- Open Access
Induction of cytopathic effect and cytokines in coxsackievirus B3-infected murine astrocytes
© Zeng et al.; licensee BioMed Central Ltd. 2013
- Received: 13 November 2012
- Accepted: 20 May 2013
- Published: 21 May 2013
Coxsackievirus commonly infects children and occasionally causes severe meningitis and/or encephalitis in the newborn. The underlying mechanism(s) behind the central nervous system pathology is poorly defined.
It is hypothesized that astrocytes may be involved in inflammatory response induced by CVB3 infection. Here we discuss this hypothesis in the context of CVB3 infection and associated inflammatory response in primary mouse astrocytes.
The results showed that coxsackievirus receptor (CAR) was distributed homogeneously on the astrocytes, and that CVB3 could infect and replicate in astrocytes, with release of infectious virus particles. CVB3 induced cytopathic effect and production of proinflammatory cytokines IL-1β, TNF-α, IL-6, and chemokine CXCL10 from astrocytes.
These data suggest that direct astrocyte damage and cytokines induction could be a mechanism of virus-induced meningitis and/or encephalitis.
- Viral infection
- Cell death
Coxsackieviruses are important human pathogens. Although most coxsackievirus infections are mild, serious complications such as meningitis, paralysis and myocarditis are not rare. Coxsackievirus B3 (CVB3) is the most frequently involved in human myocarditis. Recently, increasing cases of CVB3-associated meningitis have been reported [1, 2]. Neuroinflammation and neuronal loss have been shown in the central nervous system (CNS) infected by CVB3. Using a neonatal mouse model of CVB3 infection, a previous study has shown that neuronal precursor cells were preferentially targeted and ensuing neuronal apoptosis . Microglia and astrocytes are the major immune cells of the CNS. Our preliminary study showed that microglia were spared from CVB3 infection (unpublished data), whereas the role of astrocytes in CVB3 infection and/or its pathogenesis has not been studied.
Expression of specific receptors is often an important determinant of a cell’s susceptibility to infection. Coxsackievirus and adenovirus receptor (CAR) is used by coxsackievirus to attach cell surface . CAR is a part of the tight junction in blood–brain barrier (BBB) and appears to function in cell adhesion or intercellular recognition and participate in neural migration in the CNS [5, 6]. Viral meningitis is frequently associated with BBB disruption, thus enabling the entry of virus and inflammatory cells into the CNS . BBB is formed by endothelial cells, surrounded by basal lamina and astrocytes endfeet. As our preliminary study showed that CAR was expressed on murine astrocytes, we hypothesized that CVB3 infection process in the CNS involves astrocytes.
Damage to the CNS tissues may result from viral replication or as a consequence of inflammatory response . Cytokines are important mediators of the inflammatory response to many stimuli, including viral infections. Cytokines such as IL-1β, TNF-α and IL-6 enhance the permeability of the BBB both in vitro [9, 10] and in vivo . Therefore, in this study, we have examined the CVB3 susceptibility of astrocytes and the response of inflammation cytokines (IL-1β, TNF-α, IL-6) and chemokine CXCL10 by using primary murine astrocytes.
Isolation of murine primary astrocytes and detection of Coxsackievirus and Adenovirus receptor (CAR)
Astrocyte susceptibility and replication of CVB3
CVB3 infection induced cytopathic effect (CPE) in astrocytes
From 12 hpi, CVB3-mediated CPE was monitored microscopically. While the mock-infected cells had round phase-bright cell bodies with many neurites and smooth contours, the infected cells showed distinct morphological alterations including rounding up, appearance of granules, cytoplasmic blebbing, and detachment from the monolayer. More cells died as time went by (Figure 3B). The degree of cellular damage was estimated using the cell counting kit-8, which measures the cytoplasmic dehydrogenase activity in viable cells. We observed significant loss of cell viability by 24 hpi (58.7±3.4% viable), 48 hpi (39.0±2.1%) and 72 hpi (30.2±1.6%) (Figure 3C).
CVB3 induced proinflammatory cytokines IL-1β, TNF-α, IL-6 and chemokine CXCL10 expression both at mRNA and protein levels
Association of group B coxsackievirus (CVB) with the CNS infections have been previously shown by identification of antigens in or isolation of infectious particles of Coxsackieviruses from the brain tissues of patients with encephalitis [12, 13]. CVB can also cause CNS complications in mice and neurons are reportedly susceptible to CVB in a mouse model . However, no study has implicated major CNS immune cells astrocytes or microglia in the CVB pathogenesis. In this study, we report the CVB3 infectivity in murine primary astrocytes and the corresponding inflammatory response.
We used one- or two-day-old neonatal Balb/c mice because newborn pups are inherently more susceptible to coxsackievirus infection than are older mice and the susceptibility drops dramatically with age [3, 14]. Cellular receptors are major determinants of viral pathogenesis, and thence a previous report that CAR expression level is significantly higher in the brain of newborn mice than adult mice  and the deduced amino acid sequence of a murine CAR homolog was 91% identical to that of the human CAR . The presence of CAR in the murine astrocytes in this study suggests astrocytes could mediate CVB pathogenesis in the CNS. Besides, that CVB3 replicated in astrocytes and induced pronounced CPE (Figure 3) further suggests that CVB3 could cause direct damage to astrocytes.
Activated astrocytes are known to produce a wide variety of cytokines and chemokines [16, 17]. Cytokine production in response to CVB3 has been described in other cell types, such as insulinoma cell line  and myocardial cells . We observed upregulated mRNA expression levels in response to CVB3 infection of IL-1β, TNF-α, IL-6 and CXCL10 in astrocytes (Figure 4 and 5). Induced IL-1β mRNA expression was not correlated with the appearance of mature IL-1β in the supernatant, which could be due to impaired synthesis and liberation of IL-1β from infected cells and requires further research. Generally, cytokine release initiates a beneficial inflammatory and immune response although an exaggerated release is commonly detrimental and associated with adverse effects such as CNS disorders. IL-6 has been shown to be beneficial in the CNS because of its neurotrophic and neuroprotective effects. However, IL-6 and TNF-α production by astrocytes can lead to increased permeability of the BBB . Many factors, particularly IL-1β and TNF-α, have been shown to induce IL-6 expression by astrocytes . In consistent with this finding, TNF-α and IL-1β were stimulated before IL-6 release in our study. Marked increase in the expression of CXCL10 at both gene and protein level could be a part of innate immunity against CVB3. Previous studies have shown that the CXCL10 and its receptor CXCR3 play a vital role in the inflammatory response by attracting activated T lymphocytes to the CNS following viral infections such as Lymphocytic Choriomeningitis virus, Japanese encephalitis virus, and West Nile virus [22–24]. In addition to chemotaxis that contributes to neuropathology, CXCL10 has been reported to induce neuron apoptosis or direct damage in neuronal cells [25, 26].
It is notable that CVB3 induced the death of infected astrocytes (Figure 3). As astrocytes are essential for providing trophic support to neurons and maintain synaptic functions, loss of astrocytes can induce significant neuronal dysfunction and damage. Certain cytokines such as TNF-α and CXCL10 are known to cause cell death directly [27, 28]. In fact, when activated in an uncontrolled manner, astrocytes can release various substances, such as NO, superoxide anion, and inflammatory cytokines, triggering the cascade of events leading to neuron degeneration in the CNS . Glial cells such as astrocytes and microglia cells, although are responsible for maintenance of brain integrity, may develop noxious effects upon their activation. The situation is exacerbated as the cytokines released from the infected astrocytes may induce secondary cytokine and inflammatory responses in the uninfected astrocytes, which could further promote cell death. Although we did not investigate full cytokine profile upon CVB3 infection in astrocytes, other direct treatment studies indicate that TNF-α triggers apoptosis in astrocytes , supporting the notion that CVB3-induced cell death could be related to the dysregulation of cytokines expression. It can be postulated that CVB3 infection lead to cell death via cytokine/chemokine-mediated pathways.
In conclusion, CVB3 is capable of infecting and replicating in primary murine astrocytes with resultant cytopathic effect and induction of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) and chemokine (CXCL10). Our findings suggest that i) CVB3 infection may contribute to encephalitis and/or meningitis via astrocyte destruction, and ii) permeability of the BBB and recruitment (not invasion) of inflammatory cells are a consequence of the cytokine/chemokine production.
This study was approved by the Ethics Committee of Shantou University Medical College and conducted in conformity with the Experimental Animal Management Bill issued on November 14, 1988 (Decree No.2 of National Science and Technology Commission, China), and the National Institute of Health Guide for the Care and Use of Laboratory Animals (NIH Publications No.80-23, revised 1996). One- or two-day-old specific pathogen free Balb/c mice were purchased from Shantou University Medical College Laboratory Animal Center, Shantou, Guangdong, P.R. China.
Virus enrichment and titration
Coxsackievirus B3 (Nancy strain) was kindly provided by Dr. Qihan Li (Institute of Medical Biology, Chinese Academy of Medical Science & Peking Union Medical College). CVB3 was propagated in Vero cells with Dulbecco’s Eagle’s minimum essential medium (DMEM) (Gibco, Life Technologies, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco, Life Technologies, USA), Penicillin (20 U/ml) and Streptomycin (20 μg/ml). Monolayer of Vero cells was inoculated with the virus at a multiplicity of infection (MOI) of 0.1 and incubated at 37°C with 5% CO2 in a humidified incubator for 24 h. The viral culture supernatant was collected after centrifugation at 1500 g for 10 min and stored at −80°C until used.
Virus titer was determined based on the 50% tissue culture infectious dose (TCID50) as described previously . Briefly, a 10-fold serial dilution of virus supernatant was added in duplicate to 80-90% confluent Vero cells in 96-well culture plates (Greiner Bio-One, FrickenHausen, Germany). The virus-infected cells were inspected daily for the appearance of typical Coxsackievirus-induced CPE using an inverted light microscope (IX750, Olympus, Japan). The TCID50 titer was calculated using Reed and Munch calculation method . A batch of uninfected cells was used as control.
Preparation of primary astrocytes and purity assay by immunofluorescence
Isolation of astrocytes from neonatal mice was performed as previously described . Astrocytes were probed with Anti-Glial Fibrillary Acid Protein (GFAP) antibody. Nuclei were stained with Hoechst 33258 (1:1000, Beyotime, China). The purity of astrocytes was calculated by counting GFAP-positive cells in 10 random fluorescence fields under a Nikon 90i microscope.
Detection of coxsackievirus receptor (CAR) and Glial Fibrillary Acid Protein (GFAP) on astrocytes by fluorescence staining
Monolayer astrocytes were grown on Poly-L-lysine coated glass cover slips. For fluorescence staining, cells were washed twice with phosphate buffered saline (PBS) and fixed in 4% paraformaldehyde. Cells were blocked and permeabilized with 0.1% Triton-X100/1% bovine serum albumin/PBS (PH 7.4) and incubated with Anti-Glial Fibrillary Acid Protein (GFAP) (1:500, eBioscience, CA, USA), followed by Alexa Fluor 488 goat anti-rabbit IgG (1:1000, Invitrogen, NY, USA) to identify astrocytes. The purity of astrocytes was determined by observing 10 random fluorescence fields.
To identify CAR expression on astrocytes, Anti-CAR (H-300, 1:200, Santa Cruz, CA, USA) was used as primary antibody, followed by Cy3 goat anti-mouse IgG (1:200, Beyotime, China). Nuclei were stained with Hoechst 33258 (1:1000, Beyotime, China) and examined with a Nikon 90i laser microscope.
Virus infection of primary astrocytes
Astrocytes were cultured in a 12-well plate with DMEM-F12 supplemented with 10% FBS (105 cells/well) at 37°C with 5% CO2 in a humidified incubator. We used MOI=0.1 for CVB3 replication assay and MOI=2 for CPE and cytokine assays, in which 99% of astrocytes were expected to get infected. At 90% confluence, the cultures were inoculated with CVB3. After adsorption for 1 h, the cultures were washed three times with PBS and replenished with fresh medium. At different post-infection time points, the supernatants were aliquoted and stored at −80°C until used for virus titration and analysis of cytokine production.
Determination of astrocyte viability
Astrocytes were placed in a 96-well plate at density of 5000 cells/well. This density was chosen to ensure that cells are just confluent at the end of the assay. CVB3 was added to all wells at MOI of 2 except control wells. After adsorption for 1 h, the cultures were washed three times with PBS and replenished with fresh medium. The cell counting kit-8 (Dojindo, Kumamoto, Japan) was used to assay cell viability at different post-infection time points according to the manufacturer’s instructions.
Quantification of mRNA by real time quantitative RT-PCR
Primers used in real-time PCR
Forward / Reverse primer sequences
GenBank acc. no.
Measurement of cytokines and chemokine production by ELISA
Levels of IL-1β, TNF-α, IL-6, and CXCL10 were assessed using ELISA kits: IL-1β (Cat.No. BM6002), TNF-α (Cat.No. BM607/2), and IL-6 (Cat.No. BM603/2) were purchased from eBioscience. CXCL10 was purchased from Bender Medsystems (Cat.No. BM6018), ELISA assay was performed according to manufacturer’s instructions. Plates were read using SPECTRA max 340PC (Molecular Devices, USA) at 450 nm wavelength. To inactivate virus infectivity before assay, the supernatants of infected and uninfected culture were irradiated with UV light for 30 min. Ultraviolet irradiation had no effect on theses cytokines concentration (data not shown).
The data are presented as mean ± SD. The significance of difference between values was estimated by means of one-way analysis of variance (ANOVA) with Fisher’s LSD post-hoc test. A p-value of less than 0.05 was considered statistically significant. The statistical analyses were done using the SPSS 13.0 for windows (Chicago, USA).
The authors are grateful to Dr. William Ba-Thein for providing invaluable suggestions and critically reviewing the manuscript. We thank Dr. Qihan Li for providing CVB3 strain. The study was supported by grants National Natural Science Foundation of China (81001322, 30972766, 30771988); Guangdong Natural Science Foundation (9451503102003499); Specialized Research Fund for the Doctoral Program of Higher Education (20094402110004); State Key Lab of Agriculture Microbiology Open Foundation (AML200910); Shantou University Medical College Research Foundation, 211 Project of Guangdong Province (Mechanism and Prevention of Emerging Infectious Diseases).
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