猪圆环病毒3型衣壳蛋白通过抑制雷帕霉素靶蛋白的磷酸化诱导HEK293T细胞自噬

Porcine circovirus 3 capsid protein induces autophagy in HEK293T cells by inhibiting phosphorylation of the mammalian target of rapamycin 猪圆环病毒3型衣壳蛋白通过抑制雷帕霉素靶蛋白的磷酸化诱导HEK293T细胞自噬 1 2 first-author 1 2 1 2 corresp ‡Corresponding Author ‡Corresponding Author †E-mail:whfang@zju.edu.cn †E-mail:whfang@zju.edu.cn whfang@zju.edu.cn Institute of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, China Institute of Preventive Veterinary Medicine, Zhejiang University, Hangzhou 310058, China Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Hangzhou 310058, China Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine, Hangzhou 310058, China Porcine circovirus 3 (PCV3) has been detected in major pig-producing countries around the world since its first report in the US in 2016. Most current studies have focused on epidemiological investigations and detection methods of PCV3 because of lack of live virus strains for research on its pathogenesis in porcine cells or even in pigs. We constructed a recombinant plasmid pCMV-Cap carrying the PCV3 orf2 gene to investigate the effects of capsid (Cap) protein expression on autophagic response in human embryonic kidney cell line 293T (HEK293T). We demonstrate that PCV3 Cap protein induced complete autophagy shown as formation of autophagosomes and autophagosome-like vesicles as well as LC3-II conversion from LC3-I via inhibiting phosphorylation of the mammalian target of rapamycin (mTOR) in HEK293T cells. The ubiquitin–proteasome pathway is also involved in the autophagy process. These findings provide insight for further exploration of PCV3 pathogenetic mechanisms in porcine cells. 目的 2 探明猪圆环病毒3型衣壳(Cap)蛋白如何诱导细胞自噬. 创新点 2 首次证明猪圆环病毒3型Cap蛋白诱导细胞自噬,泛素-蛋白酶体途径也参与其中. 方法 2 构建过表达猪圆环病毒3型Cap蛋白的真核表达载体,转染HEK293T细胞,采用免疫印迹检测LC3、p62和mTOR等自噬通路的关键分子.利用激光扫描共聚焦显微镜和透射电镜,观察表达Cap蛋白的细胞是否有EGFP-LC3B点状聚集和自噬泡生成.利用氯喹抑制溶酶体酸化,探究衣壳蛋白是否诱导完整的自噬流.利用MG132抑制蛋白酶体途径,探究泛素-蛋白酶体途径是否参与自噬过程. 结论 2 猪圆环病毒3型Cap蛋白通过抑制雷帕霉素靶蛋白的磷酸化诱导HEK293T细胞自噬,泛素-蛋白酶体途径也参与这一过程. Porcine circovirus 3 (PCV3) Capsid (Cap) protein Autophagy 猪圆环病毒3型(PCV3) 衣壳(Cap)蛋白 自噬 Introduction 1 Porcine circoviruses (PCVs) are single-stranded, non-enveloped circular DNA viruses, belonging to the genus Circovirus in the family Circoviridae (Ellis, 2014 2014 ). Three types of PCVs (PCV1 (Tischer et al., 1974 1974 ), PCV2 (Allan et al., 1998 1998 ), and PCV3 (Phan et al., 2016 2016 ; Palinski et al., 2017 2017 )) have been reported in pigs. PCV1 was a contaminant of the PK-15 cells and nonpathogenic to pigs (Tischer et al., 1974 1974 ), while PCV2 is associated with porcine circovirus-associated diseases (PCVADs) and poses a serious threat to the pig industry (Ellis, 2014 2014 ). Since the first report in the US in 2016 (Phan et al., 2016 2016 ), PCV3 has been discovered in major pig-producing countries (Faccini et al., 2017 2017 ; Ku et al., 2017 2017 ; Kwon et al., 2017 2017 ; Stadejek et al., 2017 2017 ; Franzo et al., 2018 2018 ; Hayashi et al., 2018 2018 ; Kedkovid et al., 2018 2018 ; Tochetto et al., 2018 2018 ; Ye et al., 2018 2018 ; Yuzhakov et al., 2018 2018 ). The PCV3 genome is 2000 nucleotides in length with three predicted open reading frames (ORFs). The gene orf1 encodes the replicase (Rep) protein of 296 amino acids (aa) and orf2 , the capsid (Cap) protein of 241 aa, while the initiation codon of orf3 and the function of its encoded protein are not yet clear (Phan et al., 2016 2016 ). Cap is the major structural protein of PCV3 and shares 24% and 26% identity to that of PCV1 and PCV2, respectively, at the amino acid level (Phan et al., 2016 2016 ; Palinski et al., 2017 2017 ). A recent report indicates that PCV3 Cap inhibited type I interferon signaling by interacting with signal transducer and activator of transcription 2 (STAT2) (Shen et al., 2020 2020 ). Pigs infected with PCV3 are associated with clinical symptoms, such as porcine dermatitis and nephropathy syndrome (PDNS), reproductive failure, multi-systemic inflammation, and cardiac pathology (Phan et al., 2016 2016 ; Palinski et al., 2017 2017 ). However, PCV3 is also found in pigs with no clinical signs nor disease conditions (Stadejek et al., 2017 2017 ; Zheng et al., 2017 2017 ). Autophagy is a highly conserved recycling process in eukaryotes, in which double-membrane autophagosomes sequester proteins, cytoplasmic organelles, and macromolecules, and fuse with lysosomes or vacuoles for degradation and turnover (He and Klionsky, 2009 2009 ; Parzych and Klionsky, 2014 2014 ). It is a dynamic multi-step cellular process from nucleation to formation of autophagosomes and to degradation upon fusion with lysosomes that is termed “autophagy flux” to reflect the progression of the complete autophagic process (Mizushima et al., 2010 2010 ; Parzych and Klionsky, 2014 2014 ). Autophagy is induced by intra-or extra-cellular stresses or signals such as endoplasmic reticulum (ER) stress, starvation, and bacterial or viral infections (He and Klionsky, 2009 2009 ), and regulated by mammalian target of rapamycin (mTOR)-dependent pathway and mTOR-independent pathway (He and Klionsky, 2009 2009 ; Ravikumar et al., 2010 2010 ; Sarkar, 2013 2013 ; Parzych and Klionsky, 2014 2014 ). mTOR is a serine/threonine kinase belonging to the phosphoinositide-3-kinase (PI3K)-related kinase (PIKK) family and forms two distinct protein complexes, namely mTOR complex 1 (mTORC1) and 2 (mTORC2) (Saxton and Sabatini, 2017 2017 ). mTORC1 is the master regulator of autophagy, and inhibition of mTORC1 is needed for initiation of the autophagy process, including nucleation, elongation, and maturation of autophagosomes via downstream targets, such as uncoordinated (UNC)– 51-like-kinase 1 and 2 (ULK1/2), autophagy-related gene 13 (ATG13), and others (Dossou and Basu, 2019 2019 ). Viruses have evolved diverse strategies to interact with the autophagic machinery or subvert autophagy to counteract the host antiviral effects (Yin et al., 2019 2019 ). Some viruses, such as classical swine fever virus (Pei et al., 2014 2014 ) and pseudorabies virus (Xu et al., 2018 2018 ), can induce complete autophagy during infection. There are viruses that induce incomplete autophagy. Rabies virus infection, for instance, induced incomplete autophagy shown as increased accumulation of autophagosomes due to inhibition of the autophagy flux (Liu et al., 2017 2017 ). Hepatitis B virus infection led to incomplete autophagy by impairing lysosomal acidification (Zhong et al., 2015 2015 ). Coxsackievirus B3 infection inhibited autophagic flux by limiting the fusion of autophagosomes with lysosomes (Mohamud et al., 2018 2018 ). In addition, some viruses can inhibit autophagy to facilitate viral replication. African swine fever virus infection inhibited autophagosome formation in Vero cells by interaction of its A179L protein, a viral homolog of B-cell lymphoma 2 (Bcl2), with Beclin 1 (Hernaez et al., 2013 2013 ). Thus the autophagy process in the host varies among viruses. A better understanding of the interactions between host autophagic responses and viruses will provide insight into the pathogenesis of viruses and an avenue for the development of antiviral drugs. Our laboratory and other researchers have recently proved that PCV2 induces complete autophagy, most likely by its Cap protein, and the virus employs autophagy machinery to enhance its replication in PK-15 cells (Zhu et al., 2012a 2012a , 2012b 2012b ; Qian et al., 2017 2017 ; Zhai et al., 2019 2019 ). Although a recombinant PCV3 virus has been rescued (Jiang HJ et al., 2019 2019 ), most of the recent studies on PCV3 focus on epidemiological investigations and detection methods, for the reason that there are no live PCV3 virus strains for research. There has been no report so far on the involvement of autophagy in PCV3 pathogenesis. In the absence of PCV3 virus for research, we constructed a recombinant plasmid pCMV-Cap carrying the orf2 gene of PCV3 to investigate whether the Cap protein induces a cellular autophagic response. Here, we provide the first evidence that the Cap protein of PCV3 induced autophagy by inhibiting phosphorylation of mTOR in human embryonic kidney cell line 293T (HEK293T). Materials and methods 1 Cell culture 2 HEK293T cell line was used and the cells were cultured at 37 °C with 5% CO 2 in Dulbecco’s modified Eagle’s medium (DMEM; HyClone, Thermo Scientific, MA, USA) containing 10% heat-inactivated fetal bovine serum (FBS; Gibco, Thermo Scientific) with 1% L -glutamine, 1% nonessential amino acids, and antibiotics (100 U/mL penicillin G and 100 μg/mL streptomycin). Plasmid construction and transfection 2 The full-length of orf2 gene encoding Cap of the PCV3 strain (PCV3-US/MO2015, GenBank accession No. KX778720.1) was synthesized by BioSune Co., Ltd. (Shanghai, China), cloned into the pCMV plasmid (Clontech, CA, USA) using ClonExpress II One Step Cloning Kit (Vazyme, Nanjing, China), and confirmed by DNA sequencing (BioSune). Delivery of the recombinant and control plasmids into HEK293T cells was performed by using Lipofectamine 3000 (Invitrogen, CA, USA) according to the manufacturer’s instructions. Construction of the plasmid pcDNA3.1-EGFP-LC3B (pEGFP-LC3B) has been described elsewhere (Zhu et al., 2012a 2012a ). All the primers used in this study are listed in Table 1 1 . Cap: capsid; F: forward; R: reverse Primer Sequence (5'→3') Cap-F CCCAGGCCCGAATTCATGAGACACAGAGCTATATTCAGAA Cap-R CCCCGCGGCCGCTTACTTATCGTCGTCATCCTTGTAATCTCCACCGCTTCCACCGAGAACGGACTTGTAACGAATC Antibodies and chemicals 2 Rabbit anti-PCV3 Cap polyclonal antibody was produced in our laboratory. Antibodies against β-actin, sequestosome 1 (SQSTM1/p62) and mTOR were purchased from DiagBio Technology Co., Ltd. (Hangzhou, China). Antibodies against lipid-conjugated 3 (LC3A/B) and phosphorylated mTOR (p-mTOR; phospho S2448) were purchased from Cell Signaling Technology (Danvers, MA, USA). Alexa fluor 555-conjugated goat anti-rabbit IgG, goat anti-rabbit IgG, and goat anti-mouse IgG secondary antibodies conjugated to horseradish peroxidase (HRP) were purchased from Sangon Biotech (Shanghai, China). The chemicals rapamycin (Rapa; as autophagy inducer; Merck, Germany), chloroquine (CQ; as lysosomal inhibitor; MCE, USA), and MG132 (as proteasome inhibitor; MCE) were used in appropriate experiments. Nuclear stain 2-(4-amidinophenyl)-6-indolecarbamidine dihydrochloride (DAPI) was purchased from Beyotime (Hangzhou, China). Protein extraction and western blotting 2 Western blotting was performed to detect changes of the expression of target proteins in HEK293T cells transfected with plasmids or treated with chemicals. Briefly, cells in 24-well plates were harvested at indicated time points by using a pre-cooled lysis buffer (Beyotime) supplemented with protease inhibitor cocktail (Roche, Mannheim, Germany). The cell lysates were centrifuged and the supernatant samples were collected. Protein concentration in the samples was quantified using the Bradford assay kit (Beyotime). Equal amounts of the protein samples were loaded and separated on 8%–15% (8% (0.08 g/mL) for mTOR and p-mTOR; 12% (0.12 g/mL) for β-actin, p62, and Cap; 15% (0.15 g/mL) for LC3) sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gels after boiling for 10 min in the presence of the loading buffer. The proteins in the gels were transferred to polyvinylidene difluoride (PVDF) membranes (Merck Millipore, Darmstadt, Germany), blocked at 37 °C for 1 h with Tris-buffered saline (25 mmol/L Tris at pH 7.5, 150 mmol/L NaCl) containing 0.05% Tween-20 (TBST) and 5% skim milk, and incubated with different primary antibodies at 4 °C overnight. The membranes were washed five times with TBST and incubated at 37 °C for 1 h with HRP-conjugated goat anti-rabbit or goat anti-mouse antibodies. The blots were visualized using the SuperSignal West Pico chemiluminescent substrate (Thermo Scientific), and images were captured with the Gel 3100 Chemiluminescent Imaging System (Sagecreation, Beijing, China) as described (He et al., 2019 2019 ). The bands were quantified by densitometric analysis using the ImageJ software (National Institutes of Health, USA). Ratios of the target proteins to the reference proteins were used for relative quantitative purposes. Confocal microscopy 2 For detection of autophagosomes by confocal microscopy, HEK293T cells were cultured on coverslips in 29-mm dishes (Cellvis, USA). Cells were co-transfected with the plasmids pEGFP-LC3B and pCMV-Cap or the control plasmid pCMV, or transfected only with pEGFP-LC3B (mock) or treated with 2 μmol/L Rapa after 5 h of transfection with pEGFP-LC3B (positive control). After 36 h of transfection, cells were washed with phosphate-buffered saline (PBS; pH 7.4), fixed with 4% paraformaldehyde fix solution for 30 min at room temperature, permeabilized with 0.1% Triton X-100 for 15 min, and then blocked with 5% skim milk for 1 h at 37 °C. Following this, the cells were immuno-stained with rabbit anti-PCV3 Cap polyclonal antibody for 1 h at 37 °C, washed with PBS, and incubated with Alexa Fluor 555-conjugated goat anti-rabbit IgG for 1 h at 37 °C. Nuclei were counterstained with DAPI. Fluorescent EGFP-LC3B punctae were observed and captured by laser scanning confocal microscopy (IX81-FV1000; Olympus, Hamburg, Germany) as described (Shan et al., 2018 2018 ). Transmission electron microscopy 2 For ultrastructural visualization of autophagy, HEK293T cells transfected with pCMV-Cap, Rapa-or mock-treated were harvested by centrifugation and washed with PBS. Samples were fixed in 2.5% glutaraldehyde in phosphate buffer (PB, 0.1 mol/L, pH 7.0) at 4 °C overnight and post-fixed with 1% OsO 4 in PB for 1 h. The samples were then dehydrated in graded ethanol (30%, 50%, 70%, 80%, 90%, 95%, and 100%) and transferred to pure acetone for 20 min. After placing in 1:1 mixture of Spurr resin (SPI-CHEM, PA, USA) and acetone for 1 h at room temperature, samples were transferred to 3:1 mixture of Spurr resin and acetone for 3 h and finally placed in pure Spurr resin overnight. Ultrathin sections (70–90 nm) were sliced by LEICA EM UC7 ultrathin slicer (Vienna, Austria) and stained with uranyl acetate and lead citrate. Autophagosomes were observed under a transmission electron microscope (TEM; H-7650, Hitachi, Tokyo, Japan). Statistic analysis 2 All results are presented as mean±standard error of the mean (SEM) from three independent experiments. Statistical analyses were performed using GraphPad Prism 7 (GraphPad Inc., CA, USA). Differences were considered significant with P values of < 0.05 and highly significant with P values of < 0.01 using the Student’s t -test (Song et al., 2019 2019 ). Results 1 Effect of PCV3 Cap protein on induction of autophagy 2 In order to investigate whether PCV3 Cap could trigger autophagic machinery, cells were co-transfected with recombinant plasmids expressing LC3B and PCV3-Cap for confocal imaging to visualize the LC3B punctae. Fig. 1a 1a shows that overexpression of PCV3 Cap induced formation of autophagosomes shown as EGFP-LC3B punctae around the nuclei of HEK293T cells, similar to Rapa treatment, while the control cells did not show apparent LC3B punctae. To further confirm that PCV3 Cap could induce autophagy, we examined LC3 lipidation (LC3-II), a protein marker of autophagy (Mizushima et al., 2010 2010 ), and SQSTM1/p62, known as autophagy substrate (Bjørkøy et al., 2005 2005 ; Pankiv et al., 2007 2007 ). Western blotting showed that PCV3 Cap expression and Rapa treatment significantly increased the conversion of LC3-I to LC3-II ( P < 0.01) and reduced the ratio of p62 to β-actin ( P < 0.05) relative to control cells, with statistical significance at 36 h post-transfection (hpt) (Fig. 2 2 ). TEM revealed typical autophagosome-like vesicles with double or single membrane in cells expressing PCV3 Cap or treated with Rapa. Autophagosome-like vesicles were rarely seen in the mock-treated cells (Fig. 1b 1b ). These results indicate that PCV3 Cap protein induced autophagy in HEK293T cells. (a) Cells were co-transfected with pEGFP-LC3B and pCMV-capsid (Cap) or the control plasmid pCMV, or transfected only with pEGFP-LC3B (mock), or treated with 2 μmol/L rapamycin (Rapa) after 5 h of transfection with pEGFP-LC3B (positive control). After 36 h of transfection, cells were immuno-stained with the rabbit anti-PCV3 Cap polyclonal antibody and counterstained with 2-(4-amidinophenyl)-6-indolecarbamidine dihydrochloride (DAPI) for nuclei, and then examined for formation of EGFP-LC3B punctae under the confocal microscope. (b) Cells were transfected with pCMV-Cap for 36 h or mock-treated (negative control) or treated with 2 μmol/L Rapa (positive control). Autophagosome-like vesicles were observed by transmission electron microscope. Black arrows indicate the characteristic structures of autophagosomes. Scale bar=1 μm Cells were first transfected with pCMV-capsid (Cap) or the control plasmid pCMV. Rapamycin (Rapa) was used as positive control. After 36 h of transfection, the whole cell lysates were subjected to western blotting for β-actin, LC3, p62, and PCV3 Cap. (a) A representative blot showing the effects of PCV3 Cap on target proteins. (b, c) Ratios of LC3-II to LC3-I and p62 to β-actin normalized to mock transfection set at 1.0. Data were expressed as mean±standard error of the mean (SEM), n =3. * P < 0.05; ** P < 0.01 Complete autophagy flux induced by PCV3 Cap protein 2 Autophagy flux reflects progression of the autophagic response (Mizushima et al., 2010 2010 ). In order to investigate whether PCV3 Cap induces complete autophagy flux, we examined the protein level of p62 in the absence or presence of CQ, a downstream autophagy inhibitor, by inhibiting acidification of lysosomes (Poole and Ohkuma, 1981 1981 ) and repressing lysosomal degradation of autophagic substrates such as LC3-II and p62 (Mizushima et al., 2010 2010 ). In cells treated with CQ, the ratios of LC3-II to LC3-I and p62 to β-actin were significantly higher than those of the untreated cells (Figs. 3a–3c 3a–3c ; P < 0.05). These findings reveal that PCV3 Cap induced complete autophagy in HEK293T cells and p62 proteins were degraded via the autophagic lysosomal pathway. Involvement of ubiquitin–proteasome pathway in the autophagy process induced by PCV3 Cap protein 2 Considering that the autophagy–lysosomal pathway and the ubiquitin–proteasome pathway are two main machineries for protein degradation in the eukaryote (Hara et al., 2006 2006 ; Komatsu et al., 2006 2006 ), we examined whether ubiquitin–proteasome pathway participated in the autophagy process induced by PCV3 Cap. In the ubiquitin–proteasome pathway, ubiquitinated proteins are degraded by the 26S proteasome complex and the degradation process can be blocked by the peptide-aldehyde proteasome inhibitor MG132 (Han et al., 2009 2009 ; Wiegering et al., 2019 2019 ). When cells were treated with MG132 after 5 h of transfection with pCMV-Cap, the ratios of LC3-II to LC3-I (Fig. 3e 3e ; P < 0.05) and p62 to β-actin (Fig. 3f 3f ; P < 0.01) were significantly increased relative to the untreated cells, indicating that the ubiquitin–proteasome pathway might be involved in the autophagy process induced by PCV3 Cap. Cells were first transfected with pCMV-capsid (Cap) for 5 h and then treated either with 5 μmol/L chloroquine (CQ) or MG132, or left untreated as control. Rapamycin (Rapa) was used as a positive control. After 36 h of transfection, the whole cell lysates were subjected to western blotting for β-actin, LC3, p62, and PCV3 Cap. (a, d) Representative blots showing the effects of CQ or MG132 on target proteins. (b, e) Ratio of LC3-II to LC3-I normalized to mock transfection set at 1.0. (c, f) Ratio of p62 to β-actin normalized to mock transfection set at 1.0. Data were expressed as mean±standard error of the mean (SEM), n =3. * P < 0.05; ** P < 0.01 Decreased phosphorylation of mTOR by PCV3 Cap protein 2 Since mTOR signaling is the main pathway that regulates autophagy (Díaz-Troya et al., 2008 2008 ; Jung et al., 2010 2010 ), we investigated whether mTOR was inhibited in HEK293T cells transfected with pCMV-Cap using Rapa as positive control. Fig. 4 4 shows that expression of PCV3 Cap or Rapa treatment downregulated the ratio of p-mTOR to the total mTOR ( P < 0.01), suggesting that mTOR signaling is involved in the autophagy process mediated by the PCV3 Cap protein. Cells were transfected with pCMV-capsid (Cap) or the control plasmid pCMV. Rapamycin (Rapa) was used as a positive control. After 36 h of transfection, the whole cell lysates were subjected to western blotting for mammalian target of rapamycin (mTOR), phosphorylated-mTOR (p-mTOR) (S2448), β-actin, LC3, p62, and PCV3 Cap. (a) A representative blot showing the effects of PCV3 Cap expression on target proteins. (b) Ratio of p-mTOR (S2448) to mTOR normalized to mock transfection set at 1.0. Data were expressed as mean±standard error of the mean (SEM), n =3. ** P < 0.01 Discussion 1 Previous studies in our laboratory have shown that PCV2 induced autophagy, most probably by the Cap protein, and PCV2 exploited the autophagic machinery to enhance its replication in PK-15 cells (Zhu et al., 2012a 2012a , 2012b 2012b ). Here, we provide evidence that the Cap protein from PCV3 induced autophagy in HEK293T cells. Initially, the recombinant plasmid pCMV-Cap was transfected into PK-15 cells and porcine intestinal epithelial cells (IPEC-J2). However, the transfection efficiency was only 10%–20% in PK-15 and IPEC-J2 cells such that it prevented us from further study (data not shown). Low transfection efficiency may be related to the cell types. Considering that HEK293T cells have the advantage of high transfection efficiency, we attempted to explore whether PCV3 Cap expression could induce autophagy in this cell line. By confocal imaging, TEM, and western blotting, we found that PCV3 Cap protein induced autophagy in HEK293T cells (Figs. 1 1 and 2 2 ). Autophagy flux is often used to monitor the process of autophagy (Mizushima et al., 2010 2010 ; Yin et al., 2019 2019 ). CQ is known to inhibit lysosome acidification (Poole and Ohkuma, 1981 1981 ) and repress autophagy by inhibiting lysosome-mediated degradation of the autophagic debris. CQ used at 5 μmol/L for 36 h did not affect the viability of the HEK293T cells as determined by the Cell Counting Kit-8 (CCK-8; data not shown). The fact that the autophagy process induced by PCV3 Cap was blocked by CQ treatment (Fig. 3 3 ) indicates that complete autophagy flux had occurred, a finding similar to PCV2 (Zhu et al., 2012a 2012a ). One phenomenon that needs to be pointed out from the experiment is that, whenever the plasmid pCMV-Cap was transfected to PK-15, IPEC-J2, or HEK293T cells, two protein bands at 10–15 kDa and 15–25 kDa were always present by immunoblotting with the rabbit anti-PCV3 Cap polyclonal antibody or specific anti-Flag monoclonal antibody. In order to verify whether the Cap protein was partially degraded into two bands by the host proteasomes, MG132 was added to the cells transfected with pCMV-Cap to inhibit the activity of proteases. Two protein bands were still detected, indicating that these two bands were not degraded by the cellular proteasome pathway (Fig. 3 3 ). To further explore the two protein bands of the PCV3 Cap protein, we constructed two recombinant plasmids, one with full-length orf2 and the other with deletion of the region coding for the nuclear localization signal (NLS). Each peptide was fused on both ends: the N-terminus with 6×His tag and the C-terminus with Flag tag. HEK293T cells were transfected and collected for western blotting. Only one protein band (25–35 kDa) was seen in the cells expressing the His-tagged Cap as probed with the anti-His monoclonal antibody, while there were two bands in cells expressing the Flag-tagged Cap when probed with the anti-Flag monoclonal antibody (data not shown), similar to the results shown in Fig. 3 3 . This indicates that the two in-frame initiation codons in the orf2 gene of PCV3 might functionally operate to generate two peptides, one as the full-length Cap protein and the other an N-terminally “truncated” peptide. With 5 μmol/L of MG132 treatment, the cell viability was above 80% (data not shown), similar to published reports such as the one by Harhouri et al. ( 2017 2017 ). Because MG132 treatment further increased the ratios of LC3-II to LC3-I and p62 to β-actin (Figs. 3d–3f 3d–3f ), it is apparent that the ubiquitin–proteasome pathway is also involved in the autophagy process induced by PCV3 Cap protein. This is consistent with reports that exposure of MG132 impaired autophagic flux (Ji et al., 2016 2016 ) and even led to activation of autophagy (Harhouri et al., 2017 2017 ). LC3 could be degraded by the proteasomes in a stepwise manner (Gao et al., 2010 2010 ). A recent report indicates that proteasomal degradation of LC3-I, but not directly of LC3-II, could be promoted by BRUCE, a protein containing ubiquitin-conjugating E2 domain with anti-apoptotic effect, leading to decreasing levels of LC3-II and autophagy (Jiang TX et al., 2019 2019 ). This could be the reason why LC3-II was significantly increased in MG132-treated cells, because MG132 inhibited degradation of LC3-I by proteasomes without affecting its lipidation in the presence of an autophagy inducer, namely PCV3 Cap protein in this study. Because MG132 treatment could also induce autophagy (Harhouri et al., 2017 2017 ), both PCV3 Cap protein and MG132 might have contributed to the increased level of LC3-II (Figs. 3c and 3d 3c and 3d ). Reduced expression of PCV3 Cap protein in MG132-treated cells (Fig. 3d 3d ) could be due to inhibition of protein synthesis because MG132 has been shown to inhibit general protein synthesis (Ding et al., 2006 2006 ) possibly by increased phosphorylation of eukaryotic initiation factor 2α (eIF2α) (Jiang and Wek, 2005 2005 ). Since autophagy is regulated by a number of signaling pathways and the mTOR pathway is the major one (Díaz-Troya et al., 2008 2008 ; Jung et al., 2010 2010 ; Parzych and Klionsky, 2014 2014 ), we examined whether PCV3 Cap expression affected mTOR phosphorylation, a key step in mTOR-mediated signaling of autophagy (Díaz-Troya et al., 2008 2008 ; Jung et al., 2010 2010 ). Fig. 4 4 shows that Cap expression reduced p-mTOR level, similar to treatment with Rapa known to induce autophagy while total mTOR remained essentially unchanged. For PCV2 and simian virus 40 small T antigen, mTOR was also inhibited in autophagy induction (Kumar and Rangarajan, 2009 2009 ; Zhu et al., 2012b 2012b ). We believe that the PCV3 Cap protein induces autophagy in HEK293T cells by inhibiting phosphorylation of mTOR. Conclusions 1 In summary, PCV3 Cap protein induces complete autophagy in HEK293T cells by inhibiting mTOR phosphorylation. 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Porcine circovirus type 2 induces autophagy via the AMPK/ERK/TSC2/mTOR signaling pathway in PK-15 cells We thank Dr. Ying SHAN in the Core Facility Platform of the College of Animal Science, Zhejiang University (Hangzhou, China), for assistance with confocal microscopy, and the staff in the Bio-ultrastructure Analysis Center of the Agrobiology and Environmental Sciences, Zhejiang University, for assistance with transmission electron microscopy. Compliance with ethics guidelines Shi-chao GENG, Xiao-liang LI, and Wei-huan FANG have declared no conflict of interests. This article does not contain any studies with human or animal subjects performed by any of the authors. 10.1631/jzus.B1900657 Project supported by the Zhejiang Provincial Department of Science and Technology (No. 2018C02028), China 2019-11-23 2020-02-16 2022-01-05 Copyright © Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2020 2020 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 07 21