Publications

4504

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 Citrus Huanglongbing (HLB), caused by ‘ Candidatus Liberibacter asiaticus’ ( Ca Las), is the most devastating disease affecting the global citrus industry. Here, we reported that the Ca Las effector SDE70 promotes HLB pathogenicity by targeting the citrus ubiquitination pathway. Transgenic expression of SDE70 in Wanjincheng orange ( Citrus sinensis Osbeck) accelerated early Ca Las proliferation, aggravated HLB symptoms, and increased susceptibility to citrus canker induced by Xanthomonas citri subsp. citri ( Xcc ). These results demonstrate that SDE70 functions as a broad‐spectrum suppressor of citrus immunity. Mechanistically, SDE70 physically interacts with CsRUB2, a citrus ubiquitin‐related protein. Furthermore, CsRUB2 overexpression in Wanjincheng oranges reduced resistance to HLB but enhanced resistance to citrus canker. Both SDE70 and CsRUB2 elevated salicylic acid (SA) and hydrogen peroxide (H 2 O 2 ) levels in transgenic plants while lowering methyl salicylate (MeSA) levels. CsRUB2 also decreased jasmonic acid (JA). In contrast to the suppressive effect of SDE70, CsRUB2 enhanced the transcription of citrus immunity genes. Transient expression assays further demonstrated that the SDE70–CsRUB2 interaction dysregulates citrus immunity by perturbing SA, MeSA, JA, and H 2 O 2 signals. These findings provide a theoretical basis for understanding citrus– Ca Las interactions and breeding citrus varieties with broad‐spectrum resistance to both HLB and citrus canker.

Abstract ‘Candidatus Mycoplasma haemolamae’ (CMhl) is a hemotropic bacterium infecting South American Camelids (SAC), whose epidemiology and clinical significance are still not fully elucidated. This study investigated CMhl by qPCR in blood samples of alpacas ( Vicugna pacos ) and llamas ( Lama glama ) in Italy in 2021–2024, characterizing CMhl haplotypes based on partial 16 S rRNA sequences and defining haematological findings in a subset of CMhl-infected animals. Statistical analysis was performed to detect potential risk factors associated with CMhl positivity. Out of 206 animals (200 alpacas and 6 llamas), CMhl was detected by qPCR in 88 (42.7%) animals. CMhl haplotype #1 and #2 were detected in 42.2% and 0.5% of the animals, respectively. Binary logistic regression analysis showed that higher CMhl positivity was significantly associated with larger herd size ( P  = 0.011), Northern Italy area of origin ( P  = 0.031) and warmer seasons ( P  = 0.003). The detection of two CMhl haplotypes confirms the high diffusion of CMhl in SAC farmed in Italy. Results confirm that CMhl usually causes subclinical infections, suggesting that antimicrobial treatment is likely not necessary based on qPCR positivity alone. Results focusing on the association of CMhl positivity with warm temperatures and large herd size suggest the need of further studies on the genetic features, epidemiology and immune response in CMhl-positive SAC from Italy, with emphasis on understanding potential vector transmission.

Persian lime (Citrus latifolia Tan.) is a crop of high economic and social relevance in Mexico due to its nutritional properties, associated health benefits, and particularly the foreign exchange generated through exportation. In recent years, the state of Veracruz has become the leading production region for this species at the national level. However, this crop is susceptible to several vascular diseases that cause significant economic losses in the citrus industry. Among these, Huanglongbing (HLB) is considered the most destructive disease, exerting the greatest impact on Persian lime production. This study involved the collection of Persian lime leaf tissues from different sources: field-grown plants, certified nursery plants, and plants previously sanitized through micrografting and thermotherapy processes. Genomic DNA was extracted from the collected samples. DNA integrity was verified by agarose gel electrophoresis and quantified using a NanoDrop One-C spectrophotometer. Quantitative Real-Time Polymerase PCR (qPCR) was performed using a QuantStudio One thermocycler and SYBR Green Master Mix as the fluorescent detection system. Samples were considered HLB-positive when the cycle threshold (Ct) value was below 35 during the quantification of Candidatus Liberibacter asiaticus. The results support the early, precise, and efficient detection of CLas by qPCR in Persian lime plants, thereby contributing to improved diagnostic and phytosanitary management strategies for this crop.

Shorea assamica is an evergreen to semi-evergreen tree in the family Dipterocarpaceae. It is widely distributed in China, India, Myanmar, Malaysia, Indonesia, the Philippines, and other regions. In China, it is found in western Yunnan and southeastern Tibet. The species is valued for its aromatic white resin, which serves as an important chemical raw material (Ang and Maruyama 1997). In May 2025, S. assamica trees exhibiting symptoms of witches'-broom disease and plexus bud disease were found at Mengmao, WanDing, Nongdao, Jiegao, and Jiexiang in RuiLi County (97°31′-98°02′ E, 23°38′-24°14′ N), Dehong Prefecture, Yunnan Province, China. Following disease onset, the overall growth of infected plants was significantly slower compared to healthy individuals. Infected plants exhibited excessive branching, shortened internodes, and a clustered growth symptom. Lateral buds on diseased tree frequently developed into abnormal twigs, with many buds forming dense clusters and only a few producing leaves. The disease was designated as S. assamica witches'-broom (SAWB). Across the seven surveyed areas, over 74% of trees displayed symptoms, while the disease incidence in nursery-cultivated seedlings was 66%. The disease was found to be spreading actively. A total of 56 samples were collected from seven areas, including 42 symptomatic plants and 14 asymptomatic plants. The lateral stem tissues of 30 samples were observed under a scanning electron microscope (Hitachi S-3000N). Spherical bodies were found in the phloem sieve cells of symptomatic plants. Total DNA was extracted from 56 plant samples using the CTAB method (Porebski et al. 1997) and subjected to nested PCR testing. Double-distilled water was used as negative control, and the DNA extracted from Dodonaea viscosa affected by D. viscosa witches’-broom disease was used as a positive control. Nested PCR was employed to amplify the pathogen’s 16S rRNA gene (Lee et al. 1993; Schneider et al. 1993), and 1.2 kb segment was produced (GenBank accessions: PZ025091, PZ025092, and PZ025093). PCR specific to the ribosomal protein (rp) gene yielded a segment of approximately 1.2 kb (Lee et al. 2003) (GenBank accessions: PZ028767, PZ028768, and PZ028769). The fragment size from 31 samples was consistent with the positive control, confirming the association of phytoplasma with the disease. A BLAST analysis of the 16S rRNA sequences of S. assamica witches’-broom phytoplasma showed that it shared 99.68% identity with that of Rice orange leaf phytoplasma (GenBank accession: JQ965690). The rp sequence shared 99.83% identity with that of Salix tetradenia witches'-broom phytoplasma (GenBank accession: KC117314). An analysis with iPhyClassifier (Zhao et al. 2013) showed that the virtual RFLP pattern derived from the 16S rDNA fragment of SAWB phytoplasma was identical (similarity coefficient 0.98) to the reference pattern of 16Sr group I, subgroup B (OY-M, GenBank accession AP006628). The SAWB phytoplasma is a variant of 16SrI-B. The phylogenetic tree was reconstructed based on 16S rRNA and rp gene sequences using MEGA (Tamura et al. 2013). The analysis was conducted using the neighbor-joining method with 1,000 replicates of bootstrap analysis. The results indicated that the SAWB phytoplasmas grouped into clades including phytoplasmas belonging to 16SrI-B and rpI-B, respectively. In addition, 1-year-old S. assamica were used for grafting assays in nursery, the twigs from infected S. assamica under natural conditions were used as a scion, and the phytoplasma was detected using nested PCR after grafting for 40 days. To the best of our knowledge, S. assamica is a new host of ‘Ca. P. asteris’-related strain (16SrI-B) in China. The newly emerged disease is a threat to S. assamica.

Among citrus diseases, Huanglongbing (HLB) is recognized as the most destructive and economically damaging worldwide. It is mainly associated with ‘ Candidatus Liberibacter asiaticus’ ( C Las) being transmitted by Diaphorina citri . There are no curative treatments or commercial citrus varieties resistant to C Las. Wild Aurantioideae species have been widely screened and, recently, Oceanian genotypes graft- and sexually compatible with Citrus were identified as HLB-resistant; however, there is no information regarding their use as interstocks of commercial varieties yet. Under greenhouse conditions, six HLB-resistant genotypes were evaluated as interstocks between ‘Valencia’ sweet orange scion and ‘Rangpur’ lime rootstock, both susceptible to HLB, with ‘Valencia’ interstock as the control. Rootstocks were nucellar seedlings, and the scion was a commercial accession preimmunized with a mild CTV strain. Plants were assessed for C Las infection and titer in leaves, stem bark, and roots up to 12–24 months after graft-inoculation in the scion and compared to non-inoculated controls. Furthermore, molecular, anatomical, and biometric variables were investigated. As expected, the scion variety was colonized by C Las regardless of the genotype evaluated as interstock. Although bacteria were detected in the roots of most C Las-inoculated plants, C Las movement from the scion to the roots was blocked in 42% and 86% of composite plants when using a F1 hybrid of C. australis × C. inodora or an admixture hybrid of C. glauca , C. australis , and C. australasica as interstocks. Overall, C Las titers were similar in infected plant tissues among the evaluated genotypes, but titers were lower in interstock bark tissues compared to scion and rootstock ones. After one-two years of C Las + CTV infection (experiments I and II, respectively), the dry weight of the root system decreased by 50% in infected trees compared to control trees for most genotypes, and C Las + CTV infection was associated with changes in the sieve phloem and gene expression. These findings suggest that, despite CTV infection, interstocks derived from some hybrids of Australian citrus types have the potential to restrict the movement of C Las from the scion into the roots of infected citrus trees. Long-term evaluation of composite plants in field conditions is necessary to assess tree performance and, ultimately, the impact of C Las blockage by interstocking on HLB disease damage.

‘Candidatus Liberibacter solanacearum’ (Lso) haplotype D, transmitted by the carrot psyllid Bactericera trigonica, is a major threat to carrot production, particularly in the Mediterranean Basin and the Middle East. We investigated the impact of plant age at the time of inoculation on symptom development and yield under greenhouse and outdoor conditions. In greenhouse trials, 1- and 2-month-old plants were inoculated with psyllids harboring Lso. Both age groups showed reduced taproot weight compared to controls, but younger plants were more severely affected, exhibiting 90% yield reduction, while 2-month-old plants showed a 30% reduction. Witches’ broom symptoms appeared earlier in plants inoculated at 1-month-old (5 weeks post-inoculation); however, within two weeks, plants inoculated at two months reached comparable levels of symptom incidence and severity. Additional greenhouse experiments using Lso-free psyllids confirmed that yield losses and disease symptoms were specifically due to Lso infection, and not psyllid feeding. In outdoor trials, we tested the effects of inoculation at 7, 11, 15, and 19 weeks post-sowing (wps) on disease incidence and yield. Significant yield losses occurred only in plants inoculated at 7 and 11 wps, with up to 45% reduction by harvest time. Symptoms began to appear at 20 wps in plants inoculated at 7 and 11 wps. At 23 wps, symptoms also appeared in plants inoculated at 15 wps, with a similar incidence to that observed in the earlier inoculation groups. Molecular detection of Lso at harvest (23 wps) confirmed that all plants inoculated at 19 wps or earlier were infected. These results demonstrate that carrots are highly susceptible to Lso-induced yield losses at the earlier stages of growth and highlight the importance of managing early-season vector pressure to minimize economic damage.