Publications

4606

Abstract Background ‘ Candidatus Liberibacter solanacearum’ (Lso) is a phloem-limited bacterial pathogen causing significant diseases in solanaceous crops. In the United States, haplotypes A and B are transmitted by the potato psyllid Bactericera cockerelli . We previously identified differences in their acquisition and transmission between adults and nymphs. The present study characterized the dynamics of LsoA and LsoB acquisition and transmission by nymphs and examined the transcriptional responses of the nymphal gut upon their acquisition. Methods and results Nymphs were exposed to LsoA- or LsoB-infected plants for 1, 3, 5, or 7 days to measure the bacterial accumulation and for 8 days to assess the transmission efficiency following sequential inoculation of tomato plants. Quantitative PCR showed that LsoB accumulated to higher levels than LsoA after 3 days of acquisition. Following the sequential inoculation, LsoB was transmitted earlier than LsoA indicating a shorter latency period. RNA-seq analysis of the guts following a 1- and 5-day acquisition access periods revealed a greater transcriptional regulation at 5 days than at 1 day. Furthermore, the responses were haplotype-specific: LsoA primarily affected genes involved in protein translation, ER stress, and cell cycle regulation, whereas LsoB regulated genes involved in autophagy, apoptosis, and immune pathways. Conclusions This study revealed haplotype-specific gene regulation potentially leading to LsoB being transmitted more efficiently by psyllid nymphs.

Abstract Bovine hemoplasmas, including Mycoplasma wenyonii (M. wenyonii) and Candidatus Mycoplasma haemobos (C. M. haemobos) , are vector-borne pathogens that can cause significant clinical diseases in cattle. This case report from Türkiye describes the clinical findings, hematological analysis, and serum biochemistry results of a cow presenting with hemoglobinuria caused by C. M. haemobos . Blood samples from the infected animal were analyzed using hematological, biochemical, microscopic, and molecular methods. Multiplex polymerase chain reaction assay confirmed the infection, and microscopic analysis revealed a parasitemia rate of 6.99%. Clinical signs included hemoglobinuria, icterus, and anemia. The treatment included fluid therapy, antibiotic (oxytetracycline), and antianemic drugs. The cattle died 1 month post-treatment, reportedly due to a lower respiratory tract infection. This case report describes the diagnostic methods, clinical findings, and laboratory results. A widescale molecular survey of C. M. haemobos in cattle is warranted, with investigation of its pathogenicity and pathogenies.

The Asian citrus psyllid, Diaphorina citri, transmits the putative causal agent of citrus greening disease, ‘ Candidatus Liberibacter asiaticus’. The transmission occurs in a propagative, circulative manner. Specific protein–protein interactions are required for the accomplishment of the transmission process. We employed the far-Western technique, also known as protein overlay assay, and mass spectrometry to identify D. citri proteins that specifically recognize membrane proteins of ‘ Ca. L. asiaticus’. Whole-body protein extracts of D. citri were separated by electrophoresis and blotted onto polyvinylidene difluoride membranes. The membranes were overlayed with sonicated leaf midrib extracts from ‘ Ca. L. asiaticus’-infected citrus plants. The protein complexes were detected using different antibodies against ‘ Ca. L. asiaticus’ membrane proteins and peptidoglycans associated with lipoproteins. By comparison, spots were extracted from a polyacrylamide gel for liquid chromatography-tandem mass spectrometry analysis. Identified proteins included ATP synthase alpha and beta subunits, actin, alpha- and beta-tubulins, transitional endoplasmic reticulum ATPase TER94, 78 kDa glucose-regulated protein, and arginine kinase. These findings emphasize the involvement of energy machinery and muscle proteins in the ‘ Ca. L. asiaticus’– D. citri interactions. Understanding the pathogen–vector interactions will lead to better-designed control strategies based on the interference with specific interactions and/or blocking transmission.

Ticks are important vectors of bacteria belonging to the order Rickettsiales, several of which are causes zoonotic diseases. Amblyomma triste is the main vector of Rickettsia parkeri , the etiological agent responsible for most cases of human spotted fever rickettsiosis in Argentina. However, information on the circulation of rickettsial agents in protected areas of the La Plata River Hydrographic Basin, a region that includes highly urbanized environments and frequent contact between wildlife, domestic animals and humans, remains limited. The aim of this study was to investigate the presence of rickettsial bacteria in A. triste collected in protected areas of Buenos Aires Province, (La Plata River Hydrographic Basin, Argentina). Between September and December 2021, ticks were collected by vegetation flagging in four protected areas and analyzed individually. Polymerase chain reactions (PCR) for detecting the genus Rickettsia was initially performed using a simple PCR to amplify a variablesized fragment of the 23S-5S rRNA intergenic spacer. An initial PCR was performed with primers for a 16S rRNA fragment for the Anaplasmataceae family. A total of 247 adult ticks were examined. Twelve specimens (4.9%) tested positive for Rickettsia , and sequence analysis confirmed their identity as R. parkeri . Positive ticks were detected in Ciervo de los Pantanos National Park and Campos del Tuyú National Park. In addition, two specimens yielded sequences corresponding to Candidatus Midichloria sp. These findings confirm the presence of R. parkeri in A. triste populations from protected areas of the La Plata River Hydrographic Basin and provide the first evidence of Ca. Midichloria sp. in this tick species in Argentina. The results highlight the need for continued surveillance of tick-borne microorganisms in protected areas located near densely populated regions, where human exposure to infected ticks may occur.

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.

‘ 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.