32 research outputs found

    Genetic variation and recombination of RdRp and HSP 70h genes of Citrus tristeza virus isolates from orange trees showing symptoms of citrus sudden death disease

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Citrus sudden death (CSD), a disease that rapidly kills orange trees, is an emerging threat to the Brazilian citrus industry. Although the causal agent of CSD has not been definitively determined, based on the disease's distribution and symptomatology it is suspected that the agent may be a new strain of <it>Citrus tristeza virus </it>(CTV). CTV genetic variation was therefore assessed in two Brazilian orange trees displaying CSD symptoms and a third with more conventional CTV symptoms.</p> <p>Results</p> <p>A total of 286 RNA-dependent-RNA polymerase (RdRp) and 284 heat shock protein 70 homolog (HSP70h) gene fragments were determined for CTV variants infecting the three trees. It was discovered that, despite differences in symptomatology, the trees were all apparently coinfected with similar populations of divergent CTV variants. While mixed CTV infections are common, the genetic distance between the most divergent population members observed (24.1% for RdRp and 11.0% for HSP70h) was far greater than that in previously described mixed infections. Recombinants of five distinct RdRp lineages and three distinct HSP70h lineages were easily detectable but respectively accounted for only 5.9 and 11.9% of the RdRp and HSP70h gene fragments analysed and there was no evidence of an association between particular recombinant mosaics and CSD. Also, comparisons of CTV population structures indicated that the two most similar CTV populations were those of one of the trees with CSD and the tree without CSD.</p> <p>Conclusion</p> <p>We suggest that if CTV is the causal agent of CSD, it is most likely a subtle feature of population structures within mixed infections and not merely the presence (or absence) of a single CTV variant within these populations that triggers the disease.</p

    Orange jasmine as a trap crop to control Diaphorina citri

    Full text link
    [EN] Novel, suitable and sustainable alternative control tactics that have the potential to reduce migration of Diaphorina citri into commercial citrus orchards are essential to improve management of huanglongbing (HLB). In this study, the effect of orange jasmine (Murraya paniculata) as a border trap crop on psyllid settlement and dispersal was assessed in citrus orchards. Furthermore, volatile emission profiles and relative attractiveness of both orange jasmine and sweet orange (Citrus¿×¿aurantium L., syn. Citrus sinensis (L.) Osbeck) nursery flushes to D. citri were investigated. In newly established citrus orchards, the trap crop reduced the capture of psyllids in yellow sticky traps and the number of psyllids that settled on citrus trees compared to fallow mowed grass fields by 40% and 83%, respectively. Psyllids were attracted and killed by thiamethoxam-treated orange jasmine suggesting that the trap crop could act as a `sinkÂż for D. citri. Additionally, the presence of the trap crop reduced HLB incidence by 43%. Olfactometer experiments showed that orange jasmine plays an attractive role on psyllid behavior and that this attractiveness may be associated with differences in the volatile profiles emitted by orange jasmine in comparison with sweet orange. Results indicated that insecticide-treated M. paniculata may act as a trap crop to attract and kill D. citri before they settled on the edges of citrus orchards, which significantly contributes to the reduction of HLB primary spread.This work was supported by Fund for Citrus Protection (Fundecitrus) and by Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) (Proc. 2015/07011-3). We thank Moacir Celio Vizone, Felipe Marinho Martini and Joao Pedro Ancoma Lopes for technical support with experiments. Furthermore, we thank Cambuhy Agricola Ltda. and University of Araraquara (Uniara) for providing the areas in which the field experiments were performed. Second author received scholarship from National Council for Scientific and Technological Development (CNPq)/Brazil (Proc. 300153/2011-2).Tomaseto, AF.; Marques, RN.; Fereres, A.; Zanardi, OZ.; Volpe, HXL.; AlquĂ©zar-GarcĂ­a, B.; Peña, L.... (2019). Orange jasmine as a trap crop to control Diaphorina citri. Scientific Reports. 9:1-11. https://doi.org/10.1038/s41598-019-38597-5S1119BovĂ©, J. M. Huanglongbing: a destructive, newly-emerging, century-old disease of citrus. J Plant Pathol. 88, 7–37 (2006).Alvarez, S., Rohrig, E., SolĂ­s, D. & Thomas, M. H. Citrus greening disease (Huanglongbing) in Florida: economic impact, management and the potential for biological control. Agric. Res. 5, 109–118 (2016).Belasque, J. Jr. et al. Lessons from huanglongbing management in SĂŁo Paulo state, Brazil. J. Plant Pathol. 92, 285–302 (2010).Boina, D. R., Meyer, W. L., Onagbola, E. O. & Stelinski, L. L. Quantifying dispersal of Diaphorina citri (Hemiptera: Psyllidae) by immunomarking and potential impact of unmanaged groves on commercial citrus management. Environ. Entomol. 38, 1250–8 (2009).Lewis-Rosenblum, H., Martini, X., Tiwari, S. & Stelinski, L. L. Seasonal movement patterns and long-range dispersal of Asian citrus psyllid in Florida citrus. J. Econ. Entomol. 108, 3–10 (2015).Hall, D. G. & Hentz, M. G. Seasonal flight activity by the Asian citrus psyllid in east central Florida. Entomol. Exp. Appl. 139, 75–85 (2011).Tomaseto, A. F., Krugner, R. & Lopes, J. R. S. Effect of plant barriers and citrus leaf age on dispersal of Diaphorina citri (Hemiptera: Liviidae). J. Appl. Entomol. 140, 91–102 (2016).Gottwald, T. R. Current epidemiological understanding of citrus huanglongbing. Annu. Rev. Phytopathol. 48, 119–139 (2010).Bassanezi, R. B. et al. Efficacy of area-wide inoculum reduction and vector control on temporal progress of huanglongbing in young sweet orange plantings. Plant Dis. 97, 789–796 (2013).SĂ©tamou, M. & Bartels, D. W. Living on the edges: spatial niche occupation of Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Liviidae), in citrus groves. PLoS One 10, 1–21 (2015).Gottwald, T., Irey, M., Gast, T. & Parnell, S. Spatio-temporal analysis of an HLB epidemic in Florida and implications for spread. In Proceedings of the 17 th Conference of International Organization of Citrus Virologists, IOCV, University of California, Riverside, CA, 84–97 (2010).Shelton, A. M. & Badenes-Perez, F. R. Concepts and applications of trap cropping in pest management. Annu. Rev. Entomol 51, 285–308 (2006).Hokkanen, H. M. T. Trap cropping in pest management. Annu. Rev. Entomol. 36, 119–138 (1991).Stern, V. M., Mueller, A., Sevacherian, V. & Way, M. Lygus bug control in cotton through alfalfa interplanting. Calif. Agric. 8–10 (1969).Godfrey, L. D. & Leigh, T. F. Alfalfa harvest strategy effect on lygus bug (Hemiptera: Miridae) and insect predator population density: Implications for use as trap crop in cotton. Environ. Entomol. 23, 1106–1118 (1994).Gonsalves, D. & Ferreira, S. Transgenic papaya: a case for managing risks of Papaya ringspot virus in Hawaii. Plant Heal. Prog. 1–6, https://doi.org/10.1094/PHP-2003-1113-03-RV (2003)Aubert, B. Trioza erytheae del Guercio and Diaphorina citri Kuwayama (Homoptera: Psylloidea), the two vectors of citrus greening disease: biological aspects and possible control strategies. Fruits 42, 149–162 (1987).Leong, S. C. T., Fatimah, A., Beattie, A., Heng, R. K. J. & King, W. S. Influence of host plant species and flush growth stage on the Asian citrus psyllid, Diaphorina citri Kuwayama. Am. J. Agric. Biol. Sci. 6, 536–543 (2011).Patt, J. M. & SĂ©tamou, M. Responses of the Asian citrus psyllid to volatiles emitted by the flushing shoots of its rutaceous host plants. Environ. Entomol. 39, 618–24 (2010).Damsteegt, V. D. et al. Murraya paniculata and related species as potential hosts and inoculum reservoirs of ‘Candidatus Liberibacter asiaticus’, causal agent of huanglongbing. Plant Dis. 94, 528–533 (2010).Lopes, S. A. et al. Liberibacters associated with orange jasmine in Brazil: Incidence in urban areas and relatedness to citrus liberibacters. Plant Pathol. 59, 1044–1053 (2010).Cifuentes-Arenas, J. C. Huanglongbing e Diaphorina citri: Estudos das relaçÔes patĂłgeno-vetor-hospedeiro. Ph.D. Thesis. Faculdade de CiĂȘncias AgrĂĄrias e VeterinĂĄrias/Universidade Estadual Paulista (UNESP), Jaboticabal, SP, Brazil. 1–133 (2017).Morilla, G. et al. Pepper (Capsicum annuum) is a dead-end host for Tomato yellow leaf curl virus. Phytopathology 95, 1089–1097 (2005).Midega, C. A. O., Pittchar, J. O., Pickett, J. A., Hailu, G. W. & Khan, Z. R. A climate-adapted push-pull system effectively controls fall armyworm, Spodoptera frugiperda (J. E. Smith), in maize in East Africa. Crop Prot. 105, 10–15 (2018).Miranda, M. P. et al. Processed kaolin affects the probing and settling behavior of Diaphorina citri (Hemiptera: Liviidae). Pest Manag. Sci. 74, 1964–1972 (2018).Kobori, Y., Nakata, T., Ohto, Y. & Takasu, F. Dispersal of adult Asian citrus psyllid, Diaphorina citri Kuwayama (Homoptera: Psyllidae), the vector of citrus greening disease, in artificial release experiments. Appl. Entomol. Zool. 46, 27–30 (2011).SĂ©tamou, M. et al. Diurnal patterns of flight activity and effects of light on host finding behavior of the Asian citrus psyllid. J. Insect Behav. 25, 264–276 (2012).Wenninger, E. J., Stelinski, L. L. & Hall, D. G. Roles of olfactory cues, visual cues, and mating status in orientation of Diaphorina citri Kuwayama (Hemiptera: Psyllidae) to four different host plants. Environ. Entomol. 38, 225–234 (2009).Miranda, M. P., Dos Santos, F. L., Felippe, M. R., Moreno, A. & Fereres, A. Effect of UV-blocking plastic films on take-off and host plant finding ability of Diaphorina citri (Hemiptera: Liviidae). J. Econ. Entomol. 108, 245–251 (2015).Visser, J. H. Host odor perception in phytophagous insects. Annu. Rev. Entomol. 31, 121–144 (1986).Robbins, P. S., Alessandro, R. T., Stelinski, L. L. & Lapointe, S. L. Volatile profiles of young leaves of Rutaceae spp. varying in susceptibility to the Asian citrus psyllid (Hemiptera: Psyllidae). Florida Entomol. 95, 774–776 (2012).Fancelli, M. et al. Attractiveness of host plant volatile extracts to the Asian citrus psyllid, Diaphorina citri, is reduced by terpenoids from the non-host cashew. J. Chem. Ecol. 44, 397–405 (2018).AlquĂ©zar, B. et al. ÎČ-caryophyllene emitted from a transgenic Arabidopsis or chemical dispenser repels Diaphorina citri, vector of Candidatus Liberibacters. Sci. Rep. 7, 5639 (2017).Jones, R. A. C. Effects of cereal borders, admixture with cereals and plant density on the spread of bean yellow mosaic potyvirus into narrow‐leafed lupins (Lupinus angustifolius). Ann. Appl. Biol. 122, 501–518 (1993).Beloti, V. H., Alves, G. R., Coletta-Filho, H. D. & Yamamoto, P. T. The Asian citrus psyllid host Murraya koenigii is immune to citrus huanglongbing pathogen ‘Candidatus Liberibacter asiaticus’. Phytopathology 108, 1089–1094 (2018).Walter, A. J., Duan, Y. & Hall, D. G. Titers of ‘Ca. Liberibacter asiaticus’ in Murraya paniculata and Murraya-reared Diaphorina citri are much lower than in Citrus and Citrus-reared psyllids. HortScience 47, 1449–1452 (2012).Walter, A. J., Hall, D. G. & Duan, Y. P. Low incidence of ‘Candidatus Liberibacter asiaticus’ in Murraya paniculata and associated Diaphorina citri. Plant Dis. 96, 827–832 (2012).Ammar, E.-D. D., Ramos, J. E., Hall, D. G., Dawson, W. O. & Shatters, R. G. Acquisition, replication and inoculation of Candidatus Liberibacter asiaticus following various acquisition periods on huanglongbing-infected citrus by nymphs and adults of the Asian citrus psyllid. PLoS One 11, e0159594 (2016).Inoue, H. et al. Enhanced proliferation and efficient transmission of Candidatus Liberibacter asiaticus by adult Diaphorina citri after acquisition feeding in the nymphal stage. Ann. Appl. Biol. 155, 29–36 (2009).Pelz-Stelinski, K. S., Brlansky, R. H., Ebert, T. A. & Rogers, M. E. Transmission parameters for Candidatus Liberibacter asiaticus by Asian citrus psyllid (Hemiptera: Psyllidae). J. Econ. Entomol. 103, 1531–1541 (2010).Canale, M. C. et al. Latency and persistence of ‘Candidatus Liberibacter asiaticus’ in its psyllid vector, Diaphorina citri (Hemiptera: Liviidae). Phytopathology 107, 264–272 (2017).Li, W., Hartung, J. S. & Levy, L. Quantitative real-time PCR for detection and identification of Candidatus Liberibacter species associated with citrus huanglongbing. J. Microbiol. Methods 66, 104–115 (2006).Nakata, T. Effectiveness of micronized fluorescent powder for marking citrus psyllid. Diaphorina citri. Appl. Entomol. Zool. 43, 33–36 (2008).Tomaseto, A. F. et al. Environmental conditions for Diaphorina citri Kuwayama (Hemiptera: Liviidae) take-off. J. Appl. Entomol. 142, 104–113 (2018).Paris, T. M., Croxton, S. D., Stansly, P. A. & Allan, S. A. Temporal response and attraction of Diaphorina citri to visual stimuli. Entomol. Exp. Appl. 155, 137–147 (2015).Zanardi, O. Z. et al. Putative sex pheromone of the Asian citrus psyllid, Diaphorina citri, breaks down into an attractant. Sci. Rep. 8, 455 (2018).Metsalu, T. & Vilo, J. ClustVis: A web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap. Nucleic Acids Res. 43, W566–W570 (2015).Fournier, D. A. et al. AD Model Builder: using automatic differentiation for statistical inference of highly parameterized complex nonlinear models. Optim. Methods Softw. 27, 233–249 (2012).Bates, D., MĂ€chler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Softw. 67, 1–48 (2015).Nelder, J. A. & Wedderburn, R. W. M. Generalized linear models. J. R. Stat. Soc. 135, 370–384 (1972).DemĂ©trio, C. G. B., Hinde, J. & Moral, R. A. In Ecological Modelling Applied to Entomology (eds Ferreira, C. P. & Godoy, W. A. C.) 219–259 (Springer, 2014).Lenth, R. V. Least-Squares Means: the R package lsmeans. J. Stat. Softw. 69, (2016).R Core Team R: A language and environment for statistical computing. 2015. R Foundation for Statistical Computing, Vienna, Austria (2015). Available at, http://www.r-project.org/ . (Accessed: 20th July 2017)

    Early detection surveillance for an emerging plant pathogen : a rule of thumb to predict prevalence at first discovery

    No full text
    Emerging plant pathogens are a significant problem for conservation and food security. Surveillance is often instigated in an attempt to detect an invading epidemic before it gets out of control. Yet in practice many epidemics are not discovered until already at a high prevalence, partly due to a lack of quantitative understanding of how surveillance effort and the dynamics of an invading epidemic relate. We test a simple rule of thumb to determine, for a surveillance programme taking a fixed number of samples at regular intervals, the distribution of the prevalence an epidemic will have reached on first discovery (discovery-prevalence) and its expectation E(q*). We show that E(q*) = r/(N/Δ), i.e. simply the rate of epidemic growth divided by the rate of sampling; where r is the epidemic growth rate, N is the sample size and Δ is the time between sampling rounds. We demonstrate the robustness of this rule of thumb using spatio-temporal epidemic models as well as data from real epidemics. Our work supports the view that, for the purposes of early detection surveillance, simple models can provide useful insights in apparently complex systems. The insight can inform decisions on surveillance resource allocation in plant health and has potential applicability to invasive species generally
    corecore