- Research article
- Open Access
Effects of leaf colorness, pigment contents and allelochemicals on the orientation of the Asian citrus psyllid among four Rutaceae host plants
BMC Plant Biology volume 19, Article number: 254 (2019)
Asian citrus psyllid (ACP) is the primary vector responsible for the transmission of the phloem-limited bacteria Candidatus Liberibacter spp., associated with huanglongbing (HLB), which causes great loss to the citrus industry. Although the roles of leaf color and volatile compounds in the orientation of ACP have been proven, the quantification of color and allelochemicals in the host plant are kept unclear, especially in wild citrus germplasms.
Chongyi wild mandarin significantly attracted more ACP than wild Hong Kong kumquat, ‘Gannan zao’ navel orange and orange jasmine did in the four-choice and olfactometer assays. The color parameters of the tender leaves from Chongyi wild mandarin and ‘Gannan zao’ were similar. The yellow color in both of them was less saturated than that of the other two plants species, but Chongyi wild mandarin had significant lower carotenoid content (P < 0.05). Notably metabolic profiling differences were observed among the healthy tender shoots from the four tested plants via UPLC-QQQ-MS and GC-MS analyses. Comparing with the other three plant species, 66 and 50 metabolites with significantly different contents in Chongyi wild mandarin were selected as UPLC-identified and GC-identified metabolites of interest (P < 0.05), respectively. Flavonoids accounted for a large group of secondary metabolites of interest, which may function as stimulants or repellents of ACP. Higher content of salicylic acid o-hexoside and lower content of (+)-jasmonic acid in Chongyi wild mandarin may lead to higher amount of methyl salicylate (an ACP attractant) and lower amount of trans-ocimene (an attractant to herbivores’ natural enemies) as well as the suppression of JA-mediated wounding response. This kind of synergistic or antagonistic effect among the metabolites differentially accumulated in Chongyi wild mandarin made it a more attractive host plant to ACP.
Less saturated yellow color, high amount of attractants, low amount of repellents and insensitivity of JA-mediated wounding response are the four possible reasons why Chongyi wild mandarin attracted more ACP. This work may shed light on the olfactory and visual response of ACP to wild citrus germplasm hosts, and suggest the feasibility of developing ACP attractants or repellents patterned on potential metabolites.
Huanglongbing (HLB), also called citrus greening, is one of the most economically devastating diseases of citrus worldwide, which is caused by the phloem-limited fastidious bacteria “Candidatus Liberibacter asiaticus” (CLas), “Ca. L. africanus” and “Ca. L. americanus” . Among these three species, CLas is believed to be the most dominant one and has caused huge economic losses to citrus industry globally . At the early stage, infected trees show up blotchy-mottled or completely yellow chlorotic leaves and deformed small fruits with aborted seeds . As the pathogen manipulates, the infected trees will suffer from the dysfunction of source-sink carbohydrate translocation, which leads to significant fruit-dropping and yield reduction . Now there are no commercial citrus cultivars that are strongly tolerant to CLas [2, 5]. Numerous measures have been tested to address this dysfunction or control the manipulation of CLas, such as the application of enhanced foliar nutrition and thermotherapy [3, 6]. However, citrus growers mainly rely on three steps to reduce the incidence of HLB, namely eradication of infected trees, the use of healthy nursery stocks and control of the insect vector via pesticides [2, 7].
Although CLas can be transmitted via graft inoculation, Asian citrus psyllid (ACP), Diaphorina citri Kuwayama (Hemiptera: Liviidae), is believed to be the primary vector of the bacterial causative agent of HLB [2, 8]. The plant hosts of D. citri include Murraya paniculata (L.) Jack, M. exotica L., M. koenigii L. and nearly all the citrus species [9,10,11]. However, wild citrus species were rarely reported as the host of ACP or used in HLB study.
The overuse of pesticides application could bring ACP under control, but it could also cause severe environmental damage, insect resistance and food safety problem as well as adverse effect on ACP’ natural enemies [12,13,14]. Many environmental friendly alternatives have been suggested, such as essential oils, parasitic wasp, entomopathogenic fungi and additional tactics that affect the visual cues of ACP, such as reflective mulching and kaolin [15,16,17,18,19,20,21]. Given the fact that ACP could accurately detect, evaluate, and discriminate visual cues, such as hue, saturation level and outline of the object, yellow sticky cards have been proved to be an effective green approach to monitor and trap ACP [22,23,24]. Although it could also be conditioned to recognize a blue-colored probing substrate , D. citri is innately attracted to bright yellow and green colors in the human visible spectrum that might resemble the flushing shoots [25,26,27]. Moreover, the addition of ultra-violet light could enhance the attraction of D. citri to green or yellow colors [27, 28]. Even though the role of color in the orientation of the ACP has been substantially studied, the quantification of color and related allelochemicals in leaves are kept unclear.
Besides color stimuli, olfactory cues also are critical in the initiation of host plant selection process by D. citri . Therefore, repellents or attractants patterned on volatile compounds have also been suggested to be a potential way in the protection of citrus plants against HLB, which has been introduced in the push-pull strategy for ACP management [29,30,31]. (E)-β-caryophyllene identified from guava , trisulfides (dimethyl trisulfide) from garlic chive leaves , terpenoids from the non-host cashew all had repellent effect on ACP . These repellent volatiles were mainly identified from non-Rutaceae plants. As to attractant, analysis on curry leaf preferred by female ACP revealed 10 monoterpenes and four sesquiterpenes as well as two unknown compounds that may function as attractants . The identified metabolites were quite few. To have a better implementation of the push-pull strategy, a large number of volatiles that can influence the behavior of ACP should be identified.
In this study, first we intended to identify which host plants was the most preferred one by ACP. And then combined metabonomics techniques were applied to study the metabolite differences among the tender shoots of the four tested plants. Our goal was to identify the potential volatile chemicals or metabolites responsible for attracting or repelling ACP, which could be useful in ACP detection and monitoring.
Chongyi wild mandarin was the most preferred host of D. citri among the four tested Rutaceae plants in both four-choice and olfactometer tests
During the one-month observing period of the four-choice test, wild Hong Kong kumquat (Fortune hindisii Swingle, Y) had significantly more tender shoots, 7 – 10 per plant, than that of Chongyi wild mandarin (C), ‘Gannan zao’ navel orange (Citrus sinensis, G) and orange jasmine (Murraya exotica L., J), 2 – 3 per plant (Fig. 1a, P < 0.05). There were no significant differences in the mean numbers of tender shoots among G, J and Y at the 15 time points (Fig. 1a, P > 0.05). In addition, D. citri exclusively fed on the flushing shoots and tender leaves of G, J, and Y. But, besides the tender shoots of Chongyi wild mandarin, few D. citri also fed on the mature leaves of the upper half of the plant. The results of the four-choice test revealed that C always attracted more D. citri than the other three tested plants in every counting time point (Fig. 1b). Out of the 15 time points, there were four times that C attracted significantly more D.citri than G and Y did, but 10 times that significantly more than J did (Fig. 1b, P < 0.05). Totally, the mean number of D. citri attracted by C in one month was significantly higher than the other three plant species at the significance level of P < 0.05 (Fig. 1c).
In the 6-arm olfactometer with 2 arms blocked, the arm connected to the tender shoot of Chongyi wild mandarin always attracted significantly more female D. citri adults than the other five arms did (Fig. 2, P < 0.01). Due to peer effect, the two arms on the right and left sides of Chongyi wild mandarin always attracted more insects than the rest three arms. Similar results were obtained when orange jasmine, ‘Gannan zao’, wild Hong Kong kumquat was placed next to Chongyi wild mandarin one by one. Therefore, only one representative figure was showed. Since it was the most preferred host of D. citri among the four tested plant species, Chongyi wild mandarin was used as control in the subsequent experiments.
Chongyi wild mandarin and ‘Gannan zao’ shared similar leaf color parameters
Color parameters of L∗, a∗, b∗, C∗ and H∗ from tender leaves were analyzed in order to check the leaf color differences among the four kinds of plants. The values of a∗ and b∗ in tender leaves of the four plants were negative and positive, respectively, suggesting that these leaves were green and yellow hue system (Fig. 3). In addition, the values of H∗ of these leaves ranged between 60° (yellow) and 120° (green), around 105° (Fig. 3), further proving that the leaves of all tested plants were the combination of green and yellow color. There was no significant difference among the values of a∗ (P > 0.05), which meant that all the tested leaves were fairly green (Fig. 3). The values of L∗, b∗, C∗ of tender leaves from C and G were significantly lower than that of J and Y (P < 0.05), suggesting that the tender leaves from J and Y were brighter, more yellowish and saturated than that of C and G (Fig. 3). The value of H∗ in tender leaves of C was highest and significantly higher than that of J and Y (Fig. 3, P < 0.05).
The tender leaves of Chongyi wild mandarin had the lowest carotenoid content
The contents of Chlorophyll (Chl) a, Chl b, Carotenoid (Car) and total Chl in orange jasmine were significantly higher than that in Chongyi wild mandarin, ‘Gannan zao’ and wild Hong Kong kumquat at the significance level of P < 0.05, and Chongyi wild mandarin had the lowest Car content (Fig. 4).
Untargeted metabolic profiling revealed allelochemicals with different contents between Chongyi wild mandarin and the other three plant species
The following results of ultra high performance liquid chromatography coupled to triple quadrupole tandem mass spectrometry (UPLC-QQQ-MS) and solid-phase microextraction (SPME) combined with gas chromatography-mass spectrometry (GC-MS) indicated that significant genotypic differences were observed in the metabolic profiles among the tender shoots of Chongyi wild mandarin (C), ‘Gannan zao’ navel orange (G) and orange jasmine (J) and wild Hong Kong kumquat (Y) under normal growth condition (Additional file 1: Figure S1 and Figure S2).
UPLC-identified metabolic profiling
The non-biased UPLC-QQQ-MS detected totally 391 peaks, of which 126 were unknown metabolites and the remaining peaks were identified as known metabolites, such as eriodictyol, betaine, punicic acid and L-valine. Metabolites were highly reproducible among the three analyzed biological replications. Based on the principal component analysis (PCA) results, a separation of samples was observed and the first principal component (PC1) contributed 65.8%, 76.6%, 57.4% of variation in the data set of G/C, J/C, Y/C, respectively (Additional file 1 :Figure S1).
To identify the important metabolites associated with host preference of ACP, the first principal component of variable importance in the projection (VIP) and Student's t-test were carried out. There were totally 237, 259, 196 secondary metabolites with significantly different (VIP > 1 and P-value < 0.05) content in G, J and Y, respectively, when C was used as the control (Table 1). As the Venn diagram shown in Fig. 5i, 66 UPLC-identified metabolites were differentially accumulated in G, J and Y when compared with C. The difference of their accumulation among the four plant samples was illustrated with heatmap, indicating that the content of each metabolite in every sample varied and the data had good repeatability among the replications (Fig. 6).
These 66 metabolites were listed in Table 2 as the UPLC-identified metabolites of interest. Amino acids were the largest differentially accumulated metabolite category, two with higher contents and seven with lower contents in C (Table 2), which explained that aminoacyl-tRNA biosynthesis was the most important pathway with significant enrichment (P < 0.05) in the pathway analysis (Additional file 1: Figure S3). To our limited knowledge, except L-tyrosine (an aromatic amino acid), trans-cinnamaldehyde, apo-13-zeaxanthinone and geranyl acetate, no other UPLC-identified metabolites of interest were directly aroma-related. Therefore, we focused on finding the color-related metabolites, such as chlorophyll, carotenoid, flavonoids.
The corresponding pathways were found in the KEGG analysis: porphyrin and chlorophyll metabolism, flavonoid biosynthesis pathway, flavone and flavonol biosynthesis pathway. In pathway analysis, the latter two pathways were singled out in the bubble plot (Additional file 1: Figure S3). Since KEGG analysis and pathway analysis used two different calculating methods, porphyrin and chlorophyll metabolism was not showed up in the bubble plot, in which 5-aminolevulinate (5-ALA), a pivotal compound in the biosynthesis of chlorophyll, had significantly lower content in C.
As the second largest UPLC-identified metabolite category with significant difference, eight flavones, six with higher content and two with lower content in C, were all yellow metabolites (Table 2). It was worth noting that three flavones with higher content in C (apigenin-7-rutinoside, tricin o-rutinoside and chrysoeriol 7-o-rutinoside) were all exclusive to Rutaceae. Eriodictyol and chryso-obtusin-o-hexoside were two yellow differentially accumulated flavonoids. Moreover, a yellow terpenoid (apo-13-zeaxanthinone) and a yellow phenylpropanoid (trans-cinnamaldehyde) were also identified. These differentially accumulated yellow compounds plus 5-ALA identified via UPLC-QQQ-MS analysis may play important roles in the attractiveness of C to ACPs.
GC-identified metabolic profiling
525 peaks were detected and 522 GC-identified metabolites, namely volatile compounds (VOCs), could be left through interquartile range de-noising method in GC-MS analysis. The score scatter plot for PCA model showed that the original data of all samples were distributed within the 95% confidence interval of Hotelling’s T-squared ellipse (Additional file 1: Figure S2I). Chongyi wild mandarin, ‘Gannan zao’, orange jasmine and wild Hong Kong kumquat were separated by PC1, representing 68.2%, 71.7% and 77.5% of the variation, respectively (Additional file 1: Figure S2II, S2III and S2IV).
Comparing with C, there were totally 205, 309, 301 metabolites with significantly different (VIP > 1 and P < 0.05) content in G, J and Y, respectively (Table 1). G had 99 metabolites with significantly higher contents and 210 with significantly lower contents (Table 1). Near 74% and 68% metabolites’ contents in J and Y were significantly higher than that in C, respectively (Table 1).
Unlike the UPLC-identified metabolites, quite few GC-identified metabolites were involved in the KEGG analysis and pathway analysis. In the bubble plot of pathway analysis, pyruvate metabolism, sulfur metabolism and TAC cycle all showed up in the G/C, J/C and Y/C data set (Additional file 1: Figure S4), but actually they only had one or two hits. This result suggested that only one or two differentially GC-identified metabolites directly participated in these differentially metabolic pathways.
As the Venn diagram showned in Fig. 5b, 50 VOCs were differentially identified, 34 with higher contents and 16 with lower contents in the tender shoot of Chongyi wild mandarin. The contents of these 50 VOCs in C, G, J and Y became evident in hierarchical clustering with heatmap (Fig. 7), which were selected as the GC-identified metabolites of interest and listed in Table 3. Intriguingly, except ethane and 12 unknown compounds, other 37 GC-identified metabolites of interest were all known aromatic compounds (Table 3). Monoterpenes accounted for the largest aromatic metabolite group, such as pinene, camphor, linalool, camphene, carveol, carvone and limonene, whose contents were significantly higher in Chongyi wild mandarin (Table 3). The levels of bicyclo [3.1.1] hept-2-ene, p-mentha-1,5,8-triene and cis-(-)-1,2-epoxy-p-menth-8-ene were also higher in Chongyi wild mandarin, comparing with the other three plants (Table 3). The odors released by those GC-identified metabolites with significantly higher contents in the VOCs of Chongyi wild mandarin may contribute to its attractiveness to ACP.
Close correlation existed between UPLC-identified and GC-identified metabolites of interest
Spearman correlation coefficients between UPLC- and GC-identified metabolites of interest were calculated and the results were illustrated with Heatmap (Fig. 8), which revealed that there were evidently intimate correlations between the two groups of metabolites identified by UPLC-QQQ-MS and GC-MS. The relationship between the characteristics reached a significant level (P < 0.05) was indicated by ‘*’ (Fig. 8). Pinene, 2,3-penatedione, 3-hexen-1-ol, 2-hexen-1-ol, 2-hexanamine, linalool, camphene, unknown 2, 5, 7, 12 (GC-identified metabolites), 1,2-cydohexanediol were positively or negatively correlated to over 50 UPLC-identified metabolites of interest (Fig. 8). While xanthosine, sn-glycero-3-phosphocholine, naringenin, cytidine, 3-hydroxykynurenine were correlated to 37 of the selected GC-identified metabolites of interest (Fig. 8).
Pairs with the correlation coefficient > 0.8 and the corresponding P-value < 0.05 were visualized via Cytoscape (v3.5.1). The correlation network contained 116 nodes and 534 edges (Fig. 9). Generally, UPLC-identified metabolites and GC-identified metabolites were clustered separately. GC-identified pinene, 2-hexen-1-ol, 2-hexanamine, 2,3-penatedione, linalool, unknown 2 and 7 were strongly correlated to 38, 38, 37, 37, 36, 35 and 35 UPLC-identified metabolites of interest, respectively, which formed the biggest cycle in the lower part of Fig. 9. It was noteworthy that those seven GC-identified metabolites with correlation to over 50 UPLC-identified metabolites of interest. And those seven metabolites were divided into two groups: group A (pinene, linalool and unknown 2) and B (2-hexen-1-ol, 2-hexanamine, 2,3-penatedione and unknown 7), which had higher and lower amount in the tender shoots of Chongyi wild mandarin, respectively. The UPLC-identified metabolites that were positively correlated to group A were negatively correlated to group B and vice versa (Additional file 2: Table S1).
As to the UPLC-identified metabolites, cytidine, unknown 1, chrysoeriol, eriodictyol and geranyl acetate were strongly correlated to 27, 22, 16, 16 and 14 GC-identified metabolites of interest, respectively (Fig. 9). Cytidine and unknown 1 (UPLC-identified) had similar correlated metabolites, while chrysoeriol, eriodictyol and geranyl acetate shared similar correlated metabolites.
Now citrus growers rely heavily on the use of pesticide to control ACP, which are costly and cause great environmental concerns. Therefore, visual cues plus repellent or attractant for citrus psyllid control were powerful alternatives in ACP monitoring and control . But the efficiency of this strategy largely depends on the volatile or colored chemicals identified from ACP’ hosts, because they generally rely on vision and olfaction for the selection of hosts . Because flushing shoots can directly influence the oviposition and development of ACP [35, 36], it is easy to infer that more flushing shoots will result in larger amount of ACP to feed on. However, the results of the four-choice tests demonstrated that Hong Kong kumquat had constantly more new shoots, but Chongyi wild mandarin was constantly more attractive to ACP. Therefore, visual and olfactory stimuli generated by tender shoots of Chongyi wild mandarin may be pivotal in the stimulatory response of ACP.
ACP was more attractive to ‘Ca. L. asiaticus’-positive plants that were less saturated in yellow color than negative ones, probably due to the fact that infected leaves possessed an altered plane of polarization for yellow (591 nm) wavelengths [27, 37, 38]. These reports were in consistent with our results that the yellow color in the tender leaves of ACP-preferred Chongyi wild mandarin was less saturated. The color of yellowish green leaf is mainly dominated by chlorophyll (Chl) and carotenoid (Car) . The formation of 5-Aminolevulinate (5-ALA), derived from glutamate, is the key step in the biosynthesis of chlorophyll and other four tetrapyrroles [40, 41]. But the content of 5-ALA in Chongyi wild mandarin was significantly lower than that in the other three host plants, which did not result in the lowest total Chl content. However, lower 5-ALA content may lead to lower content of chlorophyllide a, an anti-herbivory compound in citrus , which may cause Chongyi wild mandarin to attract more ACP. In the case of Car, Chongyi wild mandarin had the lowest Car content and highest apo-13-zeaxanthinone, which was reasonable because apocarotenoids can be produced by carotenoid cleavage dioxygenases (CCDs) . Intriguingly, apocarotenoids are versatile aroma chemicals  and the volatile apo-13-zeaxanthinone may be preferred by ACP.
Other two pathways rich in yellow secondary metabolites are flavonoid biosynthesis pathway, flavone and flavonol biosynthesis pathway. Since ACP is attracted to yellow in general , it is reasonable that six out of eight identified yellow flavones plus one flavonoid had higher contents in ACP-preferred Chongyi wild mandarin. Besides their yellow color characteristics, flavonoids/flavones/flavonols have been suggested to act as feeding deterrents or stimulants in pest control experiments [45,46,47]. For instance, unsubstituted flavones/flavonoids like eriodictyol and apigenin were the strongest feeding deterrents in the choice assay of 3rd-instars of bertha armyworm (Mamestra configurata Walker), while naringenine, 7,40-dihydroxyflavone and dihydroquercetin functioned as stimulants . However, in the results revealed by UPLC-QQQ-MS, apigenin, eriodictyol and naringenine had higher accumulation in Chongyi wild mandarin, indicating that they may play the role as stimulants to ACP. In addition, 2,3-dihydroxyflavone had lower contents in Chongyi wild mandarin, suggesting it may function as a deterrent. The discrepancy could be explained that a specific flavonoid/flavone/flavonol may have a dual nature as deterrent or stimulant to different pests . The other possibility was that the behavioral response of insects to a compound could vary depending on the concentration and the stage of the insect tested .
Along with the color-related metabolites identified by UPLC-QQQ-MS, two phytohormones may also contribute to the preference of ACP to Chongyi wild mandarin: salicylic acid (SA) and jasmonic acid (JA). SA was repeatedly reported to take part in biotic and abiotic stresses [49,50,51]. JA, the de-methylated product of methyl jasmonate (MeJA), could suppress the conversion of SA into methyl salicylate (MeSA) and MeJA itself could suppress the emission of MeSA [50,51,52]. The higher content of SA o-hexoside and lower content of JA may all lead to higher amount of MeSA/SA in Chongyi wild mandarin. MeSA turned out to be a key ACP attractant [51, 53], and high level of SA can block the biosynthesis of JA, which is required for wound-inducible systemic defense responses [48, 54]. Moreover, the above-mentioned chlorophyllide a was suggested to induce the JA-mediated pathway, which plays a positive role to defend herbivore in citrus . Therefore, the lower content of JA and higher content of MeSA may make Chongyi wild mandarin a more preferred host plant.
In the four-choice test, the host preference of ACP was influenced mainly by visual and olfactory stimuli. Chongyi wild mandarin and ‘Gannan zao’ shared similar color parameters. Apart from visual stimuli, ACP host preference is strongly influenced by volatiles emitting from the host plants [28, 33, 55]. Therefore, olfactory stimuli from Chongyi wild mandarin probably made it more preferable to ACP than ‘Gannan zao’. This hypothesis has been proved in the following olfactometer assay, strongly indicating that some volatile compounds from the tender shoot of Chongyi wild mandarin could attract D. citri.
Monoterpene, together with monoterpene esters and sequiterpenes, commonly exist in the leaves of Citrus species [56, 57]. The contents of monoterpenes in Chongyi wild mandarin, such as pinene, camphor, linalool, camphene, carveol, carvone and limonene, were significantly higher than the other three plants, suggesting that they may play as stimulants in affecting the foraging behavior of D.citri. However, some of the monoterpenes, like β-pinene, linalool and camphor, were suggested to have repellent role in insect behavior [58,59,60]. Few reports have revealed that linalool, an acyclic monoterpene alcohol, could be used as insect-repellent against corn earworm (Helicoverpa armigera), spider mite (Tetranychus urticae), mosquito (Aedes aegypti) and beetles (T. castaneum and Dominica Rhyzopertha) [60,61,62]. But linalool was suggested to function as an attractant at least at the beginning of host plant searching for western flower thrips (Frankliniella occidentalis) . And a combination of terpenoids such as linalool, myricene, and pinene appeared to synergistically attract the western (Diabrotica virgifera virgifera) and northern corn rootworm beetles (D. barberi) . In addition, there was a Chinese patent (NO. 104222078A) applied by South China Agricultural University revealed that a combination of γ-terpinene, α-pinene plus linalool could trap significantly more D. citri than control, indicating that the proper concentration and combination of terpenoids or VOCs in Chongyi wild mandarin may be attractive to ACP. Moreover, D. citri may prefer these monoterpenes because they are prevalent in Rutaceae and may represent the presence of flush, which is pivotal for the mating, oviposition and development of D. citri [36, 55].
Correlation analysis revealed that close relationship existed between UPLC-identified and GC-identified metabolites of interest. The positively and negatively correlated metabolites may have synergistic and antagonistic effect on each other, which may work together to affect the host preference of D. citri. For example, β-ocimene synthase in the terpenoid pathway is under the control of the JA pathway , which agreed with our result that trans-ocimene was positively correlated to JA but negatively correlated to SA o-hexoside because negative cross-talk exists between the JA and SA pathways in citrus plants . Moreover, exogenous application of MeJA and SA enhanced and suppressed the amount of E-β-ocimene, namely trans-ocimene, respectively, which was suggested to be a volatile attractive to many herbivores’ natural enemies [51, 67]. It is acceptable that host plants with lower amount of volatiles attractive to its natural enemy will be more attractive to D. citri, such as Chongyi wild mandarin.
Taken together, Chongyi wild mandarin was more attractive to ACP than the other three host plants, indicating a great potential of wild citrus germplasm in HLB-related study. Metabolic profiling of the tender shoots from the four Rutaceae plants suggested four possible reasons. The first reason may be the less saturated yellow color of the tender shoot. The second reason may be that Chongyi wild mandarin contained more ACP-preferred metabolites, such as MeSA, apocarotenoids as well as some monoterpenes. The third reason may be lower amount of repellents, such as the compounds favored by ACP’s natural enemies (trans-ocimene) and the metabolites playing anti-herbivory role (chlorophyllide a). The fourth reason may be due to the insensitivity of JA-mediated wouding response from the host plant, which will generate negative influence on ACP’s development or oviposition. Even though ACP host plant preference is based on complex profile combinations, our results may, with further investigations, contribute to the elucidation of the underlying mechanism.
Four host plants of Asian citrus psyllid (ACP, Diaphorina citri) were analyzed in our experiments: Chongyi wild mandarin (C), orange jasmine (J, Murraya exotica L.), ‘Gannan zao’ navel orange (G, Citrus sinensis) and wild Hong Kong kumquat (Y, Fortune hindisii Swingle). They are all Rutaceae host of “Candidatus Liberibacter asiaticus” (CLas). Seeds of orange jasmine were purchased from a certified seed company in Jiangsu, China. Seeds of Chongyi wild mandarin and wild Hong Kong kumquat were collected from the mountains of Chongyi county and Anyuan county of Ganzhou, China, respectively. ‘Gannan zao’ is a new early-ripening cultivar released by National Navel Orange Engineering Research Center (NORC), China, which is grafted onto Poncirus triafoliata rootstock for propagation and the other three tested plants are seedlings. The potted plants were cultured in the nursery of NORC for one and a half years. The CLas-negative plants were moved to the negative pressure laboratory at 25±3°C with 14 h:10 h (light:dark) photoperiod cycle (60±5% relative humidity, RH) and cultured for half a year before use. Two-year-old plants were used for host preference of ACP and the following experiments. Tender shoots of uninfested plants were sampled, immediately frozen in liquid nitrogen and stored at -80 oC till use.
Asian Citrus Psyllids
Diaphorina citri adults were obtained from a laboratory-reared colony at NORC. The colony was established using psyllid eggs laid by adults collected from a mature navel orange block in 2012. Regular PCR (every two month) proved that the offspring is CLas-negative. And the culture was maintained on a mixture of caged sweet orange (C. sinensis (L.) Osbeck.) and orange jasmine in the negative pressure laboratory mentioned above.
Half a month before host preference analysis, heading-back cut was applied to promote more shooting. Each plant of orange jasmine, Chongyi wild mandarin, wild Hong Kong kumquat and ‘Gannan zao’ were placed in the four corners of the same cage made from polyvinyl chloride tubes (2 cm in diameter) with the size of 75*75*90 (length*width*height). The cage was wrapped up with 0.25 mm diameter nylon net to prevent the spread of psyllids. Another two cages of plants were prepared as replications. A vial of psyllids (about 100) without regard to gender or age was collected from the laboratory-reared colony. After being starved for 1 h, the vial of psyllids was placed on the floor at the center of the cage and let them fly to feed freely. The number of psyllids on each plant was counted without disturbing two days after the release. And then, the psyllids were removed from the plants and another 100 psyllids were released again. The releasing, counting and removing process continued a month to analyze the dynamic host preference situation of psyllids on the four kinds of plants. Because the life cycle of ACP is closely related to the growth pattern of its host plants , the numbers of the tender shoots of each tested plants were counted during the same period of four-choice test.
However, host selection is not a static process as the needs of the insect at various developing stages may vary and the suitability of the plant to the insect may vary with time . Therefore, in the one-month-long four-choice test, the plants were unchanged and ACPs were randomly collected regardless of gender and age to consider them as a population.
D. citri olfactometer assay
The preference of D. citri toward the four plant species was tested with a 6-arm olfactometer (BL6-300M, Shanghai BILON instrument corporation, China). There were two opposite entries blocked manually because only four samples were investigated and there was no 4-arm olfactometer available in NORC. Because it was the most preferred host of D. citri in the four-choice test, the location of the tender shoot from Chongyi wild mandarin was unchanged, while the other three tender shoots were placed next to it one by one to eliminate its peer effect. Individual constant charcoal-filtered air flows at the rate of 0.4 L min-1 was connected to each tender shoot. And the air flows contained the odour from each plant were converged to the activity room (35 cm*35 cm*3 cm) with a polytetrafluoroethylene tubes. The tubes were cleaned with the charcoal-filtered air flows when the places of the tender shoots were changed. Two olfactormeter bioassays were conducted. In the first experiment, 80 adult D. citri regardless of gender and age, being starved for 1 h before use, were released in the center of the activity room through a lid (6 cm in diameter), whose edge was covered with Vaseline. Ten minutes later, the numbers of insects in different arms were counted. Three replications were done for the first olfactormeter bioassay. In the other experiment, a single adult female, being starved for 1 h before use, was released in the center of the activity room. Ten minutes later, the place of the female D. citri was recorded. If the insect stayed in the arm connected to Chongyi wild mandarin, then it scored 1, and so on. Ten replications were performed each day and the dataset from 8 independent days were used in the data analysis. All the experiments were carried out at room temperature, 60±5% RH and constant light (2300 lux).
Measurement of leaf color parameters, chlorophyll and carotenoid concentration
Color parameters of tender leaves from the four tested plants were measured with a NR200 Precision Colorimeter (Shenzhen 3nh Technology Co., Ltd., China) and quantified using the CIELAB color space system. The values of L∗, a∗, and b∗ explain a 3-dimensional color space. The value of L∗ is the vertical axis and defines lightness. The values of a∗ and b∗ are perpendicular horizontal axes and define red-to-green and blue-to-yellow, respectively. Positive value of a∗ indicates red color, whereas negative one indicates green. Positive value of b∗ indicates yellow color and negative one indicates blue. The values of L∗, a∗ and b∗ were obtained directly from the Colorimeter. Chroma (C∗, color saturation) and Hue (H∗, color shading) were calculated as follows: C∗ = (a∗2 + b∗2)1/2 and H∗ = 180 + tan-1 (b∗/a∗), (if a∗ < 0 and b∗ > 0). The greater the value of C∗, more saturated the color will be. H∗ defines colors expressed on 360° grid: 0°= red; 60°= yellow; 120°= green; 180°= cyan; 240°= blue; 300°= magenta [68, 69].
Chlorophyll and carotenoid concentrations were measured as described by Liu et al. (2008) with some modifications . Fresh tender leaves from four uninfested plant materials were randomly collected, respectively. About 0.2 g fine powder of leaf tissue was homogenized in 2 mL of 80% acetone and kept for 15 min at room temperature in dark. The crude extraction was centrifuged at 10, 000 r min-1 under room temperature for 20 min, and the supernatant was used for assessing absorbance at 663, 645 and 480 nm with a spectrophotometer (Shimadzu UV-2600, Japan). The concentration (mg/L) of Chlorophyll a (Ca), Chlorophyll b (Cb), total chlorophyll (Ct) and carotenoid (Cx.c) were calculated as follows: Ca = 12.21A665 – 2.81A649, Cb = 20.13A649 – 5.03A665, Ct = Ca + Cb, Cx.c = (1000A470 – 3.27Ca – 104Cb)/229.
The freeze-dried tender shoots of four plant varieties were crushed using a mixer mill (MM 400, Retsch) with a zirconia bead for 1.5 min at 30 Hz, respectively. Then 100 mg powder was extracted overnight at 4 °C with 1.0 mL 70% methanol containing 0.1 mg L-1 lidocaine as internal standard. The mixture was vortexed for three times at intervals. After being centrifuged at 10000 g for 10 min, the supernatant was filtrated with organic phase needle filter 0.22-μm pore size (SCAA-104, ANPEL, Shanghai, China) before LC/MS analysis.
The extracts were analyzed using an LC-ESI-MS/MS system (HPLC, Shim-pack UFLC SHIMADZU CBM20A system, Japan; MS, Applied Biosystems 4000 QTRAP, USA). The separation was achieved using a VP-ODS C18 column (particle size 5.0 μm, 2 mm × 150 mm; Shim-pack, Japan). The mobile phase consisted of 0.04% acetic acid in water and 0.04% acetic acid in acetonitrile. The gradient elution program was set as follows: water: acetonitrile, 95:5 V/V at 0 min, 5:95 V/V at 11.0 min, 5:95 V/V at 12.0 min, 95:5 V/V at 12.1 min, 95:5 V/V at 15.0 min. The flow rate, temperature and injection volume were 0.4 mL min-1, 40 °C, 5 μL, respectively.
Linear ion trap and triple quadrupole scans were acquired on a 4500 Q TRAP® LC/MS/MS System (API, USA) equipped with an ESI-Turbo Ion-Spray interface. The ESI source operation parameters were set as follows: source temperature, 550 °C; ion spray voltage, 5500 V; curtain gas, 25.0 psi; the collision gas, high.
Solid-phase microextraction (SPME) combined with gas chromatography-mass spectrometry (GC-MS)-based volatiles profiling was well-known for its high efficiency in the identification of volatile aroma compounds . The freeze-dried tender shoot was taken into the 20 mL headspace vial. In the solid phase microextraction cycle of CTC rail system (CTC Analytics, Switzerland), the extraction temperature was kept at 50 °C and the vials were shaken for 15 min at the rate of 250 r/m. The fiber assembly was 50/30 μm DVB/CAR on PDMS and the extraction time was 30 min. After desorption for 4 min, the volatiles were used for GC-MS analysis directly, which was performed on an Agilent 7890 gas chromatograph system coupled with a Agilent 5975C mass spectrometer. The system utilized a DB-Wax capillary column with 30 m×250 μm inner diameter and 0.25 μm film thickness (J&W Scientific, Folsom, CA, USA). The analyte was injected in a splitless mode. Helium was used as the carrier gas with the front inlet purge flow 3 mL min-1. And the gas flow rate through the column was 1 mL min-1. The initial temperature was kept at 40 oC for 5 min, then raised to 250 oC at a rate of 5 °C min-1, and then kept at 250 oC for 5 min. The injection, transfer line, ion source and quad temperatures were 260 oC, 260 oC, 230 oC, and 150 oC respectively. The energy was – 70 eV in electron impact mode. The mass spectrometry data were acquired in full-scan mode with the m/z range of 33-459 after a solvent delay of 0 s.
The data were analyzed via SAS software package (version 9.4, SAS Institution, USA). Statistical difference was compared based on Duncan’s multiple range-tests at the significance level of P < 0.05 or 0.01.
UPLC-QQQ-MS data analysis was identified through matching accurate mass and tandem MS/MS spectra with in-house metabolite tandem MS/MS databases MWDB (metware database). Features of isotopes, adducts and mass fragments were removed in the identification of some metabolites. Metabolites annotation was applied with MassBank (http://www.massbank.jp/), KNAPSAcK (http://kanaya.naist.jp/KNApSAcK/), HMDB (http://www.hmdb.ca/), MoTo DB (http://www.ab.wur.nl/moto/), and METLIN (http://metlin.scripps.edu/index.php). The quantification of metabolites were based on multiple reaction monitoring method  and Analyst 1.6.1® software (SCIEX, USA). For the identification of metabolites from GC-MS analysis, Chroma TOF 4.3X software of LECO Corporation and NIST database were used for raw peaks exacting, the data baselines filtering and calibration of the baseline, peak alignment, deconvolution analysis, peak identification and integration of the peak area.
All the resulted three-dimensional data involving the peak number, sample name, and normalized peak area were fed to SIMCA14.1 software package (MKS Data Analytics Solutions, Umea, Sweden) for principal component analysis (PCA) and orthogonal projections to latent structures-discriminate analysis (OPLS-DA). To refine the analysis, the first principal component of variable importance in the projection (VIP) was obtained. The VIP values exceeding 1.0 were first selected as changed metabolites. In addition, the remaining variables were assessed by Student's t-test (P-value > 0.05) and variables were discarded between two comparison groups. Namely, the condition of selecting the differential metabolites was VIP > 1 and P-value < 0.05. Moreover, commercial databases including KEGG (http://www.genome.jp/kegg/) and MetaboAnalyst (http://www.metaboanalyst.ca/) as utilized to search for the pathways of metabolites.
Spearman correlation coefficient was used to evaluate the correlation between the GC-identified and UPLC-identified metabolites of interest. Those metabolite pairs with the correlation coefficient > 0.8 and the corresponding P-value < 0.05 were processed via Cytoscape (v3.5.1) to make the correlation network.
- −a * :
Asian citrus psyllid
- +b * :
Chongyi wild mandarin
- C * :
- C a :
Content of chlorophyll a
- C b :
Content of chlorophyll b
- C t :
Content of total chlorophyll
- C x.c :
Content of carotenoid
Candidatus Liberibacter asiaticus
- D. citri:
‘Gannan zao’ navel orange
- H ∗ :
gas chromatography-mass spectrometry
Kyoto encyclopedia of genes and genomes
- L * :
Lightness of the color
National Navel Orange Engineering Research Center
Orthogonal projections to latent structures-discriminate analysis
Principal component analysis
Polymerase chain reaction
Statistical analysis system
Ultra high performance liquid chromatography coupled to triple quadrupole tandem mass spectrometry
First principal component of variable importance in the projection
Wild Hong Kong kumquat
Bové JM. Huanglongbing: a destructive, newly-emerging, century-old disease of citrus. J Plant Pathol. 2006;88(1):7–37.
Gottwald TR. Current epidemiological understanding of citrus Huanglongbing. Annu Rev Phytopathol. 2010;48:119–39.
Gottwald TR, Graham JH, Irey MS, McCollum TG, Woodet BW. Inconsequential effect of nutritional treatments on huanglongbing control, fruit quality, bacterial titer and disease progress. Crop Prot. 2012;36(3):73–82.
Baldwin E, Plotto A, Bai JH, Manthey J, Zhao W, Raithore S, Irey M. Effect of abscission zone formation on orange (Citrus sinensis) fruit/juice quality for trees affected by Huanglongbing (HLB). J Agric Food Chem. 2018;66(11):2877–90.
Killiny N, Nehela Y, Hijaz F, Vincent CI. A plant pathogenic bacterium exploits the tricarboxylic acid cycle metabolic pathway of its insect vector. Virulence. 2018;9(1):99–109.
Hoffman MT, Doud MS, Williams L, Zhang MQ, Ding F, Stover E, Hall D, Zhang S, Jones L, Gooch M, Fleites L, Dixon W, Gabriel D, Duan YP. Heat treatment eliminates ‘Candidatus Liberibacter asiaticus’ from infected citrus trees under controlled conditions. Phytopathology. 2013;103(1):15–22.
Wang N, Pierson EA, Carlos JS, Xu J, Levy JG, Zhang YZ, Li JY, Thiberio LR, Martins JJ. The Candidatus Liberibacter–host interface: insights into pathogenesis mechanisms and disease control. Annu Rev Phytopathol. 2017;55:451–82.
Lopes SA, Bertolini E, Frare GF, Martins EC, Wulff NA, Teixeira DC, Fernandes NG, Cambra M. Graft transmission efficiencies and multiplication of ‘Candidatus Liberibacter americanus’ and ‘Ca. Liberibacter asiaticus’ in citrus plants. Phytopathology. 2009;99(3):301–6.
Halbert SE, Manjunath KL. Asian citrus psyllids (Sternorrhyncha: Psyllidae) and greening disease of citrus: a literature review and assessment of risk in Florida. Fla Entomol. 2004;87(3):330–53.
Zaka SM, Zeng XN, Holford P, Beattie GAC. Repellent effect of guava leaf volatiles on settlement of adults of citrus psylla, Diaphorina citri Kuwayama, on citrus. Insect Sci. 2010;17:39–45.
Alves GR, Diniz AJF, Parra JRP. Biology of the huanglongbing vector Diaphorina citri (Hemiptera: Liviidae) on different host plants. J Econ Entomol. 2014;107(2):691–6.
Chen XD, Stelinski LL. Resistance management for Asian citrus psyllid, Diaphorina citri Kuwayama, in Florida. Insects. 2017;20:8(3):103.
Belasque J Jr, Bassanezi RB, Yamamoto PT, Ayres AJ, Tachibana A, Violonte AR, Tank A Jr, Giorgis F, Tersi FEA, Menezes GM, Dragone J, Jank RH Jr, Bové JM. Lessons from Huanglongbing management in São Paulo State, Brazil. J Plant Pathol. 2010;2:285–302.
Tiwari S, Mann RS, Rogers ME, Stelinski LL. Insecticide resistance in field populations of Asian citrus psyllid in Florida. Pest Manag Sci. 2011;67(10):1258–68.
Qureshi JA, Rogers ME, Hall DG, Stansly PA. Incidence of invasive Diaphorina citri (Hemiptera: Psyllidae) and its introduced parasitoid Tamarixia radiata (Hymenoptera: Eulophidae) in Florida citrus. J Econ Entomol. 2009;102(1):247–56.
Vankosky MA, Hoddle MS. An assessment of interspecific competition between two introduced parasitoids of Diaphorina citri (Hemiptera: Liviidae) on caged citrus plants. Insect Sci. 2019;26(1):119–27.
Volpe HX, Fazolin M, Garcia RB, Magnani RF, Barbosa JC, Miranda MP. Efficacy of essential oil of Piper aduncum against nymphs and adults of Diaphorina citri. Pest Manag Sci. 2016;72(6):1242–9.
Ibarra-Cortés KH, Guzmán-Franco AW, González-Hernández H, Ortega-Arenas LD, Villanueva-Jiménez JA, Robles-Bermúdez A. Susceptibility of Diaphorina citri (Hemiptera: Liviidae) and its parasitoid Tamarixia radiate (Hymenoptera: Eulophidae) to entomopathogenic fungi under laboratory conditions. Neotrop Entomol. 2018;47(1):131–8.
Hall DGD, Lapointe SLS, Wenninger EJE. Effects of a particle film on biology and behavior of Diaphorina citri (Hemiptera: Psyllidae) and its infestations in citrus. J Econ Entomol. 2007;100(3):847–54.
Miranda MP, Zanardi OZ, Tomaseto AF, Volpe HX, Garcia RB, Prado E. Processed kaolin affects the probing and settling behavior of Diaphorina citri (Hemiptera: Lividae). Pest Manag Sci. 2018;74(8):1964–72.
Croxton SD, Stansly PA. Metalized polyethylene mulch to repel Asian citrus psyllid, slow spread of huanglongbing and improve growth of new citrus plantings. Pest Manag Sci. 2014;70(2):318–23.
Patt JM, Stockton D, Meikle WG, Sétamou M, Mafra-Neto A, Adamczyk JJ. Innate and conditioned responses to chemosensory and visual cues in Asian citrus psyllid, Diaphorina citri (Hemiptera: Liviidae), vector of Huanglongbing pathogens. Insects. 2014;5(4):921–41.
Patt JM, Meikle WG, Mafraneto A, Sétamou M, Mangan R, Yang C, Malik N, Adamczyk JJ. Multimodal cues drive host-plant assessment in Asian citrus psyllid (Diaphorina citri). Environ Entomol. 2011;40(6):1494–502.
Hall DG, Sétamou M, Mizell RFI. A comparison of sticky traps for monitoring Asian citrus psyllid (Diaphorina citri kuwayama). Crop Prot. 2010;29(11):1341–6.
Wenninger EJ, Stelinski LL, Hall DG. Roles of olfactory cues, visual cues, and mating status in orientation of Diaphorina citri kuwayama (Hemiptera: Psyllidae) to four different host plants. Environ Entomol. 2009;38(1):225–34.
Sétamou M, Sanchez A, Saldaña RR, Patt JM, Summy R. Visual responses of adult Asian citrus psyllid (Hemiptera: Psyllidae) to colored sticky traps on citrus trees. J Insect Behav. 2014;27(4):540–53.
Paris TM, Croxton SD, Stansly PA, Allan SA. Temporal response and attraction of Diaphorina citri to visual stimuli. Entomol Exp Appl. 2015;155(2):137–47.
Paris TM, Allan SA, Udell BJ, Stansly PA. Evidence of behavior-based utilization by the Asian citrus psyllid of a combination of UV and green or yellow wavelengths. PLoS One. 2017;12(12):e0189228.
Yan H, Zeng J, Zhong G. The push–pull strategy for citrus psyllid control. Pest Manag Sci. 2015;71(7):893–6.
Alquézar B, Hxl V, Magnani RF, de Miranda, MP Santos MA, Wulff NA, Bento JMS, Parra JRP, Bouwmeester H, Peña L. β-caryophyllene emitted from a transgenic Arabidopsis or chemical dispenser repels Diaphorina citri, vector of Candidatus Liberibacters. Sci Rep. 2017;7(1):5639.
Zanardi OZ, Volpe HXL, Favaris AP, Silva WD, Luvizotto RAG, Magnani RF, Esperança V, Delfino JY, de Freitas R, Miranda MP, Parra JRP, Bento JMS, Leal WS. Putative sex pheromone of the Asian citrus psyllid, Diaphorina citri, breaks down into an attractant. Sci Rep. 2018;8(1):455.
Mann RS, Rouseff RL, Smoot JM, Castle WS, Stelinski LL. Sulfur volatiles from allium spp. affect Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Psyllidae), response to citrus volatiles. Bull Entomo Res. 2011;101(1):89–97.
Fancelli M, Borges M, Laumann RA, Pickett JA, Birkett MA, Blassioli-Moraes MC. 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. 2018;44(4):397–405.
Beloti VH, Santos F, Alves GR, Bento JMS, Yamamoto PT. Curry leaf smells better than citrus to females of Diaphorina citri (Hemiptera: Psyllidae). Arthropod-Plant Inte. 2017;11:709–16.
Wenninger EJ, Hall DG. Daily timing of mating and age at reproductive maturity in Diaphorina citri (Hemiptera: Psyllidae). Flo Entomol. 2007;90(4):715–22.
Sétamou M, Flores D, French JV, Hall DG. Dispersion patterns and sampling plans for Diaphorina citri (Hemiptera: Psyllidae) in citrus. J Econ Entomol. 2008;101(4):1478–87.
Mishra AR, Karimi D, Ehsani R, Lee WS. Identification of citrus greening (HLB) using a VIS-NIR spectroscopy technique. T ASABE. 2012;55(2):711–20.
Pourreza A, Lee WS, Raveh E, Ehsani R, Etxeberria E. Citrus Huanglongbing detection using narrow-band imaging and polarized illumination. T ASABE. 2014;57:259–72.
Luo J, Shi Q, Niu L, Zhang Y. Transcriptomic analysis of leaf in tree peony reveals differentially expressed pigments genes. Molecules. 2017;22(2):324.
Ilag LL, Kumar AM, Söll D. Light regulation of chlorophyll biosynthesis at the level of 5-aminolevulinate formation in Arabidopsis. Plant Cell. 1994;6(2):265–75.
Gough SP, Westergren T, Hansson M. Chlorophyll biosynthesis in higher plants. Regulatory aspects of 5-aminolevulinate formation. J. Plant Biol. 2003;46:135.
Killiny N, Nehela Y. One target, two mechanisms: the impact of Candidatus Liberibacter asiaticus and its vector, Diaphorina citri on citrus leaf pigments. Mol Plant Microbe Interact. 2017;30(7):543–56.
Cáceres LA, Lakshminarayan S, Yeung KK, McGarvey BD, Hannoufa A, Sumarah MW, Benitez X, Scott IM. Repellent and attractive effects of α-, β-, and dihydro-β- ionone to generalist and specialist herbivores. J Chem Ecol. 2016;42(2):107–17.
Hou X, Rivers J, León P, McQuinn RP, Pogson BJ. Synthesis and function of apocarotenoid signals in plants. Trends Plant Sci. 2016;21(9):792–803.
Matsuda K. Feeding stimulation of flavonoids for various leaf beetles (Goleoptera ; Ghrysomelidae). Appl Entomol Zool. 1978;13(3):228–230.
Onyilagha JC, Lazorko J, Gruber MY, Soroka JJ, Erlandson MA. Effect of flavonoids on feeding preference and development of the crucifer pest Mamestra configurata walker. J Chem Ecol. 2004;30(1):109–24.
War AR, Sharma SP, Sharma HC. Differential induction of flavonoids in groundnut in response to Helicoverpa armigera and Aphis craccivora infestation. Int J Insect Sci. 2016;8:55–64.
Simmonds MSJ. Importance of flavonoids in insect–plant interactions: feeding and oviposition. Phytochemistry. 2001;56(3):245–52.
Tang X, Mu X, Shao H, Wang H, Brestic M. Global plant-responding mechanisms to salt stress: physiological and molecular levels and implications in biotechnology. Crit Rev Biotechnol. 2015;35(4):425–37.
Ament K, Kant MR, Sabelis MW, Haring MA, Schuurink RC. Jasmonic acid is a key regulator of spider mite-induced volatile terpenoid and methyl salicylate emission in tomato. Plant Physiol. 2004;135(4):2025–37.
Wu J, Wang L, Baldwin IT. Methyl jasmonate-elicited herbivore resistance: does MeJA function as a signal without being hydrolyzed to JA? Planta. 2008;227(5):1161–8.
Patt JM, Robbins PS, Niedz R, Mccollum G, Alessandro R. Exogenous application of the plant signalers methyl jasmonate and salicylic acid induces changes in volatile emissions from citrus foliage and influences the aggregation behavior of Asian citrus psyllid (Diaphorina citri), vector of huanglongbing. PLoS One. 2018;13(3):e0193724.
Mann RS, Ali JG, Hermann SL, Tiwari S, Pelzstelinski KS, Alborn HT, Stelinski LL. Induced release of a plant-defense volatile ‘deceptively’ attracts insect vectors to plants infected with a bacterial pathogen. PLoS Pathog. 2012;8(3):e1002610.
Koo AJK, Gao X, Jones AD, Howe GA. A rapid wound signal activates the systemic synthesis of bioactive jasmonates in Arabidopsis. Plant J. 2009;59(6):974–86.
Paré PW, Tumlinson JH. Plant volatile signals in response to herbivore feeding. Flo Entomol. 1996;79(2):93–103.
Patt JM, Sétamou M. Responses of the Asian citrus psyllid to volatiles emitted by the flushing shoots of its rutaceous host plants. Environ Entomol. 2010;39(2):618–24.
Gancel AL, Ollitrault P, Froelicher Y, Tomi F, Jacquemond C, Luro F, Brillouet JM. Leaf volatile compounds of seven Citrus somatic tetraploid hybrids sharing willow leaf mandarin (Citrus deliciosa Ten.) as their common parent. J Agr Food Chem. 2003;51(20):6006–13.
Jeon JH, Yang JY, Lee HS. Evaluation of the acaricidal toxicities of camphor and its structural analogues against house dust mites by the impregnated fabric disc method. Pest Manag Sci. 2014;70(7):1030–2.
Pajaro-castro N, Caballero-Gallardo K, Olivero-Verbel J. Neurotoxic effects of linalool and β-pinene on Tribolium castaneum Herbst. Molecules. 2017;22(12):2052.
Campos EVR, Proença PLF, Oliveira JL, Pereira AES, de Morais Ribeiro LN, Fernandes FO, Gonçalves KC, Polanczy RA, Pasquoto-Stigliani T, Lima R, Melville CC, Della Vechia JF, Andrade DJ, Fraceto LF. Carvacrol and linalool co-loaded in β-cyclodextrin-grafted chitosan nanoparticles as sustainable biopesticide aiming pest control. Sci Rep. 2018;8(1):7623.
Müller GC, Junnila A, Butler J, Kravchenko VD, Revay EE, Weiss RW, Schlein Y. Efficacy of the botanical repellents geraniol, linalool, and citronella against mosquitoes. J Vector Ecol. 2009;34(1):2–8.
Ukeh DA, Umoetok S. Repellent effects of five monoterpenoid odours against Tribolium castaneum (Herbst) and Rhyzopertha dominica (F.) in Calabar, Nigeria. Crop Prot. 2011;30(10):1351-1355.
Yang T, Stoopen G, Thoen M, Wiegers G, Jongsma MA. Chrysanthemum expressing a linalool synthase gene ‘smells good’, but ‘tastes bad’ to western flower thrips. Plant Biotechnol J. 2013;11(7):875–82.
Hammack L. Single and blended maize volatiles as attractants for diabroticite corn rootworm beetles. J Chem Ecol. 2001;27:1373–90.
Zhang PJ, Zheng SJ, van Loon JJ, Boland W, David A, Mumm R, Dicke M. Whiteflies interfere with indirect plant defense against spider mites in Lima bean. Proc Natl Acad Sci U S A. 2009;106(50):21202–7.
Agut B, Gamir J, Jaques JA, Flors V. Tetranychus urticae-triggered responses promote genotype-dependent conspecific repellence or attractiveness in citrus. New Phytol. 2015;207(3):790–804.
Kessler A, Baldwin IT. Defensive function of herbivore-induced plant volatile emissions in nature. Science. 2001;291:2141–4.
Gonnet JF. Colour effects of co-pigmentation of anthocyanins revisited—2.A colorimetric definition using the CIELAB scale. Food Chem. 1999;66(3):387–94.
Chajra H, Redziniak G, Auriol D, Schweikert K, Lefevre F. Trihydroxybenzoic acid glucoside as a global skin color modulator and photo-protectant. Clin Cosmet Investig Dermatol. 2015;8:579–89.
Liu JH, Inoue H, Moriguchi T. Salt stress-mediated changes in free polyamine titers and expression of genes responsible for polyamine biosynthesis of apple in vitro shoots. Enviro. Exp Bot. 2008;62(1):28–35.
Wei G, Tian P, Zhang F, Qin H, Miao H, Chen Q, Hu Z, Cao L, Wang M, Gu X, Huang S, Chen M, Wang G. Integrative analyses of nontargeted volatile profiling and transcriptome data provide molecular insight into VOC diversity in cucumber plants (Cucumis sativus). Plant Physiol. 2016;172(1):603–18.
Chen W, Gong L, Guo ZL, Wang WS, Zhang HY, Liu XQ, Yu SB, Xiong LZ, Luo J. A novel integrated method for large-scale detection, identification, and quantification of widely targeted metabolites: application in the study of rice metabolomics. Mol Plant. 2013;6(6):1769–80.
We would like to acknowledge the support of BIOTREE for assisting the metabolic data analyses.
This work was supported by the Natural Science Foundation of Jiangxi Province (20152ACB21005 and 2016BBF60071) and the National Natural Science Foundation of China (31760563).
Availability of data and materials
All data generated or analyzed during this study are included in this published article [and its supplementary information files]. The two wild citrus germplasms could be available through the local government. NORC can provide ‘Gannan zao’ navel orange seedlings.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Zhong, ZF., Zhou, XJ., Lin, JB. et al. Effects of leaf colorness, pigment contents and allelochemicals on the orientation of the Asian citrus psyllid among four Rutaceae host plants. BMC Plant Biol 19, 254 (2019). https://0-doi-org.brum.beds.ac.uk/10.1186/s12870-019-1818-7
- Diaphorina citri
- wild citrus germplasm
- behavioral analysis