- Research article
- Open Access
Profile of small interfering RNAs from cotton plants infected with the polerovirus Cotton leafroll dwarf virus
© Silva et al; licensee BioMed Central Ltd. 2011
- Received: 31 May 2011
- Accepted: 24 August 2011
- Published: 24 August 2011
In response to infection, viral genomes are processed by Dicer-like (DCL) ribonuclease proteins into viral small RNAs (vsRNAs) of discrete sizes. vsRNAs are then used as guides for silencing the viral genome. The profile of vsRNAs produced during the infection process has been extensively studied for some groups of viruses. However, nothing is known about the vsRNAs produced during infections of members of the economically important family Luteoviridae, a group of phloem-restricted viruses. Here, we report the characterization of a population of vsRNAs from cotton plants infected with Cotton leafroll dwarf virus (CLRDV), a member of the genus Polerovirus, family Luteoviridae.
Deep sequencing of small RNAs (sRNAs) from leaves of CLRDV-infected cotton plants revealed that the vsRNAs were 21- to 24-nucleotides (nt) long and that their sequences matched the viral genome, with higher frequencies of matches in the 3- region. There were equivalent amounts of sense and antisense vsRNAs, and the 22-nt class of small RNAs was predominant. During infection, cotton Dcl transcripts appeared to be up-regulated, while Dcl2 appeared to be down-regulated.
This is the first report on the profile of sRNAs in a plant infected with a virus from the family Luteoviridae. Our sequence data strongly suggest that virus-derived double-stranded RNA functions as one of the main precursors of vsRNAs. Judging by the profiled size classes, all cotton DCLs might be working to silence the virus. The possible causes for the unexpectedly high accumulation of 22-nt vsRNAs are discussed. CLRDV is the causal agent of Cotton blue disease, which occurs worldwide. Our results are an important contribution for understanding the molecular mechanisms involved in this and related diseases.
- Small RNAs
- Cotton Plant
- Antiviral Defense
- Silence Pathway
- Systemic Leaf
The RNA silencing pathway controls important biological processes in plants, including regulation of gene expression during development, heterochromatin formation, hormone signaling, metabolic processes, and stress responses, as well as being an important antiviral defense mechanism . In plants, antiviral silencing can be triggered by the presence of viral double-stranded RNAs (dsRNA), which are generated by the viral RNA polymerase as an intermediate in genomic replication and transcription, or are predicted to form as secondary structures along single stranded viral genomic RNA (ssRNA) . Both structures are recognized by Dicer-like (DCL) ribonucleases and are processed into virus-derived small interfering RNAs (vsRNAs) that vary in length from 21 to 24 nucleotides (nt) [3–5]. These vsRNAs are then loaded into Argonaute (AGO)-containing complexes known as RNA-induced silencing complexes (RISCs), which promote the degradation of both genomic and subgenomic viral RNAs [6, 7].
DCL ribonucleases are present in both monocot and dicot plants. Arabidopsis thaliana contains four DCLs (AtDCLs1-4) , while the Populus and rice genomes encode five and six DCLs, respectively . The diversity associated with Dicer ribonucleases, as well as other silencing-related proteins such as AGO, strongly suggest that several silencing pathways have evolved in plants. Correspondingly, in Arabidopsis, at least six silencing pathways have been identified, and the four DCLs involved are known to act hierarchically. For example, there are 21-nt vsRNAs and other small RNAs (sRNAs) associated with post-transcriptional silencing of endogenous genes generated by AtDCL4. In the absence of AtDCL4, 22-nt vsRNAs are produced by AtDCL2, and in the absence of both AtDCL4 and AtDCL2, 24-nt vsRNAs are produced by AtDCL3 [10–12]. Thus, AtDCL2-4 play essential roles in mediating the antiviral defenses of Arabidopsis. In contrast, AtDCL1 is mainly associated with the production of microRNAs, which represent a class of important regulatory RNAs derived from hairpin-like endogenous transcripts .
All of the four Dicer proteins expressed in Arabidopsis are usually present in other plants, also  (Additional file 1, figure s1). Correspondingly, 21-, 22-, and 24-nt vsRNAs have been detected in many plant hosts following infection . However, based on the hierarchical roles of DCL4 and DCL2 in antiviral silencing, 21-nt vsRNAs are by far the most abundant class of sRNA found in plants infected with RNA or DNA viruses, followed by 22-nt vsRNAs [15–18]. Previous studies have shown that the accumulation of vsRNAs is affected by viral suppressors of gene silencing [11, 19].
Suppressor proteins can directly bind vsRNAs [20–23], or inhibit key proteins of the gene-silencing pathway [24–26]. For example, the Polerovirus P0 protein and the P38 protein from Turnip crinkle virus (TCV) target AGO1, an important antiviral Argonaute protein [11, 24, 27–30]. Studies have shown that P0 preferentially targets AGO1, leading to its degradation, but does not affect the sRNA-RISC complex . A similar action has been suggested for the P38 protein, which binds to AGO1 and may prevent the assembly of RISC. However, unlike P0, P38 does not affect the stability of AGO1 . By preventing the association of AGO1 with RISC, P38 has the potential to destabilize a complex homeostatic network involving AGO1, microRNAs, and the four Dicer proteins. This would be consistent with the preferential accumulation of 22-nt vsRNAs observed following infection with TCV .
In this study, vsRNAs derived from cotton plants (Gossypium hirsutum) infected with Cotton leafroll dwarf virus (CLRDV) (genus, Polerovirus; family, Luteoviridae) were deep-sequenced and characterized. CLRDV is transmitted by the aphid, Aphis gossypii, and is the causal agent of cotton blue disease , which occurs in cotton crops world-wide. Consistent with other members of the same family, CLRDV is phloem-restricted and its genome consists of a single strand, positive sense, non-polyadenylated RNA (5.8 kb) containing six open reading frames (ORFs) . This is the first report of vsRNAs derived from a member of the family Luteoviridae and the first report of vsRNAs in cotton plants.
Characterization of CLRDV-derived sRNAs
The high accumulation of the endogenous 24-nt sRNAs, followed by 21-nt sRNAs, are consistent with sRNA profiles in other plants (33,34). These findings indicate that the cotton RNA silencing machinery responsible for biogenesis of endogenous or viral sRNAs does not tend to produce 22-nt sequences. Therefore, the high levels of 22-nt CLRDV-vsRNA seem to be a result of the antiviral RNA silencing mechanism or a specific CLRDV-host interaction.
Distribution of vsRNA abundance
An analysis of the unique reads that mapped to the CLRDV genome indicated that all Dicer ribonucleases were able to access the entire viral genome. Similar amounts of 21-24-nt vsRNAs corresponding to sense and antisense strands of viral RNA (Figure 4C) were present in our library, reinforcing that virus-derived dsRNAs are the main source of vsRNAs. Furthermore, peaks of both the abundance (Figure 4B) and diversity (Figure 4C) of 21-24 nt reads showed similar patterns of distribution along the genome. These results suggest that all DCL ribonucleases contribute to the generation of vsRNAs with similar substrate affinities and target the same regions of the genome. However, the fact that the 22-nt class of vsRNAs was the most prominent class supports the hypothesis that GhDCL2 may play a role in the generation of CLRDV-vsRNA.
Expression of Cotton DCL ribonucleases during infection
Assays of TCV infection have detected a high abundance of 22-nt vsRNAs [11, 19, 30] associated with the silencing suppressor protein, P38. During infection, P38 inactivates AGO1 by down-regulating miR162. As a result, low levels of miR162 directly and/or indirectly affect transcript levels of Dcl1, 3, and 4. To determine whether a similar mechanism might be activated in cotton-infected plants, we analyzed the expression levels of mature miR162 and Dcls in CLRDV-infected and uninfected plants.
This is the first report of the characterization of small RNAs produced from a member of the genus Polerovirus, family Luteoviridae. The profile of vsRNAs generated in cotton plants infected with CLRDV revealed some interesting features regarding their biogenesis. For example, both sense and antisense orientations of CLRDV-derived sRNAs accumulated to similar levels (Figure 1B). However, several other studies have found that sense vsRNAs accumulate to higher levels in some hosts [16, 17, 23]. In those cases, strand biases are usually attributed to preferential processing of highly structured single-stranded genomic viral RNAs by Dicer ribonucleases [15, 23]. Despite these differences and considerable experimental efforts, however, the existence of a direct correlation between vsRNA hot-spots and structured regions of genomic viral RNAs has never been proven . The accumulation of equivalent amounts of sense and antisense CLRDV-vsRNAs observed in the present study supports the hypothesis that CLRDV-dsRNAs, which are generated by viral RNA polymerases during genome replication or by the activity of host RNA-dependent RNA polymerases , are the main substrates for Dicer ribonucleases. Since the P0 silencing suppressor protein from Polerovirus was already shown to inhibit production of secondary vsRNAs in 35S-promoter-driven agroinfiltration assays [27, 28, 37], it may be speculated that the main substrate of cotton DCLs during CLRDV infection is probably the replicative intermediate forms of viral genomic RNAs. However, the mechanism of P0 protein action in the formation of the secondary siRNAs during virus infection remains unclear.
Overall, the distribution profile of CLRDV-vsRNAs within the genome varied considerably. High vsRNA densities were identified in regions coding for structural proteins, especially in the ORF5 region (Figure 4). Previously, it was shown that genes encoding structural proteins in the family Luteoviridae are expressed from subgenomic RNAs (i.e., sgRNA1 and sgRNA2) . Moreover, studies of the Polerovirus, Potato leafroll virus (PLRV), also identified two sgRNAs associated with the 3- block of the viral genome . The transcription of sgRNA1 provides for expression of ORFs 3, 4, and 5, while that of sgRNA2 (~800 nt) encodes two proteins located within the 3- proximal half of ORF5. Since sgRNAs are highly expressed during the infection cycle, an over-accumulation of vsRNAs derived from this region of the genome might be due to a greater availability of dsRNA intermediate templates for processing. Accordingly, the hot-spot of vsRNAs mapped to ORF5 might be due to the expression of sgRNA2, which is also derived from this region of the genome. Although the synthesis of sgRNA2 by CLRDV has not previously been reported, the ACAAAA motif present at the 5- end of sgRNA1 and sgRNA2 from other Poleroviruses  is also present in the ORF5 of CLRDV (position 4821-4828) (data not shown). Based on these results, it is possible that sgRNA2 is produced by CLRDV.
Depending on their length and 5- identity, sRNAs are selectively loaded into multiple AGO complexes [33, 34]. Previous studies have shown that plant virus-specific sRNAs beginning with uracil or adenine are preferentially loaded into AGO1, AGO2, and AGO4 [15–17]. In fact, AGO1 and AGO2 are required for the anti-viral silencing pathway in Arabidopsis[41–43]. However, 21-23 nt CLRDV-vsRNAs usually have a cytosine at the 5- terminal position (Figure 3), indicating that they may be loaded into a cotton homologue of AGO5. Although the AtAGO5 has no detectable anti-viral function against Cucumber mosaic virus (CMV) [8, 43, 44], CMV-vsRNAs have been detected in AtAGO5 immunoprecipitates, indicating that the protein may act in the biogenesis of secondary vsRNAs . Moreover, a predominance of 5- terminal cytosines has been observed for some viroid-derived sRNAs . In contrast, most 24-nt CLRDV-vsRNAs have adenine at the 5- terminal (Figure 3), indicating that they can be loaded into cotton AGO2 and AGO4 homologues. In Arabidopsis, the association between 24-nt sRNAs and AGO4 has been well-characterized as a mediator of transcriptional silencing for transposons and repeated sequences . In addition, the decreased number of vsRNAs that start with guanine is correlated with the absence of AGO proteins that might otherwise have an affinity for those sRNAs.
The balance between antiviral silencing and suppression mechanisms can directly influence the accumulation of vsRNAs within infected plants. While the functions of the four DCL proteins present in Arabidopsis are well characterized, Dicer ribonucleases from other species, including cotton, remain largely unstudied. However, if the mechanism(s) associated with DCL ribonucleases is conserved between cotton and Arabidopsis, then the predominance of 22-nt vsRNAs associated with CLRDV infection would be hypothesized to be the result of GhDCL2 activity. Although 22-nt CMV-vsRNAs produced by AtDCL2 are poor effectors of antiviral defense in Arabidopsis, other studies have detected a predominant population of 22-nt vsRNAs following infection with certain plant viruses and viroids [11, 15, 19, 36, 45]. For example, Cymbidium ring spot virus (CymRSV) and TCV infections are associated with an abundance of 22-nt vsRNAs, which seem to be related to the activity of the suppressor proteins P19 and P38 [11, 15, 19]. P19 can specifically sequester 21-nt duplex sRNAs , while P38 can indirectly block AtDCL4 activity by suppressing AGO1 function . During TCV infection in Arabidopsis, AtDCL1 levels are indirectly increased due to the P38-mediated down-regulation of microRNAs, including miR162, a negative regulator of AtDcl1 transcripts . Since AtDCL1 negatively regulates AtDcl4 and AtDcl3, over-accumulation of AtDCL1 generates a deficit in the levels of AtDCL4 and AtDCL3, leaving dsRNAs more accessible to AtDCL2 . The Polerovirus P0 suppressor protein is also able to destabilize AGO1 [24, 27, 28]. Although the activity of CLRDV P0 has not yet been tested, the F-Box-like domain necessary for silencing that is conserved among P0 sequences from other members of the genus is also conserved in CLRDV (data not shown). Thus, CLRDV P0 has the potential to similarly affect cotton Dicer ribonucleases during the infection process. However, in this study, there were no significant changes in the levels of GhDcl1, GhDcl2, and GhDcl3 transcripts in infected plants (Figure 5B). Furthermore, GhDcl4 transcripts and Gh-miR162 were up-regulated (Figure 5A and 5B). The up-regulation of Dcl4 has been observed in other viral infections , but the levels of mature miR162 are inconsistent with what was observed during TCV infection . It is possible that differences in tissue tropism between TCV and CLRDV, and/or differences in the silencing machinery of the host, account for the observed differences between the two viruses.
Members of the genus Polerovirus are restricted to the phloem cells of their hosts. Therefore, DCL activity in response to viral dsRNA may be cell-type dependent. Small RNAs derived from Hop stunt viroid (HSVd) infections in cucumber plants showed different sizes in different tissues . For example, most of the sRNAs from infected whole leaves were 21-nt long, while those derived from phloem-sap were more frequently 22 nt in length. Although transgene-induced silencing in phloem cells of Arabidopsis is triggered by AtDCL4 , a difference in the affinity or expression of Dicer ribonucleases, or other silencing-related proteins such as dsRNA-binding proteins in companion cells, could possibly explain the tissue-dependent shift in sRNA size.
The production of vsRNAs following virus infection can vary depending on the host. For example, sRNAs derived from Bamboo mosaic virus are mainly 21 nt in length in Arabidopsis, but 22 nt in Nicotiana benthamiana. Therefore, these data suggest that DCL recruitment for vsRNA production is a host-dependent process . This is the first report of a sRNA profile for cotton virus-infected plants. Further research is required to confirm whether the vsRNA profile observed here results from a viral silencing suppressor protein, or from factors such as phloem-restriction or cotton-specific factors that can activate an anti-viral silencing pathway.
This is the first high-throughput sequencing of a member of the Luteoviridae family, CLRDV, from virus-infected cotton plants. This study shows that RNA silencing systems against CLRDV result in the production of 22-nt sRNAs as the predominant sRNA size class. All vsRNAs, independently of the size, and that these are derived mainly from the 3- region of the viral genome. The sequence data of sense and antisense vsRNAs strongly suggest that dsRNA molecules are the main source of the vsRNAs. During CLRDV infection, we observed up-regulation of GhDcl4 and down-regulation of GhDcl2 transcripts, which are the major DCLs in antiviral defense in the model plant Arabidopsis. There is still much to learn about the molecular mechanisms underlying the prevalence of the 22-nt CLRDV-vsRNAs.
Sample preparation and sequencing
Fifty-day-old cotton (Gossypium hirsutum) plants (cultivar FM966; Fibermax966) that are susceptible to cotton blue disease were infected with CLRDV using the viruliferous aphid, Aphis gossypii. Aphids were placed on older true leaves and removed 24 h after infestation. Systemic leaves (i.e., representing the youngest completely expanded leaves) were harvested 5 days post-infection (dpi). The same leaves were harvested from mock-infected plants as the control. Total RNAs were extracted from systemic leaves using the Invisorb Spin Plant RNA Mini Kit (Invisorb®).
The quantity and quality of RNA samples obtained were determined by spectrophotometry (Nanodrop ND-1000, Thermo Fisher Scientific) and agarose gel electrophoresis (Additional file 3, figure s3), respectively. Systemic infections were confirmed using nested (RT)-PCR assays to detect the viral capsid protein-encoding gene as previously described . RNA samples were precipitated in ethanol and sequenced at the Fasteris Life Science Co. (Geneva, Switzerland) with an Illumina Genome Analyzer (Illumina, San Diego, USA). Small RNA libraries were prepared according to a modified Illumina protocol. Briefly, small RNAs of 15-30 nt were purified on an acrylamide gel; the 3- IDT miRNA cloning linker (Integrated DNA Technologies, San Diego, USA) and then the 5- Illumina adapters were single-stranded ligated with T4 RNA ligase. The constructs were purified again on an acrylamide gel to remove empty adapters and then reverse-transcribed and PCR-amplified. The primers used for cDNA synthesis and PCR were designed to insert an index in the 3- adapter. The libraries were quality controlled by cloning an aliquot into a TOPO plasmid and capillary sequencing 4-8 clones. High-throughput sequencing was performed on a Genome Analyzer GAIIx for 38 cycles plus 7 cycles to read the indexes. After demultiplexing and adapter removal, 10.5 million pass filter reads were obtained in the library.
All the deep sequencing libraries obtained are deposited at GEO (Gene Expression Omnibus) under the number GSE311062 http://www.ncbi.nlm.nih.gov/geo/info/submission.html
Data mining of the sRNA pool
CLRDV-derived sRNAs sequences were identified using a local BLAST database of the CLRDV-PV1 isolate genomic sequence (accession number HQ827780). Library characterization and mapping to the viral genome were performed using locally developed Perl scripts. Further calculations and statistical analyses were performed using R 2.7.1 software (R Foundation for Statistical Computing).
Primer sequences and amplicon characteristics of DCLs, XTH, and Gh-miR162
Forward primer sequence (5'-3')
Reverse primer sequence (5'-3')
Amplicon size (bp)
Efficiency ± SD*
Locus accession number
0.928647 ± 0.0293724
0.99522 ± 0.00361129
0.997162 ± 0.0071986
0.992603 ± 0.0051324
0.884982 ± 0.032819
173 and 392**
To measure expression levels of mature Gh-miR162, a stem-loop quantitative RT-PCR technique was used as previously described .
Complementary DNA was produced using the RevertAid First Strand cDNA Synthesis Kit (Fermentas) and 0.5 μg of total RNA previously treated with DNase I (Fermentas). cDNAs of the cotton DCL genes were synthesized by adding 100 μM Oligo (dT24V) primer. For synthesis of Gh-miR162 cDNA, 100 μM specific primer was added (Table 1). The presence of residual genomic DNA in the RNA samples was verified by PCR of the control gene xyloglucan endotransglycosylase (XTH) (accession number AY189971.2), using primers spanning two exons and RNA samples that were not reverse-transcribed (RT) (Additional file 4, figure s4).
Synthesized cDNAs were diluted 50 times and 2.5 μL of these dilutions were analyzed by quantitative PCR (qPCR). Assays were performed using a 48-well plate on an Step One Real-Time PCR system (Applied Biosystems) with Maxima™ SYBR Green/ROX qPCR Master Mix (Fermentas), following the manufacturer's instructions. The cycling conditions were as follows: 10 min at 95°C for initial denaturation, followed by 40 cycles of denaturation at 95°C for 15 s and annealing/extension at 60°C for 30 s. Results were normalized against cotton genes for polyubiquitin (accession number DW505546) and the catalytic subunit of phosphatase 2A (accession number DT545658) . The reference genes were validated experimentally in specific CLRDV-infected samples (Additional file 5, figure s5). All reactions were performed using two independent biological samples and each sample was analyzed in triplicate wells. The mean value of each Ct triplicate was used for further calculations by the 2-ΔCt method. Each PCR run included a no-template control containing water instead of cDNA.
The efficiency values of the DCLs and Gh-miR162 primers sets were estimated for each experimental set by Miner software , and are listed in Table 1. Amplification of a specific transcript was confirmed by the appearance of a single peak in the melting curve followed by agarose gel electrophoresis (Additional file 6, figure s6). The correlation coefficient (R2) was calculated for each transcript (Table 1). The values shown are averages obtained from three biological replicates, and relative expression levels were obtained by comparing infected plants with uninfected plants.
We thank the Brazilian sponsoring agencies CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) for studentships to TFS and RRSA, CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico, 150639/2010-4 -PDJ) for CEGS and postdoctoral fellowships to EAdCR, and FAPERJ for financial support. This work is part of TFS's PhD thesis for the Plant Biotechnology Program and EAdR's postdoctoral research at the Genetics Department, Federal University of Rio de Janeiro, Brazil. We thank Christelle Barras, Elisabeth Dieterle, and Patricia O. Hernandez (Fasteris) for technical assistance with deep sequencing, Tereza Galvão Carvalho (UFRJ) for assistance with plant care and RNA extractions, and Anna Karoline Fausto for helpful discussions on statistical analyses.
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