Maize plants produce direct resistance elicited by Tetranychus urticae Koch (Acari: Tetranychidae)/Plantas de milho produz resistencia elicitada por Tetranychus urticae Koch (Acari: Tetranychidae).
A wide diversity of herbivore species infests plants. Thus, over evolutionary time plants have developed constitutive and induced responses against these enemies (Price et al., 1980; Karban and Baldwin, 1997). The constitutive resistances operate continuously, complicating herbivore feeding through cuticular deposits, thickened epidermis and abundance of crystals, thorns, trichomes and fibers in the lea (Becerra, 1994). The chemical responses, such as toxic metabolites and/or repellents act, for example, minimizing damage by reducing the palatability of the plants or by toxic effects in the herbivores (Arimura et al., 2005).
Induced responses that reduce the herbivore survival and reproduction are termed as induced resistance (Karban and Baldwin, 1997). Induced resistances can be classified as induced direct resistance, that directly affect the herbivore biology (Schaller, 2008) and induced indirect resistance, which affects herbivores by promoting the attraction of natural enemies, as predators and parasitoids (Arimura et al., 2005; Dicke et al., 2009; Castro et al., 2014). The induced direct resistance against herbivores, for example, affects the production of secondary metabolites, substances involved in plant resistance mechanisms (Karban and Baldwin, 1997). For example, protease inhibitors and phytoalexins, directly affect the herbivore survival (Howe and Jander, 2008; Ryan, 1990). The responses of plants to herbivore attack can reduce subsequent herbivory via induced resistance (Karban and Carey, 1984; Agrawal et al., 2000). Thus, damage to part of the plant results in a systemic response, release of volatile compounds and, biochemical cascade into the plant (Moraes et al., 2000). Previous studies have reported direct resistance induction by Tetranychus urticae Koch (Acari: Tetranychidae) in plants, resulting in reduced performance of these organisms in previously infested plants (Karban and Carey, 1984; Kant et al., 2004).
The two-spotted spider mite, T. urticae, is a polyphagous herbivore of great economic importance in many crops, having a host range of more than 1,100 species of plants (Grbic et al., 2011). Nevertheless, the technical literature that recommends pest management strategies in maize (Zea mays L., Poaceae) in Brazil still does not refer to records of mite populations that have reached pest status (Fadini et al., 2010). Surveys of the species incidence and studies on mites as pests in maize are scarce (Moraes and Flechtmann, 2008; Fadini et al., 2012). Despite showing little importance as maize pests, herbivore tetranychide mites, and even eriophyoidea ones are endemically present and their populations can eventually increase when them find favorable resources and conditions and achieve pest status (Cruz et al., 2008).
The study of plant resistance is critical to the elucidation of factors that affect the arthropod community (e.g. herbivores and predators) in agroecosystems. The comprehension of the resistance mechanisms of plants facilitates the development of pest-resistant cultivars, as well as determination of biochemical and evolutionary relationships between plants and herbivores (Welling, 2001; Bale et al., 2008; Chen, 2008). There are no examples in literature about direct resistance in Z. mays induced by phytophagous mites. Therefore, the biochemical routes into the plant and ecological consequences in food web are a not studied area yet.
We tested the hypothesis that maize plants would be able to directly induce resistance to T. urticae after infestation. To test this hypothesis, we evaluated the effect of pre-infestation of maize plants by T. urticae on development and reproduction of conspecifics upon reinfestation.
2. Material and Methods
The experiment was conducted in a greenhouse and laboratory from December 2013 to February 2014. To verify the possibility of direct resistance induction in maize plants, we assessed the population growth of T. urticae on maize plants infested by conspecifics and on plants not previously infested.
2.1. Stock cultures of mites
Individuals of T. urticae were obtained from the leaves of maize Z. mays at Embrapa Milho e Sorgo, in Sete Lagoas, Minas Gerais State. Approximately 1,000 adults were removed from the leaves with a brush and transferred to seedlings of the bean Phaseolus vulgaris L (Poaceae), due to facilities to maintain this plant; the spider mites have a good performance on bean (Moraes and Flechtmann, 2008). Bean seed was sown in 500-gram plastic pots, using Terral Solo[R] substrate and kept isolated in screened cages. The rearing occurred in a greenhouse under natural conditions. Every 5 days, two new bean plants were added to maintain the population. Uninfested bean plants were also kept in a greenhouse and added to the rearing of the T. urticae mites, according to the need for plants for more infestations.
2.2. Maize plant infestation
The maize seeding occurred on December 21, 2013, in 500 g plastic pots, using Terral Solo[R] substrate and kept in a greenhouse. The maize seed planted was the conventional hybrid 30F35. Two seeds were sown per pot and thinned after two weeks to only one maize seedling per pot. Seven days after sowing the maize plants were fertilized with 0.2 g of ammonium sulfate per pot. The plants were kept in screened cages to prevent infestation by herbivores.
The two treatments evaluated were 30 uninfested plants (hereafter clean plants) and 30 plants infested with the two-spotted spider mite T. urticae (hereafter infested plants). A single infestation was conducted in maize plant group composed of clean plants. For each plant, a leaf on the abaxial face was infested with 10 females of T. urticae during five days that were maintained within a barrier made using entomological glue Biocontrole[R] to prevent escape. The infested leaves were marked for future identification. Entomological glue did not affect the plant.
Five days after the infestation, 10 females of T. urticae were set in infested and clear plants, and the leaves were marked. In infested plants, the spider mites were put in a non-infested leaf. The first infestations were kept on the plants. We evaluated the survival and reproduction of 10 spider mites females in infested and clean plants as follows.
Five days after the last infestation a random drawing of the plants to be evaluated in the group of infested and clean plants was conducted. The pots, numbered from 1 to 30, were drawn for a once-only reading of the plants, so that each maize plant became an independent sampling unit. Counting was done by removing the leaves from the previously drawn plants, identified and cut at its extremity with scissors and taken to the laboratory for viewing under magnifying glass (40X). The evaluations were conducted for 15 days, reading a total of two individuals per treatment (infested and clean plants) in each day. For each individuals one leaf were removed and daily we evaluated the number of live and dead females, the number of immatures and the number of eggs. For statistical, all measure in each day were the average of two plants.
2.3. Statistical analyses
Generalized Linear Models (GLM) with a negative binomial distribution were used for data analysis. This distribution is justified when the relationship between mean and variance is greater than one. The main independent variable (x) was the infestation by T. urticae and the time after the infestation. The dependent variables (y) were the number of living female mites, number of immature and number of T. urticae eggs. The fit of the models was evaluated by residual analysis and compliance tests. The R program (R Development Core Team, 2014) was used for exploratory analysis and statistical data. The package MASS was used to adjust models with negative binomial distribution for aggregated data. To test de adjustment of statistical models, the experimental error will be tested for the random distribution.
3. Results and Discussion
The infested plants showed a reduced the number of adult females when compared with the clean plants. In both treatments the number adult females reduced over time with a higher reduction rate in infested plants ([chi square] = 3.2, df = 1, p = 0.003; Figure 1A). However, the number of immatures ([chi square] = 1.0, df = 1, p = 0.323; Figure 1B) and the number of eggs ([chi square] = 0.8, df = 1, p = 0.390; Figure 1C) were not affected by treatments.
The infestation in maize plants by phytophagous mites reduced the number of conspecific individual adults a second infestation. These results suggest that plants undergoing prior infestations by T. urticae are able to induce direct resistances to injury compared to those that were not attacked (Baldwin and Schmelz, 1996). However, additional chemical analysis on infested and clean plants is necessary to confirm this hypothesis. Karban and Carey (1984) reported the induction of direct resistance by T. urticae in cotton plants, resulting in reduced performance of these phytophagous mites on previously attacked plants. In agreement with the direct resistance induction in maize plants by T. urticae hypothesis, studies conducted with tomato plants suggested that the two-spotted spider mite, T. urticae, induces direct resistance in tomato regulated by jasmonates (Li et al., 2002; Kant et al., 2004; Smart et al., 2013). Szczepaniec et al. (2013) noted an increase in resistance gene expression induced by phytophagous mites, as well as gene expression related to induced resistance and population reduction of T. urticae in tomato plants, maize and cotton. This present study also corroborates the findings, strongly suggesting the induction of direct resistance by T. urticae in maize plants.
However, the infestation of T. urticae in maize plants did not affect the number of immatures and the number of eggs of conspecifics compared to those maintained on clean plants. This possibly occurred because the resistances elicited in the plants act more quickly on the adult survival than on their reproduction. Fadini et al. (2004) did not observe changes in biological parameters of T. urticae in induced direct response in strawberry plants. One possible explanation for this result may also be due to the exposure time being insufficient to impair the juveniles. Maeda and Ishiwari (2012) tested the effect of Tianidil, an activator that induces resistances in Camellia sinensis (Theaceae) plants as a mechanism against herbivores, and they did not verify reductions in the oviposition rate, immature stage duration and sex ratio of the mite T. kanzawai. One hypothesis is that the induced direct resistances would affect adult females since they fed on the plants. However, the exposure time to the resistance was not enough to change reproduction related parameters (i.e. number of eggs and number of immature forms), as mentioned. Another hypothesis for the results obtained can be related to the developmental stage in which the plants were found (Boege and Marquis, 2005).
This is first report suggesting direct resistance induction in maize by the two-spotted spider mite T. urticae. It can serve to guide future studies, from which more conclusive information about the biochemical mechanisms involved this kind of resistance. Although T. urticae is not regarded as an abundant and damaging herbivore in maize, resistance induction can come a management component and minimize any injuries caused by this herbivore. Resistance induction may prove to be a component of herbivore mite integrated management in maize.
Financial support and scholarships were provided by the National Council of Scientific and Technological Development (CNPq) and by the Minas Gerais State Foundation for Research Aid (FAPEMIG).
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P. D. Paulo (a), C. G. Lima (a), A. B. Dominiquini (a), M. A. M. Fadini (a) *, S. M. Mendes (b) and C. G. S. Marinho (a)
(a) Department of Agricultural Science, Universidade Federal de Sao Joao del- Rei--UFSJ, Rod MG 424, Km 47, CEP 35701-970, Sete Lagoas, MG, Brazil
(b) Embrapa Milho e Sorgo, Rod MG 424, Km 45, CEP 35701-970, Sete Lagoas, MG, Brazil
* e-mail: email@example.com
Received: November 24, 2015--Accepted: August 12, 2016--Distributed: February 28, 2018
Caption: Figure 1. Mean of adult female (A), immatures (B), and eggs (C) of Tetranychus urticae on clean (o) and infested (*) maize plants recorded during 15 days.
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|Title Annotation:||Original Article|
|Author:||Paulo, P.D.; Lima, C.G.; Dominiquini, A.B.; Fadini, M.A.M.; Mendes, S.M.; Marinho, C.G.S.|
|Publication:||Brazilian Journal of Biology|
|Date:||Feb 1, 2018|
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