Abstract
The present study aimed to characterize the distribution of mealybug species along Chilean agro-ecosystems and to determine the relative impact of host plant, management strategy, geography and micro-environment on shaping the distribution and genetic structure of the obscure mealybug Pseudococcus viburni. An extensive survey was completed using DNA barcoding methods to identify Chilean mealybugs to the species level. Moreover, a fine-scale study of Ps. viburni genetic diversity and population structure was carried out, genotyping 529 Ps. viburni individuals with 21 microsatellite markers. Samples from 16 localities were analyzed using Bayesian and spatially-explicit methods and the genetic dataset was confronted to host-plant, management and environmental data. Chilean crops were found to be infested by Ps. viburni, Pseudococcus meridionalis, Pseudococcus longispinus and Planococcus citri, with Ps. viburni and Ps. meridionalis showing contrasting distribution and host-plant preference patterns. Ps. viburni samples presented low genetic diversity levels but high genetic differentiation. While no significant genetic variance could be assigned to host-plant or management strategy, climate and geography were found to correlate significantly with genetic differentiation levels. The genetic characterization of Ps. viburni within Chile will contribute to future studies tracing back the origin and improving the management of this worldwide invader.
Similar content being viewed by others
Introduction
Scale insects are worldwide-distributed agricultural pests that cause major economic losses of billions of dollars every year1,2, either through direct impact on crops or quarantine export restrictions3,4. Commonly known as mealybugs, scale insects belonging to the family Pseudococcidae are particularly difficult to manage5,6. Their small size and cryptic habits render them very inconspicuous so that they easily escape phytosanitary inspections. For example, the obscure mealybug Pseudococcus viburni (Signoret) has expanded across the globe and is now present in over 60 countries7. Chemical control of pseudococcids is often ineffective due to their concealed nature and patchy distributions4,8. As a consequence, many management programs rely on classical biological control and especially the use of encyrtid parasitoids6,9. The response to particular biological control agents varies depending on the mealybug species10, so characterizing the diversity and distribution of mealybugs becomes important for both fundamental research as well as in applied pest management.
The spatial distribution of agro-ecosystems is a key factor determining the species composition and population genetic structure of agricultural pests11,12. Chilean highly structured agricultural landscape represents an excellent case study, with 83% of fruit orchards being found in a 700 km long stretch of land (between Coquimbo and Maule regions) and 20 fruit species concentrating about 90% of the cultivated area13. Geographical and environmental features of the country also contribute to further structuring Chilean agro-ecosystems. In the Norte Chico area (26° S to 32° S), which includes the administrative regions of Atacama (partly overlapping the Atacama Desert) and Coquimbo, there are semi-desert conditions with extreme climate variations. In the Central Chile area (32° S to 37° S), comprising the administrative regions of Valparaíso, Metropolitana, O’Higgins, Maule and the Northern part of Biobío, climate is mostly Mediterranean, with reliable alternation of warm, dry summers and cooler, rainier winter seasons14. The Norte Chico climate is mostly favorable to vineyards, while the Central Chile area includes both vineyards and fruit orchards (e.g. orange trees, apple trees, plum trees and pears). By running parallel to the Ocean, the coastal mountains and Andes cordillera further enclose vineyards and fruit orchards in isolated valleys, even within administrative regions.
National production of grapes and fruit orchards in Chile has significantly increased during the last decade15. Mealybug detection after phytosanitary inspections is responsible for over 45% fruit rejections in exports and pest infestations must be controlled for the sustainability of the Chilean agro-industry16. Correct identification is essential for pest management, however previous reports on mealybugs have evidenced considerable difficulties when using morphology-based methods17,18,19. In a preliminary study using a DNA barcoding approach, Correa et al.20 found Pseudococcus viburni (Signoret) to be the most common mealybug species in Chilean vineyards, followed by Pseudococcus meridionalis Prado and Pseudococcus cribata González. In contrast with previous studies though, no Pseudococcus longispinus (Targioni Tozzetti) or Planococcus ficus (Signoret) were found, which could result from the limited area being covered (two regions) and the fact that only vineyards were sampled20.
The present study aimed at characterizing the diversity and distribution of mealybug species infesting Chilean agro-ecosystems, including both vineyards and deciduous fruit crops. In order to achieve this goal, we completed an extensive survey between Atacama and the Northern part of Biobío (covering most cultivated areas in Chile) and using DNA barcoding methods to identify mealybug samples to the species level. Moreover, a fine-scale study of Ps. viburni genetic diversity and population connectivity was carried out using microsatellite markers. A comprehensive analysis of Ps. viburni samples allowed us to determine the relative impact of host plant, management strategy, geography and micro-environment on shaping the distribution and genetic structure of the pest.
Methods
Sampling and molecular identification
A total of 38 sampling sites were surveyed along Chile in 2012 and 2013 (Table 1). Sample collection was performed by taking one mealybug specimen per plant (20 – 49 mealybugs per site) to avoid collecting individuals from a single family. Specimens were stored in absolute ethanol at −20 °C until DNA extraction. Given that mealybug species are difficult to distinguish based on their morphology, DNA barcoding identification was performed. Genomic DNA was extracted from at least five individuals per locality using the DNeasy extraction kit (QIAGEN, Hilden, Germany) and the conserved 28S ribosomal marker was PCR-amplified using the primers S3690 (5′-GAGAGTTMAASAGTACGTGAAAC-3′) and A4394 (5′-TCGGARGGAACCAGC-TACTA-3′)21. PCR reactions were performed in a total reaction volume of 25 μL and following the protocol of Abd-Rabou et al.22. The PCR mix was composed of 12.50 μL 2X Tmix (QIAGEN, Hilden, Germany), 0.125 μL of each primer (initial concentration of 100 μM) and 10.25 μL of ultrapure water. PCR conditions were: initial denaturation at 95°C for 15 min; 35 cycles of denaturation at 95 °C for 30 s, hybridization at 58 °C for 90 s, elongation for 60 s; final extension at 72 °C for 10 min. PCR products were then analyzed on a QIAxcel Advanced System (QIAGEN) and sent for sequencing to Genoscreen (Lille, France) or Beckman Genomics (Takeley, United Kingdom). PCR products were sequenced on both strands and consensus sequences and alignments were created manually with Bioedit version 7.0123.
Microsatellite Diversity Analyses
Out of the initial 38 sampling sites, a total of 16 samples were identified as Ps. viburni (see results section) and kept for further analysis using the 21 polymorphic microsatellite markers developed by Correa et al.24. Genotyping was carried out in a total of 529 individuals from those Ps. viburni populations. Individual PCRs were performed in a total volume of 10 μl, with cycling conditions as in Correa et al.24. PCR products were separated by electrophoresis using an ABI 3700 sequencer (Applied Biosystems) and 500 LIZ GeneScanTM size standard. Allelic profiles were obtained for each individual using the GenemarkerTM v1.75 software (SoftGenetics LLC).
For each sampling locality, mean number of alleles, observed (HO) and expected (HE) heterozygosity were computed using the software GeneClass v225. Allelic richness was estimated standardizing sample size with the R package standArich (available online at http://www.ccmar.ualg.pt/maree/software.php?soft=sarich). Deviations from Hardy-Weinberg Equilibrium (HWE) were tested for each locus and sampling locality using the software Genepop v4.226. Per locus p-values were corrected for multiple testing within each population using the false discovery rate (FDR) procedure27. The presence of null alleles was evaluated with the FreeNA software and 10,000 bootstrap replicates were used to test for significance28. Genetic signals of recent bottlenecks affecting Ps. viburni were analyzed using the software BOTTLENECK v.1.2.0229.
Genetic connectivity of Pseudococcus viburni populations
Pairwise FST estimates30 and Fisher’s exact probability tests for genotypic differentiation31 were performed using the software Genepop v4.226. Levels of genetic differentiation between sample sites were also estimated using the DST statistic, which includes a multiplicative partitioning of diversity, based on the effective number of alleles rather than on the expected heterozygosity32. Pairwise DST statistic estimates and their significance using 1,000 bootstrap replicates were obtained with the pair.pops.Dest function in the DEMETICS package in R (http://www.r-project.org/). Sampling localities were grouped with the neighbor-joining algorithm and the pairwise genetic chord distance33 as implemented in the software Populations v1.2.30 (http://bioinformatics.org/populations/).
Genetic clusters were then inferred by minimizing deviation from HWE and linkage disequilibrium (LD) with the Bayesian clustering approach implemented in STRUCTURE34. Parameters were estimated assuming an admixture model with correlated allele frequencies and no prior location information. We carried out 20 replicate runs for each value of the number of clusters (K), set between 1 and 16 (i.e. the number of sampling sites). Each run consisted of a burn-in period of 200,000 Markov chain Monte Carlo (MCMC) iterations, followed by 1,000,000 MCMC iterations. The highest level of genetic structure was inferred through the ΔK approach as implemented in STRUCTURE Harvester35,36. Finally, a discriminant analysis of principal components (DAPC) was used to identify clusters of genetically-related genotypes. DAPC (like the sPCA method presented below) differs from the Bayesian method in STRUCTURE by not assuming HWE or linkage equilibrium37.
Spatial genetic structure analyses
Isolation by distance (IBD) was tested by performing a linear regression of the genetic distances (FST or DST) and the geographical distances (Km) and obtaining the Pearson’s correlation coefficient. Matrices of genetic distance and geographical distance were subjected to a Mantel test with 10,000 permutations in Arlequin v.3.538. A spatially-explicit multivariate method (sPCA: spatial analysis of principal components) was used to further explore the spatial patterns of genetic variability between sites39. Spatial connectivity networks were built using the sampling location data and three common algorithms (Delaunay triangulation, relative neighbor and sphere of influence)40. In order to select for the network that better fits the genetic data, the corrected Akaike Information Criteria (AICc) was computed for each graph using the ortho.AIC function of the spacemakeR package41. The connectivity graph with the highest AICc was used to test for the presence of spatial autocorrelation against the null hypothesis that allele frequencies are distributed at random. Spatial correlation can be either positive or negative, resulting in principal components with positive or negative eigenvalues. Principal components with significant positive eigenvalues indicate that sites are genetically more similar to their neighbors than expected by chance (global structures), while those with significant negative eigenvalues highlight local differentiation among neighboring sites39. Spatial autocorrelation (Moran’s I) was tested for each component using the permutation procedure implemented in the spdep package and 1,000 permutations41.
Non-genetic factors influencing population structure
Several analyses of molecular variance (AMOVA) were performed in order to evaluate the importance of non-genetic categorical factors on the distribution of genetic diversity. In particular, sample sites were grouped according to (i) administrative region (AT, CQ, VL, MT, OH or ML), (ii) type of agricultural management (conventional or organic production) and (iii) host plant (grape, apple, plum or pear). The significance for the AMOVAs was obtained through non-parametric permutation procedures (with 20,000 permutations) as implemented in Arlequin v3.538. To examine whether non-genetic environmental factors may influence genetic differentiation levels in Ps. viburni, temperature and precipitation variables were recovered to 1-km spatial resolution from WorldClim version 1.4 (http://www.worldclim.org)42. The climate variables included temperature and precipitation parameters, namely: i) annual mean temperature, ii) maximum temperature of the warmest month, iii) minimum temperature of the coldest month, iv) annual precipitation and v) precipitation seasonality (Coefficient of Variation). A Spearman’s rank correlation (ρ) test was then carried out between pairwise genetic distances (FST or DST) and the Euclidean distance between climate variables for each pair of sampling sites. Spearman’s correlation measures association based on the rank differences between two vectors and indicates how well a monotonic function describes their relationship.
Results
Molecular identification of mealybug species
The present survey of scale insects infesting Chilean crops identified four mealybug species (Planococcus citri, Pseudococcus longispinus, Pseudococcus meridionalis and Pseudococcus viburni). Ps. viburni was the most widespread pest, being found on vineyards, apple trees, plum trees or pear trees in six out of seven administrative regions sampled: Atacama (AT), Coquimbo (CQ), Valparaíso (VL), Metropolitana (MT), O’Higgins (OH) and Maule (ML) (Table 1; Fig. 1). Ps. longispinus was also present in several regions and dominated apple fields south of Maule and in Biobío. Finally, Pl. citri and Ps. meridionalis were only found sporadically on vineyards or orange trees (Fig. 1).
Microsatellite Diversity Analyses
Ps. viburni samples showed an overall mean number of alleles of 3.06, with values ranging from 2.29 (ML1) to 3.62 (VL3). The overall mean allelic richness was 2.97 (N = 20 genotypes), with MT2 presenting the highest (3.52) and AT1 the lowest (2.20) values (Table 2). After correction by the FDR procedure, seven sites still showed significant HWE deviations (Table 2). Frequency of null alleles for each microsatellite marker ranged from 0.002 (PV071) to 0.133 (PV060). Nevertheless, the presence of null alleles did not affect global FST estimates and similar values were obtained using the raw dataset (FST = 0.126) or the corrected dataset (FST = 0.125). Similarly, pairwise FST values did not vary after FREENA correction for the presence of null alleles.
Genetic connectivity of Pseudococcus viburni populations
Pairwise FST values ranged from 0.011 (between ML2 and ML3) to 0.350 (between AT1 and ML3) (Table 3). All pairs of Ps. viburni samples showed significant differentiation levels after Fisher’s exact tests (P < 0.05). The results obtained using the distance-based neighbor-joining approach showed a clear support for the separation of AT1 and CQ1 from the remaining samples (Fig. 2a). Despite most bootstrap values were low, a strong support was found for some groups sites, such as VL1-VL2, ML2-ML3, MT1-MT2 and VL3-VL4. Structure Harvester selected K = 3 as the best representative number of clusters based on likelihood and ΔK (Ln = −16457; ΔK = 443.35). The first cluster included the two Northernmost sites (AT1 and CQ1), a second cluster was composed of samples from the Aconcagua (VL1 and VL2), Cachapoal (OH1), Colchagua (OH2 and OH3) and Curicó (ML1) valleys; and a third cluster was formed by the Casablanca (VL3 and VL4), Maipo (MT1 and MT2), Colchagua (OH5) and Curicó (ML2 and ML3) valleys (Figs 1, 2b). Finally, the DAPC method also support the presence of a cluster including AT1 and CQ1 samples, but indicated large overlapping between the samples assigned to the second (blue) and third (green) clusters given by STRUCTURE (Fig. 2c).
Spatial genetic structure analyses
AMOVA results showed that a significant 7.73% of the total genetic variability can be explained by administrative regions (FCT = 0.074; P < 0.0001). A significant positive correlation was found between geographical distance and either FST (r2 = 0.79; P < 0.0001) or DST values (r2 = 0.75; P < 0.0001) when considering all the 16 sample sites, indicating the presence of IBD. When the IBD test was performed without the two most distant localities (AT1 and CQ1), a weaker but still significant pattern was also observed both using FST (r2 = 0.068; P = 0.028) or DST values (r2 = 0.121; P = 0.004).
According to the corrected AIC criterion, the best connectivity graph for explaining the Ps. viburni allele frequency data was obtained from the Sphere of Influence (SoI) algorithm (AICc = −42.356; non-zero links = 34), which showed a lower AICc value than both the Delaunay triangulation (AICc = −41.325; non-zero links = 78) or the Relative Neighbor Graph (AICc = −41.159; non-zero links = 30) (Fig. 3A). The SoI algorithm differs from the Relative Neighbor algorithm by creating a disconnected graph despite having a larger number of nonzero links. The graphical representation of the scores of the first and second global components (with significant positive eigenvalues) showed that samples from the Valparaiso (VL3-VL4) and Metropolitana (MT1-MT2) regions have different allele composition than other clusters (negative scores shown as large white squares in Fig. 3B). A graphical representation of the components with significantly negative eigenvalues shows that local changes can be observed between the northernmost localities and within the O’Higgins area (both white and black squares present within connected sites in Fig. 3C).
Non-spatial factors influencing population structure
No significant genetic variance could be assigned to differences among organic and conventional management strategies (FCT = −0.0006; p-value = 0.402) or among host plants (FCT = −0.015; p-value = 0.587) (Table 4). As for the effect of climatic environmental factors, Spearman’s rank test indicated a strong correlation between genetic distances and differences in maximum temperature of the warmest month (ρ = 0.615; p-value <0.001), minimum temperature of the coldest month (ρ = 0.645; p-value <0.001), annual precipitation (ρ = 0.523; p-value <0.001) and precipitation seasonality (ρ = 0.537; p-value <0.001). However, the correlation between genetic distances and annual mean temperature was much smaller and non-significant after FDR correction (ρ = 0.239; p-value = 0.008).
Discussion
The distribution of insect pest species across agricultural ecosystems can be shaped by multiple factors, ranging from specific associations with the cultivated plant, environmental gradients or the use of pesticides. The study of these multiple factors, together with an accurate discrimination between mealybug species, are determinant for an adequate adjustment of management strategies. Previous morphology-based surveys of Chilean mealybugs have found Ps. viburni, Ps. meridionalis, Ps. cribata, Ps. longispinus and Pl. ficus, but the only molecular study performed up to date could not recover the last two species20. Our results establish, thanks to DNA barcoding methods, the presence of both Ps. longispinus and Pl. citri infesting Chilean crops. Therefore, previous reports of Pl. ficus could correspond in fact to Pl. citri, given the difficulties of morphology-based identification of mealybugs. The main Pseudococcus species infesting Chilean fruit crops was the obscure mealybug Ps. viburni, followed by Ps. longispinus and Ps. meridionalis.
Both Ps. viburni and Ps. longispinus were recovered from vineyards and fruit orchards. Nevertheless, while Ps. viburni occurred mainly in vineyards around the central regions of Chile (Valparaíso and Metropolitana) and became less frequent south of O’Higgins, Ps. longispinus showed an opposite pattern and was more abundant in Apple orchards south of that region. These different spatial distribution and host-plant preference patterns are in agreement with previous studies on the biology and systematics of Pseudococcidae4. Indeed, Ps. viburni belongs to the grape mealybug (Ps. maritimus) species complex, while the long-tailed mealybug (Ps. longispinus) and related species are commonly found on fruit orchards (e.g. avocado43,44 and pear45).
The host preference observed for different species did not extend to different populations within Ps. viburni, since no significant genetic variance could be assigned to host plant or management strategy. This lack of genetic structuring by host indicates that Ps. viburni populations are able to infest fruit orchards in an opportunistic way despite their preference for vines4. Rather than host plant or management strategy, our results highlight the importance of geography and environmental factors in shaping the intra-species population genetic structure of the obscure mealybug. The integrative analyses of micro-climatic variables and genetic markers show that the severity of climate (i.e. differences in the extremes of temperature or precipitation seasonality) is significantly correlated with genetic differentiation levels. Meteorological changes or edaphic factors have been previously proposed to modify the physiology of the plant and alter its resistance to scale insect attack46,47, but this is the first study to provide evidence on the importance of environmental factors on shaping scale insects distribution and genetic structure.
Climate differences might correlate with geographical distances, so that spurious genetic-climate correlations could result from an isolation by distance pattern. AMOVA, IBD and sPCA analyses all support the presence of reduced connectivity between Ps. viburni samples related to their spatial distribution. The fact that IBD remained significant even after excluding the two most distant populations indicates that genetic differentiation is also important at a local scale, where climatic differences are minimal. Therefore, geography cannot be discarded as a key factor shaping the population genetic structure of the obscure mealybug. In a recent study, the maritime pine bast scale (Matsucoccus feytaudi) was found to be highly structured geographically and the authors relate this fact to the limited dispersal capacity of the insect and the patchy distribution of the obligate host48. Mealybug species are known to present low dispersal abilities, so long distance movements could only be driven by human activities and agricultural practices4. The peculiar shape of Chile, being only 177 km wide in average but 4300 km long, together with the low mobility of mealybugs, could well explain the observed geography-driven genetic structure of P. viburni.
The identification of well-differentiated groups within Ps. viburni is an important contribution to design effective control strategies for pest management both in Chile and elsewhere. Even though the exact center of origin for the obscure mealybug remains unclear, South America has been suggested as the most likely native area. Therefore, the genetic characterization of Ps. viburni within Chile will contribute to future studies tracing back the origin and improving the management of this worldwide invader (e.g. allowing to search for specific parasitoids within the source populations).
Additional Information
How to cite this article: Correa, M. C. G. et al. Mealybug species from Chilean agricultural landscapes and main factors influencing the genetic structure of Pseudococcus viburni. Sci. Rep. 5, 16483; doi: 10.1038/srep16483 (2015).
References
Kosztarab, M. in Armored Scale Isects, Their Biology, Natural Enemies and Control (ed. Rosen, D. ) 688 (Elsevier, 1990).
Miller, D., Miller, G., Hodges, G. & Davidson, J. Introduced Scale Snsects of the United States and Their Impact on US Agriculture. Proc. Entomol. Soc. Washingt. 107, 123–158 (2005).
Franco, J. C., Zada, A. & Mendel, Z. in Biorational Control of Arthropod Pests (eds. Ishaaya, I. & Horowitz, A. R. ) 408 (Springer Netherlands, 2009).
Daane, K. M. et al. in Arthropod Management in Vineyards: Pests, Approaches and Future Directions 271–307 (Springer, 2012).
Walton, V. M., Daane, K. M. & Pringle, K. L. Monitoring Planococcus ficus in South African vineyards with sex pheromone-baited traps. Crop Prot. 23, 1089–1096 (2004).
Daane, K. M. et al. New controls investigated for vine mealybug. Calif. Agric. 60, 31–38 (2008).
Ben-Dov, Y., Miller, D. R. & Gibson, G. A. P. Scale Net (2010). at <http://www.sel.barc.usda.gov/scalenet/scalenet.htm> Date of access:20/02/2015
Noyes, J. & Hayat, M. Oriental mealybug parasitoids of the Anagyrini (Hymenoptera: Encyrtidae) with a world review of Encyrtidae used in classical biological control and an index of encyrtid parasitoids of mealybugs (Homoptera: Pseudococcidae). (CAB International on behalf of The Natural History Museum, 1994).
Charles, J. G. Using parasitoids to infer a native range for the obscure mealybug, Pseudococcus viburni, in South America. BioControl 56, 155–161 (2011).
Chong, J.-H. & Oetting, R. D. Specificity of Anagyrus sp. nov. nr. sinope and Leptomastix dactylopii for six mealybug species. BioControl 52, 289–308 (2006).
Plantegenest, M., Le May, C. & Fabre, F. Landscape epidemiology of plant diseases. J. R. Soc. Interface 4, 963–72 (2007).
Ovčarenko, I. et al. Agroecosystems shape population genetic structure of the greenhouse whitefly in Northern and Southern Europe. BMC Evol. Biol. 14, 165 (2014).
ODEPA, Oficina de Estudios y Politicas Agrarias. Estadísticas productivas. (2014). at <www.odepa.cl> Date of access:09/10/2014
INE, Instituto Nacional de Estadísticas. Compendio Estadístico. (2014). at <www.ine.cl> Date of access:18/09/2014.
Agosin, M. & Bravo-Ortega, C. The Emergence of New Successful Export Activities in Latin America: The Case of Chile. Inter American Development Bank RES Working Papers (Inter-American Development Bank, 2009).
Moore, C. Rechazos por Pseudococcidae y su estatus cuarentenario. Seminar: ‘Chanchito blanco en uva de mesa’ (2012). at <http://www.fdf.cl/biblioteca/presentaciones/2012/04_jt_chancho_fosfina/> Date of access:12/05/2014
González, R. Chanchitos Blancos de Importancia Agrícola Y Cuarentenaria En Huertos Frutales de Chile (Hemiptera: Pseudococcidae). Rev. Frutícola 24, 15–17 (2003).
Ripa, S. & Luppichini, P. Manejo de Plagas de La Vid. Colección libros INIA 26, 1–145 (2010).
Correa, M. et al. A new species of Pseudococcus (Hemiptera: Pseudococcidae) belonging to the ‘Pseudococcus maritimus’ complex from Chile: molecular and morphological description. Zootaxa 54, 46–54 (2011).
Correa, M., Germain, J.-F., Malausa, T. & Zaviezo, T. Molecular and morphological characterization of mealybugs (Hemiptera: Pseudococcidae) from Chilean vineyards. Bull. Entomol. Res. 102, 524–530 (2012).
Sequeira, A. S., Normark, B. B. & Farrell, B. D. Evolutionary assembly of the conifer fauna: distinguishing ancient from recent associations in bark beetles. Proceedings. Biol. Sci. 267, 2359–66 (2000).
Abd-Rabou, S. et al. Identification of mealybug pest species (Hemiptera: Pseudococcidae) in Egypt and France, using a DNA barcoding approach. Bull. Entomol. Res. 102, 1–9 (2012).
Hall, T. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp. Ser. 41, 95–98 (1999).
Correa, M. C. G., Zaviezo, T., Le Maguet, J., Herrbach, E. & Malausa, T. Characterization of microsatellite DNA libraries from three mealybug species and development of microsatellite markers for Pseudococcus viburni (Hemiptera: Pseudococcidae). Bull. Entomol. Res. 104, 213–20 (2014).
Piry, S. et al. GENECLASS2: a software for genetic assignment and first-generation migrant detection. J. Hered. 95, 536–9 (2004).
Rousset, F. Genepop’007: a complete re-implementation of the genepop software for Windows and Linux. Mol. Ecol. Resour. 8, 103–106 (2008).
Benjamini, Y. & Hochberg, Y. Controlling the False Discovery Rate - a Practical and Powerful Approach to Multiple Testing. J. R. Stat. Soc. Ser. B-Methodological 57, 289–300 (1995).
Chapuis, M.-P. & Estoup, A. Microsatellite null alleles and estimation of population differentiation. Mol. Biol. Evol. 24, 621–631 (2007).
Cornuet, J. M. & Luikart, G. Description and power analysis of two tests for detecting recent population bottlenecks from allele frequency data. Genetics 144, 2001–14 (1996).
Weir, B. S. & Cockerham, C. Estimating F-Statistics for the Analysis of Population Structure. Evolution (N. Y). 38, 1358–1370 (1984).
Raymond, M. & Rousset, F. An Exact Test for Population Differentiation. Evolution (N. Y). 49, 1280–1283 (1995).
Jost, L. GST and its relatives do not measure differentiation. Mol. Ecol. 17, 4015–4026 (2008).
Cavalli-Sforza, L. L. & Edwards, a W. F. Phylogenetic analysis. Models and estimation procedures. Am. J. Hum. Genet. 19, 233–257 (1967).
Pritchard, J. K., Stephens, M. & Donnelly, P. Inference of population structure using multilocus genotype data. Genetics 155, 945–959 (2000).
Evanno, G., Regnaut, S. & Goudet, J. Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol. Ecol. 14, 2611–20 (2005).
Dent, E. & VonHoldt, B. STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method. Conserv. Genet. Resour. 4, 359–361 (2012).
Jombart, T., Devillard, S. & Balloux, F. Discriminant analysis of principal components: a new method for the analysis of genetically structured populations. BMC Genet. 11, 94 (2010).
Excoffier, L. & Lischer, H. E. L. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol. Ecol. Resour. 10, 564–7 (2010).
Jombart, T. Adegenet: a R package for the multivariate analysis of genetic markers. Bioinformatics 24, 1403–1405 (2008).
Kleinberg, J. & Tardos, E. Algorithm Design. (Addison-Wesley, 2005).
Team, R. R. Development Core Team. R A Lang. Environ. Stat. Comput. (2013). at <https://www.r-project.org/> Date of access:20/02/2015
Hijmans, R. J., Cameron, S. E., Parra, J. L., Jones, P. G. & Jarvis, A. Very high resolution interpolated climate surfaces for global land areas. Int. J. Climatol. 25, 1965–1978 (2005).
Swirski, E., Izhar, Y., Wysoki, M., Gurevitz, E. & Greenberg, S. Integrated control of the long-tailed mealybug, Pseudococcus longispinus [Hom.:Pseudococcidae], in avocado plantations in Israel. Entomophaga 25, 415–426 (1980).
Ripa, R. & Larral, P. Manejo de plagas en paltos y cítricos. Colección Instituto de Investigaciones Agropecuarias (Centro Regional de Investigación, 2008).
Barrass, I., Jerie, P. & Ward, S. Aerial dispersal of first- and second-instar longtailed mealybug, Pseudococcus longispinus (Targioni Tozzetti) (Pseudococcidae: Hemiptera). Aust. J. Exp. Agric. 34, 1205 (1994).
Flanders, S. E. Observations on host plant induced behavior of scale insects and their endoparasites. Can. Entomol. 102, 913–926 (1970).
Miller, D. R. & Kosztarab, M. Recent Advances in the Study of Scale Insects. Annu. Rev. Entomol. 24, 1–27 (1979).
Kerdelhué, C., Boivin, T. & Burban, C. Contrasted invasion processes imprint the genetic structure of an invasive scale insect across southern Europe. Heredity (Edinb). 1–11 (2014).
Acknowledgements
We would like to thank Karina Buzzetti, Jennifer Cardenas and Alda Romero for their help with mealybug collection and to Elie Poulin and Eduardo Fuentes for comments on an earlier version of the manuscript. Special thanks to Aurélie Blin (INRA Sophia Antipolis) for her support with molecular biology supplies. MCG Correa received financial support from: Chile CONICYT Doctoral fellowship #21110864, CONICYT “Tesis en la Industria” #7812110011. This research was also funded by the European Union FP7 grants KBBE “PURE” #265865, Marie-Curie IRSES “IPRABIO” #269196. F Palero, MCG Correa, T. Malausa, T. Zaviezo and A. Alvear received financial support from Marie-Curie IAPP “COLBICS” #324475.
Author information
Authors and Affiliations
Contributions
T.Z., T.M. and F.P. conceived the ideas and led the writing; M.C., E.L. and F.P. analyzed the data; M.C., D.C. and A.A. collected the data. M.C. prepared Figures 1–3. All authors reviewed the manuscript.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Rights and permissions
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
About this article
Cite this article
Correa, M., Lombaert, E., Malausa, T. et al. Mealybug species from Chilean agricultural landscapes and main factors influencing the genetic structure of Pseudococcus viburni. Sci Rep 5, 16483 (2015). https://doi.org/10.1038/srep16483
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/srep16483
This article is cited by
-
Identifying cryptic species of Planococcus infesting vineyards to improve control efforts
Journal of Pest Science (2023)
-
Parasitoids (Hymenoptera) of Mealybug Pests (Hemiptera: Pseudococcidae) from Southern Brazil: Molecular and Morphological Characterization
Neotropical Entomology (2021)
-
European bridgehead effect in the worldwide invasion of the obscure mealybug
Biological Invasions (2019)
-
Genetic diversity of armored scales (Hemiptera: Diaspididae) and soft scales (Hemiptera: Coccidae) in Chile
Scientific Reports (2017)
-
Integrative taxonomy methods reveal high mealybug (Hemiptera: Pseudococcidae) diversity in southern Brazilian fruit crops
Scientific Reports (2017)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.