HighlightAssessing gall numbers in 331 cultivars of a rice diversity panel has identified two resistant landraces, 11 quantitative trait loci and good candidate genes for resistance to Meloidogyne graminicola.

Summary Strigolactones (SLs) are carotenoid‐derived plant hormones that also act in the rhizosphere to stimulate germination of root‐parasitic plants and enhance plant symbiosis with beneficial microbes. Here, the role of SLs was investigated in the interaction of rice (Oryza sativa) roots with the root‐knot nematode Meloidogyne graminicola. Genetic approaches and chemical sprays were used to manipulate SL signaling in rice before infection with M. graminicola. Then, nematode performance was evaluated and plant defense hormones were quantified. Meloidogyne graminicola infection induced SL biosynthesis and signaling and suppressed jasmonic acid (JA)‐based defense in rice roots, suggesting a potential role of SLs during nematode infection. Whereas the application of a low dose of the SL analogue GR24 increased nematode infection and decreased jasmonate accumulation, the SL biosynthesis and signaling d mutants were less susceptible to M. graminicola, and constitutively accumulated JA and JA‐isoleucine compared with wild‐type plants. Spraying with 0.1 μM GR24 restored nematode susceptibility in SL‐biosynthesis mutants but not in the signaling mutant. Furthermore, foliar application of the SL biosynthesis inhibitor TIS108 impeded nematode infection and increased jasmonate levels in rice roots. In conclusion, SL signaling in rice suppresses jasmonate accumulation and promotes root‐knot nematode infection.

The root-knot nematode Meloidogyne graminicola is a serious pest in rice affecting production in many rice growing areas. Natural host resistance is an attractive control strategy because the speed of the parasite’s life cycle and the broad host range it attacks make other control measures challenging. Although resistance has been found in the domesticated African rice Oryza glaberrima and the wild rice species O. longistaminata, the introgression of resistance genes to Asian rice O. sativa is challenging. Resistance due to a major gene in O. sativa would greatly aid breeding. Recently two accessions resistant to M. graminicola have been identified in a screen of 332 diverse O. sativa cultivars. In this study, these two resistant cultivars, LD 24 (an indica from Sri Lanka) and Khao Pahk Maw (an aus from Thailand), were crossed with a moderately susceptible cultivar, Vialone Nano (a temperate japonica from Italy). Approximately 175 F 2 progeny of both populations were screened for susceptibility to M. graminicola infection. Between 20 and 23 individuals with highest and lowest galls per plants were pooled to make susceptible and resistant bulks which were sequenced to conduct bulked segregant analysis using the QTL-seq method. This revealed a nematode resistance locus from 23 Mbp to the bottom of rice chromosome 11 in both crosses suggesting a rare introgression of the same locus is responsible for resistance in both cultivars. While this information can be used in marker-assisted breeding, analysis of available SNP data revealed candidate loci and genes worthy of further investigation for gene identification. Electronic supplementary material The online version of this article (10.1007/s10681-019-2427-0) contains supplementary material, which is available to authorized users.

The sedentary root-knot nematodes, Meloidogyne spp., and the migratory root-lesion nematodes, Pratylenchus spp., cause significant yield losses, particularly in aerobic and upland rice production systems. Recently, the Asian rice Oryza sativa accessions LD 24 and Khao Pahk Maw (KPM) were shown to be highly resistant to M. graminicola. In this study, we have analyzed the responses and broadness of resistance of these two rice genotypes to another root-knot nematode M. javanica and a root-lesion nematode P. zeae. The penetration as well as post-penetration development and reproduction of nematodes were compared including known susceptible and resistant genotypes. Our results indicate that the genotype KPM confers strong resistance to both M. javanica and P. zeae, while LD 24 was resistant to M. javanica and susceptible to P. zeae. Detailed observations revealed that similar numbers of M. javanica or P. zeae penetrated the resistant and susceptible hosts during early infection stages. However, the development and reproduction of both nematodes were arrested or reduced in resistant genotypes, implying that resistance occurs at the post-penetration stage.