Abstract:Sharpshooters (Hemiptera: Cicadellidae: Cicadellinae) and spittlebugs (Hemiptera: Aphrophoridae: Aphrophorinae) have a worldwide distribution and are often associated with many crops. Because the geographic range of sharpshooters and spittlebugs often overlaps with the range of the plant pathogenic bacterium Xylella fastidiosa, the importance of these groups of insects in spreading X. fastidiosa rises to the level of a major socioeconomic problem. Managing diseases caused by X. fastidiosa is challenging for se… Show more
“…Nevertheless, all the progress made in the understanding of the traits that contribute to vector acquisition and transmission in X . fastidiosa , reported in several reviews (Redak et al ., 2004; Chatterjee et al ., 2008; Krugner et al ., 2019), will be helpful to interpret and inform our findings in the context of X . fastidiosa detection and spread in Europe.…”
Section: Introductionmentioning
confidence: 94%
“…In the Americas, the role of X . fastidiosa 's vectors, such as sharpshooters and spittlebugs, in the epidemiology and spread of the disease has been widely studied and reviewed (Redak et al ., 2004; Chatterjee et al ., 2008; Krugner et al ., 2019). Recently in Europe, transmission testing has revealed that the spittlebugs Philaenus spumarius , Philaenus italosignus , and Neophilaenus campestris are efficient vectors in the Apulia region, Italy (Cornara et al ., 2017; Cavalieri et al ., 2019).…”
In Europe, the meadow spittlebug Philaenus spumarius is the main known vector of the quarantine bacterium Xylella fastidiosa. So far detection and identification of X. fastidiosa has more often been performed from plant matrices than insects, mainly using a realâtime PCR and multilocus sequence typing (MLST) approach. Detection of X. fastidiosa in its insect vectors would enhance knowledge of the epidemiologic situation in France, specifically in the already infected Corsica and ProvenceâAlpesâCĂŽte dâAzur (PACA) regions. The aim of this study was to validate a methodological approach to detect X. fastidiosa in P. spumarius, analysed individually or in groups of 10, using realâtime PCR and MLST, and to apply the approach to more than 4,000 individuals collected between 2015 and 2019 from infected areas. The corresponding results expanded our knowledge of the epidemiology of X. fastidiosa in France: (a) X. fastidiosa subsp. multiplex including the sequence types ST6 and ST7 were identified in the insect vector; (b) the rate of positive insects per infected area was as high as 33.3% in Corsica or 50% in the PACA region; (c) positive adults were found during winter; and (d) the bacterial load in P. spumarius (droplet digital PCR) usually ranged from 103 to 104 cells per insect, but could be as high as 105 or 106 cells per insect for some individuals (13%). The subspecies and sequence types detected in P. spumarius corresponded to the situation officially reported for plants in the same areas.
“…Nevertheless, all the progress made in the understanding of the traits that contribute to vector acquisition and transmission in X . fastidiosa , reported in several reviews (Redak et al ., 2004; Chatterjee et al ., 2008; Krugner et al ., 2019), will be helpful to interpret and inform our findings in the context of X . fastidiosa detection and spread in Europe.…”
Section: Introductionmentioning
confidence: 94%
“…In the Americas, the role of X . fastidiosa 's vectors, such as sharpshooters and spittlebugs, in the epidemiology and spread of the disease has been widely studied and reviewed (Redak et al ., 2004; Chatterjee et al ., 2008; Krugner et al ., 2019). Recently in Europe, transmission testing has revealed that the spittlebugs Philaenus spumarius , Philaenus italosignus , and Neophilaenus campestris are efficient vectors in the Apulia region, Italy (Cornara et al ., 2017; Cavalieri et al ., 2019).…”
In Europe, the meadow spittlebug Philaenus spumarius is the main known vector of the quarantine bacterium Xylella fastidiosa. So far detection and identification of X. fastidiosa has more often been performed from plant matrices than insects, mainly using a realâtime PCR and multilocus sequence typing (MLST) approach. Detection of X. fastidiosa in its insect vectors would enhance knowledge of the epidemiologic situation in France, specifically in the already infected Corsica and ProvenceâAlpesâCĂŽte dâAzur (PACA) regions. The aim of this study was to validate a methodological approach to detect X. fastidiosa in P. spumarius, analysed individually or in groups of 10, using realâtime PCR and MLST, and to apply the approach to more than 4,000 individuals collected between 2015 and 2019 from infected areas. The corresponding results expanded our knowledge of the epidemiology of X. fastidiosa in France: (a) X. fastidiosa subsp. multiplex including the sequence types ST6 and ST7 were identified in the insect vector; (b) the rate of positive insects per infected area was as high as 33.3% in Corsica or 50% in the PACA region; (c) positive adults were found during winter; and (d) the bacterial load in P. spumarius (droplet digital PCR) usually ranged from 103 to 104 cells per insect, but could be as high as 105 or 106 cells per insect for some individuals (13%). The subspecies and sequence types detected in P. spumarius corresponded to the situation officially reported for plants in the same areas.
“…The Gram-negative xylem-limited non-circulative propagative gamma-proteobacterium Xylella fastidiosa was ranked as the more serious of the two insect-transmitted bacterial pathogens [4]. This system was reviewed recently [12,87,88,89,90]. Reproduction in the vector takes place on the cuticular surface of the anterior foregut [91].…”
Insects can be effective vectors of plant diseases and this may result in billions of dollars in lost agricultural productivity. New, emerging or introduced diseases will continue to cause extensive damage in afflicted areas. Understanding how the vector acquires the pathogen and inoculates new hosts is critical in developing effective management strategies. Management may be an insecticide applied to kill the vector or a host plant resistance mechanism to make the host plant less suitable for the vector. In either case, the tactic must act before the insect performs the key behavior(s) resulting in either acquisition or transmission. This requires knowledge of the timing of behaviors the insect uses to probe the plant and commence ingestion. These behaviors are visualized using electropenetrography (EPG), wherein the plant and insect become part of an electrical circuit. With the tools to define specific steps in the probing process, we can understand the timing of acquisition and inoculation. With that understanding comes the potential for more relevant testing of management strategies, through insecticides or host plant resistance. The primary example will be Candidatus Liberibacter asiaticus transmitted by Diaphorina citri Kuwayama in the citrus agroecosystem, with additional examples used as appropriate.
“…Xylella fastidiosa is a gram-negative bacterium and the causal agent of Pierce's disease in grapevines, as well as numerous other leaf scorch diseases [1]. Restricted to the xylem tissue of plants, X. fastidiosa is transmitted to grapevine by xylem-feeding insects, including sharpshooters, leafhoppers, and spittlebugs [2,3]. The transition between colonization of the insect vector and plant host is a highly regulated process, which relies on quorum sensing to transition between an adhesive biofilm state and systemic motility dependent on type IV pili [4,5].…”
Bacterial phytopathogen Xylella fastidiosa specifically colonizes the plant vascular tissue through a complex process of cell adhesion, biofilm formation, and dispersive movement. Adaptation to the chemical environment of the xylem is essential for bacterial growth and progression of infection. Grapevine xylem sap contains a range of plant secondary metabolites such as phenolics, which fluctuate in response to pathogen infection and plant physiological state. Phenolic compounds are often involved in host-pathogen interactions and influence infection dynamics through signaling activity, antimicrobial properties, and alteration of bacterial phenotypes. The effect of biologically relevant concentrations of phenolic compounds coumaric acid, gallic acid, epicatechin, and resveratrol on growth of X. fastidiosa was assessed in vitro. None of these compounds inhibited bacterial growth, but epicatechin and gallic acid reduced cell-surface adhesion. Cell-cell aggregation decreased with resveratrol treatment, but the other phenolic compounds tested had minimal effect on aggregation. Expression of attachment (xadA) and aggregation (fimA) related genes were altered by presence of the phenolic compounds, consistent with observed phenotypes. All four of the phenolic compounds bound to purified X. fastidiosa lipopolysaccharide (LPS), a major cell-surface component. Information regarding the impact of chemical environment on pathogen colonization in plants is important for understanding the infection process and factors associated with host susceptibility.
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