- freely available
Viruses 2013, 5(1), 406-422; doi:10.3390/v5010406
Published: 22 January 2013
Abstract: Pneumovirus infections cause a wide spectrum of respiratory disease in humans and animals. The airway epithelium is the major site of pneumovirus replication. Apoptosis or regulated cell death, may contribute to the host anti-viral response by limiting viral replication. However, apoptosis of lung epithelial cells may also exacerbate lung injury, depending on the extent, the timing and specific location in the lungs. Differential apoptotic responses of epithelial cells versus innate immune cells (e.g., neutrophils, macrophages) during pneumovirus infection can further contribute to the complex and delicate balance between host defense and disease pathogenesis. The purpose of this manuscript is to give an overview of the role of apoptosis in pneumovirus infection. We will examine clinical and experimental data concerning the various pro-apoptotic stimuli and the roles of apoptotic epithelial and innate immune cells during pneumovirus disease. Finally, we will discuss potential therapeutic interventions targeting apoptosis in the lungs.
Pneumoviruses are single-stranded, negative-sense, enveloped RNA viruses belonging to the family Paramyxoviridae, subfamily Pneumovirinae, and include several closely related, but species-limited, members (reviewed by Easton et al. ). The human pneumovirus respiratory syncytial virus (hRSV) is a leading respiratory pathogen in young children and the elderly worldwide and is associated with considerable morbidity and mortality and high health care costs [2,3]. Likewise, bovine RSV (bRSV) causes outbreaks of respiratory disease in young beef and dairy cattle. Both bRSV infection in cattle and infection of mice by the rodent-specific pneumovirus pneumonia virus of mice (PVM) have been studied extensively as a model for hRSV disease in humans . Pneumovirus infections in humans and animals cause a wide spectrum of respiratory disease symptoms, ranging from mild upper airway illness, such as coryza and cough, to lower respiratory tract disease (e.g., bronchiolitis and bronchopneumonia), which may eventually lead to impaired gas-exchange and life threatening respiratory failure. Human infants with hRSV infection are prone to develop acute respiratory distress syndrome (ARDS), an acute-onset life threatening inflammatory lung condition associated with widespread lung injury [5,6]. Currently, as no specific treatment options for severe hRSV disease in humans exist, there is an ongoing research effort focusing on pneumovirus biology and host-interaction, ultimately to find novel therapies.
Apoptosis, a highly regulated energy-dependent type of cell death with distinct morphological and biochemical characteristics , is a basic biological response of cells to virus entry and replication . While apoptosis of virus-infected cells may be an important first line host defense mechanism to limit pathogen replication and spread, many viruses have evolved strategies to evade and modulate intracellular pro-apoptotic signaling in the early replication phase [9,10]. Conversely, it has become clear that viruses may also exploit the cellular pro-apoptotic machinery in the formation and spread of infectious progeny virions in the late phase or in the elimination of immune cells, thereby evading host defense [10,11]. At the same time, from the host’s perspective, extensive pro-apoptotic signaling may be beneficial in attacking a virus, but may become devastating upon the occurrence of an overshoot in apoptosis, leading to widespread loss of infected and/or uninfected bystander structural cells. Such an unbalanced extensive apoptotic response is implicated in the pathogenesis of a wide variety of diseases, including the development of diffuse lung epithelial injury in ARDS . Taken together, the outcome of apoptosis during viral infection for the host may depend on its extent, timing and cell-specificity.
The occurrence and potential role of apoptosis in pneumovirus infections have been investigated in both in vivo (human and animal) and in vitro studies. The main goal of this manuscript is to provide an overview of the existing literature on pro- and anti-apoptotic signaling in pneumovirus infections with a focus on lung (airway and alveolar) epithelial cells, neutrophils and macrophages as first line cellular responders to acute pneumovirus infection. Furthermore, we will speculate on future apoptosis-based pharmacological therapies in hRSV disease.
2. Apoptotic Signaling Pathways
Cell death in multicellular organisms occurs either by necrosis or apoptosis, however their strict distinction is somewhat artificial, because overlap of their characteristics and cellular pathways may occur [13,14,15]. Apoptosis is associated with membrane blebbing, cell breakdown into apoptotic bodies and fragmentation of DNA. “Classical” apoptosis refers to the activation of the caspase cascade, a family of intracellular substrate specific proteases of which the final executioner, caspase-3, is a commonly used marker for apoptosis. Non-classical apoptosis occurs independent of caspase activation and involves release of the flavoprotein apoptosis-inducing factor (AIF) from mitochondria. Galluzzi el al. have provided an extensive and detailed review on the use and interpretation of caspase-(in)dependent apoptosis assays in laboratory research .
Figure 1 shows the conceptual framework of the major (caspase-dependent) apoptotic pathways, which are relevant to discuss in the context of pneumovirus infection. The intrinsic or mitochondrial pathway involves the release of cytochrome c from mitochondria into the cytoplasm and is regulated by Bcl-2 protein family members. The extrinsic or death receptor pathway is triggered by ligation of transmembrane death receptors that belong to the tumor necrosis factor (TNF) death receptor family, which include TNF receptor (TNFR), Fas (CD95) and TNF-related apoptosis-inducing ligand (TRAIL) death receptors (TRAIL-R1 and -R2). Expression and activation of proteins in both these pathways can be modulated by p53, a major cell stress sensor protein. Finally, the granule-mediated cytotoxic pathway is exploited by effector lymphocytes, which can release serine proteases, known as granzymes, into the cytosol of target cells, which subsequently results in caspase-(in)dependent apoptosis. Activation and modulation of these three apoptotic pathways is associated with pneumovirus infection in humans and animals, as will be discussed below.
3. Lung (Airway and Alveolar) Epithelial Cell Apoptosis
In the lower airways, the bronchiolar epithelium is the primary site of human and animal pneumovirus infection [17,18,19,20]. In addition, viral antigen can be detected in alveolar epithelial cells in severe hRSV-, bRSV- and PVM-induced bronchopneumonia [18,19,20,21]. An interesting and consistently reported feature of severe pneumovirus disease is the sloughing of dead airway epithelial cells, which form dense plugs with mucus, fibrin and leukocytes, resulting in air trapping and ventilatory failure [18,20,21,22,23]. The loss of these epithelial cells has always been thought to occur primarily through necrosis, however Welliver et al. observed marked active caspase-3 immunostaining in bronchiolar epithelium of children with fatal hRSV disease, suggesting that apoptosis is an important mechanism of cell death as well (Figure 2A) [20,24]. Likewise, lung epithelial cells show enhanced DNA fragmentation as detected by terminal dUTP nick-end labeling (TUNEL) in bRSV infected calves and increased caspase-3 activation in PVM infected mice [19,25] (Figure 2B). The relative importance of apoptosis in cell decay in pneumovirus infected lungs is further supported by the finding of a strong correlation between caspase-3 and -7 activity and LDH concentration in the airways in children with hRSV-induced bronchiolitis; however, from this study, the exact cellular source of these markers is not clear .
The occurrence of apoptosis in the lung epithelium during the course of pneumovirus infection may serve to limit viral replication. However, the widespread and extensive scale on which this takes place, involving the whole pulmonary system, including the alveoli, may also suggests an overshoot and/or inefficiency of pro-apoptotic signaling during the late and severe phase of pneumovirus infection. This may lead to enhanced respiratory disease, e.g., diffuse alveolar epithelial injury, as seen in human ARDS  and influenza virus animal models . We believe three scenarios regarding lung epithelial cell apoptosis during pneumovirus infection may co-exist as described below (Figure 3), and the balance between them is likely to be critical for the development and outcome of host disease.
3.1. Pneumovirus Infected Cells May Undergo Apoptosis as a Result of Direct Activation of Intrinsic Pathways.
Based on the results of a number of in vitro studies in cultured primary airway epithelial cells and A549 cells (an adenocarcinomic human alveolar basal epithelial cell line) it appears that, although in the early phase of hRSV infection apoptosis does not occur, this type of cell death becomes an important response in the later phase of viral replication [28,29,30,31,32,33,34,35,36,37,38,39]. It should be noted however that several of these studies show some conflicting results with regard to the time point at which apoptosis is detected, possibly related to the use of different cell lines/cultures, multiplicity of infection, hRSV strains, early versus late apoptosis markers and assays used.
The relative paucity of apoptosis during the early phase of hRSV infection may be explained by viral-induced anti-apoptotic intrinsic pathway signaling, which ensures more time for viral replication and assembly of virions. Mechanisms of early hRSV-induced alteration of the intrinsic pathway towards an anti-apoptotic balance in Bcl-2 family proteins include post-transcriptional regulation of p53 , microRNA modulation  and three important basic cell survival/proliferation pathways involving nerve growth factor/tyrosine kinase receptor (NGF/Trk) , epidermal growth factor receptor (EGFR)  and phosphoinositide 3-kinase(PI3K)/Akt signaling . Interestingly, by using recombinant and RNA silencing techniques, it was shown that both the hRSV-encoded small hydrophobic (SH) protein and nonstructural (NS) proteins are critical regulators of the early anti-apoptotic effects [29,31]. The NS proteins have been found to interfere with interferon (IFN) signaling , which may affect apoptotic pathways in hRSV infected cells. However, Bitko et al.  suggested that the early NS protein associated anti-apoptotic effect was mediated through NF-κB and PI3K/Akt signaling, independent of the IFN pathway.
Pro-apoptotic signaling appears to predominate at a later phase of hRSV infection [29,30,34,39]. The hRSV-encoded fusion (F) protein, which is expressed at a later time point as compared to the NS proteins , has been found to be critical in the activation of apoptosis by p53-mediated activation of pro-apoptotic Bcl-2 family proteins . Apoptosis markers in hRSV-infected A549 and human primary airway epithelial cells further include caspase activation, detection of phosphatidylserine exposition by Annexin V and TUNEL staining. However, the susceptibility of epithelial cells to pneumovirus-associated apoptosis may vary depending on the specific localization (proximal versus distal) in the lungs . Importantly, in the recent study by Villenave et al. well-differentiated primary bronchial epithelial cells of children cultured in air-liquid interface showed TUNEL-positive staining in detached cells six days after hRSV infection . This supports the hypothesis that apoptosis contributes to the characteristic sloughing of epithelial cells in the airways of children during the late phase of pneumovirus infection.
3.2. Pneumovirus Infected Cells May Undergo Apoptosis by Activation of Extrinsic and Granule-Mediated Pathways
First, death receptor ligands may trigger apoptosis of virus infected epithelial cells. Several studies have shown enhanced local production of TNFα, FasL and TRAIL by recruited immune cells or neighbor epithelial cells upon pneumovirus infection [4,28,34,39,42,43]. Interestingly, in vitro studies have shown that, whereas hRSV infection results in decreased susceptibility to TNFα-induced apoptosis , it sensitizes lung epithelial cells to the pro-apoptotic effects of TRAIL , which likely occurs as a result of increased expression of death receptors TRAIL-R1 and -R2 [34,42]. Similarly, enhanced epithelial surface expression of Fas in hRSV infection has been found in both in vitro and human histopathology studies [20,28,45]. Interestingly, mice with a non-functional FasL (gld strain) have been reported to have delayed hRSV clearance , but van den Berg et al.  did not detect differences in lung viral loads in PVM-infected mice with a defective Fas (lpr strain) as compared to wild type mice. This differential effect of a dysfunctional Fas/FasL system on viral clearance in these different pneumovirus models may be explained by specific pneumovirus-host interactions, although may potentially also be related to a leaky, incomplete Fas defect in lpr mice.
Second, granzymes released from the granules of natural killer cells and cytotoxic T-lymphocytes into virus infected target cells may induce apoptosis. In children with severe hRSV disease, we have found strong release of granzymes in the lungs . Similarly, PVM infected mice show enhanced granzyme expression, however this appears not to affect local viral titers , suggesting that the granule-mediated apoptotic pathway does not have an important role in clearance of pneumovirus infected epithelial cells.
3.3. Uninfected Bystander Epithelial Cells May Undergo Apoptosis as a Result of Extensive and Non-Specific Activation of Extrinsic and Granule-Mediated Pathways
Although pneumovirus antigen can be detected in alveolar epithelium in the late and severe phase of human and animal pneumovirus disease, the primary site of replication are (small) airway epithelial cells [17,18,19,20,21]. Interestingly, histopathology studies in humans with fatal hRSV disease and animal models show epithelial cell apoptosis may occur in the entire pulmonary system, including the alveolar compartment [4,19,24,25]. In fact, we have previously detected active caspase-3 immunostaining primarily in alveolar epithelial cells in mice with severe PVM disease, while this apoptosis marker was scarce in bronchial epithelium . Such a potential disparity in the localization between pneumovirus presence and apoptosis may suggest uninfected bystander cells in the lungs are victim of an overshoot and/or inefficiency in pro-apoptotic signaling, and this may lead to enhanced pneumovirus disease.
The bystander injury hypothesis is supported by two in vivo studies in mice: Rutigliano et al.  showed that while a dysfunctional FasL results in delayed hRSV clearance, at the same time it significantly diminishes clinical illness; and, our own group showed that while a deficiency in granzymes did not affect PVM clearance, it resulted in delayed clinical disease in association with a marked decrease in lung caspase-3 activity . In addition, we have previously shown that soluble TRAIL is present in increased levels in bronchoalveolar lavage fluid of children with severe hRSV disease, and this death receptor ligand induced cell death in uninfected primary pediatric airway epithelial cells in vitro . Interestingly, similar findings for soluble FasL were found in relation to epithelial injury in human ARDS . When considering the bystander epithelial injury hypothesis, soluble death receptor ligands present in the lung microenvironment during pneumovirus disease are of particular interest due to the potential increased likelihood of non-specific signaling. They may be released into the extracellular space from recruited immune cells, such as macrophages  and neutrophils  or from (infected) neighbor epithelial cells (paracrine pathway) , although in vitro studies by Bitko et al.  suggested a minor role for the latter mechanism.
4. Neutrophil Apoptosis
Neutrophils, recruited by local production of chemoattractants, are the predominant inflammatory cells in the pulmonary compartment during acute pneumovirus infection [4,52,53,54]. They possess a wide arsenal of defensive strategies against invading microorganisms, including phagocytosis, production of toxic reactive oxygen species and release of immune defense proteins. Although the role of neutrophils in anti-viral immunity remains relatively unclarified, several studies have shown a protective effect of neutrophils against influenza virus [55,56]. Both animal and human studies demonstrated that during pneumovirus infection, recruited neutrophils contain virus, suggesting a contributive role to viral clearance [19,57]. This is further supported by in vitro studies that showed neutrophil-mediated injury and detachment of hRSV infected lung epithelial cells . On the other hand, it is well recognized that uncontrolled or prolonged neutrophil activity may cause collateral tissue injury , such as diffuse alveolar damage in human ARDS [60,61,62]. Although direct evidence of neutrophil-mediated respiratory disease in pneumovirus infection is lacking, the acute and strong neutrophil influx in the lungs coincides with peak disease severity in animal models [19,25].
To prevent their potential inadvertent harmful effect, the life span of neutrophils is limited by apoptosis. Interestingly, incubation of human neutrophils with hRSV in vitro results in activation of anti-apoptotic signaling through the Bcl-2 family proteins . Although this inhibition of neutrophil cell death by hRSV does not require live virus, it does require cellular uptake. Lindemans et al.  further suggested this effect depends on auto- or paracrine-signaling via the release of IL-6. Others, however, have suggested that the anti-apoptotic effect of hRSV on human neutrophils is primarily mediated by soluble factors via monocyte interaction and, thus, is a secondary response . Regardless of the precise mechanism involved, these in vitro studies suggest prolonged neutrophil survival in the setting of hRSV infection and, as such, this may be an important event in the development of lung injury during pneumovirus disease. In contrast, Wang et al.  reported an increased number of Annexin V positive neutrophils in nasopharyngeal aspirates and the peripheral blood of infants with hRSV disease, as compared to peripheral blood neutrophils of healthy children. This would imply that despite the pro-survival effect of hRSV on neutrophils as observed in vitro, pro-apoptotic signaling by mediators (e.g., cytokines) in the lung microenvironment during hRSV disease prevails. Whether this truly would protect against harmful prolonged neutrophil survival remains speculative. In particular, it is possible that different neutrophil apoptotic responses in functionally heterogeneous neutrophil subsets co-exist and change over time [66,67]. As such, it is clear that further research on the precise role of neutrophil apoptosis during pneumovirus infections is highly needed.
5. Macrophage Apoptosis
Macrophages are observed in high numbers in the airways and lungs of humans and animals with pneumovirus disease [4,18,19,20,22,23,52,54]. Macrophages are key innate immune cells acting in pathogen surveillance and initiation and resolution of inflammation through mechanisms involving antigen processing/presentation, phagocytosis and cytokine production. Macrophage depletion in wild-type mice infected by hRSV or PVM results in increased lung viral titers and greatly affects the local cytokine production [23,68,69]. However, paradoxically in PVM-infected mice, this results in prolonged survival, whereas in hRSV challenged mice, this is associated with enhanced airway occlusion on histopathological examination [23,69], suggesting that the role of macrophages may depend on specific host-pneumovirus interactions. Nevertheless, these findings underline the importance of macrophage biology in pneumovirus infection. As such, dysregulation of (apoptotic) cell death pathways in resident and migrated macrophages in the lungs may have profound consequences for the outcome of pneumovirus infection.
Unfortunately, very few studies have focused on macrophage apoptosis in pneumovirus disease. In the histopathological studies from Welliver et al., fatal hRSV disease in children was associated with relatively low numbers of caspase-3 immunoreactive inflammatory cells in the lungs, as compared to children with fatal influenza virus disease . In mice challenged with PVM, we observed cleaved caspase-3 positive macrophages in the alveolar spaces (unpublished observations, ); however, the exact magnitude and role of apoptosis of these cells in this model is not yet clear.
Ex vivo and autopsy studies have shown that virus antigen is detected in macrophages in the airways and lungs of hRSV infected patients [18,71]. In addition, isolated peripheral and cord blood monocytes, as well as alveolar macrophages, are susceptible to hRSV infection in vitro [72,73], and PVM was recently shown to replicate in primary mouse macrophage culture . Interestingly, hRSV presence in human monocytes and mouse macrophages results in decreased (susceptibility of) apoptosis, associated with decreased caspase-3 activity and enhanced expression of anti-apoptotic members of the Bcl-2 protein family and inhibitor of apoptosis protein (IAP) family [74,75]. These observations suggest pneumoviruses exploit strategies to escape apoptosis in macrophages and could explain the apparent paucity of evidence for macrophage apoptosis in the aforementioned histopathology studies.
6. Apoptosis-Based Pharmacological Intervention
During the last decades, much progress has been made in the development of apoptosis-based therapeutic agents, including antisense oligodeoxynucleotides, small interfering (si)RNA, peptides/proteins and antibodies (reviewed by Fischer et al. ). Much attention in this field has been directed towards cancer treatment, however inflammatory and infectious diseases are of emerging focus. The increasing knowledge in the regulation and molecular machinery of apoptotic cell death pathways involving many different target genes and proteins has set the stage for highly promising research in pharmacological intervention. Death receptors, caspases and IAP and Bcl-2 protein family members all belong to prominent targets in current drug development . However, despite the ongoing success of pre-clinical and even clinical studies exploiting the use of apoptosis-based drugs in a wide variety of diseases, many obstacles still have to be overcome, including cell-specificity and permeability, timing of intervention and potential toxicity or interference with other biological processes, such as inflammation.
To our knowledge, up to date, no published studies have directly examined the effects of apoptosis-based pharmacological treatments in pneumovirus disease in vivo. Although originally designed to study macrophage depletion rather than directly focusing on apoptosis intervention, Rigaux et al.  found that intratracheal treatment with clodronate-liposomes, which induces apoptosis upon specific uptake by macrophages , prolongs the survival of PVM-infected mice. This suggests that enhancing macrophage apoptosis in pneumovirus disease is of clinical interest. Currently, our own group is studying the use of the irreversible pan-caspase inhibitor, z-VAD-fmk, administrated by a systemic route in mice challenged with PVM (study in progress). In addition, we have shown that treatment with DR5-Fc fusion protein, which inhibits TRAIL death receptor signaling, partly attenuates cell death of primary pediatric bronchial airway cells exposed to bronchoalveolar lavage fluid from hRSV-infected children in vitro . However the effects of this compound in vivo are yet unclear. Given the strong evidence of activation of pro- and anti-apoptotic pathways during pneumovirus infection as described in the above paragraphs, more attention towards this field is highly needed.
Several critical points need to be considered in potential apoptosis-based interventions in pneumovirus disease. First is the cell-specificity. From the present overview, it becomes clear that different cell types in the lungs may show differential apoptotic responses during pneumovirus disease. Interestingly, even within a lung cell population (e.g., epithelial cells), differential responses to a single apoptotic mediator may exist [78,79], including in the setting of pneumovirus infection , which further increases the complexity of intervention. This stresses the need for insight in cell-specific pro- and anti-apoptotic targets and for development of small molecule compounds and vehicles for specific local intervention. On the other hand, even without specific target cell delivery systems, animal studies modeling ARDS have shown promising beneficial effects on survival and histopathological changes by using a number of systemic or intratracheal apoptosis-based treatments, including blockade of FasL by decoy receptor-3 , Fas:Ig fusion protein  or Fas-siRNA  and pan-caspase inhibition by z-VAD-fmk . These studies successfully aimed to inhibit lung epithelial cell apoptosis during the process of lung injury. However, it remains to be elucidated whether such strategies also effectively reduce lung epithelial cell death in pneumovirus disease and, subsequently, to what extent this affects viral replication and, most importantly, clinical outcome. Second, given the dynamic course of anti- and pro-apoptotic signaling in lung epithelial cells, timing of apoptotic interventions may be critical, as, for example, inhibitory strategies may be beneficial in the late severe phase of disease, but detrimental in the early stages of viral replication. Third, concurrent iatrogenic treatments with pro-apoptotic effects, such as mechanical ventilation and/or oxygen therapy [70,84], may interact with apoptosis-based interventions in the lungs. Fourth and finally, the effect of modulating apoptosis in the lungs needs to be considered with special focus on age, as apoptosis is an important event in lung development and maturation .
Pneumovirus infection is associated with both pro- and anti-apoptotic signaling in the lungs, depending on the cell-type, involvement of specific cell death pathway and timing during the course of infection. The balance between these events is likely to be critical for the development and outcome of pneumovirus disease. However, more research is needed to fully understand the dynamic character of apoptosis during this important respiratory illness. In particular, we need to address which factors favor the viral propagation versus host defense. Here, we have reviewed the existing literature on this topic and have speculated on future apoptosis-based pharmacological treatments.
Conflict of Interest
The authors declare no conflict of interest.
The authors thank Inge Kos-Oosterling from the AMC Medical Illustration Service for help with the figure drawings. No specific financial support or grants are reported.
- Easton, A.J.; Domachowske, J.B.; Rosenberg, H.F. Animal pneumoviruses: molecular genetics and pathogenesis. Clin. Microbiol. Rev. 2004, 17, 390–412, doi:10.1128/CMR.17.2.390-412.2004.
- Falsey, A.R.; Hennessey, P.A.; Formica, M.A.; Cox, C.; Walsh, E.E. Respiratory syncytial virus infection in elderly and high-risk adults. N. Engl. J. Med. 2005, 352, 1749–1759, doi:10.1056/NEJMoa043951.
- Nair, H.; Nokes, D.J.; Gessner, B.D.; Dherani, M.; Madhi, S.A.; Singleton, R.J.; O'Brien, K.L.; Roca, A.; Wright, P.F.; Bruce, N.; et al. Global burden of acute lower respiratory infections due to respiratory syncytial virus in young children: a systematic review and meta-analysis. Lancet 2010, 375, 1545–1555, doi:10.1016/S0140-6736(10)60206-1.
- Bem, R.A.; Domachowske, J.B.; Rosenberg, H.F. Animal models of human respiratory syncytial virus disease. Am. J. Physiol. Lung Cell Mol. Physiol. 2011, 301, 148–156, doi:10.1152/ajplung.00065.2011.
- ARDS definition task force Acute respiratory distress syndrome—The Berlin definition. JAMA 2012, 307, 256–2533.
- Dahlem, P.; van Aalderen, W.M.; Hamaker, M.E.; Dijkgraaf, M.G.; Bos, A.P. Incidence and short-term outcome of acute lung injury in mechanically ventilated children. Eur. Respir. J. 2003, 22, 980–985, doi:10.1183/09031936.03.00003303.
- Kerr, J.F.; Wyllie, A.H.; Currie, A.R. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br. J. Cancer 1972, 26, 239–257, doi:10.1038/bjc.1972.33.
- Barber, G.N. Host defense, viruses and apoptosis. Cell Death. Differ. 2001, 8, 113–126, doi:10.1038/sj.cdd.4400823.
- Benedict, C.A.; Norris, P.S.; Ware, C.F. To kill or be killed: Viral evasion of apoptosis. Nat. Immunol. 2002, 3, 1013–1018, doi:10.1038/ni1102-1013.
- Galluzzi, L.; Brenner, C.; Morselli, E.; Touat, Z.; Kroemer, G. Viral control of mitochondrial apoptosis. PLoS Pathog 2008, 4, e1000018, doi:10.1371/journal.ppat.1000018.
- Herold, S.; Ludwig, S.; Pleschka, S.; Wolff, T. Apoptosis signaling in influenza virus propagation, innate host defense and lung injury. J. Leukoc. Biol. 2012, 92, 75–82, doi:10.1189/jlb.1011530.
- Martin, T.R.; Hagimoto, N.; Nakamura, M.; Matute-Bello, G. Apoptosis and epithelial injury in the lungs. Proc. Am. Thorac. Soc. 2005, 2, 214–220, doi:10.1513/pats.200504-031AC.
- Denecker, G.; Vercammen, D.; Declercq, W.; Vandenabeele, P. Apoptotic and necrotic cell death induced by death domain receptors. Cell Mol. Life Sci. 2001, 58, 356–370, doi:10.1007/PL00000863.
- Leist, M.; Jaattela, M. Four deaths and a funeral: From caspases to alternative mechanisms. Nat. Rev. Mol. Cell Biol. 2001, 2, 589–598, doi:10.1038/35085008.
- Wang, X.; Ryter, S.W.; Dai, C.; Tang, Z.L.; Watkins, S.C.; Yin, X.M.; Song, R.; Choi, A.M. Necrotic cell death in response to oxidant stress involves the activation of the apoptogenic caspase-8/bid pathway. J. Biol. Chem. 2003, 278, 29184–29191.
- Galluzzi, L.; Aaronson, S.A.; Abrams, J.; Alnemri, E.S.; Andrews, D.W.; Baehrecke, E.H.; Bazan, N.G.; Blagosklonny, M.V.; Blomgren, K.; Borner, C.; et al. Guidelines for the use and interpretation of assays for monitoring cell death in higher eukaryotes. Cell Death Differ. 2009, 16, 1093–1107, doi:10.1038/cdd.2009.44.
- Bonville, C.A.; Bennett, N.J.; Koehnlein, M.; Haines, D.M.; Ellis, J.A.; DelVecchio, A.M.; Rosenberg, H.F.; Domachowske, J.B. Respiratory dysfunction and proinflammatory chemokines in the pneumonia virus of mice (PVM) model of viral bronchiolitis. Virology 2006, 349, 87–95, doi:10.1016/j.virol.2006.02.017.
- Johnson, J.E.; Gonzales, R.A.; Olson, S.J.; Wright, P.F.; Graham, B.S. The histopathology of fatal untreated human respiratory syncytial virus infection. Mod. Pathol. 2007, 20, 108–119, doi:10.1038/modpathol.3800725.
- Viuff, B.; Tjornehoj, K.; Larsen, L.E.; Rontved, C.M.; Uttenthal, A.; Ronsholt, L.; Alexandersen, S. Replication and clearance of respiratory syncytial virus: Apoptosis is an important pathway of virus clearance after experimental infection with bovine respiratory syncytial virus. Am. J. Pathol. 2002, 161, 2195–2207, doi:10.1016/S0002-9440(10)64496-3.
- Welliver, T.P.; Reed, J.L.; Welliver, R.C., Sr. Respiratory syncytial virus and influenza virus infections: observations from tissues of fatal infant cases. Pediatr. Infect. Dis. J. 2008, 27, 92–96, doi:10.1097/INF.0b013e318168b706.
- Cook, P.M.; Eglin, R.P.; Easton, A.J. Pathogenesis of pneumovirus infections in mice: Detection of pneumonia virus of mice and human respiratory syncytial virus mRNA in lungs of infected mice by in situ hybridization. J. Gen. Virol. 1998, 79, 2411–2417.
- Aherne, W.; Bird, T.; Court, S.D.; Gardner, P.S.; McQuillin, J. Pathological changes in virus infections of the lower respiratory tract in children. J. Clin. Pathol. 1970, 23, 7–18, doi:10.1136/jcp.23.1.7.
- Reed, J.L.; Brewah, Y.A.; Delaney, T.; Welliver, T.; Burwell, T.; Benjamin, E.; Kuta, E.; Kozhich, A.; McKinney, L.; Suzich, J.; et al. Macrophage impairment underlies airway occlusion in primary respiratory syncytial virus bronchiolitis. J. Infect. Dis. 2008, 198, 1783–1793, doi:10.1086/593173.
- Welliver, T.P.; Garofalo, R.P.; Hosakote, Y.; Hintz, K.H.; Avendano, L.; Sanchez, K.; Velozo, L.; Jafri, H.; Chavez-Bueno, S.; Ogra, P.L.; et al. Severe human lower respiratory tract illness caused by respiratory syncytial virus and influenza virus is characterized by the absence of pulmonary cytotoxic lymphocyte responses. J. Infect. Dis. 2007, 195, 1126–1136, doi:10.1086/512615.
- Bem, R.A.; van Woensel, J.B.; Lutter, R.; Domachowske, J.B.; Medema, J.P.; Rosenberg, H.F.; Bos, A.P. Granzyme A- and B-cluster deficiency delays acute lung injury in pneumovirus-infected mice. J. Immunol. 2010, 184, 931–938, doi:10.4049/jimmunol.0903029.
- Laham, F.R.; Trott, A.A.; Bennett, B.L.; Kozinetz, C.A.; Jewell, A.M.; Garofalo, R.P.; Piedra, P.A. LDH concentration in nasal-wash fluid as a biochemical predictor of bronchiolitis severity. Pediatrics 2010, 125, 225–233, doi:10.1542/peds.2009-0411.
- Herold, S.; Steinmueller, M.; von, W.W.; Cakarova, L.; Pinto, R.; Pleschka, S.; Mack, M.; Kuziel, W.A.; Corazza, N.; Brunner, T.; et al. Lung epithelial apoptosis in influenza virus pneumonia: the role of macrophage-expressed TNF-related apoptosis-inducing ligand. J. Exp. Med. 2008, 205, 3065–3077, doi:10.1084/jem.20080201.
- Bitko, V.; Barik, S. An endoplasmic reticulum-specific stress-activated caspase (caspase-12) is implicated in the apoptosis of A549 epithelial cells by respiratory syncytial virus. J. Cell Biochem. 2001, 80, 441–454, doi:10.1002/1097-4644(20010301)80:3<441::AID-JCB170>3.0.CO;2-C.
- Bitko, V.; Shulyayeva, O.; Mazumder, B.; Musiyenko, A.; Ramaswamy, M.; Look, D.C.; Barik, S. Nonstructural proteins of respiratory syncytial virus suppress premature apoptosis by an NF-kappaB-dependent, interferon-independent mechanism and facilitate virus growth. J. Virol. 2007, 81, 1786–1795, doi:10.1128/JVI.01420-06.
- Eckardt-Michel, J.; Lorek, M.; Baxmann, D.; Grunwald, T.; Keil, G.M.; Zimmer, G. The fusion protein of respiratory syncytial virus triggers p53-dependent apoptosis. J. Virol. 2008, 82, 3236–3249, doi:10.1128/JVI.01887-07.
- Fuentes, S.; Tran, K.C.; Luthra, P.; Teng, M.N.; He, B. Function of the respiratory syncytial virus small hydrophobic protein. J. Virol. 2007, 81, 8361–8366.
- Groskreutz, D.J.; Monick, M.M.; Yarovinsky, T.O.; Powers, L.S.; Quelle, D.E.; Varga, S.M.; Look, D.C.; Hunninghake, G.W. Respiratory syncytial virus decreases p53 protein to prolong survival of airway epithelial cells. J. Immunol. 2007, 179, 2741–2747.
- Groskreutz, D.J.; Monick, M.M.; Babor, E.C.; Nyunoya, T.; Varga, S.M.; Look, D.C.; Hunninghake, G.W. Cigarette smoke alters respiratory syncytial virus-induced apoptosis and replication. Am. J. Respir. Cell Mol. Biol. 2009, 41, 189–198, doi:10.1165/rcmb.2008-0131OC.
- Kotelkin, A.; Prikhod'ko, E.A.; Cohen, J.I.; Collins, P.L.; Bukreyev, A. Respiratory syncytial virus infection sensitizes cells to apoptosis mediated by tumor necrosis factor-related apoptosis-inducing ligand. J. Virol. 2003, 77, 9156–9172, doi:10.1128/JVI.77.17.9156-9172.2003.
- Monick, M.M.; Cameron, K.; Staber, J.; Powers, L.S.; Yarovinsky, T.O.; Koland, J.G.; Hunninghake, G.W. Activation of the epidermal growth factor receptor by respiratory syncytial virus results in increased inflammation and delayed apoptosis. J. Biol. Chem. 2005, 280, 2147–2158.
- Othumpangat, S.; Gibson, L.F.; Samsell, L.; Piedimonte, G. NGF is an essential survival factor for bronchial epithelial cells during respiratory syncytial virus infection. PLoS One 2009, 4, e6444.
- Takeuchi, R.; Tsutsumi, H.; Osaki, M.; Haseyama, K.; Mizue, N.; Chiba, S. Respiratory syncytial virus infection of human alveolar epithelial cells enhances interferon regulatory factor 1 and interleukin-1beta-converting enzyme gene expression, but does not cause apoptosis. J. Virol. 1998, 72, 4498–4502.
- Thomas, K.W.; Monick, M.M.; Staber, J.M.; Yarovinsky, T.; Carter, A.B.; Hunninghake, G.W. Respiratory syncytial virus inhibits apoptosis and induces NF-kappa B activity through a phosphatidylinositol 3-kinase-dependent pathway. J. Biol. Chem. 2002, 277, 492–501.
- Villenave, R.; Thavagnanam, S.; Sarlang, S.; Parker, J.; Douglas, I.; Skibinski, G.; Heaney, L.G.; McKaigue, J.P.; Coyle, P.V.; Shields, M.D.; et al. In vitro modeling of respiratory syncytial virus infection of pediatric bronchial epithelium, the primary target of infection in vivo. Proc. Natl. Acad. Sci. USA 2012, 109, 5040–5045.
- Othumpangat, S.; Walton, C.; Piedimonte, G. MicroRNA-221 modulates RSV replication in human bronchial epithelium by targeting NGF expression. PLoS One 2012, 7, e30030.
- Spann, K.M.; Tran, K.C.; Chi, B.; Rabin, R.L.; Collins, P.L. Suppression of the induction of alpha, beta and lambda interferons by the NS1 and NS2 proteins of human respiratory syncytial virus in human epithelial cells and macrophages. J. Virol. 2004, 78, 4363–4369, doi:10.1128/JVI.78.8.4363-4369.2004.
- Bem, R.A.; Bos, A.P.; Wosten-van Asperen, R.M.; Bruijn, M.; Lutter, R.; Sprick, M.R.; van Woensel, J.B. Potential Role of Soluble TRAIL in Epithelial Injury in Children with Severe RSV Infection. Am. J. Respir. Cell Mol. Biol. 2009, 42, 697–705.
- Aung, S.; Rutigliano, J.A.; Graham, B.S. Alternative mechanisms of respiratory syncytial virus clearance in perforin knockout mice lead to enhanced disease. J. Virol. 2001, 75, 9918–9924, doi:10.1128/JVI.75.20.9918-9924.2001.
- Domachowske, J.B.; Bonville, C.A.; Mortelliti, A.J.; Colella, C.B.; Kim, U.; Rosenberg, H.F. Respiratory syncytial virus infection induces expression of the anti-apoptosis gene IEX-1L in human respiratory epithelial cells. J. Infect. Dis. 2000, 181, 824–830, doi:10.1086/315319.
- O'donnell, D.R.; Milligan, L.; Stark, J.M. Induction of CD95 (Fas) and apoptosis in respiratory epithelial cell cultures following respiratory syncytial virus infection. Virology 1999, 257, 198–207, doi:10.1006/viro.1999.9650.
- Rutigliano, J.A.; Graham, B.S. Prolonged production of TNF-alpha exacerbates illness during respiratory syncytial virus infection. J. Immunol. 2004, 173, 3408–3417.
- van den Berg, E.; van Woensel, J.B.; Bos, A.P.; Bem, R.A.; Altemeier, W.A.; Gill, S.E.; Martin, T.R.; Matute-Bello, G. Role of the Fas/FasL system in a model of RSV infection in mechanically ventilated mice. Am. J. Physiol. Lung Cell Mol. Physiol. 2011, 301, 451–460.
- Bem, R.A.; Bos, A.P.; Bots, M.; Wolbink, A.M.; van Ham, S.M.; Medema, J.P.; Lutter, R.; van Woensel, J.B. Activation of the granzyme pathway in children with severe respiratory syncytial virus infection. Pediatr. Res. 2008, 63, 650–655, doi:10.1203/PDR.0b013e31816fdc32.
- Matute-Bello, G.; Liles, W.C.; Steinberg, K.P.; Kiener, P.A.; Mongovin, S.; Chi, E.Y.; Jonas, M.; Martin, T.R. Soluble Fas ligand induces epithelial cell apoptosis in humans with acute lung injury (ARDS). J. Immunol. 1999, 163, 2217–2225.
- Serrao, K.L.; Fortenberry, J.D.; Owens, M.L.; Harris, F.L.; Brown, L.A. Neutrophils induce apoptosis of lung epithelial cells via release of soluble Fas ligand. Am. J. Physiol. Lung Cell Mol. Physiol. 2001, 280, 298–305.
- Powell, W.C.; Fingleton, B.; Wilson, C.L.; Boothby, M.; Matrisian, L.M. The metalloproteinase matrilysin proteolytically generates active soluble Fas ligand and potentiates epithelial cell apoptosis. Curr. Biol. 1999, 9, 1441–1447, doi:10.1016/S0960-9822(00)80113-X.
- Everard, M.L.; Swarbrick, A.; Wrightham, M.; McIntyre, J.; Dunkley, C.; James, P.D.; Sewell, H.F.; Milner, A.D. Analysis of cells obtained by bronchial lavage of infants with respiratory syncytial virus infection. Arch. Dis. Child 1994, 71, 428–432, doi:10.1136/adc.71.5.428.
- van Woensel, J.B.; Lutter, R.; Biezeveld, M.H.; Dekker, T.; Nijhuis, M.; van Aalderen, W.M.; Kuijpers, T.W. Effect of dexamethasone on tracheal viral load and interleukin-8 tracheal concentration in children with respiratory syncytial virus infection. Pediatr. Infect. Dis. J. 2003, 22, 721–726, doi:10.1097/01.inf.0000078165.62923.15.
- McNamara, P.S.; Ritson, P.; Selby, A.; Hart, C.A.; Smyth, R.L. Bronchoalveolar lavage cellularity in infants with severe respiratory syncytial virus bronchiolitis. Arch. Dis. Child. 2003, 88, 922–926, doi:10.1136/adc.88.10.922.
- Tate, M.D.; Deng, Y.M.; Jones, J.E.; Anderson, G.P.; Brooks, A.G.; Reading, P.C. Neutrophils ameliorate lung injury and the development of severe disease during influenza infection. J. Immunol. 2009, 183, 7441–7450, doi:10.4049/jimmunol.0902497.
- Tumpey, T.M.; Garcia-Sastre, A.; Taubenberger, J.K.; Palese, P.; Swayne, D.E.; Pantin-Jackwood, M.J.; Schultz-Cherry, S.; Solorzano, A.; van, R.N.; Katz, J.M.; et al. Pathogenicity of influenza viruses with genes from the 1918 pandemic virus: functional roles of alveolar macrophages and neutrophils in limiting virus replication and mortality in mice. J. Virol. 2005, 79, 14933–14944.
- Halfhide, C.P.; Flanagan, B.F.; Brearey, S.P.; Hunt, J.A.; Fonceca, A.M.; McNamara, P.S.; Howarth, D.; Edwards, S.; Smyth, R.L. Respiratory syncytial virus binds and undergoes transcription in neutrophils from the blood and airways of infants with severe bronchiolitis. J. Infect. Dis. 2011, 204, 451–458, doi:10.1093/infdis/jir280.
- Wang, S.Z.; Forsyth, K.D. The interaction of neutrophils with respiratory epithelial cells in viral infection. Respirology 2000, 5, 1–10, doi:10.1046/j.1440-1843.2000.00219.x.
- Segel, G.B.; Halterman, M.W.; Lichtman, M.A. The paradox of the neutrophil's role in tissue injury. J. Leukoc. Biol. 2011, 89, 359–372, doi:10.1189/jlb.0910538.
- Martin, T.R. Neutrophils and lung injury: Getting it right. J. Clin. Invest. 2002, 110, 1603–1605.
- Perl, M.; Lomas-Neira, J.; Chung, C.S.; Ayala, A. Epithelial cell apoptosis and neutrophil recruitment in acute lung injury-a unifying hypothesis? What we have learned from small interfering RNAs. Mol. Med. 2008, 14, 465–475, doi:10.1007/s00894-008-0304-1.
- Ware, L.B.; Matthay, M.A. The acute respiratory distress syndrome. N. Engl. J. Med. 2000, 342, 1334–1349, doi:10.1056/NEJM200005043421806.
- Lindemans, C.A.; Coffer, P.J.; Schellens, I.M.; de Graaff, P.M.; Kimpen, J.L.; Koenderman, L. Respiratory syncytial virus inhibits granulocyte apoptosis through a phosphatidylinositol 3-kinase and NF-kappaB-dependent mechanism. J. Immunol. 2006, 176, 5529–5537.
- Coleman, C.M.; Plant, K.; Newton, S.; Hobson, L.; Whyte, M.K.; Everard, M.L. The Anti-Apoptotic Effect of Respiratory Syncytial Virus on Human Peripheral Blood Neutrophils is Mediated by a Monocyte Derived Soluble Factor. Open Virol. J. 2011, 5, 114–123, doi:10.2174/1874357901105010114.
- Wang, S.Z.; Smith, P.K.; Lovejoy, M.; Bowden, J.J.; Alpers, J.H.; Forsyth, K.D. The apoptosis of neutrophils is accelerated in respiratory syncytial virus (RSV)-induced bronchiolitis. Clin. Exp. Immunol. 1998, 114, 49–54, doi:10.1046/j.1365-2249.1998.00681.x.
- Pillay, J.; Ramakers, B.P.; Kamp, V.M.; Loi, A.L.; Lam, S.W.; Hietbrink, F.; Leenen, L.P.; Tool, A.T.; Pickkers, P.; Koenderman, L. Functional heterogeneity and differential priming of circulating neutrophils in human experimental endotoxemia. J. Leukoc. Biol. 2010, 88, 211–220, doi:10.1189/jlb.1209793.
- Simon, H.U. Neutrophil apoptosis pathways and their modifications in inflammation. Immunol. Rev. 2003, 193, 101–110, doi:10.1034/j.1600-065X.2003.00038.x.
- Pribul, P.K.; Harker, J.; Wang, B.; Wang, H.; Tregoning, J.S.; Schwarze, J.; Openshaw, P.J. Alveolar macrophages are a major determinant of early responses to viral lung infection, but do not influence subsequent disease development. J. Virol. 2008, 82, 4441–4448, doi:10.1128/JVI.02541-07.
- Rigaux, P.; Killoran, K.E.; Qiu, Z.; Rosenberg, H.F. Depletion of alveolar macrophages prolongs survival in response to acute pneumovirus infection. Virology 2012, 422, 338–345, doi:10.1016/j.virol.2011.10.031.
- Bem, R.A.; van Woensel, J.B.; Bos, A.P.; Koski, A.; Farnand, A.W.; Domachowske, J.B.; Rosenberg, H.F.; Martin, T.R.; Matute-Bello, G. Mechanical ventilation enhances lung inflammation and caspase activity in a model of mouse pneumovirus infection. Am. J. Physiol. Lung Cell Mol. Physiol. 2009, 296, 46–56.
- Midulla, F.; Villani, A.; Panuska, J.R.; Dab, I.; Kolls, J.K.; Merolla, R.; Ronchetti, R. Respiratory syncytial virus lung infection in infants: immunoregulatory role of infected alveolar macrophages. J. Infect. Dis. 1993, 168, 1515–1519, doi:10.1093/infdis/168.6.1515.
- Midulla, F.; Huang, Y.T.; Gilbert, I.A.; Cirino, N.M.; McFadden, E.R., Jr.; Panuska, J.R. Respiratory syncytial virus infection of human cord and adult blood monocytes and alveolar macrophages. Am. Rev. Respir. Dis. 1989, 140, 771–777.
- Panuska, J.R.; Cirino, N.M.; Midulla, F.; Despot, J.E.; McFadden, E.R., Jr.; Huang, Y.T. Productive infection of isolated human alveolar macrophages by respiratory syncytial virus. J. Clin. Invest. 1990, 86, 113–119, doi:10.1172/JCI114672.
- Krilov, L.R.; McCloskey, T.W.; Harkness, S.H.; Pontrelli, L.; Pahwa, S. Alterations in apoptosis of cord and adult peripheral blood mononuclear cells induced by in vitro infection with respiratory syncytial virus. J. Infect. Dis. 2000, 181, 349–353, doi:10.1086/315203.
- Nakamura-Lopez, Y.; Villegas-Sepulveda, N.; Sarmiento-Silva, R.E.; Gomez, B. Intrinsic apoptotic pathway is subverted in mouse macrophages persistently infected by RSV. Virus Res. 2011, 158, 98–107, doi:10.1016/j.virusres.2011.03.016.
- Fischer, U.; Schulze-Osthoff, K. Apoptosis-based therapies and drug targets. Cell Death Differ. 2005, 12, 942–961, doi:10.1038/sj.cdd.4401556.
- van Rooijen, N.; Sanders, A. Liposome mediated depletion of macrophages: mechanism of action, preparation of liposomes and applications. J. Immunol. Methods 1994, 174, 83–93, doi:10.1016/0022-1759(94)90012-4.
- Janssen, W.J.; Barthel, L.; Muldrow, A.; Oberley-Deegan, R.E.; Kearns, M.T.; Jakubzick, C.; Henson, P.M. Fas determines differential fates of resident and recruited macrophages during resolution of acute lung injury. Am. J. Respir. Crit. Care Med. 2011, 184, 547–560, doi:10.1164/rccm.201011-1891OC.
- Nakamura, M.; Matute-Bello, G.; Liles, W.C.; Hayashi, S.; Kajikawa, O.; Lin, S.M.; Frevert, C.W.; Martin, T.R. Differential response of human lung epithelial cells to fas-induced apoptosis. Am. J. Pathol. 2004, 164, 1949–1958, doi:10.1016/S0002-9440(10)63755-8.
- Matute-Bello, G.; Liles, W.C.; Frevert, C.W.; Dhanireddy, S.; Ballman, K.; Wong, V.; Green, R.R.; Song, H.Y.; Witcher, D.R.; Jakubowski, J.A.; et al. Blockade of the Fas/FasL system improves pneumococcal clearance from the lungs without preventing dissemination of bacteria to the spleen. J. Infect. Dis. 2005, 191, 596–606, doi:10.1086/427261.
- Matute-Bello, G.; Liles, W.C.; Frevert, C.W.; Nakamura, M.; Ballman, K.; Vathanaprida, C.; Kiener, P.A.; Martin, T.R. Recombinant human Fas ligand induces alveolar epithelial cell apoptosis and lung injury in rabbits. Am. J. Physiol. Lung Cell Mol. Physiol. 2001, 281, 328–335.
- Perl, M.; Chung, C.S.; Lomas-Neira, J.; Rachel, T.M.; Biffl, W.L.; Cioffi, W.G.; Ayala, A. Silencing of Fas, but not caspase-8, in lung epithelial cells ameliorates pulmonary apoptosis, inflammation and neutrophil influx after hemorrhagic shock and sepsis. Am. J. Pathol. 2005, 167, 1545–1559, doi:10.1016/S0002-9440(10)61240-0.
- Kawasaki, M.; Kuwano, K.; Hagimoto, N.; Matsuba, T.; Kunitake, R.; Tanaka, T.; Maeyama, T.; Hara, N. Protection from lethal apoptosis in lipopolysaccharide-induced acute lung injury in mice by a caspase inhibitor. Am. J. Pathol. 2000, 157, 597–603, doi:10.1016/S0002-9440(10)64570-1.
- Altemeier, W.A.; Sinclair, S.E. Hyperoxia in the intensive care unit: why more is not always better. Curr. Opin. Crit. Care 2007, 13, 73–78.
- Bem, R.A.; Bos, A.P.; Matute-Bello, G.; van, T.M.; van Woensel, J.B. Lung epithelial cell apoptosis during acute lung injury in infancy. Pediatr. Crit. Care Med. 2007, 8, 132–137, doi:10.1097/01.PCC.0000257207.02408.67.
© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).