistance to fenoxaprop-P-ethyl. In this study, we aimed to confirm the metabolic fenoxaprop-P-ethyl resistance in AHHY and uncover the potential herbicide metabolism-related genes in this economically damaging weed species. RESULTS Liquid chromatography-tandem mass spectrometry (LC-MS/MS) assays indicated the metabolic rates of fenoxaprop-P-ethyl were significantly faster in resistant (R, AHHY) than in susceptible (S, SDTS) plants. The amount of phytotoxic fenoxaprop-P peaked at 12 h after herbicide treatment (HAT) and started to decrease at 24 HAT in both biotypes. R and S plants at 24 HAT were sampled to conduct isoform-sequencing (Iso-Seq) and RNA-sequencing (RNA-Seq). A reference transcriptome containing 24 972 full-length isoforms was obtained, of which 24 329 unigenes were successfully annotated. Transcriptomic profiling identified 28 detoxifying enzyme genes constitutively and/or herbicide-induced up-regulated in R than in S plants. Real-time quantitative polymerase chain reaction (RT-qPCR) confirmed 17 genes were consistently up-regulated in R and its F1 generation plants. They were selected as potential fenoxaprop-P-ethyl metabolism-related genes, including ten P450s, one glutathione-S-transferase, one UDP-glucosyltransferase, and five adenosine triphosphate (ATP)-binding cassette transporters. CONCLUSION This study revealed that the enhanced rates of fenoxaprop-P-ethyl metabolism in P. fugax were very likely driven by the herbicide metabolism-related genes. The transcriptome data generated by Iso-Seq combined with RNA-Seq will provide abundant gene resources for understanding the molecular mechanisms of resistance in P. fugax.

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