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Transcriptome Dynamics Associated with Resistance and Susceptibility Against Fusarium Head Blight in Four Wheat Genotypes

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2018 Aug 31
PMID 30157778
Citations 45
Authors
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Abstract

Background: Fusarium head blight (FHB) of wheat in North America is caused mostly by the fungal pathogen Fusarium graminearum (Fg). Upon exposure to Fg, wheat initiates a series of cellular responses involving massive transcriptional reprogramming. In this study, we analyzed transcriptomics data of four wheat genotypes (Nyubai, Wuhan 1, HC374, and Shaw), at 2 and 4 days post inoculation (dpi) with Fg, using RNA-seq technology.

Results: A total of 37,772 differentially expressed genes (DEGs) were identified, 28,961 from wheat and 8811 from the pathogen. The susceptible genotype Shaw exhibited the highest number of host and pathogen DEGs, including 2270 DEGs associating with FHB susceptibility. Protein serine/threonine kinases and LRR-RK were associated with susceptibility at 2 dpi, while several ethylene-responsive, WRKY, Myb, bZIP and NAC-domain containing transcription factors were associated with susceptibility at 4 dpi. In the three resistant genotypes, 220 DEGs were associated with resistance. Glutathione S-transferase (GST), membrane proteins and distinct LRR-RKs were associated with FHB resistance across the three genotypes. Genes with unique, high up-regulation by Fg in Wuhan 1 were mostly transiently expressed at 2 dpi, while many defense-associated genes were up-regulated at both 2 and 4 dpi in Nyubai; the majority of unique genes up-regulated in HC374 were detected at 4 dpi only. In the pathogen, most genes showed increased expression between 2 and 4 dpi in all genotypes, with stronger levels in the susceptible host; however two pectate lyases and a hydrolase were expressed higher at 2 dpi, and acetyltransferase activity was highly enriched at 4 dpi.

Conclusions: There was an early up-regulation of LRR-RKs, different between susceptible and resistant genotypes; subsequently, distinct sets of genes associated with defense response were up-regulated. Differences in expression profiles among the resistant genotypes indicate genotype-specific defense mechanisms. This study also shows a greater resemblance in transcriptomics of HC374 to Nyubai, consistent with their sharing of two FHB resistance QTLs on 3BS and 5AS, compared to Wuhan 1 which carries one QTL on 2DL in common with HC374.

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References
1.
Spoel S, Koornneef A, Claessens S, Korzelius J, van Pelt J, Mueller M . NPR1 modulates cross-talk between salicylate- and jasmonate-dependent defense pathways through a novel function in the cytosol. Plant Cell. 2003; 15(3):760-70. PMC: 150028. DOI: 10.1105/tpc.009159. View

2.
Dubreuil-Maurizi C, Poinssot B . Role of glutathione in plant signaling under biotic stress. Plant Signal Behav. 2012; 7(2):210-2. PMC: 3405692. DOI: 10.4161/psb.18831. View

3.
Ravichandran S, Stone S, Benkel B, Prithiviraj B . Purple Acid Phosphatase5 is required for maintaining basal resistance against Pseudomonas syringae in Arabidopsis. BMC Plant Biol. 2013; 13:107. PMC: 3751912. DOI: 10.1186/1471-2229-13-107. View

4.
Chen X, Steed A, Travella S, Keller B, Nicholson P . Fusarium graminearum exploits ethylene signalling to colonize dicotyledonous and monocotyledonous plants. New Phytol. 2009; 182(4):975-983. DOI: 10.1111/j.1469-8137.2009.02821.x. View

5.
Biselli C, Bagnaresi P, Faccioli P, Hu X, Balcerzak M, Mattera M . Comparative Transcriptome Profiles of Near-Isogenic Hexaploid Wheat Lines Differing for Effective Alleles at the 2DL FHB Resistance QTL. Front Plant Sci. 2018; 9:37. PMC: 5797473. DOI: 10.3389/fpls.2018.00037. View