Role of Large Cabbage White butterfly male-derived compounds in elicitation of direct and indirect egg-killing defenses in the black mustard

To successfully exert defenses against herbivores and pathogens plants need to recognize reliable cues produced by their attackers. Up to now, few elicitors associated with herbivorous insects have been identified. We have previously shown that accessory reproductive gland secretions associated with eggs of Cabbage White butterflies (Pieris spp.) induce chemical changes in Brussels sprouts plants recruiting egg-killing parasitoids. Only secretions of mated female butterflies contain minute amounts of male-derived anti-aphrodisiac compounds that elicit this indirect plant defense. Here, we used the black mustard (Brassica nigra) to investigate how eggs of the Large Cabbage White butterfly (Pieris brassicae) induce, either an egg-killing direct [i.e., hypersensitive response (HR)-like necrosis] or indirect defense (i.e., oviposition-induced plant volatiles attracting Trichogramma egg parasitoids). Plants induced by P. brassicae egg-associated secretions expressed both traits and previous mating enhanced elicitation. Treatment with the anti-aphrodisiac compound of P. brassicae, benzyl cyanide (BC), induced stronger HR when compared to controls. Expression of the salicylic (SA) pathway- and HR-marker PATHOGENESIS-RELATED GENE1 was induced only in plants showing an HR-like necrosis. Trichogramma wasps were attracted to volatiles induced by secretion of mated P. brassicae females but application of BC did not elicit the parasitoid-attracting volatiles. We conclude that egg-associated secretions of Pieris butterflies contain specific elicitors of the different plant defense traits against eggs in Brassica plants. While in Brussels sprouts plants anti-aphrodisiac compounds in Pieris egg-associated secretions were clearly shown to elicit indirect defense, the wild relative B. nigra, recognizes different herbivore cues that mediate the defensive responses. These results add another level of specificity to the mechanisms by which plants recognize their attackers.


Introduction
Plants form the base of most terrestrial ecosystems and are under attack by a diverse community of insect herbivores. Natural selection has shaped interactions between these two trophic levels such that plants have evolved anti-herbivore defenses, and herbivores have evolved strategies to better exploit their hosts. To understand the evolution of plant -insect interactions it is crucial to know how insect attack is perceived and in particular which signals are involved in this dialog (Bonaventure et al., 2011). Upon feeding damage, plant cells produce damage-associated molecular patters (DAMPs) which trigger a general plant wound response (Heil, 2009). Recognition of more specific effectors in these interactions is based on so-called herbivore-associated molecular patterns (HAMPs), which may be present in, e.g., oral or oviposition secretions (Felton and Tumlinson, 2008;Mithöfer and Boland, 2008;Acevedo et al., 2015;Hilker and Fatouros, 2015). Several effectors like amino acid-lipid conjugates, peptides, or enzymes originating from herbivore salivary glands have been shown to elicit direct plant defenses that can reduce herbivore performance or indirect defenses that improve the foraging of natural enemies (Schoonhoven et al., 2005;Bonaventure et al., 2011;Felton et al., 2014). The plant hormones jasmonic acid (JA), ethylene (ET), and salicylic acid (SA) have been shown to be the main players in orchestrating the downstream production of defense compounds effective against chewing insects (Wu and Baldwin, 2010;Erb et al., 2012;Thaler et al., 2012). Yet, relatively little is known on the recognition of HAMPs by plants compared to interactions between plants and microbes, oomycetes, or nematodes, for which hundreds of elicitors have been described (Felton et al., 2014).
Many plant-insect interactions do not start with a feeding herbivore, but with an ovipositing female. As a cue that signals future damage, egg recognition and triggering of the appropriate response might provide plants with fitness benefits (Pashalidou et al., 2015). Several plant species have been shown to respond to herbivore egg deposition by expressing direct or indirect egg-killing defenses (Hilker and Fatouros, 2015). The ability of recognizing this early phase of attack might be crucial for plant survival but its consequences have been often neglected when studying the ecology of associations between herbivorous insects and plants (Hilker and Fatouros, 2015). A few effectors of oviposition-induced plant defenses have been identified and isolated from egg-associated secretions and extracts from homogenized eggs (Reymond, 2013;Hilker and Fatouros, 2015). Insects have also evolved strategies to overcome plant recognition; there is evidence that eggs might contain effector molecules that suppress plant defenses (Bruessow et al., 2010). More insights into plant responses to these egg-derived elicitors is required to understand their ecological consequences and potential evolutionary importance.
In brassicaceous plants, different oviposition-induced direct and indirect defenses have been identified. Brussels sprouts plants (Brassica oleracea var. gemmifera) induced by egg deposition of two Cabbage White butterfly species, the Large Cabbage White Pieris brassicae and the Small Cabbage White P. rapae were shown to retain Trichogramma egg parasitoids by chemical modifications in the leaf surface (Fatouros et al., 2005(Fatouros et al., , 2009Pashalidou et al., 2010), a type of indirect plant defense using so-called substrate-borne chemical cues (Colazza et al., 2014). During mating, pierid males transfer speciesspecific anti-aphrodisiac compounds in their spermatophores to females. These compounds were shown to curtail courtship and decrease the likelihood of female re-mating (Andersson et al., 2000(Andersson et al., , 2003. In previous work by Fatouros et al. (2008Fatouros et al. ( , 2009, we showed that egg-associated secretions produced by accessory reproductive glands (ARGs) of mated females of Cabbage White butterflies contain minute amounts of anti-aphrodisiac compounds that induced the biosynthesis of chemical cues retaining Trichogramma wasps. A subsequent study in Arabidopsis thaliana showed that epicuticular waxes, in particular some fatty acids, might act as cues for the wasps (Blenn et al., 2012).
Brassica nigra is an annual plant that responds to P. brassicae eggs by a necrosis resembling pathogen-induced hypersensitive response (HR) (Figures 1A,B), and which can directly kill eggs by desiccating or dropping-off the plant (Shapiro and De Vay, 1987;Fatouros et al., 2012Fatouros et al., , 2014. Furthermore, B. nigra plants were shown to release volatile chemical cues induced by eggs of the gregarious P. brassicae that attract egg and larval parasitoids and repel conspecific butterflies Cusumano et al., 2015;Ponzio et al., manuscript accepted). Interestingly, in the closely related but solitary P. rapae, both HR-like necrosis and oviposition-induced plant volatiles (OIPVs) were shown to act synergistically, leading to high egg mortality in nature (Fatouros et al., 2014). However, the elicitors responsible for these two traits in B. nigra are still unknown.
The aim of this study is to investigate whether egg-killing defenses in B. nigra are induced by ARG secretions released by the ovipositing female and whether anti-aphrodisiac compounds transferred during mating play a role in the elicitation. We conducted experiments to investigate whether (i) the elicitor of HR and OIPVs induced by P. brassicae is located in the ARGs, (ii) mating plays a role in elicitation, and if so (iii) whether the malederived anti-aphrodisiac compound benzyl cyanide (BC) triggers HR and/or the emission of OIPVs attracting egg parasitoids. For a better understanding of the mechanistic basis of these interactions, we further tested whether (iv) JA and SA signaling pathways were involved in plant responses to P. brassicae egg deposition and the anti-aphrodisiac compound BC by measuring their activity using two marker genes: lipoxygenase gene2 (LOX2) and pathogenesis-related gene1 (PR1).

Plants and Insects
Seeds of black mustard plants (B. nigra L.) were either obtained from a population collected along the river Rhine in Wageningen, The Netherlands or provided by the Centre for Genetic Resources [CNG, (accession number: CGN06619), Wageningen, The Netherlands]. The latter were multiplied by exposing them to pollinators in the surroundings of Wageningen. Both plant populations have been used in previous studies on Pieris oviposition-induced defenses (Fatouros et al., , 2014. The plants were grown in a greenhouse (18 ± 5 • C, 50-70% RH, L16:D8), and used in the experiments when 3-5 weeks old. The Large Cabbage White butterfly P. brassicae L. (Lepidoptera: Pieridae) was reared on Brussels sprouts plants (B. oleracea var. gemmifera cv. Cyrus) at 21 ± 1 • C, 50-70% RH, and photoperiod L16:D8, and mated females obtained from a cage where up to 50 adults of similar age were allowed to mate. Females that were observed mating were selected and were used in the experiments either immediately or 2 days after, depending on the experiment. Virgin females were obtained by isolating females immediately after eclosion (Fatouros et al., 2009). The isofemale line ED16 of Trichogramma evanescens Westwood (Hymenoptera: Trichogrammatidae) was reared on Ephestia kuehniella eggs (Koppert, Berkel en Rodenrijs, The Netherlands) under standardized conditions in a climate chamber (25 ± 1 • C, 50-70% r.h., L16:D8). Newly emerged male and female wasps were kept together for 2-5 days to allow mating and then used in the preference experiments. All wasps used in the preference experiments lacked previous contact with any plant material or host residues and are referred to as inexperienced.

Preparation of ARG Homogenates
Accessory reproductive glands (ARGs) were dissected from mated and virgin P. brassicae females (3-6 days after eclosion) (Figures 1C,D) under a stereo-microscope (optical magnification 20×) in phosphate buffered saline (PBS). One gland was transferred to 100 µL PBS, homogenized and centrifuged and used to treat a single plant.

Plant Treatments
To obtain plants with 1-3 P. brassicae egg clutches, individual B. nigra plants were placed in a cage with ca. 50 P. brassicae males and females for up to 10 min until egg deposition was observed, and then they were transferred to the greenhouse (18 ± 5 • C, 50-70% RH, L16:D8) for either four or 24 h depending on whether they were used in the bioassays or gene expression analysis, respectively. In bioassays on the effect of P. brassicae ARG homogenate on HR, 100 µl of the ARG supernatant of either mated or virgin females and PBS as control was applied with a fine brush to the edge of three different leaves of the same plant. For bioassays or gene expression analyses with plants treated with the anti-aphrodisiac compound BC, solutions of 0.5, 1, and 1.5 ng of BC/100 µl or the solvent ethanol (70%) as control were made. The solutions were applied with a fine brush to the edge of the third or fourth leaf from the top. For all plants, development of the necrotic tissue (HR) was checked after 72 h and visually categorized as none, weak, medium, or strong necrosis (Figure 2). A total of eight replicated plants were used per treatment. For bioassays on elicitation of egg parasitoidattracting volatiles, either ARG homogenate of P. brassicae females (mated or virgin) or BC (1 or 10 ng/100 µl ethanol) was applied on B. nigra plants. Test plants were compared with control plants treated with the solvent (PBS as control for ARG or ethanol for the anti-aphrodisiac) in a Y-tube olfactometer (see below) 24 h after treatment.

Y-tube Olfactometer Tests
We tested the attraction of T. evanescens wasps to volatiles of B. nigra plants induced by either ARG homogenates of P. brassicae or their anti-aphrodisiac compound (BC). Bioassays were conducted by using a dynamic airflow Y-tube olfactometer (For details see Fatouros et al., 2012). This olfactometer was designed to track minute wasps like Trichogramma sp. so that they can be released in groups. We have previously established that group-release does not influence the behavior of Trichogramma wasps . Ten adult females were released and their choice for one of the two odor sources was recorded. Thereafter the position of the odor sources was exchanged and another group of 10 wasps was released to test their preference for the same two odor sources. After 45 min, the wasps present in the collection flasks placed at the end of the arms section of the olfactometer were counted. The wasps that did not make a choice within 45 min were recorded as "no response". The odor sources tested were plants treated with (i) ARG homogenates of either virgin or mated (2 or 48 h after mating) females against control plants treated with the solvent PBS, (ii) BC at two different concentrations (1 and 10 ng/100 µl ethanol), according to the concentrations that were detected in ARGs of mated P. brassicae females in a previous study (Fatouros et al., 2008), against control plants treated with ethanol only. In addition, we recorded the presence or absence of a hypersensitive-like response of the infested plants that were used in the bioassay. Per odor source combination 4-7 different plants with one replicate per experimental day were tested with 20 wasps released per replicate (80-140 wasps/ treatment). Each wasp was used only once.

Quantitative RT-PCR Analysis of Defense Genes
We used available or cloned primers for B. nigra of one gene encoding lipoxygenase (LOX2), a key enzyme in the biosynthesis of JA in Arabidopsis (Bell et al., 1995), and one pathogenesis-related (PR) gene, shown for Arabidopsis to function downstream of the SA signaling pathway (PR1) (Jirage et al., 2001). The used sequences of B. nigra gene specific primers were: PATHOGENESIS-RELATED GENE1 PR1 F 5 -CTTGGCCATGGGTAGCGGCG-3 and PR1 R 5 -ACACCTCGCTTTGCCACATCCA-3 , LIPOXYGENASE GENE2 LOX2 F 5 -TGCTCGTGCACGCCAGAGTC-3 and LOX2 R 5 -AGCCAGCCCCCTGCTGATGA-3 . Total RNA was extracted from app. 100 mg liquid nitrogen-ground leaf powder using the RNeasy Plant Mini kit (Qiagen). One µg of total RNA was treated with DNaseI (Invitrogen) and subsequently transcribed into cDNA using the iScript cDNA synthesis kit (Biorad) following the manufacturer's protocol. Quantitative RT-PCR was performed in a Rotor-Gene 6000 machine (Corbett Research) with a 72-well rotor. The amplification reactions were performed in 25 µl final volume containing 12.5 µl iQ SYBR Green Supermix (Bio-Rad, Hercules, CA, USA), 300 nM of the gene-specific forward and reverse primer, and 5 µl cDNA. All qRT-PCR experiments were performed in duplicate and average values were used in the analyses. The following PCR program was used for all PCR analyses: 95 • C for 3 min, followed by 40 cycles of 95 • C for 15 s, and 45 s at 62 • C. Ct values were normalized by using GAPDH as a reference gene (primer sequences: F 5 -GCTACGCAGAAGAC  AGTTGATGG-3 and R 5 -TGGGCACACGGAAGGACA TAC-3 ). Normalized gene expression was then calculated as 2 − Ct (Livak and Schmittgen, 2001). Data from 3 to 4 biological replicates were used for statistical analysis. For each biological replicate, two leaf disks 1 cm away from the treated area were collected from each plant as described above.

Statistics
The occurrence of HR on the plants and its intensity was analyzed with generalized linear models with a binomial error distribution corrected for overdispersion using the glm command and the quasibinomial family in R (R 3.0.2 http://www.r-project. org/). For both the effect of the females' gland extract and the concentration of BC, two different analyses were performed: one considering the occurrence of HR as a binomial response (i.e., no HR compared with all other categories), and another as no, or weak HR compared with medium or strong HR. To test for the effect of the females' gland extract, control, virgin, or mated females were included as categorical fixed factors, and for the effect of the BC the different concentrations were also included as categorical fixed factors. When overall differences were found, pairwise differences between factors were also tested applying the Bonferroni adjustment to the significance level. Data from the Y-tube olfactometer were analyzed by expressing the number of wasps that chose the test odor as the fraction of all responding wasps and arcsine transforming the variable. Subsequently, choices were tested against a 50:50 distribution with a one-sample t-test. Gene transcription data were log-transformed for normalization, and analyzed with one-way ANOVA for the two time points independently. Then the Dunnett test was used for post hoc comparisons between the different treatments and the control treatment.

Location of HR Elicitor and Effect of Mating and Male-derived Compounds
In comparison to controls, application of extract from female glands affected both the proportion of plants showing HR (HR vs. no HR) and the proportion of those plants showing medium or strong HR (no and weak HR vs. medium and strong HR) (X 2 2 = 15.9, p < 0.001, X 2 2 = 23.7, p < 0.001, respectively, Figure 3A). As shown by pairwise comparisons, in both cases HR occurrence or intensity was significantly higher when plants were treated with secretion of mated females (p < 0.016, Bonferroni corrected, Figure 3A). The application of BC on the plants also affected HR and its intensity (X 2 2 = 15.9, p < 0.001, X 2 2 = 23.7, p < 0.001, respectively, Figure 3B). In comparison to control plants treated with ethanol only, occurrence of HR was significantly higher at low concentration of BC (0.5 ng/100 µl ethanol; p < 0.008, Bonferroni corrected), but not when the concentration of the chemical was higher (p > 0.05, Figure 3B). The probability of medium or strong HR was significantly higher when plants were treated with the chemical in comparison to controls (p < 0.008, Bonferroni corrected), but differences among plants treated with different concentrations were not significant (p > 0.3).

Location of Elicitor of OIPVs and Effect of Mating and Male-derived Compounds
We tested volatiles of differently treated B. nigra plants against volatiles of control plants and their effect on the attraction of T. evanescens wasps. The wasps showed a preference to volatiles of plants treated with either P. brassicae eggs (One-sample t-test, t 9 = 3.10, p = 0.01, Figure 4) or ARG secretion of mated P. brassicae females (t 7 = 4.94, p = 0.002, Figure 4) when tested against clean or PBS-treated control plants, respectively. Volatiles of plants treated with ARG secretion of virgin females did not attract the wasps (t 11 = 0.66, p = 0.52, Figure 4). Volatiles of plants treated with secretion of females that mated in the previous few hours before testing (they would need few days to be able to start laying eggs) were significantly less attractive than the control plants (t 9 = 3.05, p = 0.01, Figure 4). Neither application of 1 ng of BC (t 11 = 0.07, p = 0.95, Figure 4) nor 10 ng of BC (t 11 = 0.44, p = 0.67, Figure 4) induced T. evanescens attracting volatiles when tested against ethanol-treated control plants.

Induction of Defense Genes Related to JA and SA Pathways
We measured the expression of two marker genes in the JA pathway (LOX2) or SA pathway (PR1) shown in previous studies on A. thaliana (Bell et al., 1995;Jirage et al., 2001). Deposition of P. brassicae eggs induced stronger expression of PR1 at 24 h after oviposition in plants that expressed HR (F 5,25 = 2.81; p = 0.044; Figure 5A), and this effect was neither observed in non-HR plants nor at an earlier time point. Expression levels of LOX2 were not affected by Pieris oviposition, although there was a trend of LOX2 induction in HR-expressing plants 4 h after oviposition (F 5,25 = 1.47; p = 0.242; Figure 5B). Application of the anti-aphrodisiac BC did not induce expression of these two genes.

Discussion
In the present study we show that secretion of ARGs of P. brassicae butterflies elicits both a direct (HR-like necrosis) and an indirect (emission of parasitoid-attracting OIPVs) defense response in the wild crucifer B. nigra. More importantly, we have identified one compound that plays a role as an elicitor. These results are in line with our previous studies that showed that ARG secretions of Pieris butterflies induce another type of defense, namely substrate-born chemical plant cues retaining Trichogramma wasps on egg-laden Brussels sprouts leaves (Fatouros et al., 2008(Fatouros et al., , 2009Pashalidou et al., 2010).
Exocrine secretions associated with egg deposition have been found to trigger plant defenses. For example, exocrine secretions either covering the eggs or used to glue eggs on the plant surface obtained from different insect species have been shown to elicit plant responses that resulted in egg mortality or in the emission of parasitoid-attracting plant cues (Hilker and Fatouros, 2015 and Figure 3 therein). Although the specific elicitors were not determined, leaves of Zea mays exhibit indirect defenses in response to eggs of different stemborer moths including Sesamia nonagrioidis and Chilo partellus. In the former, responses were found when both the ARG secretion and the eggs dissected from the ovaries were applied, whereas in the latter responses were triggered only after application of egg-associated secretions (Tamiru et al., 2011;Salerno et al., 2013). Similarly, dissected reproductive tracts of the smaller tea tortrix Adoxophyes honmai comprising of ovaries, oviduct, and accessory glands (see also Figure 1), were shown to elicit substrate-born chemical plant cues that retained the egg-larval parasitoid Ascogaster reticulata on tea leaves. Unlike in the case of the stemborer moth, A. reticulate crushed eggs did not elicit an indirect plant response (Deshpande and Kainoh, 2012). So far, only few studies on oviposition-induced plant defenses have identified the herbivore-associated elicitor. Bruchins isolated from pea weevils (Doss et al., 2000) and phospholipids isolated from rice planthoppers (Yang et al., 2013) have been shown to induce direct egg-killing plant defenses. Our previous studies demonstrated a role of the anti-aphrodisiac compounds BC and indole (in the butterflies P. brassicae and P. rapae, respectively) in eliciting substrate-borne chemical plant cues retaining Trichogramma wasps onto egg-infested B. oleracea leaves. Both compounds were detected in minute amounts in the egg-associated secretion of mated P. brassicae females whereas they were absent in secretion of virgin females (Fatouros et al., 2008(Fatouros et al., , 2009Pashalidou et al., 2010). Unlike B. oleracea, where wasps are retained on the leaf of an egg-infested plant, B. nigra plants emit volatiles that attract the wasps from a distance and provide a long-range cue to locate the host. These differences in parasitoid-attracting cues could be due to, e.g., differences in the morphology of the two plants. B. oleracea has a glabrous waxy leaf surface and local changes in the plant might be a strategy to improve efficiency of foraging parasitoids. B. nigra, on the other hand, has non-waxy leaves covered with trichomes. Plants use trichomes as direct defenses against herbivores which are also known for their negative effects on predators and parasitoids (Wei et al., 2013;Riddick and Simmons, 2014). Moreover, the cultivar B. oleracea var. gemmifera could have lost the OIPV trait due to a trade-off when breeding the species for other traits, e.g., yield or taste (Palmgren et al., 2015). For example, herbivore-induced volatile emission was found to be very rare in commercial hybrids of maize but common in farmer-selected landraces (Tamiru et al., 2011(Tamiru et al., , 2012(Tamiru et al., , 2015. In the present study, we found that the anti-aphrodisiac compound of P. brassicae plays a role in eliciting a direct defense trait in the form of HR-like necrosis, whereas indirect defense was not triggered. Thus, our study suggests that malederived compounds other than the anti-aphrodisiac itself may also act as elicitors. In many butterflies, males transfer a so-called nuptial gift to the female's bursa copulatrix during mating. The male ejaculate consists of a spermatophore containing sperm, accessory gland products and a diverse array of nutrients that are also associated with egg production (Wiklund et al., 1993;Karlsson, 1998;Gillott, 2003). In some lepidopteran species, chemicals of paternal origin are transmitted to the mothers by seminal infusions that act as egg defenses against natural enemies (Eisner et al., 2002). For example, pyrrolizidine alkaloids (PAs), secondary metabolites from host plants are transmitted by males of arctiid moths to the females and they partly supply the paternal PAs to the eggs in order to deter predators (Dussourd et al., 1988;Eisner et al., 2002). Eggs of P. brassicae were shown to contain mustard oils, namely allylisothiocyanate (Aplin et al., 1975), but whether they are transmitted to the females during mating has not been studied yet. In our work, ARG secretions of recently mated females induced the emission of volatiles that repelled the Trichogramma wasps. Since the butterflies commonly start laying eggs 2 days after mating (David and Gardiner, 1962), this suggests that a physiological 'switch' initiated by the mating event triggers changes in the composition of the gland secretions through time. Seminal fluid proteins (SFPs) produced in reproductive tract tissues of male insects and transferred to females during mating induce numerous physiological and behavioral post-mating changes in females (Gillott, 2003;Avila et al., 2011). Thus, we cannot exclude that those physiological changes stimulated by seminal fluids are causing the observed changes in eliciting function of the eggassociated secretions after mating.
Current knowledge on egg-induced plant responses indicates a role of two antagonistic pathways, the JA and SA pathways (Reymond, 2013). In Arabidopsis, eggs of P. brassicae, and P. rapae consistently induce the SA signaling pathway including different PR genes although a necrosis is not visible in the Col-0 ecotype (Little et al., 2007;Bruessow et al., 2010). We show here that the HR-like necrosis is strongly associated with the induction of the SA-responsive gene PR1, which confirms our earlier observations on P. rapae-egg induced HR in B. nigra (Fatouros et al., 2014). LOX2, a gene involved in the JA-signaling pathway in Arabidopsis, was not affected by egg deposition in B. nigra and only slightly but not significantly induced at 4 h after oviposition by P. brassicae when HR-like necrosis was present. Yet, egg deposition by the conspecific P. rapae induced LOX3 at 24 h after oviposition on B. nigra plants in both phenotypes (HR+/HR−) (Fatouros, unpublished data). This suggests that the JA-dependent wound-induced response might work in parallel to an SA-dependent egg-induced response (Reymond, 2013). The current study supports this hypothesis and adds an extra aspect to explain the variability of the observed response in B. nigra: the presence or absence of an HR-like necrosis.

Conclusion
Our study demonstrates that secretions obtained from ARG reservoirs of Pieris butterflies contain specific elicitors of the different plant defense responses against eggs in Brassica. Mating changed the eliciting effect of the secretion suggesting that either male-derived compounds that arrive in the secretions or physiological changes triggered by mating play a role. Antiaphrodisiac compounds of Pieris butterflies transferred during mating that were shown to induce substrate-borne chemical cues in B. oleracea plants did only partly induce egg-killing defenses in B. nigra. As a direct egg-killing trait, HR-like necrosis, involves expression of PR1 defense genes and most likely the SAdependent pathway. Other studies on OIPVs have shown that the JA-pathway is involved (Meiners and Hilker, 2000;Hilker et al., 2002;Mumm et al., 2003). It is rather unlikely that the same compounds in an egg-associated secretion elicit different defense pathways and responses. Our study adds to the information on HAMPs and increases our understanding of how plants recognize information from herbivores in a non-feeding stage to respond with insect-killing defenses before actual damage occurs. preliminary analysis and discussion of data, and the experimental farm of Wageningen University (Unifarm) for rearing and providing plants. The authors are supported by grants from The Netherlands Organization for Scientific Research (NWO/ALW Veni grant 863.09.002 to N.E.F. and NWO open competition grants), the German Research Foundation (CRC973), and the European Community (Marie Curie Intra-European Fellowship, FP7-PEOPLE-2012-IEF #329648 to E.F.)