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Peters, R. J.

Publications and source records attributed to Peters, R. J..

2 recordsLinked to original sources

Diterpenoid phytoalexins shape rice root microbiomes and their associations with root parasitic nematodes

Rice synthesizes diterpenoid phytoalexins (DPs) are known to operate in defense against foliar microbial pathogens and root-knot nematode Meloidogyne graminicola. Here, we examined the role of DPs in shaping riceassociated root microbiomes in nematode-infested rice paddy soils. Further, we assessed how DPs affect interactions between the root microbiomes and nematode communities, particularly rice root-knot nematodes from the Meloidogyne genus. We used 16S and ITS2 rRNA gene amplicon analysis to characterize the rice root-and rhizosphere-associated microbiomes of DP knock-out mutants and their wild-type parental line, at an early (17 days) and late (28 days) stage of plant development in field soil. Disruption of DP synthesis resulted in distinct composition and structure of microbial communities both relative to the parental/wild-type line but also between individual mutants, indicating specificity in DP-microbe interactions. Moreover, nematode-suppressive microbial taxa, including Streptomyces, Stenotrophomonas, Enterobacter, Massilia, and Acidibacter, negatively correlated with Meloidogyne. Comparative analysis revealed differential enrichment of microbial taxa in the roots of rice diterpenoid phytoalexin (DP) knock-out mutants versus wild-type, suggesting that DPs modulate specific taxa in the rice root microbiome. These findings indicate DPs role in plant-microbiome assembly and nematode interactions, further underscoring the potential of leveraging phytoalexins for sustainable management of crop diseases.

microbiology↗

Unraveling a tangled skein: Evolutionary analysis of the bacterial gibberellin biosynthetic operon

Gibberellin (GA) phytohormones are ubiquitous regulators of growth and developmental processes in vascular plants. The convergent evolution of GA production by plant-associated bacteria, including both symbiotic, nitrogen-fixing rhizobia and phytopathogens, suggests that manipulation of GA signaling is a powerful mechanism for microbes to gain an advantage in these interactions. Although homologous operons encode GA biosynthetic enzymes in both rhizobia and phytopathogens, notable genetic heterogeneity and scattered operon distribution in these lineages suggests distinct functions for GA in varied plant-microbe interactions. Therefore, deciphering GA operon evolutionary history could provide crucial evidence for understanding the distinct biological roles for bacterial GA production. To further establish the genetic composition of the GA operon, two operon-associated genes that exhibit limited distribution among rhizobia were biochemically characterized, verifying their roles in GA biosynthesis. Additionally, a maximum-parsimony ancestral gene block reconstruction algorithm was employed to characterize loss, gain, and horizontal gene transfer (HGT) of GA operon genes within alphaproteobacteria rhizobia, which exhibit the most heterogeneity among GA operon-containing bacteria. Collectively, this evolutionary analysis reveals a complex history for HGT of both individual genes and the entire GA operon, and ultimately provides a basis for linking genetic content to bacterial GA functions in diverse plant-microbe interactions.

microbiology↗