Duck enteritis virus activates CaMKKβ-AMPK to trigger autophagy in duck embryo fibroblast cells via increased cytosolic calcium
The results of our previous study showed that impaired cellular energy metabolism contributes to duck enteritis virus-induced autophagy via the 5`-adenosine monophosphate-activated protein kinase (AMPK)/tuberous sclerosis complex 2/mammalian target of rapamycin pathway in duck embryo fibroblast (DEF) cells. However, it remains unknown whether any other underlying mechanisms of AMPK activation are involved in autophagy induction.
The activity of CaMKKβ and AMPK in DEF cells infected with DEV were evaluated.The Effect of inhibitory activity of CaMKKβ on DEV-induced autophagy was investigated. In addtion to, the cytosolic calcium level in DEF cells infected with DEV were evaluated.The Effect of inhibitory cytosolic calcium level on DEV-induced autophagy was investigated.
In this study, duck enteritis virus (DEV) infection activated CaMKKβ and its substrate molecule AMPK at 36, 48, and 60 h post-infection (hpi). STO-609, a CaMKKβ inhibitor, or CaMKKβ siRNA significantly inhibited the activation of DEV to AMPK, LC3I to LC3II transformation, and GFP-LC3 puncta distribution. In addition, inhibition of CaMKKβ activity also significantly reduced progeny DEV titer and gB protein expression. Besides, cytosolic calcium (Ca2+) was higher in DEV-infected cells than mock controls at 36, 48, and 60 hpi, respectively. Treatment of DEV-infected cells with 1,2-Bis (2-aminophenoxy) ethane-N, N, N′, N-tetraacetic acid (BAPTA-AM) significantly reduced intracellular Ca2+ ion concentrations, as well as CaMKKβ and AMPK activities, and subsequent autophagy, in addition to viral protein synthesis and viral titer.
These results showed that elevated [Ca2+]cyto-mediated activation of CaMKKβ managed the activation of AMPK, which then positively regulated autophagy, thereby providing further insight into DEV–host interactions.
KeywordsDuck enteritis virus Autophagy Cytosolic calcium CaMKKβ AMPK
Adenosine 5′-monophosphate-activated protein kinase
1,2-Bis (2-aminophenoxy) ethane-N, N, N′, N-tetraacetic acid
Duck embryo fibroblast
Duck enteritis virus
Duck enteritis virus (DEV) is a member of the Herpesviridae family and has a typical morphology of herpesviruses and a double-stranded, linear DNA genome about 160 Kb in length. DEV can cause a variety of acute, septic, and highly fatal infectious diseases in water fowl, including duck viral enteritis (DVE), which is characterized by internal bleeding due to mucosal damage of the blood vessels and digestive tract, as well as lymphoid organ damage and lesion formation . The occurrence of DVE was first reported in the Netherlands in 1923 and has since spread to other countries. In 1957, the occurrence of the DVE was first reported in China and has since prevailed in relatively developed areas in southern and eastern China . DVE is widespread and spreads rapidly, resulting in high morbidity and mortality that results in huge economic losses to the duck industry. However, the relative lag in molecular biology research has restricted efforts in DVE prevention and control.
Virus infection can induce autophagy, which is a process of precise membrane-dependent regulation to ensure intracellular fluid balance [3, 4, 5]. This response can be either antiviral or promote virus replication, depending on the type of virus and the intracellular environment of the host cell [6, 7]. According to the type of substrate, species, regulatory mechanism, and transport process, autophagy includes macroautophagy, microautophagy, and molecular chaperone-mediated autophagy . Macroautophagy commonly refers to the process of double layer membrane formation of autophagosomes by fusion of the endoplasmic reticulum (ER) with lysosomes. In this process, commonly referred to as autophagy, the contents of autophagosomes are degraded.
Calcium (Ca2+) is a ubiquitous intracellular messenger of some important signal transduction processes, including activation of enzymes, differentiation, proliferation, and gene transcription [9, 10]. Ca2+ and calcium-sensing proteins might play a dual role in the process of autophagy regulation, depending on the cell type, intracellular environment, and Ca2+ abundance [11, 12]. Excessive cytoplasmic calcium is released from the ER, and then was reported to induce autophagy through calcium/calmodulin-dependent protein kinase kinase-beta (CaMKK)-regulated activation of adenosine 5′-monophosphate-activated protein kinase (AMPK) and the subsequent inhibition of the activity of mammalian target of rapamycin (mTOR) [13, 14].
Some viruses can take advantage of Ca2+ ion-related pathways of the host to promote replication [15, 16], such as porcine circovirus type 2, which can induce the release of Ca2+ ions from the ER via the inositol 1,4,5-trisphosphate receptor in duck embryo fibroblast (DEF) cells, which is considered to be responsible for apoptosis induction . Rotavirus coding of nonstructural protein 4, which releases Ca2+ ions into the cytoplasm, initiates autophagy to activate CaMKKβ signaling . The hepatitis B virus X protein targets the human B-cell lymphoma 2 homolog to regulate CED-9, which induces an increase in cytoplasmic Ca2+ ion concentrations and subsequent cell death in Caenorhabditis elegans . Herpes simplex virus triggers activation of calcium-signaling pathways , Elevated [Ca2+]cyto-mediated activation of CaMKKβexactly managed the activation of AMPK, which then positively regulated autophagy through suppressing mTOR in cells infected with Bluetongue virus .
Our previous studies showed that impaired cellular energy metabolism contributes to DEV-induced autophagy via the AMPK/TSC2/mTOR pathway in DEF cells [22, 23]. However, it remains unknown whether other underlying mechanisms of AMPK participate in autophagy induction. The results of the present study demonstrated that CaMKKβ is an upstream regulator of AMPK during DEV infection, which contributes to autophagy induction. Activation of CaMKKβ results from an increase in cytosolic Ca2+ content. This research lays a foundation for DEV pathogenic mechanism research and provides further insight into DEV–host cell interactions.
Cells, viruses, and plasmids
DEF cells were obtained from 9 to 11 days specific pathogen-free duck embryos, as described previously , and cultured in Dulbecco’s modified Eagle’s medium (cat. no. 8116176; Gibco, Grand Island, NY, USA) supplemented with 5% fetal bovine serum (cat. no. 1722658; Gibco) and antibiotics (0.1 mg/ml of streptomycin and 0.1 mg/ml penicillin) at 37 °C under an atmosphere of 5% CO2/95% air. DEV strain CSC was kept in our laboratory.
To construct a GFP-LC3 recombination plasmid, the LC3 gene was amplified from DEF cells with the primer pair LC3F 5`-ATG CAA CCG CCT CTG-3` and LC3R 5`-TCG CGT TGG AAG GCA AAT C-3`, corresponding to the GenBank sequence for duck LC3B gene (NW_004676873.1), and cloned into the pEGFP-C1 vector, to express LC3B protein with the GFP protein.
Virus infection and drug or small interfering RNA (siRNA) treatment
DEF cells were infected with DEV for 2 h at 37 °C, washed three times with sterile phosphate-buffered saline (pH 7.4), then maintained in 2% in culture medium supplemented with fetal bovine serum for various time points until samples were harvested. The cells were then cultured in 2% culture medium supplemented with fetal bovine serum with or without pre-treatment with the same drug for the indicated times. The optimal concentrations of chemicals used in this experiment were 10 mM 1,2-Bis(2-aminophenoxy)ethane-N,N,N′,N-tetraacetic acid (BAPTA-AM; Abcam, Cambridge, UK), 5 μM STO-609 (Merck-Millipore, Darmstadt, Germany),4 μM ionomycin and 2.5 μM Fluo-3 AM (Beyotime Institute of Biotechnology, Haimen, China). The toxicities of both drugs and siRNAs were tested using the WST-1 Cell Proliferation and Cytotoxicity Assay Kit (Beyotime), according to the manufacturer’s instructions. At 36, 48, and 60 h post-infection (hpi), DEF cells were collected for subsequent analysis.
Western blot analysis
Proteins from cells treated with either drugs or siRNAs, or infected with DEV were extracted using immunoprecipitation lysis buffer (Beyotime) with the protease inhibitor phenylmethylsulfonyl fluoride (Beyotime), then boiled for 10 min in 5× loading buffer, separated by 12% sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and transferred onto nitrocellulose membranes (GE Healthcare Life Sciences, Little Chalfont, UK), according to manufacturers’ instructions. The membranes were blocked with 3% bovine serum albumin (Sigma-Aldrich Corporation, St. Louis, MO, USA) for 2 h at room temperature and then incubated with the following primary antibodies for 2 h at room temperature: rabbit anti-LC3B antibody (Sigma-Aldrich Corporation), mMouse anti-CaMKKβ antibody (Sigma-Aldrich Corporation), rabbit anti-p-AMPK antibody (Thermo Fisher Scientific, Waltham, MA, USA), mouse anti-AMPK antibody (Thermo Fisher Scientific), mouse anti-β-actin antibody (Sigma-Aldrich Corporation).Then, the membranes were incubated with IRDye 800 CW goat anti-mouse or goat anti-rabbit immunoglobulin IgG as secondary antibodies for 1 h at room temperature. Antibody detection was conducted using an Odyssey Infrared Fluorescence Scanning Imaging System (LI-COR Biosciences, Lincoln, NE, USA). Quantitation from western blot image intensity was achieved by adding rectangle to the image to gain data directly using the Odyssey Infrared Fluorescence Scanning Imaging System Application Software Version3.0.
Confocal fluorescence microscopy
For the detection of autophagosomes, DEF cells at 70–80% confluence in culture dishes were transfected with 2.5 μg of the GFP-LC3 plasmid using the Calcium Phosphate Transfection Kit (cat. no. K2780–01; Invitrogen Corporation, Carlsbad, CA, USA). At 24 hpi, chemical-treated or virus-infected DEF cells at different time points were fixed with absolute ethanol for 30 min and the cell nuclei were stained with 4′-6-diamidino-2-phenylindole (cat. no. D1306; Beyotime). The green fluorescence of GFP-LC3 was observed by confocal laser microscopy using a Leica SP2 confocal system (Leica Microsystems, Wetzlar, Germany).
In order to further study the effects of cell autophagy on viral replication, siRNA targeting the autophagy-related gene beclin-1 was synthesized (Shanghai GenePharma Co., Ltd., Shanghai, China). The sequence of the siRNA was GCC UAC AAC GAG GAC GAU ATT (sense) and UAU CGU CCU CGU UGU AGG CTT (antisense). Six-well plates were transfected with siRNA and negative control (NC)-siRNA using transfection reagents for 24 h and then infected with DEV. Cell samples were collected to detect the effects of siRNA.
Median tissue culture infective dosed (TCID50)
DEF cells were cultured in covered 96-well plates and then infected with DEV virus diluted to 10− 1 to 10− 8. At 72 hpi, the cells were observed and pathological changes were recorded. Viral titers were determined according to the Reed–Muench method.
Intracellular Ca2+ detection by flow cytometry
Cytosolic free Ca2+ ions were detected by using Fluo-3 AM. Fluo-3 AM itself is not combined with Ca2+ ions, but once dye is added to the cells, it can hybridize with Fluo-3 AM, and Fluo-3 AM will fluorescence upon binding to Ca2+. DEF cells were infected with DEV or treated with BAPTA-AM for the indicated times, then incubated with Fluo-3 AM in the dark at 37 °C for 1 h. Afterward, the cells were suspended in phosphate-buffered saline. To observe fluorescence, as an indicator of intracellular Ca2+ ions, the cells were monitored using a flow cytometer (BD FACSAria™; BD Biosciences, San Jose, CA, USA) at an excitation wavelength of 488 nm.
All experimental results are expressed as the mean ± standard deviation (SD) of three independent experiments. The Tukey’s test was used for statistical analysis. A probability (p) value of < 0.05 was considered statistically significant.
CaMKKβ-AMPK may be involved in DEV-induced autophagy
CaMKKβ is an upstream activator of AMPK involved in DEV-induced autophagy
To eliminate nonspecific effects of chemical drugs, siRNA was used to inhibit CaMKKβ expression. As shown in Fig. 2b, as compared to cells transfected with the NC-siRNA, DEF cells transfected with siRNA, expression levels of CaMKKβ, activated AMPK, and LC3II were significantly reduced (Fig. 2b). The number of GFP-LC3 puncta decreased dramatically in siCaMKKβ -treated DEV-infected cells, as compared to control cells (Fig. 2c).
Due to the decreased expression of viral proteins in response to CaMKKβ inhibition by chemical drugs or siRNA, we further checked whether inhibition of CaMKKβ reduces viral replication. Viral titers were significantly decreased in DEV-infected DEF cells treated with STO-609 or siCaMKKβ. The TCID50, as compared to control cells, at 48 hpi is shown in Fig. 2 d, e These results indicated that autophagy is related to CaMKKβ activation in DEV-infected DEF cells, and CaMKKβ is an upstream activator of AMPK involved in DEV-induced autophagy (Fig. 2d, e).
DEV infection increased intracellular Ca2+ content to activate CAMKKβ
BAPTA-AM is a well-established chelator of intracellular Ca2+ ions. Mock- or DEV-infected DEF cells were treated with 25 μm BAPTA-AM for 30 h, and intracellular Ca2+ was detected by flow cytometry. As expected, the results suggested that the addition of BAPTA-AM reduced intracellular Ca2+ levels (Fig. 3 c). Accordingly, CaMKKβ and AMPK activities were significantly decreased in BAPTA-AM-treated cells. After the addition of BAPTA-AM, LC3II expression and viral protein synthesis were significantly reduced (Fig. 3d). GFP-LC3 distribution was also observed by a confocal fluorescence microscopy as discrete puncta associated with autophagic vacuoles. The change in GFP-LC3 puncta number after drug treatment may response to changes in autophagic activity. As speculation, the number of GFP-LC3 puncta remarkable decreased in BAPTA-AM-treated DEV-infected cells, as compared to control cells, suggesting the inhibition of autophagy (Fig. 3e).
The expression of gB protein was reduced in BAPTA-AM-treated DEF cells, as compared with control cells. Consistent with the result, virus titers were significantly reduced in BAPTA-AM-treated DEF cells, as compared with control group cells. TCID50 assay was used to measure the DEV viral titers (Fig. 3f). Together, these data reflect that Ca2+ is necessary for the function of autophagy in DEV-infected DEF cells in a CaMKKβ- and AMPK-dependent process.
Cell viability unaffected by pharmacological treatment
Autophagy is a tightly regulated and evolutionarily conserved intracellular process in which cells destroy and recycle cellular components in lysosomes. Much evidence indicates that virus-induced autophagy plays an important role in the viral life cycle and pathogenicity . Many viruses have been reported to induce autophagy through multiple pathways [6, 27]. The results of our previous study showed that DEV induced autophagic activation through impaired cellular energy metabolism via the AMPK–TSC2–MTOR signaling pathway. Two signaling molecules upstream from AMPK were involved cellular energy and Ca2+-mediated CAMKKβ activation. However, it remains unknown whether Ca2+-mediated CaMKKβ can activate AMPK and a series of downstream signaling pathways during DEV-induced autophagy. The results of the present study suggested that DEV activates CAMKKβ and its substrate molecule APMK to trigger autophagy in DEF cells by increasing cytosolic Ca2+ concentrations.
Autophagy was first associated with intracellular Ca2+ regulation. Subsequent studies found that the removal of intracellular or extracellular Ca2+ ions inhibited autophagy . Although the association between Ca2+ signaling and autophagy regulation has been reported, the underlying mechanisms remain unknown. Ca2+ ion control of autophagy is divided into two opposing view, that is, Ca2+ ions inhibit autophagy and promote autophagy. In this study, DEV infection induced an increase in intracellular Ca2+ and activated the formation of autophagosomes in DEF cells.
CaMKKβ is one of the most potent Ca2+-dependent protein kinases and is involved in a variety of signal transduction process. It is well known that AMPK (Thr172), CaMKI (Thr172), and CaMKIV (Thr200) can be directly phosphorylated by CaMKKβ to participate in autophagy . In addition, activation of CaMKKβ is mainly dependent on conformational changes caused by the binding of Ca2+ and calmodulin. Therefore, the level of free Ca2+ in cytoplasm is essential for the activation of CaMKKβ .
Ca2+ and CaMKKβ are related with the activation of AMPK in T cells, hypothalamic neurous cells and endothelial cells,implying that Ca2+ metabolism may play an important role in AMPK-mTOR-regulated autophagy process . Recent studies have found that in rotavirus-infected cells, CaMKKβ is activated by increased Ca2+ levels, further activating AMPK, which leads to subsequent autophagy . Human cytomegalovirus infection can activate the CaMKKβ/AMPK pathway to promote cellular glucose metabolism and viral replication . Here, although DEV infection indeed increased the cytoplasmic content of Ca2+ ions, the underlying mechanism is not clear. However, it has been speculated that the virus may encode one or more proteins that change biomembrane permeability to Ca2+, causing an increase in [Ca2+]cyto originating from ER or Golgi [Ca2+] stores, or the extracellular environment [18, 32]. The results of our previous study confirmed that the ER stress response is involved in DEV-induced autophagy, suggesting that there might be some links between ER stress and elevated [Ca2+]cyto.
The results of the present study demonstrated that CaMKKβ is an upstream regulator of AMPK during DEV infection, which contributes to autophagy induction. Activation of CaMKKβ results from an increase in cytosolic Ca2+ content. This research lays a foundation for DEV pathogenic mechanism research and provides further insight into DEV–host cell interactions.
This work was supported by the Natural Science Foundation of Heilongjiang Province (QC2018033), the Key Program of Natural Science Foundation of Heilongjiang Province (ZD2016006) and Central Public-interest Scientific Institution Basal Fund (NO.1610302017013; NO.1610302018013).
HC, LZ and HY conceived and designed the study. HY and SL performed the experiments and analyzed the data. YW and HH drew the graphs. HY and LZ wrote the paper. All authors read and approved the final manuscript.
Availability of data and materials
The datasets analyzed during the current study available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study was approved by Harbin Veterinary Research Institute and performed in accordance with animal ethics guidelines and approved protocols. The animal Ethics Committee approval number is Heilongjiang-SYXK-2006-032.
Consent for publication
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