INTRODUCTION

Genital herpes is one of the most common, persistent and highly infectious sexually transmitted viral infections mostly caused by herpes simplex virus-2 (HSV-2) and in many emerging first time cases, by HSV-1 [1]. Primary and recurrent genital herpes infections most commonly result in lesions and inflammation around the genital area. In women, the sites of infection are mainly the vulva and the vagina, with some cases involving the regions of cervix and perianal. In heterosexual men infection is typically on the glans or the shaft of the penis, whereas anal infection is also reported with homosexual men. More than 500 million people are infected worldwide and most cases reported are among the age groups between 16-40 years that coincides with increased sexual activity among this age group [2]. While these numbers are an estimate, the actual numbers may be underestimated as many people are either asymptomatic or are unaware of the infection [3]. This review provides an insight into the epidemiology, pathology, our current understanding of the molecular mechanisms of infection and the currently available and upcoming treatments for genital herpes.

EPIDEMIOLOGY AND PREVALENCE

Herpesviruses are among the most ubiquitous of human infections. After infection with HSV, it is thought that the virus and the immune response to the virus persist through the life of the host. HSV infections are measured by testing various populations for the presence of antibodies specific to the virus. An estimated 90% of all people worldwide have one or both viruses [4][5]. HSV-1 is the more prevalent virus with 65% of persons in the United States having antibodies to HSV-1 [6], while HSV-2 infections are markedly less frequent, with 15%–80% of people in various populations infected [7]. HSV-1 and HSV-2 infection rates widely vary between countries. The increase in genital HSV-1 is mainly attributed to an increase in oral sex among youngsters and adults which is viewed safer than intercourse [8]. Due to this, in the USA, Canada, and other European countries, at least half of the first episodes for genital herpes have been caused by HSV-1 in the past decade [9][10][11][12]. In a study performed by the CDC it is estimated that about one in six Americans aged 14 to 49 are infected with HSV-2 and the prevalence in women was 20.9%, twice as high as among men [13]. While a surge of HSV-2 seroprevalence from 16.4% to 21.8% was observed from 1976 to 1994 [14], this trend has reversed, dropping to 17.2% in 2004 [15]. In Africa and other developing countries, there is a high burden of HSV-2 infections with >50% prevalence in the population [16]. Around 82% of women and 53% of men in the Sub-Saharan Africa are seropositive for HSV-2 [17]. HSV-2 infection rates also depend on the rates of sexual activity and are more prevalent in heavily exposed populations, such as commercial sex workers, who are nearly 100% positive, suggesting an urgent need for education and new measures for prevention [18].

MOLECULAR MECHANISMS OF INFECTION

FIGURE 1: Schematic of HSV-1/HSV-2 lytic infection. The HSV-1/HSV-2 virion recognizes and attaches to the heparan sulfate proteoglycan via glycoproteins on the viral envelope. By a process called ‘surfing’, the virus particles can travel along filopodia-like membrane extensions to reach the surface of the cell. On the surface of the cell, viral capsid penetration can occur by fusion of envelop with the plasma membrane (I), or alternatively by endocytosis of enveloped virions with eventual fusion of the envelope with a vesicular membrane (II). In either case, gD on the virus envelope is required via its interaction with one of the receptors (shown in red): herpesvirus entry mediator (HVEM) or nectin-1 and-2. In the cytoplasm, the capsid (brown) travels to the nucleus where the viral DNA is released. Multiple rounds of replication result in multiple copies of viral DNA and other components that get packaged and assembled in the nucleus. During egress, the newly assembled capsid gets its primary envelope at the peri-nuclear membrane, which is lost during egress from the outer nuclear membrane. Naked capsid travels through the cytoplasm where it receives the tegument and the viral envelope (presumably from the Golgi or the ER). Heparanase (denoted as pink spots) is an enzyme that was recently described in aiding viral egress. The enzyme cleaves of cell surface heparan sulfate (dotted black) which clears the path for the virus to exit the cell.

HSV are linear, double stranded DNA viruses capable of establishing latency in humans. They belong to the family of Herpesviridae and more specifically to the sub-family of Alphaherpesvirinae. There are two sub-types: HSV-1 and HSV-2 that are closely related but differ slightly in tissue tropism and antigenic properties. The viral DNA is present in the core that is enclosed in a protein shell called the capsid (Fig. 1). The icosahedral shaped capsid is ~125 nm in diameter, which is connected to and surrounded by a glycoprotein expressing lipid bilayer membrane envelope via a protein coat called the tegument. The viral envelope contains at least 12 glycoproteins many of which play major roles in the entry and egress of the virus. A list of HSV glycoproteins along with their reported functions is provided in Table 1.

TABLE 1. List of HSV glycoproteins and their reported functions. [19][20][21][22][23][24][25][26][27][28][29][30][31][32]

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The lifecycle of HSV has been mostly studied and characterized using HSV-1 infections. However, HSV-2 infections are considered similar to HSV-1 infections. Different stages in the HSV lifecycle can be broadly classified into:

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i. Attachment: Initiation of infection begins with the attachment of viral glycoproteins to the cell surface. Heparan sulfate proteoglycans (HSPGs) on the cells serve as attachment sites for HSV [19]. Glycoproteins B and C (gB and gC) on the HSV envelop bind to the HSPGs and are essential to initiate attachment. A study by Herold et al., using a gB and gC null virus showed reduction in the overall virus attachment to the cells as well as reduction in virus infectivity [20]. Moreover, it has been shown that in the absence of gC gB can take over and help in attachment to cells, indicating a gC-independent mode of viral attachment [21]. HSV was shown to bind to HS (heparan sulfate) on the filopodia, which are plasma membrane protrusions, and use filopodial interaction to migrate towards the cell body to initiate entry. This process was termed “viral surfing” [22]. In this study, viral particles were shown to surf along the filopodia and the formation of filopodial structures increased upon HSV infection, possibly due to activation of Rho GTPase signaling during virus attachment to cells. Fluorescence imaging revealed that HSPG expression is higher along the filopodial structures. This mode of attachment has also been reported for vaccinia virus, human papilloma virus type 16, hepatitis C virus, and human immunodeficiency virus (HIV) [23].

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ii. Entry: After the initial attachment to the cell surface, virus entry is the next step in the lifecycle. Various modes of viral entry have been established. The virus is taken into the cells by either direct fusion with the plasma membrane, which is independent of pH change, or through endocytosis mediated by specific cellular receptors. The glycoprotein D (gD) on HSV plays an important role in both of the aforementioned uptake processes and glycoproteins H and L (gH and gL) act in concert to complete the fusion machinery. To date the following receptors have been identified for gD: herpes virus entry mediator (HVEM), nectin-1 and -2 and 3-O sulfated heparan sulfate (3-OS HS) [24]. HVEM was the first identified HSV receptor that belongs to the tumor necrosis factor (TNF) superfamily. The next set of receptors identified is represented by nectin-1 and -2. They belong to the immunoglobulin superfamily. The last receptor is a rare modification of the large sugar molecule HS mediated by the 3-O-sulfotransferase 3 (3-OST-3). 3-OST-3 belongs to the family of 3-O sulfotransferases (3-OSTs) that place sulfate groups at the 3-OH position on the glucosamine in HS. This specific and rare modification of HS dictates the biological activity of HS and occurs during the last step of HS biosynthesis. As an example, modification of HS by 3-OST-1 serves as a binding site for antithrombin, a major player in anticoagulation [25]. 3-OST-3 modified HS serves as an entry receptor for HSV and addition of soluble form of 3-OS HS in HSV resistant cell lines showed increased viral entry [26][27]. Interestingly, 3-OST-3 generated receptor fails to mediate HSV-2 entry but may probably help in the attachment of HSV-2 [19][26].

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Viral entry can occur in the presence of any one of the aforementioned receptors and absence of all three receptors abolishes viral entry. Even though gD is needed for receptor-mediated endocytosis and also for the direct fusion of viral envelop to the plasma membrane, there seems to be no clear consensus on how and which mode of entry the viruses use in human hosts or animal models. While entry into some cultured cells like CHO, HeLa and HCEs are reported to be through receptor mediated endocytosis, entry into Vero and neuronal cell lines are through direct fusion with the plasma membrane [28][29]. In addition to gD playing a vital role in viral entry, accumulating evidence also suggests the important role of gB in HSV entry as a gB null virus was unable to enter and cause infection in target cells [30]. Paired immunoglobulin-like type 2 receptor α (PILRα) has been shown to associate with gB to function as a co-receptor in aiding HSV-1 entry. Mutations on the sites where gB attaches to PILRα not only reduced viral entry but also reduced viral replication and neuroinvasiveness [31][32][33]. Furthermore, another protein that belongs to the sialic acid-binding Ig-like lectin family which shares a similar homology to PILRα called the myelin-associated glycoprotein (MAG) acts as a co-receptor for HSV-1 entry when expressed exogenously [34]. Another co-receptor called non-muscle myosin IIA (NMIIA) was also identified to bind gB on the cell surface and aide in the viral entry [35]. As an actin binding motor protein, NM-IIA plays a critical role in cell adhesion and migration. The glycoproteins gH and gL together with gB and gD form the fusion complex [36][37]. gH exists as a hetero-oligomeric complex with gL. This complex is essential for the processing and cell surface expression of gH [38][39] and is conserved in many of the herpesviruses [40]. Apart from playing a role in the fusion machinery, the gH/gL complex plays a role in virus entry by interacting with various cell surface proteins [41], integrins being the most common. Interaction of gH with integrin αvβ3 facilitates HSV-2 viral entry and calcium signaling in human genital tract epithelial cells [42]. Another study shows that αvβ6 and αvβ8 serve as interchangeable receptors for gH/gL that promote endocytosis and activation of membrane fusion [43]. A recent study by the same group also found that conformational changes in the above mentioned integrin receptors are essential to promote the dissociation of gL from the gH/gL complex, a proposed new mechanism in HSV viral entry [44].

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Other alternative modes of viral entry have also been identified. A phagocytosis-like uptake of the virus particles was reported to be observed once the virus particles have attached to the filopodia; it is believed to exhibit mixed traits of endocytosis and phagocytosis [45]. Cytoskeleton rearrangement and their associated cellular signaling pathways have also been implicated in facilitating HSV entry into cells [46]. Rho-GTPase signaling pathway involving Rho-A and cdc42, key modulators in the formation of filopodia, were shown to be activated and aide in the phagocytic-like uptake of the virus [45]. Another signaling pathway called phosphoinositide 3 kinase (PI3K) pathway, which is involved in the downstream of the filopodial formation, was also found to affect multiple steps in the HSV entry [47]. This same pathway is also implicated to control the activity of cofilin, a family of actin-binding proteins, in facilitating entry of virus into neuronal cells [48]. The activation of Akt signaling in triggering calcium release which aids in HSV viral entry has also been shown [49].

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iii. Capsid Transport and Replication: Upon successful entry into cells, the viral capsid and tegument proteins are released into the cytoplasm. The virion host shutoff protein (vhs) is a viral tegument protein that is released into the cytoplasm after entry and degrades host mRNAs that regulate stress response. The capsid then translocates to the nucleus along microtubules via the dynein and dynactin motor proteins and releases the viral DNA into the nucleoplasm [50][51][52]. A recent study reported the role of heat-shock protein 90 (Hsp90) to be involved with HSV capsid transport to the nucleus via interaction with acetylated α-tubulin [53]. The uncoating of viral DNA occurs at the nuclear pore.

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iv. Replication and Assembly: Once inside the nucleus, several viral genes are expressed in an ordered fashion. The proteins of the α genes or intermediate early (IE) genes are the first to be transcribed. The products of these genes are termed as infected cell protein (ICP) and there are five ICPs: 0, 4, 22, 27 and 47. The virus encodes a tegument protein: VP16 that aids in the transcription of the α genes. The expression of ICP4 is then thought to drive the expression of the β genes or the early genes. The β genes encode for various proteins that promote viral DNA replication, including the enzyme thymidine kinase (TK). The virus utilizes TK for replication leading to the expression of the γ or late genes. The proteins of the γ genes encode for several components of the viral structure including capsid and envelop proteins. Various viral components are formed which then assemble and the viral DNA is repackaged into a new capsid. Fully assembled capsid exits from the nucleus by acquiring a glycoprotein-containing envelop at the inner nuclear membrane and losing it at the outer membrane when the naked capsid is released in the cytoplasm for re-envelopment using a Golgi-derived membrane (Fig. 1).

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v. Autophagy Modulation during Active Replication: The role of autophagy, a cellular process involved in maintaining the metabolic and homeostatic activity, in HSV replication has been widely studied. The ICP34.5 protein, a neurovirulence factor, regulates the replication of HSV by controlling the autophagic pathway via inhibition of either PKR/eIF2a signaling pathway [54][55] or beclin-1, a protein involved in the formation of autophagosomes [56]. A recent study showed that a basal level of autophagy is needed for efficient replication of virus and disrupting the basal level would lead to reduced viral titers [57]. Another recent study showed the role of a host cytoplasmic protein called axin in controlling autophagy and HSV replication [58]. The results from this study indicate that axin expression reduces the levels of cellular autophagy induced by HSV, resulting in enhanced HSV replication.

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vi. Latency and Reactivation: One of the key traits of this family of viruses is to go latent for the life of the host after primary infection. How and why the virus goes latent is only partially understood and is one of the hot topics in herpes research. After a lytic infection the virus has the ability to evade and mask itself from the host defense. Latency is established when the virus migrates to the sensory ganglia via a retrograde fashion and invades the nucleus of the neurons (Fig. 2). In the nucleus the HSV genome is maintained in a circular form and remains in a silent state. During this state, a region of the genome that encodes for the latency associated transcripts (LATs) remains active [59]. Kramer et al. also showed the presence of HSV transcripts using RT-PCR analyses in latently infected mouse ganglia [60][61]. The exact role and function of the LATs also remains to be completely understood. However, research over the last decade has revealed the common functions of LAT: they help in reducing the expression of the viral genome thereby maintaining them in a latent state protected from the immune system [62] and they protect infected neurons from apoptosis, thus increasing the amount of latent transcripts that would eventually increase the viral load upon reactivation [63][64]. In addition, the host immune system has also been implicated to play a vital role in viral latency. Studies in the mouse models of latent HSV infection revealed the presence of infiltrating immune cells and cytokines in latently infected ganglia [65][66][67] while some suggest that the presence of low viral transcript levels could lead to a local milieu of immune effectors that could repress HSV gene expression [68][69]. Some evidence also suggests the role of neuronal functio in maintaining latency [70][71][72]. Furthermore, during latent infection, the ability of some parts of the HSV genome to remain transcriptionally active and inactive suggested the presence of epigenetic control. Two studies that used computational analysis and latently infected mice revealed that DNA methylation, a most common epigenetic mechanism, did not regulate HSV latent gene expression [73][74], leading to the investigation of other epigenetic mechanisms.

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Figure 2: Schematic of Primary Infection and Reactivation. Primary infection occurs when a host is exposed to the virus for the first time. When a person is exposed to HSV, the virus infects the epithelial cells. Depending on the immune system of the host, lytic infection leads to virus shedding that can cause symptoms such as ulcers or remain asymptomatic. After lytic infection, the virions reach the nerve endings and through a retrograde transport, reach the sacral ganglion where it establishes latency till the life of the host. Recurrent infections occur when the virus gets reactivated due to stress, environmental conditions and other unknown factors. Reactivation causes the virus from the sacral ganglion to travel to the site of primary infection or high nerve endings via an anterograde fashion where virus shedding can cause symptoms or remain asymptomatic depending on the host immune system.

The role of chromatin and HSV latency has gained increasing popularity as the HSV DNA is devoid of histones [75] but upon infection gets assembled into the nucleosome [76] and associates with histones [77]. However whether heterochromatin or euchromatin play a role in HSV latency was not known. Only recently, using various molecular techniques, the presence of heterochromatin or euchromatin in HSV-infected cells has been studied to provide a basis for a chromatin-based epigenetic mechanism of HSV gene regulation in different cell types [78]. In a study by Kubat et al., their findings showed that active chromatin was associated with LAT gene as increasing levels of acetylated H3 histone were found to be associated with the LAT promoter and enhancer compared with the ICP0 gene [79]. In another study by Wang et al., it was shown that as latent infection is established the HSV lytic genes are progressively associated with chromatin that contains dimethylation of H3K9me2, which is an indicator of heterochromatin [80]. Thus there is a general notion that during latent infection the LAT gene is associated with euchromatin whereas the lytic genes are associated with heterochromatin. The study by Amelio et al. gave insights into how and why different chromatin are maintained and regulated separately on the latent viral genome [81]. Their study identified candidate insulator elements, DNA sequences that bind protein factors that maintain chromatin boundaries. These contain CCCTC sites that are bound by the CCCTC-binding factor (CTCF) upstream of the LAT promoter boundary and in the LAT intron. They proposed that insulators keep the LAT euchromatin activity within a boundary and heterochromatin outside of the same boundary.

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Reactivation of the latent virus occurs when an external stimuli or ‘stress’ is applied to the neuron. Various factors such as environmental conditions, fever, exposure to sunlight and other unknown conditions have been attributed to cause reactivation but their exact targets at the molecular level remain unknown. When the virus reactivates it travels from the sensory ganglia via anti-retrograde fashion to the primary infection site or sites of high neuron innervations where active virus replication and shedding occur and symptoms like pain, inflammation and lesions develop. In an effort to understand the exact role of LATs in the reactivation of HSV, LAT encoded micro RNAs (miRNA) were discovered. miRNAs are a family of non-coding RNA that is approximately 22 nucleotides in length. They usually function at a post-transcription level by inhibiting protein synthesis via mRNA degradation. HSV miRNAs have been shown to be expressed during productive infection, which helps degrade host immune responses as well as during latency, which helps in establishing latency or helps in reactivation [82].

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vii. Egress: Upon formation of capsid and packaging of the virus DNA, the virions eventually have to egress or leave the nucleus and the cell to get into the extracellular environment. While the process of HSV egress still requires some clarity due to varying experimental models and complexity in studying the virus-nuclear interactions, the following is the accepted model for viral egress. Budding is the initial step in the nuclear egress of HSV. In this process the capsid acquires the envelope from the inner nuclear membrane and two viral proteins: UL31 and UL34 are reported to be necessary for the budding process [83]. Once the virus reaches the perinuclear region, it is thought to lose the primary envelope or undergoes de-envelopment and evidence suggests that the final assembly of tegument, envelope and the glycoproteins occur within the cytoplasmic compartments (presumably in the Golgi or Endoplasmic Reticulum, ER). During productive infection either in primary infection or after reactivation, for efficient transmission and infection, the virus needs to spread to neighboring cells. The release of the virus from infected cells requires both host factors and viral components. Among the viral components, glycoproteins E and I (gE and gI) are needed for efficient spread of viruses in certain polarized and non-polarized epithelial cells and neuronal cells [84][85]. Among the host factors, a HS degrading enzyme: heparanase (HPSE) has been recently shown to aide in viral egress [86]. The study shows how the levels of HPSE increase over time with HSV infection as active form of HPSE is translocated to the plasma membrane of infected cells to remove HS for smoother release of newly generated virions. The role of myosin motor proteins such as NMIIA and myoVa have also been implicated in HSV egress [87] [88].

SYMPTOMS AND PATHOLOGY

Genital herpes is predominantly transmitted through sexual contact. Viral transmission by oro-genital contact is mostly HSV-1 and therefore the number of genital HSV-1 cases is on the rise [89][90][91]. Virus shedding is more predominant in sites like mouth and mucosal surfaces such as the vagina. Contact with any one of these increases the risk of being infected with HSV.

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An episode or outbreak is termed as the phase in which individuals experience symptoms and the severity of these episodes depends on previous immunity to HSV. Notably, almost 25% of people presenting with a first clinical episode of genital herpes have serological evidence of past HSV-2 infection at the time of presentation, suggesting initial infection was asymptomatic [92]. In many other instances of primary infections where the patient encounters HSV for the first time the first episode may occur anywhere between 2 days to 2 weeks after primary infection. Primary infections are clinically most severe and most likely symptomatic [93]. Symptoms like fever, itching and muscle pains usually in the lower part of the body are most common in primary infection; 40% of men and 70% of women also report fever, headache, malaise, and myalgias [94]. Papule formulation followed by a wide distribution of blisters or lesions appear around the genital areas that eventually break to form ulcers (Fig. 2). Over a period of time the ulcers crust and heal. In women common sites for lesion are the cervix, vagina, labia majora and minora and perianal region through infected vaginal fluid and in men it is mostly on the shaft or the glans of the penis. Anal lesions are also reported in homosexual men. Primary infections either by HSV-1 or by HSV-2 cannot be differentiated just by clinical symptoms; additional laboratory testing is needed to differentiate between the two viruses.

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At the tissue and molecular level, HSV-2 infects the epithelial cells on the genital mucosa leading to an increase in inflammatory response and cell death at the site of infection. Multinucleated cells and syncytia formation are the most common observation in cells infected with HSV. The recruitment of macrophages, natural killer cells, B-cell and T-cell mediated immunity [95][96] and the release of cytokines has been reported to play a role in innate and adaptive immunity to HSV infections. This contributes to a chronic inflammatory state in genital skin and mucosa. Histopathologic studies of foreskin in HIV-seronegative men after adult circumcision have shown a higher concentration of CD4⁺ and CD8⁺ T-cells in HSV-2–seropositive compared with HSV-2–seronegative men [97]. During the course of primary infection, the virus spreads via a retrograde fashion along the microtubules lining the axons to the dorsal root ganglia (DRG) where the neuronal cells act as reservoirs for the virus to remain latent [98]. Upon reactivation due to factors such as stress and other unknown conditions, the virus spreads from the DRG to the epithelial cells via an anterograde fashion where a lytic replication of the virus follows, resulting in virus shedding. This is the cause of recurrent infections and these infections are usually asymptomatic or may be associated with a classic genital ulcer. While the innate immune system, specifically the CD8⁺ T-cells and the plasmacytoid dendritic cells, are attributed in controlling latency and reactivation of the virus [69][99][100], recent reports suggest otherwise. Studies have shown that CD8α dendritic cells help drive the establishment of HSV-1 latency [101][102]. At a clinical and subclinical level, the severity of viral reactivation varies widely from person to person and depends on cell mediated immunity that is considered important for control of viral replication [103][104].

DIAGNOSIS

Diagnosis of genital herpes based purely on clinical presentation is often not accurate and could be misleading. Symptoms occurring from other bacterial infections like Treponema pallidum or Haemphilus ducreyi could be confused with HSV resulting in wrong diagnosis [105]. Genital herpes may also cause atypical symptoms that occur at unusual sites such as the thighs or the buttocks. HSV-2 is also found to be a co-factor for HIV-1, which is one of the leading causes of sexually transmitted infections and at times it becomes difficult to diagnose the symptoms that occur due to HIV-1 co-infections [106]. Hence, along with clinical diagnosis, laboratory tests are required to accurately diagnose genital herpes. To determine the presence of HSV in laboratory, swabs from the genital lesions are taken and tested by the following common techniques:

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i. Viral culture of HSV has been a gold standard for laboratory diagnosis of HSV for the past two decades. Using the swabs from the genital lesions, the virus can be grown on tissue culture, usually within 5 days, that is then detected using immunofluorescence assays or by enzyme immunoassay. The limitation with this method is that it lacks sensitivity as more viruses are usually obtained from patients with primary infection (80%) but less from patients with recurrent infections (20-50%) or patients whose lesions have begun to heal [107].

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ii. Polymerase Chain Reaction (PCR): This method of nucleic acid amplification has emerged as the next common method to assess the presence of HSV. Determining HSV by PCR is faster and four times more sensitive compared to viral culture [108][109]. Based on this method, three assays have been approved by the US Food and Drug Association for the detection of HSV in genital lesions. These include IsoAmp HSV Assay, BioHelix Corporation; MultiCode-RTx Herpes Simplex Virus 1 & 2 Kit, EraGen Biosciences, Inc. and BD ProbeTec Herpes Simplex Viruses (HSV I & 2) QX Amplified DNA Assays, BD Diagnostic Systems. With increasing technology and advances in kit developments for HSV detection and typing using PCR, this method is rapidly replacing the viral culture assay.

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iii. Serotyping: This method can not only be used to detect the presence of HSV but can also be used to differentiate between genital herpes originating from HSV-1 or HSV-2. Type-specific IgG against the glycoprotein G (gG) of HSV-1 and HSV-2 are available that can be used to distinguish between the two viruses [110]. Serotyping has another advantage in that it detects the presence of HSV to confirm if the infection is a primary or recurrent infection. In primary infection, type-specific HSV antibodies can take from 2 weeks to 3 months to develop. Therefore, an initial absence of IgG antibodies specific for gG and subsequent development of such antibodies after 12 weeks confirms new HSV infection. Clinicians also recommend this method to diagnose genital herpes when there are no lesions or the above mentioned detection tests do not provide substantial results.

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While this review only mentions the above common techniques to diagnose genital herpes in a laboratory setting, there are currently other methods and techniques being developed by research institutes and companies. For example, LeGoff et al. provide a detailed description of other available and upcoming diagnostic methods [111].

TREATMENT AND PREVENTION

Genital herpes conditions are primarily treated with antivirals that aim at controlling viral replication. Acyclovir, its analogue Valacyclovir and Famcyclovir (prodrug of Pencyclovir) are currently prescribed for genital herpes treatment. These drugs are nucleoside analogues that specifically inhibit the herpesvirus DNA polymerase. While cyclovir is available in oral and intravenous formulations, Valacyclovir and Famcyclovir are available only as oral formulations. For primary infections where the symptoms can be severe, antiviral therapy is usually started even before the symptoms are confirmed by laboratory diagnosis and the duration of the therapy is 7-10 days or till the lesions are healed [112]. In severe cases, to relieve pain, clinicians recommend the use of analgesics or sitz baths where the patients’ hips and buttocks are immersed in lukewarm water [107].

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Preventive strategies to efficiently reduce the transmission of the virus also exist and in combination with the above mentioned treatments there could probably be a significant reduction of viral transmission. In the case of people that have symptomatic viral shedding, the most common preventive strategy is to abstain from sexual activity or to use condoms. A prospective study showed significantly lowered levels of viral acquisition among partners that used male condoms [113]. Although it is thought that female condoms can also reduce virus transmission, this has not been clinically investigated. Applications of topical microbicides to prevent genital herpes infections are also being investigated. This strategy involves the use of natural or synthetic products that either increase the natural vaginal defenses or inactivate the HSV virions [114][115]. A recent study showed that vaginal application of tenofovir gel, an antiviral microbicide which functions as a nucleotide reverse-transcriptase inhibitor, reduced the levels of HSV-2 acquisition among women in South Africa [5].

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Various other therapeutic and prevention strategies that target different stages of virus lifecycle are currently being investigated. Peptide therapeutics is fast rising owing to the ease of synthesis, modifications and their high specificity [116]. They are being synthesized and used as inhibitors against HSV infections [117]. The TAT (transactivator of transcription)-peptide, derived from HIV, has been shown to inhibit infection of HSV in the in vitro and in vivo models of HSV infections [118][119]. A study showed the effect of a synthetic 3-OS HS specific peptide: G2 in blocking HSV-2 infections in human cervical (HeLa) cell lines. This peptide significantly blocked the entry and thereby the spread of the virus [120] and a D-enantiomer of this peptide exhibits higher stability and more promise in inhibiting HSV infection [121]. Another study designed synthetic peptides specific to the glycoproteins gD and gG and showed that these peptides can effectively recognize HSV-2 antibodies and hence may be used for serodiagnostic assays [122]. Because HSV utilizes the cytoskeleton filaments and kinases during its entry, a recent study showed that blocking the myosin light chain kinase (MLCK) with inhibitors such as blebbistatin significantly reduces HSV infection [123], providing new evidence for potential targets in blocking HSV infections. The advent of nanoparticles in drug delivery was successful, owing to their ability to provide sustained or extended delivery of drugs at a local site. Nanoparticles or nanoparticle compositions to protect against HSV-2 infections are also being actively researched. Zinc Oxide (ZnO) nanoparticles exhibited significant antiviral activity in both the in vitro model using vaginal epithelial cells and the in vivo mice model of HSV-2 infections [124]. Three different modes of treatment were used in this study: prophylaxis, therapeutic and neutralization. In all the three modes of treatment, the ZnO nanoparticles showed promising results in blocking HSV-2 infections. Another study showed the potential antiviral use of mucus-penetrating nanoparticles [125]. In this study, acyclovir monophosphate loaded mucus-penetrating nanoparticles showed an increase in drug retention and distribution thereby providing an effective protection against HSV-2 challenge.

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Protection against genital herpes infections can be enhanced by induction of protective immune responses using vaccines. Vaccines against genital herpes are underway and in the majority of clinical trials only prophylactic vaccines have seen success so far. There have been no reports of any therapeutic vaccines that show promise against genital herpes infections. These vaccines consist of subunits of glycoproteins such as gD or gB. A gD2 subunit vaccine, when administered with alum as adjuvant, showed around 39-46% efficacy in preventing HSV-2 infections in patients that were seronegative for HSV-1 and HSV-2 but did not provide protection to patients that were seropositive for HSV-1 [126][127]. Other viral glycoproteins such as gC and gE are also being used as vaccines to study their effectivity in blocking genital herpes infections [128][129]. Peptide based vaccines are also being developed to incite immune responses against HSV-2 infections. A study developed a peptide based vaccine: HerpV, which generates CD4⁺ and CD8⁺ responses when subjected to HSV-2 challenge [130][131].

CONCLUSION AND FUTURE DIRECTIONS

There is no doubt that our understanding of HSV-2 lifecycle and associated pathogenesis has improved dramatically over the last several years but challenges remain in many areas, especially those relating to disease management and prevention. The new knowledge has provided a major opportunity to develop new strategies for patient care by combining our understanding of viral infection mechanisms, host immune responses, and the viral mechanisms that subvert them. New anti-HSV drugs are on the horizon, many of which may target other herpesviruses as well. At present, the development of vaccines against HSV-2 is a highly active area of research and many innovative strategies are currently being tested for an effective vaccine generation. Future clinical trials will see many new, non-nucleoside anti-herpetic drug candidates as well as many newer approaches, including immune-based therapeutics. An area that needs extra attention is rapid diagnostics, especially since genital herpes can be caused by both HSV-1 and HSV-2. Therefore quick and easily available tests can yield much better results in reducing symptoms and lowering transmission rate. Any success in reducing transmission rate will mean a step closer to the greatest challenge for herpes virologists, which is complete elimination of this lifelong infection.

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