Microbial composition of spiny ants (Hymenoptera: Formicidae: Polyrhachis) across their geographic range
© The Author(s). 2017
Received: 21 November 2016
Accepted: 23 March 2017
Published: 5 April 2017
Symbiotic relationships between insects and bacteria are found across almost all insect orders, including Hymenoptera. However there are still many remaining questions about these associations including what factors drive host-associated bacterial composition. To better understand the evolutionary significance of this association in nature, further studies addressing a diversity of hosts across locations and evolutionary history are necessary. Ants of the genus Polyrhachis (spiny ants) are distributed across the Old World and exhibit generalist diets and habits. Using Next Generation Sequencing (NGS) and bioinformatics tools, this study explores the microbial community of >80 species of Polyrhachis distributed across the Old World and compares the microbiota of samples and related hosts across different biogeographic locations and in the context of their phylogenetic history.
The predominant bacteria across samples were Enterobacteriaceae (Blochmannia - with likely many new strains), followed by Wolbachia (with multiple strains), Lactobacillus, Thiotrichaceae, Acinetobacter, Nocardia, Sodalis, and others. We recovered some exclusive strains of Enterobacteriaceae as specific to some subgenera of Polyrhachis, corroborating the idea of coevolution between host and bacteria for this bacterial group. Our correlation results (partial mantel and mantel tests) found that host phylogeny can influence the overall bacterial community, but that geographic location had no effect.
Our work is revealing important aspects of the biology of hosts in structuring the diversity and abundance of these host-associated bacterial communities including the role of host phylogeny and shared evolutionary history.
KeywordsBlochmannia Wolbachia Lactobacillus NGS microbes amplicon sequencing
There are over 13,000 described species of ants belonging to the family Formicidae (Hymenoptera), which are widely distributed across the globe. The great diversity of the group is likely due to their ecological variability, including variation in nesting, feeding preferences and social behavior, and division of labor between castes [1, 2]. The genus Polyrhachis, Smith, 1857, is the fourth most species rich genus of ants and is characterized by its taxonomic, ecological and social diversity [3–5]. This genus contains more than 700 extant valid species , subdivided in the following recognized 13 subgenera: Aulacomyrma Emery, Campomyrma Wheeler, Chariomyrma Forel, Cyrtomyrma Forel, Hagiomyrma Wheeler, Hedomyrma Forel, Hemioptica Roger, Hirtomyrma Kohout, Myrma Billberg, Myrmatopa Forel, Myrmhopla Forel, Myrmothrinax Forel and Polyrhachis [5–7]. The genus Polyrhachis has a wide distribution across the tropical latitudes in the Old World, from Africa and Asia to Australia and a few Pacific islands, but being absent from Madagascar [7–9]. A possible reason for this restriction to the Old Word could be their late arrival to Africa, which potentially did not permit further dispersal to the New World as the continents had already drifted apart .
Nests of Polyrhachis can vary dramatically from terrestrial (present in the soil) to arboreal (in the canopy), in arid or tropical forests. Nests can be monodomous or polydomous, and colonies may be monogynous or polygynous (single or multiple breeding queens per nest). In addition colonies may vary in size from few to thousands of individuals [7, 11–13] with many species using larval silk to weave nests among plant leaves, a behavior that has been lost several times in the genus . Additionally, Polyrhachis is one of the few examples from the subfamily Formicinae known to have semiclaustral colony foundation , where the queen will exit the nest during early colony foundation to forage in an attempt to obtain food resources, despite the danger of predation, unlike claustral nest foundation . Recently Mezger and Moreau  in a large study (209 taxa) covering almost the entire distribution of the genus inferred the phylogeny and biogeography of the genus. Their molecular data support the monophyly of the genus, although some subgenera are not inferred as monophyletic. The authors were also able to estimate that the likely origin of the genus is South-East Asia, and that there were several dispersals into Australia, but only one to Africa.
In addition to the diversity of life history traits found across the ants, they also exhibit a range of associations with bacterial symbionts as seen in many other insect groups. For instance in an analysis across insect groups representing 63 species 76% were infected with associated bacteria . In fact, Buchner  considered insects the model organismal group for the study of endosymbionts, since they coexist with microorganisms internally and externally to the body. Among the Hymenoptera, ants are well known for their associations with bacterial symbionts [18–20]. Diet flexibility exhibited by many species may explain much of the evolutionary success of the group, which is achieved in part due to the presence of endosymbionts that help improve host nutrition .
One well-studied example among the ants is the association of Blochmannia in the Camponotini ants, which circumscribes eight extant genera (Calomyrmex, Camponotus, Echinopla, Forelophilus, Opisthopsis, Overbeckia, Phasmomyrmex, and Polyrhachis) including Polyrhachis, the focal genus in this study. Blochmannia is a Proteobacteria specific to the Camponotini, which has been demonstrated to assist in providing essential amino acids to their host since their diets are defficient in nutrients as a consequence of their arboreal habitats [22, 23]. The nutritional role of Blochmannia is not the only beneficial aspect to the host, as it has been shown that Blochmannia also has the necessary genes to contribute to the metabolism of nitrogen, sulfur and lipids [24–26]. In addition to Blochmannia endosymbionts, among members of the Camponotini tribe, there are other species of endosymbionts that have been documented from these hosts, including Arsenophonus spp., Cardinium hertigii, Hamiltonella defense, and Spiroplasma spp. [27, 28]. However, little work has been done on the identification, diversity, and potential coevolution of bacteria associated with Polyrhachis, leaving many remaining questions about these associations including what factors drive host-associated bacterial composition.
To better understand the evolutionary significance of this association in nature, further studies addressing a diversity of hosts across locations are necessary. Therefore to address this question, we focus our study on the bacterial community of a host that exhibits high species diversity and a wide geographic distribution, to reveal more about the factors that influence bacterial communities. Leveraging next-generation sequencing, we document the diversity of bacteria associated with Polyrhachis (in 12 of the 13 subgenera), to identify the factors that structure the diversity of bacterial communities found across a diverse and widely distributed group of animals.
DNA extraction and bacterial DNA sequencing
For this study we included 142 samples of Polyrhachis representing 12 of the 13 subgenera from the study of Mezger and Moreau . A complete list of samples used for this study can be found in Additional file 1: Table S1. The taxonomic identifications were determined by Mezger and Moreau  and vouchers were deposited in the collection of the Field Museum of Natural History, Chicago, USA during that study. Samples used for analyses were collected immediately into 95% ethanol in the field and and stored in 95% ethanol and kept at −20 °C until extraction of total DNA was performed. Total DNA was extracted from whole ant workers with Qiagen DNeasy Tissue kit following the manufacturer’s recommendations with slight modifications following Moreau  and we did not use the modification of the Quigen DNeasy kit for gram-positive bacteria. In addition, filtered pipette tips and sterile measurements were applied to avoid contamination of the samples, following recommendations of Moreau . Amplicon sequencing of the microbial community was completed using the V4 region of 16S rRNA using primers described in Caporaso et al. , following the Earth Microbiome Project (EMP) protocol (515f primer and 806r; http://www.earthmicrobiome.org/emp-standard-protocols/16s/). PCR was performed in triplicate, each 25 μl PCR reaction contained 12 μl of MO BIO PCR Water (Certified DNA-free), 10 μl of 5 Prime HotMasterMix (1×), 1 μl of forward primer (5 mM concentration, 200 final pM), 1 μl Golay barcode tagged reverse primer (5 mM concentration, 200 pM final) and 1 μL of template DNA, under the following conditions 94 °C for 3 min to denature the DNA with 35 cycles at 94 °C for 45 s, 50 °C is 60 s, and 72 °C for 90 s, with a final extension of 10 min at 72 °C. After amplification, the triplicate reactions were combined (still maintaining the individuality of samples), and to confirm the efficiency of the reaction samples were visualized using gel electrophoresis (1%). The samples were quantified via qPCR and Qubit (Thermo Fisher Scientific) (see bacterial quantification section below), and only then pooled with different samples after controlling for volume (multiplex). For purification, only 100 μL of each pool was cleaned using the UltraClean PCR Clean-Up Kit (MO BIO), following the manufacturer’s recommendations. After quantification, the molarity of the pool is determined and diluted down to 2 nM, denatured, and then diluted to a final concentration of 6.1 pM with a 10% PhiX for sequencing on the Illumina MiSeq. A 151 bp × 12 bp × 151 bp MiSeq run was performed using the custom sequencing primers and procedures described in the supplementary methods in Caporaso et al.  on the Illumina MiSeq at the Field Museum of Natural History. All raw sequence data is available publicly in Figshare [https://figshare.com/s/290531bea3dee984444e]  and also available in the NCBI Sequence Read Archive (SRA) under accession number SRR5136256 and study SRP095836 .
To optimize Illumina sequencing efficiency, we measured the amount of bacterial DNA present with quantitative PCR (qPCR) of the bacterial 16S rRNA gene using 515f (5′ - GTGCCAGCMG CCGCGGTAA) and 806r (5′ - GGACTACHVGGGTWT CTAAT) universal bacterial primers of the EMP (http://www.earthmicrobiome.org/emp-standard-protocols/16s/). All samples and each standard dilution were analyzed in triplicate in qPCR reactions. All qPCRs were performed on a CFX Connect Real-Time System (Bio-Rad, Hercules, CA) using SsoAdvanced 2X SYBR green supermix (Bio-Rad) and 2 μL of DNA. Standard curves were created from serial dilutions of linearized plasmid containing inserts of the E. coli 16S rRNA gene and melt curves were used to confirm the absence of qPCR primer dimers. The resulting triplicate amounts were averaged before calculating the number of bacterial 16S rRNA gene copies per microliter of DNA solution (see Additional file 2: Table S5).
The sequences were analyzed in QIIME 1.9.1 . First, the forward and reverse sequences were merged using SeqPrep. Demultiplexing was completed with the split_libraries_fastq.py command, commonly used for samples in fastq format. QIIME defaults were used for quality filtering of raw Illumina data. For calling the OTUs, we chose the pick_open_reference_otus.py command against the references of Silva 128 [34, 35] 97% identity with UCLUST to create the OTU table (biom format). Sequences with less similarity were discarded. Chimera checking was performed  and PyNAST (v1.2.2) was used for sequence alignment .
To test whether bacterial community composition is associated with taxonomic or geographic information, and if the taxonomic and geographic hierarchies can influence the bacterial community, we binned our data into different categories: “Subgenera” & “Species” to test taxonomic levels, and “Biogeography” & “Country”, to test the effect of geographic collection location. The summarize_taxa_through_plots.py command was used to create a folder containing taxonomy summary files (at different levels). Through this analysis it is possible to verify the total percentage of bacteria in each sample and subgenus. Additionally it is also possible to have a summary idea of the bacteria that constitute the bacterial community of Polyrhachis. In order to standardize sequencing effort all samples were rarefied to 400 reads. All samples that obtained fewer than 400 bacterial sequences were excluded from further analysis.
We used Analysis of Similarity (ANOSIM) to test whether two or more predefined groups of samples are significantly different, a redundancy analysis (RDA) to test the relationships between samples, and Adonis  to determine sample grouping. All these analyses were calculated using the compare_categories.py command in QIIME. The G test of independence (P, FDR_P and Bonferroni_P) was carried out to determine whether OTU presence/absence is associated with a host category through group_significance.py command. All these statistical tests serve to test whether the bacterial community is being influenced by any of the categories described above.
Alpha diversity was quantified using observed species richness, Shannon diversity, the Chao1 nonparametric richness estimator and whole-tree phylogenetic diversity and Simpson as implemented in equitability metric. We also compared alpha diversity based on a two-sample t-test using non-parametric (Monte Carlo) methods to test differences in OTU richness among subgenera. Unweighted and weighted UniFrac distance matrices , which uses phylogenetic information to calculate community similarity, were produced through the QIIME pipeline. The rarefaction curve was also created in QIIME and it is important to confirm if the sequencing was enough to cover the entire bacterial community associated with Polyrhachis. These beta diversity metrics were used to compare community level differences between categories. Jaccard dissimilarity metrics were calculated by beta_diversity.py command in QIIME. A matrix of community pairwise distances was generated by UniFrac and used to cluster samples by (i) the Unweighted Pair Group Method with Arithmetic Mean (UPGMA) method and (ii) principal coordinates analysis (PCoA). The UPGMA and PCoA analyzes that use the UniFrac beta diversity matrices show us which categories are influencing the bacterial community. As these analyzes have different methodologies and they will generate more robustness to the data of the study.
At a sequencing depth of 400, 64 samples passed this cutoff and were included in downstream analyses. To illustrate the relationship between ecological communities [40, 41], we implemented the analysis of multidimensional nonmetric scaling (NMDS) and related statistics in the PAST3 software package . Sorensen (Dice coefficient) and Bray-Curtis similarity indices  were used to test the variation and the structure of the bacterial community, respectively. The samples were grouped according to the host subgenera, and after viewing the plots, analyzes of similarity (ANOSIM) with Bonferroni correction was used to determine statistical significance [40, 41, 43]. As this analysis requires at least two representatives from each group, the subgenera that had only one representative were grouped into a category “Mixed”.
Networks were visualized using Cytoscape3.2.1  edge-weighted spring embedded algorithm to display the OTUs and sample nodes . Each host-bacterial network was constructed as a graph, in which each node represented a host sample. Connections were drawn between samples representing the shared significant OTUs (each color represents a different OTU). Through the network it is possible to visualize the complexity that surrounds the bacterial community associated with Polyrhachis and to look for which category may best explain the pattern found. A heatmap was constructed with all OTUs that had 400 reads represented in the main dataset using heatmap.2 and the vegan package  in R . The dendrogram of the samples shown in the heatmap was created with Bray-Curtis dissimilarity hierarchical clustering of bacterial communities in hclust. We also added a column dendrogram to cluster the genera that occur more often together. In this analysis we restrict only the most well represented OTUs and check if there is any OTU specificity within any of the categories described above. With this analysis it is also possible to verify the samples that have multiple infections as can happen with specimens infected with Wolbachia and Blochmannia .
We did analyses of correlation and coevolution: 1) compared the bacterial community following the host phylogeny of Mezger and Moreau  (coevolution/vertical transfer); 2) and similarity of bacterial community from hosts based on their locality (horizontal transfer). For this, geographic distances were calculated from sample locality information using geographical collection coordinates (latitude/longitude) of each included sample. They were transformed to UTM distance metric using the “rgdal” package  in R  and geographic distance matrix was constructed. The weighted distance of all sample were calculated through beta diversity in QIIME. The correlation between the bacterial community and geographic distances of Polyrhachis, and bacterial community and host phylogeny were calculated using the Mantel test (999 permutations) using the “vegan” package  in R. We also tested for significant associations between bacterial community dissimilarities and host genetic and geographic distances, we used partial Mantel tests, as implemented in the vegan package in R .
Bacterial 16S rRNA diversity
Illumina 16S rRNA sequencing of Polyrhachis ant hosts reveals a relatively simple microbiota that is remarkably conserved. Our analyses obtained 5443 observed OTUs from a total of 61,225 reads from 132 specimens from 12 of the 13 subgenera of Polyrhachis collected from across the Old World, which permitted analyses comparing different host categories: species, subgenera, biogeography and countries.
Statistical analyses of bacterial community diversity
We performed statistical tests (weighted and unweighted) to examine potential patterns that influence the bacterial community of Polyrhachis. From these we found subgeneric taxonomic affliation of the host (Adonis, unweight R2 = 0.23602 and P = 0.002; Anosim, unweight R2 = 0.11400 and P = 0.029; RDA, unweight Pseudo F = 1.47656 and significance = 0.001) had more influence on bacterial community composition than broader biogeographic origin, country or species, although not statistically significant.
Through the results of the G test (P, FDR_P and Bonferroni_P), we found bacteria community presence/absence is significantly different across multiple categories (species, subgenera, biogeography and country) [see in Additional file 4: Table S3]. Within the species category more bacteria were significant across samples than the other host categories. However, the bacteria Enterobacteriaceae (multiple strains, including Candidatus Blochmannia), Wolbachia (multiple strains), Nocardia, Sodalis, Thiotrichaceae and Lactobacillus were significant across all categories [Additional file 4: Table S3].
Through heatmap analysis (bacterial genera and family levels), we investigated the entire bacterial community found in this study and the abundance of OTUs found in each sample. For easy viewing, we choose to show only OTUs with more than 400 reads. It is interesting to note that more than 50% of the bacterial community consisted of Enterobacteriaceae (multiple strains). Several strains of Enterobacteriaceae were restricted to specific subgenera of Polyrhachis. This includes Candidatus Blochmannia-New.ReferenceOTU70 which was almost exclusively associated with the host subgenus Myrma from the Afrotropics, Enterobacteriaceae-New.ReferenceOTU13 which was almost exclusively with subgenus Polyrhachis, and Enterobacteriaceae-New.CleanUp.ReferenceOTU0 is found in samples from subgenus Myrmhopla.
Correlation and coevolution tests
The Mantel test verified the correlation of the bacterial community and geographic distance when analyzed with phylogenetics information from Merzer and Moreau  for Polyrhachis hosts. In addition using the Mantel test we found support for correlation between the phylogeny of the host and the bacterial community using the “vegan” package ) in R (R = 0.2289 and P = 0.0001). We also tested for the influence of locality on the bacterial community sampling, again using the Mantel test through the R software package to generate the pairwise geographical distances of each Polyrhachis sample. Our results showed that there is no correlation between the geographical location and the bacterial community overall (R = 0.08582 and P = 0.0756). Lastly through a partial mantel test of the three matrices (bacterial community, host phylogeny and geographical distances), we were able to demonstrate that the phylogeny of the host explains just part (R = 0.2279 and P = 0.0001) of the entire bacterial community, while geographical distance does not have significant influence on structuring the bacterial community of spiny ants (R = 0.09075 and P = 0.0697). While conducting more specific analysis of correlations of individual OTUs with the phylogeny of the host, we did not obtained significant results.
The use of NGS technologies to study the microbiome is relatively recent and these data are providing an unprecedented understanding of microbial diversity and putative function in many habitats and across a diversity of hosts. The bacterial communities associated with hosts can vary from simple to complex and can be influenced by environmental, genetic and other factors of the host or host’s environment which can make the task of understanding the elements determining host-association a challenge . The mechanisms that govern the ecology and evolution of the microbiota inside most hosts are still unknown and detailed studies are limited [27, 45, 51–56]. Besides revealing the bacterial community associated with hosts, studies that attempt to explain changes and what factors influence this bacterial community are still scarce . Many factors may influence the microbiota associated with the host, for example: diet, pH, host phylogeny (coevolution), life stage, and host location [58–62]. Of all these factors, the phylogeny of the host and diet has a strong effect on bacterial communities for many hosts . In a study involving ants, Anderson et al.  found similarity of the bacterial communities between species of the same trophic level, and found differences between herbivorous and predatory species. However, geographic location can also be an important mechanism influencing the microbiome . Our results are the first to characterize the bacterial community associated with the diverse spiny ant genus Polyrhachis from across their distributional range. Additionally, we were able to test whether the host phylogeny or biogeography could be influencing the diversity of bacterial communities found associated with this animal group.
Our results highlight how complex associations of different bacteria associated with Polyrhachis can be. This suggests that the evolutionary history of the host can influence the bacterial community in Polyrhachis. Ley et al.  who analyzed mammalian bacterial communities found correlations between diet and host microbiota, which they related to the gut physiology of the host. Compared to vertebrates, insects have a lower diversity of gut bacterial communities and these can be more variable [64, 65], which makes the understanding of the mechanisms that may influence communities difficult.
In a study analyzing various insects Jones et al.  also recovered low bacterial richness, as has been found in other studies [66–68]. One possible explanation is that the host has a mechanisms to prevent the establishment of new bacteria, as a way to defend against pathogens . Although the high infection with Wolbachia found in this study could also be an explanation for the low richness found in Polyrhachis, since this bacteria can reduce the diversity of bacterial communities .
Composition of the bacterial community
The bacteria most commonly found in our study were Enterobacteriacea (multiple strains). It was found present in all sampled individuals (at least one strain) across different subgenera of Polyrhachis ants, sampled from across their known geographical range (Fig. 1). Blochmannia, a member of the Enterobacteriacea, is known to possess primary interactions in Camponotini ants, which includes Polyrhachis. For symbionts of Polyrhachis the phylogenetic trees are congruent with those of their hosts across long periods of evolutionary time, indicating the coevolution of host and symbiont in previous studies [70–72] and the current study. In fact in previous studies this endosymbiont was recovered as a monophyletic group associated with Camponotini ants, showing coevolution of host and endosymbiont and suggests the acquisition of this microorganism must have occurred in the common ancestor of this ant tribe [22, 23].
The Blochmannia endosymbiont is known to play a nutritional role for the host, providing several essential amino acids , especially in early life [24, 25, 74]. Blochmannia also maintains certain genes for basic cellular functions, such as biosynthesis of the nine essential amino acids (excluding Arginine), and urease cofactors and enzymes, which allows the symbiont to recycle urea nitrogen provided by the host’s excretory system [73, 75, 76]. In addition, the nutritional role of Blochmannia is not the only potential interaction with its host, as it has also maintained genes needed to contribute to the metabolism of nitrogen, sulfur and lipids [24–26].
Overall we detected low Candidatus Blochmannia abundance, contrary to what we expected based on previous studies from this ant genus [22, 23]. But Blochmannia are known to have high mutational rates , suggesting that many if not most of the bacteria only identified as “Enterobacteriaceae” or “Enterobacteriaceae - other” may in fact be Blochmannia. This high mutation rate and the relatively short fragment of 16S rRNA that can be sequenced using NGS methods is likely responsible for our inability to assign most Enterobacteriaceae to lower taxonomic categories.
When we restricted our analysis to the bacterial genus level, 15.70% of samples included Candidatus Blochmannia. When we reduced the hierarchical level to Family, we recovered Enterobacteriaceae in more than 70% of all bacterial communities across geographical localities and host subgenera, with all individuals having at least one OTUs from this family. We also found some strains of Entecobacteriacea associated with specific host subgenera. This is potentially indicative of co-evolution and specificity of the strain to the host. For example we found Candidatus Blochmannia-New.ReferenceOTU70 associated with subgenus Myrma from the Afrotropics, Enterobacteriaceae-New.ReferenceOTU13 associated with Polyrhachis, and Enterobacteriaceae-New.CleanUp.ReferenceOTU0 associated with Myrmhopla.
This may suggest Blochmannia has undergone rapid change since its mutational rate is known to be high , which could prevent the identification of these OTUs as Blochmannia. Previous studies from the tribe Camponotini using traditional molecular techniques, i.e. Sanger sequencing of the entire 16S rRNA, showed a strong relationship of this bacterium with the host tribe [22, 23]. Even assuming that all Enterobacteriaceae found in this study belong to the bacterial genus Blochmannia, our data is still without precedent, since Brown and Wernegreen  using NGS in a study involving Camponotus found that Blochmannia typically constituted 95–98% of reads, and in our study of Polyrhachis only 70% (Blochmannia and all OTUs of Enterobacteriaceae combine). This lack of sequence conservation suggests that this bacterium may not be preforming these same fundamental roles suggested by previous studies, at least for the genus Polyrhachis. More studies are needed to reveal the function of these bacteria in the genus.
Although our results suggest that even without the modification of the Qiagen DNeasy kit for gram-positive bacteria, our DNA extraction method was able to obtain some DNA from gram-positive bacteria, but this could still influence the diversity of bacteria we are able to detect and our method may be omitting some gram positive bacteria. One interesting finding we uncovered is regarding selection of reference options for calling OTUs in Silva 128 [34, 35]. Initially we chose the pick_closed_reference_otus.py command instead of pick_open_reference_otus.py command, but this greatly reduced the number of bacteria sampled in our study. Through this command the aligned sequences are compared to the reference database, and if it does not match with any reference, the sequence was excluded from the analysis. In other words, the use of this command is not able to identify novel diversity, being restricted to already-known taxa . As it is known that Polyrhachis have Blochmannia [22, 23], and this bacterium has a high mutational rate , the pick_open_reference_otus.py command enabled the detection of unknown OTUs (i.e., those that are not represented in the reference database) compared with the closed reference of Silva 128 [34, 35]. The open reference option was able to find 429 additional OTUs (New.Reference and New.CleanUp.Reference). And when we limited our search to only OTUs with over 400 reads of 25 OTUs that met these criteria, 16 were new (Fig. 6). With that in mind, we strongly suggest that in cases where high bacterial mutational rate is known, the use of open reference instead of closed reference to insure detection of bacterial diversity is advised.
Other studies have shown Wolbachia as a major player within the bacterial community of invertebrates [19, 27, 28, 55, 78]. For example, in the screening of 24 Polyrhachis species, five (20.8%) were infected with Wolbachia . Kautz et al.  found Wolbachia in 25% of Polyrhachis analyzed from Australia. In our analysis we found Wolbachia in 65 samples of Polyrhachis (49.24%), and of these samples 25 showed multiples strain infections (38.46%). All strains have a wide distribution across our samples of Polyrhachis. Although Wolbachia is known for manipulating the reproduction of the host, its function in ants is still unclear.
The next most common bacteria associated with Polyrhachis is Lactobacillus found in 31 samples (23.48%). This bacterium was found widely distributed across host subgenera and across host locations. Recent work in the ants has shown the presence of Lactobacillus, but its function in this group is not yet fully understood. Kellner et al. , also through NGS techniques, found 56% of their samples of Mycocepurus smithii (a fungus-farming ant) contained Lactobacillales. Lactobacillus have antimicrobial properties and are widely used in the food industry and fermentation of milk products . Lactobacillus expresses antimicrobial properties through lactic acid secretion to acidify environmental conditions that some other bacteria and fungi cannot tolerate. Therefore Kellner et al.  believe that Lactobacillus may serve an important role as defense pathogens in the M. smithii system. In another study involving termites, Lactobacillus was found in the insect feces where, in addition to this protection function, it can also serve as a substrate or fertilizer [82, 83].
Polyrhachis, along with a few other ant genera, is known for the absence of a metapleural gland . Four possible functions are assigned to this gland: antimicrobials, chemical defense, recognition odor and territorial marking. The first two functions are well accepted and supported by several studies, while the last two require further investigation . This gland is essential for ground nesting ants, since they are more susceptible to infections due to the dark and sometimes damp conditions of their nesting habitat. Although many species of Camponotus and Polyrhachis nest arboreally, those with terrestrial habits should have evolved alternative antimicrobial defenses . Based on this hypothesis, another study suggested that the behavior of self-cleaning, as well as the use of venom with antimicrobial properties, are the key to disease resistance within the colony of a weaver ant species of Polyrhachis dives, Smith . With this in mind, Lactobacillus could be assisting in the defense of the colony potentially replacing the role of the metapleural gland for this genus.
In our findings Entomoplasmatales is present in only 0.80% of the bacterial community found in Polyrhachis. This result is different than those previously reported in the literature, as Kautz et al.  observed 46% infection rate by Spiroplasm (Entomoplasmatales) and Russell et al.  found 20% infection by Spiroplasm for this genus. Russell et al.  also suggested that Spiroplasm enrichment could be a feature specific to Polyrhachis and their close relatives. This may not be a genus-wide attribute, because four of the six Polyrhachis included in their study were from the Australian Wet Tropics and came from species in the subgenus Chariomyrma (4/6 species infected). Our findings do not support this as we did not find Spiroplasm strongly associated with Polyrhachis, even within the subgenus Chariomyrma.
The correlation (partial mantel and mantel tests) found in this study indicates that host phylogeny (vertical transfer) could influence the bacterial community to some extent. Our statistical tests also gave similar results to those observed for the mantel tests, suggesting that the phylogeny of the host (subgenera) explains part of the bacterial community, and host location (country or biogeography) none. This result corroborates Meirelles et al.  that also did not find any geographic signature in the bacterial community from the fungus-growing ant, Atta texana (Buckley). Certainly the specificity found in some strains of Enterobacteriaceae within subgenera of Polyrhachis contributed to our findings of correlation between bacterial community and phylogeny of the host (vertical transfer). All these data provide support for the coevolution of Polyrhachis and their microbiome, since geography can be seen as an approximation to the sum of environmental effects, such as local weather patterns and availability of food sources, which select for and influence local community assemblages. But we cannot assume that horizontal transfer does not also contribute to the diversity of bacterial communities found. Our findings of what drives the bacterial community of Polyrhachis corroborates the findings of Sanders et al.  and Ley et al. . The microbiota found in these studies also demonstrated that there is a significant effect of phylogeny of the host. Therefore, although there is a difference (both in abundance and diversity) between bacterial communities of different ants we still understand very little about the mechanisms that influence the microbiome.
These results of varing infection rates of Polyrhachis by a diversity of bacteria demonstrate the power of next-generation sequencing to uncover host-associated bacteria. In addition, our data uncovered novel bacteria, showing that with this technique it is possible to explore and discover bacterial diversity never before studied from hosts. We also recovered some species or groups of bacteria associated with only one host subgenus suggesting host-specificity and host-phylogeny could be a determining factor in the distribution of bacterial community in these associations. Furthermore, we did not recover any patterns of bacterial diversity correlated with a specific host geographic region, suggesting these microbes are not just being picked up in the environment. In the general context, we observed the complexity of an entire bacterial community associated with Polyrhachis throughout their geographic range. We focused our discussion on the most commonly recovered bacteria because we believe that these bacteria described above have an important role and may be able to influence the evolution and ecology of the host. General knowledge about the host united with information on the host’s microbiome are important tools to understand more about the evolutionary complexity of these associations in nature.
Earth microbiome project
Next generation sequencing
Multidimensional nonmetric scaling
Operational taxonomic unit
Universal transverse mercator
We thank Dirk Mezger for use of DNA extractions of Polyrhachis for this project and Matt Boot, Kevin Feldheim, Estefany Romero, Andrea Thompson, Max Winston, Brian Wray, and Erica Zahnle, for their invaluable assistance in the laboratory. For advice regarding the experimental design and analyses we thank Sarah Owens, Benjamin Rubin, Jon Sanders, Max Winston and Brian Wray. All work was completed in the Pritzker Laboratory for Molecular Systematics and Evolution at the Field Museum of Natural History, Chicago, Illinois, USA. We thank all members of the Moreau Lab for various advice and help. We thank Bruce and René Lauer and the Lauer Foundation for Paleontology, Science and Education NFP for generous support of the Pritzker Laboratory, which made this research possible. M.O.R thank Marcelo Simões Sanchez for his very generous support and encouragement during all parts of the study. We thank three anonymous reviewers that helped improve this manuscript.
M.O.R. thanks CAPES Foundation (process no. 007343/2014–00), and the Ministry of Education of Brazil, (Brasília DF 70.040–020) for their financial support. C.S.M. acknowledges the National Geographic Society (NGS Committee for Research & Exploration grant #9451–14) and the Field Dreams program of The Women’s Board of The Field Museum for financial support.
Availability of data and materials
All raw sequence data is available publicly in https://figshare.com/s/290531bea3dee984444e and NCBI SRA accession number SRR5136256 and study SRP095836.
MOR and CSM designed the experiments, analyzed the data and wrote the manuscript. MOR performed the experiments. OCB assists in data analysis and discussions. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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