4.6 Article

Improved phenotyping procedure for evaluating resistance in rice against gall midge (Orseolia oryzae, Wood-Mason)

Journal

PLANT METHODS
Volume 17, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13007-021-00823-5

Keywords

Rice gall midge (RGM); Chewing insect; High-throughput phenotyping method (HTPM); Gene mapping

Funding

  1. Guangxi Natural Science Foundation [2020GXNSFDA297008]
  2. Central Government Guiding Local Scientific and Technological Development Foundation [ZY21195040]
  3. Guangxi Key Laboratory of Biology for Crop Diseases and Insect Pests [2020-KF-02]
  4. Science and Technology Development Fund of Guangxi Academy of Agricultural Sciences [2015JZ57]

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This study developed and improved a highly efficient and reliable procedure for evaluating rice resistance to the rice gall midge (RGM), which was verified through mutant screening, gene mapping, genetic analysis, and insect growth and development observations. It provided a high-throughput phenotyping method for assessing 60 lines/varieties infested with 36 female RGM adults in one tray, along with successfully detecting an RGM resistance gene and offering adequate samples for further studies.
Background The rice gall midge (RGM, Orseolia oryzae, Wood-Mason), an important stem-feeding pest worldwide, has caused serious production losses over the past decades. Rice production practices indicate that the most reliable method for managing RGM is the deployment of cultivars that incorporate host resistance. However, the conventional phenotypic screening method of rice resistance to RGM suggested by the International Rice Research Institute (IRRI) has been used for approximately 30 years, and only 12 rice varieties/lines (including controls) can be evaluated in one tray. It is not suitable for high-throughput phenotyping of rice germplasm. Moreover, a suitable method to prepare samples for molecular biological studies of rice resistance against RGM is imperative with the rapid development of modern molecular techniques. Results The proper density of seedlings/RGM was determined for four seeding arrangements. A high-throughput phenotyping method (HTPM) for 60 lines/varieties infested with 36 female RGM adults in one tray, as described by method 4-3 (seeded 60 lines/varieties), was developed and verified using mutant screening. Furthermore, one RGM resistance gene flanked by markers 12RM28346 and 12RM28739 on chromosome 12 was simultaneously detected using method 2-2 (seeded 30 lines/varieties in one tray) treated with 24 RGM and analyzed using conventional and simplified grading systems. Genetic analysis of the RGM resistance gene was confirmed using a method identical to that suggested by IRRI. Finally, one bucket with 24 seedlings treated with at least five female RGM adults was efficacious and could offer adequate samples for insect development observation or molecular biological studies. Conclusion A highly efficient and reliable procedure for evaluation of resistance in rice to RGM was developed and improved, and was verified through mutant screening, gene mapping, genetic analysis, and insect growth and development observations.

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