MINI REVIEW article
Extracellular Vesicles in Herpes Viral Spread and Immune Evasion
- 1Departamento de Biología Molecular, Universidad Autónoma de Madrid, Madrid, Spain
- 2Centro de Biología Molecular Severo Ochoa, CSIC-UAM, Madrid, Spain
Extracellular vesicles (EVs) are involved in numerous processes during infections by both enveloped and non-enveloped viruses. Among them, herpes simplex virus type-1 (HSV-1) modulates secretory pathways, allowing EVs to exit infected cells. Many characteristics regarding the mechanisms of viral spread are still unidentified, and as such, secreted vesicles are promising candidates due to their role in intercellular communications during viral infection. Another relevant role for EVs is to protect virions from the action of neutralizing antibodies, thus increasing their stability within the host during hematogenous spread. Recent studies have suggested the participation of EVs in HSV-1 spread, wherein virion-containing microvesicles (MVs) released by infected cells were endocytosed by naïve cells, leading to a productive infection. This suggests that HSV-1 might use MVs to expand its tropism and evade the host immune response. In this review, we briefly describe the current knowledge about the involvement of EVs in viral infections in general, with a specific focus on recent research into their role in HSV-1 spread. Implications of the autophagic pathway in the biogenesis and secretion of EVs will also be discussed.
Extracellular vesicles (EVs) are a heterogeneous group of membrane vesicles, derived from endosomes or from the plasma membrane, secreted by almost all cell types belonging to the three domains of cellular life: Bacteria, Archaea, and Eukarya (Yañez-Mo et al., 2015; Sedgwick and D’Souza-Schorey, 2018; van Niel et al., 2018). EVs have been isolated from numerous biological fluids such as blood, saliva, urine, cerebrospinal fluid, amniotic fluid, ascetic fluid, breast milk, and seminal fluid (Yañez-Mo et al., 2015; Zaborowski et al., 2015; Kalra et al., 2016). Initially considered to be mostly cell debris, EVs have now emerged as key mediators of intercellular communication, and are currently associated with numerous physiological and pathological processes (Gyorgy et al., 2011; van der Pol et al., 2012; Yuana et al., 2013) such as cancer (Muralidharan-Chari et al., 2010; Barros et al., 2018; Nogues et al., 2018; Xu et al., 2018), infection (Silverman and Reiner, 2011; Lai et al., 2015; Schorey et al., 2015), inflammation and immune response (Robbins et al., 2016), and myelination and neuron-glia communication (Fruhbeis et al., 2013; Basso and Bonetto, 2016; Lopez-Leal and Court, 2016; Pusic et al., 2016; Holm et al., 2018).
Although the classification and nomenclature of EVs is complex, two major categories of EVs can be broadly established: (1) microvesicles (MVs) derived from shedding of the plasma membrane (Cocucci et al., 2009; Cocucci and Meldolesi, 2015); and (2) exosomes, vesicles released to the extracellular space upon fusion of multivesicular bodies (MVBs) with the plasma membrane (Colombo et al., 2014; Yañez-Mo et al., 2015; Maas et al., 2017). While exosomes are between 30 and 100 nm in diameter, MVs are much more heterogeneous, ranging from 100 nm to 1 μm in diameter (Raposo and Stoorvogel, 2013; Yuana et al., 2013). MVs are enriched in lipid rafts and commonly associated proteins such as flotillin-1, and expose phosphatidylserine (PS) on the outer plasma membrane leaflet (Scott et al., 1984; Del Conde et al., 2005; Wei et al., 2016). Exosomes, on the other hand, are enriched in tetraspanins (CD9, CD63 and CD81, among others), which are frequently used as exosomal markers (Andreu and Yañez-Mo, 2014) and also in endosomal markers such as ALIX and TSG101 (Kowal et al., 2016; Willms et al., 2016). Although the presence of PS exposed in exosomes has been postulated (Thery et al., 2009; Colombo et al., 2014; De Paoli et al., 2018) other studies question that exosomes expose PS just after secretion from cells (Lai R.C. et al., 2016; Skotland et al., 2017), remaining this point to be fully clarified.
Extracellular vesicles are also involved in viral infection (Meckes and Raab-Traub, 2011; Wurdinger et al., 2012; Alenquer and Amorim, 2015; Altan-Bonnet, 2016; Anderson et al., 2016), influencing viral entry, spread and immune evasion (Schorey et al., 2015; Kouwaki et al., 2017). Thus, EVs operate as an important system of intercellular communication between infected and uninfected cells (Meckes, 2015; Raab-Traub and Dittmer, 2017). Indeed, due to their common biogenesis pathways, EVs and viruses are considered to be close relatives, and EVs secreted by infected cells can either enhance viral spread or, on the contrary, trigger an antiviral response (Nolte-’T Hoen et al., 2016). The great variability of the role of EVs during the viral life cycle is evident, as they can produce such opposite effects as the blockage or increase of infection, as well as modulate the immune response (Wurdinger et al., 2012). Two key biological activities of EVs during viral infections are the transport of viral genomes into target cells and the intervention in cell physiology to facilitate infection (van Dongen et al., 2016).
This review will briefly describe the current knowledge about the involvement of EVs in viral infections, with a specific focus on recent research on their role in herpes simplex virus type-1 (HSV-1) spread.
Viruses and EVs
Extracellular vesicles have been implicated in numerous processes during infections by both enveloped and non-enveloped viruses. For example, EVs play a relevant role in hepatitis C virus (HCV) spread, as virions contained in exosomes can be transported to hepatocyte-like cells, establishing a productive infection (Ramakrishnaiah et al., 2013). Likewise, the release of hepatitis A virus (HAV) enclosed in infectious EVs derived from cellular membranes (Feng et al., 2013) permits viral escape from antibodies and facilitates viral spread. Several picornaviruses can be transported in EVs; the secretion of exosomes containing enterovirus 71 (EV71) has been shown to establish a productive infection in human neuroblastoma cells (Mao et al., 2016), and coxsackievirus B can exit infected cells in MVs derived from mitophagosomes (Robinson et al., 2014; Sin et al., 2017). Gastroenteric pathogens such as noroviruses and rotaviruses have also been detected enclosed in EVs that can transfer a high inoculum to the next host, contributing, therefore, to fecal-oral transmission and enhancing the viral propagation (Santiana et al., 2018). Thus, infection with non-enveloped viruses can induce the release of MVs containing viral proteins and infectious virus, indicating novel routes of virus dissemination.
Human immunodeficiency virus 1 (HIV-1) modulates vesicle secretion through its Nef protein, which is secreted in exosomes and modifies the intracellular trafficking pathways to enhance viral infectivity (Lenassi et al., 2010; Pereira and daSilva, 2016). For retroviruses in general, the Trojan exosome hypothesis states that these viruses use the cellular exosome biogenesis pathway for formation of infectious virions and the exosome uptake pathway for a receptor-independent, Env-independent route of infection (Gould et al., 2003). According to this model, dendritic cells (DCs) capture and internalize retroviruses by endocytosis and, subsequently, some of the non-degraded virions may infect the DC-interacting CD4+ T cells, contributing to viral spread through a mechanism known as trans-infection. Both direct infection and trans-infection might coexist to a different extent depending on the maturation stage of DC subsets (Izquierdo-Useros et al., 2010).
Herpesviruses also modulate the secretion pathway of EVs to exit cells; in fact, the exosome pathway is exploited by the three subfamilies: alpha-, beta- and gamma- (Liu et al., 2017; Sadeghipour and Mathias, 2017). Thus, the secretion of exosomes by HSV-1-infected cells carrying viral RNA and stimulator of IFN genes (STING) to uninfected cells has recently been reported (Kalamvoki et al., 2014; Kalamvoki and Deschamps, 2016). The exosome secretion pathway also plays an important role in the life cycle of human herpesvirus 6 (HHV-6), whose virions are released along with intraluminal vesicles via the exosomal pathway, by fusion of the limiting membrane of MVBs—in which virus particles and exosomes are enclosed—with the plasma membrane (Mori et al., 2008). A similar role for MVBs in the release of human cytomegalovirus (HCMV) has been also suggested (Fraile-Ramos et al., 2007; Schauflinger et al., 2011). The human gamma-herpesviruses Kaposi’s sarcoma-associated herpesvirus (KSHV) and Epstein–Barr virus (EBV) also alter the protein content of exosomes, probably to modulate the tumor microenvironment, enhance viral efficiency and promote tumorigenesis (Vazirabadi et al., 2003; Meckes et al., 2010, 2013). In addition, exosomes can also transfer functional miRNAs from EBV-infected cells to subcellular sites of gene repression in uninfected recipient cells (Pegtel et al., 2010).
HSV-1: A Brief Overview
Herpes simplex virus type-1 is a highly prevalent neurotropic human pathogen belonging to the alphaherpesvirus subfamily that can infect neurons and establish latency in these cells (Roizman et al., 2011; Miranda-Saksena et al., 2018). HSV-1 causes oral, labial and, occasionally facial lesions, and is an increasingly important cause of sexually transmitted genital herpes (Horowitz et al., 2010; Bernstein et al., 2013), producing a significant percentage of cases (Wald and Corey, 2007). This virus may also cause serious pathologies such as encephalitis or keratoconjunctivitis (Whitley, 2006). HSV-1 infects epithelial cells and subsequently travels to neurons, establishing latent infection in the trigeminal ganglia.
Herpes simplex virus type-1 has the ability to infect many different host and cell types (Karasneh and Shukla, 2011), using several different receptors and pathways. This virus can enter cells by fusion of the viral envelope with the plasma membrane, a pH-independent process, or by endocytosis, which can either be low pH-dependent or low pH-independent (Reske et al., 2007; Heldwein and Krummenacher, 2008; Akhtar and Shukla, 2009; Agelidis and Shukla, 2015; Nicola, 2016). Regardless of the pathway, HSV glycoproteins such as the receptor-binding glycoprotein D (gD), the fusion modulator complex gH/gL and the fusion effector gB are essential for virion entry. Maturation and egress follow four major stages: (a) capsid assembly and DNA packaging; (b) primary envelopment and de-envelopment; (c) tegumentation and secondary envelopment; (d) exocytosis of viral particles and/or cell-to-cell transmission (Owen et al., 2015). Secondary envelopment may also occur using the endocytic pathway, and in fact, it has been proposed that endocytosis from the plasma membrane into endocytic tubules represents the main source for HSV-1 envelopment (Hollinshead et al., 2012). According to this mode of envelopment, viral glycoproteins are exported to the plasma membrane via the secretory pathway and are subsequently endocytosed in endocytic tubules that are then used to wrap the viral nucleocapsid, forming the double-membraned intracellular virion (David, 2012; Hollinshead et al., 2012). This endocytic process is dynamin-dependent, and it plays a major role for transporting HSV-1 envelope proteins to intracellular sites of virus assembly (Albecka et al., 2016).
Herpes simplex virus type-1 may use several mechanisms to spread from infected to uninfected cells (Agelidis and Shukla, 2015). Several viral glycoproteins, such as the heterodimer gE/gI or glycoprotein gK, are necessary for release of virions from parent cells, and it has been recently reported that the host enzyme heparanase-1 is also required for viral release (Hadigal et al., 2015). On the other hand, HSV-1 can disseminate in human tissues by cell-to-cell spread—the direct passage of progeny virus from an infected cell to a neighboring one—, a mechanism that might be considered as an immune evasion strategy, since it protects the virus from immune surveillance (Campadelli-Fiume, 2007). However, many aspects concerning mechanisms of viral spread are still unidentified. In this context, secreted vesicles are interesting candidates to consider, because of their ability to participate in intercellular communications during viral infections.
HSV-1 and EVs
Production of secreted vesicles by HSV-1-infected cells has been previously reported. Light particles (L-particles) (Szilagyi and Cunningham, 1991; McLauchlan and Rixon, 1992), the first to be described, are vesicles secreted by human and animal cells after infection with every alpha-herpesviruses tested (Heilingloh and Krawczyk, 2017). They are similar to virions in appearance, but lack the viral nucleocapsid and genome (Szilagyi and Cunningham, 1991) and are thus non-infectious. L-particles have been shown to facilitate HSV-1 infection by transfer of viral proteins and cellular factors required for viral replication and also immune evasion (Dargan and Subak-Sharpe, 1997; Kalamvoki and Deschamps, 2016). Another type of particles, pre-viral DNA replication enveloped particles (PREPs), are morphologically similar to L-particles, but differ in their relative protein composition (Dargan et al., 1995).
As mentioned above, recent studies have shown that cells infected with HSV-1 can use exosomes to export STING to uninfected cells, along with virions, viral mRNAs, microRNAs and the exosome marker protein CD9. Those results suggested that HSV-1 might limit the spread of infection from cell-to-cell in order to control its virulence and facilitate the dissemination between individuals (Kalamvoki et al., 2014; Kalamvoki and Deschamps, 2016; Deschamps and Kalamvoki, 2018). On the other hand, previous studies carried out by our group indicated that Rab27a, a small GTPase implicated in exosomes secretion (Ostrowski et al., 2010), plays an important role in HSV-1 infection of oligodendrocytic cells (Bello-Morales et al., 2012). In fact, our results showed a drastic reduction not only in viral production, but also in plaque size of Rab27a-silenced cells infected with HSV-1, suggesting that Rab27a depletion might be affecting viral egress. In addition, this GTPase seems to affect the viral assembly of other viruses, such as HIV-1 (Gerber et al., 2015) and HCMV (Fraile-Ramos et al., 2010).
More recent findings (Bello-Morales et al., 2018) have suggested the participation of MVs in HSV-1 spread. Our study described the features of MVs released by the human oligodendroglial (HOG) cell line infected with HSV-1 and their participation in the viral cycle, indicating for the first time that MVs released by HSV-1-infected cells contained virions, were endocytosed by naïve cells, and led to a productive infection. This suggests that HSV-1 spread might use MVs to expand its tropism and possibly evade the host immune response (Bello-Morales et al., 2018).
EVs in Viral Immune Evasion
The release of virus from cells mediated by EVs plays a relevant role in viral spread and pathogenesis, and may help to expand the natural tropism of viruses to include target cells which lack canonical viral receptors. On the other hand, EVs may also transfer virus-encoded proteins and nucleic acids independently of the viral particles. For instance, both simian immunodeficiency virus (SIV) (McNamara et al., 2018) and HIV-1 (Lenassi et al., 2010; Pereira and daSilva, 2016; Puzar Dominkus et al., 2017) induce the release of Nef protein in exosomes; EBV LMP1 is also secreted in EVs (Meckes et al., 2010; Nkosi et al., 2018) and functional exosomes containing miRNAs have been detected in human clinical samples and mouse models of KSHV-associated malignancies (Chugh et al., 2013).
However, EVs also have an equally important role: to protect virions against the action of neutralizing antibodies and thus increasing their stability within the host during hematogenous spread. In this sense, acquisition of an envelope can provide resistance to neutralizing antibodies, and therefore reinforce viral spread (Sin et al., 2015), since neutralizing antibodies would be ineffective against virions protected within vesicles (Robinson et al., 2014). Systemic circulation of viruses enclosed in EVs would allow them to modulate host cells without exposing their proteins or progeny virions to the immune system (Raab-Traub and Dittmer, 2017). This is especially relevant for non-enveloped viruses; thus, acquisition of an envelope helps coxsackievirus to evade the immune system, permitting an efficient non-lytic viral spread (Sin et al., 2015). But enveloped viruses may also benefit from MV-mediated spread, as HCV transmission is enhanced by exosomes (Masciopinto et al., 2004; Bukong et al., 2014), and HCV-related exosomes seem to be involved in immune escape (Shen et al., 2017). In fact, hepatic exosomes—partially resistant to antibody neutralization—can transport HCV to cells and establish a productive infection (Ramakrishnaiah et al., 2013). Likewise, HAV exploits EVs as vehicles to escape antibody-mediated neutralization (Feng et al., 2013).
Regarding HSV-1, it is accepted that this virus influences the EV pathway to enhance infection and/or evade the immune system. For example, it has been demonstrated that HSV-1 may manipulate the MHC class II processing pathway by altering the endosomal sorting and trafficking of HLA-DR, hijacking these molecules from normal transport pathways to the cell surface and diverting them into the exosome pathway (Temme et al., 2010). In addition, and as already mentioned, functional HSV-1 proteins can be transferred to uninfected cells via L-particles, a process that suggests a viral immune escape strategy (Heilingloh et al., 2015). Likewise, the results obtained in our laboratory have shown that infection of Chinese hamster ovary (CHO) cells with virus-containing MVs was not completely neutralized by anti-HSV-1 antibodies, suggesting that they shield the virus (Bello-Morales et al., 2018).
EVs and the Autophagic Pathway
Conventional autophagy is a eukaryotic degradative pathway in which cytoplasmic components are sequestered in autophagosomes that finally will fuse with the lysosome, degrading its contents by lysosomal hydrolases (Nakatogawa et al., 2009; Ohsumi, 2014). Autophagy plays an essential role in several physiological and pathological processes, such as xenophagy, the removal of intracellular pathogens including viruses (Wirawan et al., 2012). Autophagy significantly restrains HSV-1 infection in various cell types (Yakoub and Shukla, 2015), though some viruses have acquired the ability to modulate autophagy for their own benefit (Choi et al., 2018). In this way, HSV-1 and HIV interact with Beclin-1, thereby inhibiting autophagosome maturation (Orvedahl et al., 2007; Kyei et al., 2009).
Autophagy, however, may also have a non-degradative role: in secretory autophagy, a newly discovered pathway, autophagosomes fuse with the plasma membrane instead of lysosomes, releasing vesicles enclosing cytoplasmic cargo to the extracellular environment (Rabouille et al., 2012; Jiang et al., 2013; Zhang and Schekman, 2013; Ponpuak et al., 2015).
Many other studies have shown that viruses may use autophagic Atg proteins for morphogenesis and viral egress (Munz, 2017), for example EBV (Lee and Sugden, 2008; Granato et al., 2014; Fotheringham and Raab-Traub, 2015; Hurwitz et al., 2018), varicella zoster virus (VZV) (Buckingham et al., 2016; Grose et al., 2016) or picornaviruses (Jackson et al., 2005; Taylor and Kirkegaard, 2008; Klein and Jackson, 2011; Robinson et al., 2014; Mutsafi and Altan-Bonnet, 2018). Coxsackievirus B, for instance, may use the autophagic pathway to exit cells enclosed in LC3-II-positive shedding MVs (Robinson et al., 2014), a process similar to the autophagosome-mediated exit without lysis (AWOL) observed in poliovirus (Taylor et al., 2009; Lai J.K. et al., 2016). According to this model, fusion between autophagosomes and endosomes generates amphisomes, LC3-II-positive vesicles enclosing viral particles which can fuse with the plasma membrane to secrete virions (Lai J.K. et al., 2016). Remarkably, due to the complexity of their replication cycles, viruses may exert a dual role on this kind of process: on one hand, subversion of autophagy in infected cells and on the other, induction of hyper-autophagy in bystander cells (Killian, 2012).
In a recent study carried out by our group (Bello-Morales et al., 2018) we have shown the presence of virions in MVs released by infected cells. Although the exact process of HSV-1 targeting to MVs remains to be fully unraveled, we suggested that autophagy may be involved in that process, since MVs isolated from HSV-1-infected cells were positive for the autophagy marker LC3-II. Therefore, these results suggest a role for the autophagic pathway in MV-mediated HSV-1 spread, although more data is necessary to confirm that crucial point. On the other hand, this particular study suggested different models of biogenesis and secretion of MV-associated HSV-1 depending on the cell type. According to the canonical model of HSV-1 egress, the nucleocapsid is wrapped in vesicles/tubules from trans-Golgi network (TGN)/endosomes, giving rise to an enveloped virion surrounded by a double membrane that, after fusion with the plasma membrane, gives rise to an extracellular free enveloped virion (Figure 1A). However, the egress of this structure by membrane shedding cannot be excluded, which would produce a three-membraned viral particle corresponding to an enveloped virion enclosed within a shedding MV (Figure 1B). Such triple-membraned virions have been observed upon infection of Mewo cells (Bello-Morales et al., 2018); however, nucleocapsids might also obtain their envelopes from the autophagic pathway. In this way, vesicles/tubules from the autophagic pathway would cover the nucleocapsid, giving rise to a viral particle surrounded by a double membrane. Then, this structure would reach the plasma membrane and, after fusion, a viral particle surrounded by a single membrane would exit the cell (Figure 1C). This type of structure has been observed upon infection of HOG and Hela cells (Bello-Morales et al., 2018). Alternatively, double-membraned particles might exit the cell not by fusion, but by shedding of the plasma membrane, originating a three-membraned viral particle (Figure 1D). Further work will have to unveil whether viral glycoproteins are targeted to vesicles/tubules from autophagic pathway (Figures 1C,D) before wrapping of nucleocapsids. Finally, our results highlight the relevance of the cellular model when attempting the study of viral modulation of autophagy and, as different cell types may give different autophagy responses, it can be difficult to directly compare different virus-cell systems, especially when studying viruses that infect more than one cell type (Lin et al., 2010).
FIGURE 1. Models of biogenesis and secretion of MV-enclosed HSV-1 virions. (A) The canonical egress of HSV-1 entails the fusion of a two-membraned viral particle with the plasma membrane, giving rise to an extracellular free enveloped virion. In this model, the viral envelope is derived from the TGN/endosomes. (B) Alternatively, this structure might exit the cell after shedding of the plasma membrane, resulting in a three-membraned viral particle, which would correspond to an enveloped virion enclosed within a shedding MV. (C) According to this model, vesicles/tubules originating from the autophagic pathway wrap around the nucleocapsid, giving rise to a viral particle surrounded by a double membrane. Then, this structure would reach the plasma membrane and, after fusion, a viral particle surrounded by a single membrane would exit the cell. (D) In an alternative model, the two-membraned viral particle might exit the cell not by fusion, but by shedding of the plasma membrane, giving rise to a three-membraned viral particle.
Several herpesviruses may modulate the secretory pathway of EVs in order to enhance viral egress or evade the immune response. EVs may also increase viral stability during hematogenous spread by protecting virus from exposure to neutralizing antibodies. Recent studies have shown that MVs released by HSV-1 infected cells contained virions which were endocytosed by naïve cells, leading to a productive infection, suggesting that the virus uses EVs to expand its tropism and possibly evade the host immune response. In addition, growing evidence is demonstrating the importance of autophagy in viral infections, which several viruses use for morphogenesis and viral egress. We suggest that HSV-1 might use MVs for viral spread and propose different models of biogenesis and secretion of MVs-associated HSV-1 depending on the cell type.
Both authors conceived and wrote the manuscript.
Fundación Severo Ochoa-Aeromédica Canaria provided financial support. The funders had no role in study design, decision to publish, or preparation of the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We thank Fundamentium (https://fundamentium.com/) for infographics. The professional editing service NB Revisions was used for technical preparation of the text prior to submission.
Albecka, A., Laine, R. F., Janssen, A. F., Kaminski, C. F., and Crump, C. M. (2016). HSV-1 glycoproteins are delivered to virus assembly sites through dynamin-dependent endocytosis. Traffic 17, 21–39. doi: 10.1111/tra.12340
Bello-Morales, R., Crespillo, A. J., Fraile-Ramos, A., Tabares, E., Alcina, A., and Lopez-Guerrero, J. A. (2012). Role of the small GTPase Rab27a during herpes simplex virus infection of oligodendrocytic cells. BMC Microbiol. 12:265. doi: 10.1186/1471-2180-12-265
Bello-Morales, R., Praena, B., De La Nuez, C., Rejas, M. T., Guerra, M., Galan-Ganga, M., et al. (2018). Role of microvesicles in the spread of herpes simplex virus 1 in oligodendrocytic cells. J. Virol. 92:e00088-18. doi: 10.1128/JVI.00088-18
Bernstein, D. I., Bellamy, A. R., Hook, E. W. III, Levin, M. J., Wald, A., Ewell, M. G., et al. (2013). Epidemiology, clinical presentation, and antibody response to primary infection with herpes simplex virus type 1 and type 2 in young women. Clin. Infect. Dis. 56, 344–351. doi: 10.1093/cid/cis891
Buckingham, E. M., Jarosinski, K. W., Jackson, W., Carpenter, J. E., and Grose, C. (2016). Exocytosis of varicella-zoster virus virions involves a convergence of endosomal and autophagy pathways. J. Virol. 90, 8673–8685. doi: 10.1128/JVI.00915-16
Bukong, T. N., Momen-Heravi, F., Kodys, K., Bala, S., and Szabo, G. (2014). Exosomes from hepatitis C infected patients transmit HCV infection and contain replication competent viral RNA in complex with Ago2-miR122-HSP90. PLoS Pathog. 10:e1004424. doi: 10.1371/journal.ppat.1004424
Campadelli-Fiume, G. (2007). “The egress of alphaherpesviruses from the cell,” in Human Herpesviruses: Biology, Therapy, and Immunoprophylaxis, eds A. Arvin, G. Campadelli-Fiume, E. Mocarski, P. S. Moore, B. Roizman, R. Whitley, et al. (Cambridge: Cambridge University Press), 151–163. doi: 10.1017/CBO9780511545313.013
Chugh, P. E., Sin, S. H., Ozgur, S., Henry, D. H., Menezes, P., Griffith, J., et al. (2013). Systemically circulating viral and tumor-derived microRNAs in KSHV-associated malignancies. PLoS Pathog. 9:e1003484. doi: 10.1371/journal.ppat.1003484
Colombo, M., Raposo, G., and Thery, C. (2014). Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annu. Rev. Cell Dev. Biol. 30, 255–289. doi: 10.1146/annurev-cellbio-101512-122326
Dargan, D. J., Patel, A. H., and Subak-Sharpe, J. H. (1995). PREPs: herpes simplex virus type 1-specific particles produced by infected cells when viral DNA replication is blocked. J. Virol. 69, 4924–4932.
Dargan, D. J., and Subak-Sharpe, J. H. (1997). The effect of herpes simplex virus type 1 L-particles on virus entry, replication, and the infectivity of naked herpesvirus DNA. Virology 239, 378–388. doi: 10.1006/viro.1997.8893
De Paoli, S. H., Tegegn, T. Z., Elhelu, O. K., Strader, M. B., Patel, M., Diduch, L. L., et al. (2018). Dissecting the biochemical architecture and morphological release pathways of the human platelet extracellular vesiculome. Cell. Mol. Life Sci. 75, 3781–3801. doi: 10.1007/s00018-018-2771-6
Del Conde, I., Shrimpton, C. N., Thiagarajan, P., and Lopez, J. A. (2005). Tissue-factor-bearing microvesicles arise from lipid rafts and fuse with activated platelets to initiate coagulation. Blood 106, 1604–1611. doi: 10.1182/blood-2004-03-1095
Deschamps, T., and Kalamvoki, M. (2018). Extracellular vesicles released by herpes simplex virus 1-infected cells block virus replication in recipient cells in a STING-dependent manner. J. Virol. 92:JVI.01102-18. doi: 10.1128/JVI.01102-18
Feng, Z., Hensley, L., Mcknight, K. L., Hu, F., Madden, V., Ping, L., et al. (2013). A pathogenic picornavirus acquires an envelope by hijacking cellular membranes. Nature 496, 367–371. doi: 10.1038/nature12029
Fraile-Ramos, A., Pelchen-Matthews, A., Risco, C., Rejas, M. T., Emery, V. C., Hassan-Walker, A. F., et al. (2007). The ESCRT machinery is not required for human cytomegalovirus envelopment. Cell Microbiol. 9, 2955–2967. doi: 10.1111/j.1462-5822.2007.01024.x
Fruhbeis, C., Frohlich, D., Kuo, W. P., Amphornrat, J., Thilemann, S., Saab, A. S., et al. (2013). Neurotransmitter-triggered transfer of exosomes mediates oligodendrocyte-neuron communication. PLoS Biol. 11:e1001604. doi: 10.1371/journal.pbio.1001604
Gerber, P. P., Cabrini, M., Jancic, C., Paoletti, L., Banchio, C., Von Bilderling, C., et al. (2015). Rab27a controls HIV-1 assembly by regulating plasma membrane levels of phosphatidylinositol 4,5-bisphosphate. J. Cell Biol. 209, 435–452. doi: 10.1083/jcb.201409082
Granato, M., Santarelli, R., Farina, A., Gonnella, R., Lotti, L. V., Faggioni, A., et al. (2014). Epstein-barr virus blocks the autophagic flux and appropriates the autophagic machinery to enhance viral replication. J. Virol. 88, 12715–12726. doi: 10.1128/JVI.02199-14
Grose, C., Buckingham, E. M., Carpenter, J. E., and Kunkel, J. P. (2016). Varicella-zoster virus infectious cycle: ER stress, autophagic flux, and amphisome-mediated trafficking. Pathogens 5:67. doi: 10.3390/pathogens5040067
Gyorgy, B., Szabo, T. G., Pasztoi, M., Pal, Z., Misjak, P., Aradi, B., et al. (2011). Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles. Cell Mol. Life Sci. 68, 2667–2688. doi: 10.1007/s00018-011-0689-3
Hadigal, S. R., Agelidis, A. M., Karasneh, G. A., Antoine, T. E., Yakoub, A. M., Ramani, V. C., et al. (2015). Heparanase is a host enzyme required for herpes simplex virus-1 release from cells. Nat. Commun. 6:6985. doi: 10.1038/ncomms7985
Heilingloh, C. S., Kummer, M., Muhl-Zurbes, P., Drassner, C., Daniel, C., Klewer, M., et al. (2015). L particles transmit viral proteins from herpes simplex virus 1-infected mature dendritic cells to uninfected bystander cells, inducing CD83 downmodulation. J. Virol. 89, 11046–11055. doi: 10.1128/JVI.01517-15
Hollinshead, M., Johns, H. L., Sayers, C. L., Gonzalez-Lopez, C., Smith, G. L., and Elliott, G. (2012). Endocytic tubules regulated by Rab GTPases 5 and 11 are used for envelopment of herpes simplex virus. EMBO J. 31, 4204–4220. doi: 10.1038/emboj.2012.262
Horowitz, R., Aierstuck, S., Williams, E. A., and Melby, B. (2010). Herpes simplex virus infection in a university health population: clinical manifestations, epidemiology, and implications. J. Am. Coll. Health 59, 69–74. doi: 10.1080/07448481.2010.483711
Hurwitz, S. N., Cheerathodi, M. R., Nkosi, D., York, S. B., and Meckes, DG Jr (2018). Tetraspanin CD63 bridges autophagic and endosomal processes to regulate exosomal secretion and intracellular signaling of epstein-barr virus LMP1. J. Virol. 92:e01969-17. doi: 10.1128/JVI.01969-17
Izquierdo-Useros, N., Naranjo-Gomez, M., Erkizia, I., Puertas, M. C., Borras, F. E., Blanco, J., et al. (2010). HIV and mature dendritic cells: trojan exosomes riding the Trojan horse? PLoS Pathog. 6:e1000740. doi: 10.1371/journal.ppat.1000740
Jackson, W. T., Giddings, TH Jr, Taylor, M. P., Mulinyawe, S., Rabinovitch, M., Kopito, R. R., et al. (2005). Subversion of cellular autophagosomal machinery by RNA viruses. PLoS Biol. 3:e156. doi: 10.1371/journal.pbio.0030156
Jiang, S., Dupont, N., Castillo, E. F., and Deretic, V. (2013). Secretory versus degradative autophagy: unconventional secretion of inflammatory mediators. J. Innate. Immun. 5, 471–479. doi: 10.1159/000346707
Kalamvoki, M., Du, T., and Roizman, B. (2014). Cells infected with herpes simplex virus 1 export to uninfected cells exosomes containing STING, viral mRNAs, and microRNAs. Proc. Natl. Acad. Sci. U.S.A. 111, E4991–E4996. doi: 10.1073/pnas.1419338111
Kouwaki, T., Okamoto, M., Tsukamoto, H., Fukushima, Y., and Oshiumi, H. (2017). Extracellular vesicles deliver host and virus rna and regulate innate immune response. Int. J. Mol. Sci. 18:666. doi: 10.3390/ijms18030666
Kowal, J., Arras, G., Colombo, M., Jouve, M., Morath, J. P., Primdal-Bengtson, B., et al. (2016). Proteomic comparison defines novel markers to characterize heterogeneous populations of extracellular vesicle subtypes. Proc. Natl. Acad. Sci. U.S.A. 113, E968–E977. doi: 10.1073/pnas.1521230113
Kyei, G. B., Dinkins, C., Davis, A. S., Roberts, E., Singh, S. B., Dong, C., et al. (2009). Autophagy pathway intersects with HIV-1 biosynthesis and regulates viral yields in macrophages. J. Cell Biol. 186, 255–268. doi: 10.1083/jcb.200903070
Lai, R. C., Tan, S. S., Yeo, R. W., Choo, A. B., Reiner, A. T., Su, Y., et al. (2016). MSC secretes at least 3 EV types each with a unique permutation of membrane lipid, protein and RNA. J. Extracell. Vesicles 5:29828. doi: 10.3402/jev.v5.29828
Lenassi, M., Cagney, G., Liao, M., Vaupotic, T., Bartholomeeusen, K., Cheng, Y., et al. (2010). HIV Nef is secreted in exosomes and triggers apoptosis in bystander CD4 + T cells. Traffic 11, 110–122. doi: 10.1111/j.1600-0854.2009.01006.x
Mao, L., Wu, J., Shen, L., Yang, J., Chen, J., and Xu, H. (2016). Enterovirus 71 transmission by exosomes establishes a productive infection in human neuroblastoma cells. Virus Genes 52, 189–194. doi: 10.1007/s11262-016-1292-3
Masciopinto, F., Giovani, C., Campagnoli, S., Galli-Stampino, L., Colombatto, P., Brunetto, M., et al. (2004). Association of hepatitis C virus envelope proteins with exosomes. Eur. J. Immunol. 34, 2834–2842. doi: 10.1002/eji.200424887
McLauchlan, J., and Rixon, F. J. (1992). Characterization of enveloped tegument structures (L particles) produced by alphaherpesviruses: integrity of the tegument does not depend on the presence of capsid or envelope. J. Gen. Virol. 73( Pt 2), 269–276. doi: 10.1099/0022-1317-73-2-269
McNamara, R. P., Costantini, L. M., Myers, T. A., Schouest, B., Maness, N. J., Griffith, J. D., et al. (2018). Nef secretion into extracellular vesicles or exosomes is conserved across human and simian immunodeficiency viruses. mBio 9:e02344-17. doi: 10.1128/mBio.02344-17
Meckes, D. G. Jr., Gunawardena, H. P., Dekroon, R. M., Heaton, P. R., Edwards, R. H., Ozgur, S., et al. (2013). Modulation of B-cell exosome proteins by gamma herpesvirus infection. Proc. Natl. Acad. Sci. U.S.A. 110, E2925–E2933. doi: 10.1073/pnas.1303906110
Meckes, D. G. Jr., Shair, K. H., Marquitz, A. R., Kung, C. P., Edwards, R. H., and Raab-Traub, N. (2010). Human tumor virus utilizes exosomes for intercellular communication. Proc. Natl. Acad. Sci. U.S.A. 107, 20370–20375. doi: 10.1073/pnas.1014194107
Miranda-Saksena, M., Denes, C. E., Diefenbach, R. J., and Cunningham, A. L. (2018). Infection and transport of herpes simplex virus type 1 in neurons: role of the cytoskeleton. Viruses 10:E92. doi: 10.3390/v10020092
Mori, Y., Koike, M., Moriishi, E., Kawabata, A., Tang, H., Oyaizu, H., et al. (2008). Human herpesvirus-6 induces MVB formation, and virus egress occurs by an exosomal release pathway. Traffic 9, 1728–1742. doi: 10.1111/j.1600-0854.2008.00796.x
Muralidharan-Chari, V., Clancy, J. W., Sedgwick, A., and D’souza-Schorey, C. (2010). Microvesicles: mediators of extracellular communication during cancer progression. J. Cell Sci. 123, 1603–1611. doi: 10.1242/jcs.064386
Nkosi, D., Howell, L. A., Cheerathodi, M. R., Hurwitz, S. N., Tremblay, D. C., Liu, X., et al. (2018). Transmembrane domains mediate intra- and extracellular trafficking of epstein-barr virus latent membrane protein 1. J. Virol. 92:e00280-18. doi: 10.1128/JVI.00280-18
Nogues, L., Benito-Martin, A., Hergueta-Redondo, M., and Peinado, H. (2018). The influence of tumour-derived extracellular vesicles on local and distal metastatic dissemination. Mol. Aspects Med. 60, 15–26. doi: 10.1016/j.mam.2017.11.012
Nolte-’T Hoen, E., Cremer, T., Gallo, R. C., and Margolis, L. B. (2016). Extracellular vesicles and viruses: Are they close relatives? Proc. Natl. Acad. Sci. U.S.A. 113, 9155–9161. doi: 10.1073/pnas.1605146113
Orvedahl, A., Alexander, D., Talloczy, Z., Sun, Q., Wei, Y., Zhang, W., et al. (2007). HSV-1 ICP34.5 confers neurovirulence by targeting the Beclin 1 autophagy protein. Cell Host Microbe 1, 23–35. doi: 10.1016/j.chom.2006.12.001
Ostrowski, M., Carmo, N. B., Krumeich, S., Fanget, I., Raposo, G., Savina, A., et al. (2010). Rab27a and Rab27b control different steps of the exosome secretion pathway. Nat. Cell Biol. 12, 19–30; sup pp 1–13. doi: 10.1038/ncb2000
Pegtel, D. M., Cosmopoulos, K., Thorley-Lawson, D. A., Van Eijndhoven, M. A., Hopmans, E. S., Lindenberg, J. L., et al. (2010). Functional delivery of viral miRNAs via exosomes. Proc. Natl. Acad. Sci. U.S.A. 107, 6328–6333. doi: 10.1073/pnas.0914843107
Pusic, K. M., Pusic, A. D., and Kraig, R. P. (2016). Environmental enrichment stimulates immune cell secretion of exosomes that promote CNS myelination and may regulate inflammation. Cell Mol. Neurobiol. 36, 313–325. doi: 10.1007/s10571-015-0269-4
Puzar Dominkus, P., Ferdin, J., Plemenitas, A., Peterlin, B. M., and Lenassi, M. (2017). Nef is secreted in exosomes from Nef.GFP-expressing and HIV-1-infected human astrocytes. J. Neurovirol. 23, 713–724. doi: 10.1007/s13365-017-0552-x
Ramakrishnaiah, V., Thumann, C., Fofana, I., Habersetzer, F., Pan, Q., De Ruiter, P. E., et al. (2013). Exosome-mediated transmission of hepatitis C virus between human hepatoma Huh7.5 cells. Proc. Natl. Acad. Sci. U.S.A. 110, 13109–13113. doi: 10.1073/pnas.1221899110
Robinson, S. M., Tsueng, G., Sin, J., Mangale, V., Rahawi, S., Mcintyre, L. L., et al. (2014). Coxsackievirus B exits the host cell in shed microvesicles displaying autophagosomal markers. PLoS Pathog. 10:e1004045. doi: 10.1371/journal.ppat.1004045
Roizman, B., Zhou, G., and Du, T. (2011). Checkpoints in productive and latent infections with herpes simplex virus 1: conceptualization of the issues. J. Neurovirol. 17, 512–517. doi: 10.1007/s13365-011-0058-x
Santiana, M., Ghosh, S., Ho, B. A., Rajasekaran, V., Du, W. L., Mutsafi, Y., et al. (2018). Vesicle-cloaked virus clusters are optimal units for inter-organismal viral transmission. Cell Host Microbe 24:e208. doi: 10.1016/j.chom.2018.07.006
Schauflinger, M., Fischer, D., Schreiber, A., Chevillotte, M., Walther, P., Mertens, T., et al. (2011). The tegument protein UL71 of human cytomegalovirus is involved in late envelopment and affects multivesicular bodies. J. Virol. 85, 3821–3832. doi: 10.1128/JVI.01540-10
Shen, J., Huang, C. K., Yu, H., Shen, B., Zhang, Y., Liang, Y., et al. (2017). The role of exosomes in hepatitis, liver cirrhosis and hepatocellular carcinoma. J. Cell Mol. Med. 21, 986–992. doi: 10.1111/jcmm.12950
Silverman, J. M., and Reiner, N. E. (2011). Exosomes and other microvesicles in infection biology: organelles with unanticipated phenotypes. Cell Microbiol. 13, 1–9. doi: 10.1111/j.1462-5822.2010.01537.x
Sin, J., Mangale, V., Thienphrapa, W., Gottlieb, R. A., and Feuer, R. (2015). Recent progress in understanding coxsackievirus replication, dissemination, and pathogenesis. Virology 484, 288–304. doi: 10.1016/j.virol.2015.06.006
Szilagyi, J. F., and Cunningham, C. (1991). Identification and characterization of a novel non-infectious herpes simplex virus-related particle. J. Gen. Virol. 72( Pt 3), 661–668. doi: 10.1099/0022-1317-72-3-661
Temme, S., Eis-Hubinger, A. M., Mclellan, A. D., and Koch, N. (2010). The herpes simplex virus-1 encoded glycoprotein B diverts HLA-DR into the exosome pathway. J. Immunol. 184, 236–243. doi: 10.4049/jimmunol.0902192
van der Pol, E., Boing, A. N., Harrison, P., Sturk, A., and Nieuwland, R. (2012). Classification, functions, and clinical relevance of extracellular vesicles. Pharmacol. Rev. 64, 676–705. doi: 10.1124/pr.112.005983
van Dongen, H. M., Masoumi, N., Witwer, K. W., and Pegtel, D. M. (2016). Extracellular vesicles exploit viral entry routes for cargo delivery. Microbiol. Mol. Biol. Rev. 80, 369–386. doi: 10.1128/MMBR.00063-15
Vazirabadi, G., Geiger, T. R., Coffin, W. F. III, and Martin, J. M. (2003). Epstein-Barr virus latent membrane protein-1 (LMP-1) and lytic LMP-1 localization in plasma membrane-derived extracellular vesicles and intracellular virions. J. Gen. Virol. 84, 1997–2008. doi: 10.1099/vir.0.19156-0
Wald, A., and Corey, L. (2007). “Persistence in the population: epidemiology, transmission,” in Human Herpesviruses: Biology, Therapy, and Immunoprophylaxis, eds A. Arvin, G. Campadelli-Fiume, E. Mocarski, P. S. Moore, B. Roizman, R. Whitley, et al. (Cambridge: Cambridge University Press).
Wei, X., Liu, C., Wang, H., Wang, L., Xiao, F., Guo, Z., et al. (2016). Surface phosphatidylserine is responsible for the internalization on microvesicles derived from hypoxia-induced human bone marrow mesenchymal stem cells into human endothelial cells. PLoS One 11:e0147360. doi: 10.1371/journal.pone.0147360
Willms, E., Johansson, H. J., Mager, I., Lee, Y., Blomberg, K. E., Sadik, M., et al. (2016). Cells release subpopulations of exosomes with distinct molecular and biological properties. Sci. Rep. 6:22519. doi: 10.1038/srep22519
Wurdinger, T., Gatson, N. N., Balaj, L., Kaur, B., Breakefield, X. O., and Pegtel, D. M. (2012). Extracellular vesicles and their convergence with viral pathways. Adv. Virol. 2012:767694. doi: 10.1155/2012/767694
Xu, R., Rai, A., Chen, M., Suwakulsiri, W., Greening, D. W., and Simpson, R. J. (2018). Extracellular vesicles in cancer - implications for future improvements in cancer care. Nat. Rev. Clin. Oncol. 15, 617–638. doi: 10.1038/s41571-018-0036-9
Yañez-Mo, M., Siljander, P. R., Andreu, Z., Zavec, A. B., Borras, F. E., Buzas, E. I., et al. (2015). Biological properties of extracellular vesicles and their physiological functions. J. Extracell. Vesicles 4:27066. doi: 10.3402/jev.v4.27066
Zaborowski, M. P., Balaj, L., Breakefield, X. O., and Lai, C. P. (2015). Extracellular vesicles: composition, biological relevance, and methods of study. Bioscience 65, 783–797. doi: 10.1093/biosci/biv084
Keywords: extracellular vesicles, microvesicles, exosomes, viral spread, immune evasion, HSV-1, autophagy
Citation: Bello-Morales R and López-Guerrero JA (2018) Extracellular Vesicles in Herpes Viral Spread and Immune Evasion. Front. Microbiol. 9:2572. doi: 10.3389/fmicb.2018.02572
Received: 30 July 2018; Accepted: 09 October 2018;
Published: 25 October 2018.
Edited by:Anthony Nicola, Washington State University, United States
Reviewed by:Maria Kalamvoki, University of Kansas, United States
Dirk Dittmer, University of North Carolina at Chapel Hill, United States
David Meckes, Florida State University, United States
Copyright © 2018 Bello-Morales and López-Guerrero. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.