The draft genome of the specialist flea beetle Altica viridicyanea (Coleoptera: Chrysomelidae) provides insight into host plant specialization

doi:10.21203/rs.3.rs-47391/v1

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The draft genome of the specialist flea beetle Altica viridicyanea (Coleoptera: Chrysomelidae) provides insight into host plant specialization

https://doi.org/10.21203/rs.3.rs-47391/v1

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published 07 Apr, 2021

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Background

Altica (Coleoptera: Chrysomelidae) is a highly diverse and taxonomically challenging flea beetle genus that has been used as a model system in which to address questions related to host plant specialization, reproductive isolation, and ecological speciation. To further evolutionary studies in this important group, here we present a high-quality draft genome of a representative specialist, Altica viridicyanea, the first Alticinae genome and the fourth chrysomelid genome reported thus far.

Results

The genome is 864.8 Mb and consists of 4,490 scaffolds with a N50 size of 557 kb, which covered 98.6% complete and 0.4% partial insect Benchmarking Universal Single-Copy Orthologs. Repetitive sequences accounted for 62.9% of the assembly, and a total of 17,730 protein-coding gene models and 2,462 non-coding RNA models were predicted. To provide insight into host plant specialization of this monophagous species, we examined the key gene families involved in chemosensation, detoxification of plant secondary chemistry, and plant cell wall-degradation.

Conclusions

The high-quality genome assembled in this work provides an important resource for further studies on host plant adaptation and functionally affiliated genes. Moreover, this work also opens the way for comparative genomics studies among closely related Altica species, which may provide insight into the molecular evolutionary processes that occur during ecological speciation.

Epigenetics & Genomics

Altica

genome

annotation

host plant adaption

chemosensory

detoxification

The high rate of diversification among host-specific herbivorous insects is thought to result from their shift and specialization to distinct host-plant species, creating conditions that promote reproductive isolation and contribute to the process of speciation [1–3]. A model herbivore that has been used to address questions about host plant specialization, reproductive isolation, and ecological speciation is the leaf beetle genus Altica (Coleoptera: Chrysomelidae) [4–10]. This group has undergone rapid divergence that is largely associated with host plant use. For example, studies of three closely related species, Altica viridicyanea, A. cirsicola, and A. fragariae, have demonstrated that although these species are broadly sympatric and quite similar in morphology, they feed on distantly related host plants from different plant families [6]. Consequently, their divergence is likely the result of dietary shifts to unrelated host plants [6]. Further, their close relationship is supported by crossing studies that show that interspecific hybrids can be generated under laboratory conditions [4–6, 8, 10], and phylogenetic analysis indicates that these species diverged over a relatively short period of time. Although Altica has been pivotal for understanding the linkages between host plant use and speciation [6, 11–13], the lack of a representative Altica genome hinders our ability to more thoroughly investigate the molecular mechanisms underlying the processes of ecological adaptation and diversification within this interesting group.

Key aspects of host plant adaptation and speciation among Altica beetles involves at least two major evolutionary changes. First, a host plant shift will require behavioral adaptations that alter both feeding preference and oviposition preference for the novel host [14–15]. Both the adults and larvae of Altica species feed on the host plant, and this has been posited as a mechanism of reproductive isolation in herbivorous insects as an insect is more likely to encounter mates while feeding [7, 16–17]. Second, the insects will also require physiological adaptations that allow them to feed on novel plant secondary compounds. This may involve new detoxification mechanisms that allow insects to avoid the deleterious effects of defensive chemistry [15, 18]. One aspect of host plant adaptation, then, is the prediction that the gene families involved in the detection of host chemical cues and those involved in xenobiotic detoxification will be key in facilitating successful shifts onto new host plant species. As a result, if we are to understand how host plant adaptation has played a role in speciation of Altica beetles, we require a reference genome to make comparisons of candidate gene families involved in the diversification process.

The wealth of genetic and behavioral studies that have been conducted on A. viridicyanea makes it an excellent starting point for genomic investigations of host plant adaptation and speciation among Altica species. This species is an extreme host specialist of the plant Geranium nepalense (Sweet) (Geraniaceae), and these beetles will not feed or lay eggs on alternative hosts even in no-choice laboratory trials [4, 5, 7]. Reproductive isolation of A. viridicyanea is driven by the presence of species-specific cuticular hydrocarbons that determine mating preferences [8, 9]. In fact, these chemical signals are so specific that they allow beetles to assess sexual maturity of conspecifics [9]. Studies of F₁ hybrids between A. viridicyanea and a close relative have shown that these cuticular hydrocarbon profiles can also be modified by the beetle’s diet [8, 10]. Consequently, host plant use and mating preferences are intrinsically linked through chemistry.

Here we provide the genome assembly of A. Viridicyanea (Fig. 1), the first genome of the subfamily Alticinae, and the fourth for the Chrysomelidae. Chrysomelids are a large and highly diverse family of beetles, with approximately 40,000 described species in the world [19], many of which are economically important pests of agricultural crops [20]. To date, genomes have been assembled for three oligophagous species, the Colorado potato beetle, Leptinotarsa decemlineata [21], the cowpea weevil, Callosobruchus maculatus [22] and the ragweed leaf beetle, Ophraella communa [23]. Consequently, the genome for A. viridicyanea will add to our genomic resources for a monophagous member of the Chrysomelidae. Furthermore, this assembly will also expand our knowledge of beetles in general as we currently have only 21 published beetle genome assemblies [22, 24–33] (Table S1) which is a comparably small number for a diverse insect group with nearly 400,000 described species [34–36]. Finally, the high-quality genome assembled here will provide an important resource for further studies on host plant adaptation and functionally affiliated genes.

De novo genome assembly

Flow cytometry revealed that the genome size of A. viridicyanea ranged from 836.3 ± 13.8 Mb in females to 795.7 ± 8.3 Mb in males. We generated and assembled 187.3 × coverage from Illumina short reads and 72.7 × coverage via PacBio long reads from 157 female adults, thus creating a draft genome reference assembly of 864.8 Mb consisting of contig and scaffold N50s of 92.8 kb and 557.2 kb, respectively (Table 1). The GC content was 31.67%. The size of the A. viridicyanea genome was larger than 85% of the currently published beetle genomes (Table S1). The draft genome assembly of A. viridicyanea was contained within 17,580 contigs that were assembled into 4,490 scaffolds, with the longest scaffold size of 5.6 Mb. Using the reference set of 1,658 insect BUSCOs, the genome contains 98.6% complete single-copy orthologs and multi-copy orthologs; using the reference set of 2,442 Endopterygota BUSCOs, our genome contains 95.8% complete single-copy orthologs and multi-copy orthologs (Table 2). Together, the results of the above analyses indicate that the genome of A. viridicyanea is a high-quality assembly.

Table 1

Summary statistics of *Altica viridicyanea* draft genome assembly.
Statistics	Value
Illumina (genome coverage)	187.3×
PacBio (genome coverage)	72.7×
Assembly size (Mbp)	864.8
Number of contigs	17,580
Longest contig (Kbp)	1,351
Contig N50 (Kbp)	92.8
Number of Scaffolds	4,490
Longest scaffold (Kbp)	5,675
Scafflod N50 (Kbp)	557.3
Gap	2.36%
GC content	31.67%
Number of protein-coding genes	17,730
Number of non-coding RNAs	2,462

Table 2

BUSCO results showing completeness of the *Altica viridicyanea* genome assembly and annotation.
	Insect		Endopterygota
	Counts	Percentage	Counts	Percentage
Complete BUSCOs	1,635	98.6%	2340	95.8%
Complete and single-copy BUSCOs	1,540	92.9%	2211	90.5%
Complete and duplicated BUSCOs	95	5.7%	129	5.3%
Fragmented BUSCOs	7	0.4%	52	2.1%
Missing BUSCOs	16	1.0%	50	2.1%
Total BUSCO groups searched	1,658		2,442

Genome annotation

Prior to gene prediction using the assembled sequences, repeat sequences were identified in the genome of A. viridicyanea. The repetitive sequence content was about 62.91% of the assembly, which was similar to that of the cowpea weevil Callosobruchus maculatus (64%), lower than that of the ladybird Propylea japonica (71.33%), and much higher than that of other beetle species (Table S1). Most of the repetitive sequences were transposable elements. According to a uniform classification system for eukaryotic transposable elements [37], retrotransposons (Class I) accounted for 41.27% whereas DNA transposons (Class II) accounted for 26.24% of the genome (Table 3).

Table 3

Composition of repetitive sequences in the *Altica viridicyanea* genome assembly.
Repeat type		Number of elements	Length (bp)	Rate (%)
Retrotransposons (transposable element class I)		1,033,903	356,902,348	41.27
	DIRS	12,458	7,468,113	0.86
	LINE	3,17,300	97,559,643	11.28
	LTR/uncertain	45,604	28,406,497	3.28
	LTR/Copia	15,362	7,752,670	0.9
	LTR/Gypsy	143,535	83,332,210	9.64
	LTR or DIRS	91	14,310	0
	PLE or LARD	485,362	155,872,484	18.02
	SINE	78	80,868	0.01
	TRIM	13,553	6,401,760	0.74
	Unknown	560	58,144	0.01
DNA transposons (transposable element class II)		803,681	226,943,053	26.24
	TIR	550,895	150,574,911	17.41
	MITE	10	635	0
	Crypton	145,294	43,476,772	5.03
	Helitron	29,008	8,403,268	0.97
	Maverick	51,701	31,213,827	3.61
	Unknown	26,773	5,423,361	0.63
SSR		583	165,863	0.02
Unknown		77,813	23,953,352	2.77
Total		1,848,679	544,002,544	62.91
Notes: DIRS, dictyostelium intermediate repeat sequence; LINE, long interspersed nuclear element; LTR, long terminal repeat; PLE, penelope-like elements; SINE, short interspersed nuclear element; LARD, large retrotransposon derivative elements; TIR, terminal inverted repeat.

The integration of de novo, RNA-seq-based and homology-based gene prediction methods identified 17,730 protein-coding genes in A. viridicyanea (Table 4, Fig. S1), a number slightly less than the average of beetle species with available genomes (~ 18,600 genes on average, Table S1). In total, 16,625 genes were assigned to putative functions, accounting for approximately 93.77% of the predicted genes (Table S2), and 750 putative pseudogenes were identified (Table S3). There were 2,462 non-coding RNA models identified, including 45 miRNAs, 1093 rRNAs, and 1324 tRNAs, corresponding to 32, four and 24 gene families, respectively.

Table 4

Statistics of gene prediction of *Altica viridicyanea*.
Method	Software	Gene number
ab initio	Genscan v1.1.0	15,170
	Augustus v2.4	31,813
	GlimmerHMM v3.0.4	58,872
	GeneID v1.4	14,970
	SNAP v2006-07-28	72,679
homology-based	GeMoMa v1.3.1 Drosophila melanogaster Tribolium castaneum Dendroctonus ponderosae Anoplophora glabripennis	9,310
		14,234
		13,066
		18,274
transcriptome-based	TransDecoder v2.0	73,432
	GeneMarkS-T v5.1	29,645
	PASA v2.0.2	23,200
Integration	EVidenceModeler v1.1.1	17,730

Phylogenetic analysis

The phylogenetic analysis identified 15,240 orthologs in A. viridicyanea that clustered with the other eight beetle species. We identified 1,609 A. viridicyanea specific genes, corresponding to 529 gene families, a number far greater than the other species included in this analysis (Table S4). The phylogenetic relationships were consistent with the results inferred from large datasets [38–40]. For example, A. viridicyanea and Leptinotarsa decemlineata, both chrysomelids, were sister taxa, and these species clustered with Anoplophora glabripennis, a member of the superfamily Chrysomeloidea (Fig. 2). The estimated divergence time between A. viridicyanea and L. decemlineata was about 98.2 million years ago. From this analysis, we also identified 165 gene families that expanded and 47 gene families that contracted along the A. viridicyanea lineage (Fig. 2). Some of these gene families were related to chemosensory and detoxification functions.

Chemosensory gene families

In many herbivorous insects, feeding, mating and oviposition behaviors are mediated by chemical cues [41]. The chemosensory system may also play important roles in speciation of some insects [42–44]. This is likely the case in A. viridicyanea as previous work has shown that this monophagous beetle primarily uses chemical cues to achieve sexual isolation from its sibling species [8]. Furthermore, these contact chemicals also act as a mating signal to discriminate intraspecific variation in sexual maturity [9]. In addition, chemical cues are modified by and likely involved in host plant choice [8, 10]. Consequently, we investigated A. viridicyanea gene families known to be involved in chemosensory signaling in insects.

There are at least five gene families involve in the detection of chemicals, including three receptor families, odorant receptors (ORs), gustatory receptors (GRs) and ionotropic receptors (IRs), and two protein binding families, odorant binding proteins (OBPs) and chemosensory proteins (CSPs). These receptor families are usually expressed in insect olfactory sensory neurons and are involved in the detection of a suite of chemicals. For instance, volatile chemicals are detected by ORs [45–47], contact chemicals or carbon dioxide are detected by GRs [48], and nitrogen-containing compounds, acids, and aromatics are identified by IRs [49]. In contrast, the binding protein gene families are highly abundant in the sensillar lymph of insects and usually function as carriers of hydrophobic scent molecules to the receptors [50, 51].

In the genome of A. viridicyanea, we identified 195 putative chemosensory genes and two pseudogenes. Perhaps not surprisingly, the gene repertoire of the monophagous A. viridicyanea was considerably reduced as compared to that of polyphagous species such as T. castaneum (630 genes plus 103 pseudogenes) and A. glabripennis (451 genes plus 65 pseudogenes). In contrast, the gene number is greater than the oligophagous Agrilus planipennis (132 genes and two pseudogenes), but smaller than other oligophagous species such as Dendroctonus ponderosae (240 genes plus 10 pseudogenes) and L. decemlineata (> 300 genes) (Table S5). These findings generally support the hypothesis that chemosensory gene content and host specificity should correlate in phytophagous beetles [52].

Insect ORs are proteins with seven transmembrane domains that are involved in the detection of volatile chemicals [46, 53, 54]. The number of ORs in beetle species varies widely from 30 to hundreds of ORs [55]. When we examined the A. viridicyanea genome for the presence of ORs, we found a diversity of gene families. There were 64 ORs and one pseudogene (PseudoGene48) that were classified into eight subfamilies: Group 1, 2A, 2B, 3, 4, 5A, 5B and 7 (Fig. 3; Table S5). Following the new OR classification scheme [55], we also identified one highly conserved olfactory co-receptor, Orco, that has been found in other beetle species. Interestingly, we also found a large expansion in A. viridicyanea in Group 4 that contained 17 ORs. By comparison, no more than four Group 4 OR genes have been previously identified in any other surveyed beetle species [52, 55].

In addition to ORs, we also compared GRs across beetle taxa. Most GRs are expressed in gustatory receptor neurons in taste organs and are involved in contact chemoreception and detection of CO₂ [48]. We annotated 38 GRs in A. viridicyanea, including three conserved candidate CO₂ receptors, seven candidate sugar receptors, and the remaining were candidate bitter taste receptors. Simple orthology of GRs is generally rare in beetles [52], and not surprisingly, no single-copy orthologs were revealed in the species that we compared. The phylogenetic analysis showed that 2–7 GRs from each of the seven species grouped within the clade of conserved sugar receptors. Additionally, two or three genes from five of the seven species formed a clade of CO₂ receptors (Fig. S2).

The number of GRs varied from 10 to 245 in the ten surveyed beetles (Table S5). Comparisons with A. viridicyanea identified as many as 147 GRs in an oligophagous chrysomelid species Leptinotarsa decemlineata, whereas fewer than 20 GRs were annotated in four other chrysomelids (Colaphellus bowringi, Ophraella communa, Pyrrhalta aenescens and Pyrrhalta maculicollis). The extremely low numbers of GRs in the latter four species is likely the result of differences in data collection—those species only had transcriptomic data available, and that approach generally does not describe the full complement of chemosensory genes. For example, a study in the longhorn beetle Anoplophora glabripennis found 11 GRs when using transcriptomic data, however, genomic data revealed 234 GRs [36, 56].

The next chemosensory receptor group that we examined was the IRs, a conserved family that evolved from a family of synaptic ligand-gated ion channels, ionotropic glutamate receptors (iGluRs) [49, 57, 58]. In insects, the IRs include two groups: the conserved “antennal IRs” that have an olfactory function, and the species-specific “divergent IRs” which are candidate gustatory receptors [59]. Our genome annotations revealed 33 ionotropic receptors (IRs). Only the members of the conserved antennal IR21a group were identified in all seven of the beetle species that we surveyed, whereas the clades IR8a, IR25a and IR76b were formed by single-copy orthologs from five species, excluding P. aenescens and P. maculicollis (transcriptomic data are available for both of these species) (Fig. 4). Furthermore, IRs from all seven species fell within the well-supported non-single-copy IR75 clade (Fig. 4). Remarkably, for A. viridicyanea, 18 of 33 IRs were clustered into a “Galerucinae + Alticinae” specific lineage that consisted of genes from O. communa, P. aenescens, P. maculicollis and A. viridicyanea (Fig. 4). These four species belong to the sister groups, Galerucinae and Alticinae, two closely related subfamilies of Chrysomelidae [60].

Finally, we examined the protein binding gene families. OBPs and CSPs are generally regarded as carriers of pheromones and odorants in insect chemoreception, and a multitude of additional functions have also been suggested such as carrying semiochemicals and visual pigments, promoting development and regeneration, and digesting insoluble nutrients [61]. OBPs are small, soluble proteins with six conserved cysteines [50]. Although the detailed mechanisms remain unclear [62], it is believed that OBPs deliver hydrophobic molecules to the receptors [50]. In A. viridicyanea, we annotated 48 putative OBP genes and one pseudogene (PseudoGene855). Among these, 34 genes belonged to the Minus C OBPs. We found four clades of classic OBPs, which include single-copy orthologs from each of the seven species in the analysis, e.g., Classic I, IV, VIII and IX. In clades VII and X, two copies from Dendroctonus ponderosae were clustered with single-copy orthologs from other six species. The clades of Classic II, III, V and VI were formed by single-copy orthologs from 5–6 species (Fig. S3). Plus-C OBPs were not found in A. viridicyanea, and are also absent in the Pyrrhalta species that belong to the “Galerucinae + Alticinae” taxonomic group.

CSPs are characterized by the presence of four cysteines that form two disulfide bridges [63]. We annotated 12 CSP genes in A. viridicyanea. The phylogenetic analysis revealed that only one clade (clade 1) was formed by single-copy orthologs from the eight species surveyed. Clades 2–7 were formed by single-copy orthologs from 5–7 beetle species. In these lineages, the absence of IRs from transcriptomic sources (e.g., P. aenescens, P. maculicollis and O. communa) was more common whereas the orthologs of A. viridicyanea also lacked members of clade 5 (Fig. S4).

Similar to previous work on GRs, transcriptomes often fail to describe the full set of chemosensory genes due to low expression, spatiotemporal variation in expression, or shallow sequencing depth. For instance, 106 chemosensory genes were detected in Anoplophora glabripennis using transcriptomic sequencing [56] whereas more than 500 chemosensory genes (65 pseudogenes included) were annotated from its genome [52].

Detoxification supergene families

Novel plant secondary compounds often present a challenge for herbivorous insects, and physiological adaptation to novel plant secondary metabolites is a key problem. The detoxification and metabolism of most xenobiotics occurs via a common set of detoxification-related enzymes, all of which belong to multigene families [64]. The cytochrome P450s (P450s), carboxyl/cholinesterases (CCEs), and glutathione S-transferases (GSTs) are widely regarded as the major insect gene/enzyme families involved in xenobiotic detoxification [65–67]. In addition, the UDP-glucuronosyltransferases (UGTs) and ATP binding cassette transporters (ABCs) can also play a role in detoxification [68–70]. This diversity of detoxification enzymes is critical for many herbivorous insects [18, 71] as their diets often contain a suite of plant chemicals that can be toxic, reduce palatability, or slow development time.

The host plant of A. viridicyanea is Geranium nepalens which has a number of chemical defenses such as tannins, flavonoids and organic acids [72]. As a strict specialist, then, A. viridicyanea likely has adaptations that allow them to detoxify these chemicals. Indeed, we annotated 225 detoxification enzymes spanning all three families (101 P450s, 97 CCEs and 27 GSTs). Expansion and contraction of these gene families are considered important in adaptive phenotypic diversification [73]. Furthermore, meta-analyses have established that the size of the P450, CCE and GST gene families are correlated with insect diet breadth [66, 67, 74]. Consistent with these ideas, in A. viridicyanea, the number of detoxifying genes is larger than that of the closely-related oligophagous Leptinotarsa decemlineata (197 genes) [21, 67], but smaller than that of the seed feeding T. castaneum (275 genes) [26, 75].

Insect cytochrome P450 proteins are important in both xenobiotic detoxification and synthesis and degradation of endogenous molecules such as ecdysteroids and juvenile hormone [76–78]. In insects, the cytochrome P450 family is divided into four major clades: the mitochondrial P450 clade, the CYP2 clade, the CYP3 clade, and the CYP4 clade [79]. We found 101 P450s in Altica viridicyanea spanning all four clades: five in the mitochondrial clade, seven in the CYP2 clade, 53 in CYP3 clade, and 36 in CYP4 clade (Fig. 5, Table S6). We found that a majority of these genes belonged to the CYP6 and CYP9 subfamilies of the CYP3 clade and the CYP4 subfamily of the CYP4 clade (Table S7). These P450 subfamilies are known to be involved in detoxification of plant allelochemicals as well as resistance to pesticides [21, 80–82].

In addition to the cytochrome P450s, the A. viridicyanea genome also contained 97 genes encoding putative CCEs (Fig. S5), which is slightly fewer than that of L. decemlineata (102), but more than that of the other eight beetle species that were included in the analysis (ranged from 44 to 82) [67]. The dietary/detoxification group included two clades: coleopteran xenobiotic metabolizing CCE (clade A) and ɑ-esterase type CCEs (clade B) [83]. In A. viridicyanea, there is a noteworthy expansion (62 genes) in clade A, whereas we did not identify any genes from Clade D (integument esterase), F (juvenile hormone esterase), or I (unknown function) (Fig. S5; Table S8).

Another group of detoxification enzymes that we examined are the GSTs. GSTs are involved in many cellular physiological activities, such as detoxification of endogenous and xenobiotic compounds, intracellular transport, biosynthesis of hormones and protection against oxidative stress [75, 84]. Insect GSTs are divided into two major groups, the cytosolic and the microsomal GST genes. The cytosolic group is further divided into six classes: Delta, Epsilon, Sigma, Omega, Theta, and Zeta [85]. The Delta and Epsilon classes are thought to be insect-specific [75, 84, 86], and members of the Epsilon subfamily are commonly involved in detoxification of xenobiotics [87]. We detected a total of 27 GST genes in A. viridicyanea (Fig. S6; Table S9). Both the total number and the number of detoxification-related Epsilon subfamily in A. viridicyanea were lower than that of most beetles [67]( Table S9).

UDP-glycosyltransferases (UGT) catalyze the conjugation of a range of diverse small lipophilic compounds with sugars to produce glycosides, playing an important role in the detoxification of xenobiotics and in the regulation of endobiotics in insects [68]. From 17 (Oryctes borbonicus) to 65 (Anoplophora glabripennis) UGTs were identified in the nine beetle species surveyed [3, 67]. Currently, the largest repertoire of UGTs in beetles was found in the polyphagous longhorn beetle Anoplophora glabripennis, with 65 putative UGT genes and 7 pseudogenes [36]. The expansion of UGTs in A. glabripennis is thought to be related to its ability to feed on a broad range of host plants [36]. In line with this, we annotated 32 UGTs in the A. viridicyanea genome. A number of UGT50s were identified in this species, which has been suggested as the most conserved UGT in insects [68], and we also observed a remarkable expansion in the UGT324 family (Fig. S7, Table 10).

Most ABC proteins engage in active transport of molecules across cell membranes. The ABC transporters are well-known components of various detoxification mechanisms across all phyla [88, 89]. In the present study, we identified 69 putative ABCs in A. viridicyanea, belonging to eight subfamilies (A to H). This is a similar number to two specialist species of chrysomelids, Chrysomela populi and Diabrotica virgifera virgifera, (65 in each based on transcriptomic data) (Table S11). The gene numbers of the conserved subfamilies D, E and F were consistent with other beetles analyzed (Table S11); however, the number of genes in subfamilies B and C in A. viridicyanea (46) are the highest among the five species with which we compared (Table S11; Fig. 6). These subfamilies are known to be involved in detoxification processes [64, 90].

Plant cell wall-degrading enzymes

Early views of insect digestion postulated that insects lack the endogenous enzymes required for plant cell wall (PCW) digestion, and that PCW digestion by insects depended on exogenous enzymes from symbiotic microorganisms [91]. Recent studies, however, have revealed that endogenous PCW degrading enzymes are present in many insects and are important in the digestion of cellulose, hemicelluloses, and pectin in PCW [40, 92]. In fact, these enzymes are likely a key innovation in the adaptive radiation of herbivorous beetles. Some insect PCW-degrading enzymes are also involved in immune-defense responses and detoxification [40, 92].

Beetle-encoded plant cell wall-degrading enzymes are carbohydrate esterases (CE), polysaccharide lyases (PL), and mainly glycoside hydrolases (GH) [40]. In A. viridicyanea, we identified 65 putative glycoside hydrolases, including 35 GH1 genes, 10 GH45 genes, two GH48 genes and 18 GH28 genes (Table S12). Genes of GH1 originated anciently in animals and are ubiquitous in beetles. The species of Phytophaga (i.e., Chrysomeloidea and Curculionoidea) examined thus far have a greater number of GH1 genes than A. viridicyanea, for example, 228 were found in Diabrotica undecimpunctata, 135 in Mastostethus salvini, and 136 in Rhynchitomacerinus kuscheli [21, 36, 40]. For another ancient and ubiquitous gene family, GH9, there are at least a dozen independent losses in beetles [40]. GH9 was not detected in A. viridicyanea, along with 4 of 7 other chrysomelid species (Callosobruchus maculatus, Donacia marginata, Diabrotica undecimpunctata and Leptinotarsa decemlineata) [21, 40].

The other plant cell wall-degrading gene families (CE8, PL4, GH32, GH5, GH10, GH43, GH44, GH45, GH48 and GH28) are suggested to be obtained from bacteria and fungi via horizontal gene transfer, and are mainly found in Buprestoidea and Phytophaga, with scattered genes in a few other taxa [40]. In A. viridicyanea, in addition to the ubiquitous GH1 genes, three families of PCW-degrading enzymes were identified, including cellulose degrading GH45 and GH48, and pectin degrading GH28. These observed gene numbers are similar to that of closely related species in the Chrysomelinae (Oreina cacaliae and Leptinotarsa decemlineata) and Galerucinae (Diabrotica undecimpunctata) [21, 40].

In the present study, we combined short Illumina reads and long PacBio reads to decrease sequencing errors. From the genome annotation we found that A. viridicyanea, a host specialist herbivore, has a reduced number of chemosensory and detoxification genes as compared to more generalist herbivorous beetles, consistent with the idea that diet breadth should positively correlate with chemosensory and detoxification gene content. Although A. viridicyanea had fewer chemosensory and detoxification genes than more polyphagous beetles, we did observe expansions in some gene families that may be related to host plant adaptation. As a result, the high-quality genome assembled here provides an important resource for further studies on host plant adaptation and functionally affiliated genes. Additionally, this work will also open the opportunity for comparative genomics studies among closely related Altica species that may provide insights into the molecular evolutionary processes that occur during ecological speciation.

Beetles

Altica viridicyanea is a highly specialized herbivore of Geranium nepalense. They are elongate-ovate beetles with a length of 3–4 mm. The dorsal surface is black with metallic blue (Fig. 1). Equipped with dilated hind legs, these beetles typically jump in a flea-like fashion to escape predators.

To make genome sequencing easier, we created a laboratory colony by collecting adult A. viridicyanea in Changping (40.28’N, 116.05’E), Beijing, China. Adults were maintained in growth chambers held at 16:8 LD and 25ºC and fed with leaves of their host plant, Geranium nepalense (Sweet). A subset of these collected adults was used for genome size estimation (see below). We maintained the colony through successive single-pair sibling matings to create third generation lines for whole genome sequencing. When we were ready to sequence the beetles, beetles were starved for two days and then killed in liquid nitrogen. The samples were stored at -80 °C until DNA extraction. In total, we used 157 virgin females for sequencing.

Genome size estimation

In preparation for whole genome sequencing, we first determined the genome size of A. viridicyanea. Genome size was estimated via flow cytometry [93] on four adult males and four adult females. The thoracic muscle of living beetles was dissected with sterilized fine forceps, and cut into small pieces in Galbraith buffer. The ground suspension was filtered through 40-mm nylon mesh (Easystrainer™) to remove cellular debris and the flow-through was collected in a 5-ml round-bottomed tube placed on ice. Propidium iodide was add to samples to a final concentration of 50 mg/ml and stained in the dark at 4 °C for 2 hours. Then fluorescence intensity was estimated for each beetle using a superfluid cell sorting system (MoFol XDP, Beckman Coulter Life Sciences). Genome size was calculated using the following formula:

GS_b = GS_standard × PI-fluor_unknown / PI-fluor_standard, where GS is genome size and PI-fluor is the channel number of the PI fluorescence for both the unknown sample and the standard. Chicken (Gallus gallus domesticus) blood was used as the standard to estimate genome size.

DNA extraction and sequencing

Genomic DNA (gDNA) was extracted from whole beetles using DNeasy Blood & Tissue Kit (Qiagen, Germany) following the manufacturer’s instructions. The total amount of gDNA was measured using QubitFluorometer (Invitrogen), and the integrity of the gDNA was verified on an agarose gel that had reference lanes containing high molecular weight ladders (GeneRuler High Range DNA Ladder and D2000 DNA Ladder). From these extractions, seven Illumina sequencing libraries were prepared, with insert sizes and genome coverage of 270 bp (55.5×), 500 bp (29.4×), 800 bp (19.0×), 3 kb (12.5×), 5 kb (two libraries, 49.7×), to 10 kb (21.1×) (Table S13). The libraries were sequenced with 150 bp paired-end reads on the Illumina HiSeq 2500 platform. We also sequenced two PacBio libraries with 72.7 × genome coverage, with N50 read lengths of 9.1 kb (Table S13).

Data pre-processing

For Illumina Data, FastQC v0.11.6 (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/) was used to check the quality of the raw reads, and then TrimGalore v0.4.5 (https://github.com/FelixKrueger/TrimGalore) was used to filter out the adapters and low-quality reads using the parameters “--length 36 -q 20 --trim-n”. Because A. viridicyanea are quite small, we used the entire body of adults for sequencing. As a result, the likelihood of microbial contamination was high; therefore, we used BBDuk in the BBMap v37.80 (https://sourceforge.net/projects/bbmap) to filter microbial contaminants. To do this, we first built a reference library which included all sequences of archaea, bacteria, fungi, protozoa, and viruses available in RefSeq (accessed on August 15, 2019). The remaining reads were used for downstream genome assembly and analysis.

To simplify the genome assembly process, we also excluded reads originating from microbial sources that were present in the PacBio data. To accomplish this, we mapped all the raw PacBio reads to the above Illumina library using minimap2 v2.12 [94], using the parameters “-x map-pb -a -Q --split-prefix”. To improve the mapping specificity, we included 11 available coleopteran genomes [28] in the reference library. Then we removed the reads that mapped to the microbial sequences.

Genome assembly

A hybrid assembly strategy was used to assemble the PacBio and Illumina reads. PacBio reads were first assembled using Flye v2.3.5b [95] to obtain contigs. Then Redundans v0.14a [96], which uses an iterative scaffolding approach by calling SSPACE [97], was used to scaffold the PacBio contigs with the Illumina short reads. After that, SSPACE-Long v1.1 [98] was used to further scaffold with PacBio long reads (Table S14).

Estimation of genome completeness

Benchmarking Universal Single-Copy Orthologs (BUSCO v3.0.1) [99]analyses against Insecta (n = 1,658) and Endopterygota (n = 2,442) were used to evaluate the integrity and quality of the genome assembly with parameters "-sp tribolium2012 -m geno".

RNA-seq library construction and sequencing

We produced transcriptomic data to facilitate gene prediction analyses. To obtain more full-length or near full-length gene sequences, we generated sequence data by combining PacBio full-length transcriptome sequencing (8 Gb clean data) and Illumina sequencing (10 Gb clean data). Whole bodies of four males and four females with three libraries (1–2 kb, 2–3 kb and > 3 kb lengths) were used for PacBio sequencing. To enrich for chemosensory genes, heads from 30 females and 30 males were also used for Illumina sequencing.

Genome annotation

Prior to gene prediction using the assembled sequences, we identified repeat sequences in the genome of A. viridicyanea. LTR FINDER v1.05 [100], RepeatScout v1.0.5 [101] and PILER-DF v2.4 [102] were used to construct a library of repetitive sequences based on the A. viridicyanea genome. PASTEClassifier v1.0 [103] was used to classify these repeats, and the Repbase database [104] was used to merge them. Finally, RepeatMasker v4.0.5 [105] was used to identify and mask the genomic repeated sequences. All the parameters were set to “default” except RepeatMasker where the parameters were set to “-nolow -no_is -norna -engine wublast”.

We combined the de novo, homology-based, and transcriptome-based predictions to identify protein-coding genes in the A. viridicyanea genome. The default settings for Genscan v1.1.0 [106], Augustus v2.4 [107], GlimmerHMM v3.0.4 [108], GeneID v1.4 [109] and SNAP (v2006-07-28) [110] were used to generate the de novo predictions. For the homology-based prediction, protein sequences of Drosophila melanogaster, Tribolium castaneum, Dendroctonus ponderosae and Anoplophora glabripennis were downloaded from NCBI and aligned to the assembled A. viridicyanea genome with GeMoMa v1.3.1 [111, 112] using default parameters. For transcriptome sequencing-based prediction, we firstly assembled the Illumina short reads into unigenes using Hisat v2.0.4 with parameters “--max-intronlen 20000,--min-intronlen 20” [113] and StringTie v1.3.4 set to default parameters [113]. Second, we combined the unigenes with the PacBio full-length transcripts, then we predicted genes based on these combined sequences with PASA v2.0.2 using the parameters “-align_tools gma༌-maxIntronLen 20000” [114]. EVidenceModeler v1.1.1 was used to integrate all of the gene predictions [115]. Finally, to obtain a final gene dataset, PASA v2.0.2 was used for further modification including adding 5’-UTR and 3’-UTRs, obtaining alternative splicing, and extending or shortening, adding or subtracting exons for the EVM-predicted results.

We predicted the non-coding RNAs based on the Rfam v12.1 [116] and miRBase v21.0 [117] databases. Putative microRNAs (miRNAs) and ribosomal RNAs (rRNAs) were predicted using Infernal v1.1 [118], and transfer RNAs (tRNAs) were predicted with tRNAscan- SE v1.3.1 [119]. Based on homology to known protein-coding genes, putative pseudogenes were first searched in the intergenic regions of the A. viridicyanea genome using genBlastA v1.0.4 [120]. Then GeneWise v2.4.1 [121] was used to search for premature stop codons or frameshift mutations in those sequences.

The predicted genes were annotated by aligning them to the NCBI non-redundant protein (nr) [122], non-redundant nucleotide (nt) [122], Swissprot [123], TrEMBL [123], KOG [124], and KEGG [125] databases using BLAST v2.2.31 [126] with a maximal e-value of 1e^− 5. We assigned gene ontology (GO) terms [127] to the genes using the BLAST2GO v2.5 pipeline [128].

Species phylogenetic analysis

We estimated the phylogenetic relationships of A. viridicyanea and an additional eight representative beetle species for which genomic data were available (Anoplophora glabripennis, Aethina tumida, Agrilus planipennis, Dendroctonus ponderosae, Leptinotarsa decemlineata, Nicrophorus vespilloides, Onthophagus taurus and Tribolium castaneum). We used 3,256 conserved single copy orthologs for this analysis. The analysis was implemented in PhyML v3.0 [129] with parameters “-gapRatio 0.5 -badRatio 0.25 -bootstrap 1000”.

We also estimated divergence times among the species using MCMCtree (PAML v4.8 package) (http://abacus.gene.ucl.ac.uk/software/paml.html) [130, 131] with parameters set to a burn-in time of 10,000, the sample number was 100,000, and the sampling frequency was 2. We used the time divergence data in timetree (http://www.timetree.org/) for calibration. To examine gene family expansion and contraction among species, we used CAFE v4.1 [132] with “lambda -l 0.002” to automatically search for birth and death parameters (λ) of genes.

Gene family evolution

To provide insights into host plant specialization, we specifically focused on the evolution of chemosensory gene families, chemical detoxification supergene families, and plant cell wall-degrading enzymes. We first conducted multiple sequence alignment using Mafft (online version 7.305) [133] (http:// mafft.cbrc.jp/alignment/server/), applying the L-INS-I algorithm. The best-fit models for amino acid sequence evolution were selected using the Akaike Information Criterion (AIC) in Prottest v3.4.2. [134] (Table S15). Maximum likelihood trees were reconstructed using RaxML v8.2.9 [135] in the CIPRES Science Gateway v3.3 (https://www.phylo.org/) [136], with 1000 non-parametric bootstrap replicates. The resulting tree was viewed and edited with FigTree v1.3.1 [137] and Adobe Illustrator CS5.

ABC: ATP binding cassette transporter; bp:base pairs; BUSCO:Benchmarking Universal Single-Copy Orthologs; CCEs:carboxyl/cholinesterases; CE:carbohydrate esterases; CSP:chemosensory protein; Gb:gigabase pairs; GH:glycoside hydrolases; GR:gustatory receptor; GST:glutathione S-transferase; IR:ionotropic receptor; kb:kilobase pairs; LINE:long interspersed nuclear element; LTR:long terminal repeat; Mb:megabase pairs; ML:maximum likelihood; OBP:odorant binding protein; OR:odorant receptor; P450:cytochrome P450; PCW:plant cell wall; PL:polysaccharide lyases; RAxML:Randomized Axelerated Maximum Likelihood; RNAseq:RNA sequencing; SINE:short interspersed nuclear element; TE:transposable element; UGT:UDP-glucuronosyltransferases.

Availability of data and materials

The raw sequence data reported in this paper are available at the Genome Sequence Archive [138] in National Genomics Data Center [139] (https://bigd.big.ac.cn/gsa; accession number: CRA002741). And the whole genome sequence data have been deposited in the Genome Warehouse in National Genomics Data Center [139] (https://bigd.big.ac.cn/gwh; accession number: GWHAMMQ00000000).

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing Interests

The authors declare that they have no competing interests.

Funding

This study was supported by National Natural Science Foundation of China (Grant Nos. 31472030, 31672334).

Author’s Contributions

H.J.X, X.K.Y. and R.S.C. designed and managed this project. H.J.X. and W.Z.L. maintained the beetle colony used for sequencing. Y.W.N.,Y.J.H., L.L.Z, X.C.C, X.W.Z and H.J.X performed genome assembly and genome annotation. H.J.X. and R.E.N. performed the phylogenetic analysis. H.J.X., K.A.S and Y.W.N. wrote the paper.

Acknowledgements

Not applicable.

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The draft genome of the specialist flea beetle Altica viridicyanea (Coleoptera: Chrysomelidae) provides insight into host plant specialization

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