Transcriptome of the adult female malaria mosquito vector Anopheles albimanus
- Jesús Martínez-Barnetche1Email author,
- Rosa E Gómez-Barreto1,
- Marbella Ovilla-Muñoz1,
- Juan Téllez-Sosa1,
- David E García López1,
- Rhoel R Dinglasan2,
- Ceereena Ubaida Mohien2, 3,
- Robert M MacCallum4,
- Seth N Redmond5,
- John G Gibbons6,
- Antonis Rokas6,
- Carlos A Machado7,
- Febe E Cazares-Raga8,
- Lilia González-Cerón9,
- Salvador Hernández-Martínez1 and
- Mario H Rodríguez López1
© Martinez-Barnetche et al.; licensee BioMed Central Ltd. 2012
Received: 15 February 2012
Accepted: 30 May 2012
Published: 30 May 2012
Human Malaria is transmitted by mosquitoes of the genus Anopheles. Transmission is a complex phenomenon involving biological and environmental factors of humans, parasites and mosquitoes. Among more than 500 anopheline species, only a few species from different branches of the mosquito evolutionary tree transmit malaria, suggesting that their vectorial capacity has evolved independently. Anopheles albimanus (subgenus Nyssorhynchus) is an important malaria vector in the Americas. The divergence time between Anopheles gambiae, the main malaria vector in Africa, and the Neotropical vectors has been estimated to be 100 My. To better understand the biological basis of malaria transmission and to develop novel and effective means of vector control, there is a need to explore the mosquito biology beyond the An. gambiae complex.
We sequenced the transcriptome of the An. albimanus adult female. By combining Sanger, 454 and Illumina sequences from cDNA libraries derived from the midgut, cuticular fat body, dorsal vessel, salivary gland and whole body, we generated a single, high-quality assembly containing 16,669 transcripts, 92% of which mapped to the An. darlingi genome and covered 90% of the core eukaryotic genome. Bidirectional comparisons between the An. gambiae, An. darlingi and An. albimanus predicted proteomes allowed the identification of 3,772 putative orthologs. More than half of the transcripts had a match to proteins in other insect vectors and had an InterPro annotation. We identified several protein families that may be relevant to the study of Plasmodium-mosquito interaction. An open source transcript annotation browser called GDAV (Genome-Delinked Annotation Viewer) was developed to facilitate public access to the data generated by this and future transcriptome projects.
We have explored the adult female transcriptome of one important New World malaria vector, An. albimanus. We identified protein-coding transcripts involved in biological processes that may be relevant to the Plasmodium lifecycle and can serve as the starting point for searching targets for novel control strategies. Our data increase the available genomic information regarding An. albimanus several hundred-fold, and will facilitate molecular research in medical entomology, evolutionary biology, genomics and proteomics of anopheline mosquito vectors. The data reported in this manuscript is accessible to the community via the VectorBase website (http://www.vectorbase.org/Other/AdditionalOrganisms/).
KeywordsAnopheles albimanus Transcriptome Malaria RNA-Seq
Human malaria transmission is dependent on efficient development of Plasmodium parasites within anopheline mosquito vectors. Anopheline mosquitoes are a large subfamily comprising nearly five hundred species distributed in subtropical and tropical areas around the world, but only a small percentage (10-20%) are malaria vectors . Intriguingly, malaria infection rates among anopheline species do not correlate with mosquito phylogenetic relationships, suggesting that genetic traits associated with vectorial capacity have quickly and independently evolved in different species .
Vectorial capacity is a highly complex biological phenomenon depending on mosquito behavior, lifespan and innate refractoriness or susceptibility to Plasmodium infection, which may result from the co-evolutionary forces driving the tripartite interaction between humans, mosquitoes and parasites . As a result of the sequencing of the Anopheles gambiae and Plasmodium falciparum genomes, a great deal of information regarding our understanding of mosquito-pathogen interactions at a molecular level has been gained [4, 5]. Post genome research has highlighted the role of the An. gambiae innate immune response in determining mosquito refractoriness to Plasmodium[6–8].
In addition to the mosquito’s innate ability to transmit malarial parasites, critical aspects of mosquito biology, like adaptation to diverse niches, host seeking behavior, and resistance to insecticides are still unknown. Novel strategies for control, based on a deep understanding of mosquito biology and evolution, will be required to achieve the goal of eventual malaria eradication. Rapid technological advances in DNA sequencing, protein characterization by mass spectrometry and bioinformatics offer unique opportunities to generate large catalogs of genes, proteins and biological networks that may enable the identification of potential mosquito control targets beyond the An. gambiae-P. falciparum dyad , which can be harnessed by novel strategies such as transgenesis, mosquito-based transmission blocking vaccines [10, 11] and alternative insecticides .
Plasmodium vivax malaria still represents a major health and socio-economic burden in Asia, the Western Pacific and the Americas [13, 14]. Malaria in the Americas is transmitted by several anopheline species, including species belonging to the Nyssorhynchus subgenus, which is unique to the New World. Anopheles (Nyssorhynchus) albimanus is a major vector in southern México, Central America and the northern region of South America [15, 16]. The Nyssorhynchus subgenus is thought to be the earliest diverged branch of the anopheline radiation, which probably occurred more than one hundred million years (My) ago when the supercontinent Gondwana separated to give rise to the actual South American and African continents . The proposed independent emergence of vectorial traits in conjunction with their rapid evolution may imply different molecular strategies involved in P. vivax and P. falciparum refractoriness and susceptibility in this subgenus. However, very little molecular information exists for any of the New World anopheline vectors, except for Anopheles (Nyssorhynchus) darlingi whose genome draft was recently released . The An. albimanus genome is scheduled for genome sequencing in the near future .
We describe herein the results of a gene discovery based cDNA sequencing project combining conventional Sanger with Next Generation Sequencing (NGS) platforms to analyze cDNA samples derived from An. albimanus tissues including the midgut, cuticular fat body, dorsal vessel and salivary gland, which are critical organs involved in the Plasmodium life cycle [6, 19, 20] (Hernández-Martínez, Unpublished observations). The main objective of our study was to construct a reference transcriptome that will facilitate molecular and applied studies of An. albimanus refractoriness to Plasmodium infection and other biological processes relevant for disease transmission. Finally, to maximize accessibility for this and future transcriptome sequencing projects in the absence of a genome sequence, we developed an open-source sequence annotation browser called GDAV (Genome-Delinked Annotation Viewer; http://funcgen.vectorbase.org/gdav). The An. albimanus transcriptome annotations are available via the VectorBase website (http://www.vectorbase.org/Other/AdditionalOrganisms/).
Results and discussion
The An. albimanus transcriptome assembly
Libraries, sequencing metrics and assembly
A: Tissue and sequencing platform
Abdominal cuticle a
Whole female b
210 x10 6
B: Transcript composition
Transcripts with Illumina reads
Transcripts with 454 reads
Transcripts with Sanger reads
C: Transcript assembly summary
Total bases (Mbp)
Mean contig length (bp)
An initial transcriptome assembly was performed by combining all sequence reads described in Table 1A, which generated 15,764 contigs. Re-mapping the Sanger and 454 reads to the initial assembly revealed that a substantial number of 454 (53%) and Sanger reads (44%) were not represented in the initial transcriptome assembly, so they were re-assembled using GS Assembler, generating an additional set of 935 contigs. The total transcript dataset included 16,699 contigs with a mean contig length of 970 bp and a N50 of 1,434 bp (Table 1C). Our assembly metrics closely resemble the recently published NGS and Sanger data on the An. funestus transcriptome, which yielded 15,527 contigs with a N50 of 1,753 bp . Similar results were also reported in de novo transcriptome assembly studies for the planarian worm, Schmidtea mediterranea in which 454 reads were pre-assembled to serve as scaffolds for Illumina paired-end assembly, yielding 17,465 contigs with a N50 of 1.6 kb , and 18,619 contigs with a mean length of 1,118 bp .
Genome mapping results to An. gambiae and An. darlingi
Transcript mapping to Anopheles genomes a
Aligned bases (Mbp)
Number of transcript with introns
Transcripts mapping to genes
Single transcript per An. gambiae gene
Single Illumina-only per An. gambiae gene
Single composite per An. gambiae gene
An analysis of the protein length coverage for An. albimanus-An.gambiae BLASTX alignments showed a considerable proportion of transcripts with only partial coverage of their corresponding An. gambiae match (Figure 2B), indicating the possibility of multiple hits per An. gambiae gene. The extent of multiple transcripts mapping to a single An. gambiae gene was estimated by comparing transcript to genome and An. gambiae gene coordinates. Anopheles albimanus transcripts mapped partially or fully within the sequences of 6,305 An. gambiae genes, and 62% of these transcripts did so within a single An. gambiae gene (Table 2. Figure 2C). Based on our protein length coverage observations (Figure 2B), we noted a higher proportion of single gene hits in the composite subset (80%) than in the Illumina-only subset (68%) (Figure 2C).
As an additional approach to estimate transcript completeness, we used reference genome mapping to analyze exon coverage. As expected from the phylogenetic relationships, transcript mapping to the An. darlingi genome showed higher average exon coverage (2.1 exons per transcript) than to the An. gambiae genome (1.9 exons per transcript), which falls below the 4.4 exons per transcript in An. gambiae (Figure 3C). However, there was no proportional difference in the exon coverage using An. gambiae or An. darlingi relative to the number of significant alignments (data not shown). More than half (54.1%) of our mapped transcript dataset covers at least two exons, whereas in An. gambiae, more than 86% of the genes are composed of at least two exons (Figure 3C). Only ten and thirty-one transcripts that mapped to An. gambiae and An. darlingi, respectively, had more than 10 exons, compared to 742 for An. gambiae. The An. albimanus transcript that covered most exons (23) when mapped to the An. darlingi genome was Locus_3073_Length_3,997, and corresponds to the An. gambiae AGAP000009 homolog, which is predicted to have 25 exons (data not shown).
In summary, transcript mapping to reference genomes and the derived analysis of exon structure of our transcript dataset revealed a degree of incompleteness when using An. gambiae as our reference. The increased proportion of genome alignments without a spanning intron (single exon transcripts) observed in An. albimanus could result from incorrect splitting of the transcript during the assembly of transcriptional units having more than one exon. Correct exon representation is relevant because alternative splicing is a means to increase proteome diversity and this phenomenon has been observed frequently among dipterans [29, 30]. Incomplete exon-exon structure across An. albimanus transcripts could underestimate the diversity of protein configurations and thus, may limit protein identification by proteomic approaches in the absence of the genome, and empirical studies to assess this possibility are required to fill in this gap in knowledge. Despite the limitations in our dataset, information regarding exon-exon structure may be useful for experimentalists when designing primers and probes for one gene-targeted analysis.
Estimated proteome coverage
As a starting point for transcript annotation, the proportion of the An. albimanus transcriptome that was homologous to a predicted protein sequence in other genomes was analyzed. Protein similarity to other insect proteomes and the NCBI nr databases was assessed using BLASTX (using an e-value threshold of 1.0E-5). A total of 10,000 sequences (62%) in our dataset had a significant match with at least one species. However, we note that probably due to methodological differences, this proportion is lower than the 84% match described by Crawford, when the An. funestus transcriptome was compared with the An. gambiae proteome .
BLASTX comparisons to other Insect predicted proteomes
An. albimanus matchs
Average identity %
Median Identity (%)
Reference proteome size
Reference Proteome coverage (%)
Considering the total amount of protein coding genes in each of the sequenced vector genomes, 51% of An. gambiae and 48% of the An. darlingi protein coding genes matched at least one transcript in An. albimanus, whereas An. darlingi covered 62% of the An. gambiae proteome. Proteome coverage tended to decrease according to phylogenetic distance (Figure 4B). However, the proportion of significant best hits decreased according to phylogenetic relatedness, so that protein percent identity among best BLASTX hits was the highest with An. darlingi (average identity 85%), and decreased according to phylogenetic distance (Table 3. Figure 4A-B).
The lower number of transcript matches observed between An. albimanus and An. darlingi than between An. albimanus and An. gambiae is likely the consequence of both the incompleteness of the An. albimanus dataset due to sampling of only a limited set of tissues from adult mosquitoes, and the current incomplete assembly status of the An. darlingi genome (Figure 4B). Moreover, the An. gambiae genome annotation relied heavily on homology based annotation approaches , and thus is very conservative. This implies that rapidly evolving genes may escape identification by such conservative approaches. Combining conservative and ab initio gene prediction strategies increased considerably the amount and quality of the An. gambiae protein coding genes . Given the fact that most of the An. albimanus transcripts mapped to the An. darlingi genome, many transcripts may in fact be derived from true protein coding genes. Additionally, many of the sequences could represent non-protein coding transcripts of potential biological significance .
Proportion of the core eukaryotic genome
CEGs in 1:1:1 BRH dataset
CEGs in 1:1 BRH.An. albimanus
CEGs in 1:1 BRH.An. gambiae
CEGs in 1:1 BRH.An. darlingi
To further validate the accuracy of our ortholog assignment, we compared protein length coverage, using pair-wise alignments between translated An. albimanus proteins and their corresponding best match in An. gambiae. A considerable improvement of protein length coverage was observed in orthologs (average protein length coverage was 74%), when compared to the protein coverage of the overall dataset (average protein length coverage of 53%). As described previously (Figure 2B), protein coverage displayed a bimodal distribution where 40% of the translated An. albimanus products covered at least two thirds of their corresponding An. gambiae matches and another 40% covered less than one third (Figure 5B). A significant and expected improvement was observed in the ortholog dataset, which was biased toward higher coverage, resulting in 66% of the orthologs covering more than two thirds of their corresponding An. gambiae matches (Figure 5B).
If our BLAST best reciprocal hit ortholog prediction strategy was accurate, we would expect that all the core eukaryotic genes (CEGs) found would be represented in the 1:1:1 ortholog dataset. As shown in Table 4, only 283 of the identified An. albimanus CEGs were included in the three species ortholog dataset, which corresponds to 61% of the core eukaryotic genome. However, the proportion of CEGs found between two species best reciprocal hits was higher and ranged from 70 to 83%. Together, our data indicate that although there is a relatively high coverage of the core eukaryotic genome, the anopheline ortholog assignment remains incomplete (i.e., it is missing a considerable amount of true orthologs), and may be inaccurate (i.e., includes a significant proportion of paralogs).
Functional annotation of the An. albimanus transcriptome
To gain insight into the predicted functional characteristics of the current dataset, translated products were functionally annotated using the Gene Ontology (GO) classification as implemented in the Blast2GO software , as well as using the InterPro classification . A total of 5,086 transcripts were annotated according to biological process, and 5,792 transcripts were annotated according to molecular function, which corresponds roughly to one third of all the transcripts in the dataset for both categories, and to one half of the total BLASTX matches in the vectors’ predicted proteomes (Table 3).
According to molecular function, the best protein matches, those that were involved in translation, structural functions, calcium and actin binding were the most conserved, which agrees with the initial biological process categorization. The least conserved putative proteins were categorized as electron carrier and proteases, whose conservation was significantly lower than that observed for the translation, actin binding and calcium binding (P < 0.05) ontologies. Proteases were significantly less conserved than the whole set of annotated predicted proteins (Figure 6B). Proteases have been reported as being subjected to positive selection in the Drosophila genus . Also, trypsin family proteases have been significantly expanded in An. gambiae compared to D. melanogaster, suggesting faster evolution in anophelines that may be related to hematophagy [28, 39]. Similarly, electron carrier activity is related to cytochrome function and is overrepresented in our dataset. The cytochrome P450 family, involved in insecticide resistance, is also expanded in An. gambiae and may be also evolving rapidly in New World anophelines.
Top 50 InterPro Annotations in the An. albimanus transcriptome
Rank inAn. albimanus
Rank inAn. gambiae
Zinc finger, C2H2-type
Protein kinase-like domain
Serine/cysteine peptidase, trypsin-like
Major facilitator superfamily transporter
RNA recognition motif, RNP-1
ATPase, AAA + type, core
Glycoside hydrolase, catalytic core
Src homology-3 domain
Short-chain dehydrogenase/reductase SDR
Protein of unknown function DUF227
DEAD-like helicase, N-terminal
Small GTPase, Rho type
Glutathione S-transferase, C-terminal-like
Heat shock protein DnaJ, N-terminal
Concanavalin A-like lectin/glucanase
General substrate transporter
Cellular retinaldehyde-binding, C-terminal
Ubiquitin-conjugating enzyme, E2
Fibronectin type III domain
Chitin binding protein, peritrophin-A
Peptidase M1, membrane alanine aminopeptidase, N-terminal
Fibrinogen, alpha/beta/gamma chain, C-terminal globular
GPCR, rhodopsin-like superfamily
Carboxylesterase, type B
7TM GPCR, rhodopsin-like
Protease inhibitor I4, serpin
C-type lectin fold
Protein-tyrosine phosphatase, receptor/non-receptor type
Peptidase M14, carboxypeptidase A
Structurally, the DUF227 domain overlaps with the SCOP Protein kinase-like (PK-like) superfamily (IPR011009). The presence of DUF227 containing predicted homologs was investigated by querying electronically inferred orthology in the BioMart database  and found that DUF227 is present in a family of proteins well represented in dipterans, nematodes, and to a lesser extent in other insects, but absent in other invertebrates such as the sea urchin. The number of DUF227 containing orthologs according to BioMart decreased with phylogenetic distance so that between An. gambiae and Ae. aegypti there were sixteen 1:1 orthologs and between An. gambiae and D. melanogaster or Pediculus humanus there were only nine and five, respectively. Using VectorBase and MozAtlas for microarray data mining to identify significant changes in gene expression (P < 1.E-5) for those An. gambiae genes containing the DUF227 domain, we found predominant expression in the Malpighian tubules, midgut and head of adult mosquitoes, with expression levels higher in males than in females . In the midgut, 34 out of 43 genes had a significantly modified expression pattern after a blood meal . Five genes were enriched in hemocytes and another five were enriched in the carcass . Two genes were induced during P. berghei midgut invasion .
Conversely, certain annotations that are abundantly represented in An. gambiae such as Insect cuticle proteins (IPR000618); Tropomyosin (IPR000533); 7TM chemoreceptor (IPR013604); Mitochondrial Rho-like (IPR013684); Olfactory receptor, Drosophila (IPR004117); Pollen allergen Poa pIX/Phl pVI, C-terminal (IPR001778) were substantially scarce in our dataset (Table 5). As expected, olfactory receptors, 7TM chemoreceptors, and pollen allergen were underrepresented protein annotations since they are not expressed in the midgut . Similarly, insect cuticle proteins that are involved in adult cuticle synthesis show a peak during metamorphosis and are under-expressed in adults .
Immunity related genes
Mosquito immune responses are thought to play an important role in influencing vectorial competence. Higher protein divergence in genes implicated in stress response (Figure 6) is in agreement with the observation of higher divergence rate in immunity related genes (IRGs) than in genes involved in other core cellular processes [33, 36–38]. Thus, we searched for potential immunity related genes by comparing our transcript sequences to a manually curated dipteran IRG dataset, which includes 385 genes classified into 27 families implicated in recognition, regulation, signal transduction and effector phases of the immune response [38, 51]. We found 413 best BLASTX reciprocal matches between our dataset and the ImmunoDB, representing all 27 families. However, this number may be an overestimation of the true number of IRGs in our dataset, because it includes a large number of structurally homologous proteins that may not be involved in insect immune responses (for example many proteases and tyrosine kinases). To refine our IRG search, we considered a rather conservative approach that contemplated the putative orthology as described in the previous section (Figure 5A), as well as structural signatures derived from the InterPro annotation. Among our 3,772 ortholog 1:1:1 dataset, 79 ortholog groups have matches in the ImmunoDB (Additional file 1) and 73 were consistently supported by InterPro annotation or other protein family classification system. This set was further increased by the inclusion of three unannotated genes of the Toll and Imd pathways (TOLLPATH1 IMDPATH5 and IMDPATH8) with supporting structural evidence based on InterPro annotation. This 82 IRG putative ortholog dataset exhibited 75% average identity to their corresponding An. gambiae proteins, which is very similar to the average identity of all An. albimanus: An. gambiae matches. However, average identity was lower than the average identity of GOslim annotated ortholog proteins (84%).
Gene duplication has been a major evolutionary force shaping immunity related genes in dipterans . Thus, the identification of putative IRGs in our dataset based solely on the inclusion of ortholog groups may be missing putative IRGs. Thus, by considering InterPro annotations, we found representative matches in 25 out of 27 families, representing the recognition, signaling, regulation and effector immune response processes.
The major immune response signal transduction pathways in dipterans are the Toll and the Imd pathways. Gene members of these pathways tend to be better conserved in different mosquito species than genes implicated in the recognition or effector phases [38, 58]. Although transcripts containing LRR or Toll/interleukin-1 receptor homology (TIR) domain (IPR000157) were found, a clear Toll receptor homolog was not. However, we found important members of the Toll pathway such as PELLE MYD88 and TRAF6; the Imd pathway such as CASPAR IKK1 and IKK2 and STAT pathway such as DOME SOCS and STAT2[59, 60] (Additional file 1), as well as REL2 transcription factor .
Autophagy was originally described as a cellular response to starvation. However, it has recently been shown to be a critical process related to immune and stress responses, clearance of intracellular pathogens and damaged organelles, as well as cell survival. There are several genes involved in the induction of autophagy, autophagosome nucleation, autophagosome expansion and autophagosome recycling . There are 20 An. gambiae entries in the ImmunoDB related to autophagy. Given the importance of all the mentioned processes in malaria transmission, we searched the ImmunoDB for orthologs and found 12. In the induction of the pathway, only the TOR homolog was found. Similarly, the only homolog involved in the nucleation phase that we found was the BCL-2 homolog DEBCL (buffy in D. melanogaster) . The remaining ten corresponded to genes involved only in autophagosome expansion such as APG3 APG4A APG4B APG7A APG7B APG8 and APG16 orthologs or autophagosome recycling such as APG2 APG9 and APG18 (Additional file 1). In contrast, we found a relative depletion of caspases (only CASPS7 and CASPL1, of 14 caspases in An. gambiae) and the absence of caspase activators (AKR and Michelob_x), suggesting that, as in larvae midgut , autophagy could be a more active homeostatic tissue process than apoptosis in adult mosquitoes.
We have explored the adult female transcriptome of an important New World malaria vector, An. albimanus, by sequencing cDNA libraries generated from different tissue sources related to the Plasmodium life cycle such as midgut, cuticular fat body, dorsal vessel and salivary gland. Merging Sanger and NGS data into a single assembly generated a robust dataset with adequate transcript lengths that could be effectively mapped to the An. darlingi genome, covered 90% of the core eukaryotic genome and half of the predicted proteome of other mosquito vectors. We identified protein-coding transcripts involved in biological processes such as immune recognition, immune signaling pathways, insecticide resistance and autophagy that may be relevant to the Plasmodium cycle or may represent targets for novel control strategies. As a result of this work, the genomic information available for An. albimanus has increased several hundred-fold, thus providing molecular inputs for research in this species: 1) from a single gene perspective; 2) to gain insight into the anopheline radiations in the New World; 3) facilitating further genomic and proteomic approaches; and 4) assisting gene finding and validation of the An. albimanus genome in the context of the Anopheles cluster genome sequencing project . Sequence information, predicted proteome comparisons, transcript mapping to the An. gambiae genome and InterPro annotations described in this manuscript are accessible to the community through the VectorBase website (http://www.vectorbase.org/Other/AdditionalOrganisms/).
Materials and methods
Mosquitoes and mosquito infections with P. vivax
All the mosquito samples used in the present work were 3-5 day post-emergence female An. albimanus of the white-stripe strain  obtained from the insectary of the National Institute of Public Health (INSP) in Cuernavaca, México. Mosquitoes were fed with 10% sucrose ad libitum and reared in a 12:12 h light cycle maintained at 28 °C and 80% relative humidity.
Mosquito infections with P. vivax CSP-VK210 and extraction of midgut epithelium of 24 h and seven days after an infectious blood meal were performed as described  in the insectary of the Centro Regional de Investigación en Salud Pública (CRISP) in Tapachula, Chiapas, México, according to Institute ethical guidelines and approval.
cDNA libraries for Sanger sequencing
To capture transcripts from mosquito organs that are relevant for the Plasmodium sp life cycle, three cDNA libraries were generated for Sanger sequencing: A sucrose-fed female midgut (site of invasion) and a salivary gland (site of sporozoite maturation and inoculation to vertebrate host) cDNA libraries were constructed from 5 μg of total RNA. cDNA was ligated to Uni-ZAP XR vector (Stratagene). The phage library was mass excised and plated into LB-agar plates. Individual colonies were replicated in 384-well plates. A third cDNA library was constructed from 0.5 μg of Poly A + RNA extracted from whole female An. albimanus 12 h after inoculation with 0.0004 OD of Serratia marcescens in the hemocoel, which elicits an immune response that limits the development of P. vivax. cDNA synthesis and library construction was done using the Creator SMART cDNA Library Construction Kit (Clontech) according to the manufacturer instructions. The library was transformed in Escherichia coli by electroporation and plated in LB-Agar with chloramphenicol (30 μg/mL). Individual colonies were replicated in 384-well plates.
Template preparation and Sanger sequencing
E. coli clones were inoculated in CIRCLEGROW® (Krackler scientific) liquid media with either chloramphenicol (pDNA-lib) or ampicilin (pBluescript) at 37 °C in 96-well plates for 16 h. Plasmid DNA was prepared by alkaline lysis in Millipore filters and ethanol-precipitated and suspended in sterile deionized water. Sequencing was performed with fluorescent dye terminators in a 3100 Genetic Analyzer (Applied Biosystems).
Raw chromatogram files were quality assessed and trimmed with Phred using the trim_alt command with default parameters  and then converted to FASTA files using PH2FASTA. Vector sequence and linker sequences were removed using CrossMatch  and SeqClean . Identification of mitochondrial and ribosomal protein transcripts was done by BLASTn searches to mosquito mitochondrial genomes or ribosomal protein sequence databases and filtered out. ESTs were submitted to dbEST at NCBI (Accession Numbers EV406110.1 - EV410194.1).
Abdominal cuticles and the underlying fat body were obtained from 20 female adult mosquitoes and total RNA was extracted with TRIzol (Life Technologies). Integrity of RNA was verified in the Agilent Bioanalyzer standard RNA chip. One μg of RNA was used for full length RT-PCR amplification using the Super-SMART PCR cDNA synthesis kit (Clontech) according to the manufacturer’s instructions. The PCR amplified cDNA library was fragmented by nebulization and subjected to library preparation according to the 454 shotgun sequencing protocol. After emulsion PCR titration and amplification, the library was sequenced in a full picotiter plate using the Genome Sequencer FLX platform. A similar approach was used to generate additional midgut libraries from P. vivax infected-mosquitoes at 24 h post-infective blood meal (PIBM) and seven days PIBM, but sequenced as pooled bar-coded libraries in half picotiter plate. A third sequencing 454 run was performed with two cDNA libraries from dissected dorsal vessels, obtained at 18 h post-inoculation (intra-hemocoelic) with 0.25 μl of soluble fraction of zymosan (10 μg glucose-equivalents/ml, Sigma) as described  and saline-inoculated mosquitoes respectively. Dorsal vessels were collected in RNAlater (Ambion) and stored at -80°C. After RNAlater removal, total RNA was extracted with the RNAeasy Kit (Qiagen) and amplified with the SMARTER Pico PCR cDNA synthesis Kit (Clontech), and sequenced in a full picotiter plate (one region per library) using the GS FLX Titanium platform. Primer adaptors used for cDNA library generation were trimmed after signal processing using SeqClean. 454 sequence data was submitted to the Sequence Read Archive (SRA) (Accession number: SRA052091).
Total RNA from 50 An. albimanus midguts was extracted using TRIzol, DNased and cleaned with an RNAeasy column (Qiagen) according to the manufacturer’s instructions. Total RNA was then quality controlled for integrity on a Bioanalyzer (Agilent Technologies). mRNA libraries were constructed and sequenced, as previously described [72–74] on a single lane of a Illumina HiSeq 2000, which generated ~210 million 101 bp paired end reads. Illumina sequence data was submitted to the Sequence Read Archive (SRA) (Accession number: SRA051893).
The entire Illumina read set was split into eight equal sized read sets. Each one of these Illumina read sets was merged with the 454 and Sanger data and assembled using the Velvet  and Oases  software packages using three different kmer sizes (43, 45 and 47). The resulting contigs for each assembly were run again through Velvet and Oases to produce a final assembly. We then filtered the final assembly to retain only those loci that contained a single transcript, that were longer than 300 bp, and that had confidence scores of 1.0. To address which contigs contained 454 or Sanger reads, all 454 and Sanger reads were re-mapped to the initial assembly using the GS Reference Mapper v.2.5.3 using default parameters. Unmapped reads were re-assembled using the GS assembler v2.5.3 on cDNA mode to yield an additional set of 935 contigs.
The An. gambiae (AgamP3)  and An. darlingi genomes  were softmasked with RepeatMasker . An. albimanus transcripts were aligned to either genome using Exonerate v. 2.2  with the EST2 Genome mode, and a threshold score of 300, and maximum intron length of 20,000 bp.
Gene ontology annotations were performed using Blast2Go . For the Initial BLASTX against the NCBI-nr database the command-line option “-e1-e-6” was used. Additionally, transcripts were annotated according to the InterPro databases using InterProScan  in six-frame translation mode. Kruskal-Wallis test followed by Dunn’s correction was performed to calculate statistical differences within GO classes and protein percent identity with the Graph Pad PRISM software.
In silico proteome comparison
The entire assembled transcript dataset was used to search for the best hit homologous proteins (BLASTX cut-off e-value 1.0E-5) in the An. gambiae (AgamP3.6), Ae. aegypti (AaegL1.2); Culex quinquefasciatus (CpipJ1.2), P. humanus (PhumU1.2) and Ixodes scapularis (IscaW1.1) predicted proteomes present at VectorBase , as well as the An. darlingi and D. melanogaster proteomes. Ortholog prediction was done by performing BLASTX and TBLASTN bidirectional comparisons between An. albimanus An. darlingi and An. gambiae (e value 1.0E-5) to identify the best reciprocal hits within the three species.
To identify the proportion of the core eukaryotic genome covered by the An. albimanus transcriptome, we used HMM profiles corresponding to the 458 core eukaryotic proteins as provided by the CEGMA algorithm . Local HMMER3 searches  were calibrated using the An. gambiae core eukaryotic protein validated dataset consisting of 453 sequences . HMMER3 was performed using hmmscan command and the “-T 40” and “--domT 40” filters against the An. albimanus predicted proteome, as well as the predicted proteomes of An. darlingi An. gambiae Ae. aegypti C. quinquefasciatus and D. melanogaster.
Many web-based genome browsers [83–85] are available as open source software and are well suited to displaying transcript annotations. However they are heavily dependent on the availability of a genome sequence to act as a coordinate system. It is possible to adapt genome browsers to work without genomes  but it is not easy to keep them synchronized with developments in the “parent” software. In this work, we chose to develop a standalone “genome-free” web application, called GDAV (Genome-Delinked Annotation Viewer). It was designed with flexibility in mind; it can handle any kind of sequence annotations and integrates with genome browsers of closely related species via the DAS protocol . The free open source code is available at https://github.com/VectorBase/GDAV and the software was developed within the auspices of VectorBase .
The key to GDAV’s flexibility is its use of three simple, open text file formats for loading data: FASTA for sequences, tab-delimited files for annotations and GFF3 for genome alignments. Only the loading of one or more FASTA files is mandatory, thereafter zero or more annotation and alignment files may be loaded into GDAV’s small MySQL schema using the supplied Perl scripts. The annotation file consists of rows of data identified by the sequence ID in the first column, and subsequent named columns providing arbitrary text annotations. The Java-based web interface is simple to deploy within a Java web server such as Apache Tomcat. The web interface, with its integrated search facility, treats all annotations as plain text—no special treatment of numeric data (e.g. range queries or unit conversions) is provided. Link-outs to third party databases from specific columns containing suitable IDs are possible through the configuration file. A Java-based DAS server based on Dazzle  is bundled with GDAV. It can be used to display GFF3 file-derived gapped alignments (e.g. exon-intron structure) of the sequences stored in GDAV with respect to the genomes of one or more closely related species. Any alignment features shown via DAS in genome browsers link back to the sequence report page in GDAV.
In this study, the annotation files loaded into the system include the InterPro domain assignments and the BLASTX results providing “best hits” to several other proteomes. The GFF3-format exonerate alignments described above were also loaded into the system.
JMB conceived the study, participated in the generation of some cDNA libraries, performed data analysis, helped in designing web application specification and drafted the manuscript. MHR, RRD, AR and CAM contributed to study conception and design and helped drafting the manuscript. JGG performed transcriptome assembly. RMM performed InterPro annotation and in conjunction with SNR designed the web application specification and developed the web application, database and curation tools. CU, CAM and DEG participated in data analysis and interpretation. REG, JTS, MOM, LGC, SHM and FCR participated in mosquito experiments design, cDNA library generation, 454 and Sanger sequencing and data analysis. All authors read and approved the final manuscript.
β-glucan Binding Proteins
Core Eukaryotic Gene
Distributed Annotation System
Fibrinogen Related Protein
Genome De-linked Annotation Viewer
High Scoring Pair
Immune Response Genes
Leucine Rich Repeat Immune Protein
Leucine Rich Repeat
Next Generation Sequencing
Peptidoglycan Recognition Protein
We thank Gabriel Hernandez of ROCHE technical support for help with 454 sequencing; Travis Clark and Chelsea Baker of the Vanderbilt Genome Technology Core for help with Illumina sequencing; Bruno Arce for SQL database support, Bernardo Cortina and Kelly Scoggins for manuscript assistance; and Fidel de la Cruz Hernandez for critically reviewing the manuscript. The authors are very grateful to Imperial College London for high performance computing facilities. We also thank the anonymous reviewers for their suggestions improving the manuscript. This investigation received financial support from the UNICEF/UNDP/WORLD BANK/WHO Special Programme for Research and Training in Tropical Diseases (TDR), project ID: A50256 (for JMB) and CONACyT-SEP-2007SEP-62389 (for MHR); from the Bloomberg Family Foundation and the Johns Hopkins Malaria Research Institute (JHMRI) (for RRD) and grant HHSN268201000032C (N01-HV-00240) from NHLBI, NIH (CU); the Advanced Computing Center for Research and Education at Vanderbilt University. JGG is funded by the Graduate Program in Biological Sciences at Vanderbilt University and the National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH, NIAID: F31AI091343-01). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIAID or the NIH. Research in AR’s lab is supported by the Searle Scholars Program and the National Science Foundation (DEB-0844968). VectorBase is supported by National Institutes of Health/National Institute for Allergy and Infectious Diseases contracts HHSN266200400039C and HSN272200900039C). Experimental mosquito infections received support from the CONACYT SALUD-2004-C01-119 grant (for LGC).
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