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Occurrence, Density, and Transcriptomic Response of the Leafhopper Erythroneura sudra (Hemiptera: Cicadellidae) When Confronted With Different Fruit Tree Species

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Wang; Yueyue; Huang; Xunbing; Li; Hui; Chen; Guangyan

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Occurrence, Density, and Transcriptomic Response of the Leafhopper Erythroneura sudra (Hemiptera: Cicadellidae) When Confronted With Different Fruit Tree Species

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OUP Academic (oup.com)

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https://academic.oup.com/jinsectscience/article/22/3/18/6619154

Date

2022-05-01

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Abstract. The leafhopper, Erythroneura sudra (Distant) is becoming a dominant insect pest, and usually can cause significant damage to fruit production in north

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Abstract

The leafhopper, Erythroneura sudra (Distant) is becoming a dominant insect pest, and usually can cause significant damage to fruit production in northern China. We studied the occurrence and density of E. sudra on three fruit tree species and its transcriptomic responses when it was fed on leaves of these tree species. A higher density and survival rate of E. sudra were recorded when it fed on leaves of peach (Amygdalus persica L.) (Rosales: Rosaceae) and cherry (Cerasus pseudocerasus Lindl) (Rosales: Rosaceae) than on apple (Malus domestica Mill) (Rosales: Rosaceae). Also, feeding on M. domestica induced the largest variation in transcriptomic profiles in E. sudra. In total, 166 genes were differentially expressed (89 upregulated and 77 downregulated) in E. sudra when it fed on M. domestica, compared to when it fed on the other two tree species. The upregulated genes were mainly related to ‘response to oxidative stress’, ‘stress-resistance’, and ‘xenobiotic metabolic process’. The downregulated genes were mainly related to ‘structural constituent of cuticle’, ‘biosynthetic process’, and ‘development regulation’. These results suggested that M. domestica significantly changed the expression of many genes and consequently caused lower occurrence and density of E. sudra. Such information could enhance our understanding of the leafhopper–host plant relationship. Additionally, it can contribute to the improvement of current control strategies for this pest.

The co-evolutionary history of plant–insect interactions is estimated to be about 400 million years (Richards et al. 2016). Consequently, almost all aspects of herbivorous insects, including growth, population dynamics, and gene expression, etc., can be influenced by host plants (Qin et al. 2017). Generally, herbivorous insects have specific food utilization spectrums (Schoonhoven et al. 2005, Poelman et al. 2008, Wetzel et al. 2016). The occurrence, density and growth of herbivores are influenced by access to suitable plant food (Ibanez et al. 2013, Yang et al. 2013). And, this may also promote pest plague or outbreaks (Cease et al. 2012, Huang et al. 2017a). For example, the plague population of Locusta migratoria manilensis (Meyen) (Orthoptera: Oedipodidae) was found to have strongly correlated with the plant species, Phragmites australis (Cav.) Trin (Poales: Poaceae) (Ji et al. 2007). The desert locusts, Schistocerca gregaria, grew larger, developed faster, had higher survival, and reproduced more and earlier when reared on high-nitrogenous plant leaves. This may possibly contribute to the successful buildup of the desert locust populations, which subsequently could lead to upsurges and plagues (White 1976, van Huis et al. 2008). Also, the egg hatching rate, larval survival, and reproductive rates of Spodoptera frugiperda reared on corn were all higher than those reared on Fagopyrum esculentum (Moench.) (Polygonales: Polygonaceae), Coix chinensis (Tod.) (Poales: Poaceae), and Phaseolus vulgaris (Linn.) (Rosales: Leguminosae) (Li et al. 2019).

Growth and occurrence of herbivorous insects are significantly influenced by host plants, which is in turn underpinned by genetic mechanisms (Roy et al. 2016, Turlings and Erb 2018). Such genes in herbivorous insects may be associated with signaling, transporters, development, stress resistance, digestion, immunity, nutrition metabolites, or detoxification (Qin et al. 2017, Chang et al. 2019). For example, the grasshopper, Oedaleus asiaticus (Bey-Bienko) (Orthoptera: Oedipodidae) had a large variation in gene profiles when fed on unsuitable food plants. Genes related to DNA replication (endonuclease-reverse transcriptase, DNA primase large subunit, DNA polymerase alpha catalytic subunit, et al.), biosynthesis, and metabolism (6-phosphogluconate dehydrogenase, lipoyltransferase 1, putative fatty acyl-CoA reductase, peptidyl-prolyl isomerase-1, protein disulfide-isomerase, et al.) were downregulated significantly and some genes related to detoxification (cytochrome P450 6k1 and carboxylesterase) were upregulated significantly (Huang et al. 2017a,b). Studies on such change could enhance our understanding of the relationship between herbivorous insects and their host plants.

Erythroneura sudra (Hemiptera: Cicadellidae) is a serious sucking pest, especially for Rosaceae fruit tree species in China (Xin 2008). Attacked leaves can reduce tree photosynthesis and consequently decrease fruit production (Chen 2012, Fornasiero et al. 2016). So far, knowledge on the gene response of E. sudra to feeding on different host plants is currently limited. Therefore, it is required that more studies are conducted to provide detailed information on this relationship. We used RNA-Seq to explore the possible transcription mechanisms underlying responses in E. sudra when it fed on three different plant species. Our goal was to unravel how different host plants affected the regulation of gene expressions in E. sudra. Further, it was also to apply such knowledge for the development of improved management strategies to control this pest.

Materials and Methods

Field Survey

The study site was located in Yi county (43.862°N, 116.028°E), southern Shandong province, China. In this region, E. sudra is becoming a major leaf pest of fruit trees (Supp Fig. 1 [online only]). Three plots, respectively, planted by peach (Amygdalus persica), apple (Malus domestica), and cherry (Cerasus pseudocerasus) for 5 yr, were selected to survey the occurrence density of E. sudra in 2020. No insecticides were applied to the plots during the survey.

In total, 10 trees were randomly selected in each plot, to survey E. sudra occurrence and density. In each tree, we randomly selected 15 leaves from the top (5 leaves), middle (5 leaves), and bottom (5 leaves) to record the numbers of E. sudra. Then, we derived a relative E. sudra density for each tree (number of individuals per 15 leaves). The field survey was conducted from 6.00 a.m. to 8.00 a.m. when the E. sudra were less active (Xin 2008, Chen 2012). This survey was conducted two times per month from May to September.

Feeding Trial

A 2-yr feeding trial were conducted during mid-July and late-August in 2019 and 2020 to determine how C. pseudocerasus, M. domestica, and A. persica affected the survival and development time of E. sudra. In each year, a total of 300 first-instar nymphs of E. sudra were starved for 24 h and assigned to 15 plastic insect-breeding cages. Then, all boxes were maintained under an 13:11 (L:D) h light regime at a RH of 70% and a temperature of 28°C.

To obtain fresh leaves to feed leafhoppers, we used gauze to protect leaves of the fruit tree species from March to August in each year. Fresh leaves (5 g) were harvested daily from each tree species and supplied as food to the leafhoppers. Each treatment was conducted five times. The leaves were replaced every 24 h and leafhoppers were inspected daily until all surviving individuals became adults. Developmental time (days) of leafhoppers was calculated using the same method described by Li et al. (1987). Survival rate (%) of leafhoppers was calculated by the number of surviving adults/the initial number of first-instar nymphs.

Transcriptome Sequencing

We collected three samples of leafhoppers from each of three treatments in 2020. Each sample consisted of five E. sudra adults (one chosen randomly from each of the five replicates). In total, nine samples were prepared. RNA of these samples was extracted using TRIzol reagent (Invitrogen, Carlsbad, CA). Then, the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs, Ipswich, USA) was used to generate the sequencing libraries. Finally, the Illumina HiSeqTM 4000 platform (Illumina Inc., San Diego, CA) was used to sequence the libraries.

To obtain high-quality clean reads, we removed the adaptor-containing sequences, poly-N, and low-quality reads. The remaining clean reads were further used in the assembly and gene abundance calculation. Trinity was used to carry out de novo assembly of the transcriptome (Grabherr et al. 2011). All nine transcriptomes were de novo assembled. Unigenes were used for BLASTX searches with an E-value < 10−5 in the following databases: Nt, KOG, Nr, Swiss-Prot, KO, PFAM, and Gene Ontology (GO).

Differential Expression Analysis

SOAPaligner/soap2 was used to remap the sequenced reads for each sample to the assembled transcriptome (Li et al. 2009). Gene expression values were quantified as FPKM by RSEM (Li et al. 2011). Differentially expressed genes (DEGs) were detected using the DESeq2 package in R (Anders et al. 2010). Transcripts with a minimum two-fold difference (|log2·Fold_change| > 1) in expression and adjusted P-values < 0.05 were considered differentially expressed.

DEGs were annotated to the GO database using the GOseq R packages (Young et al. 2010), and mapped to pathways in the KEGG database using the KOBAS software according to P-value < 0.05 (Mao et al., 2005).

Validation by Quantitative Real-Time PCR

In total, 12 candidate DEGs (Supp Table 1 [online only]) were chosen for validation by quantitative real-time PCR (qRT-PCR). The gene-specific primers are provided in Supp Table 2 (online only). We collected one adult randomly from each replicate cage, and extracted their total RNA and synthesized their cDNA using the AMV reverse transcriptase (Invitrogen). We conducted the qRT-PCR according to the following conditions: denaturation (95°C, 2 min; 40 cycles, 94°C, 10 s), annealing (59°C, 10 s), and extension (72°C, 40 s). β-Actin was used as the reference gene. Relative expression of each gene was analyzed by the 2−ΔΔCT method. Three technical replicates were conducted for each gene.

Data Analysis

Tukey’s HSD post hoc (one-way ANOVA, SAS version 8.0 software) was used to compare the relative density, developmental time, and survival rate of leafhopper after verifying normality. Holm–Sidak post hoc test was used to compare the relative gene expression levels between groups. P < 0.05 was considered statistically significant.

Results

Occurrence

The field survey from May to September in 2020 (Fig. 1) showed that the occurrence density of E. sudra on the tree species had two peaks. The first peak occurred on 15 July, with recorded relative densities on A. persica, C. pseudocerasus, and M. domestica as 59.37 ± 9.66, 51.32 ± 8.96, and 21.26 ± 5.92, respectively. The second peak occurred on 30 August, with recorded relative densities on A. persica, C. pseudocerasus, and M. domestica as 45.27 ± 6.69, 51.39 ± 8.25, and 12.36 ± 3.68, respectively. The relative densities of E. sudra on M. domestica were significantly lower at the two peaks, compared to the other two fruit trees (the first peak: F = 10.68, df = 2, 447, P < 0.001; the second peak: F = 13.32, df = 2, 447, P < 0.001).

Growth Performance

The 2-yr feeding trial showed that E. sudra had significant higher survival rates (2019: F = 5.65; df = 2, 12; P = 0.003; 2020: F = 7.91; df = 2, 12; P < 0.001) and faster developmental times (2019: F = 2.68; df = 2, 12; P = 0.035; 2020: F = 3.96; df = 2, 12; P = 0.021) on A. persica and C. pseudocerasus than on M. domestica (Fig. 2).

Transcriptome Analysis

Transcriptomes (accession number SRR14224867) of E. sudra when it was fed on the three tree species generated 40,411 unigenes (Table 1; Supp Table 3 [online only]). Of these, 17,585 (43.51%) were successfully annotated by NCBI Nr, 13,534 (33.49%) by Swiss-Prot, 14,028 (34.71%) by GO, 14,030 (34.71%) by PFAM, 20,989 (51.94%) by KO, 8,141 (20.15%) by KOG, and 6,538 (16.17%) by Nt (Supp Table 4 [online only]).

Group name . Number .
Total assembled bases 186,785,416
Total number of unigenes 40,411
GC percentage (%) 46.18
Unigene N50 (bp) 1,466
Unigene N90 (bp) 438
Maximum unigene length (bp) 27,603
Minimum unigene length (bp) 301
Average unigene length (bp) 1,100
Group name . Number .
Total assembled bases 186,785,416
Total number of unigenes 40,411
GC percentage (%) 46.18
Unigene N50 (bp) 1,466
Unigene N90 (bp) 438
Maximum unigene length (bp) 27,603
Minimum unigene length (bp) 301
Average unigene length (bp) 1,100
Group name . Number .
Total assembled bases 186,785,416
Total number of unigenes 40,411
GC percentage (%) 46.18
Unigene N50 (bp) 1,466
Unigene N90 (bp) 438
Maximum unigene length (bp) 27,603
Minimum unigene length (bp) 301
Average unigene length (bp) 1,100
Group name . Number .
Total assembled bases 186,785,416
Total number of unigenes 40,411
GC percentage (%) 46.18
Unigene N50 (bp) 1,466
Unigene N90 (bp) 438
Maximum unigene length (bp) 27,603
Minimum unigene length (bp) 301
Average unigene length (bp) 1,100

DEGs in E. sudra

DEGs were generated by comparing ES-Md (sample feeding on M. domestica) versus ES-Ap (sample feeding on A. persica) (677 downregulated, 197 upregulated), ES-Md versus ES-Cp (sample feeding on C. pseudocerasus) (645 downregulated, 265 upregulated), and ES-Cp versus ES-Ap (66 downregulated, 108 upregulated) (Table 2). Erythroneura sudra’s feeding on M. domestica generated the highest number of upregulated or downregulated genes. The cluster analysis of DEGs (Fig. 3) also showed a significant genetic variation in E. sudra’s feeding on M. domestica. In total, 166 genes (77 downregulated, 89 upregulated) were differentially expressed when E. sudra fed on M. domestica, compared separately to when it fed on the other two plant species (Fig. 4; Supp Tables 5 and 6 [online only]).

Leafhopper comparison . Downregulated genes . Upregulated genes .
ES-Md vs ES-Ap 677 197
ES-Md vs ES-Cp 645 265
ES-Cp vs ES-Ap 66 108
Leafhopper comparison . Downregulated genes . Upregulated genes .
ES-Md vs ES-Ap 677 197
ES-Md vs ES-Cp 645 265
ES-Cp vs ES-Ap 66 108

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persica), respectively.

Leafhopper comparison . Downregulated genes . Upregulated genes .
ES-Md vs ES-Ap 677 197
ES-Md vs ES-Cp 645 265
ES-Cp vs ES-Ap 66 108
Leafhopper comparison . Downregulated genes . Upregulated genes .
ES-Md vs ES-Ap 677 197
ES-Md vs ES-Cp 645 265
ES-Cp vs ES-Ap 66 108

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persica), respectively.

The DEGs between when E. sudra fed on M. domestica and when it fed on the other two trees were assigned to 10 GO terms using the GOseq packages in R (corrected P-value < 0.05) (Table 3). Downregulated GO terms included ‘structural constituent of cuticle’, ‘carbohydrate metabolic process’, ‘chitin binding’, ‘starch metabolic process’, and ‘biosynthetic process’. Upregulated GO terms included ‘antioxidant activity’, ‘regulation of apoptotic process’, ‘response to oxidative stress’, ‘response to reactive oxygen species’, and ‘xenobiotic metabolic process’.

GO terms . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Structural constituent of cuticle Down 16 14
Carbohydrate metabolic process Down 13
Chitin binding Down 8 10
Starch metabolic process Down 15 11
Biosynthetic process Down 13
Antioxidant activity Up 13 12
Regulation of apoptotic process Up 10
Response to oxidative stress Up 12
Response to reactive oxygen species Up 12
Xenobiotic metabolic process Up 11 9
GO terms . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Structural constituent of cuticle Down 16 14
Carbohydrate metabolic process Down 13
Chitin binding Down 8 10
Starch metabolic process Down 15 11
Biosynthetic process Down 13
Antioxidant activity Up 13 12
Regulation of apoptotic process Up 10
Response to oxidative stress Up 12
Response to reactive oxygen species Up 12
Xenobiotic metabolic process Up 11 9

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persica), respectively. ‘—’ indicates the corrected P-value > 0.05 and therefore not significantly different.

GO terms . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Structural constituent of cuticle Down 16 14
Carbohydrate metabolic process Down 13
Chitin binding Down 8 10
Starch metabolic process Down 15 11
Biosynthetic process Down 13
Antioxidant activity Up 13 12
Regulation of apoptotic process Up 10
Response to oxidative stress Up 12
Response to reactive oxygen species Up 12
Xenobiotic metabolic process Up 11 9
GO terms . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Structural constituent of cuticle Down 16 14
Carbohydrate metabolic process Down 13
Chitin binding Down 8 10
Starch metabolic process Down 15 11
Biosynthetic process Down 13
Antioxidant activity Up 13 12
Regulation of apoptotic process Up 10
Response to oxidative stress Up 12
Response to reactive oxygen species Up 12
Xenobiotic metabolic process Up 11 9

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persica), respectively. ‘—’ indicates the corrected P-value > 0.05 and therefore not significantly different.

The DEGs between when E. sudra fed on M. domestica and when it fed on the other two trees were assigned to 11 pathways using the KOBAS software (q-value < 0.05) (Table 4). The downregulated pathways included ‘carbohydrate digestion and absorption’, ‘insulin signaling pathway’, ‘glycolysis/luconeogenesis’, ‘fatty acid metabolism’, ‘ribosome’, ‘N-glycan biosynthesis and cutin’, ‘suberine and wax biosynthesis’. The upregulated pathways included ‘peroxisome’, ‘metabolism of xenobiotics by cytochrome P450’, ‘FoxO signaling pathway’, and ‘apoptosis’.

Pathway . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Carbohydrate digestion and absorption Down 8 12
Insulin signaling pathway Down 13 9
Glycolysis/gluconeogenesis Down 10
Fatty acid metabolism Down 13 7
Ribosome Down 17 15
N-glycan biosynthesis Down 11
Cutin, suberine and wax biosynthesis Down 9 6
Peroxisome Up 7
Metabolism of xenobiotics by cytochrome P450 Up 9 8
FoxO signaling pathway Up 6
Apoptosis Up 6
Pathway . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Carbohydrate digestion and absorption Down 8 12
Insulin signaling pathway Down 13 9
Glycolysis/gluconeogenesis Down 10
Fatty acid metabolism Down 13 7
Ribosome Down 17 15
N-glycan biosynthesis Down 11
Cutin, suberine and wax biosynthesis Down 9 6
Peroxisome Up 7
Metabolism of xenobiotics by cytochrome P450 Up 9 8
FoxO signaling pathway Up 6
Apoptosis Up 6

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persic). ‘—’ indicates a corrected P-value > 0.05 and therefore not significantly different.

Pathway . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Carbohydrate digestion and absorption Down 8 12
Insulin signaling pathway Down 13 9
Glycolysis/gluconeogenesis Down 10
Fatty acid metabolism Down 13 7
Ribosome Down 17 15
N-glycan biosynthesis Down 11
Cutin, suberine and wax biosynthesis Down 9 6
Peroxisome Up 7
Metabolism of xenobiotics by cytochrome P450 Up 9 8
FoxO signaling pathway Up 6
Apoptosis Up 6
Pathway . Upregulation/downregulation . Number of genes for ES_Md vs ES_Ap . Number of genes for ES_Md vs ES_Cp .
Carbohydrate digestion and absorption Down 8 12
Insulin signaling pathway Down 13 9
Glycolysis/gluconeogenesis Down 10
Fatty acid metabolism Down 13 7
Ribosome Down 17 15
N-glycan biosynthesis Down 11
Cutin, suberine and wax biosynthesis Down 9 6
Peroxisome Up 7
Metabolism of xenobiotics by cytochrome P450 Up 9 8
FoxO signaling pathway Up 6
Apoptosis Up 6

ES_Md (E. sudra feeding on M. domestica), ES_Cp (E. sudra feeding on C. pseudocerasus), and ES_Ap (E. sudra feeding on A. persic). ‘—’ indicates a corrected P-value > 0.05 and therefore not significantly different.

Gene Expression by qRT-PCR

The stress-resistant or detoxification enzyme-related POD, CAT, CYP450, GST, HSP, UGT, and GLU were all upregulated in E. sudra when it fed on M. domestica (Fig. 5A). The cuticle biosynthesis and development regulation-related VG, IGFP, CP, FAT, and INSR were downregulated (Fig. 5B). The qRT-PCR results and the RNA-Seq data showed significant correlations (r2 = 0.9783, P < 0.05).

Discussion

The occurrence and growth of herbivorous insects are closely associated with their host plants (Agrawal et al. 2015, Wetzel et al. 2016). In this study, we also found that the biological adaptability of E. sudra to their host plant is variable. Erythroneura sudra had higher population densities and superior growths when it fed on C. pseudocerasus and A. persica, which suggested that these tree species were more preferred by E. sudra than M. domestica. This implies that mass plantings of C. pseudocerasus and A. persica in the study area may promote a high occurrence of E. sudra population or even outbreaks. Hence, farmers should strengthen the management of E. sudra populations to avoid population explosions in this area. However, the reduced growth performance and lower density of E. sudra recorded on M. domestica compared to C. pseudocerasus and A. persica does not necessarily qualify it as undesirable, as it nevertheless supported a lower population of E. sudra that fed on it.

Variations in insect growth and occurrence on different host plants are underpinned by gene regulation (Turlings and Erb 2018). In this study, we also found that E. sudra had specific genetic adaptability to different host plants. Erythroneura sudra had significant variation in gene expressions when fed on M. domestica. Not surprisingly, little variation was observed in gene expression of leafhoppers that fed on A. persica and C. pseudocerasus, because their growth performance and density were not significantly different.

Erythroneura sudra feeding on M. domestica had many up-regulated genes related to ‘response to oxidative stress’, ‘stress-resistance’, and ‘xenobiotic metabolic process’. This was probably in response to stress from feeding on M. domestica. For example, the candidate gene for qRT-PCR, HSP (heat shock proteins), POD (peroxiredoxin), and CAT (catalase) are widely known to be highly induced when animals are confronted with environmental stress (Despres et al. 2007, Powell et al. 2011, Kumar et al. 2016, Li et al. 2016, Nojima et al. 2019). The upregulation of stress-resistance genes from the feeding on M. domestica corresponded to a significant lower growth and density of E. sudra. Generally, upregulation of these genes ameliorates stress in organisms (King and Macrae 2015). The CYP450 (cytochrome P450s), GST (glutathione-S-transferases), UGT (UDP-glycosyltransferases), and GLU (membrane beta-glucosidase) in herbivorous insects can modify the host plant’s toxic compounds, which are ingested, to render them less toxic (Zhang et al. 2012, Schuler and Berenbaum 2013, Xu et al. 2015, Poreddy et al. 2015, Pan et al. 2020). Undoubtedly, E. sudra has evolved complex strategies, such as the induction of many stress resistance-related genes to overcome the adverse effects from diet stress. Also, these genes were mainly enriched in the pathways of metabolism of xenobiotics by cytochrome P450, apoptosis, peroxisome, and FoxO signaling pathway, which have been confirmed to be related to stress-resistance regulation (Aparna et al. 2004, Lehtinen et al. 2006, Despres et al. 2007, Davies et al. 2013). Upregulation of such genes or pathways is beneficial for leafhoppers to overcome the potential diet stress for survival.

In addition, we found that leafhoppers that fed on M. domestica had many downregulated genes related to ‘structural constituent of cuticle’, ‘carbohydrate metabolic process’, ‘biosynthetic process’, and ‘development regulation’. For example, the candidate gene for qRT-PCR, VG (vitellogenin), IGFP (insulin-like growth factor-binding protein), CP (cuticle protein), FAT (fatty acid synthase), and INSR (insulin receptor) have been identified to be involved in insect development (Taguchi and White 2008, Charles 2010, Badisco et al. 2013, Hu et al. 2019). The downregulation of these genes and their enriched pathways (e.g., insulin signaling pathway, carbohydrate digestion and absorption) also may be responses to toxic substances or nutritional deficits in such plants and that can reduce insect development or reproduction. These genes and pathways may have played a role in the reduced growth performance of E. sudra. Such responses to M. domestica may also be vital for leafhopper survival. Future studies should identify the role of these significantly changed genes in leafhopper feeding on different plant foods.

The biological and genetic adaptations, including growth, density, and gene expressions of the leafhopper E. sudra to different host plants, are variable. The underlying factors may be related to plant defense responses or nutritive compounds (Richards et al. 2016, Züst and Agrawal 2017). For example, A. persica and C. pseudocerasus may have important nutrients, such as fatty acids or vitamins, or have appropriate C/N ratio (Ibanez et al. 2013), that are vital for leafhopper growth. Malus domestica, on the other hand, may have nutritional deficits or possess some special substances that induced stress in the leafhoppers. Future research should focus on the potential effects of such chemicals on gene expressions in the leafhopper. Undoubtedly, such information could enhance our understanding of the relationship between herbivorous insects and their host plants. Additionally, it could contribute to improvements in current control and management strategies for this pest.

We demonstrated by transcriptome analysis that E. sudra had a lower density and decreased growth when it fed on leaves of M. domestica than on A. persica or C. pseudocerasus. Here, we only studied the same 166 DEGs between E. sudra that had fed on M. domestica compared to that which fed on the other two tree species. We also found other DEGs between E. sudra when it fed on A. persica and C. pseudocerasus. Determination of the selective factors that influenced these different expression patterns requires future study.

Acknowledgments

This study was supported by the Science and Technology Fund Project of Shandong Provincial Department of Agriculture and Rural Affairs (2019LY005), and the National Natural Science Foundation of China (31700553 and 32102199). We also thank the DBMediting for language services.

Author Contributions

Y.W., X.H., and H.L. planed and designed the work, conducted experiments and statistical analyses, and wrote the manuscript. G.C. conducted experiments. All authors have read and agreed to the published version of the manuscript.

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Author notes

These authors contributed equally to this work.

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