14 research outputs found

    Estimating epidemiological parameters from experiments in vector access to host plants, the method of matching gradients.

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    Estimation of pathogenic life-history values, for instance the duration a pathogen is retained in an insect vector (i.e., retention period) is of particular importance for understanding plant disease epidemiology. How can we extract values for these epidemiological parameters from conventional small-scale laboratory experiments in which transmission success is measured in relation to durations of vector access to host plants? We provide a solution to this problem by deriving formulae for the empirical curves that these experiments produce, called access period response curves (i.e., transmission success vs access period). We do this by writing simple equations for the fundamental life-cycle components of insect vectors in the laboratory. We then infer values of epidemiological parameters by matching the theoretical and empirical gradients of access period response curves. Using the example of Cassava brown streak virus (CBSV), which has emerged in sub-Saharan Africa and now threatens regional food security, we illustrate the method of matching gradients. We show how applying the method to published data produces a new understanding of CBSV through the inference of retention period, acquisition period and inoculation period parameters. We found that CBSV is retained for a far shorter duration in its insect vector (Bemisia tabaci whitefly) than had previously been assumed. Our results shed light on a number of critical factors that may be responsible for the transition of CBSV from sub- to super-threshold R0 in sub-Saharan Africa. The method is applicable to plant pathogens in general, to supply epidemiological parameter estimates that are crucial for practical management of epidemics and prediction of pandemic risk

    Different plant viruses induce changes in feeding behavior of specialist and generalist aphids on common bean that are likely to enhance virus transmission

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    Bean common mosaic virus (BCMV), bean common mosaic necrosis virus (BCMNV), and cucumber mosaic virus (CMV) cause serious epidemics in common bean (Phaseolus vulgaris), a vital food security crop in many low-to-medium income countries, particularly in Sub-Saharan Africa. Aphids transmit these viruses “non-persistently,” i.e., virions attach loosely to the insects' stylets. Viruses may manipulate aphid-host interactions to enhance transmission. We used direct observation and electrical penetration graph measurements to see if the three viruses induced similar or distinct changes in feeding behaviors of two aphid species, Aphis fabae and Myzus persicae. Both aphids vector BCMV, BCMNV, and CMV but A. fabae is a legume specialist (the dominant species in bean fields) while M. persicae is a generalist that feeds on and transmits viruses to diverse plant hosts. Aphids of both species commenced probing epidermal cells (behavior optimal for virus acquisition and inoculation) sooner on virus-infected plants than on mock-inoculated plants. Infection with CMV was especially disruptive of phloem feeding by the bean specialist aphid A. fabae. A. fabae also experienced mechanical stylet difficulty when feeding on virus-infected plants, and this was also exacerbated for M. persicae. Overall, feeding on virus-infected host plants by specialist and generalist aphids was affected in different ways but all three viruses induced similar effects on each aphid type. Specifically, non-specialist (M. persicae) aphids encountered increased stylet difficulties on plants infected with BCMV, BCMNV, or CMV, whereas specialist aphids (A. fabae) showed decreased phloem ingestion on infected plants. Probing and stylet pathway activity (which facilitate virus transmission) were not decreased by any of the viruses for either of the aphid species, except in the case of A. fabae on CMV-infected bean, where these activities were increased. Overall, these virus-induced changes in host-aphid interactions are likely to enhance non-persistent virus transmission, and data from this work will be useful in epidemiological modeling of non-persistent vectoring of viruses by aphids

    A new method for the analysis of access period experiments, illustrated with whitefly-borne cassava mosaic begomovirus.

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    Reports of low transmission efficiency, of a cassava mosaic begomovirus (CMB) in Bemisia tabaci whitefly, diminished the perceived importance of whitefly in CMB epidemics. Studies indicating synergies between B. tabaci and CMB prompt a reconsideration of this assessment. In this paper, we analysed the retention period and infectiousness of CMB-carrying B. tabaci as well as B. tabaci susceptibility to CMB. We assessed the role of low laboratory insect survival in historic reports of a 9d virus retention period. To do this, we introduced Bayesian analyses to an important class of experiment in plant pathology. We were unable to reject a null hypothesis of life-long CMB retention when we accounted for low insect survival. Our analysis confirmed low insect survival, with insects surviving on average for around three days of transfers from the original infected plant to subsequent test plants. Use of the new analysis to account for insect death may lead to re-calibration of retention periods for other important insect-borne plant pathogens. In addition, we showed that B. tabaci susceptibility to CMB is substantially higher than previously thought. We also introduced a technique for high resolution analysis of retention period, showing that B. tabaci infectiousness with CMB was increasing over the first five days of infection

    The role of pathogen-mediated insect superabundance in the East African emergence of a plant virus.

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    One of the major crops for food security is cassava. Superabundant Bemisia tabaci whitefly, comprising unusually high landscape populations of the insect, have been implicated in cassava virus emergence. Studies have been unable to select from several hypotheses, however, as to the dynamic drivers of superabundant whitefly associated with the emergence in East Africa of severe cassava mosaic disease. One possibility is that pathogenic modification of infected plants can itself increase the growth of insect vector colonies on infected plants.Through the modelling of population processes at the landscape scale we introduce a framework for analysing patterns in the association of disease and insect waves.Our analyses demonstrate the role of pathogen-mediated insect superabundance in a plant disease invasion. Synthesis. An elevated abundance of insects at the landscape scale is frequently implicated in invasions of the plant pathogens that they carry. We advance ecological understanding of plant disease invasions by showing how landscape data can be used to investigate the causes of insect vector superabundance

    Estimating epidemiological parameters from experiments in vector access to host plants, the method of matching gradients.

    No full text
    Estimation of pathogenic life-history values, for instance the duration a pathogen is retained in an insect vector (i.e., retention period) is of particular importance for understanding plant disease epidemiology. How can we extract values for these epidemiological parameters from conventional small-scale laboratory experiments in which transmission success is measured in relation to durations of vector access to host plants? We provide a solution to this problem by deriving formulae for the empirical curves that these experiments produce, called access period response curves (i.e., transmission success vs access period). We do this by writing simple equations for the fundamental life-cycle components of insect vectors in the laboratory. We then infer values of epidemiological parameters by matching the theoretical and empirical gradients of access period response curves. Using the example of Cassava brown streak virus (CBSV), which has emerged in sub-Saharan Africa and now threatens regional food security, we illustrate the method of matching gradients. We show how applying the method to published data produces a new understanding of CBSV through the inference of retention period, acquisition period and inoculation period parameters. We found that CBSV is retained for a far shorter duration in its insect vector (Bemisia tabaci whitefly) than had previously been assumed. Our results shed light on a number of critical factors that may be responsible for the transition of CBSV from sub- to super-threshold R0 in sub-Saharan Africa. The method is applicable to plant pathogens in general, to supply epidemiological parameter estimates that are crucial for practical management of epidemics and prediction of pandemic risk

    Cucumber mosaic virus 2b proteins inhibit virus-induced aphid resistance in tobacco.

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    Cucumber mosaic virus (CMV), which is vectored by aphids, has a tripartite RNA genome encoding five proteins. In tobacco (Nicotiana tabacum), a subgroup IA CMV strain, Fny-CMV, increases plant susceptibility to aphid infestation but a viral mutant unable to express the 2b protein (Fny-CMV∆2b) induces aphid resistance. We hypothesized that in tobacco, one or more of the four other Fny-CMV gene products (the 1a or 2a replication proteins, the movement protein, or the coat protein) are potential aphid resistance elicitors, whilst the 2b protein counteracts induction of aphid resistance. Mutation of the Fny-CMV 2b protein indicated that inhibition of virus-induced resistance to aphids (Myzus persicae) depends on amino acid sequences known to control nucleus-to-cytoplasm shuttling. LS-CMV (subgroup II) also increased susceptibility to aphid infestation but the LS-CMV∆2b mutant did not induce aphid resistance. Using reassortant viruses comprising different combinations of LS and Fny genomic RNAs, we showed that Fny-CMV RNA 1 but not LS-CMV RNA 1 conditions aphid resistance in tobacco, suggesting that the Fny-CMV 1a protein triggers resistance. However, the 2b proteins of both strains suppress aphid resistance, suggesting that the ability of 2b proteins to inhibit aphid resistance is conserved among divergent CMV strains.This work was supported by grants from the UK Biotechnological and Biological Sciences Research Council (SCPRID grant number BB/J011762/1, and GCRF grant number BB/P023223/1) and the Leverhulme Trust (F/09741/F, RPG-2012-667), and QL was funded by the China Scholarship Council
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