Publications

4721

‘ Candidatus Liberibacter asiaticus’ ( C Las), the causal agent of citrus huanglongbing, is transmitted by the Asian citrus psyllid Diaphorina citri . While C Las-positive ( C Las+) females exhibit increased fecundity and metabolic demands, their neuroendocrine regulation mechanisms remain unclear. We propose C Las manipulates dopamine (DA) signaling to enhance psyllid fecundity and C Las proliferation. Metabolomics revealed elevated DA in C Las+ females. Silencing DA synthesis genes and receptor DcDop2 via RNAi reduced lipid reserves, fecundity, and ovarian C Las titers. Through combined in vivo and in vitro experiments, we demonstrated that the microRNA miR-31a suppresses DcDop2 expression by binding to its 3’ untranslated region. Overexpression of miR-31a resulted in decreased DcDop2 expression and C Las titers in the ovaries, eliciting phenotypic defects akin to DcDop2 knockdown. Furthermore, DcDop2 knockdown and miR-31a overexpression reduced juvenile hormone (JH) levels and adipokinetic hormone (AKH) signaling in fat bodies and ovaries. Consequently, C Las regulates the DA- DcDop2 signaling axis to improve D. citri lipid metabolism and fecundity, while simultaneously promoting its replication. These findings reveal a coevolution between C Las proliferation and ovarian development in the insect host. This discovery enhances our understanding of the molecular interplay between plant pathogens and vector insects and offers novel targets and strategies for HLB field management.

Understanding plant-vector-pathogen interactions is essential for explaining the persistence of stolbur diseases associated with the plant pathogenic bacterium ‘ Candidatus Phytoplasma solani’ (CaPsol) in agroecosystems. This study investigates the role of crop-associated Reptalus planthoppers (Insecta: Hemiptera: Cixiidae) in shaping CaPsol epidemiology within a four-crop rotation system (sunflower, wheat, sugar beet, and maize) in Serbia under field and experimental conditions. Over a three-year period (2023–2025), nymphal surveys, adult monitoring, emergence-cage experiments, molecular identification of planthoppers, assessment of CaPsol in crops, and vector transmission assays were conducted, with a particular focus on the sunflower-wheat sequence. Sunflower was identified as a developmental host for Reptalus quinquecostatus and Reptalus panzeri , with high CaPsol infection rates detected in both the host plant and associated vectors. In contrast, wheat appeared to primarily support nymphal overwintering, while its significance as a CaPsol reservoir remains inconclusive. Furthermore, the maize-wheat sequence supported the development of R. quinquecostatus while confirming its role in the life cycle of R. panzeri . Experimental trials demonstrated efficient CaPsol transmission to sunflower but limited transmission to wheat. Despite high infection levels under field conditions, sunflower remained asymptomatic, suggesting its role as a cryptic pathogen reservoir. The findings indicate that the sunflower-wheat sequence may sustain CaPsol-infected Reptalus spp. populations across seasons, facilitating pathogen persistence within cropping systems. The study highlights the importance of integrating vector life cycle dynamics into epidemiological frameworks of stolbur diseases, particularly in crop rotations where major cultivated hosts may support in-field CaPsol pathosystems.

‘ Candidatus Liberibacter asiaticus’ ( C Las), the causal agent of citrus huanglongbing, is transmitted by the Asian citrus psyllid Diaphorina citri . While C Las-positive ( C Las+) females exhibit increased fecundity and metabolic demands, their neuroendocrine regulation mechanisms remain unclear. We propose C Las manipulates dopamine (DA) signaling to enhance psyllid fecundity and C Las proliferation. Metabolomics revealed elevated DA in C Las+ females. Silencing DA synthesis genes and receptor DcDop2 via RNAi reduced lipid reserves, fecundity, and ovarian C Las titers. Through combined in vivo and in vitro experiments, we demonstrated that the microRNA miR-31a suppresses DcDop2 expression by binding to its 3’ untranslated region. Overexpression of miR-31a resulted in decreased DcDop2 expression and C Las titers in the ovaries, eliciting phenotypic defects akin to DcDop2 knockdown. Furthermore, DcDop2 knockdown and miR-31a overexpression reduced juvenile hormone (JH) levels and adipokinetic hormone (AKH) signaling in fat bodies and ovaries. Consequently, C Las regulates the DA- DcDop2 signaling axis to improve D. citri lipid metabolism and fecundity, while simultaneously promoting its replication. These findings reveal a coevolution between C Las proliferation and ovarian development in the insect host. This discovery enhances our understanding of the molecular interplay between plant pathogens and vector insects and offers novel targets and strategies for HLB field management.

Chokecherry (Prunus virginiana L.) is a native shrub that is widely found across North America and is a host of ‘Candidatus Phytoplasma pruni’ associated with X-disease of stone fruits. This pathogen is of major concern to U.S. cherry and peach growers, with the most recent and ongoing outbreak in the Pacific Northwest causing major economic harm. To investigate the role of chokecherry as a potential reservoir and source of orchard-associated strains, we surveyed wild chokecherry trees across 12 U.S. states, and compared the strains present to those in commercially cultivated Prunus species. Approximately 47% of chokecherry sampled tested positive for a ‘Ca. P. pruni’-related strain and phylogenetic analysis revealed high strain diversity, including six distinct clades and four newly identified lineages. In contrast, ‘Ca. P. pruni’ strains isolated from cultivated cherry and peach trees exhibited lower diversity and were infected by known disease outbreak-associated strains such as NWX. These data suggest limited transmission between wild and cultivated hosts in the western U.S., with patterns indicating spillover from orchards into nearby chokecherry populations rather than the reverse. However, in states east of the Rocky Mountains, chokecherry likely functions as a reservoir for orchard infections.

Abstract A comprehensive polyphasic taxonomic strategy was applied to the systematic characterization of strain DNPG3 T , which was isolated from the river Ganges, Hooghly, West Bengal, India. The Gram-positive, halotolerant, heavy-metal-tolerant strain exhibited the ability to degrade p -nitrophenol (PNP). Cellular fatty acid analysis revealed that the predominant components were anteiso-C 15:0 (24.61%), C 11:0 (21.06%), iso-C 16:0 (11.89%), C 16:0 (11.58%), and anteiso-C 17:0 (11.24%). Notably, the presence of C 11:0 , C 10:0 2-OH as major fatty acids differentiate strain DNPG3 T from its closely related members of the genus Brachybacterium . The predominant respiratory quinone was identified as menaquinone-7 (MK-7). Analysis of 16S rRNA gene sequence indicated that B. zhongshanense strain JB T was the closest relative of DNPG3 T , sharing 97.08% sequence similarity. Genome-based ANI value calculated using the EzBioCloud server revealed that B. zhongshanense JCM 15471 T was the closest genomic relative (85.49%). These values were further substantiated by digital DNA–DNA hybridization (dDDH) estimates calculated using the GGDC server. Taxonomic assignment using the GTDB database further indicated that strain DNPG3 T constitutes a previously unrecognized species within the genus Brachybacterium . Genome analysis of strain DNPG3 T identified eleven genomic islands, along with a rich repertoire of 194 carbohydrate-active enzyme (CAZyme) families, comprising 95 glycoside hydrolases and 53 glycosyltransferases. In addition, five biosynthetic gene clusters were detected. Collectively, these genomic features indicate the involvement of horizontal gene transfer events and highlighted the pronounced metabolic versatility of the strain, underscoring its potential for industrial enzyme production and secondary metabolite biosynthesis. Pan-genome analysis further indicates that the Brachybacterium pan-genome is open, reflecting substantial genetic diversity and ongoing gene acquisition within the genus. Comprehensive biochemical, physiological, chemotaxonomic, and phylogenetic analyses supported the assignment of strain DNPG3 T to the genus Brachybacterium while clearly distinguishing it from all currently described species within the genus. Accordingly, strain DNPG3 T was proposed to represent a novel species, for which the name Brachybacterium netajii sp. nov. is suggested. The type strain was DNPG3 T (= MTCC13125 T ).