» Articles » PMID: 36145736

Co-Transcriptomic Analysis of the Maize-Western Corn Rootworm Interaction

Overview
Journal Plants (Basel)
Date 2022 Sep 23
PMID 36145736
Authors
Affiliations
Soon will be listed here.
Abstract

The Western corn rootworm (WCR; ) is an economically important belowground pest of maize. Belowground feeding by WCR is damaging because it weakens the roots system, diminishes nutrient uptake, and creates entry points for fungal and bacterial pathogens and increases lodging, all of which can significantly suppress maize yields. Previously, it was demonstrated that belowground herbivory can trigger plant defense responses in the roots and the shoots, thereby impacting intraplant communication. Although several aspects of maize-WCR interactions have been reported, co-transcriptomic remodeling in the plant and insect are yet to be explored. We used a maize genotype, Mp708, that is resistant to a large guild of herbivore pests to study the underlying plant defense signaling network between below and aboveground tissues. We also evaluated WCR compensatory transcriptome responses. Using RNA-seq, we profiled the transcriptome of roots and leaves that interacted with WCR infestation up to 5 days post infestation (dpi). Our results suggest that Mp708 shoots and roots had elevated constitutive and WCR-feeding induced expression of genes related to jasmonic acid and ethylene pathways, respectively, before and after WCR feeding for 1 and 5 days. Similarly, extended feeding by WCR for 5 days in Mp708 roots suppressed many genes involved in the benzoxazinoid pathway, which is a major group of indole-derived secondary metabolites that provides resistance to several insect pests in maize. Furthermore, extended feeding by WCR on Mp708 roots revealed several genes that were downregulated in WCR, which include genes related to proteolysis, neuropeptide signaling pathway, defense response, drug catabolic process, and hormone metabolic process. These findings indicate a dynamic transcriptomic dialog between WCR and WCR-infested maize plants.

Citing Articles

Trichoplusia ni Transcriptomic Responses to the Phytosaponin Aglycone Hederagenin: Sex-Related Differences.

Chen Y, Lafleur C, Smith R, Kaur D, Driscoll B, Bede J J Chem Ecol. 2024; 50(3-4):168-184.

PMID: 38443712 PMC: 11041752. DOI: 10.1007/s10886-024-01482-1.


Maize OPR2 and LOX10 Mediate Defense against Fall Armyworm and Western Corn Rootworm by Tissue-Specific Regulation of Jasmonic Acid and Ketol Metabolism.

Huang P, Grunseich J, Berg-Falloure K, Tolley J, Koiwa H, Bernal J Genes (Basel). 2023; 14(9).

PMID: 37761872 PMC: 10530937. DOI: 10.3390/genes14091732.


Comparative Transcriptome Analysis of Defense Response of Potato to Infestation.

Zhu C, Yi X, Yang M, Liu Y, Yao Y, Zi S Plants (Basel). 2023; 12(17).

PMID: 37687339 PMC: 10490199. DOI: 10.3390/plants12173092.

References
1.
Gassmann A, Shrestha R, Kropf A, St Clair C, Brenizer B . Field-evolved resistance by western corn rootworm to Cry34/35Ab1 and other Bacillus thuringiensis traits in transgenic maize. Pest Manag Sci. 2019; 76(1):268-276. DOI: 10.1002/ps.5510. View

2.
Staswick P, Tiryaki I . The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. Plant Cell. 2004; 16(8):2117-27. PMC: 519202. DOI: 10.1105/tpc.104.023549. View

3.
Baldwin I, Schmelz E, Ohnmeiss T . Wound-induced changes in root and shoot jasmonic acid pools correlate with induced nicotine synthesis inNicotiana sylvestris spegazzini and comes. J Chem Ecol. 2013; 20(8):2139-57. DOI: 10.1007/BF02066250. View

4.
Wang K, Li H, Ecker J . Ethylene biosynthesis and signaling networks. Plant Cell. 2002; 14 Suppl:S131-51. PMC: 151252. DOI: 10.1105/tpc.001768. View

5.
Pereira A, Wang H, Zukoff S, Meinke L, French B, Siegfried B . Evidence of Field-Evolved Resistance to Bifenthrin in Western Corn Rootworm (Diabrotica virgifera virgifera LeConte) Populations in Western Nebraska and Kansas. PLoS One. 2015; 10(11):e0142299. PMC: 4643967. DOI: 10.1371/journal.pone.0142299. View