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A trypsin-like serine protease is involved in pseudorabies virus invasion through the basement membrane barrier of porcine nasal respiratory mucosa
© Glorieux et al; licensee BioMed Central Ltd. 2011
- Received: 25 August 2010
- Accepted: 14 April 2011
- Published: 14 April 2011
Several alphaherpesviruses breach the basement membrane during mucosal invasion. In the present study, the role of proteases in this process was examined. The serine protease-specific inhibitor AEBSF inhibited penetration of the basement membrane by the porcine alphaherpesvirus pseudorabies virus (PRV) by 88.1% without affecting lateral spread. Inhibitors of aspartic-, cysteine-, and metalloproteases did not inhibit viral penetration of the basement membrane. Further analysis using the Soybean Type I-S trypsin inhibitor for the serine protease subcategory of trypsin-like serine proteases resulted in a 96.9% reduction in plaque depth underneath the basement membrane. These data reveal a role of a trypsin-like serine protease in PRV penetration of the basement membrane.
- Basement Membrane
- Herpes Simplex Virus
- Serine Protease
- Herpes Simplex Virus Encephalitis
- Serine Protease Activity
The basement membrane (BM) constitutes part of the extracellular matrix and creates a formidable barrier to invading pathogens . Crossing the BM may facilitate viral access to blood vessels and nerves in the lamina propria whereafter it may spread to internal organs. Following infection of respiratory epithelial cells, different alphaherpesviruses are able to cross the BM facilitating viral invasion in the body and leading to viremia, virus dissemination and aggravated general clinical signs [2–12]. Using porcine nasal respiratory mucosal explants, we have previously confirmed that the porcine alphaherpesvirus pseudorabies virus (PRV) efficiently breaches the BM . The underlying mechanism of herpesvirus passage across the BM is unknown.
Breach of the BM in disease states is best characterized in metastatic progression in oncology following neoplastic establishment and often involves disruption of the BM by proteolytic enzymes [13, 14]. Therefore, in the current study, we investigated whether proteases are involved in alphaherpesvirus invasion through the BM. We reported previously an in vitro model that enables study and quantitative analysis of PRV invasion through the BM in nasal respiratory mucosa [3, 15]. Porcine nasal respiratory explants were obtained as described previously . Briefly, explants were stripped from the surfaces of ventral turbinates and septum, and incubated with the epithelial surface upwards on fine-meshed gauze and cultured at the air-liquid interface with serum-free medium (50% RPMI (Invitrogen, Paisley, UK)/50% DMEM (Invitrogen) supplemented with 1 μg/mL gentamycin (Invitrogen), 0.3 mg/mL glutamin (VWR, West Chester, PA, USA), 0.1 mg/mL streptomycin (Certa, Braine l'Alleud, Belgium) and 100 U/mL penicillin (Continental Pharma, Puurs, Belgium)). Explants were cultivated for 10 h before inoculation with 600 μL medium containing 107 TCID50 of PRV field strain 89V87 . After incubation for 1 h, explants were washed three times with serum-free medium.
Proteases are classified according to their catalytic activity: serine-, cysteine-, metallo- and aspartic peptidases [17, 18]. The effect of inhibition of these protease types on PRV penetration through the BM was investigated using Complete Mini Protease Inhibitor Cocktail Tablets containing a proprietary mixture of several protease inhibitors with broad inhibitory specificity for serine, cysteine, and metalloproteases (Roche Diagnostics Corporation, Basel, Switzerland). To investigate the involvement of aspartyl proteases, pepstatin A (Sigma, St. Louis, MO, USA), was used. Inhibitor concentrations were used as recommended by the manufacturer's instruction, one tablet complete Mini protease inhibitor cocktail per 10 mL and 1 μg/mL pepstatin A. At 1 h post inoculation (pi), medium was replaced by medium with and without inhibitor for inhibitor-treated and mock-treated explants respectively. Explants were immersed for 1 h and then transferred again to the gauze and cultivated with medium in the presence or absence of inhibitor for inhibitor-treated and mock-treated explants respectively until sampling. Samples were collected at 20 h pi, embedded in methocel® (Sigma) and frozen at -70°C. The time point of sampling was specified at 20 h pi because PRV was found to cross the BM between 12 and 16 h pi (data not shown). Cryosections were made, fixed in methanol, stained for collagen IV (BM component) and PRV and analyzed by confocal microscopy. Viral invasion across and lateral spread above the BM were analyzed using ImageJ, as reported previously . For each condition, maximal plaque latitude and depth underneath the BM were measured for 10 plaques; triplicate independent experiments were performed.
Interactions of herpesviruses with respiratory mucosa remain poorly understood. Invasion of different alphaherpesviruses towards the lamina propria involves passage of the BM barrier. This facilitates viral access to blood capillaries and nerve endings which enables further dissemination throughout the body [2–12]. To date, the mechanism of the alphaherpesvirus invasion process through the BM barrier is unknown.
The current study shows that serine protease activity is involved in PRV invasion through the BM. Over one third of all known proteolytic enzymes are serine proteases which mediate diverse biological processes requiring timely and specifically regulated proteolytic activity, where insufficient or excessive proteolysis can cause pathological processes [22, 23]. To date, knowledge of the role of serine proteases in the pathology of herpesvirus infections remains limited to the intracellular viral replication cycle itself. Proteolytic cleavage of viral proteins by cellular or viral proteases has been described in different stages of the herpesvirus life cycle . An observation suggesting that proteases may modulate herpesvirus pathogenesis was made by Riteau et al. . These authors suggest that herpesviruses can take advantage of mediators of inflammatory processes, namely extracellular proteases. Exposure of PRV-infected cells to trypsin increases virus production through activation of the extracellular signal-regulated kinase (ERK)1/2 signaling pathway. Reports describing protease-mediated extracellular matrix remodeling in association with viral infection are limited. Human papilloma virus (HPV) has been reported to induce both matrix metalloproteinase 2 (MMP-2) and MMP-9, two type IV collagenases. Type IV collagenases degrade the collagen type IV component of the basement membrane [26, 27]. Two herpesviruses, Epstein-Barr virus (EBV) and herpes simplex virus (HSV), have also been reported to induce MMP-9 [14, 28]. Whether this MMP-9 induction plays a role in EBV pathogenesis is unclear at present . HSV encephalitis is characterized by an early MMP-9 increase and collagen type IV degradation causing disruption of the neurovascular matrix. This overexpression in proteolytic activity is believed to result from central nervous system inflammation, rather than from the viral infection itself and its role in pathogenesis is unclear .
More specifically, in the current study, we demonstrate that a trypsin-like serine protease is involved in viral penetration of the BM. Since serine protease activity involvement has been described in different stages of the herpesvirus life cycle , the effect of the Soybean trypsin-like protease inhibitor on general PRV replication was tested in ST and MDCK cells. No defect in viral replication was observed (data not shown), which is consistent with the observation that none of the inhibitors tested affected lateral viral spread above the BM in explants (Figures 1, 2, 3 and 4). Inhibition of trypsin-like serine protease activity strongly reduced the plaque depth underneath the BM. The time course of trypsin-like serine protease inhibitor treatment revealed less prominent reductions in plaque depth underneath the BM when explants were treated at later time points pi. These results are in line with our observation that PRV already crosses the BM between 12 and 16 h pi. In addition to trypsin-like proteases, serine proteases also encompass chymotrypsin-like and elastase-like proteases . Therefore, a similar time course experiment was performed using inhibitors for chymotrypsin-like (TPCK) or elastase-like (elastatinal) serine proteases. No plaques were observed after treatment with TPCK, except for some small plaques in two conditions of one of the 3 piglets (3 h pi and 6 h pi). This perhaps may point to side or toxic effects of this inhibitor. Therefore, the involvement of chymotrypsin-like serine protease activity in PRV BM penetration could not be examined. Elastatinal did not reduce the plaque depth underneath the BM. However, since working solutions of elastase-like serine protease inhibitors have a relatively low stability (datasheet), we cannot formally exclude the possible involvement of either chymotrypsin-like or elastase-like serine protease activity in BM passage of PRV.
We can conclude that trypsin-like serine protease activity is involved in PRV invasion through the BM towards the lamina propria. We hypothesize that this trypsin-like serine protease activity is involved in local degradation of BM barrier components, thereby enhancing BM penetration. An important question that remains is whether the proteases involved are of cellular and/or viral origin. Interestingly, transcriptome studies have indicated that several cellular components involved in trypsin-like serine protease activity are differentially regulated upon infection with alphaherpesviruses like PRV and HSV, including factor IX, tissue-type plasminogen activator (t-PA) and urinary plasminogen activator receptor 1 (uPAR1) [30, 31]. Further research will be aimed at identifying the proteases involved and elucidating the exact molecular mechanism of viral penetration through the BM.
This research was supported by a Concerted Research Action of the Research Council of Ghent University and by the Agency for Innovation by Science and Technology in Flanders (IWT)) [IWT/OZM/090644]. David Lefebvre, Nick De Regge, Marc Geldhof, Geert Opsomer and Fernand De Backer are acknowledged for their help with handling and euthanizing the piglets.
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