- Research article
- Open Access
In vitro and in vivo silencing of plasmodial dhs and eIf-5a genes in a putative, non-canonical RNAi-related pathway
© Schwentke et al.; licensee BioMed Central Ltd. 2012
Received: 22 January 2012
Accepted: 31 May 2012
Published: 13 June 2012
Deoxyhypusine synthase (DHS) catalyzes the first step in hypusine biosynthesis of eukaryotic initiation factor 5A (eIF-5A) in Plasmodium falciparum. Target evaluation of parasitic DHS has recently been performed with CNI-1493, a novel selective pro-inflammatory cytokine inhibitor used in clinical phase II for the treatment of Crohn's disease. CNI-1493 prevented infected mice from experimental cerebral malaria by decreasing the levels in hypusinated eIF-5A and serum TNF, implicating a link between cytokine signaling and the hypusine pathway.
Therefore we addressed the question whether either DHS itself or eIF-5A is required for the outcome of severe malaria. In a first set of experiments we performed an in vitro knockdown of the plasmodial eIF-5A and DHS proteins by RNA interference (RNAi) in 293 T cells. Secondly, transfection of siRNA constructs into murine Plasmodium schizonts was performed which, in turn, were used for infection.
293 T cells treated with plasmodial DHS- and eIF-5A specific siRNAs or control siRNAs were analyzed by RT-PCR to determine endogenous dhs -and eIF-5A mRNA levels. The expressed DHS-shRNA and EIF-5A-shRNA clearly downregulated the corresponding transcript in these cells. Interestingly, mice infected with transgenic schizonts expressing either the eIF-5A or dhs shRNA showed an elevated parasitemia within the first two days post infection which then decreased intermittently. These results were obtained without drug selection. Blood samples, which were taken from the infected mice at day 5 post infection with either the expressed EIF-5A-shRNA or the DHS-shRNA were analyzed by RT-PCR and Western blot techniques, demonstrating the absence of either the hypusinated form of eIF-5A or DHS.
Infection of NMRI mice with schizonts from the lethal P. berghei ANKA wildtype strain transgenic for plasmodial eIF-5A-specific shRNA or DHS-specific shRNA resulted in low parasitemia 2–9 days post infection before animals succumbed to hyperparasitemia similar to infections with the related but non-lethal phenotype P. berghei strain NK65. RT-PCR and Western blot experiments performed with blood from the transfected erythrocytic stages showed that both genes are important for the proliferation of the parasite. Moreover, these experiments clearly demonstrate that the hypusine pathway in Plasmodium is linked to human iNos induction.
RNA interference (RNAi) is an evolutionary conserved mechanism found across a range of eukaryotes, where it plays a key role in post-transcriptional gene regulation and protection of genomes. The process of RNAi is triggered by the recognition of double-stranded RNA (dsRNA), which is then processed into 21–25 nucleotide sequences by Dicer, a cytoplasmic dsRNA specific RNaseII endonuclease . The generated RNAs associate with an RNA-induced silencing complex (RISC) and unwind in a strand-specific manner . The resulting short interfering RNAs (siRNAs) then target homologous mRNA for degradation in combination with the RNase H enzyme Argonaute (Slicer) . The stage of double stranded (ds) RNA processing may be surpassed by experimentally introducing sequence-specific siRNAs directly into cells.
Given the immense Public Health costs for malaria disease and the need for new drug targets a silencing approach employing RNAi might be extremely beneficial for the development of novel and advanced therapeutic strategies. Moreover, the ability to use RNAi for gene silencing in Plasmodium would provide a powerful means to gain insight into pathogenic blood stages.
Recent experiments performed by molecular genetics suggested that RNAi is not functional in malaria parasites . These authors showed that expression of the analyzed proteins continued despite the application of a variety of RNAi-based strategies to target genes which are non-essential to either growth or development of P. falciparum or P. berghei. In good agreement, control experiments with Trypanosoma brucei, a protozoan parasite with validated RNAi, were successful. Furthermore, to determine whether a primitive RNAi machinery exists in Apicomplexa a comparative analysis of Apicomplexan and other protozoan genomes was undertaken. Taken together these data argued that RNAi is absent in malaria parasites .
Several studies, however, reported the successful application of RNAi for gene silencing in the erythrocytic stages of Plasmodium. A series of experiments has been performed by introducing long dsRNAs by electroporation into infected erythrocytes. Gissot and coworkers  performed silencing experiments with MybB1, a transcription factor in Plasmodium thereby demonstrating its essential role in the erythrocytic stage. Kumar and colleagues  showed in a similar manner the requirement of a serine-threonine phosphatase for DNA-replication in Plasmodium. Tuteja and colleagues  identified a signal peptidase that is required for intra-erythrocytic growth by RNAi. Apart from electroporation , siRNAs have also been added directly to the culture medium. Cysteine proteases falcipain-1 and falcipain-2, which are necessary for haemoglobin degradation, have been shown to be essential for the blood stages . However, this finding is in question since standard disruption techniques showed no effect on parasitic development in the blood stages . While the latter authors suggested RNAi to be functional in Plasmodium, most of these cases resulted in parasitic death or significant growth defects due to unspecific downregulation of multiple genes by RNAi.
Deoxyhypusine synthase (DHS) catalyzes the first step in the biosynthesis of the amino acid hypusine (Hyp), a novel amino acid present in eukaryotic initiation factor 5A (eIF-5A) to form the deoxyhypusinylated intermediate. DHS transfers the aminobutyl moiety from the triamine spermidine to the є-amino group of Lys50 present in the hypusine loop. Both genes have been identified in P. falciparum and P. vivax[11, 12]. Hitherto, the biological function of this posttranslational modification is unknown. Recent studies have implicated a permissive role of eIF-5AHyp in various diseases. In diabetes type 2 pancreatic stressed ß-cells  and in HIV-infected T cells, eIF-5AHyp is functional as a nucleocytoplasmic shuttle protein for the transport and translation of specific mRNAs .
Particularly in HIV, eIF-5AHyp is essential for the nucleocytoplasmic transport and translation of incompletely-spliced mRNAs encoding viral proteins [15, 16]. In diabetes type2 eIF-5AHyp enables cytokine-mediated islet dysfunction through the direct posttranscriptional regulation of the mRNA encoding iNos2 (Nos2) in both rodent and human cells [13, 17]. Importantly, the immunological events which lead to severe malaria are complex and parallel events present in HIV-infection and pancreatic stressed ß-cells. Exogenous NO administration [18, 19] prevents the syndrome of severe malaria. Since a parasite specific nitric oxide synthase does not exist, the defense response may be attributed to the host specific iNos.
Cerebral malaria (CM) is characterized by clinical features like cognitive dysfunctions, seizures, coma and clinical parameters like anemia, metabolic acidosis, renal insufficiency and hypoglycaemia. Although the understanding of malaria pathogenesis is rudimentary, different theories have been accepted to understand the pathological process . The sequestration theory suggests that seizures might be caused by the adherence of parasites to red blood cells and subsequent expression of parasite specific antigens which in turn lead to obstruction of blood flow, cerebral hypoxia and decreased removal of waste. For the neurological symptoms there is growing evidence that parasite-induced sequestration of infected and uninfected erythrocytes changes blood—brain barrier function. Moreover, host-specific immune mechanisms may be important in response to the presence of parasites in the CNS.
In a first step of the infection process parasitized red blood cells adhere to brain microvascular endothelial cells through the erythrocyte membrane protein . After release of merozoites parasitic glycosylphosphatidylinositol (GPI) is released which induces a local inflammatory response involving natural killer and subsequently CD4+ T cells. At this stage of the infection, proinflammatory cytokines including tumor necrosis factor α (TNF-α interferon γ (IFN-γ and interleukin (IL)-1ß are produced locally before the entry of the systemic phase in which cytokines activate macrophages and CD8+ T cells . In the systemic phase, more platelets and microparticles are released inducing perforin-mediated lesions in the endothelium .
Recently, metabolic changes in the central nervous system caused by the parasite, have been characterized as a third theory in explaining the pathology of malaria. During CM an increase of lactate and alanine concentration and alterations in tryptophane metabolites like the kynurenine pathway lead to an increased permeability of the blood brain barrier for plasma proteins.
DHS has been recently validated as a druggable target by the small molecule CNI-1493, a synthetic guanylhydrazone , which significantly extends the survival rate of Plasmodium berghei ANKA-infected C57BL/6 mice . Initial studies with the compound suggested that the mechanism of action can be attributed to the inhibition of parasitic DHS and the translation of host specific TNFα-mRNA , indicating a link between host cell proinflammatory cytokine production and the hypusine pathway.
To study the outcome after an in vivo knockdown of this enzyme and its target protein eIF-5A in the erythrocytic stages of Plasmodium in more detail , we transfected siRNA constructs targeted to both genes based on in vitro knockdown experiments into P. berghei ANKA schizonts, using standard transfection methods .
In vitro knock-down of P. falciparum DHS and eIF-5A by RNAi
Control reactions with non-transfected cells (Figure 2A, lane 1) and eIF-5A shRNA #18 cotransfected with the aquaporin-specific siRNA (Figure 2A, lane 4) did not change the silencing effect. Although eIF-5A is a highly conserved protein in eukaryotes its nucleic acid sequence is significantly divergent in comparison to its human orthologue and thus amplificates from endogenous eIF-5A are not expected. Again, we monitored the presence of GAPDH by RT-PCR in all transfections (Figure 2B) independently of the presence of the siRNA construct.
To further validate the RT-PCR experiments the limit of detection for the corresponding mRNAs i.e. eIF-5A and dhs was determined. Titrated dhs-specific mRNA resulted in a limit of detection of 20 ng while eIF-5A-specific mRNA could only be detected at a concentration of 200 ng. Optimal primer binding was determined for eIF-5A-specific primers at a cDNA concentration of 130 ng and for dhs-specific primers at a cDNA concentration of 650 ng (data not shown).
In sum, these data demonstrated that Plasmodium-specific eIF-5A and DHS sequences can in principal be silenced by RNAi.
Monitoring in vivo silencing of eIF-5A and DHS in erythrocytic stages after infection of NMRI mice with transgenic schizonts from P. berghei
With regard to the in vitro results, we investigated the silencing effect of the expressed DHS-specific and eIF-5A specific shRNAs in an in vivo rodent model of P. berghei ANKA strain . Infection of NMRI mice with P. berghei ANKA wild type strain leads to experimental cerebral malaria within 6 to 10 days p. i. although the parasitemia is only in the range of 3–5% infected erythrocytes. In case of the infectious but non lethal phenotype P. berghei strain NK56, the infected mice succumb to high parasitemia within 80 days p.i. without cerebral malaria.
Next we monitored the effect of in vivo eIF-5A silencing on the protein level. As shown in Figure 3B, eIF-5A protein was absent in NMRI infected mice with transgenic schizonts expressing the #18 eIF-5A-specific shRNA. In these experiments a polyclonal anti-eIF-5A antibody raised against the highly conserved P. vivax protein (96% identity) was used. NMRI mice infected with transgenic schizonts expressing the #176 DHS-specific shRNA construct showed that the unmodified or hypusinated eIF-5A protein was present (Figure 3B, lane 2). This result implies that the #176 DHS-specific shRNA construct exclusively affects the DHS protein. Although eIF-5A is not modified and is mostly abundant in its unhypusinated form, it is recognized by the polyclonal anti-eIF-5A antibody (Figure 3B, lane 2). The results further support the observation that the RNA encoding the eIF-5A gene is present in the erythrocytic stages after infection with schizonts expressing the DHS -shRNA #176 (Figure 3A, lane 4). The polyclonal antibody detected the eIF-5A protein with a size of 17,75 kDa in the P. berghei ANKA strain (Figure 3B, lane 3) as well as in the mock control strain (Figure 3B, lane 4), while the eIF-5A protein from P. vivax displayed the expected molecular mass of approximately 20 kDa (lanes 5 and 6).
To further support the specificity of the polyclonal anti-EIF-5A antibody, protein extracts obtained from the infected NMRI mice expressing the #18 eIF-5A-specific shRNA were spiked with purified eIF-5A protein from P. vivax (Figure 3C, lane 1). The P. vivax anti-eIF5A antibody clearly detected the EIF-5A protein in the respective extract (lane 1) while EIF-5A protein was absent in the crude extract of P. berghei ANKA strain (Figure 3C, lane 3). Moreover, the purified, recombinant eIF-5A protein was clearly recognized by the antibody (Figure 3C, lane 2). These data suggest that an in vivo knockdown of eIF-5A is possible.
Again, as already performed with eIF-5A, the specificity of the human anti-DHS antibody was confirmed. Protein extracts prepared from the infected NMRI mice harbouring the expressed sh-RNA construct #176 were supplemented with recombinant, human DHS protein (Figure 4C, lane 1). The human anti-DHS antibody clearly detected the recombinant human protein (lane 3) and the added DHS protein (lane 1). However, in the extract with the plasmodial shRNA #176 a DHS signal was absent (lane 2). These data demonstrate the validity of this antibody.
Monitoring parasitemia after infection of schizonts transfected with eIF-5A- and DHS-specific siRNA
With respect to the in vitro silencing data, P. berghei purified schizonts were transfected with either the eIF-5A shRNA construct (P #18) or the DHS shRNA (P #176) construct. In both cases, transfected cells were tracked for infection in recipient outbred NMRI mice without any selection pressure.
Studies on the effect of cytokines on iNos production due to posttranslational modification of eIF-5A
There was no difference in signal intensity between induced and uninduced cells probably due to the induction by ionomycin/PMA (phorbol 12-myristate 13-acetate), which might not be the correct inductor to stimulate cytokine cell signaling.
Colorimetric determination of nitric oxide formation as nitrate and nitrite in sera from infected mice obtained after P.berghei ANKA strain infection and after infection with schizonts harbouring the expressed plasmodial DHS shRNA #176 or plasmodial EIF-5A shRNA #18
Nitrate and nitrite [μmol/L]
Wild type and transfectants
P. berghei ANKA wild type
DHS-specific shRNA # 176
EIF-5A-specific shRNA # 18
Hitherto, the biological function of the unusual amino acid hypusine has not been studied in Plasmodium. Previous studies showed that hypusination of eIF-5A is important for cell proliferation of the parasite . Deoxyhypusine synthase (DHS), which catalyzes the first step in the hypusine pathway has been recently targeted by a small molecule inhibitor, CNI-1493, which blocked parasitic growth in vitro and in vivo. Another excellent way to study the biological function of this posttranslational modification in more detail is a genetic analysis by loss of function of the proteins involved in hypusine biosynthesis.
For the future it will be an important issue to pursue a targeted, stable gene disruption of the dhs and eIF-5Agenes in Plasmodium, since their exact function in the erythrocytic life cycle stages is still unknown. To date gene disruption by insertion strategy has been successfully shown in the rodent model of P. berghei and it is partly working in the intraerythrocytic schizogeny of P. falciparum[24, 25].
The understanding of cerebral malaria (CM) pathogenesis is still rudimentary . Our results clearly demonstrate that the hypusine pathway in Plasmodium supports at least two different hypotheses in the pathogenesis of cerebral malaria i.e. the sequestration theory and the inflammation hypothesis. One of the underlying mechanisms of cerebral malaria pathogenesis is the adherence of parasitized red blood cells to vascular endothelial cells by parasite specific proteins. Infected NMRI mice transfected with schizonts transgenic for plasmodial eIF-5A- or DHS-specific shRNA showed a 50% reduced parasitemia in comparison to the untransfected control within 2 to 9 days post infection. This may indicate the preventing of parasitic sequestration.
In a first approach to test the possibility whether a knockdown of DHS and its precursor protein eIF-5A is possible in Plasmodium, an in vitro knockdown by RNAi was performed since an unequivocal demonstration that the Plasmodium genome contains any of the conserved RNAi machinery genes or enzymes is to date missing. In the past, RNAi in circulating malaria parasites was performed showing 50% reduction at the expression level of berghepains which are homologues of cysteine proteases in Plasmodium. For the siRNA experiments, a strategy to reduce gene expression in cultured cell lines with pSilencer1.0-U6 vectors producing the respective shRNAs from the U6 promotor was selected.
The data indicate that an in vitro knockdown of eIF-5A with four different shRNAs was not completely ablating eIF-5A expression except for the shRNA # P18 in 293 T cells (Figure 2A, lane 3) which markedly reduced the eIF-5A transcript level. These four shRNA constructs of eIF-5A were targeted all over the eIF-5A sequence. The eIF-5AshRNA #18, which targets positions 163–184 in the eIF-5A nucleic acid sequence, caused a complete decrease in eIF-5A mRNA levels. These results are in agreement with the structural model of human eIF-5A1 , which consists of two domains, a basic N-terminal domain with the hypusine loop and an acidic -terminal domain connected by a hinge. Within the basic N-terminus, the hypusine modification covers amino acid positions 46–54 i. e. nucleic acid positions 138–162 which are very close to the 3’ prime end of the hypusine loop.
By contrast eIF-5A shRNA #7 targets position 115–136, which is proximal to the 5’-end of the loop, does not affect mRNA abundance. It is likely that the secondary structure of the hypusine loop at this position might block the degradation of the specific mRNA . Taken together, from four tested shRNAs, only one, the eIF-5A-specific shRNA #18 caused a considerable decrease of the eIF-5A transcript in vitro.
Two DHS-shRNAs, #43 and #176, targeting nucleotide positions from 337–358 bp and 1269–1290 bp, respectively, were employed for an in vitro knockdown of DHS from Plasmodium. Surprisingly, the DHS-shRNA construct #176 was successful to downregulate the dhs transcript significantly (Figure 1A, lane 5), although the targeted sequence did not cover the active site of the enzyme within the amino acid region between Lys287 and Glu323[28, 29].
Subsequently, monitoring of in vivo silenced P. berghei blood stage parasites transgenic for either eIF-5A-shRNA or DHS-shRNA post transfection was performed by RT-PCR. In case of the eIF-5A-shRNA containing blood stages the eIF-5A transcript was not present (Figure 3, lane 2), while in erythrocytes with the DHS-shRNA (Figure 3A, lane 2) the dhs cDNA was not abundant (Figure 4A, lane 1). However, the eIF-5A transcript was detectable, suggesting that the silencing effect is rather specific.
Moreover, these results were confirmed by Western blot analysis where the 17,75 kDa eIF-5A protein was absent in the transgenic P. berghei ANKA parasites harbouring the eIF-5A-specific siRNA. Both proteins, i.e. the P. falciparum and the P. berghei homolog share amino acid identities of 73%. In a control experiment the antibody raised against the eIF-5A protein from P. vivax crossreacted with the eIF-5A homologue from the mock strain and the P. berghei ANKA strain resulting in a protein of 17,75 kDa  (Figure 3B, lanes 3 and 4). To monitor suppressed DHS expression a polyclonal human antibody was applied which detected the P. berghei orthologue of 49 kDa (Figure 4B, lanes 3 and 4) in the mock control and the P. berghei ANKA strain. By contrast a faint band was detected in the DHS siRNA mutant suggesting that the gene may not be silenced completely.
The inflammation hypothesis in cerebral malaria implies that brain damage is a result of the inflammatory response of the human host to the parasite in the central nervous system (CNS). The production of proinflammatory cytokines like IL-1β, TNF-α, IFN-γ leads to secretion of nitric oxide which kills the parasite. It has been recently reported that hypusinated eIF-5A is required in part for the nuclear export and translation of iNos-encoding mRNAs in pancreatic, stressed ß-cells after release of proinflammatory cytokines . To test this hypothesis the host iNos2 protein levels were monitored in serum after infection with P. berghei ANKA strain and the two transfected shRNAs P #176 (DHS) and P #18 (EIF5A), since a parasitic nitric oxide synthase is absent. We could clearly demonstrate that in both mutants there is no response to cellular stress i.e. induction of inducible nitric oxide synthase (iNos2) of the human host once modification of eIF-5A is interrupted by silencing of either parasitic DHS or eIF-5A. However, nitric oxide synthase is induced 20-fold after infection with the wild type P. berghei ANKA strain in comparison to the shRNA mutants P #176 (DHS) and P #18 (EIF5A) with a 18-fold and 20-fold lowered formation of nitric oxide. These findings do not only prove a link between the hypusine pathway and iNos production but also broaden our understanding of the CM malaria pathology and implicate alternative strategies for therapy. Similar results have been obtained in DHS heterozygous knockout mice with attenuated cytokine signalling as evidenced by reduced nitric oxide synthase production .
Malaria patients often present with hypoargininemia , and metabolomic studies of Plasmodium falciparum during its 48 h intraerythrocytic life cycle reveal nearly complete depletion of L-arginine levels. Nitric oxide synthase is induced by arginine and catalyzes the reaction to nitric oxide (NO) and urea. However, in cerebral malaria there is a lack of nitric oxide due to the presence of parasite-specific arginase which leads to a depletion of arginine and subsequent downregulation of host-specific nitric oxide synthase. This may allow the parasite to evade a NO-dependent immune response in the host since NO is deleterious to parasite proliferation . During Plasmodium berghei ANKA infection in mice exogenous nitric oxide decreases brain vascular inflammation, leakage and venular resistance [17, 18] and protects against cerebral malaria.
Finally, the crystal structure of Plasmodium arginase has been resolved recently and indicates a low complexity region  which is largely disordered and its deletion does not significantly compromise enzyme activity. Moreover, disruption of P. falciparum arginase led to an apparent reduction in liver stage infection.
Although it has been previously suggested that RNAi is not functional in Plasmodium, a putative, non-canonical RNAi pathway might exist in malaria parasites. In vivo knockdown of eIF-5A and DHS by expression of shRNAs after infection in a rodent model decreased parasitemia intermittently in the development of cerebral malaria. The data are similar to the related but non-lethal phenotype P. berghei ANKA NK 65. These results might be of further interest to study the function of hypusine modification with respect to malaria infection and therapy.
Materials and methods
All animal experiments were performed under FELASA category B and GV-SOLAS standards. Animal experiments were approved by German authorities (Regierungspräsidium Karlsruhe, Germany).
siRNAs (small interfering RNAs) for targeting DHS and eIF-5A
The following double stranded siRNAs were used and synthesized by Ambion, Karlsruhe, Germany: RNAi for DHS and EIF5A knockdowns, siRNA duplexes were used which were obtained by annealing the RNA oligonucleotides synthesized by Ambion, Karlsruhe, Germany. The oligonucleotides (3000 mM for dhs, 1500 mM for eIF-5A) were phosphorylated in a reaction volume of 20 μl with 3 Units polynucleotide kinase (10 U/μl) (Roche Diagnostics, Penzberg, Gemany) at 37°C for 45 min. The reaction was stopped on ice for 1 min. An annealing reaction was performed at 95°C with subsequent cooling of the reaction to room temperature overnight.
After annealing the siRNA duplexes were cloned into pSilencer 1.0-U6 vector before transfection into 293T cells or schizonts.
For the DHS knockdown #43, RNA oligonucleotides 5’- UGUUAGUGAAGAUCUUAAUtt-3’ and 5’-AUUAAGAUCUUCACUAACAtt-3’ were applied targeting the nucleotide positions 337–358 in the plasmodial dhs cDNA. For the DHS knockdown #176, RNA oligonucleotides 5’- UGAGGAAUGGUGCUGAUUUtt-3’ and 5’-AAAUCAGCACCAUUCCUCAtt-3’ were applied which targeted nucleotide positions 1269–1290 in the dhs cDNA.
For the eIF-5A knockdowns 4 different siRNA duplexes were generated. For the EIF-5A knockdown #5, RNA oligonucleotides 5’- ACGGCCACGUGAUGCUAAAtt-3’ and 5’- UUUAGCAUCACGUGGCCGUtt-3’ were applied targeting nucleotide positions 81–102 in the P. vivax eIF-5A cDNA. For the EIF-5A knockdown #6, RNA oligonucleotides 5’- AGGAGCAUCCUUGCAAAGUtt-3’ and 5’- ACUUUGCAAGGAUGCUCCUtt-3’ were applied which targeted nucleotide positions 99–120; for EIF-5A knockdown #7, RNA oligonucleotides 5’-AGUGGUAGAUUACUCCACGtt-3’ and 5’- CGUGGAGUAAUCUACCACUtt-3’ were used for targeting nucleotide positions 115–136. For eIF-5A knockdown #18, RNA oligonucleotides 5’- CUGAGUUGCAGCUGAUUGAtt-3’ and 3’- UCAAUCAGCUGCAACUCAGtt-5’ were applied which targeted the eIF-5A gene at nucleotide positions 163–184.
Construction of pSilencer1.0-U6 vector with double stranded siRNA of DHS and eIF-5A
20 μg of (Ambion/Invitrogen, Karlsruhe, Germany) was double digested with EcoRI/ ApaI (20 U) in a reaction volume of 20 μl and dephosphorylated with calf intestine alkaline phosphatase (CIP) (MBI Fermentas, St. Leon Rot, Germany) (1 U/μl) for 1 hour at 37°C. The double digested vector was gel-purified according to the Mini Elute Gel Extraction Kit protocol from Qiagen, (Hilden,Germany). Ligation of the annealed oligos was performed with the ligation kit from Roche Diagnostics, (Penzberg, Germany). Positive constructs were analysed after double digestion with ApaI and HindIII.
Cloning the full length dhs cDNA and eIF-5A cDNA into eukaryotic pcDNA3 vector
Amplification of the dhs gene was performed from the recombinant pet- Blue1 plasmid (Novagen, Darmstadt,Germany) from Plasmodium falciparum with primers containing recognition sites for EcoRI (restriction site is underlined) dhs forward 5’-TTT GAATTCATGGTGGATCACGTTTC-’3’ and NotI dhs reverse 5’- TTT GCGGCCGCTCACATATCTTTTTTCCTC- 3’. The resulting fragment of 1491 bp was digested with EcoRI and NotI and ligated into EcoRI/ NotI treated pc DNA3 vector (Invitrogen, Darmstadt, Germany) and re-sequenced. For construction of an eIF-5A cDNA containing pcDNA3 vector, the eIF-5A nucleic acid sequence was amplified from a recombinant plasmid pSTBlue-1 Acceptor™ vector (Novagen, Darmstadt, Germany) with primers containing EcoRI eIF-5Aforward 5’ -AAA GAA TTC ATG TCA GAC CAC GAA AC-3’ and NotI eIF-5Areverse 5’-TTT GCG GCC GCC TAG GAG GAC AAC TCC-3’ restriction sites.
Cotransfection of pSilencer1.0-U6 vectors into 293 T cells
In a 6 well microtiter plate 7x105 293T cells were seeded in all 6 wells. Four different sets of cotransfections were performed: DHS; i) P. falciparum dhs cDNA in pcDNA3 (0.3 μg), ii) P. falciparum dhs cDNA in pcDNA3 and premade scramble II duplex negative control siRNA (1.0 μg), iii) P. falciparum dhs cDNA in pc DNA3 and DHS- specific shRNA construct #43 (1.0 μg), iv) P. falciparum dhs cDNA in pcDNA3 and DHS-specific shRNA construct #176 (1.0 μg). The various transfections were mixed with transfection mix (total vol. 400 μl), which contained Opti-MEM® (Invitrogen, Karlsruhe, Germany) and polyethylenimine (PEI) (4 μl/μg), and were added to the cultures. After 10 min of incubation at room temperature, the culture supernatants were substituted by 2 ml of DMEM (Dulbecco's Modified Eagle's Medium) (Invitrogen, Karlsruhe, Germany) and the cell cultures were incubated overnight at 37°C. The next day, medium was changed and supplemented with streptomycin (60 μg/ml). Prior to transfection, the cells were washed with PBS-buffer (phosphate buffer saline).
Cotransfection of P. falciparum eIF-5A pcDNA3-based expression vector in combination with 4 different sets of siRNA vectors was performed according to a protocol from Invitrogen (Karlsruhe, Germany): i) P. falciparum eIF-5A expression vector (0.3 μg) and aquaporin-5 specific-siRNA (2.7 μg) ii) P. falciparum eIF-5A expression vector (0.3 μg) and eIF-5A-specific shRNA construct #18 (2.7 μg), iii) P. falciparum eIF5A expression vector (0.3 μg) and eIF-5A-specific shRNA #6 (2.7 μg), iv) P. falciparum eIF-5A expression vector (0.3 μg) and eIF-5A shRNA construct #7 (2.7 μg), v) P. falciparum eIF-5A expression vector (0.3 μg) and eIF-5A shRNA #5 (2.7 μg).
Isolation of cellular RNA
Isolation of total cellular RNA was performed according to the RNeasy Plant Mini Kit (Qiagen, Hilden, Germany). The quality of the isolated RNA was verfied by agarose gel electrophoresis and the quantity and purity was determined by UV spectrometry.
RT-PCR analysis of eIF-5A and DHS silencing in vitro and in vivo
To monitor the silencing of eIF-5A and DHS, RT-PCR was performed according to a protocol from the AccessQuick™ RT-PCR System (Promega, Mannheim, Germany). For the RT-PCR reaction gene specific primers for eIF-5Aforward 5’-ATGTCAGACCACGAAACGT-3’/eIF-5A reverse 5’-CTAGGAGGACAACTCCTTCACCGC- 3’ and dhs forward 5’-ATAGTGCCTAATGATAATTA -3’/dhs reverse 5’-AACCTCCTCCGAGAATAATAATACCAG -3’ were used. For control, human GAPDH-specific sequences were amplified using the following primers: GAPDH forward 5’-ATGGGGAAGGTGAAGGTCGG-3’ and GAPDH reverse 5’-TTACTCCTTGGAGGCCATGTGG-3’. For RT-PCR reactions monitoring cDNA formation in in vivo experiments after P.berghei infection the following P. berghei-specific PCR primers were used: eIF-5A forward 5’-ATGTCAGACCACGAAACGT-3’/ eIF5A reverse 5’- TATGATGACATTTCTTTAAGC-3’ and dhs forward 5’-ATGGATGGGGTATTCAAAGA-3’/ dhs reverse 5’-CTAATCACTTTTTTCTCCTTTT-3’. To analyze the quality of the cellular total RNA i α-tubulin forward 5’-ATGAGAGAAGTAATAAGTAT-3’ and α-tubulin reverse 5’-TGTTGATAAAACTGAATTAT-3’ primers were applied, resulting in a specific α-tubulin fragment of 548 bp.
Plasmodium transfection using shRNA expressing vectors
Parasite transfection using sh expression vectors without Pyrimethamine selection was performed as described in .
Preparation of protein extracts from transfected P. berghei parasites
To detect eIF-5A and DHS expression in transfected and wildtype P. berghei parasites, intraerythrocytic stages were purified by CF11 Cellulose (Whatman) (Millipore, Schwalbach, Germany) to remove platelets and leukocytes. Parasites were lysed in 0.2% saponin and resuspended in PBS (LifeTechnologies/Invitrogen, Karlsruhe, (Germany). After determination of the protein concentration by Bradford assay , extracts were adjusted to the same protein concentration (20 μg) with PBS. Alternatively, for the detection of iNos protein, serum was applied from whole blood without anticoagulant according to a protocol from Proimmune .
Western blot analysis
Western blots were performed using the i-Blot dry blotting device system from Invitrogen (Karlsruhe, Germany) for 5 min at 5.5 amp and 25 V. Protein extracts from blood stages of transfected parasites were resuspended in 1-fold Nupage buffer (Invitrogen, Karlsruhe, Germany) boiled and loaded onto a 12% SDS-polyacrylamide gel. Immunodetection was performed according to the protocol from the immunodetection kit from Amersham (Munich, Germany). Polyclonal anti-eIF5A antibodies (Eurogentec, Cologne, Germany) raised against the eIF-5A from P. vivax and anti-DHS antibodies against P. falciparum DHS were applied in dilutions of 1:1000 and 1:5000, respectively. Previous results had shown that the human DHS protein cross-reacts with the P. berghei DHS protein due to highly conserved regions and an overall amino acid identity of 56% (see within the results section) . Dilutions of 1:1000 and 1:5000 of the antibody raised against the eIF-5A from P. vivax were used, since both proteins i.e. eIF-5A from P. vivax and P. berghei, share 97% amino acid identity .
Induction of HeLa, jurkat and monomac cells and preparation of protein extracts
HeLa, Jurkat and Monomac were maintained in Dulbecco’s modified Eagle medium (DMEM) (Sigma Aldrich, Munich, Germany), supplemented with 10% (v/v) fetal bovine serum (FBS), L-glutamine (2 mM), sodium pyruvate (1 mM) penicillin (50000 U/ml) and streptomycin (5 mg/ml)).
For stress induction HeLa, Jurkat or Monomac cells were grown in overnight cultures under starving conditions (i.e. 1% FCS-containing medium). Thereafter, culture supernatants were substituted by DMEM containing 10% FCS and cells were further incubated for 3 hours. Finally, cell cultures were exposed for 4 hours to 50 ng/mL phorbol 12-myristate 13-acetate (PMA) and 1 μM of the calcium ionophore ionomycin. Subsequently, the respective cell cultures were washed several times with PBS.
In total 106-107 cells were lysed with CelLytic M solution (Sigma Aldrich, Munich, Germany) for 15 minutes on a rocker platform. The lysed cells were centrifuged at 12,000-20,000 x g to pellet the cellular debris. The supernatant, containing the cell lysate, were used for further analysis.
Determination of total nitric oxide
Concentrations of nitric oxide were determined by colorimetric detection according to the kit protocol from Enzo Life Sciences. Nitric oxide is converted to nitrate which is reduced to nitrite by the enzyme nitrate reductase followed by the colorimetric detection of nitrite as a coloured azo dye product which absorbs visible light at 560 nm. The determination allows the determination of both nitric oxide products nitrate and nitrite.
The work was supported in main parts by a grant from the German Academic Exchange Service (DAAD) to AK (432/lz (2006).
- Hammond SM: Dicing and Splicing. The core machinery of the RNA interference pathway. FEBS Lett. 2005, 579: 5822-5829. 10.1016/j.febslet.2005.08.079.PubMedView ArticleGoogle Scholar
- Bernstein E, Caudy AA, Hammond SM, Hannon GJ: Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature. 2001, 409: 363-366. 10.1038/35053110.PubMedView ArticleGoogle Scholar
- Nykanem A, Haley B, Zamore PD: ATP requirements and small interfering RNA structure in the RNA interference pathway. Cell. 2001, 107: 309-321. 10.1016/S0092-8674(01)00547-5.View ArticleGoogle Scholar
- Baum J, Papenfuss AT, Mair GR, Janse CJ, Vlachou D, Waters AP, Cowman AF, Crabb CJ, Koning-Ward TF: Molecular genetics and comparative genomics reveal RNAi is not functional in malaria parasites. Nucl. Acid Res. 2010, 37 (11): 3788-3798.View ArticleGoogle Scholar
- Gissot M, Brique S, Refour P, Boschet C, Vaquero C: PfMyb1, a Plasmodium falciparum transcription factor, is required for intra-erythrocytic growth and controls key genes for cell cycle regulation. J Mol Biol. 2005, 34: 29-42.View ArticleGoogle Scholar
- Kumar R, Adams B, Oldenburg A, Musiyenko A, Barik S: Characterisation and expression of a PP1 serine/threonine protein phosphatase (PfPP1) from the malaria parasite, Plasmodium falciparum: demonstration of its essential role using RNA interference. Malar J. 2002, 145: 1245-1254.Google Scholar
- Tuteja R, Pradhan A, Sharma S: Plasmodium falciparum signal peptidase is regulated by phosphorylation and required for intra-erythrocytic growth. Mol Biochem Parasitol. 2008, 157: 137-147. 10.1016/j.molbiopara.2007.10.007.PubMedView ArticleGoogle Scholar
- McRobert L, McConkey GA: RNA interference (RNAi) inhibits growth of P. falciparum. Mol. Chem. Parasitol. 2002, 119: 273-278. 10.1016/S0166-6851(01)00429-7.View ArticleGoogle Scholar
- Dasaradhi PV, Mohammed A, Kumar A, Hossain MJ, Bhatnagar RK, Chauhan VS, Malhotra P: A role of falcipain-2, principle cysteine proteases of Plasmodium falciparum in merozoite egression. Biochem Biophys Res Commun. 2005, 336: 1062-1068. 10.1016/j.bbrc.2005.08.213.PubMedView ArticleGoogle Scholar
- Sijwali PS, Rosenthal PJ: Gene disruption confirms a critical role for the cysteine protease falcipain-2 in haemoglobin hydrolysis by Plasmodium falciparum. Proc. Natl. Acad. Sci. USA. 2004, 101: 4384-4389. 10.1073/pnas.0307720101.PubMedPubMed CentralView ArticleGoogle Scholar
- Kaiser A, Gottwald A, Maier W, Seitz HM: Targeting enzymes involved in spermidine metabolism of parasitic protozoa-a possible new strategy for anti-parasitic treatment. Parasitol Res. 2003, 91 (6): 508-516. 10.1007/s00436-003-0970-y.PubMedView ArticleGoogle Scholar
- Njuguna JT, Nassar M, Hoerauf A, Kaiser AE: Cloning, expression and functional activity of deoxyhypusine synthase from Plasmodium vivax. BMC Microbiol. 2006, 6: 91-96. 10.1186/1471-2180-6-91. 16PubMedPubMed CentralView ArticleGoogle Scholar
- Maier B, Ogihara T, Trace AP, Tersey SA, Robbins RD, Chakrabarti SK, Nunemaker CS, Stull ND, Taylor CA, Thompson JE, Dondero RS, Lewis EC, Dinarello CA, Nadler JL, Mirmira RG: The unique hypusine modification of eIF5A promotes islet beta cell inflammation and dysfunction in mice. J Clin Invest. 2011, 20 (6): 2156-2170.Google Scholar
- Hauber I, Bevec D, Heukeshoven J, Krätzer F, Horn F, Choidas A, Harrer T, Hauber J: Identification of cellular deoxyhypusine synthase as a novel target for antiretroviral therapy. J Clin Invest. 2005, 115 (1): 76-85.PubMedPubMed CentralView ArticleGoogle Scholar
- Bevec D, Kappel B, Jaksche H, Csonga R, Hauber J, Klier H, Steinkasserer A: Molecular characterization of a cDNA encoding functional human deoxyhypusine synthase and chromosomal mapping of the corresponding gene locus. FEBS Lett. 1996, 378 (2): 195-198. 10.1016/0014-5793(95)01456-X.PubMedView ArticleGoogle Scholar
- Hofmann W, Reichart B, Ewald A, Müller E, Schmitt I, Stauber RH, Lottspeich F, Jockusch BM, Scheer U, Hauber J, Dabauvalle MC: Cofactor requirements for nuclear export of Rev response element (RRE)- and constitutive transport element (CTE)-containing retroviral RNAs. An unexpected role for actin. J Cell Biol. 2001, 152 (5): 895-910. 10.1083/jcb.152.5.895.PubMedPubMed CentralView ArticleGoogle Scholar
- Maier B, Tersey SA, Mirmira RG: Hypusine: a new target for therapeutic intervention in diabetic inflammation. Discov. Med. 2010, 10 (50): 18-23.PubMedGoogle Scholar
- Zanni GM, Cabrales P, Barkho W, Frangos J, Carvalho L: Exogenous nitric oxide decreases brain vascular inflammation, leakage and venular resistance during Plasmodium berghei ANKA infection in mice. J Neuroinflamm. 2011, 66 (Zanni GM, Cabrales P, Barkho W, Frangos J, Carvalho L): 1-9. 8Google Scholar
- Hawkes M, Opoka R, Namasopo S, Miller C, Thorpe KE, Lavery JV, Conroy AL, Liles WC, John CC, Kain KC: Inhaled nitric oxide for the adjunctive therapy of severe malaria. Trials. 2011, 12: 176-10.1186/1745-6215-12-176.PubMedPubMed CentralView ArticleGoogle Scholar
- de SA Miranda, Brant F, Machado FS, Rachid MA, Teixera AL: Improving cognitive outcome in cerebral malaria: Insights from Clinical and Experimental Research. Cent Nerv Syst Agents Med Chem. 2011, 11 (4): 285-295. 11View ArticleGoogle Scholar
- Schofield L, Grau GE: Immunological processes in malaria pathogenesis. Nat Rev Immunol. 2005, 5 (9): 722-735. 10.1038/nri1686.PubMedView ArticleGoogle Scholar
- Specht S, Sarite SR, Hauber I, Hauber J, Görbig UF, Meier C, Bevec D, Hoerauf A, Kaiser A: The guanylhydrazone CNI-1493: an inhibitor with dual activity against malaria-inhibition of host cell pro-inflammatory cytokine release and parasitic deoxyhypusine synthase. Parasitol Res. 2008, 102 (6): 1177-1184. 10.1007/s00436-008-0891-x.PubMedView ArticleGoogle Scholar
- Cohen PS, Nakshatri H, Dennis J, Caragine T, Bianchi M, Cerami A, Tracey KJ: CNI-1493 inhibits monocyte/macrophage tumor necrosis factor by suppression of translation efficiency. Proc Natl Acad Sci U S A. 1996, 93 (9): 3967-3971. 10.1073/pnas.93.9.3967.PubMedPubMed CentralView ArticleGoogle Scholar
- Janse CJ, Ramesar J, Waters AP: High-efficiency transfection and drug selection of genetically transformed blood stages of the rodent parasite Plasmodium berghei. Nat Protoc. 2006, 1: 346-356. 10.1038/nprot.2006.53.PubMedView ArticleGoogle Scholar
- Mueller AK, Camargo N, Kaiser K, Andorfer C, Frevert U, Matuschewski K, Kappe SH: Plasmodium liver stage developmental arrest by depletion of a protein at the parasite - host interface. Proc Natl Acad Sci U S A. 2005, 102 (8): 3022-3027. 10.1073/pnas.0408442102.PubMedPubMed CentralView ArticleGoogle Scholar
- De Miranda AS, Brant F, Machado FS, Rachid MA, Teixeira AL: Improving cognitive outcome in cerebral malaria: insights from clinical and experimental research. Cent Nerv Syst Agents Med Chem. 2011, 1 (4): 285-295.View ArticleGoogle Scholar
- Mohmmed A, Dasaradhi PV, Bhatnagar RK, Chauhan VS, Malhotra P: In vivo gene silencing in Plasmodium berghei--a mouse malaria model. Biochem Biophys Res Commun. 2003, 309 (3): 506-511. 10.1016/j.bbrc.2003.08.027. 26PubMedView ArticleGoogle Scholar
- Tong Y, Park I, Hong BS, Nedyalkova L, Tempel W, Park HW: Crystal structure of human eIF5A1: insight into functional similarity of human eIF5A1 and eIF5A2. Proteins. 2009, 75 (4): 1040-1050. 10.1002/prot.22378.PubMedView ArticleGoogle Scholar
- Kaiser AE, Gottwald AM, Wiersch CS, Maier WA, Seitz HM: Spermidine metabolism in parasitic protozoa- a comparison to the situation in prokaryotes, plants and fungi. Folia Parasitol. (Praha). 2003, 50 (1): 3-18.View ArticleGoogle Scholar
- Hall N, Karras M, Raine JD, Carlton JM, Kooij TW, Berriman M, Florens L, Janssen CS, Christophides GK, James K, Rutherford K, Harris B, Harris D, Churcher C, Pain A, Quail MA, Ormond D, Doggett J, Trueman HE, Mendoza J, Bidwell S, Rajandream MA, Carucci DJ, Yates JR, Kafatos FC, Janse CJ, Barrel B, Turner CM, Waters AP, Sinden RE: A comprehensive survey of the Plasmodium life cycle by genomic, transcriptomic, and proteomic analyses. Science. 2005, 30 (5706): 82-86.View ArticleGoogle Scholar
- Templin AT, Maier B, Nishiki Y, Tersey SA, Mirmira RG: Deoxyhypusine synthase haploinsufficiency attenuates acute cytokine signaling. Cell Cycle. 2011, 10 (7): 1043-1049. 10.4161/cc.10.7.15206.PubMedPubMed CentralView ArticleGoogle Scholar
- Yeo TW, Lampah DA, Gitawati R, Tjitra E, Kenangalem E, McNeil YR, Darcy CJ, Granger DL, Weinberg JB, Lopansri BK, Price RN, Duffull SB, Celermajer DS, Anstey NM: Impaired nitric oxide bioavailability and L-arginine-reversible endothelial dysfunction in adults with falciparum malaria. J. Exp. Med. 2007, 204: 2693-2704. 10.1084/jem.20070819.PubMedPubMed CentralView ArticleGoogle Scholar
- Dowling DP, Ilies M, Olszewski KL, Portugal S, Mota MM, Llinás M, Christianson DW: Crystal structure of arginase from and implications for L-arginine depletion in malarial infection. Biochemistry. 2010, 49 ((26): 5600-5608. 6PubMedPubMed CentralView ArticleGoogle Scholar
- Bradford MM: A rapid and sensitive for the quantitation of microgram quantitites of protein utilizing the principle of protein-dye binding. Analytical Biochem. 1976, 72: 248-254. 10.1016/0003-2697(76)90527-3.View ArticleGoogle Scholar
- ,: Protocols for the preparation of blood plasma and serum. www.proimmune.com
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.