Abstract

Cotton leaf curl virus (CLCuV) disease is one of the major limiting factors in cotton production, particularly in widely cultivated Gossypium hirsutum varieties that are susceptible to attack by this virus. Several approaches have been employed to explore putative resistance genes in another cotton species, G. arboreum. However, the exact mechanisms conferring disease resistance in cotton are still unknown. In the current study, we used various approaches to identify possible resistance genes against CLCuV infection. We report the identification and isolation of a set of genes involved in the resistance response to viral infestation. PCR products containing genomic DNA gave multiple amplifications with a single primer in most reactions, and 38 fragments were cloned from G. arboreum and G. hirsutum. The sequences of cloned fragments belonged to various pathway genes and uncharacterized proteins. However, five amplified fragments (RM1, RM6, RM8, RM12 and RM31) showed similarity with R genes. Maximum homology (94 %) was observed with G. raimondii toll/interleukin receptor-like protein. BLAST search showed the homology of all resistance gene analogues (RGAs) with more than one chromosome, and multiple hits were observed on each chromosome for each RGA. Expression analysis through RT–PCR identified variable expression levels of the different RGAs in all tested genotypes. The expression level of RGAs differed between symptomatic and asymptomatic plants, with the exception of RGA 395, whose expression level was the same in both diseased and healthy plants. Knowledge of the interaction of these genes with various cotton pathogens could be utilized to improve the resistance of susceptible G. hirsutum and other plant species.

Highlights

  • Analogous to the vertebrate immune system, the resistance (R) genes in plants recognize pathogen effectors and awaken the defence system of plants to combat attack (Ellis and Jones 1998; Chen et al 2015)

  • The aim of the current study was to explore the disease resistance genes in the published literature/GenBank and to screen for them in G. arboreum using degenerate primers on genomic DNA and RT–PCR on resistance gene analogues (RGAs) detected from Expressed sequence tags (ESTs)

  • The fragments appearing in Cotton leaf curl virus (CLCuV)-resistant G. arboreum and partly tolerant G. hirsutum genotypes that differed with respect to totally susceptible Coker were selected and cloned for sequencing

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Summary

Introduction

Analogous to the vertebrate immune system, the resistance (R) genes in plants recognize pathogen effectors (avirulence factors) and awaken the defence system of plants to combat attack (Ellis and Jones 1998; Chen et al 2015). To date the largest class of R genes are nucleotide-binding site leucine-rich repeats (NBS-LRR) (Dangl and Jones 2001; Chen et al 2015). Other classes of R genes produce surfacelocalized pattern recognition receptors (PRR). These include receptor-like kinases and receptor-like proteins (Monaghan and Zipfel 2012). Sixty-three resistance gene analogue (RGA) clusters have been reported in the diploid D-genome of G. raimondii, while Wang et al (2013) and Wei et al (2013) identified 355 NBS-encoding genes in the raimondii genome

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