Figures
Abstract
Sustainable management of crop productivity and health necessitates improved understanding of the ways in which rhizosphere microbial populations interact with each other, with plant roots and their abiotic environment. In this study we examined the effects of different soils and cultivars, and the presence of a soil-borne fungal pathogen, Verticillium dahliae, on the fungal microbiome of the rhizosphere soil and roots of strawberry plants, using high-throughput pyrosequencing. Fungal communities of the roots of two cultivars, Honeoye and Florence, were statistically distinct from those in the rhizosphere soil of the same plants, with little overlap. Roots of plants growing in two contrasting field soils had high relative abundance of Leptodontidium sp. C2 BESC 319 g whereas rhizosphere soil was characterised by high relative abundance of Trichosporon dulcitum or Cryptococcus terreus, depending upon the soil type. Differences between different cultivars were not as clear. Inoculation with the pathogen V. dahliae had a significant influence on community structure, generally decreasing the number of rhizosphere soil- and root-inhabiting fungi. Leptodontidium sp. C2 BESC 319 g was the dominant fungus responding positively to inoculation with V. dahliae. The results suggest that 1) plant roots select microorganisms from the wider rhizosphere pool, 2) that both rhizosphere soil and root inhabiting fungal communities are influenced by V. dahliae and 3) that soil type has a stronger influence on both of these communities than cultivar.
Citation: Nallanchakravarthula S, Mahmood S, Alström S, Finlay RD (2014) Influence of Soil Type, Cultivar and Verticillium dahliae on the Structure of the Root and Rhizosphere Soil Fungal Microbiome of Strawberry. PLoS ONE 9(10): e111455. https://doi.org/10.1371/journal.pone.0111455
Editor: Kevin McCluskey, Kansas State University, United States of America
Received: June 10, 2014; Accepted: October 2, 2014; Published: October 27, 2014
Copyright: © 2014 Nallanchakravarthula et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All pyrosequencing data files are available from the European Nucleotide Archive database (accession number PRJEB6260) http://www.ebi.ac.uk/ena/.
Funding: This work was funded by Grant No. 2007-1689 to RF from The Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Plants roots influence the structure and diversity of soil microbial communities through their energy-rich exudates [1], [2], creating diverse rhizosphere communities in close proximity to the roots [3]. The roots are colonized by a subset of these microorganisms, creating both a rhizoplane community on the surface and an endophytic compartment. Discrimination between pathogens and beneficial mutualists or commensals is controlled by an immune system [4], but the mechanisms underlying the selection of different core microbiomes [5] by different plant species are still poorly understood. Recent studies of bacteria associated with the roots or rhizosphere of Arabidopsis thaliana grown in geochemically distinct soils [6] have shown that they are both strongly influenced by soil type but that the root endophytic compartments from two soils contain overlapping, low complexity communities that are enriched in Actinobacteria and specific families belonging to the Proteobacteria. Differential relative abundance of Actinocorallia sp. has also been shown in different ecotypes of A. thaliana [7].
Plant host genetics plays a significant role in the selection of microbial communities associated with roots [8]–[10]. This selection has important implications for plant health and growth since rhizosphere microorganisms are known to have a variety of positive or negative effects. These include plant growth stimulation, antagonism against pathogens and effects on carbon sequestration and phytoremediation. Rhizosphere and root endophyte microorganisms are increasingly being used on a commercial scale for plant protection as biocontrol agents and biofertilizers [11]–[13]. Management of such microorganisms requires a thorough understanding of their interaction with other microorganisms sharing the same ecological niche. Some attempts have been made to study the effect of biocontrol agents on microbial communities [14]–[17], however studies focusing on the influence of soil-borne fungal plant pathogens on microbial community structures are less frequent [18]–[21]. Most of the inoculation studies with pathogens or biocontrol agents have been more focused on bacterial communities than on fungal communities.
The rhizosphere is a dynamic region for many biological processes and interactions [1], [11], [12], [22]–[25] and empirically-based management strategies for sustainable cultivation need to be based on a more rigorous understanding of the functional basis of the mechanisms underlying the various biotic interactions taking place [26].
Microbial community structure in the rhizosphere and the root endophytic compartment is shaped by soil characteristics as well as by plant genotype [6], [7], [20], [27]–[31]. Soils in organically managed strawberry fields have been shown to have greater functional activity and higher functional gene diversity than soils in conventionally managed fields [32]. The strawberry rhizosphere has been shown to harbour distinct microbial communities containing Streptomyces, Rhizobium and Nocardia [28], [31] and in the presence of Verticillium dahliae, a soil-borne fungal pathogen, it is dominated by Pseudomonas spp. populations [27]. Studies have also shown that strawberry cultivars respond differently to the inoculation of arbuscular mycorrhizal fungi (AMF) [33], [34]. Sporulation of Phytophthora fragariae associated with strawberry plants colonized by AMF has also been shown to be reduced in comparison to that in non-AMF colonized plants [35].
Strawberry (Fragaria×ananassa) is grown for its berries in many countries and different cultivars have been developed for commercial production. Rhizosphere bacterial biomass and activity, fruit quality and yield have all been shown to vary under different management systems. Soil microorganisms have been shown to be indirectly involved in determining the fruit quality [32], [36]. Verticillium dahliae is one of several plant pathogens that affect plant growth and yield in different plant species, including strawberry [37]–[41]. The pathogen forms conidia and microsclerotia that germinate in the presence of the root exudates, whereupon germ tubes enter the plant roots. The pathogen can persist as microsclerotia on dead plant tissues, or in the soil for more than 10 years [39]–[41]. In strawberry as few as two microsclerotia per gram of soil can cause 100% wilt [42] and this pathogen is difficult to combat with current management strategies. In a field trial, biocontrol using Trichoderma harzianum and Trichoderma viride against V. dahliae reduced wilting in strawberry by 60%. An indirect effect against V. dahliae through induced systemic resistance by Paenibacillus alvei K165 has also been observed in Arabidopsis sp. [43], [44].
Studies have shown that the presence of fungal (Phytophthora cinnamomi) and bacterial pathogens, (Liberibacter asiaticus and Erwinia carotovora (Pectobacterium carotovorum)) increases the diversity of Bacteroidetes and Alphaproteobacteria in particular [18], [20], [21]. Such changes also facilitate the selection, by the plant, of taxa including those with antimicrobial properties [27], [45].
Plant resistance is one of the effective strategies in plant protection and attempts have been made to study effects of resistant and susceptible cultivars on microbial communities [46]–[48]. The results of these studies demonstrate that plant genotype can have a significant impact on soil microbial community structure, and differences in the rhizosphere microbial community have been suggested to contribute to the differences in resistance to disease. Whether this impact is independent of the soil type is not evident from these studies.
Many earlier studies involving soil microbial community analyses have been conducted using either cultivation-dependent approaches or molecular methods such as T-RFLP, DGGE, cloning and Sanger sequencing which are now proven to underestimate the total microbial diversity [49], [50]. More recent studies using high throughput techniques have revealed taxa that were not detected with previous methods [51].
In this study we investigated the impact of plant genotype on the fungal community structure in different soil types in the presence and absence of the soil-borne fungal pathogen, V. dahliae. We used 454 pyrosequencing to analyze the rhizosphere soil- and root fungal communities in different strawberry cultivars, grown in differently managed soils. We hypothesized that the structure of microbial communities in the rhizosphere soil and roots is determined by both the cultivar and soil type, and may also be re-structured in the presence of the pathogen.
Materials and Methods
Experimental soils and plant material
Four cultivars of strawberry, Florence, Honeoye, Senga Sengana, and Zephyr, and two of the three different soils used in this study were the same as those described in a previous study by Santos-González et al. [30]. The cultivars were selected on the basis of their breeding year, yield level and disease tolerance. Honeoye and Florence were bred after 1978, Zephyr and Senga Sengana before 1966. Honeoye is considered to be a high yielding cultivar and Florence and Senga Sengana are considered to be tolerant to V. dahliae [52]–[54]. In our figures the conventionally managed soil from Kristianstad is referred to as “conventional” and the organically managed soil from Hörby as “organic” [30]. The field in Hörby was managed organically with appropriate crop rotations since 1983 and pre-cropped with potatoes prior to sampling in 2009. The experimental field in Kristianstad is conventionally managed and was planted with strawberry in 2008. The two agricultural fields are located 38 km apart in Southern Sweden. These sites are on private land and permission to collect soil was obtained from the owners Sune Abrahamsson (Kristianstad) and Ingvar Åkesson (Hörby). The soil collection did not involve endangered or protected species. The Kristianstad site at (56° 06′ N, 14° 01′ E) and the Hörby site at (55° 50′ N, 13° 35′ E) have different soil properties. The physico-chemical traits of the two field soils are described by Santos-González et al. [30]. The soils had similar textural properties (8.5–11% clay, 29–35% silt, 51–58% sand) and bulk density (1.05–1.07 g cm−3). However the pH, C, N and P levels of the Hörby soil were significantly (P<0.05) higher than those of the Kristianstad soil (6.36 vs. 5.97; 2.1% vs. 1.61%; 0.17% vs. 0.14%; 181 mg kg−1 vs. 113 mg kg−1). The third “soil” was a peat-based growth substrate (Hasselfors Garden Special, Hasselfors Garden AB, Örebro, Sweden) containing 60% light peat, 25% black peat, 15% sand (0.5–4 mm) and 0.050 kg m−3 multisport/FTE36, 2.0 kg m−3 dolomite and 4.5 kg m−3 limestone, amended with 1.3 kg m−3 fertilizer (N14:P7:K15, pH-6.0), and is used for commercial greenhouse cultivation in Sweden.
Pathogen inoculum
The pathogen isolate used was V. dahliae 12086, originating from strawberry roots and available from the Food and Environment Agency, York, UK (see http://www.q-bank.eu/). It was purified and grown in potato dextrose broth (PDB per L, 12 g Accumedia, Michigan, USA) as stationary cultures for 20 days at 24°C. The mycelial mat thus obtained was macerated carefully in diluted potato dextrose broth (1:10 water v/v). A preparatory study was conducted with the suspension thus obtained to confirm the pathogenicity of the test pathogen. On the basis of the results from the preparatory study (data not shown), 30 ml mycelial suspension was inoculated in V. dahliae-treatments. The plant roots were injured by inserting a 0.9 cm diameter cork borer into the root volume in three locations to stimulate the pathogen infection. No dead-cell, or chitin controls were used but the control plants without the pathogen were treated in a similar manner but with suspension medium not containing fungal mycelium.
Experimental design
An outdoor experiment was conducted by growing the four cultivars in the three soils as specified in a previous study [30]. In brief, the soils were prepared before planting with one plantlet per pot (13×13 cm×25 cm deep), placed outdoors and irrigated as needed. The plantlets were taken from storage under refrigeration and were about 5 cm tall with three to four leaves and roots about 15 cm long.
The cumulative fresh berry weight per plant was recorded during the experimental period of 14 weeks. The rhizosphere soil was collected from three replicates 12 weeks after planting and 14 weeks after planting. To sample the rhizosphere soil, the plants were carefully removed from the pots and roots with tightly adhering soil were suspended in phosphate-buffered saline solution (PBS, 0.14 M NaCl, 0.0027 M KCl, 0.010 M phosphate buffer, pH 7.4, Medicago, Sweden) for 30 minutes. The rhizosphere soil thus collected was centrifuged at 8000 RPM for 10 minutes at 4°C (Biofuge PrimoR, Heraeus Sorvall), the roots were once again washed carefully under aerated tap water. The soil pellet and the roots were stored at −20°C for further analyses.
Analysis of fungal communities
DNA extraction and selection of samples for pyrosequencing.
DNA extraction methods differ in their efficiency of extraction from different taxa and for the rhizosphere samples, we used two different nucleic acid extraction methods and the resultant DNA extracts were checked individually for quality and reproducibility on a DGGE (denaturing gradient gel electrophoresis) gel following PCR amplifications. The first method was based on ‘CTAB’ (hexadecyltrimethylammonium bromide) [55] that involved extraction of nucleic acids from 0.5 g of soil. The soil samples were weighed in 2 ml ‘Lysing matrix B’ tubes (Fisher Scientific, USA) containing 0.5 ml CTAB buffer (120 mM and pH 8.0) and 0.5 ml phenol: chloroform: isoamylalcohol (25:24:1 V/V). The cells were lysed at 5000 RPM for 30 seconds in a bead beater (Precellys 24; Bertin Technologies, France). Proteins and solvent residues were removed using chloroform and isoamyl alcohol (24:1) followed by further precipitation using polyethylene glycol (30%). The precipitated DNA was washed with ice-cold ethanol (70%), air dried and re-suspended in 30 µl of MilliQ water and stored at −20°C for further analysis.
The second nucleic acid extraction method was based on MOBIO ‘RNA power soil’ total RNA isolation and DNA elution accessory kits (MOBIO laboratories, California, USA) according to manufacturer’s recommendations. The concentration and quality of extracted DNA were assessed using NanoDrop (ND-1000 Nanodrop technologies, USA). The banding profiles of these two methods differed so the DNA from these two extraction methods was pooled and used as a mixed template for generating PCR amplicons for pyrosequencing. Prior to pyrosequencing, the control samples were subjected to DGGE-based analysis following PCR amplification. The DGGE banding profiles showed higher numbers of bands at the first sampling, 12 weeks after planting, than at 14 weeks (data not shown). Pyrosequencing was therefore carried out on samples from 12 weeks.
For the analysis of root-associated fungi we chose to analyze two cultivars Honeoye, susceptible to V. dahliae, and Florence, tolerant to V. dahliae, growing in each of the two field soils. Nucleic acids from roots were extracted using DNeasy plant mini kit (Qiagen, Germany) according to the manufacturer’s recommendations. Roots were carefully washed to remove the soil particles attached to the roots and soil removal was microscopically confirmed. They were gently washed three times with 0.1% Triton x100 for two minutes, thereafter washed with sterile milliQ water. All collected roots were subsequently freeze-dried for 48 h (CoolSafe, ScanLaf A/S, Denmark), homogenised by milling in 2 ml tubes containing 2.38 mm diameter stainless steel beads (MOBIO laboratories, California, USA) in a bead-beater for 30 s twice. 50 mg of the homogenised root material was used for nucleic acid extraction. The extracted DNA was quantified and used as a template for generating PCR amplicons for pyrosequencing.
Pyrosequencing
Pyrosequencing analysis of the fungal communities was carried out as described by Ihrmark et al. [56] using primers fITS7 (5′GTGARTCATCGAATCTTG-3′) and ITS4 (5′TCCTCCGCTTATTGATATGC-3′) [57]. In brief, each 50 µl reaction mixture consisted of 200 µM of dNTPs, 2.75 mM MgCl2, primers at 500 nM and 300 nM, 0.025 U polymerase (DreamTaq Green, Thermo Scientific, Waltham, MA) in buffer. The thermocycling conditions were: 5 min at 94°C; 35 cycles (30 s at 94°C; 30 s at 57°C; 30 s at 72°C); 7 min at 72°C. Three technical replicates were run for each sample. To ascertain PCR amplification efficiency and to rule out any possible contamination, all reactions were run with positive and negative controls. The PCR amplification products were analyzed on 1% (w/v) agarose gels pre-stained with Nancy red-520 (Sigma Aldrich, USA). The triplicate PCR products of each sample were pooled, purified using Agencourt AMPure, PCR purification kit (Beckman Coulter, Massachusetts, USA) and quantified using a Qubit Fluorometer (Invitrogen, USA). Equimolar concentrations of samples were pooled and the resultant mixture was freeze-dried (CoolSafe, ScanLaf A/S, Denmark) overnight. Pyrosequencing was carried out on 2×1/8th of a GS FLX Titanium Pico Titer Plate (LGC Genomics, Germany and MACROGEN, South Korea) according to the manufacturer's instructions (Roche, Branford, CT).
Bioinformatic analysis
The SCATA pipeline (Sequence Clustering and Analysis of Tagged Amplicons, http://www.scata.mykopat.slu.se) was used to analyze the sequence data from 72 rhizosphere samples and 24 root samples. The quality control and data filtering involved removal of singletons, low quality sequences, tags and primer missing sequences, followed by removal of sequences shorter than 200 base pairs (after primer and tag trimming). We used default parameters of the SCATA pipeline except that the proportion of primer match was set at 0.9. Sequences were assembled into clusters by single-linkage clustering with a 98.5% sequence similarity threshold. The most common genotype/sequence of the cluster was used to represent the operational taxonomic units (OTUs). All the representative sequences of the clusters were identified using the NCBI (National Center for Biotechnology Information) database and the nucleotide blast ‘BLASTn’ program. The most common sequence from each cluster was analyzed manually for blasting. With the exception of rarefaction analysis, only sequences with ≥95% identity were chosen for these analyses.
The pyrosequencing data have been deposited at ENA (European Nucleotide Archive) under accession number PRJEB6260.
Statistical analyses
Statistical analyses were conducted using a significance level of p≥0.05. The Chao-1 index (PAST (PAleontological STatistics), version 2.17b) was calculated to obtain the number of OTUs present in the four cultivars grown in three different soils with and without V. dahliae. The bar diagrams were generated using Microsoft Excel and the significance of the OTU data was estimated using ANOVA with MINITAB. The relative abundance of OTUs was used for Non-metric multi-dimensional scaling (NMDS) ordination performed with ‘PAST’ using Bray-Curtis dissimilarity indices. Numbers of OTUs were calculated for selected phyla and plotted in Microsoft Excel and their significance was calculated by using ANOVA. SIMPER (similarity percentage) analysis (PAST ver 2.17b) was performed using relative abundance data in order to identify the OTUs that were contributing to the differences among treatments. The rarefaction was estimated using Analytic Rarefaction (Ver 1.3, UGA Stratigraphy Lab, USA).
Results and Discussion
Bioinformatic analysis of root and rhizosphere material associated with the cultivars Honeoye and Florence revealed a total of 577 unique OTUs following quality control filtering and removal of singletons. In total 360 OTUs were associated with rhizosphere soil and 307 OTUs were associated with roots, with an overlap of 90 OTUs between the two compartments. Analysis of the rhizosphere soil associated with roots of all four cultivars revealed 128 OTUs common to both the field soils but only 16 fungal OTUs that were common to all three soils. In conventionally managed soil 63 OTUs were common to all four cultivars, with 28 common OTUs in organically managed soil and 18 common OTUs in peat-based growth substrate.
Cluster analysis of the community structure of the 50 most abundant fungal taxa was performed. These taxa constituted 90% of the reads in roots and 70% of the reads in rhizosphere soil. The analysis (Figure 1) revealed a clear separation between fungal communities from the rhizosphere soil and those from the roots. Within each of these compartments there was a clear separation according to soil type (ANOSIM p = 0.0001). The root associated community structure of the organically managed soil showed a statistically significant (ANOSIM p = 0.015) separation between Verticillium inoculated and uninoculated treatments. Rhizosphere soil communities in a peat-based substrate formed a distinct cluster with a clear separation between V. dahliae inoculated and equivalent, non-inoculated treatments. In a similar analysis of rhizosphere soil communities associated with four different strawberry cultivars, Honeoye, Florence, Senga-Sengana and Zephyr (Figure S1) clear effects of soil type were visible. Differences due to cultivar were less evident. These results are consistent with the finding of Santos-González et al [30] that soil type, but not cultivar, shapes the assemblages of arbuscular mycorrhizal fungi associated with strawberry roots in these soils.
These OTUs constituted 90% of the total reads in roots and 70% of the reads in rhizosphere soil. The clustering is based on paired group linkage using the Bray-Curtis similarity measure. Only OTUs with ≥95% identity are included.
Additional NMDS analysis of the fungal community structure in the rhizosphere soil of all four cultivars (Figure S2) showed a statistically significant effect of Verticillium inoculation in conventionally managed soil (ANOSIM p = 0.005) and peat based substrate (ANOSIM p = 0.0004). No such clear separation was evident in organically managed soil.
Rank abundance plots of the 30 most abundant fungal taxa in each of the rhizosphere and root compartments in the absence of Verticillium (Figure 2) revealed that the structure of the fungal microbiome in these two compartments is markedly different, with little overlap. The dominant OTUs from the roots were found at low frequencies in the rhizosphere, while OTUs that were dominant in the rhizosphere were absent or occurred at very low frequencies in the roots, in both field soils (Figure 2a–d). These results are in agreement with other recent studies of bacterial microbiomes of Arabidopsis thaliana and the fungal microbiome of Pisum sativum [6], [7], [58] that also show distinct communities in the rhizosphere and root endophyte compartments. Within each soil this pattern was the same for both Honeoye and Florence, however there were large differences between the rank abundance distributions of taxa between the two soils. The same lack of overlap between root and rhizosphere soil fungal communities was found in the presence of Verticillium (data not shown).
Only OTUs with ≥95% identity are included.
The top seven most abundant taxa in conventionally managed rhizosphere soil, irrespective of strawberry cultivar were Cryptococcus terreus, Mortierella elongata, Cryptococcus terricola, Panaeolus foenisecii, Phoma eupyrena, Gibellulopsis nigrescens and an unidentified Leptosphaeria species, together accounting for 33% and 37% of the total reads for the Honeoye and Florence treatments respectively. In the organically managed rhizosphere soil the top six fungal taxa accounted for 50% of the reads but Trichosporon dulcitum was the dominant taxon, accounting for 35% and 30% of the total reads in the Honeoye and Florence treatments respectively. Trichosporon dulcitum was also detected in the conventionally managed soil, but at much lower frequencies (3% and 2%). Trichosporon dulcitum is a soil-borne basidiomycetous yeast. Utilization of benzene compounds [59] and biodegradation of phenol [60] have been shown in T. dulcitum, but the ability of this yeast to interact with plants and fungal pathogens is still unclear. Other members of the Trichosporonales have been found in the rhizosphere and ectomycorrhizosphere in soil from a Nothofagus pumilio forest [61]. In the latter study T. dulcitum was found in the bulk soil but not in the rhizosphere and no other information appears to be available concerning the possible associations of this species with plant roots.
The most common fungal taxa found in roots included Entrophospora sp shylm 131, Leptodontidium sp. C2 BESC 319 g, Ilyonectria macrodidyma, Fusarium spp., Phoma sp BEA-2010, Scytalidium lignicola, Acremonium strictum, Exophiala sp. O 1 LILB 26 5 g, and Paraconiothyrium sporulosum. The composition of fungal taxa in roots of plants growing in the organically managed soil was characterised by high abundance of Leptodontidium, whereas both Leptodontidium and Entrophospora were dominant in roots of plants growing in the conventionally managed soil. Differences in the abundance of fungal taxa in relation to soil types and strawberry cultivar are discussed below in a separate SIMPER analysis.
The total numbers of fungal OTUs in the absence of Verticillium inoculation, were generally highest in the rhizosphere of plants grown in conventionally managed soil, intermediate in organically managed soil and lowest in peat-based growth substrate, indicating a strong effect of soil type on fungal diversity. The lowest fungal diversity in the peat based growth substrate is most likely due to its simple composition [62]. In the presence of Verticillium no clear difference between the field soils was evident but numbers of OTUs were lower in the peat-based growth substrate (ANOVA p≤0.05) (Figure 3a).
Only OTUs with ≥95% identity are included. Asterisks indicate statistical significance between control and Verticillium dahliae treatments within each soil (* = p≤0.05, ANOVA). Vertical bars represent mean values and error bars show ±1 SE (n = 3).
In conventionally managed soil, Verticillium inoculation resulted in a consistent reduction (20–45%) in the number of fungal OTUs in the rhizosphere that was statistically significant (p≤0.05) in Senga Sengana and Zephyr (Figure 3a). In contrast, in the organically managed soil, inoculation with Verticillium resulted in significant (p≤0.05) increases (114% and 125%) in the total numbers of ascomycete and basidiomycete OTUs respectively in the rhizosphere of Florence (Figure 3a). The reasons for this increase are not clear but may reflect differences in the quality and quantity of root exudates of Florence, which is considered to be a Verticillium tolerant cultivar [63]. Basidiomycota were less abundant in the rhizosphere but also showed a consistent reduction in response to Verticillium in plants grown in conventionally managed soil. This was statistically significant only in Honeoye, but evident as a trend in the other cultivars.
Ascomycota dominated, both in roots and in rhizosphere (Figure 3a & b). Verticillium inoculation had no statistically significant effects on the number of Ascomycotan OTUs in roots of Honeoye and Florence grown in conventional soil but these were significantly reduced by 21% in Honeoye in response to Verticillium inoculation in organically managed soil. The mean number of Ascomycotan taxa in the roots of Florence was 38% lower in the presence of Verticillium but this reduction lacked statistical support.
Numbers of Basidiomycotan OTUs in roots were negligible, but 17 Glomeromycotan OTUs were found, including Entrophospora sp. shylm 131, Rhizophagus intraradices and Rhizophagus clarus. Numbers of Glomeromycotan OTUs in Honeoye roots in organically managed soil were significantly increased by 50% (Figure 3b) in response to Verticillium inoculation. Xu et al [58] have also shown that the relative abundance of different fungal phyla varies in root and rhizosphere samples of Pisum sativum depending upon whether the plant is healthy or infected with the pathogen Aphanomyces euteiches.
Rarefraction analysis of the numbers of OTUs associated with different numbers of sequences from root and rhizosphere samples are shown in Figure S3. The root treatment samples approached saturation, with asymptotes between 80 and 120 OTUs, although fewer root treatments were analysed in this study since only the roots of Honeoye and Florence plants were examined. The species accumulation curves for rhizosphere soil samples included three growth substrates and four cultivars and were not saturated, suggesting that not all taxa were detected. However there was a high degree of consistency between the most abundant taxa in the rhizosphere for both soils (Figure 2), suggesting that the dominant taxa in these communities were adequately described.
SIMPER (Similarity Percentage) analysis of OTUs from rhizosphere and root samples was performed to identify the species primarily contributing to the difference in community structure between the two compartments and the results are summarized in Table S1.
In Florence the effect of Verticillium inoculation on fungal community structure was stronger in roots (71% in organically managed soil, 60% in conventionally managed soil) than in the rhizosphere, (46% in organically managed soil, 52% in conventionally managed soil). In Honeoye the contribution to Verticillium induced differences was lower but the values for roots (53% in organic soil and 54% in conventionally managed soil) were still higher than in the rhizosphere (41% in organic soil and 48% in conventionally managed soil).
The numbers of reads matching Verticillium genera were 564 in roots compared to only 35 in the rhizosphere soil suggesting that V. dahliae was more abundant in the roots than the rhizosphere. This is not surprising since V. dahliae is a root pathogen but the low number of reads in rhizosphere soil may reflect primer bias against V. dahliae or low template concentrations at the time of sampling. Van der Mark et al [64] reported detection of significantly more pathogen DNA of Aphanomyces euteiches and Phytophthora medicaginis in a susceptible variety of alfalfa than in the resistant variety [64]. In our study, in the conventionally managed soil, significantly higher numbers of reads (345) matching Verticillium were detected in Verticillium inoculated treatments of Honeoye, the susceptible cultivar, than in Florence, a tolerant cultivar (17 reads). In the organically managed soil the numbers of reads were lower than 17 in both cultivars, suggesting that this soil was possibly suppressive in character, while the conventionally managed soil was more conducive to Verticillium.
The top ten OTUs contributing to the differences between control and Verticillium treatments across all treatments, identified using SIMPER analysis, are shown in Figures 4a–b. The dominant OTUs in roots occur at low frequencies in the rhizosphere soil while OTUs that dominate in the rhizosphere soil are either absent or occur at low frequencies in the roots. This discrepancy between root and rhizosphere soil communities is in agreement with recent observations in other plants [6], [7], [58]. Cryptococcus spp., Gibellulopsis sp., Mortierella spp. and Phoma sp. were abundant in rhizosphere in the conventionally managed soil while Trichosporon dulcitum and Fusarium equiseti were abundant in rhizosphere of organically managed soil. In contrast, Leptodontidium sp. dominated the roots in organically managed soil, while Entrophospora sp. dominated the roots of plants in conventionally managed soil (Figure 4a, b).
A) Rhizosphere soil (29–39%), B) Roots (61–74%).
Verticillium dahliae was among the top ten species contributing to differences in fungal community structure between inoculated and uninoculated roots of Honeoye plants growing in conventionally managed soil and had a higher relative abundance in inoculated treatments than in uninoculated treatments (1.7%, 4.6%). The relative abundance of Verticillium dahliae was much lower in roots of Florence plants (0.56%, 0.27%). This result is consistent with the greater tolerance of Florence to Verticillium than Honeoye. The fungus was not present amongst the top ten taxa in organically managed soil, irrespective of strawberry cultivar or inoculation treatment.
Leptodontidium sp C2 BESC319g was one of the main contributors to differences in community structure in response to inoculation with Verticillium. In conventionally managed soil its relative abundance varied between 12 and 14% and was not affected by Verticillium inoculation. However in organically managed soil its relative abundance was much higher, increasing from 28.5% to 45.6% in Honeoye and from 17.3% to 49% in Florence, in the presence of Verticillium inoculation. This suggests that Leptodontidium sp C2 BESC319g may be one of the biological factors associated with the suppressive character of the organically managed soil. Leptodontidium orchidicola has been shown to decrease the negative effect of V. dahliae in tomato, but only at low levels of pathogen inoculation [65].
Root endophytes are known to produce secondary metabolites that may have anti-microbial effects on plant pathogens and biological control of Verticillium dahliae by root endophytes has been successfully demonstrated [66]–[70]. In the present study the absence of V. dahliae associated with increased abundance of Leptodontidium in roots of plants grown in organically managed soil, suggests that this fungus may be of functional significance in protection against vascular pathogens. Further research on root endophytic communities should provide new biological control strategies for improving plant health [25].
OTUs of other broadly pathogenic taxa were also detected in our study. Examples of these include species belonging to the genera Scytadilium, Fusarium, Pyrenochaeta, Phoma and Cephalosporium but their pathogenicity to strawberry remains largely unknown. The relative abundance of these taxa was affected by both cultivar and soil type in the presence of Verticillium (Figure 4 a–b).
The effect of soil type, cultivar and pathogen inoculation on OTUs was also reflected in the plant performance measured as berry yield in this study (Figure S4). The strawberry yield differed significantly between the four cultivars in all three soils (conventional p = 0.0014, organic p = 0.0087 and peat p = 0.0022) in the absence of V. dahliae. Honeoye and Zephyr were selected because of their high yielding potential. In the present study these two cultivars produced the highest yields in the conventionally managed soil and peat based growth substrates but their mean yields decreased in response to inoculation with V. dahliae. The response of Florence to inoculation with the pathogen varied according to the soil type demonstrating a significant positive effect in conventionally managed soil and a significantly negative response in organically managed soil. Senga Sengana had the poorest yields in all three soils irrespective of the presence or absence of V. dahliae (Figure S4).
Concluding remarks
The results of this study show a marked difference between the fungal community structure in rhizosphere soil and that of fungi growing on or within the root tissues of strawberry plants. This suggests that plant roots select microorganisms from the wider rhizosphere soil pool, but further experiments with sampling at multiple time points are necessary to shed further light on this phenomenon. Strong differences in community structure were also observed between different soils, but differences between fungal communities colonizing roots of different cultivars were less clear. Inoculation with the pathogen V. dahliae had a significant influence on community structure and decreased the number of rhizosphere soil- and root-inhabiting fungi in several treatments. Lower numbers of Verticillium reads were detected in the roots of Florence, a tolerant cultivar, than in roots of Honeoye. Significant decreases in the number of ascomycete fungal OTUs occurred in roots of both Honeoye and Florence cultivars in response to V. dahliae in organically managed soil. The rhizosphere soil of these plants was characterised by high relative abundance of Trichosporon dulcitum, while the roots were dominated by Leptodontidium sp. C2 BESC 319 g. It is possible that the high abundance of these fungi may cause some suppression of pathogens such as V. dahliae but the role of these two fungi in plant protection is still unclear.
Supporting Information
Figure S1.
Cluster analysis of the 50 most abundant fungal operational taxonomic units (OTUs) in the rhizosphere of four strawberry cultivars, Honeoye, Florence, Senga Sengana and Zephyr, grown in conventionally and organically managed soils or a peat-based growth substrate, with and without Verticillium dahliae. These OTUs constituted 90% of the total reads in roots and 70% of the reads in rhizosphere soil. The clustering was based on paired group linkage using the Bray-Curtis similarity measure. All OTUs with ≥95% identity are included.
https://doi.org/10.1371/journal.pone.0111455.s001
(TIF)
Figure S2.
Non-metric multidimensional scaling (NMDS) analysis of the effects of inoculation with Verticillium dahliae on community structure of fungi colonising the rhizosphere of four different strawberry cultivars, Honeoye, Florence, Senga Sengana and Zephyr, grown in three different soils.
https://doi.org/10.1371/journal.pone.0111455.s002
(TIF)
Figure S3.
Sample based rarefaction curves of all fungal operational taxonomic units (OTUs) in rhizosphere soil and roots of strawberry using Analytic Rarefaction (Ver 1.3, UGA Stratigraphy Lab, USA).
https://doi.org/10.1371/journal.pone.0111455.s003
(TIF)
Figure S4.
Fresh berry weight (g/pot) of four different strawberry cultivars, Honeoye, Florence, Senga Sengana and Zephyr, grown in conventionally and organically managed soils or a peat-based growth substrate, with and without Verticillium dahliae. Asterisks indicate statistically significant differences (p<0.05) between control and Verticillium dahliae inoculated treatments within each soil. Vertical bars represent mean values and error bars indicate ±1SE (n = 6).
https://doi.org/10.1371/journal.pone.0111455.s004
(TIF)
Table S1.
Similarity percentage (SIMPER) analysis of all fungal operational taxonomic units (OTUs) in rhizosphere and roots of four different strawberry cultivars, Honeoye, Florence, Senga Sengana and Zephyr, grown in conventionally and organically managed soils or a peat-based growth substrate, with and without Verticillium dahliae. All OTUs with ≥95% identity are included. (ND = not determined).
https://doi.org/10.1371/journal.pone.0111455.s005
(DOCX)
Acknowledgments
Prof. Christina Dixelius, Swedish University of Agricultural Sciences, Uppsala is acknowledged for providing the pathogen isolate.
Author Contributions
Conceived and designed the experiments: SN SM SA RDF. Performed the experiments: SN. Analyzed the data: SN SM SA RDF. Contributed reagents/materials/analysis tools: SN SM SA RDF. Contributed to the writing of the manuscript: SN SM SA RDF.
References
- 1. Morgan JAW, Bending GD, White PJ (2005) Biological costs and benefits to plant-microbe interactions in the rhizosphere. J Exp Bot 56: 1729–1739.
- 2.
Drigo B, Pijl AS, Duyts H, Kielak AM, Gamper HA, et al.. (2010) Shifting carbon flow from roots into associated microbial communities in response to elevated atmospheric CO2. P Natl Acad Sci 107: 10938 −10942.
- 3. Philippot L, Raaijmakers JM, Lemanceau P, van der Putten WH (2013) Going back to the roots: the microbial ecology of the rhizosphere. Nat Rev Microbiol 11: 789–799.
- 4. Jones JDG, Dangl JL (2006) The plant immune system. Nature 444: 323–329.
- 5. Shade A, Handelsman J (2012) Beyond the Venn diagram: the hunt for a core microbiome. Env Microbiol 14: 4–12.
- 6. Lundberg DS, Lebeis SL, Paredes SH, Yourstone S, Gehring J, et al. (2012) Defining the core Arabidopsis thaliana root microbiome. Nature 488: 86–90.
- 7. Bulgarelli D, Rott M, Schlaeppi K, Ver Loren van Themaat E, Ahmadinejad N, et al. (2012) Revealing structure and assembly cues for Arabidopsis root-inhabiting bacterial microbiota. Nature 488: 91–95.
- 8. Wissuwa M, Mazzola M, Picard C (2008) Novel approaches in plant breeding for rhizosphere-related traits. Plant Soil 321: 409–430.
- 9. Smith KP, Goodman RM (1999) Host variation for interactions with beneficial plant associated microbes. Ann Rev Phytopathol 37: 473–491.
- 10. Andreote FD, Rocha UND, Araújo WL, Azevedo JL, Van Overbeek LS (2010) Effect of bacterial inoculation, plant genotype and developmental stage on root-associated and endophytic bacterial communities in potato (Solanum tuberosum). Antonie van Leeuwenhoek 97: 389–399.
- 11. Lodewyckx C, Vangronsveld J, Porteous F, Moore ERB, Taghavi S, et al. (2002) Endophytic bacteria and their potential applications. Crit Rev Plant Sci 21: 583–606.
- 12. Ryan RP, Germaine K, Franks A, Ryan DJ, Dowling DN (2008) Bacterial endophytes: recent developments and applications. FEMS Microbiol Lett 278: 1–9.
- 13. Berg G (2009) Plant-microbe interactions promoting plant growth and health: perspectives for controlled use of microorganisms in agriculture. App Microbiol Biotechnol 84: 11–18.
- 14. Edel-Hermann V, Brenot S, Gautheron N, Aimè S, Alabouvette C, et al. (2009) Ecological fitness of the biocontrol agent Fusarium oxysporum Fo47 in soil and its impact on the soil microbial communities. FEMS Microbiol Ecol 68: 37–45.
- 15. Gao G, Yin D, Chen S, Xia F, Yang J (2012) Effect of biocontrol agent Pseudomonas fluorescens 2P24 on soil fungal community in cucumber rhizosphere using T-RFLP and DGGE. PLoS ONE. 7(2): e31806.
- 16. Zhao Y, Li W, Zhou Z, Wang L, Pan Y, et al. (2005) Dynamics of microbial community structure and cellulolytic activity in agricultural soil amended with two biofertilizers. Eur J Soil Bio 41: 21–29.
- 17. Hoitink H, Boehm M (1999) Biocontrol within the context of soil microbial communities: A substrate-dependent phenomenon. Ann Rev Phytopathol 37: 427–446.
- 18. Trivedi P, Duan Y, Wang N (2010) Huanglongbing, a systemic disease, restructures the bacterial community associated with citrus roots. Appl Environ Microb 76: 3427–3436.
- 19. Trivedi P, He Z, Van Nostrand JD, Albrigo G, Zhou J, et al. (2012) Huanglongbing alters the structure and functional diversity of microbial communities associated with citrus rhizosphere. ISME J 6: 363–383.
- 20. Reiter B, Pfeifer U, Schwab H, Sessitsch A (2002) Response of endophytic bacterial communities in potato plants to infection with Erwinia carotovora subsp. atroseptica. Appl Environ Microb 68: 2261–2268.
- 21. Yang C, Crowley DE, Menge JA (2001) 16S rDNA fingerprinting of rhizosphere bacterial communities associated with healthy and Phytophthora infected avocado roots. FEMS Microbiol Ecol 35: 129–136.
- 22. Kent AD, Triplett EW (2002) Microbial communities and their interactions in soil and rhizosphere ecosystems. Ann Rev Microbiol 56: 211–236.
- 23. Johansson JF, Paul LR, Finlay RD (2004) Microbial interactions in the mycorrhizosphere and their significance for sustainable agriculture. FEMS Microbiol Ecol 48: 1–13.
- 24. Hartmann A, Schmid M, Tuinen D van, Berg G (2008) Plant-driven selection of microbes. Plant Soil 321: 235–257.
- 25. Rodriguez RJ, White JF Jr, Arnold AE, Redman RS (2009) Fungal endophytes: diversity and functional roles. New Phytol 182: 314–330.
- 26. Mendes R, Kruijt M, de Bruijn I, Dekkers E, van der Voort M, et al. (2011) Deciphering the rhizosphere microbiome for disease-suppressive bacteria. Science 332: 1097–1100.
- 27. Berg G, Zachow C, Lottmann J, Gotz M, Costa R, et al. (2005) Impact of plant species and site on rhizosphere-associated fungi antagonistic to Verticillium dahliae Kleb. Appl Environ Microb 71: 4203–4213.
- 28. Costa R, Götz M, Mrotzek N, Lottmann J, Berg G, et al. (2006) Effects of site and plant species on rhizosphere community structure as revealed by molecular analysis of microbial guilds. FEMS Microbiol Ecol 56: 236–249.
- 29. Weller DM, Raaijmakers JM, Gardener BBM, Thomashow LS (2002) Microbial populations responsible for specific soil suppressiveness to plant pathogens. Ann Rev Phytopathol 40: 309–348.
- 30. Santos-González JC, Nallanchakravarthula S, Alström S, Finlay RD (2011) Soil, but not cultivar, shapes the structure of arbuscular mycorrhizal fungal assemblages associated with strawberry. Microb Ecol 62: 25–35.
- 31. Smalla K, Wieland G, Buchner A, Zock A, Parzy J, et al. (2001) Bulk and rhizosphere soil bacterial communities studied by denaturing gradient gel electrophoresis: plant-dependent enrichment and seasonal shifts revealed. Appl Environ Microb 67: 4742–4751.
- 32. Reeve JR, Schadt CW, Carpenter-Boggs L, Kang S, Zhou J, et al. (2010) Effects of soil type and farm management on soil ecological functional genes and microbial activities. ISME J 4: 1099–1107.
- 33. Fan L, Dalpé Y, Fang C, Dubé C, Khanizadeh S (2011) Influence of arbuscular mycorrhizae on biomass and root morphology of selected strawberry cultivars under salt stress. Botany 89: 397–403.
- 34. Norman JR, Atkinson D, Hooker JE (1996) Arbuscular mycorrhizal fungal-induced alteration to root architecture in strawberry and induced resistance to the root pathogen Phytophthora fragariae. Plant Soil 185: 191–198.
- 35. Norman JR, Hooker JE (2000) Sporulation of Phytophthora fragariae shows greater stimulation by exudates of non-mycorrhizal than by mycorrhizal strawberry roots. Mycol Res 104: 1069–1073.
- 36. Reganold JP, Andrews PK, Reeve JR, Carpenter-Boggs L, Schadt CW, et al. (2010) Fruit and soil quality of organic and conventional strawberry agroecosystems. PLoS ONE 5: e12346
- 37.
Ellis MA (2008) Verticillium wilt of Strawberry. Ohio State University Extension.
- 38. Fradin EF, Thomma BPHJ (2006) Physiology and molecular aspects of Verticillium wilt diseases caused by V. dahliae and V. albo-atrum. Mol Plant Pathol 7: 71–86.
- 39.
Lord, Cheryl A S (1994) Verticillium wilt of Strawberry. Fact sheet. Durham, New Hampshire, USA: The University of New Hampshire Cooperative extension.
- 40. Heale J, Karapapa V (1999) The Verticillium threat to Canada’s major oilseed crop: Canola. Can J Plant Pathol 21: 1–7.
- 41. Klosterman SJ, Atallah ZK, Vallad GE, Subbarao KV (2009) Diversity, pathogenicity, and management of Verticillium Species. Ann Review Phytopathol 47: 39–62.
- 42. Harris DC, Yang JR (1996) The relationship between the amount of Verticillium dahliae in soil and the incidence of strawberry wilt as a basis for disease risk prediction. Plant Pathol 45: 106–114.
- 43. Meszka B, Bielenin A (2009) Bioproducts in control of strawberry Verticillium wilt. Phytopathologia 52: 21–27.
- 44. Tjamos SE, Flemetakis E, Paplomatas EJ, Katinakis P (2005) Induction of resistance to Verticillium dahliae in Arabidopsis thaliana by the biocontrol agent K-165 and pathogenesis-related proteins gene expression. Molr Plant-Microb Interact 18: 555–561.
- 45. Rudrappa T, Czymmek KJ, Paré PW, Bais HP (2008) Root-secreted malic acid recruits beneficial soil bacteria. Plant Physiol 148: 1547–1556.
- 46. Azad HR, Davis JR, Schnathorst WC, Kado CI (1987) Influence of Verticillium wilt resistant and susceptible potato genotypes on populations of antagonistic rhizosphere and rhizoplane bacteria and free nitrogen fixers. Appl Microbiol Biotechnol 26: 99–104.
- 47. An M, Zhou X, Wu F, Ma Y, Yang P (2011) Rhizosphere soil microorganism populations and community structures of different watermelon cultivars with differing resistance to Fusarium oxysporum f. sp. niveum. Can J Microbiol 57: 355–365.
- 48. Yao H, Wu F (2010) Soil microbial community structure in cucumber rhizosphere of different resistance cultivars to Fusarium wilt. FEMS Microbiol Ecol 72: 456–463.
- 49.
Rastogi G, Sani RK (2011) Molecular techniques to assess microbial community structure, function, and dynamics in the environment. In: Ahmad I, Ahmad F, Pichtel J, editors. Microbes and Microbial Technology. New York, NY: Springer New York. 29–57.
- 50. Torsvik V, Øvreås L (2002) Microbial diversity and function in soil: from genes to ecosystems. Curr Op Microbiol 5: 240–245.
- 51. Weinert N, Piceno Y (2011) Ding (2011) Meincke R, Heuer H, et al. (2011) PhyloChip hybridization uncovered an enormous bacterial diversity in the rhizosphere of different potato cultivars: many common and few cultivar-dependent taxa. FEMS Microbiol Ecol 75: 497–506.
- 52. Simpson D, Bell JA, Hammond K, Whitehouse AB (2002) The latest strawberry cultivars from horticultural research international, Tampere, Finland: Acta horticulturae. 567: 165–168.
- 53.
Olbricht K, Hanke M (2008) Strawberry breeding for disease resistance in Dresden. Small fruit: breeding and testing of cultivar. Hohenheim, Germany: Eco Fruit. 144–147.
- 54. Davik J, Daugaard H, Svensson B (2000) Strawberry production in the Nordic countries. Advances in Strawberry Research 19: 13–18.
- 55. Griffiths RI, Whiteley AS, O’Donnell AG, Bailey MJ (2000) Rapid method for co-extraction of DNA and RNA from natural environments for analysis of ribosomal DNA- and rRNA-based microbial community composition. Appl Environ Microb 66: 5488–5491.
- 56. Ihrmark K, Bödeker ITM, Cruz-Martinez K, Friberg H, Kubartova A, et al. (2012) New primers to amplify the fungal ITS2 region – evaluation by 454-sequencing of artificial and natural communities. FEMS Microbiol Ecol 82: 666–677.
- 57.
White T, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. PCR protocols: a guide to methods and applications. Innis MA, Gelfland DH, Sninsky JJ and White TJ. San Diego, CA, USA: Academic press. 315–322 p.
- 58. Xu L, Ravnskov S, Larsen J, Nicolaisen M (2012) Linking fungal communities in roots, rhizosphere, and soil to the health status of Pisum sativum. FEMS Microbiol Ecol 82: 736–745.
- 59. Middelhoven WJ, Koorevaar M, Schuur GW (1992) Degradation of benzene compounds by yeasts in acidic soils. Plant Soil 145: 37–43.
- 60. Margesin R, Fonteyne PA, Redl B (2005) Low-temperature biodegradation of high amounts of phenol by Rhodococcus spp. and basidiomycetous yeasts. Res Microbiol 156: 68–75.
- 61. Mestre MC, Rosa CA, Safar SVB, Libkind D, Fontenla SB (2011) Yeast communities associated with the bulk-soil, rhizosphere and ectomycorrhizosphere of a Nothofagus pumilio forest in northwestern Patagonia, Argentina. FEMS Microbiol Ecol 78: 531–541.
- 62. Girvan MS, Bullimore J, Pretty JN, Osborn AM, Ball AS (2003) Soil type is the primary determinant of the composition of the total and active bacterial communities in arable Soils. Appl Environ Microb 69: 1800–1809.
- 63. Wu Y, Fang W, Zhu S, Jin K, Ji D (2008) The effects of cotton root exudates on the growth and development of Verticillium dahliae. Frontiers of Agriculture in China 2: 435–440.
- 64. Vandemark GJ, Ariss JJ, Hughes TJ (2010) Real-time PCR Suggests that Aphanomyces euteiches is associated with reduced amounts of Phytophthora medicaginis in Alfalfa that is co-inoculated with both pathogens. J Phytopathol 158: 117–124.
- 65. Andrade-Linares DR, Grosch R, Restrepo S, Krumbein A, Franken P (2011) Effects of dark septate endophytes on tomato plant performance. Mycorrhiza 21: 413–422.
- 66. Raaijmakers JM, Mazzola M (2012) Diversity and natural functions of antibiotics produced by beneficial and plant pathogenic bacteria. Ann Rev Phytopathol 50: 403–424.
- 67.
El-Deeb HM, Arab YA (2013) Acremonium as an endophytic bioagent against date palm Fusarium wilt. Arch Phytopathol Plant Prot: 1–8.
- 68. Fávaro LC, Sebastianes FL, Araújo WL (2012) Epicoccum nigrum P16, a sugarcane endophyte, produces antifungal compounds and induces root growth. PloS ONE 7(6): e36826
- 69. Mousa WK, Raizada MN (2013) The diversity of anti-microbial secondary metabolites produced by fungal endophytes: an interdisciplinary perspective. Frontiers Microbiol 4: 65.
- 70. Aly AH, Debbab A, Proksch P (2011) Fungal endophytes: unique plant inhabitants with great promises. Appl Microbiol Biotechnol 90: 1829–1845.