Chikungunya virus (CHIKV) is a re-emerging arthropod-borne (arbo)virus that causes chikungunya fever in humans and is predominantly transmitted by Aedes aegypti mosquitoes. The CHIKV replication machinery consists of four non-structural proteins (nsP1-4) that additionally require the presence of a number of host proteins for replication of the viral RNA. NsP3 is essential for CHIKV replication and has a conserved macro, central and C-terminal hypervariable domain (HVD). The HVD is intrinsically disordered and interacts with various host proteins via conserved short peptide motifs: A proline-rich (P-rich) motif that has affinity for SH3-domain containing proteins and duplicate FGDF motifs with affinity for G3BP and its mosquito homologue Rasputin. The importance of these motifs for infection of mammalian cells has previously been implicated. However, their role during CHIKV infection of mosquito cells and transmission by mosquitoes remains unclear.
Methodology / Principal findings
Here, we show that in-frame deletion of the P-rich motif is lethal for CHIKV replication in both mosquito and mammalian cells. However, while mutagenesis of the P-rich motif negatively affects replication both in mammalian and mosquito cells, it did not compromise the infection and transmission of CHIKV by Ae. aegypti mosquitoes. Mutagenesis of both FGDF motifs together completely inactivated CHIKV replication in both mammalian and mosquito cells. Importantly, mutation of a single FGDF motif attenuated CHIKV replication in mammalian cells, while replication in mosquito cells was similar to wild type. Surprisingly, CHIKV mutants containing only a single FGDF motif were efficiently transmitted by Ae. aegypti.
Conclusions / Significance
The P-rich motif in CHIKV nsP3 is dispensable for transmission by mosquitoes. A single FGDF motif is sufficient for infection and dissemination in mosquitoes, but duplicate FGDF motifs are required for the efficient infection from the mosquito saliva to a vertebrate host. These results contribute to understanding the dynamics of the alphavirus transmission cycle and may help the development of arboviral intervention strategies.
Chikungunya virus (CHIKV) is a re-emerging arthropod-borne virus that is transmitted predominantly by Aedes aegypti mosquitoes. In 2016 alone CHIKV caused over 100.000 infections in South-America, exemplifying the impact of CHIKV disease. Previous research has suggested that the CHIKV non-structural protein 3 (nsP3) may determine the infection of mosquitoes. NsP3 is known to interact with several host proteins through a conserved proline (P)-rich and duplicate FGDF motifs that are present in its C-terminal domain. Here we investigated the importance of these conserved motifs for the infection and replication of CHIKV in both Aedes mosquito cells and mammalian cells. Furthermore, we assessed the role of these motifs for the transmission by Ae. aegypti mosquitoes via infectious bloodmeal experiments. We show that mutation of the P-rich motif negatively affects the replication of CHIKV in both mammalian and mosquito cells. In contrast, mutating the P-rich motif did not affect the transmission by Ae. aegypti. Mutation of both FGDF motifs together completely inactivated CHIKV in mammalian and mosquito cells, while mutation of a single FGDF motif negatively affected replication only in mammalian cells. Importantly, CHIKV containing only a single FGDF motif was still efficiently transmitted by Ae. aegypti mosquitoes. These results contribute to understanding the key interactions between alphaviruses and their mosquito vector.
Citation: Göertz GP, Lingemann M, Geertsema C, Abma-Henkens MHC, Vogels CBF, Koenraadt CJM, et al. (2018) Conserved motifs in the hypervariable domain of chikungunya virus nsP3 required for transmission by Aedes aegypti mosquitoes. PLoS Negl Trop Dis 12(11): e0006958. https://doi.org/10.1371/journal.pntd.0006958
Editor: Lyric C. Bartholomay, University of Wisconsin Madison, UNITED STATES
Received: August 3, 2018; Accepted: October 29, 2018; Published: November 9, 2018
Copyright: © 2018 Göertz et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Alphaviruses (family Togaviridae), such as chikungunya virus (CHIKV) and Mayaro virus, are (re-)emerging arthropod-borne (arbo)viruses that impose a global threat on human health . Mayaro virus recently emerged in South America, where a large outbreak was reported in Brazil [1,2]. CHIKV is responsible for several large outbreaks in the Americas  and over 150.000 cases of infection were reported in the Americas in 2016 alone . CHIKV disease is characterized by acute fever combined with severe arthralgia, myalgia or rash, and symptoms can last from weeks to several months . Transmission of CHIKV occurs predominantly by Aedes aegypti mosquitoes, although some CHIKV strains have incorporated an amino acid substitution in the envelope protein (A226V) that allows transmission by Ae. albopictus .
Alphaviruses have a single-stranded positive-sense RNA genome that contains two open reading frames, which encode the non-structural proteins (nsP)1-4 and the structural proteins, respectively. NsP4 is the viral RNA-dependent RNA polymerase that together with nsP1-3 forms the viral replication complex. While the roles of nsP1 and nsP2 in viral replication have been extensively documented and reviewed [6–8], the exact functions of nsP3 are less clear [9,10]. During infection, nsP3 localizes partially to viral replication complexes [11,12], in accordance with the necessity of nsP3 for virus replication, as well as cytoplasmic foci [13–16]. Additionally, nsP3 interacts with several host-proteins in mammalian and mosquito cells [14,17]. Unravelling the significance and mechanisms of the interactions between nsP3 and these host-proteins in mammalian cells has been the focus of several recent studies [17–23], while the role of these interactions during infection of mosquitoes remains to be assessed.
NsP3 consists of three domains: an N-terminal, conserved macro domain, which possesses phosphatase and RNA-binding activity , a conserved zinc-binding central domain , and a highly phosphorylated [15,26,27], intrinsically disordered , hypervariable domain (HVD) at the C-terminus . Despite the lack of conservation in the HVD between the nsP3 of alphaviruses , it contains several conserved motifs, of which the Proline-rich (P-rich) PxxPPR or PxPxPR, and the duplicate FGDF motifs have been studied most extensively (reviewed in [9,10]). In mammalian cells, the P-rich motifs of Sindbis virus (SINV), Semliki Forest virus (SFV) and CHIKV nsP3 interact with the SH3 domain of the membrane modulating proteins amphiphysin-1/2, and this interaction has been shown to be important for efficient virus replication [18,19]. CHIKV nsP3 has two FGDF motifs that can bind to the NTF2-like domain of the stress granule components G3BP1 and G3BP2 in mammalian cells [17,20,29]. This interaction inhibits the formation of cellular stress granules that would otherwise stall host and viral translation, and as a consequence may facilitate virus replication [13,21,30]. In mammalian cells, mutations in the alphavirus nsP3 HVD that disrupt both of the FGDF motifs result in complete inactivation of CHIKV and also attenuates SFV and SINV [17,20,21,31]. Furthermore, deletion of a single FGDF motif in CHIKV or SFV nsP3 decreases the affinity for G3BP and attenuates the virus, suggesting that alphaviruses require duplicate FGDF motifs for their successful replication in mammalian cells [17,20].
While the importance of the conserved motifs in the nsP3 HVD for alphavirus replication in mammalian cells has been well-established, little is known about their role during alphavirus transmission by the mosquito vector . Recently, nsP3 and its mosquito interaction partner Rasputin (Rin), the mosquito homologue of G3BP, have been identified as important determinants for alphavirus transmission [33,34]. Chimeric CHIKV equipped with the nsP3 from the Anopheles-transmitted alphavirus ONNV showed an increase in infection rate in the CHIKV-refractory vector An. gambiae from 0 to 64% . Interestingly, CHIKV chimeras that contained just the C-terminal region of ONNV nsP3, including the HVD, already reached an infection rate of 9–18% , suggesting that the nsP3 HVD is an important determinant of mosquito vector specificity. Furthermore, CHIKV nsP3 was shown to co-localize with Rin , and Rin co-precipitated with SINV nsP3 , indicative of a direct interaction between Rin and nsP3. Interestingly, mutating both FGDF motifs in CHIKV nsP3 together results in complete loss of co-localization of transiently expressed nsP3 and Rin , similar to the interaction with G3BP in mammalian cells. However, co-localisation was maintained when only one of the FDGF motifs was mutated . Importantly, knock-down of Rin severely decreased the infection and transmission rates as well as the viral titers of CHIKV in the heads of Ae. albopictus after an infectious bloodmeal . Thus, the conserved motifs in the nsP3 HVD may play a crucial role in infection of the mosquito vector, potentially through their interaction with mosquito host proteins, and ultimately enable the virus to establish a disseminated infection.
Here, we investigated the role of the P-rich and FGDF motifs in the HVD of CHIKV nsP3 during virus replication in mosquito cells and infection of and transmission by in the natural CHIKV vector Ae. aegypti. Infectious cDNA clones were used to generate CHIKV variants with mutations in either the P-rich or FGDF motif(s). The mutant viruses were assessed for replication kinetics in mammalian (Vero) and Ae. aegypti (Aag2) cells. We investigated the infection and transmission of the CHIKV mutants in Ae. aegypti mosquitoes through infectious bloodmeal experiments. These experiments elucidate whether the evolutionary basis for conservation of the P-rich and duplicate FGDF motifs in alphavirus nsP3 lies solely in infection of the mammalian host, or whether these motifs are also required for alphavirus transmission by the mosquito vector.
Materials and methods
African green monkey kidney Vero E6 cells (ATCC CRl-1586) were cultured at 37°C with 5% CO2 in Dulbecco’s Modified Eagle medium (DMEM; Gibco) supplemented with 10% fetal bovine serum (FBS; Gibco), penicillin (100 U/ml; Sigma-Aldrich) and streptomycin (100 μg/ml; Sigma-Aldrich). Ae. albopictus C6/36 (ATCC CRL-1660) cells were cultured at 28°C in Leibovitz L-15 medium (Gibco) supplemented with 10% FBS, 2% tryptose phosphate broth (Gibco) and 1% nonessential amino acids (Gibco). Ae. aegypti Aag2 cells were cultured at 28°C in Schneider’s Drosophila medium (Lonza) supplemented with 10% FBS. During experiments gentamicin (50 μg/ml; Life technologies) was added to the culture medium of C6/36 and Aag2 cells.
Previously reported infectious clone derived chikungunya virus 37997 strain (CHIKV37997)  was used in all experiments. Gateway-compatible pIB vectors with CHIKV nsP3 sequences containing the mutations P398A, PPR401AAA, FG479AA, FG497AA and FG479AA/FG497AA were described previously . To insert an internal fluorescent reporter gene into nsP3, mCherry was PCR amplified from CHIKrep-nsP3mC  with primers 1,2 (Primer sequences are listed in Table 1) containing BspEI overhangs and cloned as BspEI fragment into the pIB-nsP3 vectors. This introduces the mCherry sequence between amino acids 367–368 of the CHIKV nsP3 gene. The Firefly luciferase gene was amplified from the previously described pCHIKrep-FlucEGFP  with primers 7,8 and used to replace the FlucEGFP sequence in the same pCHIKrep-FlucEGFP to generate pCHIKrep. Mutant nsP3 containing mutations P398A and PPR401AAA in the P-rich motif were cloned from the corresponding pIB vectors as AgeI/NheI fragment into pCHIKrep-Fluc to create pCHIKrep-nsP3mCP398A and pCHIKrep-nsP3mCPPR401AAA. NsP3 containing mutations in the FGDF motifs were PCR amplified using primers 3,4, nsP4 was PCR amplified using primers 5,6 and the two PCR products were fused by overlapping-PCR using primers 3,6. Subsequently, the nsP3-nsP4 fusion PCR products were cloned as AgeI/AscI fragment into pCHIKrep-Fluc to create pCHIKrep-nsP3mC-FGN (FG479AA), pCHIKrep-nsP3mC-FGC (FG497AA) and pCHIKrep-nsP3mC-FGNC (FG479AA & FG497AA). The Fluc sequence was replaced with the CHIKV37997 structural cassette from pCHIKIC through AscI/EcoRI cloning to generate pCHIKIC-nsP3mC infectious clones of all mutants. The internal mCherry was removed by BspEI digestion and vector self-ligation. An overview of the recombinant CHIKV encoding plasmids used in this study is shown in Fig 1A. Recombinant viruses were generated from the pCHIKIC infectious clones as described previously . Briefly, pCHIKIC plasmids were linearized by PacI digestion to serve as template for an SP6 RNA polymerase (NEB) transcription reaction and the resulting in vitro transcribed RNA was used to transfect pre-seeded Vero cell monolayers with Lipofectamine 2000 (Invitrogen) to generate the P0 stock. Subsequent passages were performed on C6/36 cells.
(A) Schematic overview of the viruses used in these experiments. Shown are DNA plasmids used as template for the in vitro transcription of chikungunya virus infectious clone (IC) or replicon (rep) RNA. Additionally, the location of deletions and amino acid substitutions used in mutant IC and rep constructs is displayed. (B) Alignment of alphavirus nsP3 amino acid sequences indicates conserved proline rich and FGDF motifs in the HVD. Top: zoom-in on the proline rich region of the nsP3 HVD. Red boxes indicate the PxxPPR motif, while blue boxes indicate the PxPxPR motif. Bottom: Zoom-in on the FGDF motif-containing region of the nsP3 HVD. CHIKV chikungunya virus; BFV Barmah forest virus; SFV Semliki Forest virus; WHAV Whataroa virus; EILV Eilat virus; RRV Ross River virus; MAYV Mayaro virus; BeBV Bebaru virus; TALV Taï Forest alphavirus; EEEV Eastern equine encephalitis virus; VEEV Venezuelan equine encephalitis virus; WEEV Western equine encephalitis virus.
Gateway-compatible and OpIE-2 promoter driven pIB insect-cell expression plasmids expressing EGFP, nsP3EGFP, nsP3EGFP-FGN, nsP3EGFP-FGC and nsP3EGFP-FGNC were reported previously . The Ae. aegypti poly-ubiquitin (PUB) promoter was amplified from pPUB-Fluc  using primers 9,10 (Table 1) containing BspHI and SacI restriction sites and cloned as BspHI/SacI fragment into pIB to generate the Gateway-compatible pPUB vector. Gateway-cloning (Invitrogen) was used to generate pPUB-EGFP, pPUB-nsP3EGFP, pPUB-nsP3EGFP-FGN, pPUB-nsP3EGFP-FGC and pPUB-nsP3EGFP-FGNC. Plasmid pIB-Rin-mC, expressing the mosquito Rin fused C-terminally to an mCherry red fluorescent reporter gene, was reported previously . EGFP was PCR amplified from pEGFP-N1 with primers 13,14 (Table 1) containing KpnI and SacII overhangs and cloned as KpnI/SacII fragment into pIB-Rin-mC to generate pIB-Rin-EGFP. The PUB-promoter was amplified from pPUB-EGFP with primers 11,12 (Table 1) containing EcoRI overhangs and cloned as EcoRI/EcoRI fragment into pIB-Rin-mC and pIB-Rin-EGFP to generate pPUB-Rin-mC and pPUB-Rin-EGFP respectively.
Virus growth curves
Vero or Aag2 cell monolayers were seeded one day prior to infection in a 6-wells plate. The amount of inoculum for the specific multiplicity of infection (MOI) was calculated based on end-point dilution assay (EPDA) on either Vero or Aag2 cells. Cell monolayers were infected with 1 ml of inoculum in either DMEM- 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) (Gibco) supplemented with 10% FBS, streptomycin and penicillin (DMEM-supplemented) or Schneider’s Drosophila medium supplemented with 10% FBS and gentamycin (50 μg/ml) (Schneider’s-supplemented). After 2 h the inoculum was aspirated, monolayers were washed with phosphate-buffered saline (PBS) and 2 ml of fresh culture medium was added. Vero cells were incubated at 37°C with 5% CO2 and Aag2 cells were incubated at 28°C. At the indicated time points post infection 30 μl supernatant samples were taken and after one freeze-thaw cycle (-80°C) the infectious virus titre was determined by EPDA on either Vero or Aag2 cells.
End-point dilution assays
Vero cells were detached by incubation with Trypsin-EDTA (Gibco) and diluted 1:4 in DMEM-supplemented, while Aag2 cells were detached by force and diluted 1:8 with Schneider’s supplemented. Samples were thawed, vortexed and 10-fold serial dilutions were made in either DMEM-supplemented or Schneider’s-supplemented. Cell suspensions were added to the dilutions 1:1 and 10 μl of inoculated dilution was plated 6-fold in micro-titer plates (Nunc). When samples from mosquitoes were titrated, Fungizone (50 μg/ml; Invitrogen) and gentamycin (50 μg/ml; Life Technologies), was added to the medium and cell fractions prior to titrations (DMEM-complete, Schneider’s-complete). Titrations on Vero cells were scored by CHIKV-induced CPE, while titrations on Aag2 cells were scored by α-CHIKV-E2 based immunofluorescence assay.
Vero or Aag2 cells were fixed by >10 min incubation in 4% paraformaldehyde in PBS. Cells were permeabilized by >10 min incubation in 0.1% sodium dodecyl sulphate in PBS, washed three times with PBS and blocked by incubation in 5% FBS in PBS for 30 min. Primary antibody binding was performed with α-CHIKV-E2 (rabbit polyclonal; 1:5000 ) or α-G3BP1 (1:500; G6046 Sigma Aldrich) diluted in 5% FBS in PBS for 1 h at room temperature (RT). Cells were washed three times with PBS and incubated with the secondary antibody goat-α-rabbit-Alexa Fluor 488 (1:1000; Invitrogen) in 5% FBS in PBS for 1 h at 37°C. Cells were washed three times with PBS and visualized using an Axio Observer Z1m inverted microscope (Zeiss) in combination with an X-Cite 120 series lamp.
Infectious blood meal experiments
Ae. aegypti mosquitoes (Rockefeller strain, obtained from Bayer AG,) were reared as described previously  and transported to the Biological Safety level 3 facility in buckets (diameter: 12.2 cm, height: 12.2 cm; Jokey) for virus infection assays. Mosquitoes were starved for one day and then offered an infectious bloodmeal from a 1:1 mixture of virus and human blood (Sanquin) in a total volume of 1 ml via a Hemotek feeder covered with a Parafilm membrane. Mosquitoes were allowed to feed for 1 h under light conditions at 24°C and 70% relative humidity (RH). Mosquitoes were anesthetized with CO2 and fully engorged females were selected and maintained in buckets at 28°C, 12:12 light:dark cycle, 70% relative humidity and provided with a cotton pad soaked in 6% glucose solution. After 7 or 14 days, mosquitoes were anesthetized with 100% CO2, and immobilized by removing their legs and wings. The proboscis of each stripped mosquito was inserted into a 200 μl pipet tip containing 5 μl of a 1:1 mixture of 50% glucose and FBS. Mosquitoes were allowed to salivate for >45 min, after which the bodies were individually transferred to 1.5 ml Safe-Seal micro tubes (Sarstedt) that contained a small scoop of 0.5 mm zirconium beads (Next Advance). Saliva samples were added to 1.5 ml micro tubes (Sarstedt) that contained 60 μl DMEM-complete. All samples were stored at -80°C until further processing. For most experiments, transmission was determined at 7 days post infection (dpi), as wild type CHIKV reaches relatively high transmission rates at this time-point. This therefore presents a good resolution for the detection of a putative attenuation of a mutant virus.
Frozen mosquito bodies were homogenized for 2 min at maximum speed in a Bullet Blender Storm (Next Advance). Homogenized bodies were centrifuged for 1 min at 14.500 rpm, after which 100 μl of DMEM-complete was added and the homogenization was repeated. Finally the mosquito debris was pelleted by 1 min centrifugation at 14.500 rpm. Thirty microliters of mosquito body supernatant or saliva samples were used to inoculate either Vero or Aag2 cell monolayers in 96-wells plates. After 2–3 h incubation the inoculum was removed and replaced with fresh DMEM-complete or Schneider’s-complete. Infectivity was scored at 3 dpi through virus-induced CPE in Vero cells or by CHIKV-E2-based immunofluorescence in Aag2 cells, as described above.
Verification of nsP3 mutants
Mosquitoes with CHIKV-positive saliva were selected from mosquitoes inoculated with CHIKIC, CHIKICP398A, CHIKICPPR401AAA, CHIKIC-FGN or CHIKIC-FGC. A selection of mosquitoes was made to represent each replicate experiment. Thirty μl of mosquito sample supernatant was used to inoculate a well of a 96-wells plate pre-seeded with C6/36 cells. At 3 days post infection RNA was isolated with TRIzol reagent (Invitrogen) and 300 ng total RNA was subjected to one-step RT-PCR with primers 3,4 using SuperScript III one-step RT-PCR system with Platinum Taq DNA polymerase (Invitrogen) following the manufacturer’s protocol. RT-PCR products were observed on agarose gel to confirm the infection of mosquitoes with CHIKV. To investigate the presence and preservation of the expected mutations, RT-PCR products were subjected to digestion with SacII (NEB), NotI (NEB) or ApeKI (NEB) according to the manufacturer’s protocol. Digestions were observed on agarose gel.
Transfections of mosquito cells with DNA plasmids were performed with Fugene-HD (Promega) in serum-free media following the manufacturer’s protocol. Transfections of Vero cells with DNA plasmids and transfections of C6/36, Aag2 and Vero cells with in vitro transcribed RNA were performed using Lipofectamine 2000 (Invitrogen) in Opti-MEM (Gibco). At 4 hours post transfection (hpt) with Lipofectamine 2000 the transfection mix was replaced with fresh culture media.
The cell culture volume was aspirated and cells were lysed by 20 min incubation in 1X passive lysis buffer (Promega) at RT. Ninety μl of cell lysate was pipetted into an opaque 96-wells plate and 90 μl of Steady-Glo reagent (Promega) was added. After 10 min the luciferase activity was measured using a FLUOstar Optima microplate reader (BMG Labtech).
Co-immunoprecipitation and western blotting
Pre-seeded Vero or Aag2 cells were transfected with plasmids expressing nsP3 or Rin or both. One day post-transfection cells were detached, washed once with PBS and lysed by 30 min incubation in lysis buffer (10 mM Tris/Cl pH 7.5; 150 mM NaCl; 0.5 mM EDTA; 0.5% NP-40) supplemented with Complete protease inhibitors (Roche) and 1 mM phenylmethylsulfonyl fluoride (PMSF). Lysates were cleared by 10 min 20.000 g centrifugation at 4°C and diluted 5:2 with dilution buffer (10 mM Tris/Cl pH 7.5; 150 mM NaCl; 0.5 mM EDTA). Twenty-five μl GFP-Trap_A beads (Chromotek) were added to 500 μl dilution buffer and pelleted by 2 min 2,500 g centrifugation at 4°C. Washing was repeated twice. Cell lysates were added to the equilibrated beads and incubated for 1–2 h at 4°C with overhead rotation. Beads were washed thrice by resuspension in dilution buffer followed by 2 min 2,500 g centrifugation at 4°C. Bound protein complexes were eluted by resuspension in 2X SDS-loading buffer containing 10% β-mercaptoethanol followed by 10 min incubation at 95°C. Beads were removed by 5 min 3,000 g centrifugation and eluates were subjected to western blotting. Briefly, proteins were size-separated by SDS-PAGE and semi-dry blotted onto Immobilon-P membranes (Merck Millipore). Membranes were blocked overnight at 4°C by incubation in 1% milk powder/PBS-0.05%-Tween-20 (PBST). Blocked membranes were probed for 1 h at RT with primary antibodies α-G3BP (1:1000; G6046 Sigma Aldrich), α-GFP (1:2000; A6455 Molecular Probes), α-mCherry (1:1000; ab183628 Abcam) diluted in 1% milk powder/PBST. Membranes were washed thrice for 5 min with PBST and probed for 1 h at RT with alkaline phosphatase (AP) conjugated secondary antibody goat-α-rabbit-AP (1:2500; D0487 Dako) diluted in PBST. Membranes were washed thrice for 5 min in PBS-T and developed with nitroblue tetrazolium (NBT)/BCIP (5-bromo-4-chloro-3-indolylphosphate) (Roche) until the desired signal was achieved.
Statistical analysis were performed in SPSS Statistics 23. Virus titers in mosquito bodies and supernatants from growth curve experiments were checked for normality by Kolmogorov-Smirnov test. Data that did not follow a normal distribution was Log10 transformed and confirmed for normality. Means were compared by one-way ANOVA with Tukey post-hoc test (α = 0.05). Data that did not follow a normal distribution, despite Log10 transformation was analysed by Kruskal-Wallis test with Dunn’s post-hoc test (α = 0.05). Two-tailed Fisher’s exact tests were used to compare infection and transmission rates and performed with GraphPad QuickCalcs (α = 0.05). Ns non-significant; * P < 0.05; ** P ≤0.01; *** P ≤0.001.
The CHIKV nsP3 P-rich motif is required for efficient virus replication in mammalian and mosquito cells
For SINV, SFV and CHIKV it has been shown that deletion or mutation of the conserved P-rich motif (Fig 1B) results in decreased replication in mammalian cells [13,18]. To investigate whether the P-rich motif is similarly indispensable for alphavirus replication in mosquito cells luciferase assays were performed on cells transfected with in vitro transcribed RNA of a CHIKV replicon (CHIKrep) with an in-frame deletion of the P-rich motif (ΔPVA) (Fig 1A, Fig 2A). The mutant replicon CHIKrepΔPVA was unable to replicate in either mammalian Vero or Aag2 Ae. aegypti mosquito cells, whereas wild type CHIKrep was able to replicate in both cell types. We also transfected cells with a CHIKV infectious clone containing the same deletion of the P-rich motif (CHIKICΔPVA), but again we were unable to produce infectious virus in either mammalian and mosquito cells. Together, these results clearly indicate that the P-rich motif is essential for CHIKV replication in both mammalian and mosquito cells.
(A) Vero and Aag2 cells were transfected with in vitro transcribed RNA of CHIKrep or CHIKrepΔPVA and the relative luciferase expression was quantified at 24 hpt. Bars indicate the mean relative light units (RLU) ±standard error of the mean from three independent experiments. (B/C) Vero (B) and Aag2 (C) cells were infected in duplicate with CHIKIC, CHIKICP398A or CHIKICPPR401AAA at a multiplicity of infection (MOI) of 0.01. TCID50/ml was determined by EPDA on Vero cells at the indicated time-points. (D) Aag2 cells were infected in duplicate with CHIKIC, CHIKICP398A or CHIKICPPR401AAA at an MOI of 5 and the TCID50/ml was determined by EPDA on Vero cells at the indicated time-points. Asterisks indicate significant differences compared to the wild type virus by one-way ANOVA with Tukey’s post-hoc test on Log10 transformed data at each time-point (α = 0.05). The dotted line in panels B-D indicates the EPDA detection limit.
To investigate whether the entire, intact P-rich motif is required for virus production in mammalian or mosquito cells, amino acid substitutions were made in the CHIKV infectious clone (CHIKIC) to produce CHIKICP398A and CHIKICPPR401AAA (Fig 1A). These specific mutations are designed to disrupt the residues in the P-rich motif that are conserved among old-world alphaviruses (PxxPPR; Fig 1B red boxes). Viral growth curves were determined in duplicate using an MOI of 0.01 and viral titers were determined by EPDA on Vero cells. The results show that both mutants displayed significantly delayed growth kinetics compared to the wild type virus in both Vero (Fig 2B) and Aag2 cells (Fig 2C). Even when virus infections were performed at a higher MOI of 5 this attenuating effect was observed at 24 hpi, although both CHIKICP398A and CHIKICPPR401AAA still reached a titer of ~1.0 × 106 TCID50/ml (Fig 2D). Together, these results indicate that an intact P-rich motif in CHIKV nsP3 is important, but not essential, for virus replication in mammalian and mosquito cells.
The P-rich motif is not required for the transmission of chikungunya virus by Ae. aegypti mosquitoes
The P-rich motif is conserved in most if not all mosquito transmitted alphaviruses and also in the insect-specific alphaviruses Tai Forest Alphavirus (TALV) and Eilat virus (EILV) (Fig 1B). As TALV and EILV are proposedly unable to replicate in a vertebrate host [38,39], conservation of a P-rich motif for these viruses suggests its importance for alphavirus infection in the invertebrate vector. To investigate whether the P-rich motif of CHIKV nsP3 is involved in virus transmission by mosquitoes, female Ae. aegypti were offered an infectious bloodmeal containing either CHIKIC, CHIKICP398A or CHIKICPPR401AAA (Fig 3A). After 14 days, the infection and transmission rates were determined by infectivity assay on Vero cells (Fig 3B). For all three viruses, similar infection (88–96%; P > 0.37) and transmission (6–7.7%; P = 1.00) rates were obtained, indicating that the P-rich motif is not required for virus transmission by mosquitoes.
(A) Schematic experimental set-up. Female Ae. aegypti mosquitoes were infected through an infectious bloodmeal containing 1.0 × 107 TCID50/ml of CHIKIC, CHIKICP398A or CHIKICPPR401AAA. At 14 days post infection (dpi) (B) or 7 dpi (C) the infection and transmission rates were determined by infectivity assay on Vero cells. Bars represent cumulative numbers from three (B) or two (C) independent experiments. n = total number of mosquitoes used per treatment. Statistics were performed by Fisher’s exact test (α = 0.05). (D) TCID50/ml of CHIKV in the bodies Ae. aegypti mosquitoes with CHIKV-positive saliva at 7 dpi were determined by end-point dilution assay on Vero cells. Statistics were performed by one-way ANOVA with Tukey’s post-hoc test on Log10 transformed data (α = 0.05).
To investigate whether putative differences could be observed earlier after infection of the mosquito vector, we also determined the infection and transmission rates after 7 days (Fig 3C). Again, infection (72–76%; P > 0.61) and transmission (18–23%; P > 0.47) rates were obtained that were not significantly different when compared to the wild type virus. In order to determine whether the mutations in CHIKICP398A and CHIKICPPR401AAA were preserved during infection of the mosquito, the nsP3 sequences were amplified by RT-PCR for a selection of mosquitoes with CHIKV-positive saliva. Presence of the expected mutations in nsP3 was confirmed, indicating that the mutant viruses did not revert to wild type during replication in the mosquito vector (S1 Fig). To assess whether the titers in the mosquito bodies would perhaps be decreased due to the mutations in the P-rich motif, CHIKV titers were determined in the bodies of mosquitoes with virus-positive saliva (Fig 3D). However, no difference in viral titer between CHIKIC, CHIKICP398A and CHIKICPPR401AAA (P > 0.99) was observed. Together, these results indicate that the CHIKV nsP3 P-rich motif is not required for the transmission by Ae. aegypti mosquitoes.
Chikungunya virus nsP3 requires duplicate FGDF motifs for replication in mammalian cells and a single FGDF motif in mosquito cells
Research has indicated that mutating both FGDF motifs together significantly attenuates SFV and renders CHIKV unable to replicate in mammalian cells [17,20]. Here, we investigated whether mutations in one (nsP3-FGN, nsP3-FGC) or both (nsP3-FGNC) FGDF motifs would interfere with the replication of CHIKV in mosquito cells. These amino acid mutations were previously shown to disrupt the interaction of nsP3 with G3BP [20,40], and the co-localization of nsP3 with Rin . We tested the effect of mutating the FGDF motifs on CHIKV replication using an infectious clone that contains an in-frame insertion of the mCherry reporter gene in nsP3 (CHIKICnsP3mC; Fig 1A). In vitro transcribed, capped RNA from CHIKICnsP3mC, CHIKICnsP3mC-FGN, CHIKICnsP3mC-FGC or CHIKICnsP3mC-FGNC was used to transfect Vero and C6/36 mosquito cells. At 36 hpt, the cells were fixed and analysed for mCherry fluorescence as a marker for virus replication (Fig 4A). Red fluorescence was observed in cells transfected with RNA from the infectious clones with mutations in a single FGDF motif (CHIKICnsP3mC-FGN and CHIKICnsP3mC-FGC) and wild type CHIKV. However, mammalian and mosquito cells transfected with RNA from CHIKICnsP3mC-FGNC did not show any red fluorescence, indicating that a minimum of one functional FGDF motif is essential for CHIKV replication in both mammalian and mosquito cells.
(A) Vero and C6/36 cells were transfected with in vitro transcribed RNA of CHIKICnsP3mC, CHIKICnsP3mC-FGN, CHIKICnsP3mC-FGC, or CHIKICnsP3mC-FGNC. Cells were fixed at 36 hours post transfection, stained with Hoechst, and fluorescence was observed by fluorescence microscopy. (B) Vero cells were transfected with in vitro transcribed RNA of CHIKICnsP3mC or CHIKICnsP3-FGNC either individually or co-transfected with in vitro transcribed RNA of CHIKIC. Cells were fixed at 36 hpt, stained with Hoechst and fluorescence was observed by fluorescence microscopy. (C) Vero and C6/36 cells were transfected with in vitro transcribed RNA of CHIKrep or CHIKrep-FGNC and the relative luciferase expression was quantified at 24 hpt. Bars indicate the mean relative light units (RLU) ±SEM, normalized to the wild type replicon from at least three independent experiments. (D) Growth curves of CHIKVIC, CHIKVIC-FGN and CHIKVIC-FGC on Vero cells infected in duplicate with an MOI of 0.01 based on end-point dilution assay (EPDA) on Vero cells. At the indicated time-points the TCID50/ml was determined by EPDA on Vero cells. (E) Growth curves of CHIKVIC, CHIKVIC-FGN and CHIKVIC-FGC on Aag2 cells infected in duplicate with an MOI of 0.01 based on infectivity on Aag2 cells. At the indicated time-points the TCID50/ml was determined by EPDA on Aag2 cells. Statistics were performed by one-way ANOVA with Tukey’s post-hoc test on Log10 transformed data at each time-point (α = 0.05). Asterisks indicate significance compared to the wild type virus. The dotted line in panels D-E indicates the EPDA detection limit.
To assess whether the RNA of CHIKICnsP3mC-FGNC was of sufficient quality, we co-transfected replication-competent RNA from CHIKIC, which does not express mCherry. In this experiment, CHIKIC RNA is able to complement the CHIKICnsP3mC-FGNC RNA, leading to mCherry expression. Indeed, upon co-transfection red fluorescence could be observed in some cells (Fig 4B), indicating that the quality of CHIKICnsP3mC-FGNC RNA was fine but that the RNA was replication-incompetent due to the mutation of both FGDF motifs. To confirm this result using a more sensitive assay, Vero and C6/36 cells were transfected with CHIKV replicons expressing firefly luciferase CHIKrep or CHIKrep-FGNC (Fig 1A) and firefly luciferase activity was measured at 24 hpt (Fig 4C). In both Vero and C6/36 cells, only the wild type replicon CHIKrep produced above-background luciferase levels, indicating that indeed mutation of both FGDF motifs together results in complete inactivation of CHIKV in mammalian and mosquito cells.
To assess the effect of single FGDF mutations on virus production in mammalian and mosquito cells, we performed viral growth curves on Vero and Aag2 cells at an MOI of 0.01 using CHIKIC, CHIKIC-FGN and CHIKIC-FGC (Fig 4D and 4E). These viruses do not contain the mCherry reporter gene (Fig 1A). It is important to note that we determined the viral titers for the inoculum and the samples for the mammalian growth curves by EPDA on Vero cells. For the growth curves on mosquito cells, the titrations were performed by EPDA on Aag2 cells. As expected, CHIKIC-FGN and CHIKIC-FGC were severely attenuated in Vero cells (Fig 4D). However, the result was very different in Aag2 cells; CHIKIC-FGN and CHIKICFGC displayed remarkably similar growth rates as compared to CHIKIC (Fig 4E). In summary, duplicate FGDF motifs are very important for CHIKV replication in mammalian cells, while a single FGDF motif is sufficient, but required, for efficient CHIKV replication in mosquito cells.
Requirement of FGDF motifs for chikungunya virus transmission by Aedes aegypti
While duplicate FGDF motifs do not appear to be required for virus replication in mosquito cells (Fig 4E), they might be important to sustain transmission of CHIKV by mosquitoes. Therefore, we infected Ae. aegypti mosquitoes via an infectious bloodmeal with 2.8 × 105 TCID50/ml CHIKIC, CHIKIC-FGN or CHIKIC-FGC and determined the infection and transmission rates at 7 dpi by infectivity assay on Vero and Aag2 cells (Fig 5A). When scored on Vero cells the mosquito infection rate of CHIKIC-FGC (54.8%; P <0.001) was significantly lower as compared to CHIKIC (73.7%), while the infection rate of CHIKIC-FGN (72.6%; P = 0.89) was similar to wild type (Fig 5B). Next, the saliva of infected mosquitoes was tested for the presence of virus. This showed that the transmission rates of both CHIKIC-FGN (7.4%; P <0.001) and CHIKIC-FGC (9.6% P <0.001) were significantly lower as compared to CHIKIC (25.7%), indicating that duplicate FGDF motifs are important for CHIKV transmission by Ae. aegypti to the vertebrate host.
(A) Schematic experimental set-up. Female Ae. aegypti mosquitoes were infected through an infectious bloodmeal containing 2.8 × 105 TCID50/ml of CHIKIC, CHIKIC-FGN, CHIKIC-FGC. At 7 days post infection (7dpi) the infection and transmission rates were determined by infectivity assay on (B) Vero and (C) Aag2 cells. Bars represent cumulative numbers from three independent experiments. n = total number of mosquitoes used per treatment. Statistics were performed by Fisher’s exact test (α = 0.05). (D) Ratio between the number of positive bodies or salivas in Vero compared to Aag2 cells. Statistics were performed by Kruskal-Wallis test with Dunn’s post-hoc test (α = 0.05). (E) TCID50/ml in the bodies of Ae. aegypti mosquitoes with CHIKV-positive saliva at 7 dpi were determined by end-point dilution assay on Aag2 cells. Statistics was performed by one-way ANOVA with Tukey’s post-hoc test on Log10 transformed data (α = 0.05).
However, given that CHIKIC-FGN and CHIKIC-FGC were severely attenuated on Vero cells (Fig 4D), we also determined the infection and transmission rates by infectivity assay on Aag2 cells, using exactly the same mosquito bodies and salivas (Fig 5C). The infection rate did not change much, and CHIKIC-FGC (57%; P <0.01) still reached a lower infection rate than CHIKIC (74.7%) or CHIKIC-FGN (78.5%; P = 0.49). Interestingly, however, when scored on Aag2 cells the transmission rates were very similar for CHIKIC (19.3%), CHIKIC-FGN (16.3%; P = 0.54) and CHIKIC-FGC (13.7%; P = 0.21). To directly compare the infectivity of the mosquito bodies and salivas between Vero and Aag2 cells, the ratio between the number of positive samples on Vero and Aag2 cells was determined for each replicate and normalized to the ratio for mosquitoes inoculated with wild type CHIKIC (Fig 5D). Indeed, the ratio of Vero/Aag2 positive samples was lower for CHIKIC-FGN and CHIKIC-FGC as compared to wild type CHIKIC (FGN 0.18; FGC 0.33). To determine whether the mutations in CHIKIC-FGN and CHIKIC-FGC were preserved during replication in the mosquito, the nsP3 sequences of a selection of mosquitoes with CHIKV-positive saliva were amplified by RT-PCR. Presence of the expected mutations in nsP3 was confirmed, indicating that the mutant viruses did not revert to wild type (S1 Fig). Together, these results imply that, while CHIKIC-FGN and CHIKIC-FGC are perfectly able to infect the mosquito body and disseminate to ultimately reach the mosquito saliva, their virions are less able to replicate in vertebrate cells. These results are in agreement with the observed differences between the growth curves on Vero and Aag2 cells (compare Fig 4D with Fig 4E). To assess the effect of mutating one FGDF motif on the viral load in the mosquito body, the viral titers in mosquito bodies of which the saliva was virus positive were determined by EPDA on Aag2 cells (Fig 5E). Viral loads of mosquitoes infected with CHIKIC, CHIKIC-FGN or CHIKIC-FGC were not significantly different (2.7–5.0 × 106 TCID50/ml; P > 0.65). Thus, a single FGDF motif in nsP3 is sufficient for the infection and dissemination of CHIKV in Ae. aegypti mosquitoes, but duplicate FGDF motifs are required for efficient infection of the vertebrate host by mosquito bite.
The interaction with mammalian G3BP and mosquito Rasputin depends on the presence of FGDF motifs in the HVD of chikungunya virus nsP3
We have previously shown that mutations in a single FGDF motif do not abrogate the co-localization of CHIKV nsP3 and the mosquito homolog of G3BP, Rin, in insect cells . However, in mammalian cells it has been suggested that mutation of just the N-terminal FGDF motif of nsP3 already dismantles the interaction with G3BP [17,20]. We therefore investigated the effect of mutating either of the two FGDF motifs on the co-localization of CHIKV nsP3 with G3BP in mammalian cells and Rin in mosquito cells. Because there is no anti-Rin antibody available, Aag2 cells were first transfected with a plasmid expressing an EGFP-tagged Rin (pPUB-Rin-EGFP, Fig 6A). Vero (Fig 6B) and Aag2 (Fig 6C) cells were infected with CHIKICnsP3mC, CHIKICnsP3mC-FGN or CHIKICnsP3mC-FGC. At 24 hpi, cells were fixed and permeabilized and Vero cells were immuno-stained for G3BP-1. In both mammalian and mosquito cells mutation of either the N-terminal or the C-terminal FGDF motif did not abrogate the co-localization of nsP3 with G3BP and Rin.
(A) Schematic overview of the used plasmids expressing Rasputin (Rin) fused to EGFP Rin-EGFP or mCherry Rin-mC and CHIKV nsP3 EGFP fusion proteins of wild type and FGDF single- and double-mutant nsP3. CMV cytomegalovirus promoter; PUB Aedes aegypti poly-ubiquitin promoter; NTF2 nuclear transport factor 2-like domain; RRM RNA recognition motif; RGG arginine glycine rich region; HVD hypervariable domain. (B) Vero cells were infected with CHIKICnsP3mC, CHIKICnsP3mC-FGN or CHIKICnsP3mC-FGC. At 24 hours post infection (hpi) cells were fixed, permeabilized, stained with α-G3BP and visualized by fluorescent microscopy. (C) Aag2 cells were transfected with pPUB-Rin-EGFP and at 24 hours post transfection (hpt) cells were infected with CHIKICnsP3mC, CHIKICnsP3mC-FGN or CHIKICnsP3mC-FGC. At 24 hpi cells were fixed and visualized by fluorescence microscopy. (D) Vero cells were transfected with CMV driven plasmids expressing EGFP, nsP3EGFP, nsP3EGFP-FGC, nsP3EGFP-FGN or nsP3EGFP-FGNC. At 24 hpt cells were lysed and lysates were subjected to co-immunoprecipitation with α-GFP beads. Lysates and co-precipitates were subjected to western blot with α-G3BP and α-GFP antibodies. (E) Aag2 cells were transfected with PUB driven plasmids expressing EGFP, nsP3EGFP, nsP3EGFP-FGN, nsP3EGFP-FGC or nsP3EGFP-FGNC and co-transfected with pPUB-Rin-mC. At 24 hpt cells were lysed and lysates were subjected to co-immunoprecipitation with α-GFP beads. Lysates and co-precipitates were subjected to western blot with α-GFP and α-mCherry antibodies.
As co-localization observed by fluorescent microscopy does not prove that there is a physical protein-protein interaction we investigated the importance of the FGDF motifs for interaction of nsP3 with G3BP in mammalian cells and Rin in mosquito cells by co-immunoprecipitation (co-IP). First, Vero cells were transfected with CMV-driven plasmids expressing the nsP3EGFP fusion proteins nsP3, nsP3-FGN, nsP3-FGC, nsP3-FGNC or just EGFP as a control (Fig 6A). At 24 hpt cells were lysed and lysates were subjected to co-IP with α-GFP beads followed by western blot detection of nsP3EGFP and G3BP in both the cell lysates and co-IP samples (Fig 6D). The expression of the nsP3 fusion proteins was similar for nsP3-FGN, nsP3-FGC and nsP3-FGNC while expression of wild type nsP3 was lower. Yet after co-IP, G3BP was only enriched for wild type nsP3, despite the presence of less nsP3 in the co-IP fraction. G3BP was not enriched for nsP3-FGN, nsP3-FGC or nsP3-FGNC, suggesting that nsP3 requires duplicate FGDF motifs to establish high-affinity for G3BP in mammalian cells.
Next, Aag2 cells were transfected with PUB-driven plasmids expressing the nsP3EGFP fusion proteins nsP3, nsP3-FGC, nsP3-FGN or nsP3-FGNC and co-transfected with pPUB-Rin-mC, encoding a Rin-mCherry fusion protein (Fig 6A). Cells were lysed, subjected to co-IP with α-GFP beads followed by detection of nsP3EGFP and Rin-mC in the cell lysates and precipitated samples (Fig 6E). Expression of the nsP3EGFP fusion proteins was similar for nsP3, nsP3-FGN, nsP3-FGC, nsP3-FGNC. Expression of Rin-mC was similar for nsP3, nsP3-FGN, nsP3-FGC transfected samples, while Rin-mC expression was highest in cells transfected with nsP3-FGNC. Similar amounts of nsP3, nsP3-FGN and nsP3-FGC but more nsP3-FGNC was precipitated. Interestingly, however, Rin-mC was only enriched for nsP3, nsP3-FGN and nsP3-FGC, but not for nsP3-FGNC. This demonstrates that nsP3 requires only one FGDF motif for interaction with Rin. These results suggest that differences in the affinities of FGDF motifs for G3BP and Rin may underlie the difference for the required number of FGDF motifs between mammalian and mosquito cells.
The delicacy of alphavirus-vector interactions has been well-illustrated by the discovery that a single A→V mutation in the CHIKV E1 envelope protein could change the viral vector specificity from Ae. aegypti to Ae. albopictus . Additionally, for VEEV a single amino acid substitution in the E2 protein could determine its potential to infect Ochlerotatus taeniorhynchus mosquitoes . Here, we investigated the importance of the conserved P-rich and FGDF motifs in the HVD of CHIKV nsP3 for infection of mosquito cells and transmission by Ae. aegypti mosquitoes.
Deletion of the P-rich motif in the nsP3 HVD renders CHIKV unable to replicate in both mammalian and mosquito cells, while amino acid substitutions of the core residues in the P-rich motif resulted in a significant decrease of replication in both cell types. This is similar to previous findings with SINV where deletions in the SINV nsP3 HVD that disrupt the P-rich motif were reported to decrease growth kinetics and plaque size in C7/10 mosquito cells , an indication for reduced replication potency or cytopathicity, or both. However, mutations of the P-rich motif did not affect CHIKV infection or transmission by Ae. aegypti mosquitoes. The nsP3 P-rich motif has high affinity for SH3-domain containing proteins and is known to interact with amphiphysin-I/II [18,23] in mammalian cells, and proposedly also with the Drosophila homolog of amphiphysin , although no evidence has so far been reported for this interaction in insect cells. We indeed demonstrate that mutation of the P-rich motif results in decreased virus production in mosquito cells, which suggests that nsP3 interacts with mosquito SH3-domain containing proteins, although these interactions do not appear to be essential for transmission by the mosquito vector. It was previously shown that deletions of the P-rich motif of SFV and SINV result in decreased affinity for amphiphysins and lowered replication efficiencies in mammalian cells . Therefore, the decrease in replication of CHIKICP398A and CHIKICPPR401AAA in mammalian cells may be due to reduced affinity for amphiphysins or other cellular proteins that contain an SH3 domain. Of note, both the P398A and PPR401AAA mutations do not mutate all prolines in the CHIKV PxxPPR motif, thus the remaining prolines may still partially interact with host proteins. This may underlie the strong attenuation of CHIKICP398A and CHIKICPPR401AAA after low MOI infection, but not after high MOI infection where the remaining proline(s) may be sufficient to establish successful replication. Complete inactivation of CHIKV after deletion of the entire P-rich motif implies that such interactions are crucial to establish successful virus infection. It has been demonstrated that the arginine residues downstream of the P-rich motif of CHIKV, which are not conserved in SFV and SINV nsP3, partially determine the affinity for amphiphsyin-2 . This might explain why deletion of the whole P-rich motif, including the C-terminal arginines downstream of PxxPPR completely abrogates CHIKV replication, while mutating just the core residues in the P-rich motif results in a less dramatic effect.
Mutation of both FGDF motifs together fully abrogated CHIKV replication in both mammalian and mosquito cells. This indicates that the FGDF motifs not only play an important role during infection of mammalian cells, as previously reported [17,19–22,30], but that they also determine the successful infection of mosquito cells. Furthermore, we show for CHIKV that a single FGDF motif is sufficient to infect mammalian cells, although the replication and infection efficiencies are dramatically decreased compared to wild type CHIKV. In contrast, in mosquito cells, CHIKIC-FGN and CHIKIC-FGC replicated similarly to the wild type CHIKIC and were efficiently transmitted by Ae. aegypti mosquitoes after an infectious bloodmeal. This indicates that CHIKV requires only a single FGDF motif for infection of the mosquito vector. Thus, duplicate FGDF motifs appear to be required for the efficient infection from the mosquito’s saliva to a subsequent vertebrate host, which supports the conservation of duplicate FGDF motifs for most mosquito-borne alphaviruses.
The mosquito protein Rin, a homolog of mammalian G3BP, was previously identified as an important regulator of CHIKV transmission, as knock-down of Rin severely decreased the transmission of CHIKV by Ae. albopictus mosquitoes . In our study, we confirmed that, during CHIKV infection, a single FGDF motif is sufficient for the co-localization of nsP3 with Rin, similar to previous experiments with transiently expressed nsP3 . Mutation of both FGDF motifs in nsP3 together abolished its ability to co-localize and interact with Rin, suggesting that the inability of CHIKVIC-FGNC to replicate in mosquito cells is due to absence of the nsP3-Rin interaction. Furthermore, we demonstrate that only one FGDF motif is required for the interaction between nsP3 and Rin, in contrast to mammalian cells where the interaction between nsP3 and G3BP was only observed for wild type nsP3 and not for nsP3 with one mutated FGDF motif. For SFV nsP3 it has been shown that mutation of just the phenylalanine of FGN largely abrogates the interaction with G3BP while mutating the phenylalanine of FGC only decreases the affinity of nsP3 for G3BP . We mutated not only the first phenylalanine of FGC but also the glycine to alanine, both of which have been shown to be important for G3BP binding . This may explain why we could not observe an interaction between G3BP and either nsP3-FGN or nsP3-FGC.
G3BP can be present in monomeric, dimeric and polymeric forms  and the two FGDF motifs of alphavirus nsP3 each bind one NTF2-like domain of two separate G3BP monomers [20,40]. As a result, mutation of one FGDF motif results in decreased affinity for G3BP and attenuates alphavirus replication [17,20,21]. It is uncertain whether mosquito Rin forms a dimer, although the crystal structure of the Drosophila Rin NTF2-like domain was demonstrated in dimeric form . Thus, a single FGDF motif might be sufficient for the interaction with monomeric Rin to support CHIKV replication in mosquito cells and in Ae. aegypti mosquitoes. Alternatively, the FGDF motifs of nsP3 might have a higher affinity for Rin as compared to G3BP, resulting in sufficient recruitment of Rin to replication complexes in mosquito cells with only a single FGDF motif. As Vero and Aag2 cells were cultured at 37°C and 28°C respectively, lowered affinity of the FGDF motifs for G3BP as compared to Rin may partially be explained by the higher incubation temperature. Potentially, the higher temperature at which mammalian Vero cells are cultured decreases the stability of the nsP3-G3BP interaction, thus resulting in lower affinity of nsP3 for G3BP as compared to Rin.
The exact reason for recruitment of Rin/G3BP by nsP3 is still speculative, although several hypotheses such as recruitment of viral gRNA followed by shielding of the viral replication complex from degrading enzymes  and prevention of antiviral stress granule formation [13,21] have been brought forward. Possibly, the interaction with G3BP/Rin is particularly crucial early after infection and a certain level of G3BP/Rin has to be bound by nsP3 to successfully form viral replication complexes. Interestingly, while arthritogenic-alphaviruses recruit G3BP via their FGDF motifs, neurotropic alphaviruses lack FGDF motifs and instead recruit members of the Fragile X syndrome (FXR) family via a different motif in the nsp3 HVD [17,19]. Proteins of the FXR family are abundantly expressed in neuronal cells , which may therefore be more susceptible to infection by alphaviruses that use FXR family proteins for their replication. Whether a direct correlation exists between the use of FXR or G3BP for replication and the symptoms caused by alphavirus infection should be the focus of future research. Mosquitoes possess a homolog of one FXR family protein, called Fragile X syndrome-related protein 1 (FMR1). Based on our results, we hypothesize that the nsP3 of neurotropic alphaviruses may interact with mosquito FMR1, similarly to the CHIKV nsP3-Rin interaction. Future research should investigate the possibility of an interaction between nsP3 and mosquito FMR1 and its importance for the transmission of neurotropic alphaviruses by mosquitoes.
Concluding, our results increase the understanding of the functionality of conserved motifs in the alphavirus nsP3 HVD in the context of the arboviral dual-host life cycle. Understanding the underlying mechanisms of G3BP/Rin recruitment by alphavirus nsP3 remains the focus of future research and may well contribute to the development of antiviral drugs and compounds that target this crucial interaction.
S1 Fig. Verification of CHIKIC nsP3 mutants in vivo in Ae. aegypti mosquitoes.
RNA was isolated from the bodies of mosquitoes with CHIKV-positive saliva. The nsP3 gene was amplified by RT-PCR and digested with SacII, NotI or ApeKI to screen for preservation of the expected mutations.
We thank Dr. Esther Schnettler for providing us the pPUB-Fluc plasmid, Dr. Jelke Fros for useful comments on the experimental procedures, Sandra Abbo for assistance in processing the mosquitoes, Julian Bakker for assistance in producing the pPUB-Rin-mCherry plasmid, Winnie van den Boogaard for assistance in constructing the infectious clones and replicons, and the reviewers for valuable suggestions to improve this manuscript.
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