Limited effect of planting transgenic rice on the soil microbiome studied by continuous 13CO2 labeling combined with high-throughput sequencing

Appl Microbiol Biotechnol. 2019 May;103(10):4217-4227. doi: 10.1007/s00253-019-09751-w. Epub 2019 Mar 25.

Abstract

The planting of transgenic rice has aroused ongoing controversy, due to the public anxiety surrounding the potential risk of transgenic rice to health and the environment. The soil microbial community plays an important environmental role in the plant-soil-microbe system; however, few studies have focused on the effect of transgenic rice on the soil rhizospheric microbiome. We labeled transgenic gene rice (TT51, transformed with Cry1Ab/1Ac gene), able to produce the Bt (Bacillus thuringiensis) toxin, its parental variety (Minghui 63), and a non-parental variety (9931) with 13CO2. The DNA of the associated soil rhizospheric microbes was extracted, subjected to density gradient centrifugation, followed by high-throughput sequencing of bacterial 16S rRNA gene. Unweighted unifrac analysis of the sequencing showed that transgenic rice did not significantly change the soil bacterial community structure compared with its parental variety. The order Opitutales, affiliated to phylum Verrucomicrobia and order Sphingobacteriales, was the main group of labeled bacteria in soil planted with the transgenic and parental varieties, while the orders Pedosphaerales, Chthoniobacteraceae, also affiliated to Verrucomicrobia, and the genus Geobacter, affiliated to class Deltaproteobacteria, dominated in the soil of the non-parental rice variety. The non-significant difference in soil bacterial community structure of labeled microbes between the transgenic and parental varieties, but the comparatively large difference with the non-parental variety, suggests a limited effect of planting transgenic Bt rice on the soil microbiome.

Keywords: Continuous labeling; DNA-SIP; High-throughput sequencing; Transgenic rice.

MeSH terms

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins / metabolism*
  • Carbon Dioxide / metabolism
  • Carbon Isotopes / metabolism
  • Cluster Analysis
  • DNA, Bacterial / chemistry
  • DNA, Bacterial / genetics
  • DNA, Ribosomal / chemistry
  • DNA, Ribosomal / genetics
  • Endotoxins / metabolism*
  • Hemolysin Proteins / metabolism*
  • High-Throughput Nucleotide Sequencing
  • Isotope Labeling
  • Microbiota*
  • Oryza / growth & development*
  • Phylogeny
  • Plants, Genetically Modified / growth & development*
  • RNA, Ribosomal, 16S / genetics
  • Rhizosphere*
  • Sequence Analysis, DNA
  • Soil Microbiology*

Substances

  • Bacillus thuringiensis Toxins
  • Bacterial Proteins
  • Carbon Isotopes
  • DNA, Bacterial
  • DNA, Ribosomal
  • Endotoxins
  • Hemolysin Proteins
  • RNA, Ribosomal, 16S
  • insecticidal crystal protein, Bacillus Thuringiensis
  • Carbon Dioxide