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. 2011 Jun 17;4:203. doi: 10.1186/1756-0500-4-203

Expressed sequence tags from Atta laevigata and identification of candidate genes for the control of pest leaf-cutting ants

Cynara M Rodovalho 1, Milene Ferro 1, Fernando PP Fonseca 2, Erik A Antonio 3, Ivan R Guilherme 4, Flávio Henrique-Silva 2, Maurício Bacci Jr 1,✉
PMCID: PMC3132717  PMID: 21682882

Abstract

Background

Leafcutters are the highest evolved within Neotropical ants in the tribe Attini and model systems for studying caste formation, labor division and symbiosis with microorganisms. Some species of leafcutters are agricultural pests controlled by chemicals which affect other animals and accumulate in the environment. Aiming to provide genetic basis for the study of leafcutters and for the development of more specific and environmentally friendly methods for the control of pest leafcutters, we generated expressed sequence tag data from Atta laevigata, one of the pest ants with broad geographic distribution in South America.

Results

The analysis of the expressed sequence tags allowed us to characterize 2,006 unique sequences in Atta laevigata. Sixteen of these genes had a high number of transcripts and are likely positively selected for high level of gene expression, being responsible for three basic biological functions: energy conservation through redox reactions in mitochondria; cytoskeleton and muscle structuring; regulation of gene expression and metabolism. Based on leafcutters lifestyle and reports of genes involved in key processes of other social insects, we identified 146 sequences potential targets for controlling pest leafcutters. The targets are responsible for antixenobiosis, development and longevity, immunity, resistance to pathogens, pheromone function, cell signaling, behavior, polysaccharide metabolism and arginine kynase activity.

Conclusion

The generation and analysis of expressed sequence tags from Atta laevigata have provided important genetic basis for future studies on the biology of leaf-cutting ants and may contribute to the development of a more specific and environmentally friendly method for the control of agricultural pest leafcutters.

Background

The tribe Attini comprises over 200 ant species [1] which culture mutualistic fungi for their feeding [2]. The most evolutionary derived attines are the leaf-cutting ants in the genera Atta and Acromyrmex which are considered major herbivores in the tropics [3].

Some Atta species contributes to nutrient cycling, aeration and drainage of water in the soil [4], as well as maintenance of plant diversity [5,6]. Their nests were also found to host arthropods [7-9], reptiles and amphibians [4], and microorganisms [10-14].

However, despite of these ecological roles, many leafcutter species are considered agricultural pests which impose severe economic damages to agriculture [15,16]. Some of the characteristics contributing to the pest status of leafcutters are their ability of exploiting a great variety of plant species [17], reaching high population density [15] and long life spanning queens constantly laying eggs for up to 15 years [18].

Atta laevigata is a pest leafcutter distinguished by a very large and shiny head in soldiers, a characteristic which has rendered the species with the popular name "cabeça de vidro" (meaning glass head). It can be found in Venezuela, Colombia, Guyana, Bolivia, Paraguay and, in Brazil, from the Amazonian Rain Forest in the North to the Paraná state in the South [19]. It cuts leaves from many plantations, like pine tree [20], cocoa [21] and eucalyptus [22], as well as wide variety of native plants from different biomes such as the Cerrado or the Rain Forest, where its intense herbivory challenges reforestation of degraded areas [23,24].

The control of pest leafcutters in small properties can be done by biological methods [25] or even utilizing the waste material generated by the ants [26], but in extensive monocultures this control utilizes massive amounts of broad spectrum insecticides which are toxic to other animals and persist in the environment [27]. Thus, the development of a more specific and environmentally friendly process for controlling the leafcutters is required [28].

Genomic studies can contribute with that by characterizing genes involved in key functions for the leafcutters, like longevity, fertility and plasticity to exploit different vegetations, raising more specific targets for the ant control. Genomics is also a valuable resource for ecological and evolutionary studies of leaf-cutting ants.

In the present investigation, we carried out a genomic study in the pest leafcutter Atta laevigata by generating 3,203 expressed sequence tags (ESTs) which characterized 2,006 unique sequences (US). We postulate important differences in expression level among the transcripts and identified 146 potential target sequences for the control of pest leaf-cutting ants.

Methods

EST generation

Two grams of soldiers and major workers of Atta laevigata were macerated under liquid nitrogen, total RNA was extracted with the TRIzol method (Invitrogen, UK) and mRNA was purified using the PolyATract System (Promega, USA). The CloneMiner cDNA Library Construction Kit (Invitrogen, UK) and 2 μg of mRNA were utilized for the synthesis of first and second cDNA strands which were then size-fractioned in a 1.0 ml Sephacryl S-500 resin column, inserted in a pDONR222 plasmid (Invitrogen, UK) and transformed into DH10B Escherichia coli. Cells were plated onto solid Circle Grow medium (QBIO-GENE, Canada) containing 25 μg.ml-1 kanamicin and individually picked into a permanent culture plate with 96 wells. After 22 hours growth in liquid Circle Grow medium (25 mg.ml-1 kanamicin), plasmid DNA was purified by alkaline lysis [29] and sequenced in reactions containing 300 ng template DNA, 5 pmol M13 forward primer and the DYEnamic ET Dye Terminator kit reactant (GE Healthcare, UK), according to the manufacturer's protocol. The amplified products were resolved in a MEGA-BACE 1000 automated DNA sequence machine (GE Healthcare, UK).

EST analysis

The pipeline generation system EGene [30] was used to clean and assemble ESTs in contigs and singlets. Sequences were filtered by quality using phred values >20 and 90% of minimum identity percent in window. Filtered sequences were then masked against vector and primer sequences, selected by size (>100 bp) and assembled using CAP3 [31] with an overlap percent identity cutoff (p) of 90 and a minimum overlap length cutoff (o) of 50.

The program Blast2GO (B2G) [32] was used to associate every Atta laevigata singlet and contig to blastx [33] results (nr protein database; E-value ≤ 10-5), Gene Ontology (GO) terms [34], InterProScan classification [35,36] including signal peptide [37] and transmembrane regions predictions, Kyoto Encyclopedia of Genes and Genomes (KEGG) maps (http://www.genome.jp/kegg/), and Enzyme Commission (EC) numbers (IUBMB). The results generated by B2G and those obtained from Conserved Domain Database (CCD) were manually inspected, in order to group contigs and singlets in functional categories and to infer transcript abundance in Atta laevigata.

Results and Discussion

EST generation and assembly

The 5' ends of 4,704 clones from the Atta laevigata cDNA library were sequenced, resulting 4,482 reads. We were able to selected 3,203 of these reads, which presented high-quality and with average length of 418 bp (Table 1; [GenBank:JG659458 to JG662660, dbEST ID:73713535 to 73716737, Genome Project ID:63563]).

Table 1.

EST processing.

Sequence Number %
Reads 4,482 100.00
Filtered by quality 1,241 27.69
Filtered by size 38 0.85
High-quality (after filtering) 3,203 71.46
Unique Sequences (US) 2,006 100.00
Singlets 1,666 83.05
Contigs* 340 16.95
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*Contigs were composed by 1,537 reads.

The high-quality sequences were assembled in 340 contigs (619 bp average) and 1,666 singlets which we assume to represent 2,006 unique sequences (US). It is likely that some of the US came from the same gene due to non-overlapping ESTs from a single gene or products of alternative splicing [38].

Comparative analysis of Atta laevigata genes

Using Blastx we found that 1,165 (58%) of the characterized Atta laevigata US matched significantly (E-value ≤ 10-5) with GenBank sequences in the non-redundant (nr) database (Figure 1A). Most of the best hits (Figure 1B) came from the hymenopterans Apis mellifera [39] (677) and Nasonia vitripenis [40] (334) genomes, but only 10 hits came from the ants Solenopsis invicta, Lasius niger or Myrmica rubra because ant sequences are relatively poorly represented in the nr database.

Figure 1.

Figure 1

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Summary of Blastx search results for Atta laevigata sequences. (A) Percent of Atta laevigata sequences with significant matches (red, Blastx E-value ≤ 10-5) and non-significant matches (blue) in the GenBank. (B) Number of best hits found in different biological species.

We used B2G program and found GO terms (Figure 2) to 865, EC numbers to 250, predicted signal peptides in 229, and domain information for 66 Atta laevigata US, as well as KEGG information. This bulk of retrieved information and data obtained from CDD were manually inspected to annotate Atta laevigata US in 27 functional categories (Figure 3).

Figure 2.

Figure 2

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Distribution of GO terms. The graphic displays the GO terms at level 2 for each category.

Figure 3.

Figure 3

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Functional classification of Atta laevigata genes. The graphic displays the 1,165 US grouped in 27 functional categories. The colors represent major functions: blue: metabolism; green: structural; purple: regulation; orange: other; red: control candidates.

The number of US per category gives us an idea on the diversity of genes existing in each cell function. This diversity was found high within transcripts related with signaling pathways, membrane or regulation of gene expression, but very low within transcripts related to secondary metabolism, cuticular and peritrophic membranes or homeobox.

Variation of the number of reads per contig

The number of reads per contig varied from two to 123, with 73% of the contigs containing two or three reads and only 7% containing 10 or more reads (Figure 4). Therefore few contigs concentrated many reads, i.e. 1.1% (23 out of 2,006) of the contigs contained 18.8% (603 out of 3,203) of the reads. By dividing the number of reads (3,203) by the number of US (2,006) it was found the average of 1.6 reads per contig. Some of the contigs exceeding this average value are shown in Table 2. Whether the number of reads per contig is related to gene expression level, it can be assumed that Atta laevigata contains a set of 23 highly expressed genes. Sixteen of these genes are involved with three major cellular processes (Table 2): (i) ATP synthesis coupled to redox reactions in mitochondria (273 reads); (ii) muscle or cytoskeleton structure (135 reads); (iii) transcription regulatory processes through homeobox or signaling proteins (95 reads). Gene expression is energetically expensive and is accompanied by protein synthesis for the translational process which is even more expensive. The increasing of the number of transcripts of a given gene, even in a very small extent, is not a neutral process but rather strongly constrained by evolution [41], and expected to occur only if positively selected. Therefore, our results suggest that high expression levels have been positively selected in Atta laevigata for genes responsible for energy conservation, cell structure and regulation.

Figure 4.

Figure 4

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Contig amount as function of number of reads per contig. The graphic shows the number of reads used in the assembly of the 340 contigs.

Table 2.

Contigs with high read number in the Atta laevigata cDNA library.

Contig Reads Rate* Best hit (organism) Function+
311 123 76.9 COX I (Myrmica rubra) 1
235 52 32.5 Similar to paramyosin CG5939-PA (Apis mellifera) 2
183 47 29.4 ATP synthase F0 subunit 6 (Camponotus sayi) 1
037 43 26.9 COX III (Bombyx mandarina) 1
294 40 25.0 Similar to muscle protein 20 CG4696-PA (Apis mellifera) 2
056 30 18.8 COX II (Atta colombica) 1
330 30 18.8 Actin-5 (Bactrocera dorsalis) 2
289 25 15.6 Similar to limpet CG32171-PD (Apis mellifera) 3
337 20 12.5 Muscle LIM protein (Nasonia vitripennis) 3
273 19 11.9 Cytochrome b (Formica pratensis) 1
268 14 8.8 Similar to muscle LIM protein at 84B (Apis mellifera) 3
046 14 8.8 Similar to CG5023-PA (Apis mellifera) 3
015 13 8.1 Troponin I (Apis mellifera) 2
116 12 7.5 Similar to muscle LIM protein at 84B (Apis mellifera) 3
069 11 6.9 NADH dehydrogenase subunit 4 (Harpiosquilla harpax) 1
328 10 6.3 AGAP005400-PA (Anopheles gambiae) 3
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* Number of reads divided per 1.6 which is the mean number of reads (3,203) per US (2,006).

+1. ATP synthesis coupled to redox reactions in mitochondria (273 reads). 2. Muscle or cytoskeleton structure (135 reads). 3. Transcription regulatory processes through homeobox or signaling proteins (95 reads).

Identification of candidate genes for the control of pest leafcutters

Inhibition of the translation of genes which play essential functions in insects by feeding these insects with dsRNA [42] or using transgenic plants [43] seems a promising procedure for the control of agricultural pests [44]. One of the advantages of this procedure is that it targets mRNA molecules which may be species-specific.

In order to control pest leafcutters by inhibiting gene translation, one needs to identify and sequence target candidate genes. Our library was found to contain 146 US which represent potential target genes for the control of leafcutters, because these US are likely playing essential functions in Atta laevigata (Table 3). These target genes are related to antixenobiosis (including insecticide detoxification), queen longevity, larval development, insect immunity or resistance to pathogens, communication necessary to social tasks, polysaccharide metabolism or insecticide action.

Table 3.

Candidate genes for the control of pest leafcutter ants.

Process [GenBank Acc*] Description US
Antixenobiosis Cytochrome P450 activity 25
[JI332418-JI332429, JI332686-JI332710] Cell detoxification 12
Development and longevity Development, growth and differentiation 18
[JI332430- JI332440, JI332711-JI332736] Oxidative stress protection 13
Juvenile hormone binding and synthesis 6
Immunity and resistance to pathogens Immune response 29
[JI332441-JI332452, JI332737-JI332761] Serine protease inhibitor 4
Melanization and pathogen encapsulation 4
Communication [JI332453-JI332457, JI332762-JI332767] Pheromone/odorant binding and transport 11
Signaling Generation and stability of signaling 6
[JI332458, JI332459, JI332768-JI332773] Acetylcholine receptor 2
Behavior Courtship and behavior 5
[JI332460, JI332461, JI332774-JI332782] Learning and memory 3
Others 3
Polysaccharide metabolism [JI332462, JI332463, JI332783] Glycogen and starch degradation 3
Intermediary metabolism [JI332464, JI332465] Arginine kynase activity 2
Total 146
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*Transcriptome Shotgun Assembly database.

The function and potential utilization of these 146 US as targets for the control of pest leafcutters are considered below.

Antixenobiotic genes

Cytochrome P450, carboxylesterases, and glutathione transferases are involved in insecticide metabolism [45]. In insects, P450 also participates in the metabolism of many endogenous (including juvenile hormones, ecdysteroids, and pheromones) and exogenous compounds (plant allelochemicals and insecticides) [46].

The enzyme glutathione S-transferase catalyzes the initial conjugation of insecticides with glutathione. Both enzyme and glutathione are very abundant in the cells and essential for detoxification of electrophiles causing cytotoxic or genotoxic damage [47]. The enzyme may play a role in insecticide resistance [48], herbicide resistance in plants [49], resistance of cancer cells to chemotherapeutic agents [50], and antibiotic resistance in bacteria [51]. In our study we found 25 US in the cytochrome P450 family and 12 US probably related with detoxification of xenobiotics, including glutathione S-transferase, glutamate cysteine ligase and aldehyde oxidase (Table 3). All these genes may be important targets for the control of leafcutters.

Development and longevity genes

Of the 18 US we found (Table 3) involved with development, growth and differentiation, four are putatively related with nervous system development, two of which contained the immunoglobulin domain: one wrapper one lachesin homolog. The protein lachesin has a role in early neuronal differentiation as well in axon outgrowth, cell recognition events, cell adhesion or intercellular communication [52]. The other 14 US in this category (Table 3) may be involved in different phases of insect development like egg, or larvae, or development of tissues or organs like mesoderma, spermatechae and antennae.

Queen and worker ants develop from identical eggs, being genetically identical, but the caste system produces a long-lived queen and a short-lived worker with up to ten-fold lifespan differences [3]. Harman [53] stated that lifespan is determined by the rate at which oxidative damage occurs due to the accumulation of by-products of oxidative energy metabolism. Harman's theory implicates that long-lived organisms produce fewer reactive oxygen species or have increased antioxidant production [54], although the degree of lifespan extension can be sex- or genotype-specific [55] and sometimes poorly correlated with antioxidant levels [56].

We found 13 US likely involved in organism lifespan by protection from oxidative stress (Table 3) and which are directly involved in the degradation of superoxide radicals and hydrogen peroxide or neutralization of reactive oxygen species, such as the putative Cu/Zn superoxide dismutase, catalase, Rpd3 histone deacetylase, peroxiredoxin 5, thioredoxin reductase and phospholipid hydroperoxide glutathione peroxidase.

Our library contained four US putatively coding for juvenile hormone binding protein (JHBP) domain and two for putative proteins that participate in JHBP biosynthesis (Table 3). Juvenile hormones (JH) regulate a great number of physiological processes in insect development. Larvae requires JH to maintain larval state and JH must be absent in the last larval instar for metamorphosis to start [57,58]. They are also necessary for reproduction in adults [59].

The characterization of genes which are related to development and longevity in Atta laevigata allows future investigation on the effect of the expression of these genes on queen maturation and lifespan, which are a key features associated with leafcutter pest ability.

Genes associated with immunity and resistance to pathogens

Pathogens, parasites or injury triggers in insects innate immune responses that are in essence similar and comprise both cellular and humoral components. Cellular mechanisms include phagocytosis by special blood cells and encapsulation of large invaders [60]. Humoral responses involve events of proteolytic cascades leading to melanization [60] and the production of antimicrobial peptides initiated via two distinct signaling pathways, Toll and Immune Deficiency, which depend on the pathogen recognition [61]. There are two types of recognition proteins: peptidoglycan recognition proteins and Gram-negative bacteria-binding proteins.

We found 37 US that may be involved with immunity or pathogen resistance (Table 3), including the putative toll like interacting protein, prophenoloxidase subunit 3 and easter CG4920-PA, the last two with role in melanin synthesis. We also found sequences putatively coding for the antimicrobial peptides hymenoptaecin and defensin 2, and for the peptidoglycan recognition protein precursor, as well as transferrin and transferrin 2 which participate in response to microbial infection by sequestering iron that is an essential nutrient for some pathogens [62].

Leaf-cutting ants and their mutualistic fungus are constantly challenged by pathogenic microorganisms [63] which ultimately regulate host population [64]. Therefore, the 37 US we found probably involved in resistance to microbial pathogens are important markers for understanding antimicrobial mechanisms in leafcutters and putative targets for controlling pest leafcutters.

Communication genes

Communication plays a central part in social insects necessary for division of labor and task partitioning which are essential for harvesting food, nursing the broods and sexual reproduction [65]. Thus, targeting genes involved in communication seems a promising strategy for the control of leaf-cutting ants.

Our library contained 11 US probably related to communication, one of them putatively coding for the pheromone binding protein (PBP), which is important for chemical recognition of insect conspecifics by transporting odorant molecules from cuticular pores to receptors [66]. In Solenopsis invicta, the gene Gp-9, which is a PBP homolog, seems to have a role in worker ability to discriminate queens and regulate their numbers [67]. Other important communication gene found putatively codes for fatty acid binding protein involved in transport of communication molecules in insects [68].

Four of the communication US we found were in the lipocalin family which is composed of secreted proteins binding small hydrophobic molecules or forming macromolecular complexes associated with cell surface receptors important for transport, pheromone signaling and olfaction [69]. These sequences putatively code for the odorant binding proteins, apolipophorin III or PP238.

We also found three homologs to the chemosensory protein from Nasonia vitripennis, chemosensory protein 2 from Apis mellifera and chemosensory protein 5 from Bombyx mori. Chemosensory proteins may be specifically expressed in sensory organs which are important in ant behavior [70] and participate in cellular processes that require lipophilic compounds [71].

The putative genes gustatory receptor and dihidrooratate dehydrogenase involved in odorant reception in insects were also found.

Signaling genes

Tetraspanin is an important signaling membrane protein expressed in antennae of moths and honeybees [72], being a molecular facilitator of signal transduction and cell adhesion [73]. In our library, six US putatively coding for tetraspanin were present.

We also found two US corresponding to nicotinic acetylcholine receptor which plays a role in visual processing, learning and memory, olfactory signal processing, and mechanosensory antennal input in honeybee [74]. These receptors are targets of neonicotinoids insecticides used against piercing-sucking pests [75].

Behavior genes

Eleven Atta laevigata US in this category (Table 3) were homolog to genes involved in behavior, learning, memory and courtship in Apis mellifera, Drosophila melanogaster or Solenopsis invicta. Some of the genes controlling social behavior and complex tasks or abilities may be specific to Hymenoptera [38] and thus may be specific targets for the control of pest leafcutters.

Polysaccharide metabolism genes

Food sources for worker leafcutters relies mostly on the plant polysaccharides cellulose, xylane and starch, which are degraded by extracellular enzymes secreted by the mutualistic fungus [76], generating mono and disaccharides readily assimilated by the ants [77]. Degradation of cellulose by the mutualistic fungus generates cellobiose [10] and degradation of starch generates maltose, both disaccharides being consumed by leafcutters [77] through the production of alpha- and beta-glucosidase, respectively. In addition, workers assimilate starch at certain extent [77], which demands production of alpha-amylase.

Our library contained 59 US (Figure 3) corresponding to genes related to carbohydrate metabolism, including alpha-glucosidase-like, beta-glucosidase and alpha-amylase (Table 3) which are promising targets for leafcutters control.

Arginine kinase gene

Arginine kinase catalyses the reversible transfer of phosphate between ATP and guanidine substrates and acts in cells that need readily available energy sources [78]. This enzyme activity in cockroaches was found to be inhibited by nitrates and borates [79] which were then used as insecticides. Our library contained two US which are putative arginine kinase genes (Table 3) that may also be important for the control of leafcutters.

Future perspectives

The 146 US here proposed as targets for the control of leaf-cutting ants can be used for primer designing in order to study gene expression through real time PCR. For instance, over-expression of sequences here proposed as related to immunity or antixenobiosis in A. laevigata challenged by pathogens or insecticides should validate the protective role of the respective gene products in leafcutters exposed to adverse conditions, helping us to understand the molecular basis of pest ant resistance to hazardous chemicals. A future scenario can be envisaged in which inhibition of gene expression, gene translation or the related protein activities would make pest leafcutters more susceptible to pathogens, insecticides or anti-herbivory chemicals produced by crops. In summary, inhibition of genes or gene products related to the processes described in Table 3 may specifically hamper the colonization of crop areas by pest leafcutters.

Conclusion

Leaf-cutting ants are the major neotropical herbivores, many of which are important agricultural pests. We characterized 2,006 unique sequences (US) in Atta laevigata, one of the most geographically spread pest leaf-cutting ant in South America, and found that 16 of the genes are likely under positively selected high expression and responsible for energy conservation or cell structuring or regulation. Another set of 146 US which play important part in anti-xenobiosis, longevity, immunity, development, communication, nutrition or insecticide action were identified as putative targets for the control of pest leafcutters. Our findings provided genetic background for basic and applied studies on these ants.

List of abbreviation used

EST: Expressed Sequence Tags; US: unique sequences; mRNA: messenger RNA; cDNA: complementary DNA; bp: base pair; B2G: Blast2GO; nr: non-redundant; GO: Gene Ontology; KEGG: Kyoto Encyclopedia of Genes and Genomes; EC: Enzyme Comission; IUBMB: International Union of Biochemistry and Molecular Biology; CDD: Conserved Domain Database; JHBP: juvenile hormone binding protein; JH: juvenile hormone; PBP: pheromone binding protein; PCR: polymerase chain reaction.

Competing interests

The authors declare that they have no competing interests

Authors' contributions

Conceiving and designing of the experiments: CMR, MB. Construction and sequencing of the cDNA library: CMR, FFPP, FHS. Bioinformatic analyses: MF, EAA, IRG. Contribution with reagents, materials and analysis tools: FHS, MB. Manual annotation and manuscript preparation: CMR, MF, MB. All authors read and approved the final manuscript.

Contributor Information

Cynara M Rodovalho, Email: cynaramr@yahoo.com.br.

Milene Ferro, Email: milenef@gmail.com.

Fernando PP Fonseca, Email: fonseca.fpp@gmail.com.

Erik A Antonio, Email: aceiro@gmail.com.

Ivan R Guilherme, Email: ivan@rc.unesp.br.

Flávio Henrique-Silva, Email: dfhs@ufscar.br.

Maurício Bacci, Jr, Email: mbacci@rc.unesp.br.

Acknowledgements

We thank CAPES, CNPq 476250/2008-0 and 304661/2009-0 and FAPESP 2008/54386-9 for financial support as well as the trainees Alexandre H Takara, Cristiane P Garcia, Pamella A Malagrino, Rafael B Souza, Fernando K Cochi and Washington Luiz Pires for clone picking and miniprep and Caio C Batista for computational support.

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