The molecular interplay of the establishment of an infection – gene expression of Diaphorina citri gut and Candidatus Liberibacter asiaticus

Abstract

Background

Candidatus Liberibacter asiaticus (CLas) is one the causative agents of greening disease in citrus, an unccurable, devastating disease of citrus worldwide. CLas is vectored by Diaphorina citri, and the understanding of the molecular interplay between vector and pathogen will provide additional basis for the development and implementation of successful management strategies. We focused in the molecular interplay occurring in the gut of the vector, a major barrier for CLas invasion and colonization.

Results

We investigated the differential expression of vector and CLas genes by analyzing a de novo reference metatranscriptome of the gut of adult psyllids fed of CLas-infected and healthy citrus plants for 1-2, 3-4 and 5-6 days. CLas regulates the immune response of the vector affecting the production of reactive species of oxygen and nitrogen, and the production of antimicrobial peptides. Moreover, CLas overexpressed peroxiredoxin, probably in a protective manner. The major transcript involved in immune expression was related to melanization, a CLIP-domain serine protease we believe participates in the wounding of epithelial cells damaged during infection, which is supported by the down-regulation of pangolin. We also detected that CLas modulates the gut peristalsis of psyllids through the down-regulation of titin, reducing the elimination of CLas with faeces. The up-regulation of the neuromodulator arylalkylamine N-acetyltransferase implies CLas also interferes with the double brain-gut communication circuitry of the vector. CLas colonizes the gut by expressing two Type IVb pilin flp genes and several chaperones that can also function as adhesins. We hypothesized biofilm formation occurs by the expression of the cold shock protein of CLas.

Conclusions

The thorough detailed analysis of the transcritome of Ca. L. asiaticus and of D. citri at different time points of their interaction in the gut tissues of the host led to the identification of several host genes targeted for regulation by L. asiaticus, but also bacterial genes coding for potential effector proteins. The identified targets and effector proteins are potential targets for the development of new management strategies directed to interfere with the successful utilization of the psyllid vector by this pathogen.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12864-021-07988-2.

Background

Bacterial plant pathogens are adapted to infect and propagate in insect tissues, as many insects are used as vectors by plant pathogens to infect new host plants and spread themselves in the environment. Plant pathogenic bacteria vectored by insects that use persistent, circulative, propagative mode of transmission require plastic phenotypes to interact with the different enviroments represented by sieves and tissues of the host plant, and the diverse environments faced in the gut lumen, hemocele and different tissues of the vector insect during the processes of acquisition and vector competence development [1]. The capability of these pathogens to infect completely different hosts (plant and insect), and yet to depend on the shuttle host (insect) to locate and collect the pathogen in a diseased plant, and later transport it to new, health host plants for the establishment of new infections requires a set of strategies devoted to manipulate the host insect [2, 3]. The understanding of the interactions pathogens and hosts have at their molecular level during the processes of host invasion and infection establishment is required for a fully comprehension of the mechanisms involved in guaranteeing the host – pathogen association. Such mechanisms of close interactions in the associations of host and pathogens represent potential new targets for the development of new technologies and/or use of existing technologies to interfere with the successful association pathogens establish with their hosts.

Candidatus Liberibacter are bacteria posing serious threat to food security worldwide by causing diseases to potatoes and citrus. Citrus is certainly the most severely damaged crop by Ca. Liberibacter infections, as three different species are known to infect citrus plants (Ca. L. asiaticus, Ca. L. americanus and Ca. L. africanus), causing the incurable greening or huanglongbing (HLB) disease [4–7]. Candidatus Liberibacter did not make to the top 10 plant pathogenic bacteria [8], but HLB has caused a tremendous impact in the citrus industry and led to the complete elimination of citrus orchards and the interruption of citrus production in what used to be highly productive citrus centers [7, 9, 10].

Candidatus Liberibacter asiaticus (CLas) is the most spread in the world, currently infecting citrus in the major producing areas [11–13]. In plants, Candidatus Liberibacter reside exclusively in the phloem sieve tubes [4, 14–16], but it will infect several tissues of their host vector insect [17–20]. CLas is vectored by the worldwidely distributed Asian Citrus Psyllid (ACP) Diaphorina citri Kuwayama (Hemiptera: Psyllidae) [4].

Despite the importance of this disease to the worldwide citriculture and all of the investments and efforts of the scientific community to understand the interactions of the pathogen with its vector, much of the mechanisms involved in the pathogen-vector interplay remain unknown. We learned that CLas is transmitted from host plant to host plant by establishing a persistent, propagative transmission mode with its vector, a transmission mode that is very common to plant viruses vectored by aphids and whiteflies [19, 21, 22]. CLas was also demonstrated to alter the host plant transcriptional profile [23–25]. We also learned CLas infects salivary glands and the midgut of vectors, tissues that are often recognized as natural barriers to circulative, propagative pathogens as they can prevent translocation of pathogens within the vector host [17, 22, 26, 27]. Differential gene expression analysis of CLas-infected psyllids also demonstrated CLas alters the gene expression profile of of the gut, salivary glands and whole-body of D. citri [19, 28–30]. More recently, new information on the higher efficiency of adults than psyllid nymphs as vectors of CLas has been reported, with adults displaying a higher successful rate of infection of healthy citrus plants than nymphs [27]. Nevertheless, little information at the physiological and molecular level on the interface of the interactions of CLas with key vector tissues is available [31].

The limitations in the availability of efficient, cost-effective strategies for the management of the vector and the disease prompted a large number of investigations for the exploitation of new technologies, and promising results were mainly obtained with RNAi-based approaches [32–35].

In here we focused on investigating the metatranscriptome of the gut of adults of D. citri feeding on CLas-infected citrus plants for different periods of time in order to identify genes of CLas that are expressed during the colonization of the gut of adults and the differential gene expression in the gut of psyllids over time against psyllids feeding on healthy, CLas-free citrus plants. Our major goal was to understand the dynamics of CLas gene expression during psyllid colonization and the response mechanisms that were activated in the gut epithelium of psyllids when exposed to Ca. Liberibacter asiaticus cells. We believe our data represents a source of very specific targets for the development and implementation of new strategies of psyllid/disease control using RNAi and/or gene editing technologies such as the CRISPR-Cas9 system.

Results

De novo transcriptome assembly

Sequencing from libraries of the gut of uninfected and CLas-infected nymphs and adults of D. citri yielded 395,151,161 reads, with an average of 16,464,632 reads/library. The use of the resulting 385,677,949 trimmed, quality-filtered reads (average 16,069,915 reads/library) allowed the de novo assembly of a transcriptome with 260,612,776 nucleotides (260 Mb), with transcripts with an average size of 481 bp and a N50 of 2,095 bp. The assembly resulted in 248,850 transcripts with an average of 39.9% GC content. Annotation of the transcriptome allowed the putative identification of 90,531 transcripts (36.4%), of which 52,081 transcripts were allocated to different gene ontology categories (Additional file 1). Additional filtering using the highest score hit after BlastX allowed the identification of 66,993 transcripts belonging to D. citri, 807 belonging to Ca. Liberibacter, and 1,967 to the secondary symbiont Wolbachia, among others (Additional file 2).

CLas gene expression in the gut of adults of Diaphorina citri

Since we could not detect relevant read counts against transcripts belonging to Ca. L. asiaticus when using samples obtained from nymphs, only samples collected at the adult stage were subjected to differential expression analysis. Gene expression analysis recognized 807 transcripts belonging to Ca. L. asiaticus in the gut of adult psyllids fed on CLas-infected citrus plants in at least one of feeding exposure periods analyzed for adults (1-2 d; 3-4 d; 5-6 d - A1CLas⁺, A2CLas⁺ and A3CLas⁺, respectively), with no CLas-related transcripts being identified in gut samples from insects fed on healthy plants (CLas^-).

The detection of gene expression of Ca. L. asiaticus in adult psyllids increased in adults feeding on CLas-infected plants for 1-2 d to 5-6 d. Thus, 725 transcripts of CLas were expressed in A1CLas⁺, 766 in A2CLas⁺ and 804 in A3CLas⁺ (Fig. 1). One transcript was expressed only in A1CLas⁺ and A2CLas⁺, 22 in A1CLas⁺ and A3CLas⁺, and 63 in A2CLas⁺ and A3CLas⁺. We also identified CLas genes that were exclusively expressed at the early (1-2 d, A1CLas⁺= 1 transcript, DN14421_c0_g2_i2 = nicotinate-nucleotide adenylyltransferase), intermediate (3-4 d, A2CLas⁺= 1 transcript, DN18703_c1_g1_i24 = Flp type IVb pilin) and late stage (5-6 d, A3CLas⁺= 18 transcripts) after adult started feeding on CLas-infected citrus plants (Fig. 1). Most of these transcripts were represented by several isoforms of a gene, with different isoforms expressed in more than one of the sampled feeding times. Only A3CLas⁺ adults had transcripts represented by unique isoforms of a gene specifically expressed in their gut (Table 1).

Fig. 1.

Venn diagram of Candidatus Liberibacter asiaticus transcripts differentially expressed in gut of adults at different periods of feeding on CLas-infected citrus plant. A1CLas⁺: adults that fed on CLas-infected citrus plant for 1-2 days; A2CLas⁺: adults that fed on CLas-infected citrus plant for 3-4 days; and A3CLas⁺: adults that fed on CLas-infected citrus plant for 5-6 days.

Table 1.

Single isoforms of CLas transcripts exclusively expressed in the gut of adult psyllids in A3CLas+

Transcript ID	Annotation	TPM count
DN1443_c0_g1_i1	hypothetical protein PSGCA5_05	58.77
DN15414_c0_g1_i2	pyridoxine 5'-phosphate synthase	5.33
DN25987_c0_g1_i1	hypothetical protein	30.77
DN32802_c0_g1_i1	anti-repressor protein	38.31
DN39169_c0_g1_i1	hypothetical protein BWK56_05555	69.16
DN44737_c0_g1_i1	threonine--tRNA ligase	168.28
DN47430_c0_g1_i1	flagellar basal body rod protein FlgF	54.15
DN55271_c0_g1_i1	phage related protein	10.66
DN62541_c0_g1_i1	flagellar basal body P-ring protein FlgI	31.40
DN64078_c0_g1_i1	putative phage-related acetyltransferase	43.56

Pairwise gene expression analysis of CLas in the gut of adult psyllids after different periods of feeding on CLas-infected citrus plants revealed a high number of differentially expressed CLas genes in A3CLas⁺ as compared to A1CLas⁺ and A2CLas⁺ adults (Additional file 3). One-hundred transcripts out of the over 700 transcripts detected in the three sampling times differed in their abundance (Additional file 3). Differences in the level of expression were detected for 80 transcripts when comparing A1CLas⁺ and A3CLas⁺ and 20 transcripts in comparisons of A2CLas⁺ and A3CLas⁺ (Additional file 3). CLas expression was always higher in A3CLas⁺ when compared to the others. No differences in gene expression between A1CLas⁺ and A2CLas⁺ were detected (Additional file 3).

Differential gene expression in the gut of CLas⁺ and CLas^- adults of Diaphorina citri

Differential gene expression (DE) of the gut of adults of D. citri after feeding on CLas-infected plants for 1-2 days identified 24 DE transcripts in the gut of CLas⁺ insects, 20 of them were up-regulated and 4 were down-regulated in response to CLas infection. Most of the up-regulated transcripts (11) belong to uncharacterized proteins, while nine up-regulated transcripts were identified (Table 2). After 3-4 days of feeding on CLas-infected plants, the number of DE transcripts in the gut of CLas⁺ as compared to CLas^- adult psyllids increased to 35, most of which were up-regulated (27). Eighteen out of the 27 up-regulated transcripts, and seven out of the eight down-regulated transcripts were putatively identified (Table 2). The number of DE transcripts in the gut of adult psyllids after 5-6 days of feeding on CLas-infected plants was the highest, with 61 DE transcripts in the gut of CLas⁺ insects, 57 (33 unknown proteins) of them were up-regulated and 4 were down-regulated when compared to CLas^- adult psyllids (Table 2).

Table 2.

Comparative differential gene expression of adult psyllids fed on CLas infected and non-infected citrus plants for different periods of time (A1= 1-2 d; A2= 3-4 d; A3= 5-6 d)

Stage	DE	Annotation	Transcript ID	FC	FDR
*A1 - CLas+ x CLas-	Up-regulated	arylsulfatase B-like isoform X1	DN19237_c6_g3_i2	20.9	2.0e-2
		CLIP domain-containing serine protease 2-like isoform X1	DN16851_c1_g2_i2	119.9	3.0e-3
		kinesin-like protein KIF3B isoform X4	DN10161_c0_g1_i1	55.2	6.1e-3
		membrane metallo-endopeptidase-like 1 isoform X2	DN16798_c0_g1_i1	49.0	4.8e-4
		methylglutaconyl-CoA hydratase, mitochondrial	DN18628_c4_g1_i2	26.7	1.0e-2
		mitochondrial cytochrome c oxidase subunit IV	DN18774_c0_g1_i7	44.2	2.3e-6
		nuclear speckle splicing regulatory protein 1-like	DN17904_c2_g1_i3	133.9	4.0e-2
		uncharacterized protein LOC103515486	DN16253_c6_g2_i4	11.3	9.64e-3
		protein phosphatase 1 regulatory subunit 21	DN19112_c0_g1_i1	36.7	0.02
		putative rna-directed dna polymerase from transposon bs	DN20114_c0_g1_i11	26.6	0.05
		uncharacterized protein LOC103508016	DN17144_c6_g5_i2	83.6	2.93e-5
		uncharacterized protein LOC103508016	DN17144_c6_g5_i3	62.7	0.02
		uncharacterized protein LOC103518490	DN15191_c0_g1_i1	222.8	2.03e-3
		uncharacterized protein LOC103518490	DN15191_c0_g1_i4	41.0	6.75e-3
		uncharacterized protein LOC103519237	DN15191_c0_g1_i7	210.2	1.06e-4
		uncharacterized protein LOC113469268	DN20635_c0_g3_i1	242.2	1.06e-4
		uncharacterized protein LOC113469268	DN20635_c0_g1_i3	106.3	5.87e-4
		uncharacterized protein LOC113471433	DN20585_c3_g1_i12	167.6	5.28e-3
		uncharacterized protein PFB0145c-like	DN15546_c0_g1_i1	31.3	0.04
		uncharacterized protein YMR317W-like	DN15237_c0_g1_i1	132.6	4.69e-4
	Down-regulated	NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3	DN17549_c4_g1_i2	-32.5	6.75e-3
		protein pangolin, isoforms A/H/I/S-like	DN15424_c0_g3_i2	-28.0	0.03
		titin isoform X7	DN21409_c5_g2_i1	-36.1	0.03
		zonadhesin-like	DN14644_c0_g1_i1	-13.0	0.03
**A2 -CLas+ x CLas-	Up-regulated	Ac1147-like protein	DN18394_c1_g1_i3	19.7	0.02
		arylalkylamine N-acetyltransferase	DN20634_c1_g1_i13	45.9	0.05
		cathepsin L1-like	DN15698_c4_g11_i2	111.4	1.45e-3
		hypothetical protein DAPPUDRAFT_37179, partial	DN18534_c0_g5_i1	17.0	7.51e-4
		hypothetical protein g.47064	DN18473_c2_g1_i1	11.7	8.68e-3
		hypothetical protein g.7198	DN16128_c4_g1_i1	11.1	3.86e-3
		large neutral amino acids transporter small subunit 1	DN20157_c2_g3_i2	66.6	1.50e-4
		nocturnin isoform X1	DN15927_c10_g1_i6	15.1	2.82e-4
		predicted protein	DN21032_c17_g1_i2	27.0	2.19e-3
		predicted protein	DN21032_c17_g1_i1	23.9	6.41e-3
		uncharacterized protein LOC105736982	DN21288_c9_g7_i2	28.5	8.64e-4
		uncharacterized protein LOC103515486	DN16253_c6_g2_i4	12.6	0.04
		profilin	DN19422_c2_g2_i1	162.4	7.00e-9
		protein hu-li tai shao	DN19744_c0_g2_i2	12.2	0.01
		putative senescence-associated protein	DN18133_c2_g1_i3	28.0	1.41e-3
		Regulator of rDNA transcription protein 15	DN16244_c2_g3_i1	24.8	1.62e-3
		Regulator of rDNA transcription protein 15	DN21288_c9_g7_i1	16.4	6.43e-3
		Regulator of rDNA transcription protein 15	DN16244_c2_g3_i2	15.6	7.58e-4
		Regulator of rDNA transcription protein 15	DN16244_c2_g3_i3	13.0	5.46e-3
		reverse transcriptase-like protein	DN21162_c2_g1_i4	12.4	0.02
		sodium/potassium-transporting ATPase subunit alpha-like	DN14485_c0_g1_i1	17.9	5.33e-4
		UNC93-like protein MFSD11	DN16539_c2_g6_i1	48.5	0.04
		Uncharacterized protein ART2	DN19721_c0_g1_i3	9.8	0.02
		uncharacterized protein LOC105206152	DN18133_c2_g1_i1	22.8	1.45e-3
		uncharacterized protein LOC105693632	DN19721_c0_g4_i1	7.9	8.56e-3
		uncharacterized protein LOC113219380	DN19326_c1_g1_i2	35.7	6.21e-4
		uncharacterized protein LOC113469268	DN20635_c0_g1_i1	37.4	0.02
	Down-regulated	leptin receptor overlapping transcript-like 1	DN20058_c2_g3_i4	-26.7	0.02
		methylglutaconyl-CoA hydratase, mitochondrial	DN18628_c4_g1_i2	-11.3	1.27e-3
		putative juvenile hormone binding protein	DN21423_c1_g12_i2	-12.3	0.04
		Soluble NSF attachment protein	DN21196_c2_g1_i1	-19.8	5.64e-7
		translation elongation factor 2	DN21188_c1_g7_i2	-11.9	0.02
		tubulin-folding cofactor B	DN17504_c3_g2_i6	-4.5	1.82e-3
		uncharacterized protein LOC103513992	DN16335_c5_g1_i1	-16.7	5.18e-3
		zinc transporter ZIP10 isoform X1	DN19132_c8_g1_i5	-43.4	0.02
***A3 - CLas+ x CLas-	Up-regulated	2-oxoglutarate dehydrogenase, mitochondrial-like	DN14833_c0_g1_i1	8.6	0.03
		Ac1147-like protein	DN21090_c8_g2_i1	50.3	0.04
		BCL2/adenovirus E1B 19 kDa protein-interacting protein 3	DN20168_c2_g3_i4	21.0	0.04
		beta-1,3-galactosyltransferase 5-like	DN18243_c2_g2_i2	20.2	7.31e-3
		cleavage and polyadenylation specificity factor subunit CG7185-like	DN15201_c0_g1_i1	15.6	6.05e-3
		cytochrome P450-like TBP	DN19721_c0_g1_i4	35.7	0.05
		dynein heavy chain 7, axonemal-like	DN35915_c0_g1_i1	17.3	0.05
		gamma-glutamyl hydrolase-like	DN18300_c5_g1_i2	16.7	3.96e-5
		GATA zinc finger domain-containing protein 14-like	DN16387_c3_g2_i1	12.2	6.66e-3
		glycerophosphocholine phosphodiesterase GPCPD1-like isoform X1	DN15741_c0_g2_i2	41.6	1.10e-4
		hydrocephalus-inducing protein homolog	DN14616_c0_g1_i2	26.6	0.03
		hydrocephalus-inducing protein homolog	DN14616_c0_g2_i2	16.6	0.02
		hypothetical protein ALC57_18598	DN17391_c0_g1_i2	230.6	1.56e-4
		hypothetical protein FF38_03795	DN18516_c0_g3_i1	67.0	0.02
		hypothetical protein LOTGIDRAFT_202939	DN17968_c0_g2_i3	101.2	0.03
		hypothetical protein Phum_PHUM590900	DN17430_c2_g2_i1	24.2	0.02
		keratin-associated protein 5-3-like	DN15230_c0_g1_i2	14.2	6.76e-4
		keratinocyte proline-rich protein-like	DN20284_c2_g1_i3	11.5	0.02
		mucin-5AC-like, partial	DN16207_c6_g5_i1	7.7	0.04
		uncharacterized protein LOC103511862	DN17183_c5_g2_i3	9.4	0.04
		uncharacterized protein LOC103513455	DN17270_c3_g2_i1	46.8	0.04
		uncharacterized protein LOC103514633	DN18467_c1_g5_i1	31.7	3.61e-5
		uncharacterized protein LOC103515486	DN16253_c6_g2_i4	12.6	0.04
		uncharacterized protein LOC103518002	DN18156_c6_g2_i2	10.0	0.03
		uncharacterized protein LOC103521603	DN17270_c3_g2_i2	63.7	0.01
		uncharacterized protein LOC103521674	DN15182_c0_g1_i1	9.3	0.03
		protein AMN1 homolog	DN15340_c0_g1_i1	8.9	0.04
		protein FAM133-like isoform X1	DN19474_c1_g3_i11	15.4	8.40e-3
		protein PRRC2C-like	DN15390_c0_g1_i1	21.0	3.47e-4
		protein suppressor of forked	DN20501_c1_g1_i2	50.7	0.04
		putative juvenile hormone binding protein	DN21423_c1_g12_i1	33.0	5.4e-5
		putative juvenile hormone binding protein	DN21423_c1_g12_i2	9.4	8.34e-3
		RNA-directed DNA polymerase from mobile element jockey-like	DN19725_c3_g1_i3	14.1	6.95e-3
		senescence-associated protein	DN16041_c1_g1_i2	198.7	1.67e-4
		SWI/SNF chromatin-remodeling complex subunit SNF5-like	DN18520_c6_g1_i1	52.5	1.18e-5
		uncharacterized protein Dyak_GE27401	DN16348_c2_g1_i1	18.0	0.02
		uncharacterized protein LOC103507494 isoform X2	DN20548_c5_g2_i7	13.1	0.01
		uncharacterized protein LOC103507496	DN20260_c2_g2_i2	17.0	6.6e-4
		uncharacterized protein LOC103507787	DN20585_c3_g1_i2	60.0	8.58e-3
		uncharacterized protein LOC103512709	DN20458_c5_g2_i2	29.7	0.03
		uncharacterized protein LOC103514651	DN18692_c1_g1_i7	41.1	9.13e-4
		uncharacterized protein LOC103516995	DN14754_c0_g3_i1	39.3	2.89e-3
		uncharacterized protein LOC103518490	DN15191_c0_g1_i2	105.3	0.05
		uncharacterized protein LOC103518490	DN15191_c0_g1_i4	85.7	7.47e-3
		uncharacterized protein LOC103519237	DN15191_c0_g1_i7	36.9	0.01
		uncharacterized protein LOC103520317	DN17514_c8_g2_i1	10.7	0.01
		uncharacterized protein LOC103524424	DN14888_c0_g2_i1	7.8	0.04
		uncharacterized protein LOC108252545 isoform X1	DN16387_c3_g1_i9	7.6	0.03
		uncharacterized protein LOC113219351	DN17193_c2_g1_i6	74.5	8.74e-4
		uncharacterized protein LOC113219380	DN18715_c0_g1_i6	305.6	9.53e-5
		uncharacterized protein LOC113219380	DN21090_c7_g10_i1	82.0	0.04
		uncharacterized protein LOC113469268	DN20635_c0_g3_i2	73.8	0.03
		uncharacterized protein LOC113469268	DN20635_c0_g1_i1	37.4	0.02
		uncharacterized protein LOC113469268	DN20635_c0_g3_i1	36.9	0.02
		uncharacterized protein LOC113469388	DN14497_c0_g1_i2	8.9	0.04
		uncharacterized protein YMR317W-like	DN15237_c0_g1_i1	60.2	8.52e-4
		Zgc:165536 protein	DN19721_c0_g2_i1	186.9	8.52e-4
	Down-regulated	annexin B9-like isoform X1	DN19784_c8_g1_i2	-11.0	0.03
		cytosolic purine 5'-nucleotidase isoform X4	DN16811_c2_g1_i5	-37.4	0.02
		probable 4-coumarate--CoA ligase 1	DN19422_c2_g3_i12	-7.4	0.05
		UDP-glucuronosyltransferase 2C1-like	DN20095_c3_g1_i5	-12.4	1.92e-3

* A1- CLas+ x CLas-: Differential gene expression of adults with 1 to 2 days of feeding; ** A2- CLas+ x CLas-: Differential gene expression of adults with 3 to 4 days of feeding; *** A3- CLas+ x CLas-: Differential gene expression of adults with 5 to 6 days of feeding

From the total number of differentially expressed transcripts of CLas⁺ when compared to their respective CLas^- psyllids, only one transcript (DN16253_c6_g2_i4: uncharacterized protein LOC103515486) was differentially expressed in CLas⁺ psyllids regardless the time they were allowed to feed on CLas-infected citrus plants as compared to psyllids fed on CLas-uninfected citrus plants (Fig. 2). Most of the DE transcripts detected in CLas⁺ psyllids differed only at the specific stage they were compared. Seventeen (71%) of the DE transcripts detected in the gut of adult psyllids after 1-2 d, 31 (88%) after 3-4 d and 60 (88%) after 5-6 d of feeding in CLas-infected plants differed from controls specifically at each particular stage (Fig. 2).

Fig. 2.

Venn diagram of Diaphorina citri transcripts differentially expressed in gut of adults at different periods of feeding on CLas-infected citrus plant compared to insects that fed on healthy citrus plant. A1 - CLas⁺ x CLas^-: adults that fed on CLas-infected versus uninfected citrus plant for 1-2 days; A2 - CLas⁺x CLas^-: adults that fed on CLas-infected versus uninfected for 3-4 days; and A3 - CLas⁺x CLas^-: adults that fed on CLas-infected versus uninfected for 5-6 days.

Discussion

The differential gene expression of the gut of adult psyllids differed depending on the duration of feeding on CLas-infected citrus plants. The number of DE transcripts in the gut of psyllids increased as the time the psyllids fed on CLas-infected plants increased. Most interesting, the majority of DE transcripts detected were specific to each one of the periods of feeding psyllids remained exposed to CLas-infected plants.

Gene expression of CLas in the gut of adult psyllids after different times of feeding on CLas-infected citrus plants were quite different. CLas transcription in the gut of adult psyllids was highly active soon after adult feeding started, but expression of a large set of genes was significantly increased at later stages of feeding (A3CLas⁺).

Immune attack and immune defense responses

Bacteria that gain access to the hemocoel of insects find an easy way through the gut epithelium of the midgut, since the epithelium in this region does not have the cuticle lining protecting the fore- and the hindgut. Psyllids, as other sap-feeding insects do not carry the peritrophic membrane that protects the midgut epithelium of several other groups of insects [36, 37]. But regardless the presence of such physical barriers, the front line of defense of the gut immune system involves the activation of the epithelial innate immune system for the production of reactive oxygen species (ROS). Bacteria that survive in the gut of insects are either resistant to or are able to metabolize ROS [38, 39].

Analysis of the CLas gene expression in the gut of adult psyllids demonstrated that CLas expressed the cytoprotective antioxidant enzyme peroxiredoxin (DN17546_c4_g1_i1), capable of reducing ROS and reactive nitrogen species (RNS) produced in the process of gut infection [40, 41]. Peroxiredoxins (EC 1.11.1.15) are cysteine-dependent peroxidases targeting hydrogen peroxide, peroxynitrite and organic peroxide as substrates [42]. Peroxiredoxins utilize either 2-Cys or 1-Cys reaction catalysis mechanisms [42], with CLas showing two chromosomal 1-Cys-1 peroxiredoxin genes (CLIBASIA_RS00940 and CLIBASIA_RS00445). These genes are highly conserved in all CLas sequenced strains [42]. The DE expressed transcript detected in the gut of CLas-infected psyllids (DN17546_c4_g1_i1) shared 100% identity with CLIBASIA_RS00940 (WP_012778530). But peroxidase activity has only been reported for CLIBASIA_RS00445 (WP_012778432.1) [42, 43]. The CLas BCP endoded by this gene was demonstrated to be an extracellular 1-Cys peroxiredoxin that suppresses the signaling and accumulation of oxypilins in plants mediated by the respiratory burst oxidase homologs (RBOH). Regulation of this process was reported as essential for CLas survival and host plant colonization [42, 43].

The significant increase in the expression of peroxiredoxin from A1CLas⁺ to A3CLas⁺ (FC = 13.48) suggests this enzyme provides an increased contribution in the infection process, as CLas cells also established an intracellular interaction with the gut epithelium of psyllids. CLas expression of peroxiredoxin occurred despite the expected reduction of ROS in the gut epithelium of adult psyllids, as the major source for ROS production in the gut, NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3 (DN17549_c4_g1_i2), was down-regulated in CLas⁺ psyllids.

These results suggest that CLas can inhibit hydrogen peroxide production in the host insect, and that peroxiredoxin is certainly serving roles other than its antioxidative contribution. The adipokinetic hormone (ADK) is involved in the regulation of the oxidative stress response in insects [44]. Unfortunately, the expression levels of ADK-related genes by CLas infection could not be verified as ADK is produced and stored in neurosecretory cells of the corpora cardiaca. Nevertheless, regulation of this neuropeptide hormone in the gut epithelium of CLas⁺ psyllids could occur by the up-regulation of the metallo-endopeptidase-like 1 isoform X2 (DN16798_c0_g1_i1) neprilysin. Neprilysins are metalloproteases better known for their neuropeptide degrading activity, while also carrying peptide-degrading activity in other tissues, including the gut [45].

CLas peroxiredoxin could also be acting in the regulation of H₂O₂-mediated cell signaling processes, such as those involved in growth and immune responses [46]. The oxidative response produced by gut epithelia due to microbial infection leads to cell proliferation and modulation of the innate immune response [47], and ROS is required for inducing nitric oxide production in the gut. Nitric oxide production will in turn trigger the synthesis of antimicrobial peptides (AMP) and activate organ-to-organ communication [48]. Therefore, the down-regulation of ROS production in the gut of CLas⁺ psyllids could explain the lack of differential expression of genes belonging to the AMP production pathways. AMP synthesis can also be elicited by the recognition of peptidoglycans released by bacteria by membrane-bound peptidoglycan recognition proteins if peptidoglycans survive to amidase degradation [39].

There is very little information on insect gut phagocytosis, although proteomic analysis of anal droplets of the beetle Cryptorhynchus lapathi larvae led to the identification of several proteins to support an immune cellular response at the gut level [49]. Moreover, phagocytic receptors identified in the gut epithelium of Drosophila were proven to play crucial role in the phagocytosis of both Gram bacteria, and in controlling hemocele infection by bacteria invasion through the gut epithelium [50]. We could not detect any changes at the molecular level in CLas⁺ psyllids that would demonstrate a phagocytic response in the gut, as well as we did not observe adult psyllids to build an immune response to CLas infection by activating ROS and AMP pathways.

Nevertheless, differential gene expression analysis of the gut of A1CLas⁺ psyllids demonstrated the mounting of a defensive response of the gut epithelium based on the increased expression of a CLIP domain-containing serine protease 2-like (DN16851_c1_g2_i2). CLIP domain-containing serine protease 2-like has been recently reported to be up-regulated in the midgut of CLas-infected psyllids [29]. Serine proteases containing a CLIP domain are involved in the regulation of humoral responses through the activation of prophenoloxidases (PPO) and the Toll immune signaling pathway. Activation of Toll pathway leads to antimicrobial peptides production, while the activation of PPO results in melanogenesis [51, 52]. Toll activation requires a multi-step proteolytic cascade [53], and the lack of additional differentially expressed serine proteases and the antimicrobial peptides transcripts in the psyllid transcriptome support the argument that the up-regulation of CLIP-domain serine protease in the gut of ACP feeding on CLas-infected plants leads to the activation of melanization as an immune response against CLas infection. We also believe the activation of melanization at this stage of psyllid-CLas interaction was triggered by a local response caused by cell injury and invasion of the gut epithelium by CLas cells, resulting in the production of wound clots in order to avoid infected, damaged cells to suffer further damage, die and be replaced by nidi cells. This hypothesis is also supported by the down-regulation of pangolin (Pan) (DN15424_c0_g3_i2), a key regulator of the Wnt/Wg pathway. Wnt proteins are highly conserved and participate in the control of growth, patterning, tissue and energy homeostasis. Pangolin was reported to bind to the β-catenin homologue Armadillo, acting directly in the regulation of gene expression in response to Wnt signaling [54, 55]. The Wnt signaling in Drosophila is an important process for the homeostasis of the gut tissue as it is involved in the regeneration of adult gut epithelial cells [56, 57]. Thus, the down-regulation of pangolin interferes with the activation of the Wnt signaling to regulate gene expression involved in the replacement of CLas-infected cells by the activation of the nidi cells to differentiate into new, active cells of the gut epithelium.

Studies on the role of genotype-genotype interactions of insects and parasites demonstrated activation and differential gene expression of the host immune machinery depending on the interacting parasite genotype. Alternative splicing was also reported as a required element in the specificity of the immune response of insects to specific parasite genotypes [58]. The nuclear speckles carry pre-mRNA splicing machinery composed by nuclear speckle-related proteins that mediate alternative splice site selection in targeted pre-mRNAs [59, 60]. The detected up-regulation of proteins that mediate alternative splice site selection in targeted mRNAs, the nuclear speckle splicing regulatory protein 1-like (DN17904_c2_g1_i3) in CLas⁺ psyllids, suggests CLas acts on the regulation of gene expression of infected psyllids at the molecular level.

The psyllid initial defense response against CLas infection also included the up-regulation of arylsulfatase B (DN19237_c6_g3_i2), an enzyme stored in lysosomes that acts on large glycosaminoglycan molecules by removing attached sulfate groups [61]. Glycosaminoglycans are components of proteoglycans commonly exploited by pathogens as receptors for their adherence to different tissues [62]. Glycosaminoglycans are produced by some pathogenic bacteria as extracellular capsule and used in the process of host infection and colonization to facilitate pathogen attachment, invasion and/or evasion of host defensive mechanisms [63]. Arylsulfatases B can also participate in processes of biotransformation, mediating the sulfonation of xenobiotics by other enzymes to facilitate their excretion [64]. In this case, increase in the arylsulfatase could be related to the psyllid physiological needs to metabolize the high levels of flavonoids (hesperidin, narirutin and dydimin) produced in citrus plants infected by Ca. Liberibacter asiaticus [65–67]. Flavanoids are important metabolites produced by plants in response to abiotic and biotic stressors and play a relevant contribution in plant resistance against microbes and herbivores [68], including citrus plants in response to CLas infection [69, 70].

The overexpression of immune related genes and the required increased cell metabolism early in the process of interaction of the psyllid gut epithelium with CLas can explain the up-regulation of the mitochondrial cytochrome c oxidase subunit IV (DN18774_c0_g1_i7) in CLas⁺ insects. Mitochondrial cytochrome c oxidase subunit IV is the major regulation site for oxidative phosphorylation by catalyzing the final step of electron transfer in mitochondria [71].

Cross-talk in the colonization of the gut lumen

Bacteria that survive the harsh chemical environment and the immune barriers available in the gut will have to use strategies to avoid their rapid elimination from the gut with faeces [39, 72]. Insects are active feeders and food fastly transits through the gut. The fast transit of the food in the gut has been argued as one condition to explain the controversial lack of a resident microbiome in lepidopteran larvae, for example [73].

CLas seems to employ different strategies to colonize the gut lumen by avoiding its elimination with faeces: regulation of gut peristalsis, synthesis of adherence proteins, and biofilm formation.

CLas regulation of the psyllid gut peristalsis is thought to occur through the up-regulation of the host neprilysin as earlier discussed. Neprilysins are reported to degrade peptide hormones, and the gut of insects contains several hormone-producing cells. Peptide hormones produced in the gut act as signaling molecules that are involved in the regulation of a range of processes, including gut peristalsis [74–76]. The hypothesis that CLas modulates the gut peristalsis of psyllids is supported by the down-regulation of titin (DN21409_c5_g2_i1) transcription in CLas⁺ psyllids. Muscle degeneration is marked by a reduction in titin proteins, and gut-associated muscles are in charge of producing the peristaltic movement observed in the gut. Additionaly, the intracellular non-catalytic domain of neprilysins in excess is shown to induce muscle degeneration [77]. Thus, the degeneration of muscles associated with the gut would certainly impair gut peristalsis and consequently reduce the elimination of bacteria with faeces [39, 72].

Regulation of signaling in the gut is also evidenced by the up-regulation of arylalkylamine N-acetyltransferase (DN20634_c1_g1_i13) transcription in A2CLas⁺ psyllids. Arylalkylamine N-acetyltransferases are involved in the N-acetylation of arylalkylamines, playing an important role in the synthesis of melatonin in vertebrates and invertebrates [78, 79]. But in insects, arylalkylamine N-acetyltransferases also inactivate arylalkymines that play important roles as neuromodulators, such as octopamine, dopamine and serotonin [80, 81]. These neuromodulators are also implicated in the double brain-gut communication circuitry [82, 83].

CLas adherence to the psyllid gut was achieved by the expression of three genes of a subtype of the type IVb pilins, the tight adherence pili (Tad = Flp). Flp pilins are common to several Gram⁺ and Gram^- bacteria. Type IV pili are highly diverse and involved in a number of protein-protein interactions, but flp pili are better known for their role in adherence to living and nonliving surfaces. Pili are also involved in cell motility, secretion of exoproteins, and in host cell manipulation under extreme conditions [84, 85].

The expression of Type IVc pili of Ca. L. asiaticus was reported to be higher in psyllids than in plants, but only one (flp3 pilin) out of five flp genes was reported to be up-regulated in psyllids [86]. The flp3 pilin gene was demonstrated to be under the regulation of VisN and VisR, demonstrating these proteins are important in the colonization of the host vector [86]. In our analysis of the transcriptional profile of CLas in the gut of adult psyllids, we detected the expression of several isoforms of two flp genes (DN14425_c0_g1; DN18703_c0_g1), but both belonging to the family Type IVb pilin. Three isoforms of gene DN14425_c0_g1 (DN14425_c0_g1_i2; DN14425_c0_g1_i3; DN14425_c0_g1_i4) and two of gene DN18703_c0_g1 (DN18703_c0_g1_i21 and DN18703_c0_g1_i23) were highly and consistently expressed in the gut of psyllids in all sampling periods. Three CLas LuxR family transcriptional regulators (DN1177_c0_g1_i1, DN14940_c0_g2_i1, and DN38633_c0_g1_i1) were also observed in the gut of CLas⁺ psyllids; one of them refers to the VisR regulator (DN1177_c0_g1_i1 = CLIBASIA_02900), and the other two to the VisN regulator (DN14940_c0_g2_i1 and DN38633_c0_g1_i1 = CLIBASIA_02905) of flp3 pilin gene reported by Andrade & Wang [86].

The expression of CLas flagellins (FlgA) (DN3624_c0_g2_i1 and DN40834_c0_g1_i1) and several genes involved in the assembling and functioning of the flagellar machinery (FliE, FliF, FliG, FliK, FliN, FliR, FliP, FlgB, FlgD, FlgE, FlgF, FlgG, FlgH, FlgI, FlgK, FlhA, FlhB, MotB, and the flagellar C-ring protein) would indicate CLas assembles flagella for colonizing the gut of adult psyllids, although FlgF and FlgI were detected exclusively in A3CLas⁺. The expression of genes involved in the flagellar machinery corroborates recent data on the higher expression of genes encoding the flagellum apparatus of CLas in the gut of psyllids than in plants [87]. Although we detected a much higher number of transcripts of the flagellar system of the CLas isolate we worked with than those reported to be expressed in the gut of psyllids by Andrade et al. [87], we did not detect the expression of three genes they evaluated (fliQ, fliL, and flgA). Differences in the overall number of genes of the flagellar system among lineages are expected to occur, but not among isolates of the same species [88].

The production of flagellum in the gut by infecting CLas is also supported by transmission electron microscopy images, although most of the CLas cells observed lacked a flagellum [87]. Analysis of images of the flagellum of CLas cells clearly shows CLas carries the secondary flagellar system, producing a lateral flagellum. The secondary flagellar systems arose twice in the evolution of bacteria, once in alpha-proteobacteria and once in the common ancestor of beta/gamma-proteobacteria [89]. The primary flagellar system produces a polar flagellum and contributes with cell motility in liquid media, while the secondary flagellum system produces a lateral flagellum that is involved in adhesion and cell swarming on surfaces. Bacterial flagella serve bacteria not only as a motor apparatus, but also as a protein export/assembly apparatus. The motor apparatus of flagella can provide bacteria the movement required to remain in the gut, as demonstrated in the trypanosomatid Vickermania [90]. Moreover, the flagellum pattern can be altered by bacteria depending on the environmental conditions faced, and bacterial flagella are recognized as important virulence factors [91–93]. Chemotaxis is an important contribution of bacterial flagellum to virulence [94], and the detection of the expression of four chemotaxis protein genes (DN15199, DN31800, DN46197 and DN50630) suggests the flagellum participates in cell adhesion to and swarming on the psyllid gut epithelium. Yet, we also propose the flagellum aids CLas to become chemically oriented for the localization of suitable host cells for invasion.

Biofilm formation requires bacteria to synthesize an extracellular matrix. Biofilms include extracellular proteins, cell surface adhesins and subunits of flagella and pili proteins [95]. We did not identify the expression of adhesins in the transcriptome of CLas in the gut of adult psyllids. Nevertheless, several chaperones were highly expressed, and many chaperones can act as adhesins in bacteria. Additionally, we believe the cold shock protein (DN10086_c0_g2_i1) of CLas is also playing key roles in biofilm formation. Cold shock proteins were demonstrated not only to participate in biofilm formation but also to support cell adhesion and motility, and to stimulate cell aggregation, interfering thus with virulence [96, 97].

Cross-talk for infecting the gut epithelium

Several gut-associated bacterial symbionts of hemipterans enter in close contact with epithelial cells to establish an intracellular phase through endocytosis [98]. CLas also enters the gut epithelium of psyllids through endocytosis, remaining inside vacuoles formed from or surrounded by endoplasmic reticulum membrane [99]. The differential gene expression analysis of the gut of CLas⁺ psyllids led to the identification of transcripts involved with ultrastructural alterations of the gut epithelial cells, allowing the identification of the molecular intermediates that participate in the route CLas follows to invade the gut epithelium.

In addition to the regulation of the immune related responses earlier described in the gut epithelium of CLas⁺ psyllids, epithelial cells of the gut were altered early in the infection process (A1CLas⁺ adults). Alterations are perceived by the transcriptional down-regulation of zonadhesin-like (DN14644_c0_g1_i1), a transcriptional response already reported by Ramsey et al. [100]. Zonadhesin-like proteins represent an expansion of the zonadhesin multi-domain proteins that are implicated in the binding of sperm and egg in a species-specific manner. In the gut, zonadhesin-like proteins are thought to function as mucins, and two zonadhesin-like proteins of D. citri were previously predicted to be part of the extracellular matrix and to have a role in cell-cell adhesion. Mucins protect the gut epithelium from microbial infections and inflammation [101]. Mucins are components of the perimicrovillar layer that in psyllids and other paraneopterans [102] replaces the chitin-based matrix (peritrophic membrane) that provides a protective barrier to the gut epithelial cells from pathogenic bacteria [103].

In vertebrates the mucin composition of the mucous layer can vary among gut regions, with diet composition and gut microbial infection [104]. Mucins can also be exploited as a nutritional resource by bacteria, and degradation of mucins by a commensal microbe was demonstrated to facilitate the penetration of the epithelium by viruses [105, 106]. The role different mucins can have on the host-pathogen interaction can explain the up-regulation of the psyllid gene coding for mucin-5AC (DN16207_c6_g5_i1) in A3CLas⁺ psyllids. The higher abundance of this protein in CLas⁺ psyllids has been demonstrated in previous proteomic analysis [107]. Regulation of the host mucin-5AC has been reported in vertebrate hosts infected by Gram^- and Gram⁺ bacteria, and in one system modulation of mucin-5AC has been linked with increased adhesion of bacteria to the gut tissue [108, 109].

The differential expression of genes coding for cytoskeletal proteins involved in the regulation of the submembranous actin-spectrin network in cells of the gut epithelium of CLas⁺ psyllids demonstrates CLas interferes with the remodeling of gut epithelial junctions in adult psyllids, leading to endocytosis of intercellular junctions with cellular organelles. Adducins (protein Hu-li tai shao - DN19744_c0_g2_i2) form connections with membranes, promote spectrin-actin interactions and regulate actin filaments [110]. Internalization of apical junction and/or tight junction proteins may disrupt the epithelial barriers and favor the movement of bacterial toxins into cells [111].

The intracellular events in preparation for endocytosis can also be detected as indicated by the up-regulation of the psyllid phosphatase 1 regulatory subunit 21 (DN19112_c0_g1_i1) in the gut of A1CLas⁺. This protein participates in early (sorting process) or late (maturation) endosome pathway, which leads to the endocytosis of several types of materials, including pathogenic agents. Our hypothesis is that early endosomes will also internalize the leptin receptor overlapping protein-like 1. The leptin receptor overlapping transcript-like 1 (DN20058_c2_g3_i4) was down-regulated in the gut epithelium of A2CLas⁺ psyllids. Internalization of such receptors in early endosomes also affects cell signaling, and in this particular case can severely interferes with the gut epithelium resistance to microbial infection. Down-regulation of leptin/leptin receptor was reported to drastically affect cell resistance to amoeba and bacterial infection in several species [112–114].

The endocytic vesicles detach and become free endocytic carrier vesicles transporting their cargoes to late endosomes to finally fuse with endoplasmic reticulum, where CLas cells aggregate in associated vacuoles as indicated by ultrastructural analysis [99]. Fusion of lysosomes to cell aggregates vacuoles is inhibited by the down-regulation of soluble NSF attachment protein (SNAPs) (DN21196_c2_g1_i1) in A2CLas⁺. SNAPs are highly conserved proteins that participate in intracellular membrane fusion and vesicular trafficking [115]. Intracellular membrane fusion requires both SNAPs and NSF to act in concert, and inhibition of one of them will lead to the failure of membrane fusion and the accumulation of vesicles one cannot fuse [116].

SNAPs are characterized by the presence of a tetratricopeptide repeat (TPR) domain [117]. Tetratricopeptide repeat proteins (TRP) are directly involved in virulence, particularly due the translocation of virulence factors into host cells and in the blockage of phagolysosomal maturation, among others [118]. Three TRPs (DN11192_c0_g1_i1; DN11192_c0_g1_i2; DN14826_c0_g1_i2) were expressed in the gut of CLas⁺ psyllids, but only DN14826_c0_g1_i2 was differentially expressed. The expression of different TRPs in all sampling periods and their time-specific differential expression indicates TRPs participates in different processes of CLas interactions with the host cells, from CLas establishment in the gut lumen to epithelial cell invasion and access to the hemocoel.

The down-regulation of the psyllids annexin B9-like isoform X1 (DN19784_c8_g1_i2) in the gut of A3CLas⁺ would interferes with the development of multivesicular bodies, once annexin B9 is involved in endosomal trafficking to multivesicular bodies [119]. This change will affect the transfer of the contents of CLas-containing endosomal vesicles to lysosomes for proteolytic degradation.

We propose that the establishment of the intracellular cycle and survival of CLas within host cells was putatively aided by the expression of CLas peptidyl-prolyl isomerase (PPI) (DN14386_c0_g1_i1), a protein that has been proved to participate in intracellular infection and virulence of other Gram^- bacteria [120–122]. The Mpi PPI from Legionella pneumophila was demonstrated to require an active enzymatic site to enhance a proper host cell invasion [123], although the preservation of the active site was not a requirement for the PPI of Burkholderia pseudomallei [120]. Ghanim et al. [99] suggested earlier that CLas cells do not enter the ER, but instead CLas cells recruit ER to transform the phagosome into a host-immune free space suitable for CLas survival and multiplication. These same ER-derived structures were already observed in Legionella and Brucella [124, 125].

Early endosomes and endoplasmic reticulum share contact sites that are used to bind to microtubules at or close to their contact sites, and both organelles remain bounded as endosomes traffic and mature [126]. Endosome trafficking within the cell involves the membrane binding to motor proteins and its transport along the actin and microtubule cytoskeleton [127]. Trafficking of endosomes in CLas⁺ psyllids is provided by the up-regulation of kinesin-like protein KIF3B isoform X4 (DN10161_c0_g1_i1) in the gut of psyllids. Kinesins are motor proteins involved in the movement of multiple cytoplasmic organelles [127].

Profilin (DN19422_c2_g2_i1), another protein involved in intracellular movement of organelles, was also up-regulated in the gut of A2CLas⁺ psyllids. Profilins are actin-binding proteins capable of regulating actin polymerization and the availability of the actin cytoskeleton for binding to the endosomes; but new roles for profilins are being identified in vertebrates [128]. Additionally, profilin 1 plays an important role in host–pathogen interactions. Intracellular pathogens such as Listeria monocytogenes and Shigella flexneri use the host-cell actin cytoskeleton to propel themselves through the cytoplasm and to spread to neighboring cells without entering the extracellular space [128, 129]. Dynein (DN35915_c0_g1_i1), another motor protein, was up-regulated in the gut of A3CLas⁺ psyllids. Dyneins also contribute to microtubule-based transport in eukaryotic cells [130–132].

Cross-talk for moving to the hemocoel

After CLas inhibits the early immune response and invades the intracellular space of the gut epithelium by regulating a clathrin-independent endocytosis mechanism, hiding from the host’s immune activators within vacuoles surrounded by endoplasmic reticulum membrane, where CLas multiplies, the molecular mechanism behind the release of CLas bacteria from epithelial cells in the hemocoel may require additional data.

The higher expression in A3CLas⁺ of seven (DN15630_c0_g2_i3 = CLIBASIA_00255; DN15330_c0_g1_i2 = CLIBASIA_00880; DN14809_c0_g1_i = CLIBASIA_03170; DN14146_c0_g1_i1 = CLIBASIA = 04410; DN10141_c0_g1_i1 = CLIBASIA_00995; DN15141_c0_g1_i1 = CLIBASIA_01620; DN15414_c0_g1_i4 = CLIBASIA_01605) out of the 67 Sec-dependent proteins common to Candidatus Liberibacter species [133] indicates these candidate effector proteins play an important role in the dynamics of CLas infection of the psyllid gut epithelium at this stage. In fact, genomic analysis of Liberibacter species predicted a total of 166 proteins containing Sec-dependent signal peptides in the CLas strain psy62, from which 86 have been already experimentally validated [134]. These are potential effector proteins, and 106 of them share common homologues with Las_Ishi-1 and Las_gxpsy. But only 45 Sec-dependent proteins were shared among HLB-associated Ca. Liberibacter species (CLas, CLam and CLaf) [135, 136]. The detection of transcripts of the general secretion system provides further support for the participation of the detected Sec-dependent proteins in the late process of infection of the gut epithelium of D. citri. The Sec pathway secretion system transports proteins involved in bacterial cell functions and survival [133]. The Sec pathway is represented by two independent pathways, both detected in the gut of CLas⁺ psyllids: the post-translational pathway represented by the expression of SecA (DN14962_c0_g1_i1) and SecY (DN15568_c0_g3_i3); and the co-translational pathway represented by the signal recognition particle receptor FtsY (DN1686_c0_g1_i1) [137]. We did not detect SecB expression in the gut of adult psyllids, indicating SecA can also act as a chaperone complementing the required activity of SecB as reported in Escherichia coli [138].

Combined ultrastructure, proteomics and transcriptomics analysis of the gut epithelium of CLas-infected psyllids suggested CLas acquisition into the hemocoel would rely on the programmed cell death of CLas-infected epithelial gut cells, although CLas infection has little impact on the fitness of adult psyllids [19]. The low fitness impact of CLas infection to adult D. citri indicates CLas acquisition into the hemocoel would occur through an exocytosis process, as suggested for the Ca. Liberibacter solanacearum vectored by potato psyllids [139].

By following the proposed subroutines based on mechanistic and essential aspects of cell death proposed by the Nomenclature Committee on Cell Death [140], our transcriptomic analysis could not support the proposition that CLas-infected epithelial gut cells of psyllids would initiate the process of programmed cell death (PCD) as proposed by Kruse et al. [19]. We did not observe transcription of caspases, a very common protein to several subroutines of cell death, as well as other aspects that would allow this characterization [140]. Yet, we were unable to confidently characterize one of the subroutines of cell death described when analyzing the transcriptional profile of CLas⁺ psyllids, once the molecular mechanisms involved were not all represented. However, we can confidently report the activation/inhibition of the expression of genes involved in processes of regulated cell death. The high expression of the lysosomal cathepsin L1 (DN15698_c4_g11_i2) in A2CLas⁺ psyllids would support the activation of lysosome-dependent cell death, which requires intracellular perturbations to permeabilize the lysosomal membrane to result in the release of cytosolic cathepsins. Mitochondrial outer membrane permeabilization and caspases are not necessarily required for this process of cell death, and lysosome-dependent cell death is an important response to pathophysiological conditions induced by intracellular pathogens [140].

The overexpression of the psyllid BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 (BNIP3) (DN_20168_c2_g3_i4) in A3CLas⁺ also supports the gut epithelium of CLas⁺ psyllids go into lysosome-dependent cell death. BNIP3 are pro-apoptotic proteins that open the pores of mitochondrial outer membrane, resulting in mitochondria dysregulation due the loss of membrane potential and ROS production in mitochondria [141, 142]. But BNIP3 oligomerization with BCL2 has been demonstarted not to be required for cell death [141]. Besides, the down-regulation of the psyllid senescence-associated protein transcript (DN16041_c1_g1_i2) in the gut of A3CLas⁺ psyllids demonstrates CLas suppresses cell senescence and the further dysfunctional growth of the epithelial cells due the activation of senescence-associated secretory phenotype [143, 144]. Cellular senescence is not considered a form of regulated cell death [140].

The differential expression of a putative juvenile hormone binding protein (JHBP) (DN21423_c1_g12_i2; DN21423_c1_g12_i1) in CLas⁺ psyllids (down-regulation in the gut of A2CLas⁺; up-regulation in A3CLas⁺) demonstrates the epithelial cells count with different levels of hormonal stimulation. JHBPs are proteins that act as shuttles for juvenile hormone (JH) in the hemolymph, avoiding JH degradation by JH-esterases and JH-epoxide hydrolases [145]. JH is produced and released primarily by neurosecretory cells of the corpora allata of the central nervous system, and the availability of JHBP in the gut, if its activity in the gut is the same played in the hemolymph, indicates JH is alo available in the gut epithelial cells. JH has recently been shown to be produced by intestinal stem cells and enteroblasts of the gut epithelium of D. melanogaster, and to regulate cell growth and survival. The local JH activity was also shown relevant for damage response by gut cells, playing important roles in gut homeostasis [146]. If the pattern of expression of JHBP correlates with the availability of JH we can argue that at the same time CLas acts on the regulation of the gut epithelium by suppressing cell senescence, it can also induce the proliferation of stem cells in order to replace cells that were damaged due the release of CLas cell into the hemocoel and/or entered the lysosome-mediated cell death as discussed earlier.

The observed up-regulation of the transcriptional levels of nocturnin (DN19927_c10_g1_i6) in the gut of A2CLas⁺ psyllids suggests that this circadian rhythm effector protein may be acting together with JH in regulating gut genes, just as the joint action of the circadian genes and JH in the regulation of genes acting on the transitional states of Pyrrhocoris apterus adults to reproductive diapause or not [147]. Nocturnin is classified as a deadenylase acting on the catalysis of poly(A) tail of target mRNAs and/or targeting noncoding RNAs, and has been implicated in metabolic regulation, development and differentiation [148]. But recent studies with curled, the nocturnin ortholog in Drosophila proved nocturnin is an NADP(H)2’-phosphatase acting on the conversion of the dinucleotide NADP⁺ into NAD⁺ and NADPH into NADH, regulating mitochondrial activity and cellular metabolism in response to circadian clock [149]. NADP(H)2’-phosphatase activity of nocturnin was later reported in vertebrates, with the demonstration of the colocalization of nocturnin in mitochondria, cytosol and endoplasmic reticulum-bound pools depending on the isoform [150]. Thus, nocturnin acts as a regulator of the intracellular levels of NADP(H) and the oxidative stress response. The role of nocturnin in the regulation of cell metabolism and the oxidative stress response supports the required energy supply to sustain the increased gene expression activity in CLas⁺ gut epithelium cells.

The expression profile of CLas infecting the gut epithelium of A3CLas⁺ psyllids demonstrates CLas has an increased protein synthesis activity as expected by the overexpression of DEAD/DEAH box helicase (DN4052_c0_g1_i1), a protein involved in ribosome biogenesis, RNA turnover and translation initiation [151]. Increased protein activity is also supported by the increased expression of molecular chaperones, such as the trigger factor (DN13945_c0_g1_i1), GroEL (DN14757_c0_g1_i1) and DnaK (DN15220_c0_g1_i1), which prevent protein misfolding and aggregation [152, 153].

CLas multiprotein complexes

The protein HlyD family efflux transporter periplasmic adaptor subunit (DN11766_c0_g1_i1) and the outer membrane factor translocation protein TolB (DN15087_c0_g1_i3) are essential components for functioning the pump of tripartite efflux systems. HlyD connects primary and secondary inner membrane transporters to the outer membrane factor TolB. CLas expressed several inner membrane transporters belonging to the MSF and ABC families. TolB has been shown to interact with a range of proteins including cell-killing proteins [154, 155]. In Xylella fastidiosa TolB was shown to be involved in biofilm development as one of the members of the Tol – Pal system. TolB associates with other proteins than Pal in the outer membrane and periplasm, aiding X. fastidiosa in maintaining membrane integrity [156].

Additional CLas transcriptional regulators

The detection of several other uncharacterized response regulators (DN10585_c0_g1_i1; DN10585_c0_g2_i1; DN12200_c0_g1_i1; DN58285_c0_g1_i1) and transcriptional regulators (DN11066_c0_g1_i1; DN15145_c0_g1_i2; DN15145_c0_g1_i5) indicates other CLas two-component systems are also being activated by environmental stimuli, such as the two-component system sensor histidine kinase AtoS (DN14305_c0_g2_i1; DN15701_c0_g1_i1). The two-component system sensor histidine kinase AtoS is a member of the AtoS/AtoC regulatory system, but we did not identify the AtoC response regulator in the CLas transcriptome. This regulatory system is better known by the induction of AtoS by acetoacetate. AtoS then phosphorylates AtoC that will in turn stimulate the expression of the atoDAEB operon for the catabolism of short chain fatty acids. We could not reliably identify transcripts belonging to the atoDAEB operon to demonstrate CLas requirements for short chain fatty acids. We propose that the activation of the AtoS/AtoC regulatory system is instead acting on the regulation of the flagellar regulon, regulating the expression of CLas genes involved in cell motility and chemotaxis, as reported for Escherichia coli in response to acetoacetate or spermidine [157].

Cross-talk on nutrient deficiency

The high expression of sulfonate ABC transporter permease (DN15690_c0_g1_i2) in all CLas⁺ psyllids suggests CLas signals the host to supply its requirements for sulfur. Sulfur is a ubiquitous element involved in a number of different processes in organisms [158]. The sulfonate ABC transporter permease is involved in sulfur/sulfonate uptake, and the higher expression observed in A3CLas⁺ as compared to A1CLas⁺ points for an increased demand late in the infection process.

Sulfur is also used in the biogenesis of Fe-S clusters, which are produced in conditions of oxidative stress and iron deprivation. The biogenesis of Fe-S clusters was observed by the expression of two unclassified cysteine sulfurases (DN12917_c0_g1_i1 and DN35541_c0_g1_i1), the cysteine desulfuration protein SufE (DN1144_c0_g1_i1), the Fe-S cluster assembly protein SulfB (DN14252_c0_g1_i1), and the iron-sulfur cluster carrier protein ApbC (DN17762_c4_g2_i3) [159, 160]. All four genes had an increased expression in A3CLas⁺ as compared to A1CLas⁺. Sulfur requirements by CLas could also be used for protection against oxidative stress as demonstrated by the expression of the thioredoxin-dependent thiol peroxidase (DN10526_c0_g1_i1) [161, 162].

The high expression of CLas phosphate ABC transporter permease subunit PstC (DN40256_c0_g1_i1; DN67283_c0_g1_i1), putative two-component sensor histidine kinase transcriptional regulatory protein (DN14305_c0_g2_i1), two-component sensor histidine kinase (PhoR) (DN28075_c0_g1_i1; DN67626_c0_g1_i1), two component response regulator protein (PhoB) (DN14869_c0_g1_i1), alkaline phosphatase (DN12828_c0_g1_i2; DN39297_c0_g1_i2) and NTP pyrophosphohydrolase (DN2128_c0_g1_i1) demonstrates CLas cells are exposed to phosphate restriction while infecting the gut epithelium of adult psyllids. Phosphate is generally the major source of phosphorus to bacteria, a vital nutrient for living organisms. Phosphorus is important in several processes (energy metabolism, intracellular signaling, among others). Misregulation of phosphorus availability in bacteria is sensed by the PhoB/PhoR two-component regulatory system, leading to the activation of the Pho regulon. The Pho regulon regulates the expression of other genes, producing phenotypes that can differ in morphology and virulence in response to phosphate deprivation [163, 164]. Thus, the expression of both members of the PhoB/PhoR two component regulatory system and the phosphate ABC transporter permease subunit PstC, that is in charge to transport extracellular phosphate to the cytosol, proves CLas was exposed to phosphate concentrations below 4 μM, a threshold that generally turns on the expression of the response regulator PhoB. Furthermore, the expression of alkaline phosphatase and NTP pyrophosphohydrolase, which both act on phosphorus-containing substrates [163] demonstrates CLas increased the catabolism of substrates capable of releasing phosphorus nutrient.

The requirement of CLas for phosphate is also demonstrated by the up-regulation of the psyllid glycerophosphocholine phosphodiesterase GPCPD1 gene, as observed by the increased abundance of its transcript (DN15741_c0_g2_i2) in A3CLas⁺. The contribution of GPCPD1 in phosphate production results from the downstream processing of GPCPD1 hydrolysis products of glycerophosphocholine, choline and glycerolphosphate. At the same time glycerophosphocholine hydrolysis can provide phosphates for cell metabolism, the choline can serve as as substrate for phosphatidylcholine synthesis. Phosphatidylcholine is a major lipid component of membranes of eukaryotes, although several bacterial symbionts and pathogens carry phosphatidylcholine synthases, showing their requirement for this lipid component of cell membranes, including those belonging to Rhizobiaceae as Ca. Liberibacter. Choline serves as substrate for the osmoprotectant glycine betaine synthesis and as an energy substrate to support cell growth in Rhizobiaceae [165, 166].

The role of host-produced choline in CLas metabolism is supported by the up-regulation of CLas glycine/betaine ABC transporter substrate-binding protein (DN15178_c0_g1_i1) in the gut of A3CLas⁺. ABC transporters were reported to have several important roles in Ca. Liberibacter asiaticus, from the importation of nutrients like choline to the exportation of virulence factors [167]. Thus, we believe the increased activity of GPCPD1 in A3CLas⁺ is a result of the recycling of glycerophosphocholine for choline utilization in the recovery of membranes of the gut epithelial cells of the host psyllid as a response to cell infection and/or in the supplementation of choline to CLas metabolism.

CLas is known to induce profound physiological changes in citrus plants, affecting the nutritional content of CLas-infected plants to psyllids, which have in turn altered transcriptional profiles and protein abundance when feeding on CLas-infected and health citrus plants [24, 107]. Therefore, it is impossible to distinguish if the indication of nutritional restriction CLas encounters when infecting the gut epithelium of psyllids is an indirect effect of the host plant on the psyllids or if this is a direct response of psyllids to avoid CLas infection.

Conclusion

We conclude that CLas basically express its full arsenal of genes early in the invasion process of the gut of adults of D. citri. CLas survival in the gut of psyllids involves the regulation of ROS production and availability in the psyllid gut, and consequently the inhibition of activation ROS-dependent nitric oxide production and nitric oxide-dependent antimicrobial peptide synthesis. Our data suggests that gene expression regulation of adult psyllids is based on the up-regulation of proteins involved in alternative splice site selection. CLas regulates the peristalsis of the gut of the host and highly expresses genes involved in adherence proteins and biofilm formation to colonize the gut lumen. Our analysis also indicates the gut epithelial cells are invaded by CLas by a process mediated by the down-regulation of leptin receptor and its internalization in early endosomes in the psyllid gut cells. This process is followed by the regulation of several host genes that lead to vesicles containing CLas, which includes the suppression of the cell machinery involved in the process of cell senescence. The intense cross talk between CLas and the host cells is mediated by a high number of candidate effector proteins we identified. These proteins are potential targets for the development of management strategies directed to interfere with essential metabolic pathways to invasion, infection and multiplication of CLas in the vector D. citri.

Material and Methods

Diaphorina citri rearing and plants

A colony of CLas-free Asian Citrus Psyllid (ACP) was initiated with insects collected from Murraya paniculata (L.) Jack, syn. Murraya exotica L. (Sapindales: Rutaceae) in the state of São Paulo, Brazil in 2009.

Diaphorina citri gut collection and RNA extraction

Adults of D. citri (7 to 10 days after emergence) were transferred to uninfected and CLas-infected citrus plants [Citrus x sinensis (L.) Osbeck, grafted in ‘Rangpur’ lime (C. x limonia Osbeck)] for an exposure period (EP) of 1, 2, 3, 4, 5 and 6 days. For each exposure period, three biological replicates were collected (1 replicate = 100 individuals). Third-instars of D. citri were also transferred to CLas-infected and uninfected (control) citrus plants for collection of RNA and differential transcriptional analysis. Nymphs were allowed to feed for 4 days on CLas-infected and control plants. Afterwards, three biological replicates/treatment (1 replicate = 200 nymphs) were collected and stored in RNALater (Invitrogen/ThermoFisher Scientific, Waltham, MA, United States, USA) for further processing and analysis.

After each exposure time, adults were collected and the gut dissected under aseptic conditions. A similar procedure was used for nymphs, but in this case insects we opted by extracting RNA from whole nymphs, as initial attempts to dissect the suitable gut samples for downstream analysis were very time-consuming and had a low success rate.

The obtained guts/nymphs were stored in RNALater (Invitrogen/ThermoFisher Scientific, Waltham, MA, USA) at -80°C until RNA extraction. Total RNA extraction was performed using the SV RNA Isolation System Kit (Promega Madison, WI, USA), following the manufacturers’ recommendations. Samples were lysed in 175 μL of RNA lysis buffer added with β-mercaptoethanol and 350 μL of RNA dilution buffer for tissue disruption using a TissueLyser II LT^TM (Qiagen, Hilden, Germany). Samples were incubated at 70°C for 3 min, centrifuged (12,000 g × 10 min × 4°C), trapped in a column and washed with 95% ethanol by centrifugation (12,000 g × 10 min × 4°C). Total RNA was recovered in 350 μL of RNA wash solution following centrifugation (12,000 g × 1 min × 4°C). Afterwards, samples were treated with 50 μL of DNAse mix (40 μL buffer ‘yellow core’+ 5 μL 0.09 M MnCl₂ + 5 μL DNAse I) for 15 min at room temperature. Samples were added with 200 μL of DNAse stop solution and subjected to centrifugation (13,000 g × 1 min × 4°C). Samples were washed in 600 μL cleaning solution followed by a second wash in 250 μL following centrifugation (12,000 g × 1 min × 4°C). The pelleted RNA was recovered in 30 μL of nuclease-free water, and RNA concentration verified using NanoDrop V 3.8.1 (ThermoFischer).

RNA samples containing residual DNA contaminants were further treated with 2 μL of buffer (10×) and 2 μL of Turbo^TM DNAse (2 U/μl) (Ambion/ThermoFisher Scientific, Vilnius Lithuania). Samples were incubated at 37°C for 30 min followed by DNAse inactivation by adding 2 μL of DNAse Inactivation Reagent (Ambion/ThermoFisher Scientific, Vilnius Lithuania). After 5 min at room temperature, samples were centrifuged (13,000 g × 1.5 min × 4°C) and the supernatant collected and stored at -80°C. DNA elimination was confirmed by testing the amplification of the wingless gene (wg) of ACP [168].

All plants and insects were subjected to quantitative PCR analysis for verification of CLas infection using the TaqMan qPCR Master Mix Kit (Ambion /ThermoFisher Scientific, Vilnius Lithuania) [169]. In insects, the average Ct value found for the wg gene in the libraries was 30.7, while the average Ct value in plants for the 16S rRNA gene from CLas was 29.6. Samples with a Ct value under 35 were considered positive for CLas.

After confirmation of the Ca. L. asiaticus infection status of each sample, RNA obtained from the gut samples of adults were pooled in equimolar concentrations to yield three exposure periods: i) A1CLas^-: adults that fed on healthy citrus plant (CLas^-) for 1-2 days; ii) A2CLas^-: for 3-4 days; iii) A3CLas^-: for 5-6 days; iv) A1CLas⁺: adults that fed on infected citrus plant (CLas⁺) for 1-2 days; v) A2CLas⁺: for 3-4 days; and vi) A3CLas⁺: for 5-6 days. In the case of the whole nymphs, two samples were produced: N1CLas⁺: for nymphs after 4 days of feeding on CLas-infected citrus plants, and N1CLas^-: for nymphs after 4 days of feeding on control plants.

Samples were subjected to mRNA enrichment through eukaryote and prokaryote rRNA removal using the Ribo-Zero rRNA Removal Epidemiology Kit (Illumina, San Diego, CA, USA), following the manufacturers’ instructions. RNA integrity was confirmed using the Agilent Bioanalyzer 1000 (Agilent Technologies, Santa Clara, CA, USA).

Library preparation and sequencing

cDNA libraries were prepared for sequencing using the cDNA TruSeq RNA Library Prep Kit (Illumina, San Diego, CA, USA) following a paired-end (2 × 100 bp) strategy. The cDNA produced was end-repaired and adenosine was added at the 3′ end of each cDNA fragment to guide the ligation of specific adapters. Adapters consisted of primers for transcription and a specific index to code each sample. Samples were enriched with limited-cycle PCR and analyzed to confirm the success of sample preparation before sequencing using the Illumina HiScanSQ platform (Illumina, San Diego, CA, USA) available at the Multiusers Center of Agricultural Biotechnology at the Department of Animal Sciences, ESALQ/USP.

De novo transcriptome assembly

Reads quality were visualized in FastQC software [170] before adapters removal and quality filtering by trimming the leading (LEADING:3) and trailing (TRAILING:3) nucleotides until the quality was higher than 3, and then using a sliding window of 4 nucleotides and trimming when scores were lower than 22 (SLIDINGWINDOW 4:22). Quality filtering was done using Trimmomatic-0.36 [171].

All reads obtained were used to assemble a de novo transcriptome using the pipeline available in the Trinity-v.2.4.0 software [172]. Both paired and unpaired trimmed and quality-filtered reads were used to assemble the de novo transcriptome, which was further used as the reference transcriptome for the RNA-Seq experiments. Assemblage was obtained using normalization of the reads coverage (<50) and the minimum contig size selected was 200 nucleotides.

The transcripts obtained were functionally annotated using the BlastX algorithm for putative identification of homologous sequences, with an e-value cut-off < 10^–3. Annotated sequences were curated and grouped into categories according to their function using Blast2Go® [173] with an e-value cut-off < 10^–6 and EggNOG-mapper 4.5.1 [174]. Transcripts putatively identified as belonging to insects and Ca. L. asiaticus were checked against the KEGG database (Kyoto Encyclopedia of Genes and Genomes) [175] to verify the metabolic pathways represented in the obtained de novo transcriptome. Transcripts of Diaphorina citri, Ca. Liberibacter spp. and Wolbachia spp. were filtered using Blast2Go version Pro [176].

Differential gene expression analyses

Changes in the pattern of gene expression were evaluated separately in gut of ACP adults infected or not by Ca. L. asiaticus using the CLC Genomics Workbench 20.0 software (QIAGEN, Aarhus, Denmark). Reads from each library were counted against the de novo transcriptome, and counts were normalized as transcripts per million reads (TPM). TPM values for each sample were used to calculate fold-change ratios for comparative analyses of the gene expression of control (CLas^-) versus CLas-infected insects (CLas⁺) within each feeding interval (1-2 d, 3-4 d, 5-6 d). Only the transcript that were counted in two of the replicates of a particular treatment were further taken for comparative analysis. Data were analyzed using multifactorial statistics based on a negative binomial Generalized Linear Model (GLM). The values of fold change obtained were corrected with False Discovery Rate (FDR) method and only transcripts that showed p-value ≤0.05 and log fold change > |2| between treatments were considered differentially expressed.

Abbreviations

A1CLas

adults that fed on healthy citrus plant for 1-2 days

A2CLas

adults that fed on healthy citrus plant for 3-4 days

A3CLas^-

adults that fed on healthy citrus plant for 5-6 days

A1CLas⁺

adults of Asian Citrus Psyllid that fed on CLas-infected citrus plant for 1-2 days

A2CLas⁺

adults of Asian Citrus Psyllid that fed on CLas-infected citrus plant for 3-4 days

A3CLas⁺

adults of Asian Citrus Psyllid that fed on CLas-infected citrus plant for 5-6 days

ACP

Asian Citrus Psyllid

ADK

Adipokinetic Hormone

AMP

Antimicrobial Peptides

BLAST

Basic Local Alignment Search Tool

BNIP3

BCL2/Adenovirus E1B 19 Kda Protein-Interacting Protein 3

CLaf

Candidatus Liberibacter africanus

CLam

Candidatus Liberibacter americanus

CLas

Candidatus Liberibacter asiaticus

CLas^-

adults of Asian Citrus Psyllid that fed on healthy citrus plant

CLas⁺

adults of Asian Citrus Psyllid that fed on CLas-infected citrus plant

DE

Differential Expression

ER

Endoplasmic Reticulum

FC

Fold Change

FDR

False Discovery Rate

GLM

Generalized Linear Model

HLB

Huanglongbing

JH

Juvenile Hormone

JHBP

Juvenile Hormone Binding Protein

KEGG

Kyoto Encyclopedia of Genes and Genomes

N1CLas^-

Nymphs of Asian Citrus Psyllid fed for 4 days on healthy citrus plants

N1CLas⁺

Nymphs of Asian Citrus Psyllid fed for 4 days of feeding on CLas-infected citrus plants

PhoB

Two-component Response Regulator Protein

PhoR

Two-component Sensor Histidine Kinase

PPI

Peptidyl-Prolyl Isomerase

PPO

Prophenoloxidases

RBOH

Respiratory Burst Oxidase Homologs

RNS

Reactive Nitrogen Species

ROS

Reactive Oxygen Species

SNAP

Soluble NSF Attachment Protein

TPM

Transcripts Per Million Reads

TPR

Tetratricopeptide Repeat

Authors’ contributions

FLC and NAW designed the experiments. FLC, NAW and LP secured the funds. JCD collected insect samples and extracted RNA. BLM processed the sequencing data and assembled the de novo transcriptome. FMMB analyzed the data. FMMB and FLC wrote the paper. All authors read and approved the final manuscript.

Funding

FAPESP provided the post-doctoral fellowship to FMMB (grant number 2018/24234-4) and BLM (grant number 2018/24768-9), and a research grant to FLC, NAW and LP to support this research (grant number 2015/07011-3). CNPq provided the PhD fellowship to JCD (grant number 141042/2017-6).

Availability of data and materials

All cDNA libraries produced from RNA obtained from samples analyzed are fully available as SRA files through NCBI (https://www.ncbi.nlm.nih.gov/bioproject/) under BioProject ID PRJNA722422. All remaining data generated or analysed during this study are included in this published article and its additional information files.

Declarations

Ethics approval and consent to participate

This study did not require permits for seeds, plant and/or animal collection, and maintenance under laboratory conditions. This study complies with institutional, national and international guidelines and legislation.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.