Jassar, Ola

ABSTRACT Vector-borne transmission of plant and animal pathogens requires active engagement of the vector’s immune system, as pathogens must overcome barriers and exploit host cellular mechanisms. Candidatus Liberibacter solanacearum (CLso) and C. L. asiaticus (CLas) are gram-negative, phloem-limited bacteria transmitted by the psyllids Bactericera trigonica and Diaphorina citri , respectively. Both pathogens induce endoplasmic reticulum (ER) stress and apoptosis in the midguts of their respective vectors, promoting their transmission. The protein kinase R-like endoplasmic reticulum kinase (PERK), a key regulator of ER stress and the unfolded protein response (UPR), plays a crucial role in modulating immunity. In this study, we investigated the role of PERK in CLso-induced apoptosis. PERK expression was downregulated in CLso-infected adult psyllids and midguts, yet immunostaining revealed a significant increase in phosphorylated (active) PERK in infected midguts, despite reduced gene expression. Additionally, ER stress-inducing treatments in both infected and uninfected psyllids demonstrated that CLso infection differentially regulates PERK expression. Interestingly, similar treatments in CLas-infected and uninfected D. citri yielded different results, suggesting species-specific immune responses. Furthermore, inhibition of PERK altered the expression of apoptosis-related genes in CLso-infected psyllids, indicating its involvement in CLso-induced apoptosis. Our findings suggest that PERK and UPR play a role in initiating immune responses at the ER interface in response to CLso, ultimately contributing to apoptosis, which may aid pathogen transmission. While the precise mechanisms by which CLso controls these processes remain unclear, this study provides new insights into how vector-borne plant and potentially animal pathogens manipulate host cellular pathways to enhance their spread. IMPORTANCE This study provides valuable insights into how vector-borne pathogens manipulate host cellular pathways to promote their survival and transmission. Candidatus Liberibacter solanacearum (CLso) and C. L. asiaticus (CLas) cause severe plant diseases, such as zebra chip in potatoes, carrot yellows, and huanglongbing (citrus greening), posing significant threats to global agriculture. By revealing the role of PERK and the unfolded protein response (UPR) in CLso-induced apoptosis, our findings contribute to the growing understanding of insect immunity and pathogen-host interactions. Understanding how CLso influences ER stress and immune signaling in its psyllid vector could lead to innovative strategies to disrupt pathogen persistence and transmission, ultimately supporting disease management efforts.

ABSTRACT Autophagy plays an important role against pathogen infection in many organisms; however, little has been done with regard to vector-borne plant and animal pathogens, that sometimes replicate and cause deleterious effects in their vectors. Candidatus Liberibacter solanacearum (CLso) is a fastidious gram-negative phloem-restricted plant pathogen and vectored by the carrot psyllid, Bactericera trigonica . The plant disease caused by this bacterium is called carrot yellows and has recently gained much importance due to worldwide excessive economical losses. Here, we demonstrate that calcium ATPase, cytosolic calcium, and most importantly Beclin-1 have a role in regulating autophagy and its association with Liberibacter inside the psyllid. The presence of CLso generates reactive oxygen species and induces the expression of detoxification enzymes in the psyllid midguts, a main site for bacteria transmission. CLso also induces the expression of both sarco/endoplasmic reticulum Ca2+pump (SERCA) and 1,4,5-trisphosphate receptors (ITPR) in midguts, resulting in high levels of calcium in the cellular cytosol. Silencing these genes individually disrupted the calcium levels in the cytosol and resulted in direct effects on autophagy and subsequently on Liberibacter persistence and transmission. Inhibiting Beclin1-phosphorylation through different calcium-induced kinases altered the expression of autophagy and CLso titers and persistence. Based on our results obtained from the midgut, we suggest the existence of a direct correlation between cytosolic calcium levels, autophagy, and CLso persistence and transmission by the carrot psyllid. IMPORTANCE Plant diseases caused by vector-borne Liberibacter species are responsible for the most important economic losses in many agricultural sectors. Preventing these diseases relies mostly on chemical sprays against the insect vectors. Knowledge-based interference with the bacteria-vector interaction remains a promising approach as a sustainable solution. For unravelling how Liberibacter exploits molecular pathways in its insect vector for transmission, here, we show that the bacterium manipulates calcium levels on both sides of the endoplasmic reticulum membrane, resulting in manipulating autophagy. Silencing genes associated with these pathways disrupted the calcium levels in the cytosol and resulted in direct effects on autophagy and Liberibacter transmission. These results demonstrate major pathways that could be exploited for manipulating and controlling the disease transmission.

AbstractCandidatus Liberibacter solanacearum (CLso) transmitted by the carrot psyllid, Bactericera trigonica causes carrot yellows in Israel, and has recently gained much importance due to the excessive economical loss. Understanding the interactions between CLso and the psyllid at the cellular level is fundamental for the disease management. Here, we demonstrate the role of calcium ATPase, cytosolic calcium and most importantly Beclin1 in regulating autophagy and its association with Liberibacter. Presence of CLso generates reactive oxygen species and induces the expression of the detoxification enzymes in the psyllid midguts. CLso also induces the expression of both sarco/endoplasmic reticulum Ca2+ pump (SERCA) and 1,4,5-trisphosphate receptors (ITPR) in the midguts, followed by high levels of calcium in the cytosol. Silencing these proteins individually disrupted the calcium levels in the cytosol leading to direct effects on autophagy and thus on Liberibacter. On the other hand, inhibiting Beclin1-phosphorylation through different calcium induced kinases altered the expression of autophagy and CLso abundance. This study establishes a direct correlation between cytosolic calcium levels, autophagy and CLso in the carrot psyllid midgut.

Candidatus Liberibacter solanacerum (CLso), transmitted by Bactericera trigonica in a persistent and propagative mode causes carrot yellows disease, inflicting hefty economic losses. Understanding the process of transmission of CLso by psyllids is fundamental to devise sustainable management strategies. Persistent transmission involves critical steps of adhesion, cell invasion, and replication before passage through the midgut barrier. This study uses a transcriptomic approach for the identification of differentially expressed genes with CLso infection in the midguts, adults, and nymphs of B. trigonica and their putative involvement in CLso transmission. Several genes related to focal adhesion and cellular invasion were upregulated after CLso infection. Interestingly, genes involved with proper functionality of the endoplasmic reticulum (ER) were upregulated in CLso infected samples. Notably, genes from the endoplasmic reticulum associated degradation (ERAD) and the unfolded protein response (UPR) pathway were overexpressed after CLso infection. Marker genes of the ERAD and UPR pathways were also upregulated in Diaphorina citri when infected with Candidatus Liberibacter asiaticus (CLas). Upregulation of the ERAD and UPR pathways indicate induction of ER stress by CLso/CLas in their psyllid vector. The role of ER in bacteria–host interactions is well-documented; however, the ER role following pathogenesis of CLso/CLas is unknown and requires further functional validation.