» Articles » PMID: 38673861

NRPS-like ATRR in Plant-Parasitic Nematodes Involved in Glycine Betaine Metabolism to Promote Parasitism

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Apr 27
PMID 38673861
Authors
Affiliations
Soon will be listed here.
Abstract

Plant-parasitic nematodes (PPNs) are among the most serious phytopathogens and cause widespread and serious damage in major crops. In this study, using a genome mining method, we identified nonribosomal peptide synthetase (NRPS)-like enzymes in genomes of plant-parasitic nematodes, which are conserved with two consecutive reducing domains at the N-terminus (A-T-R-R) and homologous to fungal NRPS-like ATRR. We experimentally investigated the roles of the NRPS-like enzyme (MiATRR) in nematode () parasitism. Heterologous expression of in can overcome the growth inhibition caused by high concentrations of glycine betaine. RT-qPCR detection shows that is significantly upregulated at the early parasitic life stage (J2s in plants) of . Host-derived RNA interference (RNAi) in can significantly decrease the number of galls and egg masses of , as well as retard development and reduce the body size of the nematode. Although exogenous glycine betaine and choline have no obvious impact on the survival of free-living J2s (pre-parasitic J2s), they impact the performance of the nematode in planta, especially in -RNAi plants. Following application of exogenous glycine betaine and choline in the rhizosphere soil of , the numbers of galls and egg masses were obviously reduced by glycine betaine but increased by choline. Based on the knowledge about the function of fungal NRPS-like ATRR and the roles of glycine betaine in host plants and nematodes, we suggest that MiATRR is involved in nematode-plant interaction by acting as a glycine betaine reductase, converting glycine betaine to choline. This may be a universal strategy in plant-parasitic nematodes utilizing NRPS-like ATRR to promote their parasitism on host plants.

Citing Articles

Animal-Encoded Nonribosomal Pathway to Bursatellin Analogs.

Venugopalan A, Schmidt E J Am Chem Soc. 2025; 147(8):6623-6632.

PMID: 39933076 PMC: 11869996. DOI: 10.1021/jacs.4c15714.


Biochemical Defence of Plants against Parasitic Nematodes.

Meresa B, Matthys J, Kyndt T Plants (Basel). 2024; 13(19).

PMID: 39409684 PMC: 11479011. DOI: 10.3390/plants13192813.

References
1.
Eves-van den Akker S . Plant-nematode interactions. Curr Opin Plant Biol. 2021; 62:102035. DOI: 10.1016/j.pbi.2021.102035. View

2.
Marchler-Bauer A, Bryant S . CD-Search: protein domain annotations on the fly. Nucleic Acids Res. 2004; 32(Web Server issue):W327-31. PMC: 441592. DOI: 10.1093/nar/gkh454. View

3.
Dafny-Yelin M, Chung S, Frankman E, Tzfira T . pSAT RNA interference vectors: a modular series for multiple gene down-regulation in plants. Plant Physiol. 2007; 145(4):1272-81. PMC: 2151715. DOI: 10.1104/pp.107.106062. View

4.
Siddique S, Grundler F . Parasitic nematodes manipulate plant development to establish feeding sites. Curr Opin Microbiol. 2018; 46:102-108. DOI: 10.1016/j.mib.2018.09.004. View

5.
Lee K, Da Silva N, Kealey J . Determination of the extent of phosphopantetheinylation of polyketide synthases expressed in Escherichia coli and Saccharomyces cerevisiae. Anal Biochem. 2009; 394(1):75-80. DOI: 10.1016/j.ab.2009.07.010. View