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Authors Oh

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Oh, Junepyo


Publications
5

CitationNamesAbstract
Accumulation and transmission dynamics of ‘Candidatus liberibacter solanacearum’ haplotypes A and B by potato psyllid nymphs: bioassay and transcriptomic insights Oh et al. (2026). Molecular Biology Reports 53 (1) “Liberibacter solanacearum”
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Monitoring and manipulating autophagy in potato psyllids: impacts on accumulation and transmission of “ Candidatus Liberibacter solanacearum” haplotypes A and B Oh et al. (2025). Microbiology Spectrum 13 (10) “Liberibacter solanacearum”
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‘Candidatus liberibacter solanacearum’ protein CKC_05770 interacts in vivo with tomato APX6 and APX7 Levy et al. (2025). Scientific Reports 15 (1)
Accumulation and Transmission of ‘Candidatus Liberibacter solanacearum’ Haplotypes by the Nymphs of Two Psyllid Vectors Oh et al. (2023). Insects 14 (12) “Liberibacter solanacearum”
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A ‘Candidatus Liberibacter solanacearum’ Haplotype B-Specific Family of Candidate Bacterial Effectors Levy et al. (2023). Phytopathology® 113 (9) “Liberibacter solanacearum”
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Accumulation and transmission dynamics of ‘Candidatus liberibacter solanacearum’ haplotypes A and B by potato psyllid nymphs: bioassay and transcriptomic insights
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.
Monitoring and manipulating autophagy in potato psyllids: impacts on accumulation and transmission of “ Candidatus Liberibacter solanacearum” haplotypes A and B
ABSTRACT “ Candidatus Liberibacter solanacearum” (Lso) is a highly destructive plant pathogen within the alpha-proteobacteria group. Multiple Lso haplotypes occur worldwide, each uniquely associated with a specific psyllid vector. Haplotypes A and B, found in the United States, cause serious damage to solanaceous crops and are transmitted by Bactericera cockerelli , known as the potato psyllid in a circulative and persistent manner. The psyllid gut is the first organ encountered by Lso and may act as a barrier to its transmission; however, the immune response of the gut to Lso infection remains largely uncharacterized. In this study, we examined autophagic responses in the gut of potato psyllids at early, mid, and late infection stages. Based on gene expression analyses, microscopic observations, and Western blotting, we found no clear evidence of autophagy induction despite Lso infection. Nevertheless, during mid and late phases of LsoB infection, we observed downregulation of the mechanistic target of rapamycin and decreased accumulation of ATG8-II. Notably, inducing autophagy with rapamycin significantly reduced LsoA titers in the psyllid guts after a 5-day acquisition access period and lowered transmission efficiency, while LsoB remained unaffected. These findings suggest that modulating autophagy in the gut of potato psyllids could be a promising strategy to limit LsoA acquisition and transmission, while highlighting LsoA and LsoB possess distinct molecular regulatory mechanisms in the psyllid gut. IMPORTANCE Liberibacters are devastating plant pathogens transmitted by psyllids. Because these bacteria are fastidious, the study of the molecular mechanisms involved in plant infection and transmission is difficult. Here, we determined that inducing autophagy in the potato psyllid can affect the acquisition and transmission of Lso haplotype A but not haplotype B. Comparing the host and vector responses to different liberibacters can help identify their transmission and infection mechanisms and find targets to disrupt these processes.
Accumulation and Transmission of ‘Candidatus Liberibacter solanacearum’ Haplotypes by the Nymphs of Two Psyllid Vectors
‘Candidatus Liberibacter solanacearum’ (Lso) is a plant pathogenic bacterium transmitted by psyllids that causes significant agricultural damage. Several Lso haplotypes have been reported. Among them, LsoA and LsoB are transmitted by the potato psyllid Bactericera cockerelli and infect solanaceous crops, and LsoD is transmitted by the carrot psyllid B. trigonica and infects apiaceous crops. Several studies evaluated the transmission of these haplotypes by adult psyllids. However, fewer data are available on the transmission of different Lso haplotypes by psyllid nymphs. In this study, we investigated the transmission of these three haplotypes by psyllid nymphs to expand our basic understanding of Lso transmission. Specifically, the objective was to determine if the haplotypes differed in their transmission rates by nymphs and if LsoA and LsoB accumulated at different rates in the guts of nymphs as it occurs in adults. First, we quantified LsoA and LsoB titers in the guts of third- and fifth-instar potato psyllid nymphs. We found similar LsoA titers in the two nymphal stages, while LsoB titer was lower in the gut of the third-instar nymphs compared to fifth-instar nymphs. Second, we assessed the transmission efficiency of LsoA and LsoB by third-instar nymphs to tomato plants, revealing that LsoA was transmitted earlier and with higher efficiency than LsoB. Finally, we examined the transmission of LsoD by carrot psyllid nymphs to celery plants and demonstrated an age-related difference in the transmission rate. These findings provide valuable insights into the transmission dynamics of different Lso haplotypes by nymphal vectors, shedding light on their epidemiology and interactions with their psyllid vectors.
A ‘Candidatus Liberibacter solanacearum’ Haplotype B-Specific Family of Candidate Bacterial Effectors
‘ Candidatus Liberibacter solanacearum’ (Lso) is a phloem-limited pathogen associated with devastating diseases in members of the Solanaceae and Apiaceae and vectored by several psyllid species. Different Lso haplotypes have been identified, and LsoA and LsoB are responsible for diseases in Solanaceae crops. Our efforts are aimed at identifying pathogenicity factors used by this bacterium to thrive in different hosts. Bacterial secreted proteins can play a role in host colonization or the manipulation of the host immune responses; these proteins are called effectors. In this study, we identified six LsoB-specific proteins with a conserved secretion motif as well as a conserved N-terminal domain in the mature protein. These proteins had different expression and secretion patterns but a similar subcellular localization in Nicotiana benthamiana leaves, suggesting that they play different roles regardless of their conserved secretion motif. One of these proteins, CKC_04425, was expressed at high levels in the insect vector and the host plant, indicating that it could play a role in both the plant and insect hosts, whereas the others were mainly expressed in the plant. One protein, CKC_05701, was able to efficiently suppress programmed cell death and reactive oxygen species production, suggesting that it may have a virulence role in LsoB-specific pathogenesis.
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