Shared Escovopsis parasites between leaf-cutting and non-leaf-cutting ants in the higher attine fungus-growing ant symbiosis.

Fungus-gardening (attine) ants grow fungus for food in protected gardens, which contain beneficial, auxiliary microbes, but also microbes harmful to gardens. Among these potentially pathogenic microorganisms, the most consistently isolated are fungi in the genus Escovopsis, which are thought to co-evolve with ants and their cultivar in a tripartite model. To test clade-to-clade correspondence between Escovopsis and ants in the higher attine symbiosis (including leaf-cutting and non-leaf-cutting ants), we amassed a geographically comprehensive collection of Escovopsis from Mexico to southern Brazil, and reconstructed the corresponding Escovopsis phylogeny. Contrary to previous analyses reporting phylogenetic divergence between Escovopsis from leafcutters and Trachymyrmex ants (non-leafcutter), we found no evidence for such specialization; rather, gardens from leafcutters and non-leafcutters genera can sometimes be infected by closely related strains of Escovopsis, suggesting switches at higher phylogenetic levels than previously reported within the higher attine symbiosis. Analyses identified rare Escovopsis strains that might represent biogeographically restricted endemic species. Phylogenetic patterns correspond to morphological variation of vesicle type (hyphal structures supporting spore-bearing cells), separating Escovopsis with phylogenetically derived cylindrical vesicles from ancestral Escovopsis with globose vesicles. The new phylogenetic insights provide an improved basis for future taxonomic and ecological studies of Escovopsis.

Introduction

Symbiotic relationships are a significant source for evolutionary innovation [1-3], generating diversity in mutualistic and parasitic interactions, particularly among microbe–insect associations. During the last decades, understanding of microbe–insect interactions has significantly improved, revealing more complex interactions among an increasingly diverse set of participants than was previously appreciated. This is especially true for attine ants and their microbial symbionts, which have become among the best-studied examples for parasitic and mutualistic insect–microbe coevolution [4,5].

All known attine ants (more than 250 described species within 16 genera) cultivate basidiomycetous fungi as the primary source of food [6,7]. Since the origin of the symbiosis approximately 67 million years ago, five distinct types of fungiculture evolved [8-10]. We focus here on the phylogenetically derived higher attine fungiculture involving four ant genera: Trachymyrmex, Sericomyrmex, Acromyrmex and Atta (the last two genera comprise the leaf-cutting ants, the behaviourally most complex group within the entire tribe [9,10]). Higher attine ants cultivate phylogenetically derived fungi that exhibit hyphal swellings, called gongylidia, which are specialized structures used to feed the queen and the brood [11-13].

The gardens grown by attine ants are susceptible to invasion by fungi; some of these are only known from associations with attine ant nests and are considered specialized parasites [14] grouped within the genus Escovopsis [14-21]. Recently, a new closely related genus, Escovopsioides, was described, but the parasitic nature of this fungus is unknown [20].

Previous research argued that Escovopsis coevolved with attine ants and their cultivars [17], resulting in a clade-to-clade correspondence where different clades of the Escovopsis parasite would be specifically associated with distinct clades of ants and their corresponding fungi. For example, a monophyletic clade of three Escovopsis strains was found infecting Trachymyrmex gardens from Panama, Ecuador and Trinidad, suggesting that a specific clade of Escovopsis infects the Trachymyrmex symbiosis [17]. Based on the three strains examined (each from a single nest from each of these locations), the Trachymyrmex-associated Escovopsis was thought to be distinct from Escovopsis infecting leaf-cutting ants (Acromyrmex and Atta). However, to our knowledge to date no study has extensively explored the geographical diversity of Escovopsis associated with Trachymyrmex, especially in South America, the centre of diversity for all genera of higher attines. Studying Escovopsis strains from leaf-cutting ants, Taerum et al. [22,23] identified three main, monophyletic groups among leafcutter-associated Escovopsis, all of which were found in South and Central America. However, Taerum et al. [22,23] studied mostly Escovopsis collected in Panama (some samples from Argentina, Ecuador and one sample from Guiana and Mexico), but few representatives from across South America. Augustin et al. [20] studied Escovopsis strains associated with Acromyrmex species within a small geographical area in Brazil (Viçosa, Minas Gerais state) and showed that, even within a restricted area, three new species of Escovopsis were found infecting gardens of Acromyrmex ants. This previously unknown diversity uncovered in the small sample of Augustin et al. [20] suggests that South America might hold a significant unexplored diversity of Escovopsis.

Using an expanded collection of Escovopsis spanning almost the entire range of higher attine ants, including Brazil (n=55 strains), Argentina (n=1), Panama (n=13), Lesser Antilles (n=2), Trinidad and Tobago (n=1) and Mexico (n=3), we test here whether Escovopsis isolated from leaf-cutting colonies group separately from those isolated from Trachymyrmex colonies. Analysing Escovopsis strains isolated from 70 higher attine colonies (26 Atta colonies, 25 Acromyrmex, 18 Trachymyrmex, one Sericomyrmex), from at least 20 ant species in 31 locations, we show that leafcutter ants and other higher attine ants can share similar Escovopsis parasites, indicating no strict ant-parasite co-cladogenesis within this group of ants. We also identify several new Escovopsis strains forming previously unknown clades, which may correspond to new species. Correlations between morphological traits and phylogenetic patterns reveal a need for further taxonomic and ecological studies on these newly identified fungal pathogens.

Material and methods

Collection, isolation and morphological aspects

From 2001 to 2013, we sampled Escovopsis from Brazil (22 sites), Panama (four sites), the Caribbean island of Guadeloupe (one site), Argentina (one site) and Mexico (one site). To these collections, we added DNA sequence data from published studies of Escovopsis collected in Trinidad and Tobago by Seifert et al. [16] and in Viçosa, Brazil by Augustin et al. [20]. The combined dataset contains samples from 31 collection sites spanning the known geographical range of Escovopsis (see the electronic supplementary material, table S1, for complete information).

To isolate Escovopsis, pieces of attine fungus garden (one to five pieces with 3–5 cm3 each, depending on the size of the chamber) along with some worker ants were collected in situ from live ant colonies using a sterile spatula. Fungus gardens were maintained in ultraviolet-sterilized plastic containers until they reached the laboratory. Small fragments of the fungus garden (0.5–1 mm in diameter) were plated on potato dextrose agar (PDA) supplemented with chloramphenicol (150 mg l−1, Sigma) and incubated at 25°C in the dark for the following 14 days. Plates were checked twice daily for fungal growth and were subcultured on new PDA plates when Escovopsis growth became visible. To confirm the purity of Escovopsis cultures, monosporic cultures were obtained for each strain after isolation. Some strains were isolated from middens, but the isolation process was the same as described above (see the electronic supplementary material, table S1). We obtained 61 new Escovopsis strains from our survey and also analysed nine Escovopsis strains isolated by our research group and superficially characterized in previous studies [24,25]. Moreover, we included morphological data derived from five strains for brown-spored Escovopsis species previously identified [16,20]. Therefore, our morphological analysis comprised 75 Escovopsis strains associated with higher attine ants: 55 from Brazil, 13 from Panama, three from Mexico, two from the Caribbean island of Guadeloupe, one from Argentina and one from Trinidad and Tobago. Escovopsis strains RS019, RS020, RS030, RS053, RS055, RS061 and RS076 were superficially analysed by Rodrigues et al. [24], while strains NL007 and SES005 were used in in vitro bioassays by Meirelles et al. [25].

In addition to the 75 strains, we also analysed the morphology of five brown-spored Escovopsis strains isolated from Apterostigma by Gerardo et al. [19]; these strains were included mainly for comparison with our strains associated with higher attines. Escovopsis sampled from Brazil are stored in 10% glycerol at −80°C at UNESP—Microbial Resource Center in Rio Claro, SP, Brazil, while Escovopsis obtained from other countries are stored under the same conditions in the Section of Integrative Biology—University of Texas at Austin, Austin, TX, USA.

We performed morphological examinations on all new strains. For this purpose, the strains were grown in PDA at 25°C in the dark and, after 7 days of growth, microscopic slides were prepared to analyse the vesicle shape (globose or cylindrical).

DNA extraction, PCR and sequencing

Using a modified CTAB method [18,26], we extracted genomic DNA directly from colony mycelia of all strains after 7 days of growth in PDA. Previous studies used elongation factor 1-alpha (tef1) to reconstruct Escovopsis phylogenies [17-19,22,23]. Augustin et al. [20] showed the potential of using the internal transcriber spacer (ITS) as a phylogenetic marker for this fungus; this region is now considered the ‘barcoding region’ for fungi [27]. To increase our phylogenetic signal, we used both tef1 and ITS for phylogenetic analyses.

For tef1 amplification, we used primers derived from Taerum et al. [22]. The forward primer was the same EF6–20F (5′-AAGAACATGATCACTGGTACCT-3′); however, we modified one base on the reverse primer (‘R’ was replaced by ‘A’) and the final primer was EF6A-1000R (5′-CGCATGTCACGGACGGC-3′). This change increased the melting temperature of the primer, minimized co-amplification and improved the sequencing results. DNA was diluted 1000–10 000 × (final concentration ≅0.5–5 ng μl−1) and the PCR conditions were: 96°C for 3 min, 35 cycles at 96°C for 30 s, 61°C for 45 s and a final extension step at 72°C for 1 min following Meirelles et al. [25].

ITS amplification was performed using primers ITS1 (5′-TCCGTAGGTGAACCTGCGG-3′) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′). DNA was diluted 100× (final concentration ≅ 50–100 ng μl−1) and the PCR conditions were: 96°C for 3 min, 35 cycles at 94°C for 1 min, 55°C for 1 min and a final extension step at 72°C for 2 min [28]. Owing to the high CG content in ITS for Escovopsis (more than 65% in some strains), we prepared reactions with 5% dimethyl sulfoxide to enhance primer annealing.

PCR products were cleaned up with Kit Wizard® SV Gel and PCR Clean-up System (Promega) and the cycle sequencing reactions were prepared with 15–20 ng of template using BigDye® Terminator v. 3.1 Cycle Sequencing Kit (Life Technologies) following the manufacturer’s instructions. Sequences were generated at UNESP using ABI3500 (Life Technologies) and in a DNA sequence facility at UT-Austin. Contigs were assembled using Bioedit v. 7.1.3 [29]. Sequences of all strains were deposited in GenBank under accessions KM817043–KM817173 (see the electronic supplementary material, table S1).

Phylogenetic analysis

We included in our analysis all the 61 new strains derived from this study as well as nine Escovopsis strains from Brazil used in previous studies [24,25], all associated with higher attine ants (see the electronic supplementary material, table S1). Moreover, sequences of five brown-spored Escovopsis strains associated with Apterostigma ants [19] were included along with sequences from described species for Escovopsis and Escovopsioides [16,20,21]. Finally, three other Hypocreaceae fungi used as an outgroup by Meirelles et al. [21] were maintained here. The final dataset comprised two files, one for tef1 with 85 taxa and the other for ITS with 80 taxa (for the five Escovopsis strains derived from Gerardo et al. [19], only tef1 but no ITS sequences were available). Alignments were obtained independently for each file using MAFFT v. 7 [30]. Nucleotide substitution models were selected under separated runs for each file using the Akaike and Bayesian information criteria (AIC) with a confidence interval of 95% in jModelTest 2 [31]. The phylogeny was reconstructed by two different methods: maximum likelihood (ML) using RAxML v. 8 [32] and Bayesian Inference (BI) using MrBayes v. 3.2.2 [33].

We performed individual phylogenies for each marker, and the general phylogenetic topology was similar (data not shown) with respect to the well-supported clades and key features emphasized in the below discussion (e.g. despite the few topological differences within specific clades, both markers showed the same Escovopsis sharing between leaf-cutting and non-leaf-cutting ants). Our main analyses here therefore focus on the concatenated data (figure 1) combining information from both markers. For Escovopsis from higher attines, ITS is a phylogenetically informative marker, but tef1 provides greater phylogenetic resolution.

Figure 1.

Phylogeny of Escovopsis associated with higher attine ants based on elongation factor 1-alpha (tef1) and internal transcribed spacer (ITS) markers analysed under Bayesian criteria. Pie-graphs at key nodes show probabilities of ancestral character-states for globose (red) and cylindrical (blue) vesicles. Coloured bars on the right side indicate the observed vesicle morphology, and black arrows point to the respective vesicle structure (400×). The main clades are highlighted in different colours and were consistently supported in both ML and Bayesian analyses. The phylogenetic tree includes also strains from brown-spored Escovopsis associated with Apterostigma ants [19], Escovopsioides nivea and Escovopsis kreiselii (the only species described for the pink-spored Escovopsis, a less derived group that infects lower attine ant gardens, [21]). Three additional species of Hypocreaceae fungi were used as an outgroup. Escovopsis strains in bold indicate exceptions of the co-cladogenesis model (see text). The ant species from which an Escovopsis strain was isolated, its corresponding collection sites and identification (ID) numbers are given in parentheses. GenBank accession number for tef1 and ITS of each strain are available in the electronic supplementary material, table S1. Only posterior probabilities and bootstrap values greater than or equal to 0.5 or 50 are shown. The letter ‘T’ indicates ex-type strains (Ser., Sericomyrmex; sub., subterraneus; ARG, Argentina; BRA, Brazil; MEX, Mexico; PAN, Panama; TTO, Trinidad and Tobago).

The two different alignments were concatenated using Winclada v. 1.00.08 [34]. ML analysis was conducted in RAxML using GTR+I+G for each partition; 100 independent ML trees were reconstructed and the one with the best score was kept. To evaluate the tree reliability, 2000 bootstraps replicates were performed using the same model (bootstraps values converged at 1100 replicates [35]). For BI, GTR+I+G was also used as initial model for each partition. Two independent runs were performed; for both, three heated chains and one cold chain was used; each run consisted of Markov Chain Monte Carlo (MCMC) sampling for two million generations. Convergence occurred when the standard deviation of split frequencies fell below 0.01 and the first 25% of MCMC generations were discarded as ‘burn-in’. The final Bayesian tree was edited in FigTree v. 1.4.0 (http://tree.bio.ed.ac.uk/software/figtree/) and Adobe Illustrator CS6 (Adobe Systems) for final polishing.

Ancestral state reconstruction

One important microscopic morphological character for Escovopsis is the shape of their vesicles, which has been used in the taxonomic descriptions of new species [15,16,20]. Escovopsis vesicles are structures supporting spore-bearing cells (phialides) and two vesicle types can be distinguished, globose and cylindrical (figure 1). Because Escovopsis with globose vesicles grouped in less derived clades, whereas Escovopsis with cylindrical vesicles grouped in a derived clade, globose vesicles appeared to be the ancestral state. To test this hypothesis, we performed ancestral state reconstruction. Ancestral state inference using a phylogenetic tree assumes a single tree that is known without error. However, heuristic searches for phylogenetic tree estimation do not guarantee the discovery of the true tree topology and branch lengths. Therefore, we performed ancestral state reconstruction using the Ape package in R [36,37] over the ML topology estimated in RAxML, the Bayesian consensus topology estimated in MrBayes, a sample of trees from the Bayesian posterior sample and a sample from the RAxML bootstrap replicates to assess the robustness of our conclusions to slight variations in topology and/or branch lengths.

Ape incorporates multiple models that can be used for ancestral state reconstruction. We performed model fitting using likelihood ratio tests to determine whether a simple equal rates model could be rejected in favour of a more complex model, in which the rate of changing from globose to cylindrical vesicles differed from the rate of changing from cylindrical to globose vesicles. With an average p-value of 0.749, we could not reject the simpler model in favour of the more complex model for any tree in our sample; therefore, we performed the analysis under the equal rates model.

Results

Escovopsis strains derived from higher attine ants grouped within nine different clades, and four of them (I, II, V and VII) contain both Escovopsis from leaf-cutting ants and Trachymyrmex ants (figure 1). Representative strains from these four clades were isolated from multiple points in Brazil, Panama, Argentina, Mexico, Guadeloupe and Trinidad and Tobago (figure 1). Clades I and II consist mainly of Escovopsis isolated from leaf-cutting ants, while clades V and VII consist mostly of Escovopsis derived from Trachymyrmex, but we also found multiple exceptions to this clade-to-clade correspondence. Specifically, 12 of the 75 Escovopsis strains (16%) isolated from higher attine ants did not follow this pattern (figure 1). These results show that Escovopsis infecting leaf-cutting ants and those infecting other higher attine ants are not reciprocally monophyletic, suggesting that these insects can share infections caused by closely related strains of the parasite.

This is, to our knowledge, the first study to report the occurrence of clades IV, V, VI and VIII. These results indicate that the phylogenetic diversity of Escovopsis is much greater than what was known. This is probably owing to the inclusion of samples from a geographical range unexplored before, especially from Brazil. Our results suggest that clades IV, VI and VIII may consist of rare Escovopsis types, as strains from these clades were each found in only one locality (figure 2). Clade IV consists of three phylogenetic identical strains isolated from two different Atta cephalotes colonies in Camacan, Bahia—BRA (site no. 9); despite possible abundance at this site, representatives of this clade have not been isolated at any other collection site (figures 1 and 2) suggesting the possibility of an endemic Escovopsis strain from this region.

Figure 2.

Geographical distribution of Escovopsis sampling sites. Coloured circles correspond to clade colours in figure 1. Location number corresponds to the listing in the electronic supplementary material, table S1. For sites from which different clades of Escovopsis were sampled, more than one coloured circle is shown, but this does not indicate that different Escovopsis strains derived from the same colony (see the electronic supplementary material, table S1 for nests IDs). The green shading indicates the approximate distribution of higher attine ants [6,38]. Cartographic data (original map) were obtained using a free package for the software DIVA-GIS [39].

As demonstrated by Taerum et al. [22], there was no correlation between leaf-cutting ant genera and particular Escovopsis strains. Atta cephalotes populations from Camacan were infected by Escovopsis from clades I, II and IV. In Atta sexdens, we found Escovopsis from clades I, V and also one strain (Escovopsis UT010) that grouped with brown-spored Escovopsis associated with Apterostigma [19], called here clade IX. Finally, the type strains of E. microspora and E. moelleri, both isolated from the same ant species Acromyrmex subterraneus molestans [20], grouped in clades I and V, respectively (figure 1). These results support the low host-specificity between Escovopsis and its leaf-cutting ant hosts, demonstrated by Taerum et al. [22].

The results of our phylogenetic groupings based on two nuclear markers are further supported by the presence of two morphological characters that distinguish clades I–V and VIII from clades VI, VII and IX (figure 1). Based on our samples, all Escovopsis strains from clades I–V and VIII have cylindrical vesicles, while all strains from clades VI and VII have globose vesicles (figure 1). All the Escovopsis strains from the clade mainly associated with Apterostigma (clade IX) analysed here also have globose vesicles. Both vesicle morphotypes were previously reported by studies that described the five known brown-spored Escovopsis species [15,16,20]. However, we show here that this morphological character correlates with phylogeny (i.e. we did not find strains within the same clade exhibiting different types of vesicles), suggesting that this trait is important for taxonomic studies.

Moreover, we also performed ancestral state reconstruction to test which of the two morphotypes could be considered the ancestor state using the ‘Ape’ package in R [36,37] (see Material and methods for details). Under the equal rates model, the average support for globose vesicles as the ancestral state average is 96.99% (pie-graphs in figure 1) and in none of the trees were cylindrical vesicles supported as the ancestral state. When estimated over a sample of trees from a RAxML bootstrap sample, the average support for globose vesicles as the ancestral state was 69.04%. This is lower than the support values obtained from the Bayesian sample (96.99%). One possible cause for this discrepancy is that the RAxML trees were, on average, shorter in total branch lengths than the Bayesian trees. Shorter branch lengths decrease the possibility of change along a given branch, and the trees estimated by RAxML tend to have short branch lengths near the root of the tree. These branch lengths could inflate the probability of observing cylindrical vesicles at the root.

Additional macroscopic differences (e.g. growth, time for sporulation and intensity of sporulation) were noted between strains from different clades that warrant more careful examination by taxonomists (electronic supplementary material, figure S1).

Discussion

Escovopsis occurrence in higher attine ants

Despite the efforts of attine workers to weed out pathogens from fungal gardens, alien fungi can invade attine gardens [24,40]. Some of these invaders are cosmopolitan fungi within the genera Trichoderma, Fusarium or Syncephalastrum that also exist outside the attine symbiosis [24]. By contrast, Escovopsis are fungal parasites so far only known from attine colonies and therefore are considered specialized on attine nests [14,17]. Escovopsis parasites have stimulated broad interest due to their potential as biological control agents of leaf-cutting ants, which are major agricultural pests throughout the tropical New World [41]. To date, the largest studies considering Escovopsis diversity associated with higher attine ants are those of Taerum et al. [22,23]. However, these authors did not deeply explore geographical areas in South America (the origin of higher attine ants) as well as the diversity of the parasite associated with non-leafcutter higher attine ants (they focused mostly on Escovopsis from the leafcutter ants Acromyrmex and Atta, but not from the other higher attine genera Trachymyrmex and Sericomyrmex).

Our results do not support the phylogenetic clade-to-clade correspondence between higher attine ants (i.e. between leafcutters and non-leafcutters) and their respective Escovopsis parasites [17,22]. Escovopsis associated with higher attine ants are thought to have undergone cladogenesis in parallel with the corresponding ant lineages. This was originally supported by the apparent presence of two reciprocally monophyletic Escovopsis clades, each associated with its own clade of higher attine ants: (i) Escovopsis from the leaf-cutting ants Acromyrmex and Atta, and (ii) Escovopsis from Trachymyrmex, a non-leafcutter higher attine genus [17,22]. A similar pattern of co-cladogenesis had been suggested for the mutualistic cultivar, which likewise consists of a higher attine clade, within which ‘Attamyces’ is cultivated by leaf-cutting ants, and the so-called ‘Trachymyces’ by Trachymyrmex [42]. Our phylogenetic reconstruction (figure 1) reveals exceptions to this view, as we found 12 examples of Escovopsis (16% of our total sampling; figure 1) infecting attine colonies other than the clade with which they were thought to be exclusively associated [17,22]. Our data suggest that, rather than tight correspondence between ant genera and particular Escovopsis strains, ants from any higher attine genus can share infections by closely related Escovopsis strains. However, it is important to mention that these patterns are not inconsistent with broad congruence between Escovopsis and attine ants at higher taxonomic levels [17], for example, between higher and lower attine ants other than Apterostigma ants (i.e. we did not find pink-, white- or yellow-spored Escovopsis infecting higher attine gardens; these morphotypes seem to be less derived and restricted to lower attine ants, as indicated by previous studies [17,19,21,43]).

Cultivar switching, which is known to occur among some attine species [42,44-46-51], could be one of the mechanisms for Escovopsis sharing between leaf-cutting and other higher attine ants. In our study, we did not sequence the cultivar of the colonies from where the Escovopsis strains were isolated, which would allow a test of association-specificity between the parasite and the cultivars and would permit testing of whether phylogenetic patterns of Escovopsis are more congruent with those of the ants or the fungal cultivars. However, comparisons with data obtained in previous studies enable us to indirectly realize that cultivar switching by ants does not seem to be the only mechanism for Escovopsis infection sharing. Augustin et al. [20] found three different Escovopsis species infecting the same garden within a nest of Acromyrmex subterraneus molestans (see the electronic supplementary material, table S2, nest no. 4 in Augustin et al. [20]). Like other leafcutters, this ant is supposed to cultivate a single clone of the cultivar within its colony [52]. Strains of E. moelleri and E. microspora were found in top-portions of the garden, while strains of E. moelleri and E. lentecrescens were found on the bottom of the garden. Therefore, Escovopsis strains infecting the same garden (i.e. a single cultivar clone) grouped in three different clades shown in figure 1 (E. microspora, clade I; E. moelleri, clade V; E. lentecrescens, clade VII). These clades include Escovopsis from leaf-cutting ants as well as Escovopsis thought previously to be specialized on Trachymyrmex ants, indicating no specificity in Escovopsis infections within the higher attine group (i.e. it is possible to isolate from a single ant garden Escovopsis strains that span a broad diversity of higher attine-associated Escovopsis).

One possible interpretation of the new phylogenetic pattern (figure 1) is that some Escovopsis clades have generalist pathogenic potential (clades I, II, V and VII), infecting different higher attine ant genera, whereas other clades (IV, VI and VIII) may be more restricted to specific ant populations or geographical regions (corresponding to endemic Escovopsis species). For example, although the mechanisms of Escovopsis transmission between ant nests is still unknown, it is possible that a generalist vector might be able to transmit Escovopsis from clades I, II, V and VII between nests from the majority of higher attine ants, whereas other Escovopsis from clades IV, VI and VIII may be transmitted by vectors more specific to particular ant clades. Other explanations for the observed association patterns include that (i) Escovopsis from rare clades might be more adapted to the specific ecological conditions in the regions where they are found, or (ii) some Escovopsis from generalist clades could have been selected to have broad host ranges (this could be driven, for example, by dispersal limitations, thus increasing the need to transition between phylogenetically distant ant or fungal lineages), while Escovopsis from rare clades could have evolved to overcome specific defences of specific cultivar hosts.

The presence of Escovopsis in the Caribbean island of Guadeloupe (strains UT001 and UT002; figure 1) is particularly interesting. Acromyrmex octospinosus was recently introduced to Guadeloupe and is an invasive species there [53], which makes the presence of Escovopsis in these colonies somewhat of a curiosity. We propose three potential hypotheses for how this relationship came to be: (i) Escovopsis was present in the colony that was initially introduced, suggesting that Escovopsis sometimes do not represent a deadly disease, because the introduced colony(ies) survived; (ii) Escovopsis was present on a dispersing queen that was introduced, implying that Escovopsis can also be vertically transmitted; or (iii) Escovopsis can be dispersed or vectored widely across the Neotropics to reach remote islands, indicating that Escovopsis is able to disperse greater distances than nest-founding queens.

Despite the observed sharing of Escovopsis types between leaf-cutting and non-leaf-cutting ants, the effective pathogenic potential of such strains remains unclear. Augustin et al. [20] isolated E. moelleri from many colonies of Acromyrmex subterraneus collected at multiple sites, which indicates this fungus is consistently associated with this ant species, and it is probably a pathogen infecting the ant’s fungal cultivars. However, in our phylogenetic analysis, E. moelleri grouped within a clade composed mainly of Escovopsis strains isolated from Trachymyrmex gardens (clade V, figure 1). The consistent isolations of E. moelleri from A. subterraneus colonies and its position in a Escovopsis clade infecting mostly Trachymyrmex colonies could therefore be an indication that E. moelleri might transit readily as a generalized symbiont between local leafcutters and non-leafcutters colonies. Nevertheless, we cannot discard the possibility of transmission between leaf-cutting and non-leaf-cutting colonies with no pathogenic action yet. Future testing on the pathogenic potential of Escovopsis from different clades against cultivar strains from both leaf-cutting and non-leaf-cutting ants can distinguish between these possibilities.

Gerardo et al. [19] were the first to document exceptions to the co-cladogenesis model when they found brown-spored Escovopsis (closely related to Escovopsis associated with higher attines) infecting Apterostigma ants that cultivate ‘coral fungi’ in the family Pterulaceae, which are distantly related to the higher attine cultivars. Recently, Apterostigma ants cultivating ‘Attamyces’ fungi were found in Brazil [51]. These combined findings suggest that evidence for additional switches at higher phylogenetic levels between Escovopsis, the attine ants and their fungal cultivars may be found in South America. Future sampling of lower attine ants, especially in Brazil, may reveal further exceptions to the co-cladogenesis model of the attine ant–cultivar–parasite symbiosis.

Emerging infectious diseases can derive from novel host–parasite interactions, for example, a host jump (i.e. parasite infection of a new host species) or spread to uninfected host populations of an existing host–pathogen association [54,55]. In some fungal–insect or fungal–plant interactions, the fungal pathogens can establish generalist infections, being able to switch between different hosts, whereas in other interactions the fungal pathogen is restricted to specific host species or populations [54,56]. Because Escovopsis has been found so far only associated with attine ants, it is assumed to be specialized on the ants’ cultivars [14]. The switches documented here (figure 1) are indirect indications that Escovopsis has the ability to spread across more phylogenetically diverse hosts than was previously known, but it is still a specific parasite linked to the fungus-growing ant system. Investigations into the life cycle of Escovopsis will probably reveal mechanisms underlying this attine-specificity, as well as the observed host switching across attine ant–cultivar lineages.

Phylogenetic and morphological diversity of higher attine Escovopsis

Escovopsis diversity could be affected by climate and other environmental conditions, and may therefore follow a latitudinal diversity gradient. Four colonies of Atta cephalotes from Camacan, Bahia, Brazil (figure 2; electronic supplementary material, table S1) contained Escovopsis from three different clades (figure 1), including clade IV, currently known only from that site. Augustin et al. [20] also found Escovopsis from three different clades (I, V and VII) associated with a single colony of Acromyrmex in Viçosa (site no. 23 in figure 2), Brazil. By contrast, our sampling of Acromyrmex species from southern Brazil only revealed Escovopsis strains from clade I. This preliminary analysis therefore suggests a somewhat reduced genetic diversity at higher latitudes, but more comprehensive collections across latitudinal gradients will be needed to firmly establish this latitudinal pattern.

Until recently, Escovopsis was characterized into two types, ‘weberi morphology’ and ‘aspergilloides morphology’, corresponding to cylindrical and globose vesicles, respectively [15,16]. However, Augustin et al. [20] were the first to recognize new species within each of these two morpho-groups when describing E. microspora, E. moelleri and E. lentecrescens. Our analyses (figure 1) expand on Augustin et al.’s [20] work by identifying additional Escovopsis clades, as well as several new strains or species within the two previously known morpho-groups. To avoid taxonomic confusion, future studies should therefore consider using either ‘globose’ or ‘cylindrical’ vesicles for a morphological classification for this group (instead of using ‘weberi morphology’ and ‘aspergilloides morphology’).

Ancestral character-state reconstruction indicated that globose vesicle appears to be the ancestral state relative to the phylogenetically derived cylindrical vesicles, being present in Escovopsis that commonly infect Apterostigma gardens and in Escovopsis UT010 (clade IX; figure 1 and electronic supplementary material figure S2, prob = 0.97). Therefore, two main scenarios can explain these observed phylogenetic patterns (figure 1): (i) cylindrical vesicles arose in the ancestor of clade VIII and clades I–VII and after that, independent reversions to globose vesicles occurred for clades VI and VII, while all other clades maintained the derived character; (ii) cylindrical vesicles arose independently twice, once in clade VIII and once in the ancestor of all derived clades I–V. Our data support the second scenario more strongly (figure 1; electronic supplementary material, figure S2). However, future sampling of Apterostigma ants from Brazil (especially searching for brown-spored Escovopsis) will be necessary to better understand the morphological evolution and evolutionary transitions of associations with globose versus cylindrically vesicled Escovopsis. Such studies can then also address the predicted additional switches between Escovopsis infecting higher attine ants and the lower attine Apterostigma, as discussed above.

In addition to the defining morphological differentiation between globose versus cylindrical vesicles, we found that strains from different Escovopsis clades can exhibit very distinct growth, time of sporulation and sporulation intensity when cultivated under the same conditions (electronic supplementary material, figure S1). Such differences, as well as more detailed microscopic analyses (e.g. of conidia structure and size or conidiophore morphology) will be necessary to inform future taxonomy. The phylogenetic patterns documented here (figure 1) hint at an underappreciated diversity of Escovopsis and the complexity of its evolutionary history; and will provide a firm basis for future taxonomic and ecological studies of Escovopsis fungi associated with higher attine ants.