Transcriptomics identifies key defense mechanisms in rice resistant to both leaf-feeding and phloem feeding herbivores

Author:

Li Yi,Cheah Boon Huat,Fang Yu-Fu,Kuang Yun-Hung,Lin Shau-Ching,Liao Chung-Ta,Huang Shou-Horng,Lin Ya-Fen,Chuang Wen-Po

Abstract

Abstract Background Outbreaks of insect pests in paddy fields cause heavy losses in global rice yield annually, a threat projected to be aggravated by ongoing climate warming. Although significant progress has been made in the screening and cloning of insect resistance genes in rice germplasm and their introgression into modern cultivars, improved rice resistance is only effective against either chewing or phloem-feeding insects. Results In this study, the results from standard and modified seedbox screening, settlement preference and honeydew excretion tests consistently showed that Qingliu, a previously known leaffolder-resistant rice variety, is also moderately resistant to brown planthopper (BPH). High-throughput RNA sequencing showed a higher number of differentially expressed genes (DEGs) at the infestation site, with 2720 DEGs in leaves vs 181 DEGs in sheaths for leaffolder herbivory and 450 DEGs in sheaths vs 212 DEGs in leaves for BPH infestation. The leaf-specific transcriptome revealed that Qingliu responds to leaffolder feeding by activating jasmonic acid biosynthesis genes and genes regulating the shikimate and phenylpropanoid pathways that are essential for the biosynthesis of salicylic acid, melatonin, flavonoids and lignin defensive compounds. The sheath-specific transcriptome revealed that Qingliu responds to BPH infestation by inducing salicylic acid-responsive genes and those controlling cellular signaling cascades. Taken together these genes could play a role in triggering defense mechanisms such as cell wall modifications and cuticular wax formation. Conclusions This study highlighted the key defensive responses of a rarely observed rice variety Qingliu that has resistance to attacks by two different feeding guilds of herbivores. The leaffolders are leaf-feeder while the BPHs are phloem feeders, consequently Qingliu is considered to have dual resistance. Although the defense responses of Qingliu to both insect pest types appear largely dissimilar, the phenylpropanoid pathway (or more specifically phenylalanine ammonia-lyase genes) could be a convergent upstream pathway. However, this possibility requires further studies. This information is valuable for breeding programs aiming to generate broad spectrum insect resistance in rice cultivars.

Publisher

Springer Science and Business Media LLC

Subject

Plant Science

Reference95 articles.

1. Datta A, Ullah H, Ferdous Z. Water management in rice. In: Chauhan BS, Jabran K, Mahajan G, editors. Rice production worldwide. Switzerland: Springer; 2017. p. 255–78. https://doi.org/10.1007/978-3-319-47516-5_11.

2. Hedge S, Hedge V. Assessment of global rice production and export opportunity for economic development in Ethiopia. Int J Sci Res. 2013;2(6):257–60.

3. Ali MP, Bari MN, Haque SS, Kabir MMM, Afrin S, Nowrin F, et al. Establishing next-generation pest control services in rice fields: eco-agriculture. Sci Rep. 2019;9(1):10180. https://doi.org/10.1038/s41598-019-46688-6.

4. Pathak MD, Khan ZR. Insect pests of rice. Philippines: International Rice Research Institute; 1994.

5. Heong KL, Wong L, Reyes JHD. Addressing planthopper threats to Asian rice farming and food security: fixing insecticide misuse. Philippines: Asian Development Bank; 2013.

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