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Open Access

Transcriptional analysis of sweet orange trees co-infected with ‘Candidatus Liberibacter asiaticus’ and mild or severe strains of Citrus tristeza virus

BMC Genomics201718:837

https://doi.org/10.1186/s12864-017-4174-8

Received: 10 May 2017

Accepted: 5 October 2017

Published: 31 October 2017

Abstract

Background

Citrus worldwide is threatened by huanglongbing (HLB) and tristeza diseases caused by ‘Candidatus Liberibacter asiaticus’ (CaLas) and Citrus tristeza virus (CTV). Although the pathogens are members of the α-proteobacteria and Closteroviridae, respectively, both are restricted to phloem cells in infected citrus and are transmitted by insect vectors. The response of sweet orange to single infection by either of these two pathogens has been characterized previously by global gene expression analysis. But because of the ubiquity of these pathogens where the diseases occur, co-infection by both pathogens is very common and could lead to increased disease severity based on synergism. We therefore co-inoculated sweet orange trees with CaLas and either a mild or a severe strain of CTV, and measured changes of gene expression in host plants.

Results

In plants infected with CaLas-B232, the overall alteration in gene expression was much greater in plants co-inoculated with the severe strain of CTV, B6, than when co-infected with the mild strain of CTV, B2. Plants co-infected with CaLas-B232 and either strain of CTV died but trees co-infected with CTV-B2 survived much longer than those co-infected with CTV-B6. Many important pathways were perturbed by both CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232, but always more severely by CTV-B6/CaLas-B232. Genes related to cell wall modification and metal transport responded differently to infection by the pathogens in combination than by the same pathogens singly. The expressions of genes encoding phloem proteins and sucrose loading proteins were also differentially altered in response to CTV-B2 or CTV-B6 in combination with CaLas-B232, leading to different phloem environments in plants co-infected by CaLas and mild or severe CTV.

Conclusions

Many host genes were expressed differently in response to dual infection as compared to single infections with the same pathogens. Interactions of the pathogens within the host may lead to a better or worse result for the host plant. CTV-B6 may exert a synergistic effect with CaLas-B232 in weakening the plant; on the other hand, the responses activated by the mild strain CTV-B2 may provide some beneficial effects against CaLas-B232 by increasing the defense response of the host.

Keywords

HuanglongbingCTVHLBTristezaTranscriptomeHost-pathogen interaction

Background

Huanglongbing (HLB) and Tristeza are destructive and globally distributed citrus diseases, and are responsible for tremendous economic losses to citrus industries worldwide [8, 60]. HLB is strongly associated with ‘Ca. Liberibacter asiaticus’ (CaLas), a gram-negative and phloem-limited member of the α-Proteobacteria. CaLas has a global distribution and can be transmitted through grafting and by the citrus psyllid, Diaphorina citri [8]. Tristeza is caused by Citrus tristeza virus (CTV), a member of the Closteroviridae with a single-stranded and positive sense RNA-genome of 19.3 kb [16]. Like CaLas, CTV replicates in the phloem cells and may also be transmitted by grafting and by several aphids, most notably Toxoptera citricidus [60].

HLB has been studied for more than 100 years. Early observations of what is likely to have been HLB were made in the late 1880s by growers in Chaoshan, China and in the Pearl River Delta area of Guangdong in China. The earliest unambiguous report of HLB and association of the disease with the citrus psyllid was however made from India. Since CaLas has not been cultured in vitro, Koch’s postulates have not been completed. The first CaLas genomic sequence (Psy62) was obtained through multiple displacement amplification [22]. Genomes of additional six CaLas strains and three CaLam strains have been successively sequenced and are available at NCBI.

Considerable research has focused on host responses to infection. Transcriptome studies of host responses to HLB were conducted in leaves [24], fruits [47, 56], stems and roots [5, 92], as well as in resistant and susceptible varieties [3, 10, 26, 54]. Differentially expressed genes (DEGs) and altered metabolic pathways were described. Pathways related to sugar and starch metabolism, cell wall metabolism, secondary metabolism, hormone signaling, photosynthesis, phloem transport and ion uptake were found to be affected in citrus plants infected by CaLas.

Strains of CTV vary from very mild, which do not cause notable damage to citrus hosts, to severe strains that induce symptom patterns that include leaf yellowing, stiffening, and cupping. These symptoms are very similar to those associated with alterations in sucrose metabolism in the phloem and decline of roots [35, 41] and collapse of phloem tissue [29, 60] seen in HLB. Previously we have analyzed the transcriptome of sweet orange, Citrus sinensis, singly inoculated with CaLas-B232, mild CTV-B2 or severe CTV-B6 [30]. CTV-B2 does not induce visible symptoms in sweet orange while both CTV-B6 and CaLas-B232 are lethal. We found that the circadian rhythm system of C. sinensis and ionic balances were perturbed by all three pathogens but to differing degrees. Defense responses related to cell wall modification, regulation of transcription, hormone metabolism, secondary metabolism, kinases and both biotic and abiotic stress were activated by all three pathogens but with different patterns [30]. These results provided some valuable insight into the similarity and differences of the responses of C. sinensis to CaLas and CTV. Both CTV and CaLas are globally distributed, and are present simultaneously in most locations. Therefore, co-infection by strains of CTV and CaLas is now a common situation. In the current study, transcriptome profiles of C. sinensis co-infected with CTV-B2/CaLas-B232 (B2/B232) and CTV-B6/CaLas-B232 (B6/B232) were analyzed to identify differentially expressed gene (DEGs) and unveil how mild CTV-B2 and severe CTV-B6 affect the genome-wide gene expression changes of C. sinensis infected with CaLas-B232.

Results

40–45 million reads/sample were obtained and mapped to the C. sinensis reference genome [85], and about 60% of reads mapped successfully to the healthy, CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 sweet orange transcriptomes (Additional file 1: Figure S1). Differentially expressed transcripts (DETs) for CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 were identified by comparison with the transcriptome of the healthy controls. The number of up- or down regulated DETs varied for each co-infection (Additional file 2: Figure S2), and the overall alteration of the transcriptome was much greater in the presence of CTV-B6 than CTV-B2. We observed 402 and 420 transcripts induced and repressed respectively in response to CTV-B2/CaLas-B232, while 813 and 1009 transcripts were induced and repressed, respectively in response to CTV-B6/CaLas-B232. We compared the expression of the sweet orange genome in response to single infection and in combination after co-infection. We found that 29 transcripts were differentially regulated in response to CTV-B2 alone and in combination with CaLas-B232, while about twice that number were differentially regulated in response to CaLas-B232 alone and in combination with CTV-B2 (Fig. 1a and b). The number of transcripts that were co-regulated in response to CaLas-B232 alone and in combination with CTV-B6 was greater than the number that were co-regulated in response to CTV-B6 alone and in combination with CaLas-B232 (Fig. 1c and d).
Fig. 1

Differentially expressed transcripts in sweet orange responding to single and co-infection by CTV-B2, CTV-B6 and CaLas-B232. a venn diagram of differentially expressed transcripts (DEGs) in sweet orange responding to CTV-B2 and CTV-B2/CaLas-B232; b venn diagram of DEGs in sweet orange responding to CaLas-B232 and CTV-B2/CaLas-B232; c venn diagram of DEGs in sweet orange responding to CTV-B6 and CTV-B6/CaLas-B232; d venn diagram of DEGs in sweet orange responding to CaLas-B232 and CTV-B26CaLas-B232

The DETs were functionally placed in different Gene Ontology (GO) biological process (BP) categories. The largest numbers of genes induced by both CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 were associated with metabolic processes, followed by cellular processes, localization, biological regulation and responses to stimulus. Genes repressed by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 also had a similar distribution within GO categories (Fig. 2). Many important metabolic pathways were heavily perturbed by CTV-B2/CaLas-B232, especially by CTV-B6/CaLas-B232 (Fig. 3a and c) in the young leaves that were sampled prior to the development of symptoms. These included metabolism of carbon compounds such as starch/sucrose and amino acids. Pathways related to photosynthesis, plant-pathogen interactions, hormone metabolism, signal transduction, circadian rhythm and ribosomal structure were also perturbed (Fig. 3a, c and Additional file 3: Tables S1 and Additional file 4: Table S2). The changes in gene expression are consistent with the symptoms that developed in mature leaves (Fig. 3b and d). Sixteen months after the inoculation of CaLas and 13 months the inoculation of CTV, the trees with the most and least severe symptoms (Fig. 4) were selected and compared to the self-inoculated healthy controls. Trees confirmed to be infected with both pathogens, either CTV-B2/CaLas-B232 or CTV-B6/CaLas-B232, were all smaller than the healthy controls. Trees infected with CTV-B6/CaLas-B232 (Fig. 4b) were also much weaker and showed much more severe symptoms, including chlorosis, stunting and leaf curling than plants infected with CTV-B2/CaLas-B232 (Fig. 4a).
Fig. 2

Categorization of differentially expressed transcripts in Citrus sinensis infected with CTV-B2/CaLas-B232 or CTV-B6/CaLas-B232 based on gene ontology. a and c, Induced transcripts; b and d, Repressed transcripts; B2/232, CTV-B2/CaLas-B232; B6/232, CTV-B6/CaLas-B232

Fig. 3

Metabolic overview in young leaves and subsequent symptoms in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. a and b, CTV-B2/CaLas-B232; c and d, CTV-B6/CaLas-B232

Fig. 4

General appearance of sweet orange co-infected with CTV-B2/CaLas-B232 or CTV-B6/CaLas-B232. Pictures were taken 16 months after inoculation with CaLas and 13 months after inoculation with CTV. a, Trees co-infected with CTV-B2 and CaLas-B232; b, Trees co-infected with CTV-B6 and CaLas-B232; 1 and 2, Most and least severe symptom expression for each treatment; 3, Self-inoculated healthy control

Validation of RNA sequence data by RT-qPCR

Gene expression analyses were performed with RT-qPCR to verify RNA sequence data. In total, 60 genes involved in different biological processes were selected, including genes encoding transporters ZIP1, ZIP5, ZIP11, COPT1, PHT2;1 and OPT7, transcription factors (TF) WRKY33, WRKY46, WRKY70 and MYB77, hormone metabolism proteins LOX3, GA2OX8, TPS21, phloem protein PP2-B15, light reaction proteins LHCA4 and LHCB6, cytochrome P450 members CYP83B1 and CYP94B1, light signaling related ELIP1, lipid metabolism protein LP1, an F-box family protein, and CCT-motif family proteins related to regulation of transcription PCL1 and CBF4. Primer information is provided in Additional file 5: Table S3. Similar expression patterns were revealed by both techniques for these genes. Spearman’s rho values of 0.91 for CTV-B2/CaLas-B232 and 0.87 for CTV-B6/ CaLas-B232 (Fig. 5) and low variation within the replicated samples (Additional file 6: Figure S3) confirmed the reliability of RNA sequence data.
Fig. 5

Correlation of estimates of differential gene expression by RT-qPCR and RNA-seq. FC: Log2 Fold Change

Photosynthesis, carbohydrate and amino acid metabolism

We found that many DETs associated with the light reactions of photosynthesis, Calvin cycle and photorespiration were repressed by CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 (Fig. 6). In photosystem II these genes included chlorophyll binding proteins (LHB1B1, LHCA1 and LHCA2), light harvesting complex (LHCB3, LHCB5, LHCB6 and LHCA4) and calcium ion binding proteins (PPL1 and PSBQ). In photosystem I subunits (PSAD-1, PSAF, PSAO, PSAD-2, PSAH-1, PSAL, PSAK, PSAP and PSAO), rubisco activase (RCA) and plastid transcriptionally active14 (PTAC14) were repressed (Additional file 3: Table S1 and Additional file 4: Table S2). The repression of genes involved with the synthesis of tetrapyrrole (Additional file 7: Figure S4) and the light harvesting complex of the chloroplast is consistent with reduced capacity for photosynthesis, and is consistent with the symptoms that subsequently developed in the plants (Fig. 3). Symptoms observed following co-infection by CTV-B6 and CaLasB232 were similar to those produced by either pathogen alone (Additional file 8: Figure S5).
Fig. 6

Photosynthetic system of Citrus sinensis perturbed by co-infection with CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232

Metabolism of amino acids including aspartate, proline, arginine, methionine, cysteine, asparagine, tyrosine and tryptophan was also disrupted by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. Both nitrogen (N) and sulfur (S) assimilation are linked with amino acid metabolism. For example, SERAT1;1 (serine acetyltransferase1;1) and SERAT2;2 involved in cysteine synthesis were induced by both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). Glutamate synthase (NADH) (GLT1), involved in N-metabolism, was repressed by both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. Intriguingly, several genes associated with S-assimilation were exclusively activated by CTV-B6/CaLas-B232 rather than CTV-B2/CaLas-B232. These included APS1 (ATP sulfurylase 1), APS2 and APR1 (APS reductase 1). AKN1 (APS kinase) was repressed by CTV-B6/CaLas-B232 but was not affected by CTV-B2/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2).

Cell wall

The primary cell wall of a land plant is composed of the major carbohydrates cellulose, hemicelluloses and pectin. Genes encoding pectin methyl esterase were generally repressed, whereas genes related to cellulose synthesis were induced by CTV-B6/CaLas-B232.

Transport and heavy metal ions

The transportation system of the host plants was heavily disturbed by CTV-B6/CaLas-B232 and CTV-B2/CaLas-B232. Genes encoding sugar transporters were up-regulated in young leaves in response to co-infection. Transportation of metals was impaired by CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 as inferred from the suppression of iron, copper and zinc transporter genes (Additional file 3: Table S1 and Additional file 4: Table S2). The expression of phloem protein PP2-B15 was highly up-regulated in response to CTV-B6/CaLas-B232 (Additional file 4: Table S2), but no alteration was observed in response to CTV-B2/CaLas-B232.

The circadian system

The plant circadian clock regulates expression of as much as one-third of the Arabidopsis genome [71], including carbohydrate metabolism and defense responses [33, 37, 69]. The clock is composed of interlocking transcription-translation feedback loops. These were greatly disrupted by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Fig. 7).
Fig. 7

Disturbances in the circadian system by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. Red boxes, down- regulated genes; Green boxes, up-regulated genes

Hormones and control of defense responses

The metabolism of abscisic acid, auxins, brassinosteroids, cytokinins, ethylene, gibberellins, jasmonate and salicylic acid were all perturbed by CTV-B6/CaLas-B232 and to a lesser extent by CTV-B2/CaLas-B232 (Table 1; Additional file 9: Figure S6). A large number of transcription factors (TF) were affected by the pathogens, including AP2/EREBP, basic helix-loop-helix (bHLH), C2C2 (Zn), MYB, WRKY, bZIP, PHOR1 and Pseudo ARR (PRR) (Additional file 3: Tables S1 and Additional file 4: Table S2). An overwhelming majority of genes regulated by AP2/EREBP (APETALA/ETHYLENE RESPONSIVE ELEMENT BINDING PROTEIN) were down-regulated in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. These included ethylene-responsive element binding factor (ERF13 and ERF38) and the C-repeat-binding factors (CBF4, CBF1 and CBF2). MYB14, MYB73 and MYB77 were all repressed in response to both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. Ethylene signaling and ethylene mediated defense responses were activated in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2), as well as to CTV-B2, CTV-B6 and CaLas-B232 separately.
Table 1

Responses of hormones to infection by CTV-B2, CTV-B6 and CaLas-B232

Categories

CTV-B2a

CTV-B6a

CaLas-B232a

CTV-B2/

CaLas-B232b

CTV-B6/

CaLas-B232b

Abscisic acid (ABA)

 

Y

Y

Y

Y

Auxin

  

Y

Y

Y

Brassinosteroid

   

Y

Y

Cytokinin (CK)

    

Y

Ethylene

Y

Y

Y

Y

Y

Gibberelin (GA)

 

Y

 

Y

Y

Jasmonate (JA)

  

Y

Y

Y

Salicylic acid (SA)

Y

Y

Y

 

Y

a: sweet orange trees were singly inoculated with pathogens (Fu et al., 2016)

b: sweet orange trees were doubly inoculated with CaLas-B232 and mild CTV-B2 or severe CTV-B6

Y: hormone related pathways were disrupted by single or dual pathogen infection

Alteration of ribosomal composition

Ribosomal proteins play crucial roles in cell division, growth and metabolism in plants. Several members of ribosomal protein families were down-regulated in host plants in response to dual infection by CTV-B2/CaLas-B232 but many more by CTV-B6/CaLas-B232 (Table 2).
Table 2

Transcripts encoding ribosomal proteins were differentially regulated in Citrus sinensis in response to infection by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232

Gene symbol

Transcript id_

AGI

Gene description

Log 2 Fold-change

Citrus sinensis

CTV-B2/

CaLas-B232

CTV-B6/

CaLas-B232

RPS5

orange1.1g021869m

AT2G33800

ribosomal protein S5 family protein

 

−1.42

RPS5

orange1.1g013474m

AT1G64880

ribosomal protein S5 family protein

 

−1.03

RPS6

orange1.1g027743m

AT1G64510

ribosomal protein S6 family protein

 

−1.71

RPS9

orange1.1g042358m

AT1G74970

ribosomal protein S9

 

−1.46

RPS10

orange1.1g041275m

AT3G13120

30S ribosomal protein S10, chloroplast, putative

 

−1.70

RPS13

orange1.1g030930m

AT5G14320

30S ribosomal protein S13, chloroplast (CS13)

 

−1.39

RPS17

orange1.1g033970m

AT1G79850

ribosomal protein S17

 

−1.48

RPS20

orange1.1g029900m

AT3G15190

chloroplast 30S ribosomal protein S20, putative

−1.11

−1.69

RPS1

orange1.1g015066m

AT5G30510

ribosomal protein S1

 

−1.57

GHS1/S21

orange1.1g030080m

AT3G27160

glucose hypersensitive1, structural constituent of ribosome

 

−1.86

RPS4B

orange1.1g024793m

AT5G07090

40S ribosomal protein S4 (RPS4B)

 

−1.12

RPS5A

orange1.1g028585m

AT3G11940

ribosomal protein 5A, structural constituent of ribosome

 

−1.16

RPS8A

orange1.1g044642m

AT5G20290

40S ribosomal protein S8 (RPS8A)

 

−1.06

RPS13A

orange1.1g031857m

AT4G00100

Arabidopsis thaliana ribosomal protein S13A

 

−1.02

RPS16A

orange1.1g032049m

AT2G09990

40S ribosomal protein S16

 

−1.04

RPS19C

orange1.1g032099m

AT5G61170

40S ribosomal protein S19 (RPS19C)

 

−1.04

RPS20B

orange1.1g033482m

AT3G47370

40S ribosomal protein S20 (RPS20B)

 

−1.14

RPS23B

orange1.1g032383m

AT5G02960

40S ribosomal protein S23 (RPS23B)

 

−1.46

RPS24B

orange1.1g032727m

AT5G28060

40S ribosomal protein S24 (RPS24B)

 

−1.77

RPS25

orange1.1g033931m

AT4G34555

40S ribosomal protein S25, putative

 

−1.48

RPS26C

orange1.1g032843m

AT3G56340

40S ribosomal protein S26 (RPS26C)

 

−1.13

PSRP3

orange1.1g030605m

AT1G68590

plastid-specific 30S ribosomal protein 3, putative / PSRP-3

 

−1.33

PSRP3

orange1.1g029878m

AT5G15760

plastid-specific 30S ribosomal protein 3, putative / PSRP-3

 

−1.44

PSRP3

orange1.1g030716m

AT1G68590

plastid-specific 30S ribosomal protein 3, putative / PSRP-3

 

−1.40

RPS30A

orange1.1g020955m

AT5G24490

30S ribosomal protein, putative

−1.09

−1.39

RPL3

orange1.1g023905m

AT2G43030

ribosomal protein L3 family protein

 

−1.64

RPL5

orange1.1g024440m

AT4G01310

ribosomal protein L5 family protein

 

−1.69

RPL6

orange1.1g027306m

AT1G05190

embryo defective 2394

 

−1.58

RPL9

orange1.1g029153m

AT3G44890

ribosomal protein L9

 

−1.81

RPL10

orange1.1g027713m

AT5G13510

ribosomal protein L10 family protein

 

−1.34

RPL13

orange1.1g026067m

AT1G78630

embryo defective 1473

 

−1.37

RPL15

orange1.1g024515m

AT3G25920

structural constituent of ribosome

 

−1.39

RPL17

orange1.1g041707m

AT3G54210

ribosomal protein L17 family protein

 

−1.79

RPL18

orange1.1g030804m

AT1G48350

ribosomal protein L18 family protein

−1.08

−1.94

RPL19

orange1.1g026573m

AT4G17560

ribosomal protein L19 family protein

 

−1.53

RPL21

orange1.1g027519m

AT1G35680

50S ribosomal protein L21, chloroplast/CL21

 

−1.72

RPL24

orange1.1g029417m

AT5G54600

50S ribosomal protein L24, chloroplast (CL24)

 

−1.98

RPL27

orange1.1g029509m

AT5G40950

ribosomal protein large subunit 27

 

−1.01

RPL28

orange1.1g031725m

AT2G33450

50S ribosomal protein L28, chloroplast (CL28)

 

−1.42

RPL29

orange1.1g030809m

AT5G65220

ribosomal protein L29 family protein

 

−1.32

RPL34

orange1.1g031306m

AT1G29070

ribosomal protein L34 family protein

−1.01

−2.10

RPL35

orange1.1g031865m

AT2G24090

ribosomal protein L35 family protein

 

−1.29

RPL3A

orange1.1g038172m

AT1G43170

Arabidopsis ribosomal protein 1

 

−1.61

RPL6B

orange1.1g026764m

AT1G74060

60S ribosomal protein L6 (RPL6B)

 

−1.17

RPL7C

orange1.1g026093m

AT2G44120

60S ribosomal protein L7 (RPL7C)

 

−1.14

RPL15A

orange1.1g028730m

AT4G16720

60S ribosomal protein L15 (RPL15A)

 

−1.16

RPL17B

orange1.1g030568m

AT1G67430

60S ribosomal protein L17 (RPL17B)

 

−1.17

RPL18C

orange1.1g030771m

AT5G27850

60S ribosomal protein L18 (RPL18C)

 

−1.27

RPL24A

orange1.1g031225m

AT2G36620

ribosomal protein L24

 

−1.05

RPL32A

orange1.1g032796m

AT4G18100

60S ribosomal protein L32A

 

−1.02

RPL37C

orange1.1g034400m

AT3G16080

60S ribosomal protein L37 (RPL37C)

 

−1.22

RPL7A

orange1.1g025016m

AT2G47610

60S ribosomal protein L7A (RPL7aA)

 

−1.02

RPL7A

orange1.1g024981m

AT3G62870

60S ribosomal protein L7A (RPL7aB)

 

−1.04

RPLP1

orange1.1g033944m

AT5G24510

60s acidic ribosomal protein P1, putative

1.92

1.75

RPP3A

orange1.1g033353m

AT4G25890

60S acidic ribosomal protein P3 (RPP3A)

 

−1.14

RPL18A

orange1.1g035537m

AT1G29970

60S ribosomal protein L18A-1

 

−1.40

RPL37A

orange1.1g044880m

AT3G10950

60S ribosomal protein L37a

 

−1.04

RRL13A

orange1.1g028649m

AT5G48760

60S ribosomal protein L13A

1.12

 

BBC1/L13

orange1.1g028624m

AT3G49010

Arabidopsis thaliana breast basic conserved 1

 

−1.92

a

orange1.1g010232m

AT1G71720

S1 RNA-binding domain-containing protein

 

−1.21

a

orange1.1g034489m

AT5G40080

60S ribosomal protein-related

 

1.46

a

orange1.1g043340m

AT2G39670

radical SAM domain-containing protein

 

−1.58

a

orange1.1g044572m

AT3G27180

unknown protein

 

−1.01

Note: ‘a’ represents transcripts without gene symbol

Discussion

Differentially expressed genes and altered metabolic pathways of hosts provide a broad perspective of the host response to infection by CaLas [2, 54, 92] and by CTV [14, 49, 86]. We have compared changes in transcription in sweet orange plants in response to mild and severe strains of CTV and to CaLas-B232 when inoculated separately, which provided an overview of how susceptible hosts respond to CTV and CaLas [30]. Because CTV and CaLas are globally distributed, it is very common to have trees infected with both pathogens. Thus single pathogen studies, while essential, do not provide all of the needed data. In this study we have collected and analyzed transcriptome data from sweet orange plants co-infected with CTV-B2 and CaLas-B232 or CTV-B6 and CaLas-B232. In preliminary experiments we found that trees became PCR-positive for CTV much more quickly and more reliably than for CaLas (data not shown), so that simultaneous inoculations with the two pathogens was not effective. We therefore inoculated trees with CaLas-B232 first, and after the trees became positive for CaLas by qPCR (about 3 months after of inoculation) and we inoculated the trees with CTV-B2 or CTV-B6. In this way we observed the host response to infection by both pathogens compared with each pathogen separately [30]. The alteration of the transcriptome in response to co-infection by both pathogens was much larger than in response to infection by any single pathogen [30]. Some genes showed similar expression patterns in both circumstances but others showed different, and even opposite expression patterns (Additional file 3: Table S1 and Additional file 4: Table S2). Although all trees died eventually, trees co-infected with CTV-B2 and CaLas-B232 were slower to develop symptoms and survived longer than trees co-infected with CTV-B6 and CaLas-B232 (Fig. 4). Defense responses in trees may have been activated by CTV-B2 to provide limited protection against CaLas-B232, while CTV-B6 and CaLas-B232 acted synergistically to rapidly kill the trees.

Photosynthesis carbohydrate and amino acid metabolism

The most abundant tetrapyrrole in plants is chlorophyll, the pigment that harvests light for photosynthesis. Genes related to tetrapyrrole synthesis were repressed (Additional file 7: Figure S4) in young leaves prior to symptom development in response to CTV-B2/CaLas-B232 and especially by CTV-B6/CaLas-B232. These genes included CHLI2 (magnesium chelatase I2), FC1 (ferrochelatase 1) and HEME2 (uroporphyrinogen decarboxylase) (Additional file 3: Table S1 and Additional file 4: Table S2). These pathways were also disrupted by infection with CaLas alone [2, 14, 30, 55]. Expression of some photosynthesis-related genes was increased in response to CTV-B6 and CaLas-B232 alone but no changes were found in response to CTV-B2 [30]. This indicates that the reduced capacity for photosynthesis as the host responds to the two pathogens is primarily in response to CaLas.

The HLB syndrome also includes impaired carbohydrate metabolism [2, 54, 55, 91], and similar effects have been reported in sweet orange trees infected with Spiroplasma citri, another phloem-limited bacterial pathogen [9]. Sucrose is transported from source to sink organs and starch is the storage reserve in plants. Metabolic pathways related to energy generation from carbohydrates, including glycolysis, the oxidative pentose phosphate pathway (OPP) and the tricarboxylic acid cycle (TCA), were all repressed by both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). The OPP is the main source of NADPH. Both the respiratory TCA pathway and glycolysis are essential to produce energy and precursors of amino acids and secondary metabolites. The repression of these processes may limit plant growth and successful defense response as plant defense is energy intensive [7].

Amino acids are also involved in plant-pathogen interactions [74, 89]. Amino acid transporters are involved in plant defense responses by alteration of amino acid concentrations in balancing N pools. Our data strongly indicated that not only the metabolism of amino acids but also their related transporters were increased in response to dual infection, particularly by CTV-B6/CaLas-B232 (Additional files 3: Table S1 and Additional file 4: Table S2). Amino acid permeases (AAPs) are important for phloem transport of amino acids. AAP6, AAP7 and ProT1 (proline transporter1) were induced by CTV-B2/CaLas-B232; AAP6 and CAT8 (cationic amino acid transporter 8) were induced while AAP3 was highly repressed by CTV-B6/CaLas-B232. AAP3 transports the basic amino acids lysine and arginine [28]. AAP6 was expressed primarily in sink tissues [68] but also in xylem parenchyma in Arabidopsis and AAP6 was predicted to transfer amino acids from the xylem to the phloem [39, 63]. Some studies have found that the abundance of amino acids is correlated positively with the performance and behavior of phloem feeding insects: higher levels of amino acids increased aphid performance in potato [43, 66]. Both CaLas and CTV are transmitted by phloem feeding insects, and CaLas has to obtain nutrients such as amino acids and enzymes from the host due to its greatly reduced genome [22, 38]. The altered expression of transporter genes may result in a traffic jam of carbohydrates, amino acids and other substances in the phloem. The availability and abundance of nutrients and the composition of the amino acids in phloem would be correlated with the growth of CaLas and favor feeding by the insect vectors.

Cell wall

CSLB04 and CSLE1 associated with cellulose synthesis in cell walls were up-regulated while COBL7 (COBRA-like 7), which is thought to be required for properly oriented cell expansion [72, 73] was down-regulated in response to CTV-B6/CaLas-B232. In our earlier study, COBL7 was strongly up-regulated by CTV-B2 [30]. Genes related to cell wall degradation were generally up-regulated in response to both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. Genes encoding cell wall proteins, such as HRGP (hydroxyproline-rich glycoprotein), RGP2 (reversibly glycosylated polypeptide 2) and LRR (leucine-rich repeat family protein) were up-regulated in response to CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). Genes related to cell wall modification were differentially regulated in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232. XTR6 (xyloglucan endotransglycosylase) was down-regulated in response to both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 but was up-regulated in response to CTV-B2, CTV-B6 and CaLas-B232 when inoculated singly [30]. Expansin genes, EXP1, EXP3, EXP4, EXPB5, EXPL1, etc., were also differentially regulated by CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232. EXLB3 was especially up-regulated by CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2).

Transport and heavy metal ions

Genes encoding sugar transporters were up-regulated in young leaves in response to co-infection, as well as to CTV-B6 and CaLas-B232 alone [30]. The phloem-located SUC/SUT1 (sucrose-proton symporter2) is responsible for loading sucrose into sieve tubes [21, 75] and was induced in response to CTV-B2/CaLas-B232. Potassium ions also play a crucial role in the transport of photo assimilates in the phloem [34]. Potassium channel SKOR (cyclic nucleotide binding) was up-regulated in response to CTV-B6/CaLas-B232 (Additional file 4: Table S2). In Arabidopsis the loss of the potassium channel AKT2/3 impacted the loading of sugar into the phloem via the regulation of the phloem osmotic potential and the activity of sucrose transporters [18]. mRNAs for ATPases, CNG channels, ABC and nitrate transporters have been identified in sieve element sap of Ricinus and barley [20, 21]. These were also differentially expressed in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232.

FER1 (Ferric iron binding), radical SAM domain-containing protein, PCS2 (phytochelatin synthase 2) were down-regulated in response to CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). The over-expression of ferric reduction oxidase genes FRO6, FRO7 and PCS2 was found in response to CaLas-B232 but not to CTV-B2 or to CTV-B6 in the previous study [30]. This is consistent with iron deficiency in young leaves. 80% of leaf iron is located in the chloroplasts [78]. A shortage of iron leads to reduction of iron-containing proteins and most markedly to decreased production of chlorophyll. The deficiency of chlorophyll results in yellowing symptoms on leaves as observed on leaves infected with CaLas or CTV-B6 and also lowers the capacity for photosynthesis directly [1].

FP6 (Farnesylated protein 6) was induced by CTV-B2/CaLas-B232. FP3 and FP6 also possess the heavy metal binding MXCXXC domain and are involved in Cu(II) and Zn(II) transport in Arabidopsis roots [31]. HMA5 (Heavy metal ATPase) also contains the MXCXXC domain and functions in copper (Cu(II)) detoxification [4]. The expression of these metal handling proteins is consistent with deficiency of metal ions, which may be exacerbated by the dramatic decline of fibrous roots after infection with CaLas [35, 41]. Symptoms of zinc-deficiency are often observed on new leaves following infection by CaLas [8, 76, 84].

Up-regulation of zinc and copper transporter genes was also found in response to CTV-B6 and CaLas-B232 when inoculated alone [30, 25, 54]. The expressions of ZIP1, ZIP2, ZIP4, ZIP5 and ZIP11 were all induced by CaLas-B232 and CTV-B6/CaLas-232, while only ZIP5 and ZIP11 were induced by CTV-B2/CaLas-B232. ZIP6 was also induced by CTV-B6/CaLas-B232 and the expression level of these ZIPs was much higher in response to CTV-B6/CaLas-B232 than to CTV-B2/CaLas-B232 or CaLas-B232 alone. Interestingly, the expression of ZIP1, ZIP4 and ZIP5 was repressed by CTV-B2. Both CaLas and the severe strain of CTV, B6, cause chlorosis and symptoms of zinc deficiency on leaves, phloem collapse, and decline of roots, but the mild strain of CTV-B2 does not cause any damage or symptoms on indicator plants.

P-proteins (Phloem-proteins) are components of phloem involved both in the long-distance movement of macromolecules and in signaling [44, 52]. Several phloem proteins PP2-B10, PP2-B11, PP2-B13 and PP2-B15 were over expressed in response to CTV-B6 or CaLas-B232 alone, but PP2-B13 and PP2-B15 were dramatically down-regulated by CTV-B2 [30]. However, no change in expression of PP2-B13 and PP2-B15 was found after co-infection with CTV-B2/CaLas-B232. PP2-B15 has been previously reported to be induced in hosts in response to CaLas [45, 47, 54]. The increased expression of PP2-B13 and PP2-B15 by CaLas appears to be offset by the interaction with CTV-B2. This is also solid evidence that Zn transporters and phloem proteins were connected in a co-expression network as suggested [67, 92]. These results may also support the notion that CTV-B6 acts synergistically with CaLas-B232 to disrupt phloem transport and further stimulate the expression of ZIPs and PP2. Patterns of gene expression activated by CTV-B2 may provide some beneficial effects on infection by CaLas-B232. In addition, induction of ZIP4, ZIP5 and PP2-B15 may serve as biomarkers for HLB disease.

The circadian system

The plant circadian clock regulates expression of as much as one-third of the Arabidopsis genome [71], including carbohydrate metabolism and defense responses [33, 37, 69]. The clock is composed of interlocking transcription-translation feedback loops. These were greatly disrupted by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Fig. 7), as we observed in our previous study of the pathogens in single infections [30]. Of particular interest is GIGANTEA (GI), a key regulatory protein that is necessary to maintain the appropriate period and amplitude of cca1 and lhy gene expression in the outer feedback loop of the circadian system in Arabidopsis [64]. GI also functions in the sucrose-signaling network of Arabidopsis [15], which probably contributes to the perturbations of sucrose metabolism described above. GI is also involved in the regulatory pathway that determines wall in-growth to provide physical barriers to limit pathogen invasion [13, 23]. Deformation of phloem cell walls is observed in citrus in response to infection by CaLas [29] and stem pitting, caused by in-growths of the phloem cells is a primary symptom of CTV [16]. The expression of GI was increased in response to CTV-B2/CaLas-B232, as well as to CTV-B2, CTV-B6 and CaLas-B232 alone [30], but was repressed by CTV-B6/CaLas-B232 together. The repression of GI would limit the production of intracellular barriers and lead to a weakened defense against the invasion of CaLas-B232 and CTV-B6. Trees inoculated with CaLas-B232 and CTV-B6 together tended to die rapidly rather than linger in diseased states as when inoculated with CTV-B6 or CaLas-B232 alone. Other genes of the circadian system were also differentially regulated in response to CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232. These included ELF3 (early flowering), PIF3 (phytochrome interacting factor), and COP1 (constitutive photo morphogenesis protein 1). ELF3 and COP1 control the stability of GI and therefore mediate photoperiodic flowering and circadian function [88]. Whether plants were infected with CaLas and CTV separately or together, the circadian system was heavily disturbed. Alterations of the circadian system may contribute to the generalized reprogramming of the transcriptome observed in response to these pathogens, and has been observed previously for CaLas but not for CTV [30, 47].

Hormones and control of defense responses

The central plant immune responses associated with jasmonic acid, salicylic acid and ethylene [65] interact with plant hormones, including gibberellins [17], abscisic acid [57], auxins [40, 62, 83], cytokinins [40] and brassinosteroids 61]. Pathways leading to production of these hormones were also affected by CaLas-B232 alone [30]. The brassinosteroid, cytokinin and gibberellic acid, ethylene, abscisic acid and salicylic acid associated pathways were affected by CTV-B6 but only the ethylene and SA related pathways were affected by CTV-B2 (Table 1). Lipoxygenase 2 (LOX2) associated with JA synthesis-degradation was highly induced by CaLas-B232 alone but only slightly induced by CTV-B2/CaLas-B232 and repressed by CTV-B6/CaLas-B232 (Additional file 4: Table S2).

The WRKY factors are important regulators of SA-dependent defense responses [82] and some of them have been demonstrated in SA-JA crosstalk. Genes encoding WRKY transcription factors were mostly down-regulated in response to CTV-B2/CaLas-B232 and/or CTV-B6/CaLas-B232 (Additional file 3: Tables S1 and Additional file 4: Table S2), but WRKY 50, WRKY60 and WRKY70 were induced by CTV-B6/CaLas-B232, as well as by CTV-B2, CTV-B6 and CTV-B232 alone [30]. WRKY70, WRKY11 and WRKY17 are involved in SA/JA crosstalk as negative regulators of disease resistance in Arabidopsis [42]. WRKY70 was induced by CTV-B6/CaLas-B232 together, and also by CTV-B2, CTV-B6 and CaLas-B232 alone [30, 54] and in fruit infected with CaLas [55]. These results imply that WRKY70 plays a pivotal role in defense responses to both CaLas and CTV. WRKY33 was induced as a key regulator in modulating hormonal and metabolic responses to Botrytis cinerea infection in Arabidopsis [6], but the expression of WRKY33 was strongly repressed by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232, while slightly induced by CaLas-B232. This is consistent with different responses to necrotrophic (B. cinerea) and biotrophic (CaLas) pathogens.

Ubiquitin ligases add ubiquitin to proteins to direct them to the proteasome for degradation. Expression of PUB22 (U-box 22) and PUB24 encoding ubiquitin ligases were sharply down-regulated by both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). This suggests that the subset of proteins whose degradation is regulated by these ubiquitin ligases would accumulate to abnormally high levels in plants infected by CTV and CaLas.

ERF1 (Ethylene response factor 1) is a positive regulator mediating the jasmonate and ethylene signaling pathways [51] and many other ERF members also play important functions in defense responses in Arabidopsis [58]. The expression of ERF1 was repressed in response to both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232, whereas ERF1 was induced by CTV-B6 and CaLas-B232 and no change was found in response to CTV-B2 when the pathogens were inoculated individually. The gene that encodes jasmonate-ZIM-domain protein1 (JAZ1/TIF10A) was strongly down-regulated by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2) whereas was up-regulated in response to CaLas-B232 alone. JAZ proteins act as repressors of JA-signaling and interact with JIN1/MYC2 [12]. A reduction of JAZ protein releases transcription factor MYC2 and further stimulates the expression of JA-responsive genes [12, 77, 81]. The expression of JAZ1/TIFY10A may be inducible by auxin and crosstalk between auxin and JA signaling [36].

ABA is also an important hormone associated with plant defense responses. NCEDs (nine-cis-epoxycarotenoid dioxygenase 3) are involved in the biosynthesis of ABA and their up- or down-regulation is correlated with levels of ABA. The expression of NCED3, NCED4 and NCED5 was repressed by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 together, while NCED3 and NCED4 were over expressed in response to CTV-B6 and CaLas-B232, respectively. ABA plays a central role in plant-pathogen interactions via crosstalk with JA-SA mediated signaling pathways [27].

Auxin related genes were differentially expressed in response to CTV-B2/CaLas-B232, CTV-B6/CaLas-B232 together, and to CaLas-B232 alone, but not by either strain of CTV alone. The auxin-responsive gene GH3.1 (Gretchen Hagen3) was highly repressed by both CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 (Additional file 3: Table S1 and Additional file 4: Table S2). GH3.5 regulates both SA and auxin signaling against infection by Pseudomonas [90]. Over expression of GH3.8 reinforced resistance of rice against Xanthomonas oryzae pv. oryzae (Xoo) and reduced levels of SA and JA and expression of genes responsive to SA and JA [19], demonstrating a link between the auxin responsive pathway and the SA-JA-ET signaling network in plants. GH3.1 and GH3.6 were strongly repressed by CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232, consistent with down-regulation of auxin responsive genes in young leaves [53], but GH3.6 was slightly induced in response to CaLas-B232 alone [30]. The repression of auxin signaling may be part of the plant immune response and could potentially enhance resistance of plants to pathogens [62, 79].

Brassinosteroids (BRs) are a unique class of plant hormones involved in various developmental processes including cell division, elongation, flowering, senescence, fruit ripening and abiotic/biotic stress responses. The BRs pathways were up regulated by either strain of CTV in conjunction with CaLas, but not by any of the pathogens separately. BR increased rice resistance to Xanthomonas oryzae infection [61]. The titer of CaLas was reduced by treatment with BRs, providing a new insight for the control of HLB [11].

Plants often face multiple pests and pathogens in the natural environment and consequently they apply comprehensive regulatory mechanisms to activate defense responses against various pathogens. Signaling networks and crosstalk among plant hormone mediated defense pathways played more profound and complicated roles in response to co-infection with CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232 than to single infection with CTV-B2, CTV-B6 or CaLas-B232. The expression patterns of some genes related to plant hormones, such as LOX2, WRKY33, ERF1, JAZ1 (Additional file 3: Table S1 and Additional file 4: Table S2), in response to dual pathogen infection were opposite to the response observed with single infections by the same pathogens.

The composition of ribosomal subunits was especially affected by co-infection of CaLas-B232 and CTV-B6, in contrast with infection by the same pathogens in single pathogen infections. The down-regulation of ribosomal biogenesis was also found in both roots and leaves from Fe-deficient Arabidopsis [70]. PSI and PSII are the largest sinks for Fe and majority of Fe is stored in chloroplasts. Decreased photosynthetic performances as well as tetrapyrrole biosynthesis are hallmarks of Fe deficiency in plants [70]. The repression of ribosomal biogenesis we observed could also result from Fe deficiency in the leaves we sampled, particularly when the hosts are infected with both CTV-B6 and CaLas together [70]. A failure to properly recalibrate cellular Fe homeostasis may be responsible for the decrease of ribosomal subunits. This repression is highly organ-specific, rather than general [70, 84].

Conclusion

Carbohydrate, amino acid and lipid metabolism were deeply reconfigured in response to CTV-B2/CaLas-B232 and CTV-B6/CaLas-B232, much more so than in response to infection by any of the pathogens alone. The photosynthetic, glycolytic, oxidative pentose phosphate and tricarboxylic acid pathways were all repressed by CTV-B2/CaLas-B232 and especially by CTV-B6/CaLas-B232. The repression of these energy generating processes limited plant growth and defense responses [7]. The circadian system was also strongly perturbed by both double and single pathogen infection. Defense pathways, including those linked to the hormones jasmonic acid, salicylic acid, gibberellic acid, abscisic acid, auxin, brassinosteroids and cytokinins were all perturbed by CTV-B6/CaLas-B232, and to a lesser extent by CTV-B2/CaLas-B232, CaLas-B232, CTV-B6 and CTV-B2. Transport systems were also heavily perturbed and many transporters were activated. ZIP1, ZIP4, ZIP5 and PP2-B15 showed very different expression patterns in response to double pathogen infection compared to single pathogen infection. CTV-B6 may cooperate with CaLas-B232 in weakening the plant through root decline and phloem blockage. Defense responses activated by the mild strain CTV-B2 may provide some beneficial effects against CaLas-B232. Although many host genes were expressed differently in response to double-infections as compared to single infections with the same pathogens, the symptoms of CaLas and CTV-B6 infection were produced. The interaction of the pathogens within the host may lead to a better or worse result for the host plant.

Methods

Inoculation of experimental trees with CTV and CaLas

CTV mild strain B2 (T30 genotype, Florida), severe strain B6 (Complex genotype, SY568, California) and CaLas strain B232 (Thailand) are maintained in planta as part of the Exotic Pathogens of Citrus Collection (EPCC) at the USDA-ARS Beltsville Agricultural Research Center (BARC) in Beltsville, MD. Experimental seedling trees were ‘Valencia’ sweet orange. CaLas-B232 was inoculated by bud grafting into two groups of 10 trees. Three months later, one group of the trees was inoculated with CTV-B2 and another group was inoculated with CTV-B6. Ten trees were mock-inoculated with healthy buds as controls.

RNA preparation and qPCR

DNA and RNA extractions and RT-PCR and qPCR testing for the presence of pathogens were performed as previously described [30]. Three months after the CTV inoculations, and therefore 6 months after the CaLas inoculations, trees that tested positive for both CTV-B2 and CaLas-B232 (CTV-B2/CaLas-B232) or both CTV-B6 and CaLas-B232 (CTV-B6/CaLas-B232) by PCR were selected for analysis. Three to five young, soft, not fully expanded leaves of uniform size and without symptoms were collected, frozen in liquid nitrogen and kept at −80 °C. RNA was extracted as described [30] and assessed for quantity and quality with a Qubit 2.0 Fluorometer (Invitrogen) and Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA). Nine RNA samples (RIN ≥ 7.5), comprised of three RNA replicates, each from individual trees for each treatment (CTV-B2/CaLas-B232-infected, CTV-B6/CaLas-B232-infected and healthy citrus) were sent to Otogenetics (Norcross, GA, USA) for paired-end sequencing with the Illumina HiSeq 2500 platform.

Statistical analyses of RNA sequence libraries

Libraries of paired-end reads (2 × 100 nucleotides) for the nine citrus RNA extracts were generated with the Illumina HiSeq2500. After removing low-quality reads and adaptor sequences from the raw reads, high-quality reads were obtained and mapped to the C. sinensis reference genome [85] with Bowtie [46]. Expression levels of transcripts (log2 fold change) were calculated with DESeq2 [53]. Sequence similarity comparisons of the sequences identified in the reference genome of C. sinensis were made with both Arabidopsis thaliana and another C. sinensis genome [32]. Differentially expressed transcripts (DETs) were filtered with cut-off values, Padj ≤0.1, |log2FC| ≥ 1 and e-value ≤ e−5. DETs were enriched by Panther [59] with corresponding Arabidopsis orthologs and further assigned to metabolic pathways by reference to the Kyoto Encyclopedia of Genes and Genomes (KEGG) and functionally classified by Mapman [80].

RT-qPCR analysis

A total of 4 μg of RNA was reverse transcribed for first-strand cDNA syntheses using GoTaq® 2-step RT-qPCR system (Promega, Madison, WI) according to the manufacturer’s instructions. cDNA was diluted three fold with 1 X TE and stored at −20 °C for use. Gene-specific primers (Additional file 5: Table S3) were designed with an online tool (Integrated DNA Technologies, Coralville, IA) with melting temperatures of 60 °C ± 5 °C. qPCR reactions were performed with GoTaq® qPCR Master Mix (Promega) in a Bio-Rad CFX96 system. Twenty microliters of reaction mixture was added to each well with three replicated plant samples for each primer pair for each sample. The reaction program was set at 95 °C for 3 min, and 40 cycles of 95 °C for 10 s, 60 °C for 30 s and 72 °C for 30 s. Melting curves were analyzed to ensure that a single product was amplified. Actin was used as the internal control. The Actin gene has been verified to be relatively stable within the large number of potential references genes [48, 87]; (Additional file 10: Figure S7). The 2-Ct method was applied for relative quantification of gene expression [50].

Abbreviations

CqaLas: 

Candidatus Liberibacter asiaticus’

CTV: 

Citrus tristeza virus

DEG: 

Differentially expressed gene; GO: Gene Ontology; FC: fold change; BP: biological process; TF: transcription factor

DET: 

Differentially expressed transcript

HLB: 

Huanglongbing

Declarations

Acknowledgements

None.

Funding

The research was supported by USDA ARS project 701–8042-560. A small portion of this work was done when SMF was Ph. D candidate and sponsored by China Scholarship Council (CSC) and Southwest University.

Availability of data and materials

The datasets supporting the conclusions of this article are available in the SRA database under Submission ID SUB2613423 and BioProject ID PRJNA384780; https://www.ncbi.nlm.nih).

Authors’ contributions

SMF performed the experiments and wrote the manuscript; SMF and JS collected data and carried out all data analyses; CP prepared experimental plants; JSH conceptualized the idea; JSH and CYZ revised the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

The plant materials used were commercial varieties and seed was obtained from a commercial source. Therefore, no voucher specimens were prepared. The isolates of ‘Ca. Liberibacter asiaticus’ and Citrus tristeza virus used were from the Exotic Pathogens of Citrus Collection of the USD ARS and were obtained and maintained under permit from USDA APHIS.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interest.

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Authors’ Affiliations

(1)
Citrus Research Institute, Southwest University, Chongqing, China
(2)
United States Department of Agriculture-Agricultural Research Service, Molecular Plant Pathology Laboratory, Beltsville, USA

References

  1. Abadía J, Morales F, Abadía A. Photosystem II efficiency in low chlorophyll, iron-deficient leaves. Plant Soil. 1999;215(2):183–92.View ArticleGoogle Scholar
  2. Albrecht U, Bowman KD. Gene expression in Citrus sinensis (L.) Osbeck following infection with the bacterial pathogen Candidatus Liberibacter asiaticus causing Huanglongbing in Florida. Plant Sci. 2008;175:291–306.View ArticleGoogle Scholar
  3. Albrecht U, Bowman KD. Transcriptional response of susceptible and tolerant citrus to infection with Candidatus Liberibacter asiaticus. Plant Sci. 2012;185-186:118–30.View ArticlePubMedGoogle Scholar
  4. Andrés-Colás N, Sancenón V, Rodríguez-Navarro S, Mayo S, Thiele DJ, Ecker JR, et al. The Arabidopsis heavy metal P-type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots. Plant J. 2006;45(2):225–36.View ArticlePubMedGoogle Scholar
  5. Aritua V, Achor D, Gmitter FG, Albrigo G, Wang N. Transcriptional and microscopic analyses of citrus stem and root responses to Candidatus Liberibacter asiaticus infection. PLoS One. 2013;8(9):e73742.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Birkenbihl RP, Diezel C, Somssich IE. Arabidopsis WRKY33 is a key transcriptional regulator of hormonal and metabolic responses toward Botrytis cinerea infection. Plant Physiol. 2012;159(1):266–85.View ArticlePubMedPubMed CentralGoogle Scholar
  7. Bolton MD. Primary metabolism and plant defense-fuel for the fire. Mol Plant-Microbe Interact. 2009;22(5):487–97.View ArticlePubMedGoogle Scholar
  8. Bové JM. Huanglongbing: a destructive, newly-emerging, century old disease of citrus. J Plant Pathol. 2006;88:7–37.Google Scholar
  9. Bové JM, Renaudin J, Saillard C, Foissac X, Garnier M. Spiroplasma citri, a plant pathogenic mollicute: relationships with its two hosts, the plant and insect vector. Annu Rev Phytopathol. 2003;41:483–500.View ArticlePubMedGoogle Scholar
  10. Bowman K, Albrecht U. Comparison of gene expression changes in susceptible, tolerant and resistant hosts in response to infection with Citrus tristeza virus and huanglongbing. J Citrus Pathol. 2015;2(1). http://escholarship.org/uc/item/5qt4z9c0#page-4.
  11. Canales E, Coll Y, Hernández I, Portieles R, García MR, et al. Candidatus Liberibacter asiaticus’, causal agent of citrus huanglongbing, is reduced by treatment with brassinosteroids. PLoS One. 2016;11:e0146223.View ArticlePubMedPubMed CentralGoogle Scholar
  12. Chini A, Fonseca S, Fernandez G, Adie B, Chico J, Lorenzo O, et al. The JAZ family of repressors is the missing link in jasmonate signalling. Nature. 2007;448:666–71.View ArticlePubMedGoogle Scholar
  13. Chinnappa KSA, Nguyen TTS, Hou J, Wu Y, McCurdy DW. Phloem parenchyma transfer cells in Arabidopsis-an experimental system to identify transcriptional regulators of wall ingrowth formation. Front Plant Sci. 2013;4:102.Google Scholar
  14. Cristofani-Yaly M, Berger IJ, Targon MLP, Takita MA, Dorta S, Freitas-Astúa J, et al. Differential expression of genes identified from Poncirus Trifoliata tissue inoculated with CTV through EST analysis and in silico hybridization. Genet Mol Biol. 2007;30(3):972–9.View ArticleGoogle Scholar
  15. Dalchau N, Baek SJ, Briggs HM, Robertson FC, Dodd AN, Gardner MJ, et al. The circadian oscillator gene GIGANTEA mediates a long-term response of the Arabidopsis thaliana circadian clock to sucrose. PNAS USA. 2011;108(12):5104–9.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Dawson WO, Bar-Joseph M, Garnsey SM, Moreno P. Citrus Tristeza Virus: making an ally from an enemy. Annu Rev Phytopathol. 2015;53:137–55.View ArticlePubMedGoogle Scholar
  17. De Bruyne L, Höfte M, De Vleesschauwer D. Connecting growth and defense: the emerging roles of brassinosteroids and gibberellins in plant innate immunity. Mol Plant. 2014;7(6):943–59.View ArticlePubMedGoogle Scholar
  18. Deeken R, Geiger D, Fromm J, Koroleva O, Ache P, Langenfeld-Heyser R, et al. Loss of the AKT2/3 potassium channel affects sugar loading into the phloem of Arabidopsis. Planta. 2002;216(2):334–44.View ArticlePubMedGoogle Scholar
  19. Ding X, Cao Y, Huang L, Zhao J, Xu C, Li, X et al. Activation of the indole-3-acetic acid–amido synthetase GH3–8 suppresses expansin expression and promotes salicylate-and jasmonate-independent basal immunity in rice. Plant Cell 2008;20(1): 228-240.Google Scholar
  20. Doering-Saad C, Newbury H, Couldridge C, Bale J, Pritchard J. A phloem-enriched cDNA library from Ricinus: insights into phloem function. J Exp Botany. 2006;57(12):3183–93.View ArticleGoogle Scholar
  21. Doering-Saad C, Newbury HJ, Bale JS, Pritchard J. Use of aphid stylectomy and RT-PCR for the detection of transporter mRNAs in sieve elements. J Exp Botany. 2002;53:631–7.View ArticleGoogle Scholar
  22. Duan Y, Zhou L, Hall DG, Li W, Doddapaneni H, Lin H, et al. Complete genome sequence of citrus huanglongbing bacterium, ‘Candidatus Liberibacter asiaticus’ obtained through metagenomics. Mol Plant-Microbe Interact. 2009;22(8):1011–20.View ArticlePubMedGoogle Scholar
  23. Edwards J, Martin AP, Andriunas F, Offler CE., Patrick JW., McCurdy, DW. GIGANTEA is a component of a regulatory pathway determining wall ingrowth deposition in phloem parenchyma transfer cells of Arabidopsis Thaliana. Plant J 2010;63(4): 651-661.Google Scholar
  24. Fan J, Chen C, Achor DS, Brlansky RH, Li ZG, Gmitter FG Jr. Differential anatomical responses of tolerant and susceptible citrus species to the infection of ‘Candidatus Liberibacter asiaticus. Physiol Mol Plant Path. 2013;83:69–74.View ArticleGoogle Scholar
  25. Fan J, Chen C, Yu Q, Brlansky RH, Lia ZG, Gmitter FG Jr. Comparative iTRAQ proteome and transcriptome analyses of sweet orange infected by “Candidatus Liberibacter asiaticus”. Physiol Plant. 2011;143:235–45.View ArticlePubMedGoogle Scholar
  26. Fan J, Chen C, Yu Q, Khalaf A, Achor DS, Brlansky RH, et al. Comparative transcriptional and anatomical analyses of tolerant rough lemon and susceptible sweet orange in response to ‘Candidatus Liberibacter asiaticus’ infection. Mol Plant-Microbe Interact. 2012;25(11):1396–407.View ArticlePubMedGoogle Scholar
  27. Fan J, Hill L, Crooks C, Doerner P, Lamb C. Abscisic acid has a key role in modulating diverse plant-pathogen interactions. Plant Physiol. 2009;150(4):1750–61.View ArticlePubMedPubMed CentralGoogle Scholar
  28. Fischer WN, Loo DD, Ludewig U, Boorer KJ, Tegeder M, Rentsch D, et al. Low and high affinity amino acid H+−cotransporters for cellular import of neutral and charged amino acids. Plant J. 2002;29(6):717–31.View ArticlePubMedGoogle Scholar
  29. Folimonova SY, Achor DS. Early events of citrus greening (huanglongbing) disease development at the ultrastructural level. Phytopathology. 2010;100(9):949–58.View ArticlePubMedGoogle Scholar
  30. Fu S, Shao J, Zhou C, Hartung JS. Transcriptome analysis of sweet orange trees infected with ‘Candidatus Liberibacter asiaticus’ and two strains of Citrus Tristeza Virus. BMC Genomics. 2016;17:349.View ArticlePubMedPubMed CentralGoogle Scholar
  31. Gao W, Xiao S, Li HY, Tsao SW, Chye ML. Arabidopsis thaliana acyl-CoA-binding protein ACBP2 interacts with heavy metal binding farnesylated protein AtFP6. New Phytol. 2009;181(1):89–102.View ArticlePubMedGoogle Scholar
  32. Gmitter Jr. FG, Chen C, Machado MA, de Souza AA, Ollitrault P., Froehlicher Y et al. Citrus genomics. Tree Genet Genomes. 2012; 8(3): 611-626.Google Scholar
  33. Goodspeed D, Chehab EW, Min-Venditti A, Braam J, Covington MF. Arabidopsis synchronizes jasmonate-mediated defense with insect circadian behavior. PNAS USA. 2012;109(12):4674–7.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Gould N, Thorpe MR, Minchin PE, Pritchard J, White PJ. Solute is imported to elongating root cells of barley as a pressure driven-flow of solution. Funct. Plant Biol. 2004;31(4):391–7.Google Scholar
  35. Graham JH, Johnson EG, Gottwald TR, Irey MS. Presymptomatic fibrous root decline in citrus trees caused by Huanglongbing and potential interaction with Phytophthora spp. Plant Dis. 2013;97:1195–9.View ArticleGoogle Scholar
  36. Grunewald W, Vanholme B, Pauwels L, Plovie E, Inzé D, Gheysen G, et al. Expression of the Arabidopsis jasmonate signalling repressor JAZ1/TIFY10A is stimulated by auxin. EMBO Rep. 2009;10(8):923–8.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Harmer SL. The circadian system in higher plants. Annu Rev Plant Biol. 2009;60:357–67.View ArticlePubMedGoogle Scholar
  38. Hartung JS, Shao J, Kuykendall LD. Comparison of the ‘Ca. Liberibacter asiaticus’ genome adapted for an intracellular lifestyle with other members of the Rhizobiales. PLoS One. 2011;6(8):e23289.View ArticlePubMedPubMed CentralGoogle Scholar
  39. Hunt E, Gattolin S, Newbury HJ, Bale JS, Tseng H-M, Barrett DA, et al. A mutation in amino acid permease AAP6 reduces the amino acid content of the Arabidopsis sieve elements but leaves aphid herbivores unaffected. J exp. Botany. 2010;61(1):55–64.Google Scholar
  40. Jiang C-J, Shimono M, Sugano S, Kojima M, Liu X, Inoue H, et al. Cytokinins act synergistically with salicylic acid to activate defense gene expression in rice. Mol Plant-Microbe Interact. 2013;26(3):287–96.View ArticlePubMedGoogle Scholar
  41. Johnson EG, Wu J, Bright DB, Graham JH. Association of ‘Candidatus Liberibacter asiaticus’ root infection, but not phloem plugging with root loss on huanglongbing-affected trees prior to appearance of foliar symptoms. Plant Pathol. 2014;63:290–8.View ArticleGoogle Scholar
  42. Journot-Catalino N, Somssich IE, Roby D, Kroj T. The transcription factors WRKY11 and WRKY17 act as negative regulators of basal resistance in Arabidopsis thaliana. Plant Cell. 2006;18(11):3289–302.View ArticlePubMedPubMed CentralGoogle Scholar
  43. Karley A, Douglas A, Parker W. Amino acid composition and nutritional quality of potato leaf phloem sap for aphids. J Exp Botany. 2002;205(19):300r9–3018.Google Scholar
  44. Kehr J, Butz A. Endogenous RNA constituents of the phloem and their possible roles in long-distance signaling in phloem. In: Thompson GA, van Bel AJE, editors. Molecular cell biology, systemic communication, biotic interactions. Oxford,UK: Wiley-Blackwell. https://doi.org/10.1002/9781118382806.ch95.
  45. Kim JS, Sagaram US, Burns JK, Li JL, Wang N. Response of sweet orange (Citrus sinensis) to ‘Candidatus Liberibacter asiaticus’ infection: microscopy and microarray analyses. Phytopathology. 2009;99(1):50–7.View ArticlePubMedGoogle Scholar
  46. Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10 (R25). https://genomebiology.biomedcentral.com/track/pdf/10.1186/gb-2009-10-3-r25?site=genomebiology.biomedcentral.com.
  47. Liao HL, Burns JK. Gene expression in Citrus sinensis fruit tissues harvested from huanglongbing-infected trees: comparison with girdled fruit. J Exp Botany. 2012;63(8):3307–19.View ArticleGoogle Scholar
  48. Liu Q, Zhu A, Chai L, Zhou W, Yu K, Ding J, et al. Transcriptome analysis of a spontaneous mutant in sweet orange [Citrus sinensis (L.) Osbeck] during fruit development. J Exp Botany. 2009;60(3):801–13.View ArticleGoogle Scholar
  49. Liu Y, Wang G, Wang Z, Yang F, Wu G, Hong N. Identification of differentially expressed genes in response to infection of a mild Citrus tristeza virus isolate in Citrus aurantifolia by suppression subtractive hybridization. Sci Hort. 2012;134:144–9.View ArticleGoogle Scholar
  50. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods. 2001;25:402–8.View ArticlePubMedGoogle Scholar
  51. Lorenzo O, Piqueras R, Sánchez-Serrano JJ, Solano R. ETHYLENE RESPONSE FACTOR1 integrates signals from ethylene and jasmonate pathways in plant defense. Plant Cell. 2003;15(1):165–78.View ArticlePubMedPubMed CentralGoogle Scholar
  52. Lough TJ, Lucas WJ. Integrative plant biology: role of phloem long-distance macromolecular trafficking. Annu Rev Plant Biol. 2006;57:203–32.View ArticlePubMedGoogle Scholar
  53. Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15(12):1–21.View ArticleGoogle Scholar
  54. Mafra V, Martins P, Francisco C, Ribeiro-Alves M, Freitas-Astua J, Machado MA. Candidatus Liberibacter americanus induces significant reprogramming of the transcriptome of the susceptible citrus genotype. BMC Genomics. 2013;14(1):247.View ArticlePubMedPubMed CentralGoogle Scholar
  55. Martinelli F, Reagan RL, Uratsu SL, Phu ML, Albrecht U, Zhao W, et al. Gene regulatory networks elucidating huanglongbing disease mechanisms. PLoS One. 2013;8(9):e74256.View ArticlePubMedPubMed CentralGoogle Scholar
  56. Martinelli F, Uratsu SL, Albrecht U, Reagan RL, Phu ML, Britton M, et al. Transcriptome profiling of citrus fruit response to Huanglongbing disease. PLoS One. 2012;7(5):e38039.View ArticlePubMedPubMed CentralGoogle Scholar
  57. Mauch-Mani B, Mauch F. The role of abscisic acid in plant–pathogen interactions. Curr Opin Plant Biol. 2005;8(4):409–14.View ArticlePubMedGoogle Scholar
  58. McGrath KC, Dombrecht B, Manners JM, Schenk PM, Edgar CI, Maclean DJ, et al. Repressor-and activator-type ethylene response factors functioning in jasmonate signaling and disease resistance identified via a genome-wide screen of Arabidopsis transcription factor gene expression. Plant Physiol. 2005;139(2):949–59.View ArticlePubMedPubMed CentralGoogle Scholar
  59. Mi H, Dong Q, Muruganujan A, Gaudet P, Lewis S, Thomas PD. PANTHER version 7: improved phylogenetic trees, orthologs and collaboration with the gene ontology consortium. Nucleic Acid Res. 2010;38:D247–52.View ArticleGoogle Scholar
  60. Moreno P, Ambros S, Albiach-Marti MR, Guerri J, Pena L. Citrus tristeza virus : a pathogen that changed the course of the citrus industry. Mol Plant Pathol. 2008;9(2):251–68.View ArticlePubMedGoogle Scholar
  61. Nakashita H, Yasuda M, Nitta T, Asami T, Fujioka S, Arai Y, et al. Brassinosteroid functions in a broad range of disease resistance in tobacco and rice. Plant J. 2003;33(5):887–98.View ArticlePubMedGoogle Scholar
  62. Navarro L, Dunoyer P, Jay F, Arnold B, Dharmasiri N, Estelle M, et al. A plant miRNA contributes to antibacterial resistance by repressing auxin signaling. Science. 2006;312:436–9.View ArticlePubMedGoogle Scholar
  63. Okumoto S, Schmidt R, Tegeder M, Fischer WN, Rentsch D, Frommer WB, et al. High affinity amino acid transporters specifically expressed in xylem parenchyma and developing seeds of Arabidopsis. J Biol Chem. 2002;277(47):45338–46.View ArticlePubMedGoogle Scholar
  64. Park DH, Somers DE, Kim YS, Choy Y, Lim HK, Soh MS, et al. Control of circadian rhythms and photoperiodic flowering by the Arabidopsis GIGANTEA gene. Science. 1999;285:1579–82.View ArticlePubMedGoogle Scholar
  65. Pieterse CM, Leon-Reyes A, Van der Ent S, Van Wees SC. Networking by small-molecule hormones in plant immunity. Nature Chem Biol. 2009;5(5):308–16.View ArticleGoogle Scholar
  66. Ponder K, Pritchard J, Harrington R, Bale J. Difficulties in location and acceptance of phloem sap combined with reduced concentration of phloem amino acids explain lowered performance of the aphid Rhopalosiphum padi on nitrogen deficient barley (Hordeum vulgare) seedlings. Entomologia Experimentalis et Applicata. 2000;97(2):203–10.View ArticleGoogle Scholar
  67. Rawat N, Kiran SP, Du D, Gmitter FG, Deng Z. Comprehensive meta-analysis, co-expression, and miRNA nested network analysis identifies gene candidates in citrus against Huanglongbing disease. BMC Plant Biol. 2015;15:184.View ArticlePubMedPubMed CentralGoogle Scholar
  68. Rentsch D, Hirner B, Schmelzer E, Frommer WB. Salt stress-induced proline transporters and salt stress-repressed broad specificity amino acid permeases identified by suppression of a yeast amino acid permease-targeting mutant. Plant Cell. 1996;8(8):1437–46.View ArticlePubMedPubMed CentralGoogle Scholar
  69. Roden LC, Ingle RA. Lights, rhythms, infection: the role of light and the circadian clock in determining the outcome of plant–pathogen interactions. Plant Cell. 2009;21(9):2546–52.View ArticlePubMedPubMed CentralGoogle Scholar
  70. Rodríguez-Celma J, Pan IC, Li W, Lan P, Buckhout TJ, Schmidt W. The transcriptional response of Arabidopsis leaves to Fe deficiency. Frontiers Plant Sci. 2013;4(276). https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719017/pdf/fpls-04-00276.pdf.
  71. Rosa BA, Jiao Y, Oh S, Montgomery BL, Qin W, Chen J. Frequency-based time-series gene expression recomposition using PRIISM. BMC Syst Biol. 2012;6:69.View ArticlePubMedPubMed CentralGoogle Scholar
  72. Roudier F. The COBRA family of putative GPI-anchored proteins in Arabidopsis. A new fellowship in expansion. Plant Physiol. 2002;130:538–48.View ArticlePubMedPubMed CentralGoogle Scholar
  73. Schindelman G., Benfey P. NCOBRA encodes a putative GPI-anchored protein, which is polarly localized and necessary for oriented cell expansion in Arabidopsis. Genes Dev. 2001; 15: 1115-1127.Google Scholar
  74. Schwachtje J, Baldwin IT. Why does herbivore attack reconfigure primary metabolism? Plant Physiol. 2008;146(3):845–51.View ArticlePubMedPubMed CentralGoogle Scholar
  75. Slewinski TL, Meeley R, Braun DM. Sucrose transporter1 functions in phloem loading in maize leaves. J Exp Botany. 2009;60(3):881–92.View ArticleGoogle Scholar
  76. Spann TM, Schumann AW. The role of plant nutrients in disease development with emphasis on citrus and huanglongbing. Proc Florida State Hort Soc. 2009:169–71.Google Scholar
  77. Staswick PE. JAZing up jasmonate signaling. Trends Plant Sci. 2008;13(2):66–71.View ArticlePubMedGoogle Scholar
  78. Terry N, Low G. Leaf chlorophyll content and its relation to the intracellular localization of iron. J Plant Nutr. 1982;5:301–10.View ArticleGoogle Scholar
  79. Thilmony R, Underwood W, He SY. Genome wide transcriptional analysis of the Arabidopsis thaliana interaction with the plant pathogen Pseudomonas syringae pv. tomato DC3000 and the human pathogen Escherichia coli O157: H7. Plant J. 2006;46(1):34–53.View ArticlePubMedGoogle Scholar
  80. Thimm O, Bläsing O, Gibon Y, Nagel A, Meyer S, Krüger P, et al. MAPMAN: a user-driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes. Plant J. 2004;37(6):914–39.View ArticlePubMedGoogle Scholar
  81. Thines B, Katsir L, Melotto M, Niu Y, Mandaokar A, Liu G, et al. JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling. Nature. 2007;448:661–5.View ArticlePubMedGoogle Scholar
  82. Wang D, Amornsiripanitch N, Dong X. A genomic approach to identify regulatory nodes in the transcriptional network of systemic acquired resistance in plants. PLoS Pathog. 2006;2(11):e123.View ArticlePubMedPubMed CentralGoogle Scholar
  83. Wang D, Pajerowska-Mukhtar K, Culler AH, Dong X. Salicylic acid inhibits pathogen growth in plants through repression of the auxin signaling pathway. Curr Biol. 2007;17(20):1784–90.View ArticlePubMedGoogle Scholar
  84. Wang N, Trivedi P. Citrus huanglongbing: a newly relevant disease presents unprecedented challenges. Phytopathology. 2013;103:652–65.View ArticlePubMedGoogle Scholar
  85. Xu Q, Chen L-L, Ruan X, Chen D, Zhu A, Chen C, et al. The draft genome of sweet orange (Citrus sinensis). Nat Genet. 2013;45(1):59–66.View ArticlePubMedGoogle Scholar
  86. Yang F, Wang G-P, Jiang B, Liu Y-H, Liu Y, Wu G-W, et al. Differentially expressed genes and temporal and spatial expression of genes during interactions between Mexican lime (Citrus aurantifolia) and a severe Citrus tristeza virus isolate. Physiol Mol Plant Pathol. 2013;83:17–24.View ArticleGoogle Scholar
  87. Yan J, Yuan F, Long G. Selection of reference genes for quantitative real-time RT-PCR analysis in citrus. Mol Biol Rep. 2012;39(2):1831–8.View ArticlePubMedGoogle Scholar
  88. Yu J-W, Rubio V, Lee N-Y, Bai S, Lee S-Y, Kim S-S, et al. COP1 and ELF3 control circadian function and photoperiodic flowering by regulating GI stability. Mol Cell. 2008;32(5):617–30.View ArticlePubMedPubMed CentralGoogle Scholar
  89. Zeier J. New insights into the regulation of plant immunity by amino acid metabolic pathways. Plant Cell Environ. 2013;36(12):2085–103.View ArticlePubMedGoogle Scholar
  90. Zhang Z, Li Q, Li Z, Staswick PE, Wang M-Y, Zhu Y, et al. Dual regulation role of GH3. 5 in salicylic acid and auxin signaling during Arabidopsis-Pseudomonas syringae interaction. Plant Physiol. 2007;145(2):450–64.View ArticlePubMedPubMed CentralGoogle Scholar
  91. Zheng Z-L, Zhao Y. Transcriptome comparison and gene coexpression network analysis provide a systems view of citrus response to ‘Candidatus Liberibacter asiaticus’ infection. BMC Genomics. 2013;14(1):1.View ArticleGoogle Scholar
  92. Zhong Y, Cheng C-Z, Jiang N-H, Jiang B, Zhang Y-Y, Wu B, et al. Comparative Transcriptome and iTRAQ proteome analyses of citrus root responses to Candidatus Liberibacter asiaticus infection. PLoS One. 2015;10(6):e0126973.View ArticlePubMedPubMed CentralGoogle Scholar

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