Symbiotic relationships between hosts and bacteria are common in nature, and these may be responsible for the evolutionary success of various groups of animals. Among ants, these associations have been well studied in some genera of the Camponotini, but several questions remain regarding the generality of the previous findings across all the members of this ant tribe and if bacterial communities change across development in these hosts. This study is the first to characterize the bacterial community associated with a colony of the recently recognized genus Colobopsis and three colonies of Camponotus (two distinct species) and show how different the composition of the bacterial community is when compared across the different genera. Our data reveal that Colobopsis (species: Co. riehlii) and Camponotus (species: Ca. floridanus and Ca. planatus) have distinct microbiota, and we were able to verify that the identity of the species contributes more to the bacterial diversity. We also demonstrated that there were no significant differences between colonies of the same species (Camponotus planatus), and between stages of development from different colonies. We did find that some developmental stages have distinct bacteria, confirming that each stage of development could have a specific microbiota. Our results show species are one of the factors that shape the bacterial community in these Camponotini ants. Additional studies of the intra-colonial microbiome of other hosts and across development may reveal additional clues about the function and importance of bacteria in colony recognition, individual and colony health, and nutritional upgrading.
Citation: Ramalho MO, Bueno OC, Moreau CS (2017) Species-specific signatures of the microbiome from Camponotus and Colobopsis ants across developmental stages. PLoS ONE 12(11): e0187461. https://doi.org/10.1371/journal.pone.0187461
Editor: Brenda A. Wilson, University of Illinois at Urbana-Champaign, UNITED STATES
Received: March 17, 2017; Accepted: October 22, 2017; Published: November 22, 2017
Copyright: © 2017 Ramalho et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All raw sequence data is available publicly in https://figshare.com/s/290531bea3dee984444e and NCBI SRA accession number SRR5136256 and study SRP095836.
Funding: M.O.R. thanks CAPES Foundation (process no. 007343/2014-00) the Ministry of Education of Brazil, (Brasília DF 70.040-020) for their financial support. C.S.M. acknowledges the National Science Foundation (DEB-1442316) and Field Dreams program of The Women's Board of The Field Museum for support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Symbiotic interactions are thought to be one of the factors responsible for the ecological success of many groups of animals and plants [1–4]. Symbiotic microbes can influence the host through the manipulation of the host's reproduction or provide direct benefits to the host through nutrition, defense, or even environmental tolerance [5–8]. Social animals often interact intimately with other members of their group and offspring through grooming and trophallaxis. These activities facilitate the transmission and sharing of bacteria, often making their microbiota extremely specialized [9,10]. As these behaviors may facilitate symbiont transfer, social insects are considered models to evaluate evolutionary aspects of microbial community diversity and acquisition .
Among the Hymenoptera (bees, wasps, and ants), many species of ants (Formicidae) are known to possess diverse and stable microbial communities [12–18]. The importance of bacterial symbionts related to nutrition has been shown to be fundamental in ant species feeding low on the trophic scale [17,19,20] as is the case for the ant tribe Camponotini. One of the most well-known ant genera recognized for having symbiotic relationships with bacteria is Camponotus Mayr, 1861 [21–24]. The genus is currently subdivided into 43 subgenera, covering more than 1000 valid species and 31 fossils , with an almost world wide geographic distribution. They are popularly known as carpenter ants, have diurnal and nocturnal activity with a generalist diet, and have diverse nesting habits. Arboreal nesting species may specialize on a diet that is nutritionally deficient, since their diet is largely derived from the exudate of plants and phytophagous insects [20,26,27].
The phylogeny of Camponotini, especially within Camponotus, has always been complex, and several studies using different approaches have indicated that Camponotus is not monophyletic [28–31]. Ward et al.  in a recent phylogenetic analysis of the group elevated Colobopsis Mayr 1861, to the genus level, but still belonging to the tribe Camponotini. Prior to this it was considered a subgenus of Camponotus. Completely understanding the phylogeny and evolution of Camponotus remains a difficult task, which will require the efforts of researchers from around the world, due to their wide distribution and high species diversity. Colobopsis, now considered a distinct ant genus, has 94 valid species, with a distribution across the Australasia, Indomalaya, Neartic, Neotropical, Oceania and Paleartic regions . This genus has strictly arboreal habits, and nests inside dead branches. As in the distantly related turtle ant genus, Cephalotes, they can employ phragmotic major workers to block the nest entrance with their heads as a line of passive defense [34–36].
With the recognition of this new genus, Colobopsis, it now raises the intriguing question whether host-associated endosymbionts are tracking the host's evolutionary history. We also wanted to investigate the diversity of bacteria associated with these genera and determine how common Blochmannia is associated with both genera, as has been noted in several studies for Camponotus [21,22,37]. In a recent study Brown and Wernergreen , using next-generation sequencing (NGS) techniques, found that 95–98% of the reads of Camponotus chromaiodes were dominated by the intracellular bacteria Blochmannia and Wolbachia. However the variation across the different stages of development and for additional species and genera remains unclear.
It is known that diet [38,39], parasitic infection , host age , phylogeny of host [15,42] may contribute to changes in the bacterial community. Thus, the natural variation found across insect microbiota may indicate important influences of host biology. To this end, our understanding of factors that determine the bacterial communities of Camponotus floridanus, Camponotus planatus and Colobopsis riehlii remain unclear. In addition detailed comparative surveys of the microbiota present in different castes and across development within a colony are still lacking .
This study focuses on the bacterial community of different colonies of Camponotus and Colobopsis across their stages of development, to reveal more about the factors that influence bacterial communities. Therefore, the present work raises the following questions: 1) What exerts greater influence in these microbiomes, the colony/species or developmental stage? 2) Are Camponotus floridanus, Camponotus planatus and Colobopsis riehlii bacterial communities different? 3) Do individuals from different colonies, but the same species, have similar microbiota? 4) Are there differences between the stages of development within the same colony? And finally 5) Does the same stage of development from different colonies/species have similar bacteria? Leveraging next generation amplicon sequencing, we address these questions and document the diversity of bacteria to help identify the factors that structure the bacterial communities found across a diverse and widely distributed group of animals.
Materials and methods
Sample collection and determination of the different stages of development
All specimens used in this study were collected by authors MOR and CSM in April 2015 from the Florida Keys, USA—Watson Creek bridge, Monroe County (24.69786N, 081.3405W). These specimens were collected under the permissions of the Florida Department of Environmental Protection—Division of Recreation and Parks (permit number 0127201515 to CSM). Three Camponotus colonies, representing two species (Ca. floridanus and Ca. planatus), and one Colobopsis riehlii colony were obtained from hollow twigs of trees and brought to the lab. The samples were immediately preserved in 95% ethanol and stored at -20°C before DNA extraction. In order to determine the castes / stages of development, we selected the eggs, larva with variation of size (L1 = small larvae, below 2 mm; and L2 = large larvae–last larval instar, approx. 2–4 mm), pupae classified according to the pigmentation of the eye and body (P1, P2 and P3—from the white eye to total pigmentation, respectively), small and large workers (W1 and W2 to represent adult worker size polymorphism, with W1 as minor and W2 as major workers), queens and males [43,44]. Within each entire colony, the quantity of each caste/subcaste/stage was determined (see Table 1). The taxonomic identification were determined using taxonomic keys for Camponotus and Colobopsis species in the southeastern US (available in: http://mississippientomologicalmuseum.org.msstate.edu//Researchtaxapages/Formicidaepages/Identification.Keys.htm#.WE7qIH31-3H—from Creighton 1950, Snelling 1988; Mark Deyrup, pers. comm., William MacKay-Camponotus website) and vouchers were deposited in the collection of the USP Zoology Museum in São Paulo, Brazil.
DNA extraction and bacterial DNA sequencing
Total DNA was extracted from 85 samples (three specimens of each caste and colony, when available) of entire individuals with the Qiagen DNeasy Tissue kit following the manufacturer's recommendations with filtered pipette tips and sterile techniques were applied to avoid contamination following Moreau .
Additionally, the samples were sterilized on the surface as described in Moreau . Although we did not use the modification of the Qiagen DNeasy kit for Gram-positive bacteria, we did follow the extraction method recommended by Rubin et al. . This method is able to detect Gram positive bacteria in large quantities, but this could still influence the diversity of bacteria we are able to detect. We amplified 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/). Per sample three PCR reactions were performed (triplicate) when samples were available, each 25 μl PCR reaction contained 12 μl of MO BIO (MO BIO, Solana Beech, USA) PCR Water (Certified DNA-free), 10 μl of 5 Prime HotMasterMix (1x) (5 PRIME, Gaithersburg, USA), 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 (>0.20 ng/ μl), under the following conditions 94°C for 3 min, with 35 cycles at 94°C for 45 s, 50°C for 60 s, and 72°C for 90 s, with a final of 10 min at 72°C. After the triplicate reactions were combined we confirmed amplification efficiency using agarose gel electrophoresis (1%). The samples were quantified via qPCR and Qubit (Thermo Fisher Scientific) with High Sensitivity Assay Kit (Life Technologies Corp., Carlsbad, USA), and only then pooled with different samples after controlling for volume to include the same amount of genetic material. For purification, only 100 μL of each pool was cleaned using the UltraClean PCR Clean-Up Kit (MO BIO, Solana Beech, USA), following the manufacturer's recommendations. The molarity of the pool was 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 at the Field Museum of Natural History, Chicago. A 151 bp x 12 bp x 151 bp MiSeq Illumina run was performed using the custom sequencing primers and procedures described in the supplementary methods in Caporaso et al. . All raw sequence data are publicly available in Figshare [https://figshare.com/s/290531bea3dee984444e] and NCBI SRA accession number SRR5136256 and study SRP095836.
We measured the amount of bacterial DNA present in all samples with quantitative PCR (qPCR) of the bacterial 16S rRNA gene using 515f (5’—GTGCCAGCMGCCGCGGTAA) and 806r (5’—GGACTACHVGGGTWTCTAAT) universal bacterial primers of the EMP (http://www.earthmicrobiome.org/emp-standard-protocols/16s/) to check Illumina sequencing efficiency. All qPCRs were performed on a CFX Connect Real-Time System (Bio-Rad, Hercules, USA) 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 protocol for standardization following the recommendations of Rubin et al. . All samples were analyzed in triplicates including a blank. The results were averaged before calculating the number of bacterial 16S rRNA gene copies per microliter of DNA solution (S4 Table).
The sequences were analyzed in QIIME 1.9.1 . We merged the forward and reverse sequences through SeqPrep. Demultiplexing was completed and QIIME defaults were used for quality filtering of raw Illumina data. We implemented the pick_open_reference_otus.py command using the SILVA 128 reference database with 97% identity [49,50] to call OTUs, and UCLUST to create the OTU table. Singletons were discarded. Chimera checking was performed with UCLUST  and PyNAST (v1.2.2) was used for sequence alignment .
To test whether the composition of the bacterial community is more related to the colony/species itself, or whether it is more related to the different stages of development, we separated our analyses into two categories: different colonies/species (MOR#59, MOR#62, MOR#69, and MOR#73) and developmental stage (available in colonies/species sampled, see Table 1).
The summarize_taxa_through_plots.py command was used to create a folder containing taxonomy summary files. In order to standardize, all samples that obtained less than 400 bacterial sequences after quality filtering were excluded from the subsequent analysis. We started our analysis with 73 samples (triplicate of each caste when available, which obtained good DNA quality), and after filtering to a sequencing depth of 400, 63 samples passed this cutoff and were included in downstream analyses. Ten samples were excluded because they did not pass the cutoff of 400 sequences (see S6 Table), and they are identified with a yellow star in Fig 1. All analyzes started from the bacterial OTU data. We implemented an analysis of multidimensional nonmetric scaling (NMDS) and related statistics in the PAST3 software package  to illustrate the relationship between ecological communities [54,55]. Sorensen (Dice coefficient) and Bray-Curtis, similarity and dissimilarity indices, respectively  were used to test the variation and the structure of the bacterial communities, respectively. The samples were grouped according to the host colony/species and developmental stage. Analyses of similarity (ANOSIM) with Bonferroni correction was used to determine statistical significance [54,55]. The SIMPER analysis was conducted to verify the contribution of each OTU for grouping between colonies/species and different developmental stage .
A. Different colonies and species used in this study and their bacterial communities. B. Summary of all OTUs found in Colobopsis riehlii. The main bacterium is Enterobacteriaceae in pink, followed by Wolbachia in brown C. Summary of all OTUs found in Ca. floridanus and Ca. planatus. The main bacterium is Candidatus Blochmannia in green. The yellow stars highlight samples that were excluded after the read depth standardization of 400 reads was implemented.
The G test of independence (P, FDR_P and Bonferroni_P) was carried out to determine whether OTU presence/absence is associated with different colonies/species or different developmental stages. We also used Analysis of Similarity (ANOSIM), Adonis  to determine sample grouping and a redundancy analysis (RDA) to test the relationships between samples.
Observed species richness, Shannon diversity, the Chao1 nonparametric richness estimator, whole-tree phylogenetic diversity, Simpson, and equitability metrics were calculated to compare alpha diversities based on a two-sample t-test using non-parametric (Monte Carlo) methods to test differences in OTU richness among categories. Unweighted and weighted UniFrac distance matrices , which use phylogenetic information to calculate community similarity, were used to calculated beta diversity. These beta diversity metrics were used to compare community level differences between two categories: colonies/species and developmental stage. Jaccard dissimilarity metrics were calculated and the average was compared. A matrix of community pairwise distances was generated by UniFrac and used to cluster samples by principal coordinates analysis (PCoA).
Cytoscape v3.2.1  edge-weighted spring embedded algorithm was used to visualize networks of bacterial community . Connections were drawn between samples representing the shared significant OTUs. A heatmap was constructed with all OTUs that had 100 reads using heatmap.2 and the vegan package  in R . The dendrogram was created with Bray-Curtis dissimilarity hierarchical clustering of bacterial communities in hclust.
Phylogenetic tree reconstruction
To investigate the possible relatedness of some of our unassigned bacterial OTUs (representative sequences from the dominant OTUs), we downloaded from GenBank the closest Blast hits for our selected sequences and other strains of Blochmannia available from different Camponotini genera. We were able to include Blochmannia from all Camponotini genera except Dinomyrmex and Overbeckia. Sequences were assembled and edited using Bioedit Sequence Alignment Editor  and aligned with the Clustal W tool . We implemented a maximum likelihood analysis using PhyML 3.0  on the CIPRES web portal . The GTR+I+G model of sequence evolution was implemented. Branch lengths and bootstrap support are reported. To facilitate visualization, the clade of Wolbachia (brown) and Blochmannia (green) were colored in FigTree .
In this study we used the open reference option to assign OTUs. Open reference is an important tool for studies that want to take into account the diversity of bacteria that many not be present in the database . Since these results may return OTUs with no close species level assignments contained in the database, the open reference command assigns these OTUs to the previous taxonomic level (i.e. Genus, Family, etc.) where there is confidence in the assignment. So in our results some OTUs are only confidentially assigned to higher taxonomic levels like "Burkholderiales; Other", while others are assigned to the species level like Candidatus Blochmannia. From the four colonies analyzed we obtained 1,322 observed OTUs from a total of 152,500 reads from 73 samples from one colony of Colobopsis riehlii and three colonies of Camponotus from two species (one colony of Ca. floridanus and two colonies of Ca. planatus), which permitted analyses comparing different colonies/species and developmental stages. To visualize the diversity of OTUs found per sample we used the summarize_taxa_through_plots.py command (Fig 1). For Colobopsis, 19 samples across the stages of development were analyzed, resulting in 134 OTUs from a total of 16,591 reads, ranging from 206 to 3008 reads per samples. For analysis of the colonies of Ca. floridanus and Ca. planatus were recovered 1,188 OTUs resulting from 135,909 reads ranging from 10 to 13,989 reads, with the latter value belonging to one from the queens analyzed.
According to our results, the bacterial communities of Colobopsis riehlii and other Camponotus colonies (Ca. floridanus and Ca. planatus) are distinct. The predominant bacteria found in the samples of Camponotus were Candidatus Blochmannia (93.9%), Wolbachia (1.0%) (multiple strains), Enterobacteriaceae (0.8%), followed by other bacteria in smaller quantities. For the Colobopsis samples the predominant bacteria were Enterobacteriaceae (72.8%), Wolbachia (multiple strains) (22.2%), Pasteurellales (2.2%) mainly related to a specific stage of development, Sodalis (1.7%), Other Enterobacteriaceae (0.4%), followed by additional bacteria at low amounts (S5 Table).
By analyzing the bacteria found across different stages of development within a colony (developmental stage), we recovered bacteria associated with only a specific stage of development such as the Pasteurellales, which is present in the second larval stage of Colobopsis riehlii, and Wolbachia present only in the queens and males of Camponotus planatus. Our data also reveal that the larval stage exhibits much greater microbial diversity than the other stages of development (S3 Fig).
Patterns that influence the bacterial community
We performed statistical tests (weighted and unweighted, depth 400, 63 samples included) to examine potential patterns that influence the bacterial community of these Camponotini samples, and for this we analyzed the following two variables: differences between colonies/species and developmental stage. A list of the 10 samples that did not reach the depth of 400 reads and were excluded from the analysis are included in S6 Table. From these we found different colonies/species (Table 2), can influence the bacterial community of these Camponotini samples, although for the developmental stage we did not obtain significant results for the weighted distance.
Through analyses of beta diversity (matrices UniFrac weighted distance) we observed bacterial communities among all Camponotini samples. PCoA analysis showed that the bacterial community becomes more distinct when comparing the different species than when comparing the stages of development across all species (Fig 2). The average Jaccard dissimilarity metric was 0.90 for Camponotus colonies (one of Ca. floridanus and two of Ca. planatus), which suggests only few of the bacterial community members are shared among all individuals of different developmental stages of Camponotus, but for Colobopsis riehlii Jaccard dissimilarity of 0.65 was inferred, which suggests more of bacteria was shared among the colony.
A. Different colonies/species (axis 1 = 88.8% and axis 2 = 7.12%) and B. Developmental stage (axis 1 = 88.8% and axis 2 = 7.12%). Note that the "Colony/Species" category influences the bacterial community more than "Developmental stage".
No significant changes in the composition of the bacterial community (Sorensen index) were observed between the colonies/species and among developmental stage (S1 Table). However, when we analyzed the bacterial community structure (Bray-Curtis index, stress 0.051, for different colonies, and 0.051 for different developmental stage), we found significant results such as difference between samples MOR#73 (Ca. planatus) vs. MOR#62 (Co. riehlii) and MOR#69 (Ca. planatus) vs. MOR#62 (Co. riehlii) (Fig 3, S1 Table). For these analyses we did not recover significant differences between developmental stages.
Bray-Curtis, stress 0.081, Axis 1: 0.9817, Axis 2: 7.471E-06 and developmental stage Bray-Curtis, stress 0.085, Axis 1: 0.9807, Axis 2: 0.0002. Note that species play an important role in structuring the bacterial community.
The SIMPER between-groups analysis revealed that the OTUs recovered in the comparisons between the different colonies/species, are essentially the same OTUs responsible for structuring these bacterial communities within significance groups (S2 Table). But we also observe that there are multiple strains of Candidatus Blochmannia, Enterobacteriaceae and Wolbachia present across these samples.
To examine the complicated associations between samples with shared significant OTUs, we used Cytoscape to construct a network graph in which each node represented a host sample. Network analyzes were performed using the spring-embedded edge-weighted algorithm (Fig 4), which approaches the samples according to the number of OTUs shared, and we colored the edges according to the different colonies/species (Fig 4A), and in the different stages of development (Fig 4B). OTUs with less than 100 reads were hidden for easy viewing. From this analysis we observe greater structuring between species than across different stages of development.
A. The edges were colored according to the different colonies: MOR#59 –Camponotus floridanus in red, MOR#69 –Ca. planatus in orange, MOR#73 –Ca. planatus in green, MOR#62 –Colobopsis riehlii in blue. B. The edges were colored according to the different stages of development: egg in red, L1 in light green, L2 in green, P1 in blue, P2 in light blue, P3 in aquamarine, W1 in pink, W2 in light pink, queen in yellow and male in brown. Note that it is the same image as in A, but now colored according to the different stages of development.
Bacterial communities of Camponotus (Ca. floridanus and Ca. planatus) and Colobopsis riehlii are different
Our statistical results confirm that the bacterial community of Camponotus (Ca. floridanus and Ca. planatus) and Colobopsis riehlii are different (Table 3). This can clearly be seen in Figs 2 and 3. This result shows that even in closely related genera, the microbial communities are different, at least for the colonies/species analyzed in this study.
Camponotus planatus from distinct colonies have similar bacterial communities
Of all the colonies analyzed in the present study, the two Camponotus planatus colonies (MOR#69 and MOR#73), have the highest similarity, as observed from the statistical tests that resulted significant differences (Table 4), but a small difference if we compare with the other colonies. This result corroborates S1 Table.
There are microbiota differences in the stage of development between host species
Statistical analyzes show that there are significant differences in the development stage across two of the species, Camponotus planatus (MOR#69 and MOR#73) and Colobopsis riehlii (MOR#62). This pattern could also be true for Camponotus floridanus, but unfortunately after rarefaction only a few individuals from this colony (MOR#59) could be included and therefore we were not able to conduct beta diversity analyses on this species. As the main bacteria across all of these colonies are Blochmannia and Enterobacteriaceae (for Camponotus: Ca. floridanus and Ca. planatus, and Colobopsis riehlii respectively; S2 Table), the abundance of OTU (weighted) may not be appropriate to test for significant differences across the developmental stages within each colony. Therefore the results of unweighted distances were presented on Table 5, and there are significant differences in the development stage across two of the species.
The same stage of development in different Camponotus species have similar bacteria
To address this question we binned our Camponotus samples (Ca. floridanus and Ca. planatus) into the following groups: larva (L1 and L2), pupae (P1, P2 and P3), workers (W1 and W2) and finally a mixed group with queens, males and eggs (all directly derived from the queen). The results show that there were no significant differences when we analyzed each of these groups, (Table 6), which reveals that there is similarity in each of these stages of development, even when they were grouped from different colonies (See S1 Fig).
Bacteria responsible for differences between colonies/species and development stages
Through the results of the G test (P, FDR_P and Bonferroni_P), we found bacterial community presence/absence is significantly different across developmental stage and colonies/species (S3 Table). Between colonies/species more OTUs were significantly different across samples than the other developmental stage category (different stages of development within a colony). However, the bacteria Enterobacteriaceae (multiple strains, including Candidatus Blochmannia), Wolbachia (multiple strains) and Pasteurellales were present across all categories (S3 Table). Separate G-test analyses of the different developmental stages within each Colobopsis riehlii and Camponotus colony (Ca. floridanus and Ca. planatus) recovered the different OTUs, except for Enterobacteriaceae (S3 Table).
According to our results of measures of Alpha diversity (Chao1, PD whole tree, observed OTUs, Simpson and Shannon), we found that the samples of Camponotus floridanus, Ca. planatus and Colobopsis riehlii are not very diverse, showing few different OTUs. Likely due to this low diversity, we did not obtain significant results when comparing alpha diversities based on a two-sample t-test using non-parametric (Monte Carlo) methods. Through the rarefaction curve analysis of OTUs observed, our sequencing coverage of the bacterial communities appears satisfactory for most samples. However for some samples, it was not possible to reach a plateau (S2 Fig).
For easy viewing on our HeatMap, we are presenting only OTUs with more than 100 reads. We grouped the samples according to the quantity and type of associated bacteria. Our results revealed that there are some OTUs specific to a particular colony, such as OTU AJ245591.1.1215—Candidatus Blochmannia was restricted to the Ca. floridanus colony MOR#59. The Colobopsis colony was also distinct from the others, having specific OTUs, such as OTU EU348326.1.1455-Pasteurellales, KF249887.1.1350–Wolbachia and CP010049.668121.669704-Enterobacteriaceae.
For the colonies of Ca. planatus (MOR#69 and MOR#73) we also observed several samples from different development stage with two distinct strains of Candidatus Blochmannia: AF495758.1.1401, and the new strain New.ReferenceOTU1, suggesting possible multiple infection by this endosymbiont. For Wolbachia we found one strain with high abundance, mainly in Colobopsis (KF249887.1.1350), and we observed an infection rate of 94.73% from across our Colobopsis colony (n = 19). The OTU GAUE02014372.1.1238—Wolbachia was found only in males and queens of Camponotus present in colony MOR#69 (Ca. planatus). Lastly the CP010049.668121.669704-Enterobacteriaceae strain was recovered from larva (L2) of Camponotus planatus, colony MOR#69 (Fig 5). In less quantity the strain New.ReferenceOTU71—Wolbachia (difficult visualization in Fig 5) was found in both colony MOR#69 and colony MOR#62, at different stages of development.
These range from 0% (light yellow) to 100% (red). We choose to show only OTUs with more than 100 reads, for easy viewing. Dendrograms were generated from Bray–Curtis distance matrices. Note there are OTUs restricted to specific colonies/species.
Phylogenetic Tree: Blochmannia and Enterobacteriaceae OTUs are related
The inferred maximum likelihood phylogeny received high boostrap support across the major nodes placing our samples with their closest relatives. All the sequences of Blochmannia are grouped in a single clade with high bootstrap support (99%). In addition, the OTUs identified as Enterobacteriaceae in the present study are closely related to Blochmannia, corroborating the hypothesis that all Enterobacteriaceae are actually Blochmannia (Fig 6).
The maximum likelihood phylogeny of the 16S rRNA region of the main bacterial symbionts of this study along with the closests matches on GenBank. Bootstrap support is shown on branches. The labels are given with GenBank accession number (GenBank sequences) or collection code (sequences generated in the present study—colored in red). The branch color refers to bacteria with Wolbachia in brown and Blochmannia in green.
In Camponotini ants the presence of bacteria such as Blochmannia, considered a primary endosymbiont, and Wolbachia, as secondary, is already well known [21,22,37,67], but the diversity of the entire bacterial community has not been fully documented and differences across developmental stage have not been adequately explored. Although our study included a modest number of colonies (85 individual samples from four colonies) our results are the first to characterize the bacterial community associated with a colony of the recently recognized genus Colobopsis (species: Colobopsis riehlii) and three colonies of Camponotus (two distinct species: Ca. floridanus and Ca. planatus) and show how different the composition of the bacterial community is when compared across the different colonies/species (different genera and different species—collected in the same location), and how they are conserved when comparing across the different stages of development within a colony.
In general, our data reveal that Colobopsis riehlii and Camponotus (Ca. floridanus and Ca. planatus) have distinct microbiota, although they are closely related ant genera. The OTUs from these two host genera are distinct. We were able to verify that the identity of the species contributes more to the bacterial diversity than the stage of development. A significant difference between species is likely due to the different bacterial communities between Camponotus and Colobopsis ant species. We also demonstrated that there were no significant differences between colonies of the same species (Camponotus planatus), and between stages of development from different colonies, confirming that each stage of development may have a specific microbiota. Our results show different host species likely shape the bacterial community in Camponotini ants. Clear visual and statistical evidence also separates Colobopsis riehlii from the others Camponotus colonies, corroborating the studies by Blaimer et al.  and Ward et al.  in elevating Colobopsis as a separate genus from Camponotus.
In this study, bacterial community structure and composition in ants of the same colony were most similar to each other, a pattern recovered in other ant species [13,40,46,68]. This is likely because social insects live in densely populated colonies with highly related individuals , which may facilitate the sharing of the microbiota. In addition, it is often observed that Camponotini ants exhibits mouth-to-mouth (stomodeal) trophallaxis, i.e. the sharing of liquid nutrients through mutual feeding [70,71]. Nutrients stored in the crop or 'social stomach' are shared throughout the colony during trophallaxis , which is thought to be a primary means for horizontal bacterial transfer within a colony [26,73–75]. This intense interaction and exchange of microbiota may reinforce colony-specific signatures [40,76], and also appears to occur with Camponotini ants.
Blochmannia, a member of the Enterobacteriaceae, is known to provide important functions in Camponotini ants, which includes, Camponotus, Colobopsis, Polyrhachis and others, whose phylogenetic trees of symbionts are congruent with those of their hosts across long periods of evolutionary time, indicating the coevolution of host and symbiont [77,78]. In addition to its nutritional role , especially in early life , it has also maintained genes needed to contribute to the metabolism of nitrogen, sulfur and lipids [80–82].
The high mutational rate of Blochmannia  may influence and disrupt the identification of OTUs at the bacterial genus level for the short sequences generated by most amplicon methods, therefore Enterobacteriaceae or Other Enterobacteriaceae–may in fact be Blochmannia. For Camponotus (Ca. floridanus and Ca. planatus) we detected high Candidatus Blochmannia abundance. We also expected this bacterium in high abundance for Colobopsis riehlii but our results did not reveal this at first. Our phylogenetic analysis of the main OTUs found in our study grouped in the same clade as Blochmannia and Enterobacteriaceae with high statistical support. All the individuals of Camponotus (Ca. floridanus and Ca. planatus) and Colobopsis riehlii analyzed in the present study have some type of Enterobacteriaceae as the main bacterium in their microbiota and based on our phylogenetic analysis is likely Blochmannia. Our study also found 44 samples of Camponotus planatus, from two colonies (MOR#69 and MOR#73), with two strains of Blochmannia (double infection). This result corroborates Ramalho et al.  finding of double infections of Blochmannia in Camponotus textor Forel, an exclusively Neotropical species.
In fact the Blochmannia (strain / OTU) of Colobopsis is different from the (strain / OTU) of Camponotus, at least for the fragment of 16S rRNA that we sequenced. All these strains belong to the genus Blochmannia, corroborating what has already been found in other studies that this bacterium is established in the tribe [21, 22], but our data show that there is still a great difference / diversity of these strains of Blochmannia found in the samples of the present study (Co. riehlii, Ca. floridanus and Ca. planatus). This great diversity found within Blochmannia genus (16S rRNA gene) can be explained by its high evolutionary rate, which made possible the differences found in the present study. Functionally these distinct strains of Blochmannia are similar, supported by the genome  and the phylogenetics presented in this study. But the Blochmannia strain found in the samples of Colobopis and Camponotus of the present study are distinct, which suggests their microbiome to be distinct.
Wolbachia, a major invertebrate endosymbiont [14,84–86] famous for manipulating the reproduction of the host , was the second most common endosymbiont found in all Colobopsis riehlii samples, occurring in all individuals of the colony, across all stages of development. There are many studies associating this bacterium with Formicidae, but its function remains unclear. Interestingly OTU GAUE02014372.1.1238 of Wolbachia was found only in the reproductive castes (queen and males) in the colony MOR#69 of Camponotus planatus but was not found in the other stages of development across the colony. Another OTU of Wolbachia (New.ReferenceOTU71) although in a lower concentration was found in Colobopsis riehlii (MOR#62) and in Camponotus planatus (MOR#69). This low infection rate by Wolbachia (1%) has also been found in another North American Camponotus , although is not true across the genus as Ca. textor was found to be highly associated with Wolbachia .
The next most common bacterium associated was Pasteurellales—EU348326.1.1455 found specifically in the larval stage (L2) in Colobopsis riehlii (2.20%). Pasteurellales are one of the major orders within the class Gammaproteobacteria [88,89]. This bacterium is often present in the respiratory, alimentary and reproductive tract of various birds and mammals, including humans [89,90]. This group of bacteria has been identified from another arboreal ant, Pseudomyrmex ferrugineus , but their function in ants is not clear.
Previous studies have reported the presence of other symbionts in Camponotus, including Spiroplasma which has been reported in other species of Camponotus , but was not found in our results. Acetobacteraceae was also recently found in Camponotus, and is believed to be strongly host specific . We also recovered this bacterium (multiple strains) in 11 individuals of Camponotus (20.37%), but with few copies per individual, ranging from 1–4 reads.
Studies that try to understand the patterns that explain the association of microbiota and host inform us about the potential impacts and roles of these symbioses. In the present study we show that the Colobopsis riehlii microbiota is distinct from Ca. floridanus and Ca. planatus, a closely related genus. In general, the microbiota presented here appears as a species-specific signature, whereas most developmental stages do not have distinct microbiota. Although we present some differences across development, especially in the larval stage, the intense social interaction between individuals of a colony likely homogenizes the microbiota among colony members. Additional studies of the intra-colonial microbiome of other hosts and across development may reveal additional clues about the function and importance of bacteria in colony recognition, individual and colony health, and nutritional upgrading.
S1 Fig. Nonmetric multidimensional scaling (NMDS) plot illustrating bacterial community structure among different development stages.
Bray-Curtis, stress 0.029, Axis 1: 0.9683, Axis 2:0.0527.
S2 Fig. Rarefaction curves with OTUs by sequences per samples.
Rarefaction curves analyzed across the different stages of development. The queen was more diverse than the others and when compared between the colonies of Camponotus (Ca. floridanus and Ca. planatus) and Colobopsis riehlii.
S3 Fig. Simpsons index by developmental stage.
Through this image it is possible to visualize that the L2 larvae have a greater diversity in comparison with the other stages of development.
S1 Table. Analyses of similarity (ANOSIM).
These results are evaluating variation in the composition and structure of bacterial communities (global effect), and the colonies/species and developmental stage that showed significant differences.
S2 Table. SIMPER analysis reveals contribution of specific operational taxonomic units (OTUs).
This test indicates the contribution of specific operational taxonomic units (OTUs) to the observed differences in community structure among different colonies/species of Camponotini.
S3 Table. Analysis of G test of independence (P, FDR_P and Bonferroni_P) across Camponotini samples.
Hence, it determines whether OTU presence/absence is associated with different colonies and developmental stage.
S4 Table. Bacterial quantification through 16S rRNA gene (qPCR) of all samples.
Each sample was analyzed in triplicate therefore follows the values of average and standard deviation for each sample.
S5 Table. Bacteria found in Camponotini samples.
Bacteria and the quantities identified in Camponotini samples in the present study.
S6 Table. Samples excluded after the depth of 400 reads.
These 10 samples from different colonies did not reach our cutoff of 400 reads and they were excluded from the subsequent analyses.
We thank 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 laboratory 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 and the Field Dreams program of The Women's Board of The Field Museum, which made this research possible. We thank the following agencies for permissions and permits to collect ant specimens in the Florida Keys: Florida Department of Environmental Protection—Division of Recreation and Parks, United States Department of Interior—Fish and Wildlife Service, and The Nature Conservancy. MOR thanks Ana Maria A. O. Ramalho and Roselei Ap. Simões Sanchez for their very generous support and encouragement during all parts of the study. Lastly we thank the reviewers of this manuscript for helpful suggestions that improved this paper.
- 1. Buchner P. Endosymbiosis of animals with plant microorganisms. New York: Interscience Publishers; 1965.
- 2. Long SR. Rhizobium-legume nodulation: Life together in the underground. Cell. 1989;56: 203–214. pmid:2643474
- 3. Moya A, Peretó J, Gil R, Latorre A. Learning how to live together: genomic insights into prokaryote–animal symbioses. Nat Rev Genet. 2008;9: 218–229. pmid:18268509
- 4. Gibson CM, Hunter MS. Extraordinarily widespread and fantastically complex: comparative biology of endosymbiotic bacterial and fungal mutualists of insects. Ecol Lett. 2010;13: 223–234. pmid:20015249
- 5. Charlat S, Hurst GDD, Merçot H. Evolutionary consequences of Wolbachia infections. Trends Genet. 2003;19: 217–223. pmid:12683975
- 6. Engelstädter J, Hurst GDD. The ecology and evolution of microbes that manipulate host reproduction. Annu Rev Ecol Evol Syst. 2009;40: 127–149.
- 7. Oliver KM, Degnan PH, Burke GR, Moran NA. Facultative symbionts in aphids and the horizontal transfer of ecologically important traits. Annu Rev Entomol. 2010;55: 247–266. pmid:19728837
- 8. Feldhaar H. Bacterial symbionts as mediators of ecologically important traits of insect hosts. Ecol Entomol. 2011;36: 533–543.
- 9. Evans JD, Chen YP, Prisco G di, Pettis J, Williams V. Bee cups: single-use cages for honey bee experiments. J Apic Res. 2009;48: 300–302.
- 10. Evans JD, Lopez DL. Bacterial probiotics induce an immune response in the honey bee (Hymenoptera: Apidae). J Econ Entomol. 2004;97: 752–756. pmid:15279248
- 11. Martinson VG, Moy J, Moran NA. Establishment of characteristic gut bacteria during development of the honeybee worker. Appl Environ Microbiol. 2012;78: 2830–40. pmid:22307297
- 12. Zientz E, Feldhaar H, Stoll S, Gross R. Insights into the microbial world associated with ants. Arch Microbiol. 2005;184: 199–206. pmid:16205909
- 13. Hu Y, Łukasik P, Moreau CS, Russell JA. Correlates of gut community composition across an ant species (Cephalotes varians) elucidate causes and consequences of symbiotic variability. Mol Ecol. 2014;23: 1284–1300. pmid:24286170
- 14. Kautz S, Rubin BER, Moreau CS. Bacterial infections across the ants: frequency and prevalence of Wolbachia, Spiroplasma, and Asaia. Psyche A J Entomol. 2013;2013: 1–11.
- 15. Sanders JG, Powell S, Kronauer DJC, Vasconcelos HL, Frederickson ME, Pierce NE. Stability and phylogenetic correlation in gut microbiota: lessons from ants and apes. Mol Ecol. 2014; pmid:24304129
- 16. Kellner K, Ishak HD, Linksvayer TA, Mueller UG. Bacterial community composition and diversity in an ancestral ant fungus symbiosis. FEMS Microbiol Ecol. 2015;91. pmid:26113689
- 17. Russell JA, Moreau CS, Goldman-Huertas B, Fujiwara M, Lohman DJ, Pierce NE. Bacterial gut symbionts are tightly linked with the evolution of herbivory in ants. Proc Natl Acad Sci U S A. 2009;106: 21236–41. pmid:19948964
- 18. Russell JA, Funaro CFC, Giraldo YM, Goldman-Huertas B, Suh D, Kronauer DJC, et al. A Veritable menagerie of heritable bacteria from ants, butterflies, and beyond: broad molecular surveys and a systematic review. PLoS One. 2012;7: e51027. pmid:23284655
- 19. Anderson KE, Russell JA, Moreau CS, Kautz S, Sullam KE, Hu Y, et al. Highly similar microbial communities are shared among related and trophically similar ant species. Mol Ecol. 2012;21: 2282–2296. pmid:22276952
- 20. Davidson DW, Cook SC, Snelling RR, Chua TH. Explaining the abundance of ants in lowland tropical rainforest canopies. Science. 2003;300.
- 21. Sameshima S, Hasegawa E, Kitade O, Minaka N, Matsumoto T. Phylogenetic comparison of endosymbionts with their host ants based on molecular evidence. Zoolog Sci. 1999;16: 993–1000.
- 22. Wernegreen JJ, Kauppinen SN, Brady SG, Ward PS. One nutritional symbiosis begat another: phylogenetic evidence that the ant tribe Camponotini acquired Blochmannia by tending sap-feeding insects. BMC Evol Biol. 2009;9: 292. pmid:20015388
- 23. Feldhaar H, Straka J, Krischke M, Berthold K, Stoll S, Mueller M, et al. Nutritional upgrading for omnivorous carpenter ants by the endosymbiont Blochmannia. BMC Biol. 2007;5: 48. pmid:17971224
- 24. Williams LE, Wernegreen JJ. Genome evolution in an ancient bacteria-ant symbiosis: parallel gene loss among Blochmannia spanning the origin of the ant tribe Camponotini. PeerJ. 2015;3: e881. pmid:25861561
- 25. Bolton B. An online catalog of the ants of the world. 2016. Available: http://www.antcat.org/
- 26. Cook SC, Davidson DW. Nutritional and functional biology of exudate-feeding ants. Entomol Exp Appl. 2006;118: 1–10.
- 27. Blüthgen N, Gebauer G, Fiedler K. Disentangling a rainforest food web using stable isotopes: dietary diversity in a species-rich ant community. Oecologia. 2003;137: 426–435. pmid:12898386
- 28. Brady SG, Schultz TR, Fisher BL, Ward PS. Evaluating alternative hypotheses for the early evolution and diversification of ants. Proc Natl Acad Sci U S A. 2006;103: 18172–7. pmid:17079492
- 29. Moreau CS, Bell CD, Vila R, Archibald SB, Pierce NE. Phylogeny of the ants: diversification in the age of angiosperms. Science. 2006;312.
- 30. Moreau CS, Bell CD. Testing the museum versus cradle tropical biological diversity hypothesis: phylogeny, diversification, and ancestral biogeographic range evolution of the ants. Evolution. 2013;67: 2240–2257. pmid:23888848
- 31. Blaimer BB, Brady SG, Schultz TR, Lloyd MW, Fisher BL, Ward PS. Phylogenomic methods outperform traditional multi-locus approaches in resolving deep evolutionary history: a case study of formicine ants. BMC Evol Biol. 2015;15: 271. pmid:26637372
- 32. Ward PS, Blaimer BB, Fisher BL. A revised phylogenetic classification of the ant subfamily Formicinae (Hymenoptera: Formicidae), with resurrection of the genera Colobopsis and Dinomyrmex. Zootaxa. 2016;4072: 343. pmid:27395929
- 33. AntWeb. AntWeb 2017. Available: https://www.antweb.org
- 34. Forel A. Die Nester der Ameisen. Neujahrsblatt Naturforschende Gesellschaft in Zürich. 1892;95: 1–36.
- 35. Wheeler WM. The American ants of the subgenus Colobopsis. New York: American Museum of Natural History Press; 1904.
- 36. Creighton WS. Living doors. Nat Hist. 1967;76: 71–73.
- 37. Brown BP, Wernegreen JJ. Deep divergence and rapid evolutionary rates in gut-associated Acetobacteraceae of ants. BMC Microbiol. 2016; pmid:27400652
- 38. Kane MD, Breznak JA. Effect of host diet on production of organic acids and methane by cockroach gut bacteria. Appl Environ Microbiol. 1991;57: 2628–34. pmid:1662936
- 39. Turnbaugh PJ, Ridaura VK, Faith JJ, Rey FE, Knight R, Gordon JI. The effect of diet on the human gut microbiome: a metagenomic analysis in humanized gnotobiotic mice. Sci Transl Med. 2009;1.
- 40. Koch H, Cisarovsky G, Schmid-Hempel P. Ecological effects on gut bacterial communities in wild bumblebee colonies. J Anim Ecol. 2012;81: 1202–1210. pmid:22708631
- 41. Dillon RJ, Webster G, Weightman AJ, Keith Charnley A. Diversity of gut microbiota increases with aging and starvation in the desert locust. Antonie Van Leeuwenhoek. 2010;97: 69–77. pmid:19876756
- 42. Ramalho MO, Bueno OC, Moreau CS. Microbial composition of spiny ants (Hymenoptera: Formicidae: Polyrhachis) across their geographic range. BMC Evol Biol. 2017; pmid:28381207
- 43. Stoll S, Feldhaar H, Fraunholz MJ, Gross R. Bacteriocyte dynamics during development of a holometabolous insect, the carpenter ant Camponotus floridanus. BMC Microbiol. 2010;10: 308. pmid:21122115
- 44. Bueno OC, Cruz Landim C. Estudo do Cordão Nervoso Ventral de Camponotus rufipes (Fabricius) durante o desenvolvimento pós embrionário (Hym.:Formicidae). Stud Entomol. 1975;18: 605–613.
- 45. Moreau CS. A practical guide to DNA extraction, PCR, and gene-based DNA sequencing in insects. Halteres. 2014;5: 32–42.
- 46. Rubin BER, Sanders JG, Hampton-Marcell J, Owens SM, Gilbert JA, Moreau CS. DNA extraction protocols cause differences in 16S rRNA amplicon sequencing efficiency but not in community profile composition or structure. Microbiologyopen. 2014; pmid:25257543
- 47. Caporaso JG, Lauber CL, Walters WA, Berg-Lyons D, Huntley J, Fierer N, et al. Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J. 2012;6: 1621–1624. pmid:22402401
- 48. Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, et al. QIIME allows analysis of high-throughput community sequencing data. Nat Methods. 2010;7: 335–336. pmid:20383131
- 49. Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 2013;41: D590–D596. pmid:23193283
- 50. Yilmaz P, Parfrey LW, Yarza P, Gerken J, Pruesse E, Quast C, et al. The SILVA and “All-species Living Tree Project (LTP)” taxonomic frameworks. Nucleic Acids Res. 2014;42: D643–D648. pmid:24293649
- 51. Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics. 2010;26: 2460–2461. pmid:20709691
- 52. Caporaso J, Bittinger K, Bushman F. PyNAST: a flexible tool for aligning sequences to a template alignment. Bioinformatics. 2009;26: 266–267. pmid:19914921
- 53. Hammer Ø, Harper DAT, Ryan PD. Paleontological statistics software: package for education and data analysis. Palaeontol Electron. 2001; 1–9.
- 54. McCune B, Grace JB. Analysis of ecological communities (MjM Software Design). 2002.
- 55. Clarke KR. Non-parametric multivariate analyses of changes in community structure. Austral Ecol. 1993;18: 117–143.
- 56. McArdle BH, Anderson MJ. Fitting multivariate models to community data: a comment on distance-based redundancy analysis. Ecology. 2001;82: 290–297.
- 57. Lozupone C, Knight R. UniFrac: a new phylogenetic method for comparing microbial communities. Appl Environ Microbiol. 2005;71: 8228–35. pmid:16332807
- 58. Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003;13: 2498–504. pmid:14597658
- 59. Ley RE, Hamady M, Lozupone C, Turnbaugh PJ, Ramey RR, Bircher JS, et al. Evolution of mammals and their gut microbes. Science. 2008;320.
- 60. Oksanen J, Kindt R, Legendre P, O’Hara B. The vegan package. Community Ecol. 2007.
- 61. R Development Core Team (2015) R: A Language and Environment for Statistical Computing. Available from http://www.R-project.org/. 2016.
- 62. Hall T. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 1999.
- 63. Higgins D, Bleasby A, Fuchs R. Clustal V: improved software for multiple sequence alignment. Comput Appl. 1992.
- 64. Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol. 2010;59: 307–321. pmid:20525638
- 65. Miller M et al. The CIPRES portals. 2017.
- 66. FigTree. FigTree 2017. Available: http://tree.bio.ed.ac.uk/software/figtree
- 67. Ramalho MO, Martins C, Silva LM, Martins VG, Bueno OC. Intracellular symbiotic bacteria of Camponotus textor, Forel (Hymenoptera, Formicidae). Curr Microbiol. 2017; pmid:28261755
- 68. Koch H, Schmid-Hempel P. Socially transmitted gut microbiota protect bumble bees against an intestinal parasite. Proc Natl Acad Sci U S A. 2011;108: 19288–92. pmid:22084077
- 69. Schmid-Hempel P. Parasites in social insects. Princeton: Princeton University Press; 1998.
- 70. Hölldobler B, Engel-Siegel H. On the metapleural gland of ants. Psyche A J Entomol. 1984;91: 201–224.
- 71. de Souza DJ, Van Vlaenderen J, Moret Y, Lenoir A. Immune response affects ant trophallactic behaviour. J Insect Physiol. 2008;54: 828–832. pmid:18430435
- 72. Hölldobler B, Wilson E. The ants. Berlin: Springer—Verlag; 1990.
- 73. McMahan E. Feeding relationships and radioisotope techniques. In: Weesner FM, Krishna K, editors. Biology of Termites. New York: Academic Press; 1969. pp. 387–406.
- 74. Wilson EO. A social ethogram of the neotropical arboreal ant Zacryptocerus varians (Fr. Smith). Anim Behav. 1976;24: 354–363.
- 75. Wheeler DE. Behavior of the ant, Procryptocerus Scabriusculus (Hymenoptera: Formicidae), with comparisons to other Cephalotines. Psyche A J Entomol. 1984;91: 171–192.
- 76. Minkley N, Fujita A, Brune A, Kirchner WH. Nest specificity of the bacterial community in termite guts (Hodotermes mossambicus). Insectes Soc. 2006;53: 339–344.
- 77. Munson MA, Baumann P, Clark MA, Baumann L, Moran NA, Voegtlin DJ, et al. Evidence for the establishment of aphid-eubacterium endosymbiosis in an ancestor of four aphid families. J Bacteriol. 1991;173: 6321–4. pmid:1917864
- 78. Baumann P. Biology of bacteriocyte-associated endosymbionts of plant sap-sucking insects. Annu Rev Microbiol. 2005.
- 79. Stoll S, Feldhaar H, Gross R. Transcriptional profiling of the endosymbiont Blochmannia floridanus during different developmental stages of its holometabolous ant host. Environ Microbiol. 2009;11: 877–888. pmid:19040455
- 80. Gil R, Silva FJ, Zientz E, Delmotte F, González-Candelas F, Latorre A, et al. The genome sequence of Blochmannia floridanus: comparative analysis of reduced genomes. Proc Natl Acad Sci U S A. 2003;100: 9388–93. pmid:12886019
- 81. Degnan PH, Lazarus AB, Wernegreen JJ. Genome sequence of Blochmannia pennsylvanicus indicates parallel evolutionary trends among bacterial mutualists of insects. Genome Res. 2005;15: 1023–33. pmid:16077009
- 82. Williams LE, Wernegreen JJ. Unprecedented loss of ammonia assimilation capability in a urease-encoding bacterial mutualist. BMC Genomics. 2010;11: 687. pmid:21126349
- 83. Degnan PH, Lazarus AB, Brock CD, Wernegreen JJ. Host-symbiont stability and fast evolutionary rates in an ant-bacterium association: cospeciation of Camponotus species and their endosymbionts, Candidatus Blochmannia. Syst Biol. 2004;53: 95–110. pmid:14965905
- 84. Jones RRT, Sanchez LG, Fierer N, Dale C, Moran N, Lamelas A, et al. A cross-taxon analysis of insect-associated bacterial diversity. PLoS One. 2013;8: e61218. pmid:23613815
- 85. Russell JA, Goldman-Huertas B, Moreau CS, Baldo L, Stahlhut JK, Werren JH, et al. Specialization and geographic isolation among Wolbachia symbionts from ants and Lycaenid butterflies. Evolution. 2009;63: 624–640. pmid:19054050
- 86. Russell JA. The ants (Hymenoptera: Formicidae) are unique and enigmatic hosts of prevalent Wolbachia (Alphaproteobacteria) symbionts. Myrmecol News. 2012;16: 7–23.
- 87. Shoemaker D, Keller G, Ross KG. Effects of Wolbachia on mtDNA variation in two fire ant species. Mol Ecol. 2003;12: 1757–1771. pmid:12803629
- 88. Pohl S. DNA relatedness among members of Haemophilus, Pasteurella and Actinobacillus. In: Donachie W, Lainson FA, Hodgson JC, editors. Haemophilus, Pasteurella and Actinobacillus. London: Academic Press; 1981. pp. 245–253.
- 89. Christensen H, Bisgaard M. Molecular classification and its impact on diagnostics and understanding the phylogeny and epidemiology of selected members of Pasteurellaceae of veterinary importance. Berl Munch Tierarztl Wochenschr. 2010;123: 20–30. pmid:20135907
- 90. Bisgaard M. Ecology and significance of Pasteurellaceae in animals. Zentralblatt für Bakteriol. 1993;279: 7–26.
- 91. Eilmus S, Heil M. Bacterial associates of arboreal ants and their putative functions in an obligate ant-plant mutualism. Appl Environ Microbiol. 2009;75: 4324–32. pmid:19447959