Abstract

A previous complementary cDNA-amplified fragment length polymorphism (cDNA-AFLP) analysis examined responses to the powdery mildew pathogen Oidium neolycopersici (On) of the resistant cultivar Solanum habrochiates G1.1560, carrying the Ol-1 resistance gene, and susceptible cultivar S. lycopersicum Moneymaker (MM). Among other findings, a differentially expressed transcript-derived fragment (DE-TDF) (M14E72-213) was upregulated in near isogenic line (NIL)-Ol-1, but absent in MM. This DE-TDF showed high homology to a gene of unknown function, which we named ShORR-1 (Solanum habrochaites Oidium Resistance Required-1). However, MM homolog of ShORR-1 (named ShORR-1-M) was still found with 95.26% nucleic acid sequence similarity to ShORR-1 from G1.1560 (named ShORR-1-G); this was because the cut sites of restriction enzymes in the previous complementary cDNA-AFLP analysis was absent in ShORR-1-M and differs at 13 amino acids from ShORR-1-G. Transient expression in onion epidermal cells showed that ShORR-1 is a membrane-localized protein. Virus-induced gene silencing (VIGS) of ShORR-1-G in G1.1560 plants increased susceptibility to On. Furthermore, overexpressing of ShORR-1-G conferred MM with resistance to On, involving extensive hydrogen peroxide accumulation and formation of abnormal haustoria. Knockdown of ShORR-1-M in MM did not affect its susceptibility to On, while overexpressing of ShORR-1-M enhanced MM’s susceptibility to On. We also found that changes in transcript levels of six well-known hormone signaling and defense-related genes are involved in ShORR-1-G-mediated resistance to On. The results indicate that ShORR-1-M and ShORR-1-G have antagonistic effects in tomato responses to On, and that ShORR-1 is essential for Ol-1-mediated resistance in tomato.

Highlights

  • Plants have evolved a multilayered immune system that prevents or hinders colonization by most potential pathogens

  • In our previous cDNA-AFLP study, we found that Transcript-derived fragments (TDFs) fragment M14E72-213—designated No 25 by Li et al (2007), Appendix 1)— was present in Oidium neolycopersici (On)-resistant near isogenic line (NIL)-Ol-1, but not in the On-susceptible cultivar MM

  • We found it encodes a putative protein of 268 amino acids with a molecular weight of 30.55 kDa, isoelectric point of 9.53, and 95% identity to a protein of unknown function encoded by Solyc06g059860.2 according to a BLASTP search against the Solanaceae Genomics Network (SGN) database

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Summary

Introduction

Plants have evolved a multilayered immune system that prevents or hinders colonization by most potential pathogens. ShORR-1-Mediated Resistance to Oidium neolycopersici pattern recognition receptors (Jones and Dangl, 2006; Dodds and Rathjen, 2010; Peng et al, 2018). Tobacco rattle virus (TRV)-based virus-induced gene silencing (VIGS) constructs targeting these UniGenes were subsequently generated, and used to determine whether silencing the targeted genes altered the On resistance of relevant genotypes. These efforts revealed that acetolactate synthase (ALS) (Gao et al, 2014), a glutathione S-transferase (GST) gene (Pei et al, 2011a), and an NADP-malic enzyme gene (Pei et al, 2011b) are required for Ol-1-mediated resistance to On

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