Ethics Statement

For all the insect samples used in the study, no permission was required for the insect sampling and collection. Insect sampling and collection in Benin was performed with our collaborators at the International Institute of Tropical Agriculture (IITA). Permission was not required because the insects used for the study are common insect pests on legumes, and IITA Benin has a Memorandum of Understanding (MOU) with the government of Benin for conducting research on these insect pests. In Burkina Faso and Niger, insect sampling and collection were also carried out with our collaborators at the Institut de l’Environnement et de Recherches Agricoles (INERA) and the Institut National de la Recherche Agronomique du Niger (INRAN), respectively. Both INERA and INRAN are national government agencies in their respective countries and therefore have the mandate to work on these insect pests from their respective governments. The insects used for this study are not endangered species.

Development of Reference Transcriptome Sequence Assemblies

Insect samples were collected during the summer through fall of 2011 at 7, 11 and 9 locations in Benin, Burkina Faso and Niger respectively for A. craccivora, A. curvipes, C. tomentosicollis and M. sjostedti (Figure 1). A total of 79, 1,920, 364 and 740 individual insect samples were collected respectively for A. craccivora, A. curvipes, C. tomentosicollis and M. sjostedti from these locations. Both the larval and adult life stages were sampled for all species and stored in RNAlater (Ambion, TX, USA) immediately after collection in the field. All samples from each species, from a single location, were pooled and total RNA was extracted from the insect samples at IITA Benin and INERA Burkina Faso using QIAGEN RNeasy RNA extraction kits (CA, USA) and following the manufacturer's instructions. The RNA was shipped to University of Illinois at Urbana-Champaign (UIUC), USA in 70% ethanol where it was resuspended in water and quantified by measuring the absorbance at 260 nm using a NanoDrop spectrophotometer (Thermo Scientific, DE, USA). The samples were then stored in an ultra-low temperature freezer (-80°C).

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Figure 1. Map of Benin, Burkina Faso, and Niger showing the sites from which A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti were collected.

https://doi.org/10.1371/journal.pone.0079929.g001

Four normalized cDNA libraries were constructed and sequenced on a Roche 454 GS-FLX at the W.M. Keck Center for Comparative and Functional Genomics, Roy J. Carver Biotechnology Center, UIUC. Briefly, messenger RNA (mRNA) was isolated from 10μg of total RNA with the Oligotex kit (Qiagen, Valencia, CA). The mRNA-enriched fraction was converted to 454 barcoded cDNA libraries and normalized [45]. The barcoded libraries were pooled in equimolar concentration based on average fragment length and concentration. After library construction, the pooled libraries were quantified using a Qubit fluorometer (Invitrogen, CA, USA) and average fragment sizes were determined by analyzing 1µl of the samples on the Bioanalyzer (Agilent, CA, USA) using a DNA 7500 chip. The pooled library was diluted to 1 x 10⁶ molecules/µl. Emulsion-based clonal amplification and sequencing on a full plate on the 454 Genome Sequencer FLX+ system was performed according to the manufacturer’s instructions (454 Life Sciences, CT, USA). Signal processing and base calling were performed using the bundled 454 Data Analysis Software v2.6.

The raw sequence read data from the four insect pests were analyzed using the CLC Genomics Workbench 6.0.1 (Cambridge, MA, USA). Pre-processing of the raw reads from each of the four insect samples involved trimming each 454 read using a Phred quality score of 20 and also removing nucleotides < 50 bp from the ends. The adapter sequences were also trimmed from the raw reads. The processed read data from each of the four insect samples were assembled into contiguous sequences using parameters: mismatch cost = 2, insertion and deletion cost = 3, length fraction = 60% and similarity = 90%. After assembly, the vector contamination were removed using the UniVec database and also after assembly, human, bacterial, fish (Danio rerio), mouse (Mus musculus), Salmonella enterica, archeal and viral contamination were removed using a web-based version of DeConSeq [46] using a coverage of 90% and a sequence identity threshold of 94%. The clean transcriptomes, with the contaminations removed, were then deposited at DDBJ/EMBL/GenBank for each of the four insect species.

Functional Gene Annotation

Open reading frames (ORFs) were predicted from assembled contigs using the ORF-Predictor server [47] using all 6 possible reading frames for prediction. The assembled transcripts were used as queries to search against NCBI’s non-redundant (nr) database using the BLASTx algorithm [48], with a cut-off E-value of ≤ 10^-6 and a high scoring segment pairs (HSP) length cut-off of 33. The Blast2GO software package v2.6.5 [49] was used for automating BLASTx searches as well as to retrieve associated gene ontology (GO) terms that allowed the prediction of transcript functions [49,50]. The contigs with significant GO terms were determined with an E-value hit filter of ≤ 1 x 10^-6 and an annotation cut off of 55. Gene ontologies were categorized with respect to molecular function, biological process and cellular component.

Annotations for A. craccivora, A. curvipes, C. tomentosicollis and M. sjostedti gene functions were manually searched for those putatively involved in the expression of insecticide resistance traits, and pathogen defense and immunity, using each gene function as keywords to search GO terms. Prediction of candidate gene function was also obtained using InterProScan [51,52] and Kyoto Encyclodepia of Genes and Genomes (KEGG) pathway analyses [53] using Blast2GO v2.6.5 [49].

Prediction of Putative SNPs

The associated SNP detection software on the CLC Workbench 6.0.1 was used for putative SNP discovery among Roche 454 reads for all species. Attempts to reduce the rate of false SNP discovery included applying a read coverage cut-off of ≥ 35-fold and reporting SNPs that were present in ≥ 35% of the aligned reads. These criteria might reduce the false SNP discovery rate by potentially eliminating sequencing errors from the prediction. However, such stringent criteria likely increases type II error, therefore we also performed a comparative prediction of putative SNPs using a reduced coverage cut off of ≥ 10%. All putative indels and nucleotide variants involving > 2 nucleotides were excluded. Lastly, only SNPs located in an ORF were extracted and reported in this study. We checked whether SNPs introduced an amino acid change to differentiate non-synonymous and synonymous SNPs by using the open reading frames of each of the contigs with SNPs, identifying the codons containing the SNPs and then translating and comparing the amino acids for each allele on CLC Workbench 6.0.1. We also checked the type of substitution, whether transition or transversion, using the CLC Workbench 6.0.1.

Metagenomic Identification of Endosymbiont and Pathogen Transcripts

The bacterial endosymbiont, Buchnera aphidicola, was identified from a BLASTn search against Buchnera (Taxid: 32199) in NCBI using the assembled A. craccivora contigs as queries. The A. craccivora contigs with relevant hits to Buchnera were extracted and further confirmatory analysis was performed using InterProScan on Blast2GO v2.6.5, and the associated KEGG pathways were investigated also using Blast2GO v2.6.5.

Data Deposition

The raw Roche 454 sequence data were submitted to the National Center for Biotechnology Information (NCBI) Sequence Read Archive (SRA) with accession numbers of SRR768514, SRR768515, SRR768524 and SRR768525 for A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti, respectively. The Transcriptome Shotgun Assembly project for the four insect species were submitted to DDBJ/EMBL/GenBank under the accession numbers of GAJV00000000, GAJW00000000, GAJX00000000 and GAJY00000000 for A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti, respectively. The version of the TSA accession numbers described in this paper is the first version for each of the four species.

Development of Reference Transcriptome Sequence Assemblies

Normalized species-specific libraries were successfully constructed from mRNA isolated from pooled samples of all tissues and pooled adult and larval life stages. A total of 319,126, 176,262, 320,722 and 227,882 raw reads were respectively obtained from these A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti libraries. The bacterial and human contaminants discovered by DeConSeq were negligible across the four insect species. Seventeen, 2, 11 and 37 contigs were identified by DeConSeq as contaminants in A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti, respectively and were also subsequently removed from the transcripts. The remaining statistics for sequence and contig assemblies are reported in Table 1. After assembly and decontamination, the mean contig length ranged from 669.8 to 688.1, from which ORFs with a mean length of between 498.5 and 524.5 bp was predicted (Table 1).

Functional Gene Annotation

ORFs were predicted from ≥ 98% of A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti transcripts, and respectively showed mean lengths of 498.5, 514.3, 524.5 and 508.8 bp (Table 1). Blast2GO output indicated that BLASTx hits were obtained for 6,430 (55%), 7,647 (79.9%), 6,839 (64.2%) and 4,292 (58.4%) contigs in A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti, respectively. The contigs with significant BLASTx matches were assigned GO terms into molecular function, biological process, and cellular components (Tables S1a to S1d). The functional classification based on molecular function, biological process and cellular component are represented in Figures 2a to 2d. In the molecular function category, the most highly represented were assigned to binding (13.7% for A. curvipes, 13.6% for A. craccivora, 13.4% for C. tomentosicollis and 13.5% for M. sjostedti) and catalytic activity (14.4% for A. curvipes, 13.1% for A. craccivora, 14.9% for C. tomentosicollis and 13.5% for M. sjostedti). In the biological process category, the most highly represented were assigned to cellular process (4.7% for A. curvipes, 4.7% for A. craccivora, 4.7% for C. tomentosicollis and 4.7% for M. sjostedti) and metabolic process (5.4% for A. curvipes, 5.4% for A. craccivora, 5.8% for C. tomentosicollis and 5.6% for M. sjostedti) while in the cellular component category, the most highly represented were assigned to cell (9.3% for A. curvipes, 9.1% for A. craccivora, 9.5% for C. tomentosicollis and 9% for M. sjostedti) and cell part (8.2% for A. curvipes, 8% for A. craccivora, 8.3% for C. tomentosicollis and 8.2% for M. sjostedti) (Tables S1a to S1d).

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Figure 2. Gene ontology classification into biological process, cellular component and molecular function.

Gene ontology terms were determined using an e-value of ≤ 1.0 e-6 sorted based on level 2 classifications in all the contigs of (a) A. curvipes, (b) A. craccivora, (c) C. tomentosicollis, (d) M. sjostedti.

https://doi.org/10.1371/journal.pone.0079929.g002

The majority of the top BLASTx hits in the four insect species were from insects. In A. curvipes, the most common were from Hemiptera [Riptortus pedestris (23.6%)], Coleoptera [Tribolium castaneum (7.1%)], Phthiraptera [Pediculus humanus (6.7%)] and another Hemiptera [Acryrthosiphon pisum (6%)] (Figure S1a). The most frequent hits from A. craccivora were from Hemiptera [A. pisum (83.7%)], two fungi species [Rhizopus delemar (1.5%); Batrachochytrium dendrobatidis (0.7%)] and Phthiraptera [P. humanus (0.5%)] (Figure S1b). The most frequent in C. tomentosicollis were from Hemiptera [R. pedestris (27.7%)], Coleoptera [T. castaneum (7.7%)], another Hemiptera [A. pisum (7%)] and Phthiraptera [P. humanus (6.7%)] and (Figure S1c) while the most frequent in M. sjostedti transcripts were from Coleoptera [T. castaneum (9.7%)], Phthiraptera [P. humanus (8.4%)], Lepidoptera [Danaus plexippus (6.5%)] and Hymenoptera [Nasonia vitripennis (5.6%)] (Figure S1d). BLASTx hits also revealed matches to other fungi species, bacteria, and a plant among A. craccivora contigs (Figure S1b), but these were not analogously observed within libraries from the other three insects.

Within the libraries constructed from A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti cDNA, a combined total of 23 candidate genes for detoxification, immunity and pathogen defense, development and communication were identified including cytochrome P450, glutathione s-transferase, esterase, cathepsin, heat shock protein, chitinase, defensin, c-Jun NH (2)-terminal kinase (jnk) stimulatory phosphatase, down syndrome critical region protein, epidermal growth factor, lysozyme, nimrod, nitric acid synthase, prophenol oxidase, ubiquinol cytochrome c reductase, peptidoglycan recognition protein, toll protein, chemosensory protein, juvenile hormone inducible protein, juvenile hormone esterase and juvenile hormone epoxide hydrolase, chemosensory binding protein as well as odorant binding protein (Figures 3a to 3d).

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Figure 3. Transcripts putatively involved in responses to xenobiotic (e.g., insecticide resistance) and disease transmission in (a) A. curvipes, (b) A. craccivora, (c) C. tomentosicollis, (d) M. sjostedti.

https://doi.org/10.1371/journal.pone.0079929.g003

Metagenomic Identification of Endosymbiont- and Pathogen-Derived Transcripts

Thirty six BLASTn hits to the NCBI nr protein database were identical to the primary endosymbiont of aphids, B. aphidicola, when transcripts from A. craccivora were used as queries of which 23 unique transcripts retrieved InterProScan annotations (Table S2) and nine were predicted to be involved in nine different bacterial biochemical pathways (Table 2). Transcripts from six different fungi species were also predicted among A. craccivora transcripts, including Rhizopus delemar and Batrachochytrium dendrobatidis (Figure S1b).

Prediction of Putative SNPs

All A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti contigs, that contained a putative ORF, were included in the SNP prediction pipeline (Tables S3a to S3d; Tables S4a to S4d). From these predictions, 256, 30, 225 and 63 contigs respectively from A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti had putative SNPs, which respectively contained a total of 742, 97, 607 and 180 putative SNPs (Tables S3a to S3d; Tables S4a to S4d). The mean depth of reads aligned to the reference transcripts depth for all putative SNPs was > 60 across all species (Table 3). The density of SNPs within transcripts was measured by estimates of mean number of putative SNPs per kilobase, and were all less than 1 (0.09, 0.02, 0.08 and 0.04 respectively among A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti contigs) (Table 3). The alternate ≥ 10% coverage cut off we used comparatively predicted 2,703, 340, 2,087 and 780 putative SNPs for A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti, respectively. As a consequence of 454-based sequence by synthesis methods used, resulting reads are prone to sequencing errors known as homopolymers which comprise imprecise nucleotide numbers in long arrays of the same nucleotide. These errors can cause misalignment within contig assemblies such that incorrect SNP predictions can result in sequence regions flanking the homopolymer stretch. To compensate for these errors, the assembled contigs were filtered for 454/Ion homopolymer INDELS in the SNP detection software in the CLC Genomics Workbench before performing the SNPs prediction. To understand the effects of SNP mutations and associate them to the different transcripts obtained in our study, we differentiated synonymous SNPs from non-synonymous SNPs. Of the total number of SNPs obtained in the four insect species, there were 425, 72, 419 and 97 synonymous SNPs respectively in A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti and respectively 317, 25, 188 and 83 non-synonymous SNPs. In all four species, transitions were more frequent than transversions (Ts/Tv > 1) (Table 3).

Development of Reference Transcriptome Sequence Assemblies

Next generation sequencing technologies offer a rapid entry point into genomic research [44] and can generate valuable molecular resources for non-model species [35,54] that are a foundation from which a diversity of research questions can be addressed [54,55]. In the absence of complete genome sequences, transcriptome sequencing remain a useful molecular resource that can be applied to the identification of candidate insecticide resistance genes and mutations that can be developed into genetic markers for population genetic studies [28], as well as the identification of potential targets for RNAi knockdown. The Roche 454 platform provides long sequence read lengths that may better allow the assembly of de novo transcriptomes [54], but remain susceptible to sequencing errors in homopolymer regions. The Roche 454 transcriptome data presented in this study from A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti had a high median length (≥ 680 bp), and a majority of resulting contigs encoded a predicted ORF (= protein coding sequence, CDS). Despite this, a high number of contigs (> 35%) had ORFs with no amino acid similarity to known proteins within the NCBI nr database and was especially the case for A. curvipes, C. tomentosicollis and M. sjostedti transcripts. However, only 20.06% of the A. craccivora contigs had no similarity to known proteins in the NCBI nr database. Annotation of previous transcriptome assemblies have similarly revealed a high number of contigs with genes of unknown function [56-59] which may represent novel uncharacterized genes and reflect the limitation of inferring transcript functions by comparison to model species that have long evolutionary distances to the non-model species in question [60]. Even within whole genome sequence assemblies, species-specific genes can comprise a high percentage of predicted ORFs [61]. The presence of these genes of unknown function could similarly suggest these proteins may be species-specific and, that de novo transcriptome assemblies from non-model insect pest species are useful for phylogenetic novel gene discovery. Furthermore, the resulting assembly of sequence data allow for the identification of novel gene pathways that have potentials for RNAi targeting within a suite of species-specific control tactics.

Functional Annotation

Functional annotations of assembled A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti transcripts allowed for the identification of candidate genes encoding proteins putatively involved in insecticide resistance, and pathogen defense and immunity. Transcriptomic approaches are powerful tools to identify new genes and gene functions and have been successfully applied to many organisms. In this study, we have identified genes putatively involved in the response to and the detoxification of xenobiotics in the four insect pests. Some of these xenobiotic response/detoxification genes will likely be useful for the study of chemical insecticide resistance traits as well the role in detoxification following exposure to plant allelochemicals. For example, strains of A. craccivora have elevated esterase activities that were linked to increased resistance to the nicotinic acetylecholine receptor agonist, dinotefuran, which belongs to the third generation of neonicotinoids [62]. Our results will provide a foundation that makes the future study of the involvement of these candidate genes in field-observed insecticide resistance traits in these insects more likely, and may also represent genetic markers that can be used to screen field populations (and compare resistant vs. susceptible individuals) to determine linkage (or not) of the locus to the resistant phenotype trait.

Our current understanding of insect immunity and stress responses comes from holometabolous insects and includes flies, butterflies, beetles and bees [63]. The four insect pests under study in this paper are all hemimetabolous insects with three of them (A. curvipes, A. craccivora and C. tomentosicollis) falling into the same insect order of Hemiptera and the fourth insect M. sjostedti falling into the insect order, Thysanoptera. Because all studied species exhibit incomplete development, comparison with the genome of a hemimetabolous insect (i.e., pea aphid, A. pisum) may provide insights into immunity and defense mechanisms in these pest insects. It is also interesting to note that while the four insect species included in this study were not intentionally immunologically challenged, we still observed some transcripts putatively involved in insect defense and immunity based on studies conducted on other insects such as A. pisum. We did not observe as many immunity and defense transcripts in both A. craccivora and M. sjostedti as we observed in A. curvipes and C. tomentosicollis. The immune genes observed in this study include most genes involved in the IMD pathway in insects and includes chitinase, defensin, down syndrome critical region protein, epidermal growth factor receptor, jnk stimulatory phosphatase, lysozyme, nimrod, nitric oxide synthase, odorant binding protein, peptidoglycan-recognition protein and pro-phenol oxidase. We also observed genes involved in toll signaling pathway. It is interesting to note that none of these genes are represented across all the four insect pests. Some insects have particular genes that others lack, and vice versa. For example, A. craccivora appears to be missing the defensin gene, however, a lack of such a gene would have to be verified in the future if a genomic project were to occur for this species. This is consistent with studies conducted on A. pisum, which shows the pea aphid is lacking many of the antimicrobial peptides, such as defensin, common to other insects [64]. The reduced humoral immune system in A. pisum, including an apparently non-functional IMD signaling pathway and absence of PGRPs, has been suggested to be an adaptation for the symbiosis with the bacterium B. aphidicola [65]. The presence of defensin in the human louse, P. humanus and in the ancient apterygote insect, the fire brat, Thermobia domestica [66], suggests that defensins may have been lost during aphid evolution.

Prediction of Putative SNPs

Single nucleotide polymorphisms are rapidly becoming the marker of choice for many applications in population ecology, evolution and conservation genetics, because of the potential for high genotyping efficiency, data quality, genome-wide coverage and analytical simplicity (e.g. in modeling mutational dynamics) [42]. Transcriptome-derived SNPs have several advantages over those developed from genomic sequences [67–69], including acquisition of actual gene sequences that allow for direct mapping and comparative genome studies among organisms ([70] and references therein). SNPs derived from transcriptomes are also a source of candidate polymorphisms underlying important traits that can lead to the identification of quantitative trait nucleotides (QTN) [71] linked to ecologically relevant genes. The applicability of SNPs from sequence data for marker development has been previously reported [72–74] and has been applied for the genetic mapping of insect orders such as Lepidoptera (Bombyx mori [75]), and for population genetics of the Glanville fritillary butterfly, Melitaea cinxia [76]. The current study provides a set of at least 742, 97, 607 and 180 putative SNPs respectively for A. curvipes, A. craccivora, C. tomentosicollis and M. sjostedti (predicted using the criteria that SNPs be present in ≥ 35% of aligned reads), and the segregating mutations that can be developed into molecular genetic markers for the study of the population genetic structure of these insect pests. Although a greater number of putative SNPs were predicted using a more lenient coverage cut off value of 10%, these loci may be prone to type I error and secondary validation methods may likely be required to distinguish these from sequencing errors.

The frequency of SNPs in laboratory strains of Drosophila was reported at 5 SNP per kilobase [77] and at 1.3 SNPs per kilobase in the inbred Dazao strain of Bombyx mori [78]. Similarly, laboratory strains of the malaria mosquito, Anopheles funestus, were reported to have 7.2 SNPs per kilobase [79], and 8.0 SNPs per kilobase in An. gambiae [80]. Compared to the results obtained from the above studies, we did observe a lower amount of SNPs per kilobase in the present study. Although laboratory strains were used in those studies, we used field-collected insects in our study and usually a reduced SNP frequency is reported in laboratory strains because homozygosity may be increased by the effects of inbreeding or random genetic drift. Non-synonymous SNPs have commonly been reported to occur less frequently than synonymous SNPs, and is presumably due to the evolutionary constraints of negative selection that may eliminate deleterious substitutions from the population [81]. Non-synonymous SNPs are of particular interest because they are more likely to affect the function of the encoded protein and may influence phenotype. It has been estimated that 20–30% of non-synonymous SNPs affect protein function [82,83]. In our study, we did observe a higher number of synonymous SNPs than non-synonymous SNPs across transcripts from all the four insect species. In metazoan DNA sequences, an excess of transition vs. transversion mutations is often observed. This may be partly due to the relatively high rate of change of methylated cytosines to thymine, as well as post-mutation processes of selection on codon-usage bias within coding regions [84]. The role of population genetic and biochemical effects on the rate and direction of nucleotide changes remains unknown, but are likely factors that affect the observed level of SNP allele frequencies within natural populations.

Metagenomic Identification of Endosymbiont- and Pathogen-Derived Transcripts

Aphids are sap-feeding insects that infest a wide range of plant species. Although sap fluids from plant phloem contain high concentrations of carbohydrates, they are deficient in nitrogenous nutrients such as specific amino acids [85,86]. To overcome these nutritional deficiencies, species within Aphidoidea have established mutualistic relationships with the obligate intracellular endosymbiont, B. aphidicola [87,88]. Buchnera endosymbionts produce essential amino acids that cannot be synthesized by aphids or obtained in sufficient quantities from plant saps [65,87]. In return, aphids provide Buchnera with other nutrients required to survive [89]. Relationships between these two groups have existed for approximately 150 to 200 million years [90] resulting in drastic Buchnera genome reductions due to the loss of many genes needed for independent life and has led to the inability to survive outside host cells [91]. Therefore, aphids and associated Buchnera symbionts may be inseparable mutualistic partners. We observed 36 B. aphidicola transcripts among BLASTn hits to our A. craccivora transcripts. These 36 B. aphidicola transcripts were annotated from twelve different strains of B. aphidicola. We also observed ubiquinone in the BLASTx search of A. craccivora. Symbiotic B. aphidicola are aerobic bacterium which, due to gene reduction in metabolic pathways, cannot carry out respiration without obtaining gene products from the host [92]. The electron transport chain consists of a primary dehydrogenase and a terminal reductase, which are linked by ubiquinone [93]. Ubiquinone is an essential redox component of the aerobic respiration of bacteria and mitochondria [94], and participates in the transfer of electrons and hydrogen between flavoproteins and cytochrome b in the respiratory chain. Also, one of the 36 A. craccivora contigs with hits to B. aphidicola was annotated as the gene symbionin, which has been reported to increase the transmission of plant viruses by binding to the read-through domain of the viral coat protein [95]. Further study of these genes may likely lead to a better understanding of symbiosis and plant disease transmission by A. craccivora, and may lead to potential tactics to reduce or eliminate the disease vectoring capacity of A. craccivora.

Additionally, we observed BLASTx hits to six fungi species among A. craccivora sequences. Rhizopus oryzae (R. oryzae has been reclassified to include R. oryzae and R. delemar [96]. Rhizopus delemar was observed in the BLASTx hits in this study) was previously reported to be an entomopathogenic fungal species [97]. Batrachochytrium dendrobatidis causes chytridiomycosis and is a major cause of amphibian population decline worldwide [98] and the sequences within our aphid transcripts may be derived from a related fungal species that is capable of infecting A. craccivora in West Africa. In contrast, Melampsora larici-populina is a cause of rust in poplar trees [99]. These may have resulted from environmental contamination or were present within gut contents of whole aphids that were used for library preparations. These results suggest that application of NGS may be used for the metagenomic identification of putative pathogen species, which in turn may be useful for the biological control of pest insect species.