An effective framework for early warning and rapid response is a crucial element to prevent or mitigate the impact of biological invasions of plant pathogens, especially at ports of entry. Molecular detection of pathogens by using PCR-based methods usually requires a well-equipped laboratory. Rapid detection tools that can be applied as point-of-care diagnostics are highly desirable, especially to intercept quarantine plant pathogens such as Xylella fastidiosa, Ceratocystis platani and Phytophthora ramorum, three of the most devastating pathogens of trees and ornamental plants in Europe and North America. To this aim, in this study we developed three different loop mediated isothermal amplification (LAMP) assays able to detect each target pathogen both in DNA extracted from axenic culture and in infected plant tissues. By using the portable instrument Genie® II, the LAMP assay was able to recognize X. fastidiosa, C. platani and P. ramorum DNA within 30 min of isothermal amplification reaction, with high levels of specificity and sensitivity (up to 0.02 pg µL−1 of DNA). These new LAMP-based tools, allowing an on-site rapid detection of pathogens, are especially suited for being used at ports of entry, but they can be also profitably used to monitor and prevent the possible spread of invasive pathogens in natural ecosystems.
Invasive alien species represent a primary threat to biodiversity, economy and human health. International trade, tourism and other human activities break geographical barriers introducing non-native pathogenic organisms into new environments where they eventually find susceptible hosts and environments (Fisher et al. 2012; Migliorini et al. 2015; Santini et al. 2018). In Europe the accidental introduction of three quarantine pathogens, Xylella fastidiosa, Ceratocystis platani and Phytophthora ramorum with infected plants or wood material, has led to epidemics with heavy economic and ecological impacts.
Xylella fastidiosa is a bacterium reported on more than 350 different hosts (Denancè et al. 2017) and since 2013 is responsible for Olive Quick Decline Syndrome in Southern Italy (Apulia) (Saponari et al. 2013), more recently it has been found in Tuscany (Central Italy) (EPPO 2019); Ceratocystis platani is an ascomycetous fungus reported as the causal agent of Canker Stain Disease (CSD) of plane tree (Platanus) in urban and natural ecosystems (Lehtijärvi et al. 2018; Tsopelas et al. 2017). Phytophthora ramorum is an oomycete causing Sudden Oak Death (SOD) in the USA (Rizzo et al. 2002) but the pathogen has also been found in European ornamental nurseries (Werres et al. 2001) and in plantations of Japanese larch (Larix kaempferi) in Great Britain (Brasier and Webber 2010).
In the last decades alien plant pathogens are exponentially establishing in Europe (Santini et al. 2013). The European Union (EU) has an open-door phytosanitary system, which means that plants not specifically regulated can enter, therefore, inspections are concentrated on well-known pests and mostly limited to visual examination of aerial parts of plants. Traditional inspection methods are time consuming and labor-intensive, requiring specialized laboratories and expert operators. Furthermore, the first disease symptoms can occur after a long latent phase of the infection and they may be non-specific (e.g. X. fastidiosa), hampering detection efforts and, therefore, timely management of potential outbreaks. Serological and immunoassay-based methods are available, but their low sensitivity and specificity make them unreliable for phytosanitary inspections. For these reasons, sensitive and specific tools for effective phytosanitary inspection and interception are required to prevent new pathogen introductions. Nowadays, the high specificity and sensitivity of molecular DNA-based technologies allows detection of pathogens in the early stages of infection, when they are present at low DNA concentrations (Bilodeau et al. 2007; Chandelier et al. 2006; Harper et al. 2010; Luchi et al. 2013; Rollins et al. 2016). Although many of these methods have been used routinely in the laboratory, most of them are not transferable for field inspection, seriously limiting their adequacy for point-of-care application (Lau and Botella 2017). Point-of-care methods, besides being sensitive and specific, should also be simple and fast, producing results that are easy to interpret and demanding minimal equipment and facilities (Tomlinson et al. 2010a). For these purposes, an affordable LAMP (Loop mediated isothermal amplification) technique (Notomi et al. 2000), seems to be the most suitable. Recently several LAMP assays have been developed for both field and lab use especially for human and animal diseases and food safety control (Abdulmawjood et al. 2014; Lucchi et al. 2010). Up to now, even if many LAMP-based assays were developed for plant pathogens (Chen et al. 2013; Dai et al. 2012; Hansen et al. 2016; Harper et al. 2010; Moradi et al. 2014; Peng et al. 2013; Sillo et al. 2018; Tomlinson et al. 2007), only a few tests (Bühlmann et al. 2013; Franco Ortega et al. 2018; Harrison et al. 2017; Tomlinson et al. 2010b, 2013) were optimized and applied on portable instrument for on-site use. The use of portable detection instruments is a major driving force to achieve point-of-use, and real-time monitoring of analysed samples, allowing rapid detection.
The aim of this study was to optimize a reliable, fast and sensitive diagnostic assay using a LAMP portable instrument for early detection of X. fastidiosa, C. platani, and P. ramorum. These new protocols will be available to be used for research aims and for phytosanitary inspection, in order to prevent further introductions and spread of these pathogens.
Materials and methods
Microbial strains and DNA extraction
In addition to the targeted pathogens, fungal and bacterial species phylogenetically related to target pathogens, as well as out-group species and common host colonizers were used to optimize the molecular assay (Table 1).
Mycelium of fungal and oomycete isolates (stored at 4 °C in the IPSP-CNR collection) was grown on 300PT cellophane discs (Celsa, Varese, Italy) on potato dextrose agar (PDA; Difco, Detroit, MI, USA) in 90 mm Petri dishes and maintained in the dark at 20–25 °C according to species requirements. After 7–10 days the mycelium was scraped from the cellophane surface and stored in 1.5 mL microfuge tubes at − 20 °C.
Bacterial strains (stored at − 80 °C in the IPSP-CNR collection) were grown on Luria–Bertani (LB) agar for 24 h at 25 ± 2 °C. Single colonies were picked-up and transferred to tubes containing 5 mL of LB that were incubated in an orbital shaker at 25 ± 2 °C and 90 rpm overnight. One millilitre of each suspension was used for DNA extraction. Fungal and oomycete DNA suitable for molecular analysis was extracted from mycelium by using the EZNA Plant DNA Kit (Omega Bio-tek, Norcross, GA, USA), as described by Migliorini et al. (2015). DNA from bacteria was extracted by using EZNA Bacteria DNA Kit (Omega Bio-tek) according to the procedure described by the manufacturer. DNA from the quarantine pathogens X. fastidiosa, E. amylovora, P. ramorum and P. lateralis were kindly provided by different collectors (see Table 1). Concentration of extracted DNA was measured using a Nanodrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).
Plant DNA samples
Plant samples were analyzed from naturally infected hosts including: (i) Two symptomatic plants of each of the following Mediterranean maquis species were collected in March 2019: Rhamnus alaternus, Calicotome spinosa, Cistus incanus, Spartium junceum, Prunus dulcis, affected by X. fastidiosa subsp. multiplex (recently detected by Tuscany Regional Phytosanitary Service—EPPO 2019); (ii) 10 Platanus × acerifolia symptomatic trees infected by C. platani (Florence, Italy).
About 80 mg (fresh weight) of plant material, i.e. leaves of Mediterranean maquis species and wood of P. × acerifolia plants, were used for genomic DNA extraction by using two different extraction protocols: (i) on-site by using Plant Material DNA extraction kit (OptiGene), according to manufacturer’s instructions. Briefly, small pieces of plant material (c.a. 80 mg) were placed in a 5 mL bijou with ball bearing and 1 mL lysis buffer. Bijous were shaken vigorously for 1 min to ground the plant material. Plant material solution (10 μL) was transferred into a vial containing 2 mL dilution buffer and mixed. Finally, 3 μL of dilution buffer containing DNA has been used as template in a LAMP assay;
ii) in laboratory by using EZNA Plant DNA Kit (Omega Bio-tek). Plant material of all the collected samples for DNA extraction was transferred to 2 mL microfuge tubes with two tungsten beads (3 mm) (Qiagen) and 0.4 mL lysis buffer P1 EZNA Plant DNA Kit (Omega Bio-tek, Norcross, GA, USA) then ground with a TissueLyser (Qiagen) (30 oscillations/s for 1 min). DNA was extracted from all samples using the EZNA Plant DNA Kit (Omega Bio-tek) (Migliorini et al. 2015).
In addition to the above samples, the optimization of LAMP assay was conducted by using the following DNA samples stored at − 80 °C (IPSP-CNR DNA collection): (i) 10 DNA samples extracted from symptomatic Olea europaea leaves with X. fastidiosa subsp. pauca infections. DNA was kindly provided by M. Saponari (IPSP-CNR, Bari) and extracted in CTAB buffer (Loconsole et al. 2014); (ii) 10 DNA samples from symptomatic Viburnum tinus leaves affected by P. ramorum extracted by using EZNA Plant DNA Kit (Omega Bio-tek).
As negative control, fresh tissue collected from 10 healthy plant of each tested species (Olea europaea, Rhamnus alaternus, Calicotome spinosa, Cistus incanus, S. junceum, Prunus dulcis, Platanus × acerifolia and Viburnum tinus) were extracted by using both Plant Material DNA extraction kit (OptiGene) and EZNA Plant DNA Kit (Omega Bio-tek), as previously described.
LAMP primer design
The six LAMP primers included: two outer primers (forward primer, F3; backward primer, B3) two inner primers (forward inner primer, FIP; backward inner primer, BIP) and two loop primers (forward loop primer, FLP; backward loop primer, BLP), as required by LAMP reaction (Notomi et al. 2000). Primers were designed using LAMP Designer software (OptiGene Limited, Horsham, UK) (Table 2) on the basis of the consensus sequences of the ribosomal RNA gene (ITS1-5.8 S-ITS2) for P. ramorum (KC473522) and C. platani (EU426554.1), while for X. fastidiosa the ribosome maturation factor (RimM) gene belonging to Co.Di.Ro strain was chosen (JUJW01000001). All designed primers were synthesized by MWG Biotech (Ebersberg, Germany) and are reported in Table 2. The specificity of newly designed primers was further tested using nucleotide–nucleotide BLAST® (Basic Local Alignment Search Tool; http://www.ncbi.nlm.nih.gov/BLAST) (Altschul et al. 1990).
Real-time LAMP assay conditions
Real-time LAMP reactions were performed and optimised on the portable real-time fluorometer Genie® II (OptiGene Limited, Horsham, UK). DNA samples were amplified for 30 min in Genie® Strips (OptiGene Limited, Horsham, UK) with eight 0.2 mL isothermal reaction tubes with a locking cap providing a closed-tube system. Each isothermal amplification reaction was performed in duplicate, in a final volume of 25 μL. The reaction mixture contained 15 μL Isothermal Master Mix (ISO-001) (OptiGene Limited, Horsham, UK), 7 μL LAMP primer mixture (at final concentrations 0.2 μM of each F3 and B3, 0.4 μM of each FLP and BLP and 0.8 μM of each FIP and BIP) and 3 μL of template DNA. For each run two tubes including 3 μL dd-water were tested as No Template Control (NTC). LAMP amplification reactions were run at 65 °C for 30 min, followed by an annealing analysis from 98 to 80 °C with ramping at 0.05 °C per second that allow the generation of derivative melting curves (Abdulmawjood et al. 2014).
The main parameters used by Genie® II system to assess the positivity of a sample are: amplification time (tamp) and amplicon annealing temperature (Ta). The tamp is the time (expressed in min) where the fluorescence second derivative of the signal reaches its peak above the baseline value, while the Ta is the temperature (expressed in °C) at which double-stranded DNA product dissociates into single strands.
Specificity and sensitivity of real-time LAMP assays
For each target pathogen (X. fastidiosa, C. platani and P. ramorum) the specificity of the real-time LAMP assay was tested by using genomic DNA extracted from bacterial, fungal or oomycete strains (Table 1), at a final concentration of 10 ng μL−1. The limit of detection (LOD) of the LAMP assay was tested by using an 11-fold 1:5 serial dilution (ranging from 10 ng μL−1 to 0.001 pg μL−1) of each standard DNA template (X. fastidiosa - Co.Di.Ro strain; C. platani - isolate Cp24; P. ramorum - isolate Pram).
Real-time LAMP assay in naturally infected plants
To check the suitability of extracted plant DNA for downstream analysis the cytochrome oxidase (COX) gene was used as endogenous plant gene according to Tomlinson et al. (2010a) (Table 2).
The effectiveness of the real-time LAMP assay was then tested on DNA extracted from naturally infected hosts (Olea europaea, Rhamnus alaternus, Calicotome spinosa, Cistus incanus, S. junceum, Prunus dulcis, Platanus × acerifolia and Viburnum tinus) to detect each respective target pathogen (X. fastidiosa, C. platani and P. ramorum). For each plant species, additional healthy plants DNA were also included as negative control.
Real-time quantitative PCR assay
To validate the LAMP assay, for each target pathogen, DNA samples (from microbial and plant tissue) were also tested by real-time quantitative PCR (qPCR) based on TaqMan chemistry.
Primers and TaqMan® MGB probe for the DNA quantification of X. fastidiosa with the StepOnePlus™ Real-Time PCR System (Applied Biosystems, Forster City, CA, USA) were designed using Primer Express™ 3.0 software (Applied Biosystems). The DNA sequence of the ribosome maturation factor (RimM) gene (CoDiRO strain) was obtained from the ‘National Center for Biotechnology Information’ (NCBI) (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi) (accession number JUJW01000001). The TaqMan® MGB probe was labelled with 6-carboxy-fluorescein (FAM) at the end, and a non-fluorescent quencher (NFQ) with minor groove binder (MGB) ligands, at the 3′ end. Primers and probe are reported in Table 2. The length of the amplification product was 60 bp. The identity of the amplicon sequence was determined by comparing with other fungal species with the Standard nucleotide–nucleotide BLAST (blast n) of the NCBI.
DNA samples were assayed in MicroAmp Fast 96-well Reaction Plates (0.1 mL) closed with optical adhesive and using the StepOnePlus™ Real-Time PCR System (Applied Biosystems).
The real-time PCR reaction was performed in a final volume of 25 µL. Each tube contained: 300 nM forward primer (Eurofins MWG Operon, Ebersberg, Germany); 300 nM reverse primer (Eurofins MWG Operon); 200 nM fluorogenic probe (Applied Biosystems); 12.5 µL TaqMan™ Universal Master Mix (Applied Biosystems); 5 µL DNA template.
Each DNA sample was assayed in three replicates. Four wells containing 5 µL sterile water each were used for a No-Template Control (NTC) without any nucleic acid. The PCR protocol was 50 °C (2 min); 95 °C (10 min); 40 cycles of 95 °C (30 s), 60 °C (1 min).
For each replicate the Ct value, defined as the point at which the Reporter fluorescent signal first became statistically significant against the background, was utilised to quantify the sample. Measurements of X. fastidiosa DNA in unknown samples were achieved by interpolation from a standard curve generated with a DNA standard (Co.Di.Ro. strain), which was amplified in the same PCR run.
Real time PCR protocols for C. platani and P. ramorum were those described in Luchi et al. (2013) and Migliorini et al. (2018), respectively.
For each 1:5 serial dilution (ranging from 10 ng µL−1 to 0.128 pg µL−1) of each target pathogen, the correlation analysis was carried out between amplification time (tamp) for LAMP assay and threshold cycle (Ct) for qPCR.
Specificity of real-time LAMP assay
For each target pathogen (X. fastidiosa, C. platani and P. ramorum) the nucleotide–nucleotide BLAST ® search showed a complete homology (100%) between the LAMP amplicon sequences designed in the current study and the sequences of the same pathogen available in GenBank database (NCBI).
BLAST ® search did not find sequence identity between the LAMP X. fastidiosa amplicon and the other species present in GenBank, while the P. ramorum LAMP amplicon showed 99% homology (due to only 2 bases of differences in the ITS region) with P. lateralis sequences. Similarly, the C. platani LAMP amplicon showed complete homology (100%) with C. fimbriata and 99% homology with C. neglecta, C. ecuadoriana and C. manginecans.
LAMP assay was able to detect DNA of each target pathogen (X. fastidiosa, C. platani and P. ramorum) with positive results in the first time of the isothermal amplification (tamp c.a. 7 min for P. ramorum and X. fastidiosa; c.a. 8 min for C. platani) (Fig. 1). All DNA samples of X. fastidiosa that include X. fastidiosa (Co.Di.Ro), X. fastidiosa subsp. fastidiosa (Xff) and X. fastidiosa subsp. multiplex (Xfm) were positively amplified by LAMP assay, and the melting curve showed a specific peak (Ta ranged between 88.78 and 88.98 °C) (Table 1). Bacterial DNA extracted from the other strains were not amplified by LAMP assay (Table 1). LAMP results were also confirmed by qPCR by using the designed primers (Xf_Fw and Xf_Rev) and probe (Xf_Pr) for X. fastidiosa (Tables 1, 2).
The real-time LAMP assay designed for C. platani was able to detect C. fimbriata strains belonging to different hosts and geographic origin (Table 1), whereas the qPCR assay gave negative results for these isolates. Similarly, the LAMP primers designed for P. ramorum were able to amplify P. lateralis DNA with melting temperatures very close to each other (Table 1). The other Phytophthora species included in this work either were not amplified or showed different amplification curves (with different tamp) or melting curves (with different Ta) (Table 1). For each designed LAMP assay DNA from outgroup species and common host colonizer species were not amplified, as confirmed by qPCR (Table 1).
Sensitivity of real-time LAMP assays
The values of limit of detection of LAMP assays (LODLAMP) were always very low, ranging from 0.02 pg μL−1 for X. fastidiosa and C. platani and 0.128 pg μL−1 for P. ramorum, (Fig. 2; Table 3). P. ramorum qPCR assays had the same sensitivity as LAMP (LODqPCR = 0.128 pg μL−1). The qPCR assays for the other two pathogens were more sensitive than LAMP with lower detection limits (X. fastidiosa, LODqPCR = 0.001 pg μL−1; C. platani, LODqPCR = 0.005 pg μL−1) (Fig. 2).
We also observed a very strong correlation between the tamp of the LAMP assay and Ct value of the qPCR in the same set of DNA samples (X. fastidiosa: R2 = 0.97; C. platani R2 = 0.95; P. ramorum R2 = 0.98) (Fig. 3).
Real-time LAMP detection in plant samples
LAMP analyses carried out on plant host DNA were further validated by COX gene amplification, showing a specific melting peak at Ta = 85 °C for each analysed plant sample (both healthy and infected tissues) (Fig. 1). COX gene amplification was a reliable internal positive control, confirming host DNA extractions were successful by using both on-site DNA extraction kit (OptiGene) and laboratory commercial kit (Omega Bio-tek).
All symptomatic host plant samples (Olea europaea, Rhamnus alaternus, Calicotome spinosa, Cistus incanus, S. junceum, Prunus dulcis, Platanus × acerifolia and Viburnum tinus) were amplified successfully with the LAMP assay designed for each target pathogen (X. fastidiosa, C. platani and P. ramorum, respectively).
Symptomatic plant tissue showed similar Ta obtained from DNA of axenic cultures of each target pathogen (Table 1; Fig. 1), confirming the specificity of each LAMP assay to detect pathogens in infected plant tissues.
No amplification nor melting curve was obtained by applying the LAMP primers to healthy samples confirming the specificity of the LAMP optimized assay.
In this work LAMP assays for detecting X. fastidiosa, P. ramorum and C. platani, optimized for a portable instrument in real time were developed. LAMP-based assays optimized in this study allow a complete analysis (amplification and annealing) in only 30 min, starting to have positive amplification from ca. 7 min (Table 1). To our best knowledge no previous LAMP assay has been developed for C. platani. qPCR showed higher sensitivity with respect to LAMP in X. fastidiosa and C. platani detection, while for P. ramorum LOD was the same as that of LAMP.
The opportunity to have an accurate and rapid detection of the three quarantine pathogens considered in this study directly in the field by a portable instrument, represents a great advantage to preventing introductions and for applying control measures. Most of the LAMP-based assays recently developed for plant pathogens, including the one developed for P. ramorum by Tomlinson et al. (2007) and for X. fastidiosa by Harper et al. (2010), are based on laborious and time-consuming isothermal amplification reactions (Table 3). As an example, the LAMP protocol adopted by EPPO for X. fastidiosa detection and developed by Harper et al. (2010), requires ca. 60 min to amplify all the isolates tested by the author and to consistently amplify ca. 250 copies of template for reaction (corresponding to 1.4 pg μL−1 pathogen DNA) in host (Vitis vinifera) DNA. In comparison, the assay developed in the current study requires only ca. 15 min to amplify 0.02 pg μL−1 of X. fastidiosa DNA in dd-water. The use of a simple colour change method to assess the positive result of LAMP-tested samples (e.g. Hydroxynaphtal blue dye used in Harper et al. 2010), could be particularly suited for use in the field, but opening the tube to add the colorimetric dye makes the method extremely vulnerable to carryover contamination due to the very large amount of product generated by LAMP reaction (Tomlinson et al. 2007). Furthermore, some colorimetric dyes reagents can completely inhibit the LAMP reaction at the concentration needed to produce a colour change visible with the naked eye (Tomlinson et al. 2007) and even though they may be possible to observe in a laboratory environment, they are difficult to detect in the field due to the different light conditions at different times of the day (Lau and Botella 2017), leading to false negative results or to losses in detection sensitivity. In addition, the interpretation of positive results from colour changes in colorimetric dyes is very subjective, requiring experienced staff. On the contrary, the main parameters used to assess the positivity of a sample in a LAMP real-time assay, as the one developed in the present work, are amplification time (tamp) and annealing temperature (Ta) resulting by fluorescence analysis results provided by the instrument.
The EPPO diagnostic protocol (PM 7/24) for X. fastidiosa describes a field LAMP assay based on the paper by Yaseen et al. (2015). In this paper authors optimized the Harper et al. (2010) assay for a portable instrument, but they do not report the sensitivity of the assay, strongly limiting its application due to the risk of false negatives.
LAMP assays developed in this study are specific and able to detect the target species, both from pure DNA and from DNA obtained from plant infected tissues. Some cross reactions have been observed in species genetically closely related to target species (for C. platani/C. fimbriata and P. ramorum/P. lateralis); however, their Ta is one-two degrees higher than that of the target organisms (89–90 °C vs. 88 °C), allowing a correct detection (Table 1).
A positive amplification sharing the same Ta of that of P. ramorum and C. platani (88 °C) was obtained only with P. lateralis and C. fimbriata, respectively. These species are almost morphologically indistinguishable and phylogenetically very close (De Beer et al. 2014; Kroon et al. 2012; Martin et al. 2014), but they were reported on very different hosts: P. lateralis attacks Chamaecyparis spp. and other Cupressaceae (Hansen et al. 2000; Robin et al. 2011), and C. fimbriata is the agent of sweet potato black rot (Okada et al. 2017).
The results of LAMP assays were also validated by those obtained from qPCR assays. The new TaqMan qPCR assay developed in this study for targeting X. fastidiosa is able to amplify all the X. fastidiosa tested subspecies with high efficiency excluding other tested bacteria species (Table 1). Furthermore, its sensitivity (0.001 pg μL−1) is much higher than that of the qPCR TaqMan assays developed by Harper et al. (2010) and by Francis et al. (2006) (both EPPO official diagnostic qPCR for X. fastidiosa) which has a detection limit of 0.05 pg μL−1, corresponding to 20 copies of template for reaction.
The use of rapid, specific and sensitive point-of-care methods like the LAMP assays developed in this study could enable phytosanitary services to make immediate management decisions, helping in containing environmental and economic losses. The application of such a portable diagnostic tool, requiring minimum equipment and a few, if any, specific scientific skills could be profitably used to check the health status of live plants or plant parts at the points of entry or in field, thus reducing time of analyses, thus allowing a prompt reaction. In conclusion, the results presented in this study show how an advance in technology can provide efficient tools to prevent the introduction or limit the spread of diseases that can have severe economic, ecological and sociological consequences.
loop mediated isothermal amplification
real-time quantitative polymerase chain reaction
amplicon annealing temperature
limit of detection
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NL, AS conceived and designed the experiments. CA, NL, ALP, PB, FP, AS performed the field work and the experiments. AR provided bacterial strains. CA, NL, AS analyzed the data. CA, NL, AS wrote the paper. AR, PC made contribution to the revision of the manuscript. All authors read and approved the final manuscript.
The authors wish to thank colleagues who kindly provided DNA and isolates of fungi and bacteria species used in this work: R. Ioos and N. Schenck (ANSES, France), G.P. Barzanti (CREA, Italy), S.O. Cacciola (Università di Catania, Italy), T. Dogmus (Süleyman Demirel University, Isparta, Turkey), T. Jung (University of Algarve, Portugal), S. Leonhard, J. Schumacher (BBA, Germany), A. Pérez-Sierra (Forest Research, UK), C. Robin (INRA, France), P. Tsopelas, (NAGREF, Greece), A. Vettraino (Università della Tuscia, Italy), M. Saponari, D. Boscia (IPSP-CNR, Bari, Italy), G. Marchi (University of Florence, Italy). Authors are also grateful to Tuscany Regional Phytosanitary Service for helping to the sampling in the field. Authors wish to warmly thank Dr. Trudy Paap (FABI, University of Pretoria, South Africa) for the thorough critical review of the text and for English language editing of the manuscript. The authors would like to thank the editor and the anonymous referees for their comments and suggestions that greatly improved the manuscript.
The authors declare that they have no competing interests.
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The data supporting the conclusions of this article are included within the article. Data and materials can also be requested from the corresponding author.
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This article does not contain any studies with human participants or animals performed by any of the authors.
This study was funded by European Union’s Horizon 2020 Research and Innovation Programme (grant No 771271). Part of this work has been funded by the project “PATINVIVA—Invasive pathogens in nurseries: new tools for the certification of pathogen exemption of material for export”—Fondazione Cassa di Risparmio di Pistoia e Pescia (grant No 255).
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Authors and Affiliations
Institute for Sustainable Plant Protection, National Research Council (IPSP-CNR), Via Madonna del Piano 10, 50019, Sesto Fiorentino, Firenze, Italy
Chiara Aglietti, Nicola Luchi, Alessia Lucia Pepori, Paola Bartolini, Francesco Pecori, Aida Raio & Alberto Santini
Department of Agrifood Production and Environmental Sciences (DISPAA), University of Florence, Piazzale delle Cascine 28, 50144, Firenze, Italy
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