Abstract
Apoptosis has been recognized as a suicidal host-defense programmed cell death pathway against invading pathogens. However, recent evidences showed that viruses can employ caspases to cleave and inactivate immune signaling molecules to facilitate infection. Whether caspases can promote anti-viral immune responses is currently unknown. Here, we demonstrated that the NSs protein of RVFV triggers activation of apoptotic caspases, which cleave the mitochondrial fission factor DRP1 resulting in mitochondrial elongation. Elongated mitochondria promote MAVS aggregation leading to enhanced anti-viral immunity. Apoptotic caspases, including caspase-3, -6, -7 and -8, cleave DRP1 at the motifs of D500FAD503 and/or AEAD556, suggesting that this cleavage event may occur during infection of different viruses. Indeed, infection of H1N1, SeV and HSV-1 all triggered apoptotic caspases activation to cleave DRP1 promoting anti-viral immune responses. Compared with wild-type DRP1, introduction of caspase-resistant DRP1 strongly attenuated immune responses triggered by virus infection. These results revealed a novel mechanism through which apoptotic caspases promote anti-viral immunity by regulating mitochondrial morphodynamics.
eLife assessment
This manuscript describes an unexpected role of cellular caspases in cleaving Drp1, a protein involved in mitochondrial fission, in virus-infected cells. Drp1 cleavage augments mitochondrial fission, reinforcing MAVS-dependent type-1 IFN response against multiple viruses. The findings presented in this manuscript are important and the strength of evidence is solid. Additional studies may allow for more robust mechanistic substantiation of the proposed model.
Introduction
Rift Valley fever virus (RVFV) is an enveloped, single-stranded ambisense, tri-segmented RNA virus, belonging to the genus phlebovirus and the family Phenuiviridae within the order Bunyavirales (Noronha and Wilson, 2017). As a mosquito-borne virus, RVFV is transmitted among humans through mosquito bites and can cause serious diseases including ocular (eye) disease, meningoencephalitis or haemorrhagic fever (McMillen and Hartman, 2018). The case-fatality ratio for RVF patients developing the haemorrhagic fever can be up to approximately 50% (Sun et al., 2018). Due to the absence of effective preventive or therapeutic strategies for human use and the potential of widespread transmission, RVFV has been listed as one of the viruses causing priority diseases categorized by the world health organization (WHO) (Gerken et al., 2022). RVFV has a three-segmented RNA genome of the L (large), M (medium) and S (small) segment, of which the S segment encodes the major virulence factor nonstructural protein (NSs) (Freire et al., 2015; Leger et al., 2020). Previous studies have shown that the virulence factor NSs protein triggers apoptosis during infection and contributes to viral pathogenesis (Austin et al., 2012; Narayanan et al., 2014; Smith et al., 2010).
Apoptosis is a form of programmed cell death that functions in regulating normal embryonic development, tissue homeostasis and immune responses (Elmore, 2007; Everett and McFadden, 1999; Williams, 1994). Apoptosis is mediated through the activation of apoptotic caspases including caspase-2, -3, -6, -7, -8, -9 and -10. Apoptosis can be triggered by either extrinsic or intrinsic pathways. The extrinsic apoptosis pathway is activated by the engagement of cell surface death receptors, such as members of the tumor necrosis factor (TNF) receptor superfamily, by its ligands, leading to the activation of caspase-8 and its downstream effector caspases (Li and Yuan, 2008; Orzalli and Kagan, 2017; Zhou et al., 2017). The intrinsic apoptosis is regulated by the function of pro-apoptotic members of the B-cell lymphoma 2 (Bcl-2) family, which controls the Bax/Bak activation and induces mitochondrial outer membrane permeabilization (MOMP) (Zhou et al., 2017). MOMP results in the release of cytochrome c into the cytosol, which binds to Apaf-1 to activate caspase-9 and the downstream effector caspases -3, -6 and -7 (Li and Yuan, 2008; Zhou et al., 2017).
Many viruses, including both DNA and RNA viruses, cause infected cells to undergo apoptosis (Koyama et al., 1998). Apoptosis has long been regarded as a host defense mechanism eliminating the niche of virus amplification (Koyama et al., 1998). However, recent evidences showed that viruses can employ activated caspases to cleave and inactivate the innate immune molecules to dampen the host anti-viral immune responses and promote virus replication (Ning et al., 2019; Wang et al., 2017). For example, vesicular stomatitis virus (VSV) and Poliovirus trigger caspase-3 or caspase-7 activation to cleave and inactivate MAVS (also named as VISA, IPS-1, and Cardif) to facilitate virus replication (Ning et al., 2019; Rebsamen et al., 2008). Similarly, HIV-1 triggers caspase-3 activation to cleave IRF3 and promotes virus infection (Ning et al., 2019; Park et al., 2014). IRF3 can also be cleaved and inactivated by caspase-8 during Sendai virus (SeV) infection (Sears et al., 2011). Up till now, whether virus infection-triggered apoptotic caspases can promote antiviral innate immunity has not been reported.
Both extrinsic and intrinsic apoptosis involve regulation of mitochondria, a critical intracellular organelle participating in energy production, metabolism, cell death and differentiation (Ren et al., 2020). Recent studies revealed that mitochondria are central hubs of innate immune responses mediating both IFN-I and inflammatory responses (Sandhir et al., 2017). Mitochondria undergo dynamic morphological changes regulated by mitochondrial fusion and fission factors (Tilokani et al., 2018). Key regulators that mediate the switch between mitochondrial fusion and fission include OPA1, which is responsible for fusion of the inner membrane; MFN1 and MFN2, which are responsible for fusion of the outer membrane; and dynamin-related protein 1 (DRP1/DNM1L/DLP), which is the critical factor that participates in mitochondrial fission (Chen et al., 2020; Wei et al., 2021). The morphodynamics of mitochondria is important for regulating immune responses with the elongated mitochondria mediates enhanced immune responses through serving as the platform for immune signalosome assembly (Chen et al., 2020). Mitochondrial elongation has been reported during virus infection which is induced by inactivation of DRP1 modulated by its phosphorylation status (Chen et al., 2020). Whether virus-triggered apoptosis can regulate mitochondrial morphodynamics is currently unknown.
Here, we found that RVFV virulence factor NSs activates apoptotic caspases which then cleave and deplete mitochondrial fission factor DRP1. DRP1 depletion leads to elongated mitochondria and promotes anti-viral immune responses through facilitating MAVS aggregation. We further demonstrated that multiple apoptotic caspases can cleave and deplete DRP1 at different positions. This caspase mediated DRP1 cleavage event is observed during both DNA and RNA virus infection and appears as a general caspase-dependent host anti-viral mechanism. These results revealed a new host defense mechanism mediated by apoptotic caspase activity.
Results
RVFV infection leads to mitochondrial elongation through down-regulating DRP1
RVFV infection leads to distinctly elongated mitochondria in the infected PMA-induced THP-1 macrophage cells (THP-1PMA) (Figure 1A). The RVFV-induced mitochondrial elongation was also observed in various cell types including Huh7 cells and A549 cells (Figure 1A). Examination of ultrathin sections of RVFV infected THP-1PMA cells by transmission electron microscopy (TEM) confirmed that mitochondria were more elongated in RVFV-infected cells than those in uninfected cells (Figure 1B). To identify which viral protein induced mitochondrial elongation, RVFV viral proteins, including NSs, NP, NSm, Gn, Gc and polymerase (Pol), were transiently expressed in Huh7 cells and the mitochondrial morphology was observed. It is found that only NSs expression, but not other viral proteins, induced distinct mitochondrial elongation (Figure 2A). The expression of RVFV-NSs in A549 cells also induced mitochondrial elongation (Figure S1A). To analyze whether NSs mediates mitochondrial elongation during RVFV infection, we generated NSs-deleted RVFV encoding EGFP in the position of NSs (RVFVEGFP △ NSs) and evaluated mitochondrial morphology in infected cells. Unlike infection with wild type (WT) virus, infection with RVFVEGFP△NSs did not lead to elongated mitochondria (Figure 2B). These results suggested that the viral protein NSs induced mitochondrial elongation during RVFV infection.
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RVFV infection leads to mitochondrial elongation.
(A) Mitochondria were visualized by immunofluorescence using confocal microscopy. THP-1PMA, Huh7 or A549 cells were infected or mock infected with RVFV for 24 h at MOI = 5. Mitochondria were labeled with anti-Tom20 antibody (red), RVFV were labeled with anti-RVFV-NSs antibody (green) and Nuclei were stained with DAPI (blue). Scale bars, 5 μm (THP-1PMA and Huh7 cells) or 7.5 μm (A549 cells).
(B) Sections of mock infected or RVFV-infected THP-1PMA cells (MOI = 1) were analyzed by TEM. Black solid squares, scale bars, 1 μm. Blue dashed squares represent the magnification of regions of interest, scale bars, 250 nm. Mitochondria are circled in red shown on the right panels.
Data are representative of three experiments with similar results.
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RVFV infection induces NSs-dependent DRP1 downregulation leading to mitochondrial elongation.
(A) The effects of exogenously expressed RVFV viral proteins on mitochondrial morphology in Huh7 cells was observed by confocal microscopy. Huh7 cells were transfected with empty vector or vectors expressing strep-tagged viral proteins of RVFV for 48 h. Mitochondria were labeled with anti-Tom20 antibody (red), viral proteins of RVFV were labeled with anti-strep antibody (green) and Nuclei were stained with DAPI (blue). Scale bars, 7.5 μm.
(B) Huh7 cells were mock infected or infected with the indicated virus for 24 h. Mitochondria were labeled with anti-Tom20 antibody (red), RVFV were labeled with anti-RVFV-NSs antibody (green), RVFVEGFP△NSs were observed through detecting EGFP signal, and Nuclei were stained with DAPI (blue). Scale bars, 7.5 μm.
(C) Immunoblot analysis of the proteins that regulate mitochondrial morphology, including MFN1, MFN2, OPA1 and DRP1 in THP-1PMA cells infected with RVFV for the indicated times.
(D) Immunoblot analysis of DRP1 protein level in Huh7 cells infected or mock infected with RVFVWT or RVFVEGFP△NSs for 24 h.
(E) Immunoblot analysis of DRP1 protein level in Huh7 cells transfected with the plasmids expressing the indicated proteins for 48 h.
Data are representative of three experiments with similar results.
To explore the mechanisms underlying RVFV-NSs induced mitochondrial elongation, we first examined the abundance of host proteins that regulate mitochondrial morphology, including MFN1, MFN2, OPA1, which mediate mitochondrial fusion, and DRP1, which mediates mitochondrial fission. It is found that among these proteins the fission factor DRP1 was significantly down-regulated in RVFV infected cells, while the abundance of other proteins was unaffected (Figure 2C). Additionally, DRP1 down-regulation in RVFV infected cells showed a MOI-dependent phenotype (Figure S1B). DRP1 down-regulation was also observed in RVFV infected human Huh7 cells (Figure S1C) and A549 cells (Figure S1D), mouse bone marrow-derived macrophages (BMDMs) (Figure S1E) or liver samples harvested from RVFV-infected mice (Figure S1F). Since DRP1 functions in mitochondrial fission, it’s down-regulation might account for mitochondrial elongation triggered by RVFV infection. In line with this notion, infection with RVFVEGFP△NSs, which does not result in mitochondrial elongation (Figure 2B), did not lead to down-regulation of DRP1 in Huh7 cells (Figure 2D). Furthermore, exogenous expression of NSs leads to down-regulation of DRP1 protein level (Figure 2E). Taken together, these results suggested that RVFV infection induced NSs-dependent DRP1 down-regulation resulting in mitochondrial elongation.
DRP1 is cleaved by activated caspase during RVFV infection
We next investigated the molecular mechanisms underlying RVFV NSs-induced DRP1 down-regulation. The transcriptional level of DRP1 was not down-regulated during RVFV infection (Figure S2A), indicating down-regulation at the post-transcriptional level. We then used the inhibitors MG132 (proteasome inhibitor), Chloroquine (CQ) (autophagy-lysosome inhibitor) and Z-VAD-FMK (pan caspase inhibitor) to characterize the pathway that mediates DRP1 down-regulation. Neither MG132 (Figure 3A) nor CQ (Figure 3B) treatment inhibited DRP1 down-regulation in RVFV infected cells. In contrast, the pan caspase inhibitor Z-VAD-FMK treatment prevented DRP1 down-regulation in a dose-dependent manner (Figures 3C and 3D). These results suggested that RVFV infection triggered the caspase-mediated down-regulation of DRP1.
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DRP1 is cleaved by activated caspase during RVFV infection.
(A-C) Immunoblot analysis of DRP1 protein level in Huh7 cells infected or mock infected with RVFV for 2 h, followed by MG132 (5 μM) (A), CQ (10 μM) (B) or Z-VAD-FMK (20 μM) (C) treatment for 22 h.
(D) Immunoblot analysis of DRP1 protein level in THP-1PMA cells infected or mock infected with RVFV for 2 h, followed by Z-VAD-FMK treatment with the indicted concentration for 22 h.
(E) Immunoblot analysis of DRP1 cleavage in THP-1PMA cells infected or mock infected with RVFV for the indicted times.
(F) Immunoblot analysis of DRP1 cleavage in THP-1PMA cells infected or mock infected with RVFV for 2 h, followed by Z-VAD-FMK treatment in the indicted concentration for 22 h.
(G) Immunoblot analysis of caspases activation in THP-1PMA cells infected or mock infected with RVFV for 24 h.
Data are representative of three experiments with similar results.
Furthermore, we found that RVFV infection induced DRP1 cleavage to generate a cleaved DRP1 (∼60 kDa) (Figures 3E). Similar to RVFV infection, apoptotic inducer staurosporine (STS) can also induce DRP1 cleavage (Figures S2B). Cleavage of DRP1 showed a time- and MOI-dependent manner during RVFV infection (Figures 3E and S2C). Exogenously expressed DRP1, either through transient transfection (Figure S2D) or lentiviral transduction (Figure S2E), was also cleaved upon RVFV infection. And Z-VAD-FMK inhibited the formation of cleaved form of DRP1 in a dose-dependent manner (Figure 3F), further supporting that DRP1 might be cleaved by RVFV activated caspases. Indeed, RVFV infection induced the activation of multiple apoptotic caspases, including caspase-3, -6, -7, -8 and -9 (Figure 3G). In contrast, infection with RVFVEGFP△NSs did not trigger the activation of these caspases (Figure S2F). NSs expression alone triggered apoptotic caspases activation and PARP-1 cleavage (Figure S2G). These results together suggested that RVFV infection triggered NSs-dependent caspases activation that cleaved DRP1 in infected cells.
Apoptotic caspase-3, -6, -7 and -8 cleave DRP1 at the AEAD556 and D500FAD503 motifs
To analyze whether activated caspases cleave DRP1, we performed an in vitro caspase cleavage assay with purified caspases. Purified DRP1 was incubated with active human recombinant caspase-1, -4, -3, -6, -7, -8 or -9 protein (C1, C4, C3, C6, C7, C8 or C9). Immunoblotting analysis showed that among these caspases, apoptotic caspase-3, -6, -7 and -8, but not caspase-1, -4 or -9, cleaved DRP1 into a C terminal 20 kDa fragment recognized by the anti-strep antibody (Figure 4A). Pulldown assay showed that DRP1 interacted with caspase-3, -6, -7 and -8 protein, but not with EGFP (Figure 4B). The potential caspase cleavage sites on DRP1 were predicted with the CaspDB database (Kumar et al., 2014). The top five predicted sites were D221, D556, D260, D228 and D503 according to the probability score (Prob.score) (Figure 4C).
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Apoptotic caspase-3, -6, -7 and -8 cleave DRP1 at the AEAD556 and/or D500FAD503 motifs.
(A) Immunoblot analysis of DRP1 cleavage by the in vitro cleavage assay. The strep-tagged DRP1 protein was expressed and purified from HEK293T cells, and subjected to the in vitro cleavage assay with his-tagged caspase-1, 4, 3, 6, 7, 8 or 9 protein, followed by immunoblot analysis. Anti-strep antibody was used to determine the cleavage of DRP1. Anti-His antibody was used to identify caspases. The asterisks (*) represent non-specific bands. The blue solid rectangle represents long exposure.
(B) Immunoblot analysis of whole-cell lysates (WCL, bottom) and pull-down proteins with streptavidin magnetic beads (top) from HEK293T cells transfected with indicated plasmids for 24 h. Anti-V5 antibody was used to determine DRP1. Anti-strep antibody was used to identify EGFP or caspases.
(C) Prediction of the caspase cleavage sites for DRP1 using the CaspDB database.
(D) Immunoblot analysis of DRP1 cleavage in Huh7 cells. Cells were transfected with the DRP1- WT or DRP1-D556E mutant expressing plasmids, followed by RVFV infection or mock infection for 24 h.
(E) Immunoblot analysis of DRP1 cleavage by the in vitro cleavage assay. The strep-tagged DRP1-WT or DRP1-D556E proteins was expressed and purified from HEK293T cells, and subjected to the in vitro cleavage assay as described in (A).
(F) Immunoblot analysis of DRP1 cleavage by the in vitro cleavage assay. The strep-tagged DRP1-WT or the indicated DRP1 mutants, or his-tagged caspase-3 were expressed and purified from HEK293T cells, and incubated for the in vitro cleavage assay followed by immunoblot analysis. DRP1 fragments were detected with anti-strep antibody. Caspase-3 was detected by the anti-His antibody.
Data are representative of three experiments with similar results.
In the in vitro cleavage assay, caspases cleaved the C-terminal strep tagged DRP1 into two bands that can be recognized by the anti-strep antibody (Figure 4A). One of the cleaved bands was approximately 20 kDa, which corresponds to the potential cleavage site of D556. We therefore substituted the D556 of DRP1 with glutamate (E) to construct the mutant, DRP1-D556E, and transiently expressed the DRP1-D556E and DRP1-WT in Huh7 cells. Upon RVFV infection, DRP1-WT was cleaved, but no cleaved band was observed in DRP1-D556E expressing cells (Figure 4D), suggesting that D556 may be a key caspase cleavage site of DRP1. The in vitro caspase cleavage assay further showed that the DRP1-D556E mutant is resistant to caspase cleavage (Figure 4E), suggesting that caspase-3, -6, -7 and -8 can recognize and cleave DRP1 at the AEAD556 motif. Another cleavage band in the caspase-3 treated group was approximately 27 kDa, and there was a canonical caspase recognition motif (D500FAD503) in this region. We mutated D500 and D503 to glutamate (E) respectively or in combination on the basis of the D556E mutation. The in vitro caspase cleavage assay showed that the mutation of either D500 or D503 prevented caspase cleavage and the formation of the 27 kDa fragment (Figure 4F), suggesting that caspase-3 can also recognize and cleave DRP1 at the D500FAD503 motif and both D residues are important for this cleavage. Thus, apoptotic caspase-3, -6, -7 and -8 cleave DRP1 at the AEAD556 motif and caspase-3 has an additional cleavage site at the D500FAD503 motif (Figure S3).
Caspases-mediated DRP1 cleavage promotes anti-viral innate immunity
Mitochondria is a critical platform for regulating innate immune responses (Arnoult et al., 2011), so we reasoned that RVFV infection triggered DRP1 down-regulation and mitochondrial elongation may regulate anti-viral immune responses. To analyze this possibility, we first depleted DRP1 in THP-1 cells through knockdown (KD) by shRNA or knockout (KO) by sgRNA with CRISPR-Cas9. The RVFV-induced transcription of IFNβ and its downstream interferon-stimulated genes (ISGs), including RSAD2, CXCL10, ISG15, ISG54 and ISG56, were significantly enhanced in DRP1 knockout macrophages compared with the control cells (Figure 5A). Immunoblot analysis showed that DRP1 depletion though knockdown (Figure S4A) or knockout (Figure 5B) enhanced the phosphorylation of TBK1 and up-regulated the expression of ISGs after RVFV infection indicating elevated innate immune responses. In line with this, intracellular RVFV-NP protein expression (Figures S4A and 5B), or RVFV-NSs protein expression (Figure S4C) and infectious RVFV production (Figures 5C and S4B) were all significantly reduced in DRP1-depleted macrophages relative to the control cells. Treatment with DRP1 inhibitor mdivi-1, which inhibits DRP1 fission functionality, also inhibited RVFV replication in a dose-dependent manner (Figure S4D). Restriction of RVFV replication was also observed in mouse embryonic fibroblast (MEF) cells with DRP1 depletion by CRISPR-Cas9 mediated knockout (Figure S4E). These results indicated that DRP1 deficiency potentiated innate antiviral responses.
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DRP1 deficiency promotes antiviral innate immunity.
(A) qPCR analysis of the indicated genes in scramble or DRP1 knockout THP-1PMA cells infected or mock infected with RVFV for 12 h. ***P < 0.001 (Two-way ANOVA test).
(B) Immunoblot analysis of the indicated proteins in scramble or DRP1 knockout THP-1PMA cells infected or mock infected with RVFV for 24h.
(C) Focus forming assay to determine the titer from RVFV infected scramble or DRP1 knockout THP-1PMA cells infected for 24h. ***P < 0.001 (One-way ANOVA test).
Data are representative of three experiments with similar results.
In contrast, overexpression of DRP1 inhibited the up-regulation of IFNβ and its downstream representative ISGs (RSAD2, CXCL10, ISG15, ISG54 and ISG56) mRNA triggered by RVFV infection compared with the control cells (Figures 6A). DRP1 overexpression also reduced the phosphorylation of TBK1 and inhibited the up-regulation of ISGs after RVFV infection (Figure 6B). Consistently, intracellular RVFV-NP protein level (Figure 6B) and infectious RVFV production (Figure 6C) were significantly higher in DRP1-overexpressed macrophages relative to the control cells. These results suggested that over-expression of DRP1 dampened innate antiviral responses.
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Overexpression of DRP1 inhibits anti-viral innate immunity.
(A) qPCR analysis of the indicated genes in vector or DRP1-WT transduced THP-1PMA cells infected or mock infected with RVFV for 12 h. ***P < 0.001 (Two-way ANOVA test).
(B) Immunoblot analysis of the indicated proteins in vector or DRP1-WT transduced THP-1PMA cells infected or mock infected with RVFV for 24h.
(C) Focus forming assay to determine the titer from RVFV infected vector or DRP1-WT transduced THP-1PMA cells infected with RVFV for 24h. *P < 0.05, **P < 0.01, ***P < 0.001 (Student’s t test). Data are representative of three experiments with similar results.
To verify whether DRP1 cleavage by apoptotic caspases play a role in regulating immune responses, human DRP1-WT or caspase-resistant DRP1-3DE (a mutant of which the three D residues in the caspase cleavage motifs D500FAD503 and AEAD556 were substituted into E) was over-expressed in THP-1 cells. We found that cells expressing DRP1-3DE, which is resistant to caspase cleavage, showed further attenuated transcription of ISGs RSAD2, ISG15 and ISG54 mRNA compared with the DRP1-WT over-expressing cells, in response to RVFV infection (Figure 7A). Compared with DRP1-WT, DRP1-3DE also more strongly inhibited the phosphorylation of TBK1 and the up-regulation of ISGs after RVFV infection (Figures 7B and 7D). Additionally, intracellular RVFV-NP protein expression (Figures 7B and 7D) and infectious RVFV production (Figure 7C) were significantly higher in DRP1-3DE expressing macrophages relative to the DRP1-WT expressing cells. These data revealed that the caspase-resistant DRP1-3DE mutant showed more potent inhibition of antiviral immune responses compared with the DRP1-WT control, suggesting that caspases-mediated DRP1 cleavage plays a role in up-regulating anti-viral innate immune responses.
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Caspases-mediated DRP1 cleavage promotes antiviral innate immunity.
(A) qPCR analysis of the indicated genes in DRP1-WT or DRP1-3DE transduced THP-1PMA cells infected or mock infected with RVFV for 12 h. ***P < 0.001 (Two-way ANOVA test).
(B) Immunoblot analysis of the indicated proteins in DRP1-WT or DRP1-3DE transduced THP-1PMA cells infected or mock infected with RVFV for 24 h.
(C) Focus forming assay to determine the titer from RVFV infected DRP1-WT or DRP1-3DE transduced THP-1PMA cells infected with RVFV for 24 h. **P < 0.01 (Student’s t test).
(D) Immunoblot analysis of the indicated proteins in vector, DRP1-WT or DRP1-3DE transduced THP-1PMA cells infected or mock infected with RVFV for 24 h.
Data are representative of three experiments with similar results.
Caspases-mediated DRP1 cleavage leads to mitochondrial elongation and promotes MAVS aggregation
The above evidences suggest that the DRP1-depletion altered mitochondrial morphodynamics is linked with regulation of antiviral innate immunity. Activation and aggregation of the mitochondria-associated MAVS is a key event to mediate the activation of TBK1/IKKε and the down-stream immune responses (Chen et al., 2020; Zhang et al., 2020). We therefore analyzed whether mitochondrial elongation caused by caspases-mediated DRP1 depletion can facilitate MAVS aggregation to promote the antiviral innate immunity. Confocal fluorescence microscopy revealed that DRP1 depletion in macrophages caused significant MAVS aggregation on fused mitochondria (Figure 8A). Concomitantly, DRP1 deficiency in THP-1PMA cells either through CRISPR-Cas9 knockout showed significantly increased transcription of representative ISGs including RSAD2, ISG54 and CXCL10 mRNA compared with the scramble cells (Figure S5A). Similarly, DRP1 deficiency in MEF cells through knockout also elevated transcription of representative ISGs RSAD2, ISG56 and CXCL10 mRNA compared with the scramble cells (Figure S5B). RVFV infection of THP-1PMA led to caspase activation, DRP1 depletion and aggregation of MAVS (Figure 8B). DRP1 depletion further increased aggregation of MAVS upon SeV (Figure 8C) or RVFV infection (Figure 8D). Simultaneous knock-out (dKO) of DRP1 and MAVS strongly attenuated the elevated antiviral immune responses observed in RVFV infected DRP1 KO cells and promoted viral replication (Figures 8E and 8F). These data suggest that DRP1 depletion promotes antiviral innate immunity, at least in part, through inducing MAVS aggregation and activation. Altogether, these data indicated that virus infection can trigger caspases-mediated DRP1 depletion leading to mitochondrial elongation, which enhanced MAVS aggregation to elevate the antiviral immune responses.
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Caspases-mediated DRP1 cleavage induces mitochondrial elongation to promote MAVS aggregation and immune responses.
(A) Immunofluorescence analysis of MAVS aggregation in scramble or DRP1 knockout THP-1PMA cells. Mitochondria were labeled with anti-Tom20 antibody (red), MAVS was labeled with anti-MAVS antibody (green) and Nuclei were stained with DAPI (blue). Scale bars, 10 μm.
(B) Immunoblot analysis of caspase-8 activation, DRP1 protein level and MAVS aggregation in THP-1PMA cells infected or mock infected with RVFV or 24 h.
(C) Immunoblot analysis of MAVS aggregation in scramble or DRP1 knockout HEK293T cells. HEK293T cells were transfected with HA-tagged MAVS (HA-MAVS) plasmid for 24 h, followed by SeV infection for 12 h.
(D) Immunoblot analysis of MAVS aggregation in scramble or DRP1 knockout THP-1PMA cells infected or mock infected with RVFV for 24 h.
(E) Immunoblot analysis of the indicated proteins in DRP1 knockout or DRP1 and MAVS double knockout THP-1PMA cells infected with RVFV for 24 h.
(F) Focus forming assay to determine the titer from RVFV infected DRP1 knockout or DRP1 and MAVS double knockout THP-1PMA cells infected for 24 h. ***P < 0.001 (One-way ANOVA test). Data are representative of three experiments with similar results.
Caspases-mediated DRP1 depletion and elevation of immune responses is conserved among different viruses infection
Next, we analyzed whether caspase-dependent DRP1 depletion and promotion of innate immune responses is a general mechanism during virus infection. For this purpose, H1N1 and SeV were selected as additional RNA model viruses, and HSV-1 was selected as a DNA model virus. THP-1PMA cells were infected with H1N1, SeV or HSV-1 and the activation of multiple apoptotic caspases, including caspase-3, -6, -7, -8 and -9 were observed (Figures 9A-9C). Concomitantly with caspases activation, the cleavage of DRP1 was observed in H1N1, SeV or HSV-1 infected cells (Figures 9A-9C). Mitochondrial elongation was also observed in H1N1, SeV or HSV-1 infected cells (Figure 9D). Similar with RVFV, H1N1, SeV or HSV-1 infection induced DRP1 depletion was prevented by Z-VAD-FMK treatment (Figures 9E-9F). Additionally, infectious H1N1 or HSV-1 titers were all significantly reduced in DRP1-depleted macrophages relative to the control cells (Figures 9H and 9I), suggesting that DRP1 depletion may pose restriction effect on H1N1 and HSV-1 replication, similar with the case of RVFV infection. These results suggested that the caspase-triggered DRP1 depletion and elevation of immune responses is a general mechanism occurring during virus infection (Figure S6).
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Multiple viruses trigger caspases-mediated DRP1 cleavage.
(A-C) Immunoblot analysis of caspases activation and DRP1 cleavage in THP-1PMA cells infected or mock infected with H1N1 (A), SeV (B) or HSV-1 (C) for 24 h. The asterisks (*) represent non-specific bands.
(D) Mitochondria were visualized by immunofluorescence using confocal microscopy. THP-1PMA cells were infected or mock infected with RVFV, H1N1, SeV or HSV-1 for 18 h, respectively. Mitochondria were labeled with anti-Tom20 (red) antibody and Nuclei were stained with DAPI (blue). Scale bars, 7.5 μm.
(E) Immunoblot analysis of DRP1 cleavage in THP-1PMA cells infected or mock infected with H1N1 for 2 h, followed by Z-VAD-FMK treatment for 22 h.
(F) Immunoblot analysis of DRP1 cleavage in THP-1PMA cells infected or mock infected with SeV for 2 h, followed by Z-VAD-FMK treatment for 10 h.
(G) Immunoblot analysis of DRP1 cleavage in THP-1PMA cells infected or mock infected with HSV-1 for 2 h, followed by Z-VAD-FMK treatment for 22 h.
(H-I) Plaque assay results determining the titers from virus infected scramble or DRP1 knockout THP-1PMA cells infected with H1N1 (H) or HSV-1 (I) for 24 h. ***P < 0.001 (One-way ANOVA test).
Data are representative of three experiments with similar results.
Discussion
Virus triggered apoptotic caspase activation has recently been shown to dampen antiviral innate immunity via the cleavage of multiple key immune molecules, such as cGAS, MAVS, and IRF3 (Ning et al., 2019). Whether apoptotic caspases can promote innate immune responses to inhibit viral infection is currently unknown. Here, we demonstrated that virus-activated apoptotic caspases, including caspase-3, -6, -7 and -8, cleave and deplete the mitochondrial fission factor DRP1 leading to mitochondrial elongation, which in turn results in increased MAVS aggregation and enhanced antiviral innate immune signaling. This mitochondrial elongation driven elevation of innate immune responses can occur during multiple viruses infection and poses a broad antiviral effect against both RNA and DNA viruses. Thus, while the virus can employ host caspase activity to facilitate it’s infection, the activated caspases can also promote immune responses to inhibit viral replication serving as a host defense mechanism. It has been recognized that apoptotic caspases-mediated suicidal cell death limits virus replication through eliminating the niche of viral production. Thus, it can be speculated that apoptotic caspases can pose two-modes of anti-viral effects through cleaving DRP1 and mediating mitochondrial elongation to elevate the immune responses and, in the meantime, depleting the virus infected cells.
The dynamic balance between fission and fusion plays a critical role in maintaining the functionality of mitochondria. DRP1 is the major regulator of mitochondrial fission, and its activity is regulated by multiple post-translational modifications, including phosphorylation, ubiquitination, sumoylation, and S-nitrosylation (Khan et al., 2015). Previous reports showed that viruses can dampen the activity of DRP1 by modulating its phosphorylation state. For example, SeV infection-induced TBK1-mediated DRP1 phosphorylation and abrogates its mitochondrial fission function, leading to mitochondrial elongation (Chen et al., 2020). Moreover, DENV NS4B inhibits phospho-S616-dependent activation of DRP1 and its subsequent translocation to mitochondria, thus inducing mitochondrial elongation in virus-infected cells (Chatel-Chaix et al., 2016). Here, we discovered that cleavage by multiple caspases is a novel mechanism to dampen DRP1 functionality and enhance innate immune responses. This new layer of regulation adds to the complex regulation mechanisms of DRP1 and further indicates its critical role in maintaining mitochondrial morphodynamics and immune responses.
It is found that multiple caspases, including caspase-3, -6, -7 and -8, are capable of cleaving DRP1. Among them, caspase-8 is the initiator apoptotic caspase, while caspase-3, -6 and -7 belong to the executive apoptotic caspases. In addition, multiple sites in DRP1 are sensitive to caspase cleavage, including the D500FAD503 and AEAD556 motifs. The susceptibility of DRP1 to cleavage by different types of caspases and the presence of multiple caspase-sensitive sites in DRP1 ensure the efficient cleavage of DRP1 under different contexts. Indeed, multiple viruses and other pathogens trigger apoptotic caspases activation during infection through diverse mechanisms (Fang and Peng, 2021; Li et al., 2020b). The results that, besides RVFV, H1N1, SeV and HSV-1 infection triggered caspase-dependent cleavage of DRP1 further support the notion. It can be speculated that DRP1 potentially serves as a common sensor of pathogen invasion through sensing pathogen activated caspases and promotes innate immunity. This might be a general host defense mechanism occurring under different pathogen invasion contexts.
In summary, these results revealed a novel apoptotic caspase-DRP1 axis in promoting anti-viral immune responses through regulating mitochondrial morphodynamics. This indicates that apoptotic caspases activation can have both pro- or anti-viral effects depending on the cleaved substrates. During the course of virus infection, it is likely that the balance between pro- or anti-viral effects is controlled by multiple viral and host factors. The overall effect of how caspase activation regulates viral infection and pathogenesis may be context-dependent and awaits further characterization for different viruses. Nevertheless, the critical roles of caspases in regulating cell death and immune responses may provide novel targets for developing anti-viral therapeutics.
Materials and Methods
Plasmids
cDNAs encoding human caspase-3 (CCDS3836.1) was synthesized by Tsingke (Wuhan, China) and cloned into pRK plasmid with a C-terminal His tag. Plasmids, including C-terminal strep-tagged human DRP1 (hDRP1) and viral proteins of RVFV (NSs, NP, NSm, Gn, Gc and Pol), were constructed by standard molecular biology techniques. Point mutants were generated by using the ClonExpress II One Step Cloning Kit (#C112-01, Vazyme, China) and the construct coding the wild-type DRP1 as template. Each construct was confirmed by sequencing.
Antibodies, recombinant proteins and reagents
The anti-V5 (#V8012) antibody was purchased from Sigma (St. Louis, MO, USA). The anti-strep (#A00626) antibody was purchased from GenScript (Nanjing, China). The anti-MAVS (#sc-166583) antibody used in immunofluorescence analysis was purchased from Santa Cruz Biotechnology (Delaware, USA). The anti-Tom20 (#ab209606) was purchased from Abcam (Cambridge, UK). The anti-DRP1 (#5391), anti-caspase-3 (#9662), anti-cleaved caspase-3 (#9661), anti-caspase-6 (#9762), anti-cleaved caspase-6 (#9761), anti-caspase-7 (#9492), anti-caspase-8 (#9746), anti-cleaved caspase-8 (#9496), anti-caspase-9 (#9502), anti-PARP1 (#9542), anti-MAVS (#24930), anti-TBK1 (#38066) and anti-Phospho-TBK1/NAK (Ser172) (#5483) antibodies were obtained from Cell Signaling Technology (Beverly, MA, USA). The anti-MFN2 (#A10175) and anti-OPA1 (#A9833) antibodies were obtained from ABclonal. The anti-His tag (#66005-1-Ig), anti-MFN1 (#13798-1-AP), anti-RSAD2 (#28089-1-AP), anti-MAVS (#14341-1-AP) used in immunoblot analysis, anti-alpha Tubulin (#14555-1-AP), anti-GAPDH (#60004-1-Ig), goat anti-mouse (#SA00001-1) and goat anti-rabbit (#SA00001-2) IgG-horseradish peroxidase (HRP) secondary antibodies were purchased from Proteintech (Wuhan, China). The rabbit anti-RVFV-NP and rabbit anti-RVFV-NSs antibodies were made in-house. Alexa Fluor 488 goat anti-mouse IgG (H + L) (#A11029) and Alexa Fluor 568 goat anti-rabbit IgG (H + L) (#A11036) were purchased from Thermo Fisher.
Active human recombinant caspase-4 (#1084) and caspase-7 (#1087-25) proteins were purchased from Biovision. Active human recombinant caspase-1 (#268-10011-1), caspase-6 (#268-10016-1) and caspase-8 (#268-10018-1) proteins were obtained from Raybiotech. Active human recombinant caspase-3 (#CC119) and caspase-9 (#CC120) proteins were purchased from Merck.
PMA (#P1585) was purchased from Sigma-Aldrich (St. Louis, MO, USA). Recombinant murine M-CSF (#315-02) was obtained from PeproTech. MG132 (#S2619), Chloroquine (#S4430), Z-VAD-FMK (#S7023) and Mdivi-1 (#S7162) were obtained from Selleck (Houston, TX, USA). Staurosporine (#HY-15141) was purchased from MedChemExpress (New Jersey, USA). DAPI (#C1002) was purchased from Beyotime (Shanghai, China).
Cell lines
The HEK293T, BHK-21, Vero, A549, and THP-1 cell lines were purchased from American Type Culture Collection (ATCC). Huh7 cell was obtained from China Center for Type Culture Collection and the MDCK cell line was provided by Dr Jianjun Chen (Wuhan institute of virology, China). Adherent cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM; Gibco) supplied with 10% fetal bovine serum (FBS; Gibco) and 1% Pen Strep antibiotics (Gibco), THP-1cells were cultured in RPMI 1640 (Gibco) containing 10% FBS (Gibco) and 1% Pen Strep (Gibco). All cells were cultured at 37°C in a humidified 5% CO2 incubator.
Viruses and titer determination
Recombinant wild-type RVFV (RVFV) and the NSs deleted RVFV (RVFVEGFP△NSs) were rescued by T7 RNA polymerase-driven reverse genetics system as previously described (Li et al., 2019). And RVFV strains were propagated in BHK-21 cells under Biosafety Level-3 (BSL-3) conditions. All RVFV-related experiments were performed at the BSL-3 laboratory of the Wuhan Institute of Virology, Chinese Academy of Sciences (Wuhan, China) according to the institutional guidelines.
Titer of RVFV was determined by focus forming assay on Vero cells as previously described (Li et al., 2020a). Briefly, confluent Vero monolayers were infected with 10-fold dilutions of virus and incubated at 37°C for 1 h, then culture medium was replaced by DMEM containing 2% FBS and 1.1% (wt/vol) carboxymethyl-cellulose/ methylcellulose. After 3 days of incubation, cells were fixed with 3.6%-4% formaldehyde. And then, Foci were visualized by DAB staining after two-step immunostaining with an antibody against viral protein NP and an anti-rabbit horseradish peroxidase-conjugated secondary antibody.
Plaque assays were performed on Vero cells or MDCK cells to determine the titer of HSV-1 or H1N1, respectively. For HSV-1, confluent Vero monolayers were infected with 10-fold dilutions of virus and incubated at 37°C for 1 h, then culture medium was replaced by DMEM containing 2% FBS. After 48 h of incubation, cells were stained with 0.5% crystal violet after fixing with 3.6%-4% formaldehyde and plaques were counted. For H1N1, we referred to the protocol of Galani et al (Galani et al., 2022).
Liver samples of mice
BALB/c mice were purchased from Charles River Laboratories (Beijing, China). 6-week-old BALB/c mice were intraperitoneally injected or mock injected with 1000 plaque forming unit (PFU) of RVFV in 100 µL of PBS. Mice were monitored for 3 days and Liver samples were harvested for Immunoblot analysis. Animal experiments were performed in agreement with Regulations for the Administration of Affairs Concerning Experimental Animals in China. The procedures were approved by the Laboratory Animal Care and Use Committee of the Wuhan Institute of Virology, Chinese Academy of Sciences (Wuhan, China). The approval code was WIVA38202002.
Cell differentiation
THP-1 cells were differentiated into macrophages by treatment with 40 ng/mL of PMA in RPMI 1640 (Gibco) containing 10% FBS (Gibco) and 1% Pen Strep (Gibco) at 37°C for 24 h, and then cells were cultured in RPMI 1640 (Gibco) containing 10% FBS (Gibco) and 1% Pen Strep (Gibco) without PMA at 37°C for 24 h.
Generation of BMDMs
Bone marrow cells were isolated from tibiae and femur of mice. The bone marrow cells were cultured in RPMI 1640 medium containing 10% FBS, 1% Pen Strep and 20ng/ml M-CSF at 37°C in a humidified 5% CO2 incubator for 3-5 days to generation of BMDMs.
Knockdown, knockout, double-knockout and overexpression
Knockdown of DRP1 with shRNA was done by lentiviral transduction of THP-1 cells. Knockout of DRP1 or double Knockout of DRP1 and MAVS with sgRNA and Cas9 was accomplished by transduction of THP-1 cells. Overexpression of DRP1-WT or DRP1 mutant with coding sequence was done by lentiviral transduction of THP-1 cells. Sequences of targeting shRNAs and sgRNAs used in this study were listed in Table S1.
Fluorescence and Immunofluorescence Microscopy
THP-1PMA cells, Huh7 cells or A549 cells were infected or mock infected with RVFV, and then fixed with 4% paraformaldehyde (PFA) at room temperature for 30 min, permeabilized with 0.3% (vol/vol) Triton X-100 for 20 min, blocked in 3% bovine serum albumin in PBS for 30 min, and incubated sequentially with the indicted primary antibodies at room temperature for 1h, followed by incubation with the correspondingly fluorescent-dye conjugated secondary antibodies. Cells were stained with DAPI, mounted with ProLongTM Gold antifade reagent (Invitrogen, San Diego, CA, USA), and then analyzed using confocal microscope (Andor Dragonfly 202). Images were processed by Imaris.
Transmission Electron Microscope (TEM)
THP-1PMA cells were infected or mock infected with RVFV at MOI = 1 for 30 h. Cells were fixed with 2.5% (w/v) glutaraldehyde in 0.1 M sodium chloride and and processed for Electron Microscopy (EM). The mitochondria were observed under a transmission electron microscope (FEI Tecnai G2 microscope at 200 kV).
Pulldown assay
HEK293T cells were transfected with the indicated plasmids for 24 h. The cells were washed twice with PBS, lysed with RIPA (weak) buffer (#P0013D, Beyotime, Shanghai, China) and rotated for 30 min at 4°C. After centrifugation at 16000× g for 20 min, the whole cell lysates were incubated with streptavidin magnetic beads (#2-4090-010, Iba-Lifesciences, Germany) and rotated overnight at 4°C on a rotator. After washing three times with PBST, the pull-down complexes were eluted with 2× SDS sample loading buffer for 10 min at 95°C and applied to immunoblot analysis.
Immunoblot Analysis
Cells were lysed with buffer (#P0013, Beyotime, Shanghai, China). Cell lysates were subjected to SDS-polyacrylamide gel electrophoresis (PAGE) then transferred to polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). Proteins were incubated with primary antibodies, then secondary horseradish peroxidase-conjugated goat anti-rabbit/mouse IgG. Protein bands were detected by an enhanced chemiluminescence (ECL) kit (Millipore, Billerica, MA, USA) using a Chemiluminescence Analyzer (Chemiscope600pro, Shanghai, China).
In vitro cleavage assay
In vitro protease cleavage experiments were performed as previously described (Wang et al., 2017). Briefly, recombinant or purified caspase was incubated with DRP1-WT or DRP1 mutant in cleavage buffer (100 mM HEPES, 10% (w/v) sucrose, 0.1% (w/v) CHAPS, PH 7.0, 10mM DTT) at 37°C for 2 h and then samples were applied to immunoblot analysis.
Semi-denaturing detergent agarose gel electrophoresis (SDD-AGE)
Cells were lysed with NP-40 buffer (#P0013F, Beyotime, Shanghai, China) and mixed with 5× sample buffer (2.5× TBE, 50% glycerol, 10% SDS and 0.0125% bromophenol blue). The samples were loaded onto a 1.5% agarose gel in 1× TBE containing a final concentration of 0.1% SDS, electrophoresed at a constant voltage of 100 V at 4°C until the bromophenol blue dye reached the bottom of the agarose gel, and then transferred to PVDF membranes for immunoblot analysis.
RNA isolation and Quantitative RT-PCR analysis
Total RNAs were extracted with RNAiso Plus (Takara, Japan) following the manufacturer’s instructions. qRT-PCR was performed with a two-step procedure using the HiScript II 1st Strand cDNA Synthesis Kit (+gDNA wiper) (#R212-01, Vazyme, China) and ChamQ Universal SYBR qPCR Master Mix (#Q711-02/03, Vazyme, China). Data shown are the relative abundance of the indicated mRNA normalized to that of GAPDH. Primer sequences are available upon request. Gene-specific primer sequences were listed in Table S2.
Statistical analysis
All data are presented as mean values ± SD of three or more experiments. Statistical significance was determined with Student’s t test, One-way ANOVA or Two-way ANOVA as showed in figure legends with P < 0.05 considered statistically significant. ns, not significant; *P < 0.05, **P < 0.01, ***P < 0.001.
Software
Data were analyzed with GraghPad prism 9. Images were processed by Imaris.
Acknowledgements
This work was supported by the National Key R&D Program of China (2021YFC2300700), National Science and Technology Major Project (No. 2018ZX10101004001005), National Natural Science Foundation of China (numbers 32070179). We thank Dr. Qinxue Hu (Wuhan Institute of Virology), Dr. Jianjun Chen (Wuhan Institute of Virology) and Dr. Yuchen Xia (Wuhan University) for help with materials, and Dr. Leike Zhang (Wuhan Institute of Virology) and Dr. Peng Zhou (Wuhan Institute of Virology) for their advice and guidance. We thank Hao Tang, Jun Liu and Jia Wu from BSL-3 Laboratory of Wuhan Institute of Virology for their critical support. We thank Ding Gao and Pei Zhang from Center for Instrumental Analysis and Metrology at Wuhan Institute of Virology for their help with confocal microscopy and transmission electron microscope experiments.
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