Many heritable mutualisms, in which beneficial symbionts are transmitted vertically between host generations, originate as antagonisms with parasite dispersal constrained by the host. Only after the parasite gains control over its transmission is the symbiosis expected to transition from antagonism to mutualism. Here, we explore this prediction in the mutualism between the fungus Rhizopus microsporus (Rm, Mucoromycotina) and a beta-proteobacterium Burkholderia, which controls host asexual reproduction. We show that reproductive addiction of Rm to endobacteria extends to mating, and is mediated by the symbiont gaining transcriptional control of the fungal ras2 gene, which encodes a GTPase central to fungal reproductive development. We also discover candidate G-protein-coupled receptors for the perception of trisporic acids, mating pheromones unique to Mucoromycotina. Our results demonstrate that regulating host asexual proliferation and modifying its sexual reproduction are sufficient for the symbiont’s control of its own transmission, needed for antagonism-to-mutualism transition in heritable symbioses. These properties establish the Rm-Burkholderia symbiosis as a powerful system for identifying reproductive genes in Mucoromycotina.
Heritable mutualisms are a source of major evolutionary innovations1. However, their evolution remains elusive. Evolutionary theory suggests that many heritable mutualisms originate as antagonisms in which parasite dispersal is controlled by the host2. A transition to mutualism requires the parasite to dominate the coevolutionary race with the host by establishing control over its own transmission. However, few symbioses exist where this prediction can be explored. One such system is the mutualism between a soil fungus Rhizopus microsporus (Rm, Mucoromycotina) and a beta-proteobacterium Burkholderia, which controls asexual proliferation of its host3. Like many other Mucoromycotina, the Rm hosts of Burkholderia thrive as soil saprotrophs. They can cause food spoilage, infect plants4, and act as opportunistic pathogens of immune-compromised humans5. While the evolutionary history of the Rm-Burkholderia symbiosis is uncertain, present-day antagonistic interactions of Burkholderia endobacteria with nonhost Rm isolates naturally free of endobacteria6 suggest that it originated as an antagonism. In the Rm-Burkholderia mutualism, the partners can be separated, cultivated independently, and reassembled to form a functional symbiosis in which the endobacteria reside directly in the host cytoplasm3. Burkholderia cells are transmitted via sporangiospores, which are asexual propagules produced by the host3. Sporangiospores are generated continuously throughout colony growth in favorable environmental conditions, disseminate aerially, and germinate rapidly.
In addition to asexual propagation, fungi, like most other eukaryotes, engage in sexual reproduction. In Mucoromycotina, sex involves the union of gametangia, leading to the formation of a zygospore7. In heterothallic species, such as Rm, two compatible strains, sex plus (sexP) and sex minus (sexM), are required for mating to be successful7. Partner recognition and progression of mating are mediated by trisporic acids and their precursors8, 9, which act as sex pheromones and are synthesized in a cooperative manner from intermediates provided by the complementary mating partner10. Due to their recalcitrance to genetic analysis and manipulation, Mucoromycotina are one of the least explored major lineages of fungi, with only few reproductive genes characterized functionally thus far11. To test the hypothesis that the Burkholderia endobacteria control sexual reproduction of the Rm host and identify the control mechanism, we mated fungi that harbored endosymbionts or were cured of them, followed by transcriptional profiling and phylogenomic analyses utilizing the wealth of information on sexual reproduction in Dikarya, a lineage uniting Ascomycota and Basidiomycota. We discovered that endobacteria modify sexual reproduction of Rm, and generated insights into the reproductive biology of Mucoromycotina.
Diversity and natural loss of endobacteria
Previous observations indicated that only a single bacterial cell was present per sporangiospore in one of the Rm strains, CBS1122853. We found that bacterial loads in other strains differ, varying from on average three cells per sporangiospore in strain ATCC 52813 to four in ATCC 52814 (Supplementary Fig. 1). This observation suggests phenotypic diversity among host–symbiont pairings.
The role of endobacteria in asexual proliferation of Rm was evidenced by the loss of sporulation in mycelia treated with antibiotics that eradicate Burkholderia3. We observed that endobacteria and asexual reproduction can be lost spontaneously after as few as four generations of propagating the fungus via single spores, and after 12 generations of propagation via mycelial fragments (Supplementary Table 1). These patterns indicate that in nature, hosts can become naturally cleared of their endosymbionts, and the loss of sporulation can be attributed to endosymbiont absence.
Not all zygospores are populated by endobacteria
All asexual sporangiospores formed by Rm strains hosting endobacteria appear to harbor the symbiont. To test whether the same is true for sexually produced zygospores, we mated Rm strains ATCC 52813 sexP and ATCC 52814 sexM, which both naturally contain endobacteria in their mycelia. We then surveyed zygospores for bacterial presence by PCR targeting their 23S rRNA gene. Burkholderia was detected in 40% (±6% s.e.m.) of zygospores, suggesting that the rate of symbiont transmission through the sexual pathway is substantially lower than through the asexual pathway.
Endobacteria modify fungal mating
To test the hypothesis that Burkholderia endobacteria control sexual reproduction of Rm, we examined the interactions of wild-type B(+) strains that harbored endobacteria and B(−) isolates that were cured of endosymbionts: (1) ATCC 52813 sexP with ATCC 52814 sexM, (2) ATCC 52813 sexP with ATCC 52811 sexM, and (3) ATCC 62417 sexP with ATCC 52811 sexM. We found that in all pairs, bacteria impacted fungal ability to reproduce sexually. They either controlled it completely, with removal of endobacteria leading to total loss of mating, or incompletely, with removal of endobacteria leading to a reduced zygospore yield (Fig. 1). These two outcomes did not appear to be specific to the strains that were mated. Moreover, loss of mating was not a consequence of vigor reduction in cured isolates, as, with the exception of ATCC 62417, which grew poorly after the loss of endobacteria, the differences in the rate of mycelial expansion between the B(−) and B(+) mycelia were largely negligible (Supplementary Fig. 2).
Attempts to restore fungal mating
To examine whether the loss of host reproduction upon removal of endobacteria was reversible, we investigated the consequences of reintroducing endosymbionts into the cured host isolates that exhibited total loss of mating. Reinfection with endobacteria restored both asexual and sexual reproduction regardless of whether bacteria were introduced into their original native hosts or nonnative hosts, with all pairwise combinations of source bacteria and target fungal strains across ATCC 52811, ATCC 52813, ATCC 52814, and ATCC 62417 yielding reproduction. However, while asexual reproduction was restored immediately after reinfection, restitution of the ability to mate required an additional step of exposing the reinfected isolates to extreme cold (–80 °C), which eliminated fungal hyphae while preserving sporangiospores. This observation suggested that there was a subtle mechanistic difference in how endosymbionts interact with asexual vs. sexual reproduction of the fungus. We also attempted to restore Rm sexual reproduction in the absence of endosymbionts by exposing compatible B(−) mates to extracts of mated mycelia and to environmental conditions known to affect reproduction in Mucoromycotina (Supplementary Table 2). None of these treatments restored mating or asexual propagation in cured fungi, suggesting that for reproduction, the host is addicted to bacterial factors.
Gene networks responsible for mating in Mucoromycotina
To investigate the genetic underpinnings of fungal reproductive responses to endobacteria, we conducted an RNA-seq experiment assessing global gene expression patterns under six different conditions: (1) Rm ATCC 52813 B(+) grown alone, (2) ATCC 52813 B(−) grown alone, (3) ATCC 52814 B(+) grown alone, (4) ATCC 52814 B(−) grown alone, (5) both B(+) mates grown together, and (6) both B(−) mates grown together, with sexual reproduction completely absent. We sequenced the genomes of both mates (Supplementary Tables 3 and 4, and Lastovetsky et al.6) to facilitate mapping of RNA-seq reads to each host. Because the knowledge of molecular mechanisms underlying sexual reproduction in Mucoromycotina lags behind other fungi, we first needed to identify genes that are relevant to reproductive processes in these fungi.
We found that in Rm, 2124 genes were differentially expressed (DE) at a significant level during sexual reproduction relative to asexual growth and sporulation, with 1496 genes upregulated and 628 downregulated (false-discovery rate (FDR) corrected P ≤ 0.05, identified using DESeq12; Supplementary Data 1, Supplementary Fig. 3). Ortholog clustering revealed that, while many of these genes were conserved across most fungi (57.95%), a substantial proportion were either restricted to Mucoromycotina (42.04%) or even unique to the Rm lineage (11.67%; Fig. 2, Supplementary Table 5, Supplementary Data 2). For example, several major regulators of sexual reproduction, such as genes interacting with the pheromone mitogen-activated protein kinase (MAPK) cascade and several transcription factors appear to consistently play roles in sexual reproduction across different fungi, including Mucoromycotina (Supplementary Data 2). Conversely, genes encoding response regulators, such as PHOA/Pho8013 (phosphate response) and CpcB14 (amino acid starvation), which provide important cues for sexual reproduction in Aspergillus nidulans but are not involved in sex regulation of other Dikarya, did not show differential expression during sexual reproduction in Rm (Supplementary Table 5, Supplementary Data 1). As expected, we also observed upregulation of mating-type genes, sexM (FDR corrected P = 1.08×10−22) and sexP (FDR corrected P = 9.61×10−188), previously characterized in Mucoromycotina11. In contrast, the neighboring rhnA gene15 was not differentially expressed during reproduction in Rm. Finally, we discovered that Mucoromycotina lack all the mating pheromone recognition genes present in Dikarya (Fig. 2; Supplementary Data 2), a pattern consistent with the fact that Mucoromycotina use trisporic acids and their precursors as sex pheromones rather than the peptides and lipopeptides employed by Dikarya16.
Candidate trisporic acid receptors
As G-protein-coupled receptors (GPCRs) are involved in the perception of mating pheromones in other fungi17 and animals18, we explored Rm genes upregulated during sexual reproduction in search of GPCRs unique to the Mucoromycotina lineage. We found three such candidate trisporic acid receptor (tar) genes, encoding class C seven-transmembrane domain GPCRs, that were present in the genomes of ATCC 52813 and ATCC 52814 (Fig. 3a). Through qRT-PCR, we confirmed that expression of these three candidate genes was also upregulated during mating interactions of a different pair of Rm mates, ATCC 52813 and ATCC 52811 (Fig. 3b). In addition, we established that the expression pattern of each gene changes during the progression of mating (Fig. 3c). Through phylogeny reconstructions, we determined that these GPCRs cluster with animal γ-aminobutyric acid (GABA) receptors, a group related to animal retinoic acid-inducible class C GPCRs (Fig. 3a).
Effects of endobacteria on regulation of Rm mating
Only 80 of the 2124 Rm sex-related transcripts were impacted by the symbiont presence in the hosts (Supplementary Fig. 3, Supplementary Data 1). One of the most striking observations was an ~12-fold downregulation in the absence of endobacteria of an ortholog of ras2, which encodes a small GTPase protein. Furthermore, ras2 was downregulated in fungi cured of bacteria growing alone vegetatively and upregulated during active asexual proliferation. Despite the expansion of the ras gene family in Mucoromycotina relative to Dikarya (Fig. 4a), only the expression of the Rm ras2-1 gene (protein ID 223475 and 286484 in Rm ATCC 52813 and ATCC 52814, respectively) was affected by endobacteria. Ras2 is conserved across all fungi except Ascomycota yeasts (Fig. 4a). In the basidiomycete Ustilago maydis, it controls the initiation of the mating pheromone MAPK cascade19. Ras2 is also involved in asexual reproduction, as shown in ascomycetes in which repression of ras2 has a negative impact on sporulation20, 21. To examine whether the role of ras2-1 extends to mating in other Mucoromycotina, we conducted qRT-PCR on vegetative mycelia vs. mating interactions involving ATCC 1216b sexP and CBS 277.49 sexM strains of Mucor circinelloides, and found that expression of ras2-1 was elevated during mating relative to vegetative growth (Fig. 4b). Finally, we examined expression levels of ras2-1 in mating interactions between Rm ATCC 52813 and ATCC 52811 focusing on patterns exhibited by cured mates that experience total loss of mating vs. restricted mating. Like in the RNA-seq experiment, the levels of ras2 expression were lower in interactions between B(−) mates compared to those between B(+) mates (Fig. 4c). However, they did not differ between interactions of B(−) mates exhibiting total loss of mating vs. restricted mating (Fig. 4c), a pattern consistent with incomplete control of mating by the endobacteria.
In addition to regulating the pheromone MAPK cascade, in U. maydis, Ras2 interacts with the cyclic adenosine monophosphate (cAMP) signaling pathway and controls morphogenesis19. cAMP is a secondary messenger that, in coordination with the pheromone MAPK cascade, affects sexual development in many fungi, albeit often with contrasting effects22. We explored the impact of exogenous cAMP on Rm mating by exposing B(+) and B(−) mates to 0 mM, 1 mM, and 2 mM dibutyryl cAMP. We found that increased concentrations of cAMP reduced the rate of zygospore formation in the interactions between B(−) mates that were capable of restricted mating (Student post hoc test of the interaction between bacterial presence and cAMP level in two-way ANOVA, P = 0.02), whereas the decrease in zygospore formation in interactions between B(+) mates was not statistically significant (Fig. 1i). These results suggested that elevated levels of cAMP interfered with mating in Rm, and the endosymbiont presence buffered the negative effects of high cAMP levels on sexual reproduction.
We found that Rm is highly dependent for survival on the Burkholderia endobacteria. Although the fungus can grow vegetatively after endobacteria are lost naturally or eradicated with antibiotics23, it is unable to proliferate asexually and its ability to reproduce sexually is severely compromised. These patterns indicate that in the Rm-Burkholderia mutualism, the endosymbiont controls its own vertical transmission, which is a prerequisite for the antagonism-to-mutualism transition in heritable symbioses2. Remarkably, less than half of zygospores formed during mating interactions of wild hosts harbor endobacteria. However, as zygospore germination is extremely difficult to achieve under laboratory conditions24, it remains untested whether zygospore functionality is affected by endosymbiont absence. Zygospore germination occurs via a sporangium resembling the asexual sporangium. Therefore, it cannot be excluded that endobacteria-free zygospores may fail to germinate, further reinforcing endosymbiont dominance over host reproduction. Endosymbiont ability to control its own transmission is expected to facilitate reciprocal selection between the partners, leading to utilization of symbiont services by the host2. In the Rm-Burkholderia symbiosis, these services include endosymbiont-mediated synthesis of rhizoxin, a potent toxin that enables pathogenesis of plants by Rm23, 25.
In addition to facilitating the antagonism-to-mutualism transition, the role of endobacteria in regulating Rm asexual and sexual reproduction is consistent with the addiction model of mutualism evolution6, 26. According to this model, a host population that interacts with an antagonistic symbiont should develop mechanisms to compensate for its negative effects and become addicted to the symbiont’s continued presence27. In the case of the Rm-Burkholderia symbiosis, endobacteria have hijacked an indispensable component of the host’s developmental machinery by gaining control over expression of ras2-1, encoding a G-protein responsible for the reproductive development in Dikarya19,20,21. The exact mechanism of bacterial control over the ras2-1 expression and the evolutionary trajectory that lead to it are unknown. However, as stimulation of ras signaling induces programmed cell death in other fungi28, it is possible that in the ancestrally antagonistic relationship between Rm and Burkholderia6, establishing control over the ras2-1 expression by endosymbionts was an important component of coevolution between partners, leading to adaptive changes in host regulation of ras2-1 signaling (Supplementary Fig. 4). Evolutionary theory predicts further that once a mutualism is established, the host is favored to control mixing of symbionts29. Such control is expected to reduce harmful competition among symbionts for the host resources. It remains to be investigated whether endobacteria are able to mix in the Rm-Burkholderia symbiosis.
We exploited the endosymbiont control over Rm reproduction to reconstruct the key reproductive pathways across the fungal kingdom, including Mucoromycotina, Ascomycota, and Basidiomycota. Since many of these genes were experimentally studied in Dikarya, we were able to augment our findings with information on conservation of their sex-related function. Using this approach, we uncovered candidate genes that may be involved in perception of trisporic acid pheromones in Mucoromycotina. Unlike class D GPCRs responsible for pheromone sensing in Dikarya30, which are absent from Rm, these candidate receptors appear to represent class C GPCRs. They are encoded by genes that are conserved across all Mucoromycotina, upregulated during sexual reproduction in R. microsporus, absent from higher fungi, and closely related to retinoic acid-sensing GPCRs in animal systems. Similar to trisporic acid, retinoic acid is derived from β-carotene and is essential for the initiation of meiosis in animals31, 32. Further functional analyses are now required to test the hypothesis that these C GPCRs interact with and transduce trisporic acid pheromone signals.
Overall, our findings indicate that in the Rm-Burkholderia symbiosis, endobacteria control their vertical transmission by regulating asexual proliferation of the host and impacting its mating. Such control appears to be sufficient to have mediated the antagonism-to-mutualism transition in this heritable symbiosis. Symbiont presence correlated with expression levels of the host ras2-1 gene, a major regulator of both sexual and asexual reproduction in fungi, suggesting that endobacteria influence its activity. Finally, we took advantage of the symbiont impact on host mating to make inferences about reproductive genes in Mucoromycotina, a group of fungi recalcitrant to genetic analysis. In the process, we discovered candidate trisporic acid receptors, TARs, that may be responsible for perception of trisporic acid sex pheromones uniquely utilized by this group of fungi.
Rm strains, culture conditions, and loss of endobacteria
Strains ATCC 52811, ATCC 52813, ATCC 52814, and ATCC 62417 were cultivated on half (1/2) or full-strength potato dextrose agar (PDA) containing 2 g L−1 potato extract, 10 g L−1 dextrose, and 15 g L−1 agar. Plates were sealed with Parafilm M (Pechiney Plastic Packaging Company), unless otherwise noted. In addition to curing fungi of Burkholderia endobacteria with antibiotics as described in Partida-Martinez and Hertweck23, we experimented with the impact of their subculturing by individual spores and mycelial fragments on bacterial presence. Isolates of ATCC 52813 were propagated by mycelial fragments and by single spores, with two replicates per isolate. For mycelial fragments, a small spore-free section of ~1 × 0.5 cm was excised from the edge of the colony and transferred to fresh PDA. For single-spore propagation, sporulating colonies were flushed with 3 mL of sterile nanopure water to dislodge spores. To remove hyphae, the spore suspension was filtered through a cotton filter into a 2-mL microfuge tube, and diluted 10−3 in sterile nanopure water, followed by spreading 100 μL into a 6-cm PDA plate. After approximately 24 hours of incubation at 30 °C, one colony was removed and plated onto a PDA plate. The absence of endosymbionts was confirmed by PCR using Burkholderia-specific primers GlomGiGf33 and LSUb 483r34 as described in Mondo et al34.
Extraction, cultivation, and reintroduction of endobacteria
Young fungal mycelium (1–2-days old) containing endosymbionts was finely chopped in 500-μL Luria-Bertani (LB) broth, and pressed gently to release cellular contents into the broth, followed by filtration through a 2-μm filter to remove fungal debris. Varying amounts of filtrate were added to LB plates containing 10 mL L−1 glycerol and 100 μg mL−1 cycloheximide. Single colonies were isolated and grown at 30 °C either on LB agar or in 5-mL LB broth incubated at 250 rpm. To reinfect fungi with endobacteria, a plug of agar was removed from 1/2 PDA using the upper end of a P-1000 pipette tip and replaced with a plug of LB agar. Bacterial inoculum was placed on the LB agar plug, and a plug containing cured fungus was either positioned directly on bacterial cells, or somewhere nearby on the plate.
Visualization of endobacteria in sporangiospores
For visualization, endobacteria were transformed with either an mCherry-expressing or YFP-expressing gentamicin resistance-conferring plasmid pBS46, and introduced to cured strains ATCC 52813 and ATCC 52814. Sporangiospores were collected and embedded in polyacrylamide pads to immobilize them35. Between 70 and 100 spores were examined using the DeltaVision RT system (Applied Precision) with an Olympus IX-70 inverted microscope (Olympus America) fitted with a 100-W mercury arc bulb and a CoolsnapHQ ICX285 camera (Sony). Z-sections were acquired using 0.15-μm step size and the Z stacks were deconvolved using the softWoRx Explorer software (Applied Precision).
Rm mating interactions
Half-strength PDA plates were used for all mating experiments. Mates were placed at the edges of the plate, allowing mycelia to grow toward each other and develop an interaction zone in the center of the plate. Cultures were incubated in the dark at 30 °C. Each interaction was examined in 6–10 replicates; the entire experiment, including removal of endobacteria, was repeated three times. Prior to investigating the role of endobacteria in sexual reproduction, we examined fungal mating in both darkness and in ambient light, and found that Rm has no light preference with respect to mating. To ensure that loss of fertility in cured fungi is not due to multiple rounds of subcultivation7 required to remove endobacteria23, we generated tester lines of Rm-harboring bacteria that were subjected to the same number of subcultivation events as cured lines but without an antibiotic. We found that subculturing had no effect on sexual reproduction.
Detection of endobacteria in Rm zygospores
Mating interactions between Rm ATCC 52813 and ATCC 52814 were conducted on PDA (Sigma) as described above, and zygospores were analyzed after 7 days of incubation in the dark at 30 °C. A tuft of mycelium containing zygospores was removed from the mating zone and placed in 10% w/v chloramine T (Sigma) for 20 min to kill hyphae. The tuft was subsequently transferred to sterile water and shaken slowly for 5 min at room temperature, followed by two additional water washes lasting for 20 min. The mycelial tuft was then transferred onto a sterile 1.5% water agar and zygospores were collected with sterile forceps, taking care to remove all attached hyphae. A total of 80 zygospores from two separate mating interactions were transferred individually into 0.2-mL PCR tubes, crushed, and subjected to whole-genome amplification (WGA) with the Illustra GenomiPhi Kit v2 (GE) to generate template DNA for multiple PCR reactions per zygospore. A volume of 1 μL of the last water wash was used as a negative control during WGA and subsequent PCR, with a total of 16 negative controls. PCR was performed on the 1/20-diluted WGA products using LR1 and NDL2236 as well as Burkholderia-specific primers34 to detect the presence of fungal and bacterial DNA in zygospores.
Attempts to restore mating in the absence of endobacteria
Interactions between compatible B(−) mates ATCC 52813 and ATCC 52814 showing total loss of mating were examined on 1/2 PDA: (1) amended with mating relevant compounds, such as 3 g L−1 NaNO3, 0.5 g L−1 NaNO2, 1 mg L−1 thiamine, and 16.6 mg L−1 β-carotene as well as with extracts from successfully mating liquid cultures filtered through 0.22-μm filter, (2) at high moisture generated by adding 1-mL H2O to culture plates and sealing them with Parafilm M, and at low moisture generated by sealing plates with porous Micropore™ surgical tape (3 M Health Care), (3) in ambient light and in darkness, (4) after cold treatment of 1-week, 2-week, 4-week, and 10-week incubation at 4 °C, (5) under oxidative stress of 0.3, 0.6, 1.2, 2.4, and 10 mM H2O2, and (6) osmotic stress of 0.4, 0.8, and 1.6 M NaCl. Each treatment included three to five replicates. Exogenous dibutyryl cAMP (Enzo Life Sciences) was added at concentrations of 0 mM, 1 mM, and 2 mM to B(+) mates ATCC 52813 and ATCC 52814 and to B(−) mates ATCC 52813 and ATCC 52814 that showed restricted levels of mating. Ten mating interactions were established per condition and incubated in the dark at 30 °C for 10 days.
Six different conditions were examined in Rm ATCC 52813 and ATCC 52814: B(+) and B(−) mates grown alone, as well as both B(+) and B(−) partners grown together, respectively. We chose to analyze the interaction between B(−) mates that exhibited total loss of mating to maximize our chances of identifying genes impacted by bacteria during sexual reproduction. For each condition, fungal plugs were placed at the edge of the 1/2 PDA plate and harvested after six days, when opposite B(+) mates were undergoing sexual reproduction. Each condition had two biological replicates, each consisting of five culture plates, which were pooled prior to RNA extraction. Total RNA was extracted from a 2.5-cm-wide strip of mycelium from the middle of the plate where most mating occurred, using the Ambion ToTALLY Total RNA Isolation Kit (Life Technologies) to recover both fungal and bacterial transcripts. Fungal rRNA was removed with the Human/Mouse/Rat Ribo-Zero rRNA Removal Kit (Epicentre), whereas bacterial rRNA was treated with the Gram-negative bacteria Ribo-Zero rRNA Removal Kit (Epicentre). After rRNA removal, sequencing libraries were constructed using the TruSeq RNA Sample Preparation Kit (Illumina) and sequenced at the Cornell University Biotechnology Resource Center using the Illumina Hi-Seq 100-bp paired-end platform.
Illumina reads were quality controlled using BBDuk (https://sourceforge.net/projects/bbmap/), and then mapped to either the Rm ATCC 52813 or ATCC 52814 genomes (depending on the sample) using TopHat237. HTSeq38 was used to collect read counts per gene, followed by exploration of differential expression across several comparisons using DESeq12: (1) ATCC 52813 B(+) vs. ATCC 52813 B(−), (2) ATCC 52814 B(+) vs. ATCC 52814 B(−), (3) both B(+) mates grown together (active mating) vs. both B(−) mates grown together (no mating), and (4) both B(+) mates grown alone vs. both B(+) mates grown together (active mating). This combination of comparisons allowed us to identify genes that were significantly DE in both mates due to (1) endosymbiont presence and (2) sexual reproduction, as well as assess the overlap between them. For comparisons involving both mates, we mapped reads to a combined assembly of both genomes, and since these strains are so closely related, we allowed reads mapped twice to be retained for downstream DESeq analysis. Genes with an adjusted P ≤ 0.05 were considered DE.
Mating interactions were set up as above between Rm ATCC 52813 sexP and ATCC 52811 sexM. Expression of ras2-1 was examined in (1) B(+) mating cultures, (2) cultures of B(−) mates exhibiting complete loss of mating, and (3) cultures of B(−) mates exhibiting restricted levels of mating. Expression of candidate tar1, tar2, and tar3 genes was measured in B(+) and B(−) mates grown alone, as well as during mating interactions, with a particular focus on B(+) mating cultures at 3, 6, and 8 days after the mates reached the mating zone. To assess the expression of ras2-1 in Mucor circinelloides (Mc), ATCC 1216b sexP and CBS 277.49 sexM were grown at 20 °C on YXT medium containing 4 g L−1 yeast extract, 10 g L−1 malt extract, 4 g L−1 glucose, and 15 g L−1 agar, with the pH adjusted to 6.5. Mc mates were grown (1) individually for 3 days and harvested before the onset of asexual sporulation, and (2) together and harvested 6 days after the onset of mating. Each condition had three biological replicates, each replicate consisting of a single plate. RNA was extracted with the Ambion ToTALLY Total RNA Isolation Kit (Life Technologies) and converted to cDNA using ProtoScript II First Strand cDNA Synthesis Kit (New England Biolabs). Real-time PCR was performed on a StepOnePlusTM Real-Time PCR System (Applied Biosystems) using TaqMan® Universal PCR Master Mix. The reaction mix consisted of 0.5 μM primers, 0.2 μM TaqMan® probe, 1× Master Mix, and 10 ng of cDNA in a volume of 25 μL. All reactions were performed in technical duplicate. Nontemplate control (10 ng of RNA) and nonreaction control (RNase-free water) were included. The thermal program for the PCR consisted of Stage 1: 95 °C, 10 min; Stage 2: 95 °C, 0.5 min and 60 °C, 1 min for a total of 40 cycles; and Stage 3: hold at 4 °C. Relative quantitation was conducted using the ∆∆Ct method (StepOnePlus™ user manual of Applied Biosystems). Each RT-PCR experiment was performed in triplicate. Probes and primers were Rm ras2-1 TaqMan® probe 5′-[6-FAM] AG CAT TTT ACT CAG TTG CT [Tamra-Q]-3′, Rm ras2-1 forward primer 5′-CGC AAA GAC TTG TGC TAA TGT AGA A-3′, Rm ras2-1 reverse primer 5′-CGC GCT TGC TTG ATC TGA-3′, Rm tar1 (238519) TaqMan® probe 5′[6-Fam] ATT GCA AGA CTT GGC TAG T [Tamra-Q]3′, Rm tar1 forward primer 5′-GGT GGC CGG GAA AAG G-3′, Rm tar1 reverse primer 5′-TAG GTG TCA TCG AAC TCG TGT TAA A-3′, Rm tar2 (238870) TaqMan® probe 5′[6-FAM] AGA GTG GAG CAC GGA T [Tamra-Q]3′, Rm tar2 forward primer 5′-TCT GAA TTC GGC ACT GAC AAA CT-3′, Rm tar2 reverse primer 5′-GAT TCG CTG CGA CCA TGA T-3′, Rm tar3 (316085) TaqMan® probe 5′[6-Fam] CCT CTT CTT GGA CCT CT [Tamra-Q]3′, Rm tar3 forward primer 5′-CGT CGG CAT TAT CGG AGA TAT C-3′, Rm tar3 reverse primer 5′-TGC AAG GTG CTC GTC ATC A-3′, Mc ras2-1 (156566) TaqMan® probe 5′[6-FAM] CTC GCA CGC TTA AT [Tamra-Q]3′, Mc ras2-1 forward primer 5′-TCG AGA AGA GGG AGC GAT AAA G-3′, and Mc ras2-1 reverse primer 5′-TGC TGA CGT CTC GAC GAA AT-3′. Rm ATCC 52813 gene encoding hypothetical protein 72589 served as an internal standard for ras2-1 and tar normalization, with TaqMan® probe 5′[6-FAM] AG TGG TTG TTA ACA GCG [Tamra-Q]3′, forward primer 5′-AGG AAT TGA TCT CGA AAA ATC TGA A-3′, and reverse primer 5′-GAT CCC ACG CAG AGA AGC AT-3′. This gene was not affected by the presence/absence of endobacteria and displayed a high level of constitutive expression in the RNA-seq data. Mc actin gene (105861) was used for normalization in Mc ras2-1 reactions with TaqMan® probe 5′[6-FAM] CCG AAG TGC AAC TGT TCT TGC CTC ACT [Tamra-Q]3′, forward primer 5′-GCA GGA ATC ACA AAA CGT ATC AAG-3′, and reverse primer 5′-GTT GTG TAT CGC CTG CAT TCT C-3′.
Identification of sex-relevant genes across fungi
To identify sex-related genes conserved across fungi, we queried the genomes of Saccharomyces cerevisiae YJM78939, Schizosaccharomyces pombe 972h40, Aspergillus nidulans FGSC A441, Cochliobolus heterostrophus C442, Neurospora crassa OR74A (N150)43, Ustilago maydis 52144, Coprinopsis cinerea strain Okayama 7 #13045, Cryptococcus neoformans var. neoformans B-3501A46, Batrachochytrium dendrobatidis JAM81 (genome.jgi.doe.gov), Mucor circinelloides CBS 277.4947, Phycomyces blakesleeanus NRRL155547, R. delemar 99–88048, and Rm ATCC 52813 (genome.jgi.doe.gov) and ATCC 528146. We additionally included transcriptomic data from Rhizophagus irregularis DAOM18160249. OrthoMCL50 was conducted using default parameters (minimum E value cutoff of 1e-5, inflation 1.5) to cluster genes across all of these genomes into orthologous groups. From the genomes of S. cerevisiae, A. nidulans, N. crassa, and U. maydis, we extracted a collection of genes with experimentally validated reproductive phenotypes as a tool for further characterization of the resulting clusters, and to assess whether these known genes were also altered in expression due to reproduction in Rm. For Ras phylogeny reconstruction, full-length amino acid sequences were aligned using MUSCLE51 under default parameters, and the phylogeny was constructed with MrBayes52 under the mixed amino acid substitution model with Γ rate variation run for 2 million generations. For GPCR phylogeny reconstruction, we extracted protein sequences for the seven-transmembrane domain, aligned them with MUSCLE, and reconstructed phylogeny using FastTree53 under the WAG substitution model54 with Γ rate variation.
Rm genome sequencing, assembly, and annotation
The Rm ATCC 52813 genome was sequenced using the Illumina platform. Two Illumina libraries were sequenced: (1) fragment library with 270-bp insert size in 2 × 150-bp reads, and (2) 5.2-kb-long mate pair in 2 × 100-bp reads. Each fastq file was QC filtered for artifact/process contamination and subsequently assembled with AllPathsLG R4104355, resulting in 26-Mb assembly in 131 scaffolds and 773 contigs, with an average 143.6× read depth coverage. The assembled genome was annotated using the JGI annotation pipeline56, which combines several gene prediction and functional annotation methods, and integrates the annotated genome into JGI web-based resource for fungal comparative genomics, MycoCosm (http://genome.jgi.doe.gov/fungi)57.
Before gene prediction, assembly scaffolds were masked using RepeatMasker58, Repbase library59, and the most frequent (>150 times) repeats recognized by RepeatScout60. The following combination of gene predictors was run on the masked assembly: (1) ab initio, including Fgenesh61 and GeneMark62, (2) homology based, including Fgenesh+61 and GeneWise61 seeded by BLASTx alignments against the NCBI NR database, and (3) transcriptome based, including Fgenesh and COMBEST63. In addition to protein-coding genes, tRNAs were predicted using tRNAscan-SE64. All predicted proteins were functionally annotated using SignalP65 for signal sequences, TMHMM66 for transmembrane domains, interProScan67 for integrated collection of functional and structural protein domains, and protein alignments to NCBI NR, SwissProt68, KEGG69 for metabolic pathways, and KOG70 for eukaryotic clusters of orthologs. InterPro71 and SwissProt68 hits were used to map Gene Ontology terms72. For each genomic locus, the best representative gene model was selected based on a combination of protein homology and transcriptome support, which resulted in the final set of 10,905 gene models reported in this study. Coverage of gene models by BLAT alignments of transcriptome assemblies to the genome assembly resulted in 85% of models being covered over at least 75% of their length, and 67% of models 100% covered. The complete set (100%) of eukaryotic core genes from the CEGMA dataset73 was found in Rm, indicating a reasonably complete genome assembly.
The transcriptome data are available at the NCBI GEO database under the accession number GSE57644. The Rhizopus microsporus ATCC 52813 Whole Genome Shotgun project has been deposited at DDBJ/EMBL/GenBank under accession JOSV00000000. All other relevant data are available in this article and its Supplementary Information files, or from the corresponding author upon request.
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We thank J. Spatafora for including Rm ATCC 52813 in the 1000 Fungal Genomes project, J. Taylor for permission to analyze the unpublished genome of Batrachochytrium dendrobatidis JAM81, A. Collmer and J. Worley for the gift of pBS46:YFP and pBS46:mCherry plasmids, E. Angert, and G. Turgeon for comments on the manuscript. The work at Cornell University was funded by the National Science Foundation grants DEB-0918880, IOS-1261004, and DBI-1263103 to T.E.P., and by the National Institutes of Health grant GM-19629 to Susan A. Henry in support of M.L.G., whereas the work conducted by the U.S. Department of Energy Joint Genome Institute was sponsored by the Office of Science of the U.S. Department of Energy under contract DE-AC02-05CH11231.
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