QTL Mapping for Bacterial Wilt Resistance in Eggplant via Bulked Segregant Analysis Using Genotyping by Sequencing

Author:

Xiao Xi’ou12345,Lin Wenqiu12345,Nie Heng12345,Duan Zhe12346,Liu Ke12347

Affiliation:

1. South Subtropical Crop Research Institute, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524091, China

2. Key Laboratory of Tropical Fruit Biology Ministry of Agriculture & Rural Affairs, Zhanjiang 524091, China

3. Key Laboratory of Hainan Province for Postharvest Physiology and Technology of Tropical Horticultural Products, Zhanjiang 524091, China

4. Zhanjiang Key Laboratory of Tropical Crop Genetic Improvement, Zhanjiang 524091, China

5. National Key Laboratory for Tropical Crop Breeding, Sanya 572024, China

6. College of Tropical Crop Science, Yunnan Agricultural University, Kunming 665099, China

7. College of Horticulture, South China Agricultural University, Guagnzhou 510642, China

Abstract

The bacterial wilt disease caused by Ralstonia solanacearum is a significant threat to eggplant production. Breeding and promoting resistant varieties is one of the most effective methods to manage bacterial wilt. Conducting QTL (quantitative trait locus) mapping of resistant genes can substantially enhance the breeding of plant resistance to bacterial wilt. In this study, a population of 2200 F2 individuals derived from resistant and susceptible materials was utilized to establish extreme resistance and susceptibility pools. Following resequencing analysis of the parents and extreme pools, the QTL were examined using the DEEP-BSA software and QTLseqr R package (version 0.7.5.2). The results revealed that the detection of 10 QTL sites on chromosomes 5, 8, 9, and 11 by the five algorithms of the DEEP-BSA software. Additionally, the candidate region of 62 Mb–72 Mb on chromosome 5 was identified in all five algorithms of the DEEP-BSA software, as well as by the QTLseqr R package. Subsequent gene annotation uncovered 276 genes in the candidate region of 62 Mb–72 Mb on chromosome 5. Additionally, RNA-seq results indicated that only 13 genes had altered expression levels following inoculation with R. solanacearum in the resistant materials. Based on the expression levels, SMEL4_05g015980.1 and SMEL4_05g016110.1 were identified as candidate genes. Notably, SNP annotation identified a non-synonymous mutation in the exonic region of SMEL4_05g015980.1 and a variant in the promoter region of SMEL4_05g016110.1. The research findings have practical significance for the isolation of bacterial wilt resistance genes in eggplant and the development of resistance to bacterial wilt varieties in eggplant.

Funder

Natural Science Foundation of Hai Nan province

Key R&D Projects in Hainan Province

Central Public-interest Scientific Institution Basal Research Fund

Key R&D Projects in Guangdong Province

National Key Laboratory for Tropical Crop Breeding

Publisher

MDPI AG

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