Insect immunity is a crucial process in the interaction between host and microorganisms; presence of pathogenic, commensal, or beneficial bacteria may result in different immune responses. In Hemiptera vectors of phytoplasmas, infected insects are amenable to carrying high loads of phytopathogens, besides hosting other bacterial affiliates, which have evolved different strategies to be retained; adaptation to host response and immunomodulation are key aspects of insect-symbiont interactions. Most of the analyses published have investigated insect immune response to pathogens, whereas few studies have been focused on the role of host immunity in microbiota homeostasis and vectorial capacity. Here the expression of immune genes in the leafhopper vector of phytoplasmas Euscelidius variegatus Kirschbaum is investigated following exposure to Asaia symbiotic bacteria, previously demonstrated to affect phytoplasma acquisition by leafhoppers. The expression of four genes related to major components of immunity was tested, i.e. defensin, phenoloxidase, kazal type 1 serine protease inhibitor and Raf, a component of the Ras/Raf pathway. The response was separately tested in whole insects, midguts and cultured hemocytes. Healthy individuals were tested along with specimens undergoing early- and late-stage phytoplasma infection. Beside that, the adhesion grade of Asaia strains was examined to assess whether symbionts may establish a physical barrier against phytoplasma colonization. Our results revealed a specific activation of Raf in midguts after double infection by Asaia and flavescence dorée phytoplasma. Increased expression was observed already in early stages of phytoplasma colonization. Gut-specific localization and timing of Raf activation are consistent with the role played by Asaia in limiting phytoplasma acquisition by E. variegatus, supporting the involvement of this gene in the anti-pathogen activity. On the other hand, limited attachment capability was found for Asaia under in vitro experimental conditions, suggesting a minor contribution of physical phytoplasma exclusion from the vector gut wall. By providing evidence of immune modulation played by Asaia strains, these results contribute to elucidating the molecular mechanisms regulating its interference with phytoplasma infection in E. variegatus. The involvement of Raf is particularly interesting in hemipterans, where a reduced innate immune system was reported, suggesting that other genes of the immune systems compensate lost functions.

Activation of immune related genes in leafhoppers by phytoplasmas and symbiotic bacteria / Elena, Gonella; Mandrioli, Mauro; Rosemarie, Tedeschi; Elena, Crotti; Marianna, Pontini; Alberto, Alma. - In: FRONTIERS IN PHYSIOLOGY. - ISSN 1664-042X. - 10:(2019), pp. 795-795. [10.3389/fphys.2019.00795]

Activation of immune related genes in leafhoppers by phytoplasmas and symbiotic bacteria

MANDRIOLI, Mauro
Data Curation
;
2019

Abstract

Insect immunity is a crucial process in the interaction between host and microorganisms; presence of pathogenic, commensal, or beneficial bacteria may result in different immune responses. In Hemiptera vectors of phytoplasmas, infected insects are amenable to carrying high loads of phytopathogens, besides hosting other bacterial affiliates, which have evolved different strategies to be retained; adaptation to host response and immunomodulation are key aspects of insect-symbiont interactions. Most of the analyses published have investigated insect immune response to pathogens, whereas few studies have been focused on the role of host immunity in microbiota homeostasis and vectorial capacity. Here the expression of immune genes in the leafhopper vector of phytoplasmas Euscelidius variegatus Kirschbaum is investigated following exposure to Asaia symbiotic bacteria, previously demonstrated to affect phytoplasma acquisition by leafhoppers. The expression of four genes related to major components of immunity was tested, i.e. defensin, phenoloxidase, kazal type 1 serine protease inhibitor and Raf, a component of the Ras/Raf pathway. The response was separately tested in whole insects, midguts and cultured hemocytes. Healthy individuals were tested along with specimens undergoing early- and late-stage phytoplasma infection. Beside that, the adhesion grade of Asaia strains was examined to assess whether symbionts may establish a physical barrier against phytoplasma colonization. Our results revealed a specific activation of Raf in midguts after double infection by Asaia and flavescence dorée phytoplasma. Increased expression was observed already in early stages of phytoplasma colonization. Gut-specific localization and timing of Raf activation are consistent with the role played by Asaia in limiting phytoplasma acquisition by E. variegatus, supporting the involvement of this gene in the anti-pathogen activity. On the other hand, limited attachment capability was found for Asaia under in vitro experimental conditions, suggesting a minor contribution of physical phytoplasma exclusion from the vector gut wall. By providing evidence of immune modulation played by Asaia strains, these results contribute to elucidating the molecular mechanisms regulating its interference with phytoplasma infection in E. variegatus. The involvement of Raf is particularly interesting in hemipterans, where a reduced innate immune system was reported, suggesting that other genes of the immune systems compensate lost functions.
2019
10
795
795
Activation of immune related genes in leafhoppers by phytoplasmas and symbiotic bacteria / Elena, Gonella; Mandrioli, Mauro; Rosemarie, Tedeschi; Elena, Crotti; Marianna, Pontini; Alberto, Alma. - In: FRONTIERS IN PHYSIOLOGY. - ISSN 1664-042X. - 10:(2019), pp. 795-795. [10.3389/fphys.2019.00795]
Elena, Gonella; Mandrioli, Mauro; Rosemarie, Tedeschi; Elena, Crotti; Marianna, Pontini; Alberto, Alma
File in questo prodotto:
File Dimensione Formato  
Author's Proof.pdf

Accesso riservato

Tipologia: Versione dell'autore revisionata e accettata per la pubblicazione
Dimensione 3.59 MB
Formato Adobe PDF
3.59 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
reprint_Frontiers 2019.pdf

Open access

Tipologia: Versione pubblicata dall'editore
Dimensione 3.47 MB
Formato Adobe PDF
3.47 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1176878
Citazioni
  • ???jsp.display-item.citation.pmc??? 6
  • Scopus 14
  • ???jsp.display-item.citation.isi??? 13
social impact