Rhodnius handling and whole-mount immunostaining

Rhodnius females were dissected 10 days after the feeding regimen and ovaries were immediately placed in cold Phosphate Buffered Saline (PBS). Ovaries were fixed and immunostained as previously described [32]. The anti-γH2Ax (Millipore) and DAPI were diluted 1:1000 in PBS + Tween20 0.3% supplemented with 1% BSA. Ovaries were mounted in 70% glycerol and analyzed on a Leica Confocal Microscope.

Phylogenetic construction

The evolutionary history of PIWI proteins in Rhodnius and Drosophila was inferred applying a Maximum Likelihood method [33]. The analysis included a total of seven amino acid sequences, which were aligned by the Multiple Sequence Alignment with Log Expectation (MUSCLE, version 3.8.31) method [34], employing standard parameters. The evolutionary history was inferred by Molecular Evolutionary Genetics Analysis version 6.0 (MEGA6), and visualized using interactive Tree of Life (iTOL, v2). The tree was validated by 1000 bootstraps replications. Values higher than 90% were indicated in nodes. The amino acid alignments performed to highlight the Rp-Piwi2 PolyQ stretch in Triatominae species included the following sequences: JAI55027.1 (R. neglectus), JAP02788.1 (T. dimidiata), JAC16725.1 (T. infestans) available in NCBI, and Rp-Piwi2 of R. prolixus. The aminoacid sequences of proteins from R. prolixus and D. melanogaster were obtained from VectorBase (https://www.vectorbase.org/) and FlyBase (http://flybase.org/) respectively.

Total RNA extraction and RT-PCR assays

For the RT-PCR assays, total RNA was extracted from previtellogenic stages and, separately, from choriogenic stages dissected from 10/15 adult females. For qRT-PCR assays, total RNA was extracted from previtellogenic stages of wildtype, pRNAi and control ovaries 2 weeks after blood feeding. Tissues were ground in Trizol Reagent (Invitrogen) and processed as per manufacturer instructions. Total RNA was treated with Turbo DNA-free (Ambion) to remove genomic DNA traces. The resulting DNA-free total RNA was subjected to in vitro Reverse Transcription (RT) with Superscript III (Invitrogen). 1.0μg of DNA-free total RNA was used for each reaction and assays were conducted in biological triplicates. The oligonucleotides used in RT-PCR and qRT-PCR assays, are listed in the S1 Table.

Parental RNAi and in situ RNA hybridization assays

For in vitro transcription, T7 promoter sequences in the appropriate orientation were added to the DNA templates through a PCR-based system using the set of oligonucleotides listed in S1 Table. The same DNA templates were adopted both for in situ hybridization assays and for dsRNA production. For parental RNAi assays, sense and antisense ssRNAs for each gene were produced using the Megascript kit (Ambion). Approximately equal amounts of sense and antisense RNAs for each target were mixed in annealing buffer, precipitated and resuspended in water to a final concentration of approximately 1.5μg/μL. Two microliters of each dsRNA were injected in the abdomen of adult females three days prior blood feeding. A total of 10 adult females were injected with each dsRNA preparation. Ovaries were dissected two weeks after the feeding regimen. The DNA templates used to generate in situ hybridization probes were obtained by PCR using oligonucleotides carrying T7 promoter sequences at the 5'-end. The templates were subjected to in vitro transcription with the DIG RNA labeling kit (Roche). In situ hybridization conditions have been described elsewhere [35]. Oligonucleotides used in this study are listed in the S1 Table.

RNAseq library preparation and bioinformatic analyses

Ovaries of 10 blood-fed Rhodnius females were dissected in cold PBS and previtellogenic stages of oogenesis were manually separated from vitellogenic stages and chorionated eggs. Total RNA from two biological replicates was isolated with Trizol reagent (Invitrogen) and subjected to paired-end RNA library preparation as per manufacturer's instructions (Illumina, Truseq paired-end RNA library prep. kit). The libraries were sequenced on Illumina HiSeq platforms at the Lactad Facility (University of Campinas, Brazil). RNAseq datasets are available at NIH SRA (SRP158580).

We employed the GEMtools pipeline (https://github.com/gemtools/gemtools) of the GEM mapper [36] to align 128,411,588 paired-end reads sequenced from two replicates (76,963,784 vs. 51,447,804 reads in each of the libraries vit1 and vit2) of the ovary samples to the Rhodnius genome assembly RproC1, using the subsequently quantified transcriptome annotation RProC1.1 as a guide. Overall ~90% (89.1 vs. 89.6%) of these reads mapped, and ~80% (80.9% vs. 79.2%) of the in total sequenced reads were considered informative for the quantification at a proportion of multi-mappings of <1%. These mappings exhibited a fidelity of on average ~3 mismatches and indels (3.2 respectively 3.5) with the RproC1 reference genome sequence and were used for subsequent quantification of the RproC1.1 transcriptome as annotated by the Vectorbase community (PMID: 22135296) and obtained from the Ensembl Metazoa database (v88). The EnsMart annotation of this database to maps 1,029 of the 1,467 most abundant mRNAs bidirectionally (i.e., orthology type "one-to-one") to protein-coding loci of the Flybase RefSeq annotation [37], further 208 Flybase proteins can be rescued through "one-to-many" and "many-to-many" ortholog mappings. After evaluating the number of occurrences for each term in comparison to their occurrence in the entire Flybase reference annotation, a p-value for the statistical overrepresentation is computed according to the model implemented in the DAVID tool [38]. Based on the distribution of p-values, we control the rate of false-discoveries to be not higher than 0.05 and group the remaining terms by a fuzzy clustering procedure on their co-occurrence in gene products, calling clusters with at least 5 members. The RproC1 version of the Rhodnius genome is available at the following URL: https://www.ebi.ac.uk/ena/data/view/GCA_000181055.2.

Transcriptomic profiling of previtellogenic stages of oogenesis in Rhodnius prolixus

Adult Rhodnius females develop two ovaries, each composed of groups of seven ovarioles (Fig 1A and 1B) [39–41]. Germline stem cells are present in nymphal stages and the adult females inherit a discrete number of oocyte arrested in meiosis I and aligned at the anterior region of a lancet-like structure termed the tropharium. During oogenesis, each oocyte is surrounded by a layer of somatic follicle cells to form the mature egg chamber. Different from the meroistic polytrophic ovary found in Drosophila and other species, in the meroistic telotrophic ovary of Rhodnius the egg chambers do not harbor nurse cells. Instead, the nurse cells or trophocytes populate the tropharium, where they form a syncytium around a central region termed the trophic core (Fig 1B). The tropharium can be divided in three regions with typical cell populations (Fig 1A and 1B). Actively dividing germ cells are observed only in the Zone1 at the very anterior region [42]. These cells migrate to the Zone2, where they lose their proliferation ability, begin the endoreduplication program and turn into trophocytes (Ts), which are functionally analogous to the Drosophila nurse cells. In the Zone3, that anticipates the previtellogenic egg chambers, the Ts display large nuclei with prominent nucleoli. In this region, the cell also start to degenerate and are progressively lost and replaced by new Ts migrating from Zone2. Nutrients and possibly RNAs produced by the trophocytes accumulate in the trophic core and are subsequently transported to the growing oocytes through specialized cytoplasmic bridges termed trophic cords. The previtellogenic phase of oogenesis starts in the tropharium and ends when the egg chambers reach a diameter of 0.5mm [43]. During vitellogenesis, the egg chambers grow up to 1mm in length, the trophic cords are severed and choriogenesis begins. Mature eggs produced by Rhodnius adult females are protected by a compact and resistant chorion, which regulates the fertilization process and prevents dehydration (Fig 1A). To investigate the molecular mechanisms that coordinate and drive Rhodnius oogenesis, we performed transcriptomic profiling in ovaries of blood-fed females. Our study focused on the previtellogenic phase of oogenesis. Total RNA extracted from these tissues was used to prepare and sequence paired-end RNAseq libraries and in total 12.84 Gigabases were sequenced in two replicates (vit1 and vit2). Sequence reads were then mapped to the Rhodnius genome RproC1 (Methods) as obtained from the Ensembl Metazoa database (v83) [41]. On average ~86% of informative mappings to the genome (55,455,772 in vit1, and 36,324,980 in vit2) superimposed in the correct orientation to the RProC1.3 transcriptome annotation. These mappings provide a deep interrogation of the annotated R. prolixus transcripts, with ~84% of the 14,840 transcripts detected by >10 read mappings, ~67% by >100 mappings, ~48% by >1,000 mappings, and ~10% by 10,000 mappings. Besides six rRNA loci (RPRC015844, RPRC015846, RPRC016406, RPRC016579, RPRC016706 and RPRC016876), these highly expressed loci comprise the RNAseP (RPRC016972) and two SRP genes (RPRC017200 and RPRC017302). Interestingly, we also found a putative ortholog of the Drosophila squid gene to be highly expressed in Rhodnius ovaries. The Squid protein controls the localization and translation of the gurken mRNA, which encodes a TGFa-like morphogen involved in the axial polarization of the egg and future embryo. Of the remaining 7,172 highly expressed protein-coding (pseudo-) genes, we investigated the 1,467 genes that exhibited > 10,000 reads for common functional patterns. Since only 36 of these were annotated with known protein functions in the RproC1.3 genome version, we employed for our functional study 9,188 orthology mappings to the Drosophila melanogaster proteome. Five major groups obtained by clustering 626 functional terms are obtained from these most abundant mRNAs (Fig 1C). These have been annotated in Flybase orthologs, collected from different databases and integrated into the DAVID functional annotation platform [44,45]. Our analysis reveals that genes with high expression levels in Rhodnius ovaries are orthologs of Drosophila proteins annotated with functions related to the ribosome (group 1) and translation (group 3), to mRNA processing and splicing (group 2), to proteasome activity (group 4), and also to helicases that pave the way for transcription of genes and ATP metabolism (group 5). In agreement with our samples being depleted of vitellogenic and choriogenic egg chambers, the functional classes related to vitellogenin biogenesis and uptake as well as chorion synthesis displayed low expression levels in our datasets. Our results demonstrate that cells in the previtellogenic phase of Rhodnius oogenesis invest the major part of their energy in the biogenesis (i.e., at the level of transcription, mRNA processing and translation) and turnover of the existing proteome by elevated proteome activity.

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Fig 1. Transcriptomic analyses in early stages of Rhodnius prolixus’ oogenesis.

A) Structure of the ovariole showing the tropharium at the very anterior region, egg chambers in various stages of development and a mature chorionated egg at the very posterior end. The operculum defines the anterior pole of the egg. B) Schematic of the ovariole. The tropharium hosts mitotically active cells in zone 1 at the anterior region and the polyploid trophocytes (i.e. nurse cells) in zone 2 and 3. Oocytes arrested in Meiosis I are located at the posterior region of the tropharium. Each oocyte becomes encapsulated by follicle cells to form the budding egg chamber. Egg chambers in Rhodnius remain connected to the tropharium through the trophic cords, which ensure that nutrients and RNAs produced by the trophocytes are transferred to the growing oocytes. Z1, Zone1, Z2, Zone2, Z3, Zone3, GC, germinal vesicle. C) Functional Analysis of the previtellogenic transcriptome: Five major functional clusters (left) are identified for the 1,050 most expressed genes with high confident homologues in D. melanogaster, obtained by grouping statistically overrepresented terms (right) by their co-occurrence in gene products (x-axis). The matrix in the middle panel visualizes by colors the significance of the p-value computed for a gene.

https://doi.org/10.1371/journal.pntd.0006760.g001

Orthologs of the Drosophila piRNA pathway components are expressed during Rhodnius oogenesis

We employed our transcriptome profiling to determine the extent of evolutionary and functional conservation of the piRNA pathway in R. prolixus. Using Blast tools, we interrogated the Vectorbase platform to identify genes with homology to the Drosophila factors involved in the biogenesis and function of the piRNAs. For each putative ortholog, we then computed the expression levels as per RNAseq, as average RPKM between two biological replicates (Fig 2). We immediately noticed that the heat shock protein 83 (hsp83) and uap56 gene, which encode a nuclear-cytoplasmic RNA export factor, are expressed at higher levels (>500 RPKM) than other piRNA pathway components in Rhodnius ovaries (Fig 2A). The majority of the putative piRNA pathway genes however could be grouped in two classes: intermediate and low expression levels (Fig 2B and 2C). The first group is composed of 14 genes, whose steady state expression levels ranged between 50 and 250 RPKM (Fig 2B). These genes encode putative orthologs of several cytoplasmic factors involved in the biogenesis of the piRNAs in Drosophila, including Vas, Tudor, Maelstrom, and two putative orthologs of the Zuc endonuclease belong to this class. The remaining 15 genes displayed average RPKM lower than 50 (Fig 2C). Among them, armitage, the dSetDB1 methyl-transferase encoding eggless gene and the putative orthologs of krimper, papi and tejas, which encode Tudor domain proteins. Surprisingly, spn-E, a critical Helicase for the production of piRNAs in Drosophila, as well as the piwi ortholog Rp-piwi1 seem to be either expressed at very modest levels or not expressed in Rhodnius ovaries (average RPKM<5) (Fig 2C). The results of the RNAseq analysis were validated by qRT-PCR assays with oligonucleotides specific to a selected group of genes (S2 Fig). In the fruit fly, the expression of the piRNA clusters in germline tissues is regulated by the RDC complex, which consists of the HP1 variant Rhino (Rhi), the Rai1-like factor Cutoff (Cuff) and the Deadlock (Del) protein. Blast alignments of the Rhi aminoacid sequence with proteins encoded in the Rhodnius genome did not return a clear match. Since this protein is a member of the Heterochromatin Protein (HP) family, several putative Rhodnius HP proteins share comparable aminoacid sequence similarity with Rhi. Conversely, the Del protein appears to evolve rapidly and is restricted to the Drosophilids. In Drosophila, the cuff and the CG9125 genes code for proteins with aminoacid sequence similarity to the yeast transcription co-factor Rai1. Interestingly, blast search analyses retrieve one single gene in Rhodnius encoding a putative protein displaying 20.7% and 28.1% aminoacid sequence identity with Cuff and with the protein encoded by CG9125 respectively. The Rhodnius Rai1-like gene, which we named Rp-rai1l, is not annotated in the current version of the Rhodnius genome and lies within the first intron of the gene RPRC008241 (supercontig KQ034693) (S1 Fig). Our transcriptomic analysis reveals that Rp-rai1l displays intermediate expression levels during Rhodnius oogenesis (Fig 2B), although its role, if any, in the piRNA pathway needs to be elucidated. For several genes that have been linked to the piRNA pathway in Drosophila, our blast search did not return homologous sequences in the Rhodnius genome. For instance, the Rhodnius genome does not appear to host homologs of the Drosophila moon and squash genes, which are expressed in the germline tissues, as well as of YB, SoYB, BoYB and T2RD2 that act in the somatic branch of the piRNA pathway in the fruit fly.

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Fig 2. Steady-state expression levels of putative piRNA pathway genes in early Rhodnius oogenesis.

A) Box plot showing the highly expressed putative orthologs of the fruit fly uap56 and hsp83 genes in Rhodnius. B) Box plot displaying 14 genes with intermediate expression levels in Rhodnius oogenesis. C) Box plots showing 15 genes, including putative orthologs of spn-E and Rp-piwi1, characterized by low expression levels in Rhodnius. In the panels A-C, Y-axis represents average RPKM values over two biological replicates. D) RNAseq profiles along the Rp-vas, Rp-piwi1, Rp-piwi2, Rp-piwi3 and Rp-ago3 genes. The Y-axis displays RPKM for two biological replicates (dark and light blue). Red line indicates the position of a mariner-like element in the Rp-vas gene. PVG stands for previtellogenic.

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We then focused our study on the Rhodnius orthologs of the vas and piwi genes, which are central components of the piRNA pathway in Drosophila. Vas is a DEAD-box RNA helicase related to the translation factor eIF-4A and has been extensively used as a marker of germline tissues in distantly related organisms [46]. Importantly, studies in Drosophila showed that Vas elicits piRNA production in concert with Aub and Ago3 [16]. We found that the Rhodnius genome harbors a putative homolog of the vas gene (Vectorbase ID RPRC009661), which encodes a protein 75% identical to DmVas. Our RNAseq profiling reveals that Rp-vas is expressed at intermediate levels during Rhodnius oogenesis (Fig 2B). Interestingly, while the D. melanogaster vas hosts the vig and solo genes in its intronic sequences, this arrangement is absent in Rhodnius, where the Rp-vas intron 1 harbors an Open Reading Frame (ORF) encoding a transposase enzyme from a mariner-like element (Fig 2D). Transcripts of this ORF are readily detected in our ovarian transcriptome datasets. Previous studies reported that Rhodnius displays an amplification of the piwi genes, whereby three putative orthologs of piwi, namely Rp-piwi1, Rp-piwi2 and Rp-piwi3, in addition to the Rp-ago3 ortholog of the Drosophila ago3 gene are present in the genome [26]. The analysis of the normalized RNAseq reads shows that Rp-piwi2, Rp-piwi3 and Rp-ago3 are expressed at intermediate or low levels in Rhodnius oogenesis (Fig 2B–2D), while the Rp-piwi1 transcripts are barely detectable. Based on the absence of intronic sequences, it has been proposed that Rp-piwi1 is a pseudogene and might not be required for Rhodnius development. Our transcriptomic analyses seem to support this hypothesis, although we cannot rule out the Rp-piwi1 might be expressed in tissues other than the ovary. According to the current genome annotation, Rp-piwi2 contains a small intron of approximately 100bp. Our RNAseq analysis however reveals that this sequence is included in the mature transcript and the resulting ORF encodes a putative protein of 882aa. Furthermore, the 5' and 3' untranslated regions of the Rp-vas, Rp-piwi2, Rp-piwi3 and Rp-ago3 extend beyond the limits annotated in the current version of the genome. Thus, our datasets not only provide information on the steady-state expression levels for all the genes and loci expressed in previtellogenic stages of Rhodnius oogenesis, but will also contribute to improve gene annotation and discovery.

Evolutionary conservation of the putative Rp-PIWI proteins

The Rp-piwi1, Rp-piwi2 and Rp-piwi3 (VectorBase IDs RPRC00252, RPRC002460 and RPR001891) encode putative proteins with 38.7%, 36.1% and 43.3% aminoacid sequence identity with D. melanogaster Piwi respectively (Fig 3A and S2 Fig). While the piwi orthologs appear to have originated from duplication of an ancestral piwi gene, the Rp-ago3 gene is homologous to the Drosophila ago3 gene (Fig 3A and S2 Fig). Accordingly, the Rp-ago3 locus (Vectorbase ID RPRC013054) encodes a putative protein 43.3% identical to DmAgo3. We then analyzed the degree of sequence identity between the individual Piwi, MID and Paz domains across the PIWI proteins in Drosophila and Rhodnius (Fig 3A and S2 Fig). All the domains appear to be well conserved in all the Rhodnius orthologs including the putative PIWI protein encoded by the Rp-piwi1 gene. Interestingly, the N-terminal region of the putative Rp-Piwi2 protein features a stretch of 18 Glutamine residues (i.e. polyQ tract) (Fig 3A and S2 Fig). This characteristic has not been reported for any of the PIWI proteins so far analyzed in a range of animal species. We therefore wondered whether PolyQ stretches are present in PIWI related proteins from other insects. Using NCBI Blast search analyses, we found that the polyQ tract is present in Piwi-like proteins encoded in the genome of Rhodnius neglectus, Triatoma infestans and Triatoma dimidiata (Fig 3B), but it is absent in PIWI proteins of Drosophila and other animals (Fig 3A and S2 Fig). Thus, the acquisition of a PolyQ sequence is likely a recent evolutionary event and is restricted to certain Triatomine species.

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Fig 3. Evolutionary conservation of the putative PIWI proteins in Rhodnius.

A) Phylogenetic tree displaying the evolutionary relationship among Rp-Piwi1, Rp-Piwi2, Rp-Piwi3 and Rp-Ago3 and their Drosophila orthologs Piwi, Aub and Ago3. Schematic displaying the conservation of the typical Argonaute domains in the Drosophila and Rhodnius Piwi-clade Argonaute proteins. The conserved Piwi (yellow), PAZ (blue) and MID (grey) domains are highlighted. Argonaute linker domains 1 (green) and 2 (dark grey) are also shown. A polyglutamine stretch (orange) is present at the N-terminal region of the putative Rp-Piwi2 protein. B) Multiple aminoacid sequence alignment of the N-terminal regions of the putative Rp-Piwi2 orthologs in Rhodnius prolixus, Rhodnius neglectus, Triatoma dimidiata and Triatoma infestans. The red box highlights the position of the conserved PolyQ tract in the different Piwi orthologs.

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Expression pattern of the Rp-vas and Rp-piwi genes during previtellogenesis

Next, we wondered whether the Rp-vas and the Rp-piwi genes display stage- or tissue-specific expression patterns during Rhodnius oogenesis. To answer this question, we performed in situ hybridization assays in fixed ovaries using antisense probes corresponding to specific sequences within the ORF of Rp-vas, Rp-piwi1, Rp-piwi2, Rp-piwi3 and Rp-ago3 (Fig 4). This approach revealed that the expression of Rp-vas is restricted to the germline tissues given that the Rp-vas probe generates a signal in the tropharium and in the oocyte, but not in the somatic follicle cells (Fig 4A). Thus, RPRC009661/Rp-vas encodes a bona fide ortholog of DmVas, which allows distinguish the germ cell lineage from the somatic cell population. Previous studies reported the expression of a putative vas ortholog in the somatic follicle cells of the Rhodnius ovary [47]. Our in situ hybridization protocols did not allow preserve the vitellogenic egg chambers, thus we could not determine whether RPRC009661/Rp-vas transcripts are produced in the follicular epithelium in late stages of oogenesis. In accordance with the RNAseq data, the Rp-piwi1 probe did not produce any signals above the background levels (Fig 4B). The Rp-piwi2 transcripts instead are clearly detected in the tropharium and in the developing oocytes (Fig 4C). Interestingly, the Rp-piwi2 RNAs seem to unevenly accumulate in more mature oocytes, where they are enriched in the anterior region (Fig 4C). In addition, the Rp-piwi2 transcripts are detected also in the somatic follicle cells, thus suggesting that the expression of this gene is not restricted to the germline tissues (Fig 4C'). Similar to Rp-vas, the Rp-piwi3 and Rp-ago3 transcripts are detected in the region of the tropharium hosting the polyploid Ts and in the ooplasm of newly formed and mature egg chambers, but not in the follicle cells (Fig 4D and 4E). As control assay, we generated a sense probe corresponding to a region of the Rp-ago3 ORF (Fig 4F). This probe did not produce specific signals above the background levels.

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Fig 4. Expression pattern of the vas and piwi orthologs in Rhodnius.

A) In situ hybridization assays in early stages of oogenesis (tropharium and vitellarium) for Rp-vas (panel A), Rp-piwi1 (panel B), Rp-piwi2 (panels C and C'), Rp-piwi3 (panel D) and Rp-ago3 (panel E) genes. A sense Rp-ago3 probe was used as control for these assays (panel F). G-H) RT-PCR in previtellogenic stages of oogenesis (panel G) and in mature eggs (panel H) with oligonucleotides specific to Rp-vas, Rp-piwi1, Rp-piwi2, Rp-piwi3 and Rp-ago3 genes.

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During Rhodnius oogenesis, RNAs and nutrients produced by the nurse cells hosted in the tropharium are transported to the growing oocytes through the trophic cords. In order to determine whether piwi and vas transcripts are maternally stored in the mature eggs, we performed RT-PCR assays in ovaries with oligonucleotides specific for the piwi and vas genes by separating the previtellogenic stages of oogenesis from the chorionated mature eggs. In both stages of Rhodnius oogenesis, a clear amplification product of the expected molecular weight was detected for the Rp-piwi2, Rp-piwi3, Rp-ago3 and Rp-vas genes, while no amplification signal was produced for Rp-piwi1 (Fig 4G and 4H). These observations point to a direct role for Rp-piwi2, Rp-piwi3, Rp-ago3 and Rp-vas in Rhodnius germline development and possibly early embryogenesis.

Rp-piwi2, Rp-piwi3 and Rp-ago3 ensure female adult fertility in Rhodnius

Parental RNAi (pRNAi) was previously shown to induce the efficient reduction of gene expression in Rhodnius, where genetic tools are still lacking [48]. In order to understand the function of the Rp-piwi genes in Rhodnius, we carried on pRNAi assays by injecting dsRNA molecules targeting portions of their coding regions in the abdomen of adult females (Fig 5A). Injected females were blood-fed, their eggs were collected daily over a period of three weeks and let to develop until the first-instar nymphs emerged. After the 3-weeks period, the females were dissected and the eggs retained in the abdomen were also counted. This approach allowed us to investigate the oviposition and fertility of the injected females. Eggs were divided into three bins: 1) total number of eggs, which is given by the sum of the eggs retained in the abdomen and those that were actually oviposited, 2) oviposited eggs, 3) eggs that hatched to produce first-instar nymphs. Each group of control-injected females produced on average a total of 262 eggs of which 103 were oviposited and 67 developed into first-instar nymphs. Compared to these control animals, the Rp-piwi1 pRNAi females produced on average a slightly lower number of total eggs (~86%) and oviposited eggs (~83%). However, the hatching rates were higher than the control (~111%). It is noteworthy that in our pRNAi assays, the Rp-piwi1-KD females consistently produced a slightly higher number of first-instar nymphs than the control females, although this gene is apparently not expressed in ovaries. In contrast, oogenesis seemed to be partially impaired by pRNAi-mediated downregulation of the Rp-piwi3 and Rp-ago3 genes. Compared to the control, females from these assays respectively produced ~63% and ~48% total eggs, ~40% and ~39% deposited eggs and ~33% and ~35% first-instar nymphs. The most striking result however was obtained upon injection of Rp-piwi2 dsRNA molecules in adult females. The total number of eggs and the number of oviposited eggs produced on average by these animals was ~19% and ~13% of the control values, respectively. More importantly, the first-instar nymphs generated by Rp-piwi2 pRNAi females were only ~2% of the control values.

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Fig 5. Functional analysis of the Rp-piwi genes.

A) Parental RNAi against the piwi orthologs. Oogenesis and fertility were investigated by dividing the eggs in three groups: total number of eggs (Tot), oviposited eggs (Ovi) and hatched eggs giving rise to first-instar nymphs (Nym). Y-axis displays the percentage eggs produced by Rp-piwi pRNAi treated females compared to control pRNAi females. B) qRT-PCR assays to investigate the expression levels of the Rp-piwi genes after pRNAi treatment. The Y-axis displays the fold difference in the expression levels of the Rp-piwi1, Rp-piwi2, Rp-piwi3 and Rp-ago3 in each of the Rp-piwi KD versus control-injected ovaries. Error bars indicate standard deviation. C-E) Ovarian phenotype of Rp-piwi2 pRNAi females. Zone1 of control (C) and Rp-piwi2 pRNAi (D) ovaries. pRNAi against the Rp-piwi2 gene leads to a reduction in the number of trophocytes and abundant DAPI-positive nuclear debris (red arrows). (E) Zone 1 of Rp-piwi2 pRNAi ovaries is frequently atrophic. F-G) Immunostaining with anti-γH2Ax antibodies (red) and DAPI (blue) in Zone1 of control (F) and Rp-piwi2 pRNAi (G) ovaries. Notice the degenerating nuclei and DAPI-positive particles (red arrow). Single channels for the γH2Ax signal in control (F’) and pRNAi (G’) are shown. H-I) Zone3 and previtellogenic egg chambers of control (H) and Rp-piwi2 pRNAi (I) ovaries stained with DAPI. Degenerating nuclei appear to accumulate in the trophic core of Rp-piwi2 KD tropharia (red arrows). J-K) Control and Rp-piwi2 pRNAi egg chambers. Notice the cortical position of the germinal vesicle and the organized layer of follicle cells surrounding the oocyte in the control (J) ovaries, while egg chambers appear collapsed or atrophic upon pRNAi for Rp-piwi2 (K).

https://doi.org/10.1371/journal.pntd.0006760.g005

In order to investigate the specificity of our dsRNAs for the respective cognate Rp-piwi gene, we performed qRT-PCR assays in previtellogenic stages of pRNAi ovaries with oligonucleotides specific to Rp-piwi1, Rp-piwi2, Rp-piwi3 and Rp-ago3 (Fig 5B). As internal control for this assay, we used oligonucleotides specific to Rp-rp49 (RPRC014419), a putative Rhodnius ortholog of the Drosophila rp49 gene. These assays revealed that each dsRNA specifically downregulates the expression of the cognate gene by ~30% for Rp-piwi3, ~40% for Rp-ago3 and >50% for Rp-piwi2. As expected, the injection of Rp-piwi1 dsRNA did not produce significant changes in the expression levels of Rp-piwi1. Our results strongly point to a critical role for Rp-piwi2, Rp-piwi3 and Rp-ago3 in Rhodnius oogenesis and female adult fertility.

The Rp-piwi2 gene controls germ cell survival and egg chamber development during Rhodnius oogenesis

We then sought to determine the cellular basis of the reduced fertility observed in Rp-piwi2, Rp-piwi3 and Rp-ago3 KD females. To this aim, we immunostained ovaries from pRNAi-injected adult females with DAPI to visualize the nuclei of the germ cells and of the follicle cells (Fig 5). We immediately noticed that Rp-piwi2 pRNAi tropharia displayed abundant DAPI-positive particles in Zone1 and Zone2, which are rarely observed in the tropharia of control ovaries (Fig 5C and 5D). In some cases, the anterior tip of the tropharium corresponding to Zone1 appeared severely atrophic (Fig 5E). The γH2Ax histone variant was shown to accumulate at sites of DNA damage, induced for instance by meiotic recombination events or by transposable element mobilization [23,49]. We therefore monitored the occurrence of DSBs in control and Rp-piwi2-KD ovaries with the antibodies specific to γH2Ax (Fig 5F, 5F’, 5G and 5G’). This assay revealed that the DAPI particles observed in Zone1 of Rp-piwi2-KD tropharia as well as some nurse cell nuclei are enriched in this histone variant. In contrast, control tropharia did not display any signal beyond the background levels. In Zone 3 of control tropharia, the Ts nuclei are arranged at the periphery of the tropharium and display apparent nucleoli (Fig 5H). Instead, the Zone3 of the pRNAi-treated ovaries clearly displays a lower number of Ts nuclei and abundant nuclear debris in the trophic core (Fig 5I). In Rhodnius, each egg chamber is formed by an oocyte surrounded by a follicular epithelium (Fig 5J). pRNAi for Rp-piwi2 seems to strongly impair the progression through oogenesis and the growth of the egg chambers. We frequently observed smaller and apparently collapsed egg chambers during vitellogenesis (Fig 5K). These atrophic egg chambers were still connected posteriorly to younger egg chambers emerging from the tropharium and anteriorly to more mature choriogenic egg chambers through bridges of stalk cells. Despite the clear impact of pRNAi on Rhodnius fertility, the analysis of Rp-piwi3 and Rp-ago3 pRNAi ovaries did not display obvious abnormalities by DAPI staining and anti-γH2Ax immunostainings and additional molecular tools will be necessary to dissect their function during germline development. Our results however, demonstrate that Rp-piwi2 in fundamental for Ts survival and egg chamber development during Rhodnius oogenesis.