Insecticidal fungi represent a promising alternative to chemical pesticides for disease vector control. Here, we show that the pathogenic fungus Beauveria bassiana exports a microRNA-like RNA (bba-milR1) that hijacks the host RNA-interference machinery in mosquito cells by binding to Argonaute 1 (AGO1). bba-milR1 is highly expressed during fungal penetration of the mosquito integument, and suppresses host immunity by silencing expression of the mosquito Toll receptor ligand Spätzle 4 (Spz4). Later, upon entering the hemocoel, bba-milR1 expression is decreased, which avoids induction of the host proteinase CLIPB9 that activates the melanization response. Thus, our results indicate that the pathogen deploys a cross-kingdom small-RNA effector that attenuates host immunity and facilitates infection.
Malaria remains one of the world’s deadliest infectious diseases, with 435,000 global deaths and 219 million new cases in 2017, up from 217 million cases in 20161. Because mosquitoes are obligatory vectors for malaria transmission2, vector control represents the front-line intervention tool for preventing malaria transmission3. However, vector control efforts are being undermined by increasing insecticide resistance4, and alternative ecologically sound approaches to control mosquitoes are urgently needed. The insect pathogenic fungus Beauveria bassiana (Cordycipitaceae) offers a promising environment-friendly alternative to chemical insecticides5,6. This fungus is effective at killing both insecticide-resistant and -susceptible adult mosquitoes7,8 and considered as a next-generation mosquito control agent9,10. However, fungal pathogens kill mosquitoes relatively slow compared with chemical pesticides, which has hampered their widespread application11. Thus, better understanding of molecular interactions between the fungus and the host mosquito is of particular importance for improvement of its efficacy.
Insects employ innate immune responses to fight pathogenic infection. Toll is the principal antifungal pathway by directing the production of antifungal peptides12. Melanization is another important facet of the mosquito immune defense against fungi13. To cause infection, pathogens must counteract their host immune responses14. In case of fungi, the molecular mechanism of host immunity suppression has not been described, although the metabolites secreted by insect fungal pathogens have been implicated in this phenomenon15,16,17. Plant pathogenic fungi are known to deliver cell-entering effectors to suppress host immunity18,19. However, to our knowledge, no examples of such effector molecules have been described for insect pathogenic fungi20.
Small silencing RNAs (sRNAs) are short noncoding RNAs that regulate gene expression by binding to Argonaute (AGO) proteins and directing the RNA-induced silencing complex (RISC) to RNAs with complementary sequences. miRNAs are a class of sRNAs of ∼22 nt, and are important modulators of various biological processes, including development and host–microorganism interactions19,21,22.
Here, we report that the insect fungal pathogen B. bassiana produces a microRNA-like sRNA bba-milR1 that acts as a host cell-entering effector to modulate the expression of mosquito immune genes, demonstrating the fungal pathogen has adapted the cross-kingdom RNA interference-mediated defense mechanism during the evolutionary arms race with the insect hosts.
Beauveria bassiana expresses miRNA-like small RNAs
To explore possible roles of miRNAs in mosquito–fungus interactions, we profiled sRNA libraries generated from Beuaveria bassiana-infected Anopheles stephensi mosquitoes collected at 36, 60, and 84 h post fungal topical inoculation. We identified four miRNA-like small RNAs (milRNAs) whose sequences cannot be mapped to the A. stephensi genome, but perfectly matched the B. bassiana genome (Supplementary Fig. 1a). These 4 milRNAs (bba-milR1, bba-milR2, bba-milR3, bba-milR4) had predicted miRNA-like precursor stem-loop structures (Supplementary Fig. 1b), suggesting that B. bassiana may generate miRNA-like small RNAs during host infection. Fungi have diverse milRNA biogenesis pathways, and some milRNAs are Dicer independent23. B. bassiana has two Dicer proteins Dicer1 and Dicer2. To investigate whether B. bassiana milRNAs are produced by Dicer, we generated Dicer1 deletion mutant (ΔDcl1), Dicer2 deletion mutant (ΔDcl2), and double-mutant ΔDcl1/Dcl2 by homologous replacement (Supplementary Fig. 2a, d–f). We found that bba-milR1 could not be detected in ΔDcl2 and ΔDcl1/Dcl2 mutants (Fig. 1a), demonstrating that bba-milR1 is Dicer dependent, whereas bba-milR2, bba-milR3, and bba-milR4 are still expressed in Dcl1 or Dcl2 single- and double-mutants (Supplementary Fig. 1c).
bba-milR1 facilitates fungal infection
To investigate whether these milRNAs are involved in fungal pathogenicity, we generated deletion mutants by separately disrupting the precursor sequences of the four milRNAs in B. bassiana ARSEF252 by homologous replacement (Supplementary Fig. 2a, g–j). Pathogenicity assays against A. stephensi showed that deletion of bba-milR1 resulted in a significant reduction in fungal virulence to mosquitoes relative to wild-type B. bassiana ARSEF252 (P < 0.0001, Log-rank test) (Fig. 1b). However, deletion of bba-milR2, bba-milR3, or bba-milR4 did not alter fungal virulence (Supplementary Fig. 3). We next generated the transgenic strains that overexpress bba-milR1, bba-milR2, bba-milR3, or bba-milR4 under control of the constitutive glyceraldehyde-3-phosphate dehydrogenase (gpd) promoter. For each milRNA, a fragment of ∼400 bp primary milRNA centered on the genome sequence of B. bassiana ARSEF252 was amplified and cloned into the fungal expression vector. The overexpression vectors were separately transformed into ARSEF252 (Supplementary Fig. 2b). We validated that expression level of the four miRNAs was significantly higher in transgenic strains compared with wild-type (Supplementary Fig. 4a). These results further confirm that these milRNAs are transcribed from the genome of B. bassiana. Overexpression of the bba-milR2, bba-milR3, or bba-milR4 did not affect fungal virulence (Supplementary Fig. 4b), whereas overexpression of bba-milR1 (milR1-OV) resulted in significant decrease in virulence to adult A. stephensi mosquitoes (P < 0.0001, Log-rank test) (Fig. 1c) and had no obvious negative impact on fungal development (Supplementary Fig. 2c), suggesting that constitutive expression of bba-milR1 impacts fungal pathogenicity. To further investigate the function of bba-milR1 in fungus–mosquito interactions, we quantified its expression pattern during B. bassiana infection of A. stephensi. bba-milR1 was induced by ~30-fold at 36 h post infection (hpi), and then declined to very low levels as the fungus enters the host’s hemocoel at about 60 hpi (Fig. 1d). To investigate whether bba-milR1 is expressed by other B. bassiana strains, 5-day-old female A. stephensi mosquitoes were infected with ARSEF252 and two other B. bassiana strains ARSEF2860 and Bb-bm01. We found that bba-milR1 is also detected in mosquitoes infected with these two strains (Supplementary Fig 5), suggesting that bba-milR1 is conserved among B. bassiana strains.
bba-milR1 binds to mosquito Argonaute 1
Recent studies showed that microorganism-encoded miRNAs can act as cross-kingdom regulators of host gene expression19,21,22. Given the high expression level of bba-milR1 at early stages of infection, we hypothesized that it may play a role in the interaction between fungus and host. To investigate whether B. bassiana bba-milR1 can enter mosquito cells, we incubated Aedes albopictus C6/36 cells with Cy3-labeled bba-milR1 and tracked RNA localization. As shown in Fig. 2a, bba-milR1 was loaded in vesicles that were present outside the cells, on the cell surface, and was transported into insect cells. These results suggest that bba-milR1 enters host cells via vesicles. Similar results were observed in Drosophila S2 cells (Supplementary Fig. 6). To examine the transport of milRNA in vivo, Cy3-labeled bba-milR1 was injected into the mosquito hemocoel and found that Cy3-labeled bba-milR1 was present in the cytoplasm of fat body cells (Fig. 2b).
In insects, miRNAs are preferentially assembled with Argonaute 1 (AGO1) to form an RNA-induced Silencing Complex (RISC) that modulates gene expression24. To investigate whether bba-milR1 associates with RISC, we performed RNA immunoprecipitation (RIP) assays using an A. stephensi AGO1 (AsAGO1) antibody and assayed for AGO1-bound miRNAs using Reverse Transcription PCR (RT-PCR). As a positive control, A. stephensi derived miR-10-5p and miR-2940-3p were detected in AsAGO1-RIP samples (Fig. 2c). We found that B. bassiana milR1, milR2, milR3, and milR4 were specifically detected in AGO1-RIP samples (Fig. 2c). These results indicate that miRNAs produced by B. bassiana are exported into host cells and bind to mosquito AGO1 to hijack host the RNA interference (RNAi) machinery.
bba-milR1 targets the mosquito host genes Spz4 and CLIPB9
To investigate whether bba-milR1 targets mosquito genes, three stringent target prediction softwares (microTar, PITA, and miRanda) were used to predict potential targets in the 3′UTR, 5′UTR and coding sequences of the A. stephensi genome (Supplementary Table 1; Fig. 3a). We found that bba-milR1 could base pair with some mosquito immunity genes, including genes encoding thioester-containing protein, CLIP-domain serine protease, serine protease inhibitor, and Spätzle-like cytokine (Supplementary Table 1). To validate the interaction between bba-milR1 and the predicted immune-related target genes, we performed target verification tests ex vivo and in vivo. To verify these targets ex vivo, we cloned the DNA sequences surrounding predicted target sites using A. stephensi cDNA as templates into psiCheck2 vectors downstream Renilla luciferase stop codon. The engineered vectors and bba-milR1 mimics were co-transfected into HEK293T cells, and measured luciferase activity. Dual-luciferase reporter assays showed that bba-milR1 can suppress Spz4 and induce CLIPB9 expression (Fig. 3b, c). When the regions homologous to the seed sequence of bba-milR1 were mutated in the Spz4 and CLIPB9 reporter constructs, the luciferase activity was not affected by bba-milR1 (Fig. 3a–c). To confirm that the regulation of the two targets was indeed triggered by bba-milR1 in vivo, we injected bba-milR1 agomir, a type of chemically modified double-stranded microRNA, into adult A. stephensi mosquitoes, and examined the transcript level of the target genes by qRT-PCR. We found that the transcript levels of Spz4 and CLIPB9 were significantly suppressed and induced in agomir-treated groups, respectively (Fig. 3d, e). These results show that the host genes Spz4 and CLIPB9 are targeted in the coding regions and are suppressed and induced by B. bassiana bba-milR1, respectively. However, ex vivo and in vivo results for other predicted targets were contradictory (Supplementary Fig. 7).
bba-milR1 manipulates host immunity to facilitate infection
The Toll pathway in mosquitoes and other insects operates as a primary immune defense against fungal infection12,25. The activation of the Toll pathway requires the binding of the cytokine Spätzle (Spz) to the Toll receptor, an interaction that transduces extracellular immune signals into cells. There are six members of the Spz family in the A. stephensi genome, of which Spz4 has the highest expression in the integument and fat body (Supplementary Fig. 8). To confirm that Spz4 can be targeted by bba-milR1 during infection, we further examined the expression levels of Spz4 in mosquitoes after infection with wild-type B. bassiana (WT) and bba-milR1 overexpression strain (milR1-OV). Expression of Spz4 was significantly lower in milR1-OV-infected mosquitoes than in WT-infected mosquitoes (Fig. 4a; Supplementary Fig. 9). Meanwhile, the mRNA levels of the major antifungal effector genes encoding Cecropin 1 (CEC1) and Defensin 1 (DEF1) were also reduced in milR1-OV-infected mosquitoes (Fig. 4a; Supplementary Fig. 9), indicating that bba-milR1 can suppress Spz4 and immune response during mosquito infection. To determine whether Spz4 is involved in the mosquito Toll immune signaling pathway, we silenced Spz4 by systemic injection of Spz4 double-stranded RNA (dsSpz4). The mRNA levels of CEC1 and DEF1, which are antimicrobial peptide genes downstream of the Toll pathway, were reduced by ∼50% in dsSpz4-treated mosquitoes compared with the dsGFP-treated controls (Fig. 4b). The CEC1 and DEF1 transcript levels were decreased by ∼70% in agomir-injected mosquitoes compared with negative controls, which provides further evidence for Spz4 repression and inhibition of the Toll signaling pathway by bba-milR1 (Fig. 4c). To define the contribution of Spz4 in the mosquito immune defense against B. bassiana infection, we knocked down Spz4 by injecting dsSpz4 and then infected mosquitoes with B. bassiana. At 60 h after topical infection of B. bassiana, the formation of hyphal bodies, a proxy for fungal invasion efficiency, was significantly more abundant in dsSpz4-treated mosquitoes than the dsGFP control (Fig. 4d). The fungal biomass in dsSpz4-treated mosquitoes was 2.2-fold greater than the dsGFP controls (Fig. 4e). Moreover, silencing of Spz4 rendered mosquitoes more susceptible to the B. bassiana infection than the dsGFP-treated control, and the survival rate was significantly lower (Fig. 4f). These results indicate that Spz4, a Toll receptor ligand, regulates the expression of the antifungal peptide genes to protect mosquitoes from fungal infection. We conclude that bba-milR1 acts as a fungal effector molecule to suppress mosquito immune response by targeting host Spz4.
Melanization, another important immune mechanism of arthropods, also plays an important role in the innate immune response to encapsulate and retard invasive B. bassiana growth and dissemination in mosquitoes13. Melanization is regulated by activation of prophenoloxidase (PPO) into phenoloxidase (PO), and involves an extracellular proteinase cascade and serpin inhibitors (Fig. 5a). The clip domain serine proteinase CLIPB9 acts as a PPO-activating proteinase to regulate melanization in mosquitoes26. To confirm whether CLIPB9 is indeed modulated by bba-milR1 during infection, we examined the transcript levels of CLIPB9 in mosquitoes after infection with WT, milR1-OV, and milR1-KO strains. The results showed that there was no significant difference in the transcript levels of CLIPB9 between mosquitoes at 36 h post infection with WT, milR1-KO, and milR1-OV (Fig. 5b; Supplementary Fig. 10a), indicating that bba-milR1 does not interact with CLIPB9 during the early stages of infection when fungus penetrating the mosquito integument. However, the expression of CLIPB9 was significantly higher and lower in the mosquitoes infected by B. bassiana milR1-OV and the milR1-KO mutant, respectively, than the WT-infected mosquitoes at late stages of infection (84 hpi) (Fig. 5c; Supplementary Fig. 10b). To test the role of CLIPB9 in the defense against B. bassiana infection, we silenced CLIPB9 by systemic injection of CLIPB9 dsRNAs. The dsCLIPB9 silencing reduced CLIPB9 mRNA levels by 83% (Supplementary Fig. 11a). Then, we measured the hemolymph PO activity in dsGFP-treated and dsCLIPB9-treated mosquitoes at 3 days post injection. The PO activity was significantly lower in dsCLIPB9-injected mosquitoes than dsGFP-injected mosquitoes (Supplementary Fig. 11b). Similarly, infection of milR1-OV and milR1-KO resulted in significant increase and decrease in A. stephensi hemolymph PO activity compared with WT at 84 hpi, respectively (Fig. 5d). As a consequence of CLIPB9 knock down, the number of B. bassiana hyphal bodies was higher than in dsGFP-treated controls (Fig. 5e). qPCR analysis demonstrated that fungal load was significantly higher in dsCLIPB9-treated mosquitoes compared with the dsGFP-treated controls (Fig. 5f). Moreover, silencing of CLIPB9 rendered mosquitoes more susceptible to B. bassiana infection than dsGFP-treated controls (Fig. 5g). Taken together, these results show that B. bassiana markedly reduces bba-milR1 expression during late stages of infection to elaborately avoid induction of CLIPB9, and in this way circumvent the melanization response (Fig. 6).
Beauveria bassiana has been at the forefront of efforts to develop biocontrol alternatives to the use of chemical insecticides for vector control5,10,27,28. This fungus is also widely used as a model for studies of fungal pathogenicity and fungus–invertebrate host molecular interactions14,20. Insects possess a refined innate immune system capable of recognizing fungal pathogens12,25. To develop in insects, fungal pathogens must be able to attenuate their host immune responses. How this happens remains elusive. Here, we show that the fungal pathogen produces a sRNA effector that is translocated into host insect cells to attenuate host immunity and achieve its infection, which is an example of the evolution of a cross-kingdom RNA-mediated defense mechanism.
Small RNAs play critical roles in regulating gene expression in many organisms. In insects, miRNAs associate with AGO1 to mediate gene regulation24. Our immunoprecipitation assays demonstrated that the bba-milR1 can enter the insect cells where it associates with mosquito AGO1 and in this way hijacks the insect RNAi machinery to selectively modulate host defense genes. The bba-milR1 was found in exosome-like extracellular vesicles (EVs) from where it is transported into mosquito and fruit fly cells and fat body tissues. Recent studies suggest that EV-mediated export of sRNA represents a conserved universal mechanism for intra-kingdom and inter-kingdom communication29,30.
Insect pathogenic fungi gain access to the insect hemocoel by penetrating its chitinous integument20. B. bassiana penetrates the mosquito integument at ∼36 hpi, and invades the mosquito’s hemocoel at ∼60 hpi31. To successfully develop in their insect hosts, pathogenic fungi must be able to disable host immune responses. The cleaved ligand Spätzle activates the Toll immune pathway, which is the principal insect antifungal mechanism12. In insects, the Toll is activated early by recognizing fungal structures while traversing the external cuticle32,33. We found that A. stephensi Spz4 is highly expressed in the mosquito integument at the point of fungus penetration. Interestingly, we found that the bba-milR1 is highly induced and expressed in B. bassiana during cuticle penetration, so that it can efficiently silence Spz4 and suppress Toll-mediated mosquito immunity.
Once in the hemocoel, fungal hyphae encounter host cellular and humoral defenses. To counter these defenses, the invasive filamentous cells switch to a yeast-type proliferation strategy to form hyphal bodies that possess fewer carbohydrate epitopes, allowing fungi to avoid recognition by the host immune system14,20. The other target of bba-milR1 is A. stephensi CLIPB9 that regulates PPO activation in the melanization response26. Although bba-milR1 can induce expression of CLIPB9, we found that B. bassiana reduces bba-milR1 expression to very low level after entering the hemocoel, thus elaborately avoiding direct induction of CLIPB9. If bba-miR1 is overexpressed under the control of a constitutive promoter, it impairs fungal pathogenicity (Fig. 1c). CLIPB9 and PPO are mostly expressed in mosquito hemocytes34,35, which could explain why highly expressed bba-milR1 during fungal penetration of the insect integument did not target and induce expression of CLIPB9. These findings uncover how the fungal pathogen manipulates its host’s defense mechanisms by deploying bba-milR1 in a spatial and temporal manner at different phases of infection (Fig. 6). This study also opens a new avenue to improve fungal pathogenicity against mosquitoes, leading to better control of mosquito-borne diseases.
Anopheles stephensi (Dutch strain) mosquitoes were maintained at 27 °C with 70 ± 5% relative humidity under 12 h/12 h day–night cycle. Larvae were fed on cat food pellets and ground fish food supplement. Adult mosquitoes were maintained on 10% (wt/vol) sucrose.
Fungal culture and infection bioassay
Beauveria bassiana strains ARSEF252, ARSEF2860, and Bb-bm01 were grown and maintained on Sabouraud dextrose agar plus yeast extract (SDAY; BD Difco) at 26 °C. Conidia were obtained from 10-day-old SDAY cultures. Conidia suspensions were prepared in 0.01% (vol/vol) Triton X-100 and filtered through layers of sterile glass wool to remove hyphal fragments. To conduct fungal infection, 5-day-old female A. stephensi adult mosquitoes were sprayed with fungal conidial suspension (107–108 conidia/mL). Mosquitoes sprayed with sterile 0.01% Triton X-100 were used as a negative control. The treated mosquitoes were subsequently maintained at 26 ± 1 °C and 80 ± 5% relative humidity, with a 12-h/12-h day–night cycle, until mosquitoes died or were collected for sample preparation at the indicated time points. Each treatment was replicated three times with 50 mosquitoes per replicate, and the infection bioassays were repeated three times. Mortality was recorded every 12 h, and cadavers were transferred to moisturized filter paper to monitor the emergence of fungal hyphae.
Small RNA library construction and sRNAs sequencing
Mosquito samples were collected at 36 , 60 , and 84 h after topical infection with B. bassiana ARSEF252. For each time point, about 50 infected mosquitoes collected from two biological replicates were pooled. The fungus-infected mosquito samples were homogenized with beads in RNAiso Plus (TaKaRa). The total RNA was extracted using Direct-zol RNA Miniprep Kit (Zymo Research Corporation) and treated with DNase I (TaKaRa) following the manufacturer’s instructions. The RNA concentration and purity were assessed in an Agilent 2100 Bioanalyzer (Agilent) to verify RNA integrity. Small RNA libraries were constructed using a TruSeq small RNA sample preparation kit (Illumina) following the manufacturer’s instructions. Illumina microRNA sequencing was performed at Shanghai Biotechnology Corporation. Briefly, the 3′ and 5′ RNA adapters were ligated to the corresponding ends of small RNAs. Following adapter ligation, the ligated RNA fragments were reverse transcribed using M-MLV reverse transcriptase (Invitrogen). The resulting cDNA products were PCR amplified with two primers that were complementary to the ends of the adapter sequences. The PCR amplicons were separated by size in 6% polyacrylamide gel for sRNA (20–30 nt) enrichment and sequenced on Illummina HiSeq 2500 sequencing system.
miRNA sequence analysis
The raw reads from sequencing data were filtered by removing poor quality reads, adaptor pollution reads and reads less than 18 nt. The clean reads of small RNAs were aligned to the reference Beauveria bassiana genome. The alignment analysis was conduced using CLC Genomics Workbench 12. The sequences that correspond to known miRNAs were determined by matching to the miRNA database (miRBase 22.0). The unannotated sRNA sequences were aligned to the reference B. bassiana genome to find precursor sequences for novel miRNAs. Novel miRNAs were predicted by miRCat2 (http://srna-workbench.cmp.uea.ac.uk/mircat2/) with stem-loop structure. The R package DEGseq software was used to analyze differentially expressed miRNAs.
miRNA target prediction
Three miRNA prediction softwares miRanda (http://www.microrna.org) and PITA (http://genie.weizmann.ac.il/index.html) and microTar (http://tiger.dbs.nus.edu.sg/microtar/) were jointly used to predict miRNA targets in mosquito Anopheles stephensi. Thresholds were set to a score of ≥ 140 for miRanda (default), ddG ≤ 0 for PITA, and energy ≥ 0.5 for microTar.
Fungal small RNAs deletion and overexpression
For targeted deletion of milRNAs (bba-milR1, bba-milR2, bba-milR3, or bba-milR4), the 5′ and 3′ flanking regions of the miRNAs were amplified by PCR from B. bassiana ARSEF252 genomic DNA and then subcloned into the XbaI and EcoRV sites of the binary vector pBarGFP, respectively36. The gene disruption vectors were then transformed into Agrobacterium tumefaciens AGL-1 for targeted gene disruption in B. bassiana ARSEF252 by homologous recombination16.
To overexpress miRNAs (bba-milR1, bba-milR2, bba-milR3, or bba-milR4) in B. bassiana ARSEF252, the ~400 bp fragment surrounding primary milRNA was amplified by PCR from B. bassiana genomic DNA, and then subcloned into EcoRI and EcoRV sites of the binary vector pBarGFP-PgpdA downstream of a constitutive Aspergillus nidulans gpdA promoter (PgpdA), to generate microRNA expression vectors. The sequence of the microRNA amplicon was confirmed by sequencing. The vectors were separately transformed into wild-type B. bassiana ARSEF252 using Agrobacterium tumefaciens-mediated transformation to generate microRNA overexpression strains36.
Generation of Dicer mutants of B. bassiana
To generate Dicer1, Dicer2 single knockout mutant, the 5′ and 3′ flanking regions of the genes open-reading frame were amplified by PCR from B. bassiana ARSEF252 genomic DNA, and then subcloned into the binary vector pBarGFP. Dcl1 and Dcl2 deletion mutants were generated by using homologous recombination and the Agrobacterium tumefaciens-mediated transformation system36. To double-knockout Dcl1 and Dcl2, the 5′ and 3′ flanking regions of Dcl2 ORF were subcloned into the binary vector pSurGFP. The resulting vector was applied to A. tumefaciens-mediated transformation in a Dcl1 mutant strain as described above. The sequences of the primers are given in Supplementary Data 1.
Mosquito RNA isolation and qPCR
The total RNA was extracted from mosquitoes by using RNAiso Plus (TaKaRa) and treated with Recombinant DNase I (TaKaRa) according to the manufacturer’s instruction. For mRNA, cDNAs were synthesized from the total RNA using a PrimeScript™ RT reagent Kit (TaKaRa). Quantitative reverse transcription PCR (qPCR) reactions were performed using the AceQ qPCR SYBR Green MasterMix Kit (Vazyme). cDNAs for miRNAs were reverse transcribed by using miRcute miRNA First-Strand cDNA Synthesis Kit (Tiangen), and qRT-PCR reactions were performed using miRcute miRNA qPCR detection kit (Tiangen) according to the manufacturer’s protocol. Each sample was performed in triplicate. The housekeeping gene RPS7 (AsS7) and snRNA U6 were used as endogenous control for mRNA and miRNA, respectively.
Luciferase reporter assays
For high-transfection efficiency and low background expression of bba-milR1, the mammalian HEK293T cell line (ATCC) was used for luciferase reporter assay37. The HEK293T cells were grown in the DMEM/HIGH GLUCOSE medium (HyClone) containing 10% (vol/vol) heat-inactivated fetal bovine serum (FBS, Gibco) and 1 × antibiotic–antimycotic (Gibco) at 37 °C under 5% CO2. The ~400 bp sequences surrounding the predicted bba-milR1 target sites in CLIPB9 and Spz4 were separately cloned into the XhoI and NotI sites of the psiCheck-2 vector (Promega). Mutagenesis PCR was performed to introduce point mutations at the bba-milR1 target sites to construct psiCheck-2-mut vectors. The HEK293T cells were transfected with 100 ng of psiCheck-2 reporters with 100 nM (final concentration) of synthetic bba-milR1 Mimic (sense strand 5′-UGACUGGCUGUUAAUUGACUGG-3′, anti-sense strand 5′-AGUCAAUUAACAGCCAGUCAUU-3′, RiboBio) or Negative Control miRNA Mimic (micrON mimic NC #24, RiboBio) using Attractene Transfection Reagent (Qiagen). Cells were collected and lysed at 48 h after transfection. The activities of firefly and Renilla luciferases were measured using the Dual-Luciferase Reporter Assay System (Promega). Each sample was performed in triplicate, and transfections were repeated three times.
miRNA Agomir injection
bba-milR1 Agomir is a chemically modified double-strand stable bba-milR1 (sense strand 5′-UGACUGGCUGUUAAUUGACUGG-3′, anti-sense strand 5′-AGUCAAUUAACAGCCAGUCAUU-3′). The 3-day-old female mosquitoes were microinjected using Nanoject II microinfector (Drummond) into the thorax with 69 nl agomir (200 nM). Control mosquitoes were injected with negative control Agomir (200 nM). bba-milR1 Agomir and control Agomir (micrON agomir NC #24) were synthesized by RiboBio (Guangzhou, China). Mosquitoes were allowed to recover for 2–3 days before fungus infection.
dsRNA-mediated gene silencing in adult mosquitoes
To produce the double-stranded RNA of the genes Spz4 (dsSpz4) and CLIPB9 (dsCLIPB9), the coding regions of the Spz4 and CLIPB9 genes were separately PCR amplified from A. stephensi cDNA with forward and reverse primers containing the T7 promoter sequence at their 5′ ends (5′-TAATACGACTCACTATAGGG-3′) (Supplementary Data 1). The PCR products were purified with Cycle-Pure Kit (OMEGA) and used as the template to synthesize dsRNA in vitro using the MEGAscript RNAi kit (Life Technologies). The dsRNA was further purified using the purification column supplied with the kit, eluted with nuclease-free water, and concentrated to 3 μg/μl using a Microcon YM-100 filter (Millipore). An enhanced green fluorescent protein (eGFP)-derived double-stranded RNA (dsGFP) was synthesized and used as a negative control. For dsRNA microinjection, cold-anesthetized 3-day-old female mosquitoes were injected with 69 nl of dsRNA solution (3 ng/μl) into the hemocoel using Nanoject II microinfector (Drummond). Injected mosquitoes were allowed to recover for 2–3 days before conducting fungal infection. To compare the abundance of hyphal bodies in mosquitoes, the hemolymph was collected. An incision was made in the abdomen between the last two segments with a sterile tweezers, and 10 μl perfusion buffer [60% Schneider’s Insect Medium (Sigma), 10% FBS, and 30% citrate buffer (pH 4.5; 98 mM NaOH, 186 mM NaCl, 1.7 mM EDTA, and 41 mM citric acid)]38 was slowly injected into the throax. The diluted hemolymph was collected from the incision by a pipette tip. The hemolymph samples were added to glass slides immediately and observed under a microscope. To quantify the load of B. bassiana in the dsRNA-treated mosquitoes, 20 whole mosquitoes were collected for every group and ground in liquid nitrogen. The total DNA was extracted by DNeasy Blood & Tissue Kits (Qiagen) according to the manufacturer’s instruction. The fungal housekeeping gene 18S rRNA was used to quantify fungi by qPCR analysis.
PO activity assay
To collect mosquitoes hemolymph, 30 mosquitoes were surface-sterilized and dissected at the thorax. The hemolymph was collected into a 1.5 -mL Eppendorf tube containing 200 μl 1 × PBS and 0.2 μl of protease inhibitor solution, centrifuged for 20 min at 4 °C, 10,000 rpm. The hemolymph was recovered in supernatant at the volume about 150 μl, and protein concentration was determined using the Pierce BCA Protein Assay Kit (Thermo scientific). Five micrograms of hemolypmh protein were adjusted to 40 μl in PBS containing protease inhibitors and then added 120 μl of L-DOPA solution (20 mM). The samples were incubated at 29 °C for 30 min. The optical density at 492 nm was measured for each sample against an L-DOPA control that was incubated with PBS. Each experiment was repeated three times.
The fat body of the B. bassiana ARSEF252 infected mosquitoes at 36 , 60, and 84 hpi were dissected, mixed, and homogenized in ice-cold RIP lysis buffer39. Uninfected mosquitoes mixed with B. bassiana ARSEF252 mycelia were used as a control. Magnetic beads were pre-incubated with 5 μg of custom-made antibody against A. stephensi AGO1 (GenScript) (Supplementary Fig. 12) or normal mouse IgG (Millipore). Then, the antibody-coupled magnetic beads were incubated with 100 μl mosquito homogenates. The immunoprecipitates were pulled down and digested with protease K to release the bound sRNAs. Finally, the cDNAs were reverse transcribed using miRcute miRNA First-Strand cDNA Synthesis Kit (Tiangen). RT-PCR reactions were performed using a miRcute miRNA qPCR detection kit (Tiangen).
The total proteins from A. stehpensi and B. bassiana was extracted by RIPA lysis buffer (Beyotime) containing 1 × protease inhibitor cocktail (Beyotime). Proteins were separated in a sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto a PVDF membrane (Bio-Rad). The membrane was blocked with 5% nonfat milk in TBST buffer (pH 7.5; 100 mM Tris·HCl, 150 mM NaCl, and 0.05% vol/vol Tween 20) and incubated overnight 4 °C with AsAgo1 antibody (1:1000, GenScript). The horseradish peroxidase (HRP)-linked goat anti-rabbit IgG secondary antibody (BBI, D110058) was used at a 1:10,000 dilution. Protein bands were detected using SuperSignal West Pico PLUS Chemiluminescent Substrate (Thermo Fisher Scientific).
Immunohistochemistry to detect miRNA entering host cells
Mosquito Aedes albopictus C6/36 (ATCC) and Drosophila melanogastor S2 cell lines (Thermo Fisher Scientific) were used for miRNA transportation assay. The mosquito cells C6/36 cells were grown in the RPMI 1640 Medium (Hyclone) containing 10% (vol/vol) heat-inactivated FBS (Gibco) and 1 × antibiotic–antimycotic (Gibco) at 28 °C. S2 cells were grown in Schneider’s Insect Medium (Sigma) containing 10% (vol/vol) heat-inactivated FBS (Gibco) and 1 × antibiotic–antimycotic (Gibco) at 28 °C. To detect the transportation and subcellular localization of exogenous miRNAs in insect cells, C6/36 and S2 cells were cultured in the presence of 2 μM synthesized Cy3-labeled bba-milR1 (GenePharma) for 24 h. After incubation, all cells were terminated by washing with ice-cold PBS and fixed cells with 4% (m/vol) paraformaldehyde (PFA) for 10 min. Then, cells were washed with 1 × PBST for three times and kept in 1 × PBS. For confocal observation, cells were mounted with VECTASHIELD Antifade Mounting Medium containing DAPI (Vector Laboratories, H-1200) for 5 min and fluorescence signals were visualized with Leica SP8 confocal microscope system.
To examine the translocation and localization of bba-milR1 in mosquito for in vivo analysis, 69 nl Cy3-labeled bba-milR1 (20 μM) was injected into female mosquitoes as described above. The mosquito fat bodies were collected in 1 × PBS at 24 h post injection. The tissues were further fixed with PFA, stained with DAPI, and observed with a confocal microscope as described above.
The statistical significance of the survival data from fungal infection bioassays and Triton X-100 treated mosquitoes (control) was analyzed with a log-rank (Mantel–Cox) test. Other statistical significance was determined by Student’s t test for unpaired comparisons between two treatments. P-value of < 0.05 was regarded as statistically significant. Except for when specified in the context, the results are expressed as mean ± s.e.m. All statistics were performed using GraphPad Prism version 5.00 for Windows (GraphPad Software).
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The sRNA sequencing datasets have been deposited in the National Center for Biotechnology Information Sequence Read Archive with accession number PRJNA517599. The source data underlying Figs. 1a–d, 2c, 3b–e, 4a–f, and 5b–g, and Supplementary Figs 1c, 2d–j, 3a–c, 4a, b, 5, 7a–e, 8, 9, 10a, b, 11a, b, and 12 are provided as a Source Data file.
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We thank Prof. Marcelo Jacobs-Lorena at Johns Hopkins University School of Public Health for comments and proofreading the paper. We thank Fang Li for rearing mosquitoes. This work was supported by grants from the Strategic Priority Research Program of Chinese Academy of Sciences (grant XDB11010500), National Key R&D Program of China (2018YFA0900502, 2017YFD0200400), the National Natural Science Foundation of China (grants 31772534, 31830086, 31501703, 3170110113), and One Hundred Talents Program of the Chinese Academy of Sciences (grant 2013OHTP01).
The authors declare no competing interests.
Peer review information Nature Communications thanks Sassan Asgari, Raymond St Leger and other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
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Cui, C., Wang, Y., Liu, J. et al. A fungal pathogen deploys a small silencing RNA that attenuates mosquito immunity and facilitates infection. Nat Commun 10, 4298 (2019). https://doi.org/10.1038/s41467-019-12323-1
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