Comparison between epidemiologic and clinical data of HIV-1 and HIV-2 infections
Although sharing identical transmission routes as well as structural and genomic properties, human immunodeficiency viruses 1 and 2 (HIV-1 and HIV-2, respectively) show different pathogenic abilities in human host. Despite both HIV-1 and HIV-2 lead to immunological failure and Acquired Immunodeficiency Syndrome (AIDS), a slower rate of disease progression with a longer asymptomatic period and lower levels of viremia in general characterize HIV-2 infection (Table 1). Comparative studies measuring the progression rates of both HIV-1 and HIV-2 infections provided clear evidence that the majority of HIV-2 infected individuals fit in a definition of long-term non-progressors [1-3].
|Worldwide||Restricted to West African countries and to countries sharing economical-social links with them|
|Usually moderate to high||Usually undetectable|
|By sexual route is usually inefficient, requiring multiple exposures||Scarce data but less efficiently transmitted than HIV-1|
|Usually less than 10 years||Usually decades|
|Plenty of data regarding viral susceptibility to all anti-retroviral drugs. Resistance-conferring mutations well established and defined||Naturally resistant to non-nucleoside analogous targeting reverse transcriptase. Scarce and sometimes conflicting results regarding susceptibility to other anti-retroviral drugs|
All these findings support the notion that in HIV-2 infected individuals several factors (e.g. virologic and immunologic) should account for a best fitted response that ultimately leads to a better control of HIV-2 infection compared to HIV-1. Deciphering these factors should provide crucial information about the mechanisms underlying the delayed disease progression and may help explain how a retroviruses infection could be coped for such a long time without causing disease. This knowledge is important to clarify AIDS pathogenesis and to identify the correlates of protection crucial to develop an efficient HIV vaccine.
Despite the potential importance of HIV-2 as a model to address those issues, it has been mostly neglected and very few data exists regarding HIV-2 interaction with target cells. In this chapter I will focus on these interactions, particularly those concerning early events. Distinguishing features between HIV-1 and HIV-2 will be highlighted and their implications in viral fitness and pathogenic differences between the two viruses will be discussed.
2. Origin of HIV-2
HIV-2, as HIV-1, belongs to Family
HIV-1 and HIV-2 were introduced into human population as a consequence of multiple cross-species transmissions from simian immunodeficiency virus (SIV)-infected non-human primates. The genetic relatedness between HIV-1, HIV-2 and SIV strains, and the coincidence of natural habitats of specific simian species and geographic regions where HIV-1 and HIV-2 had probably emerged, allowed the identification of SIVcpz (infecting the chimpanzee subspecies
3. Genomic organization of HIV-2
The genomic information of HIV-2 is comprised in two identical copies of 9.2 kb single strand RNA. HIV-2 genome encodes nine open reading frames (i.e.
After integration, the HIV-2 proviral DNA is transcribed into several mRNAs by cellular RNA polymerase II, a process initiated through the binding of cellular activation factors to the viral LTR, culminating in the synthesis of viral proteins and in the production of new progeny virions. The function of each HIV-2 protein has been inferred from HIV-1 counterparts and reviewed in .
Compared to HIV-1, HIV-2 lacks the
Vpx is a protein only present in HIV-2 and SIVsm lineage. Sequence analysis suggests that the
4. HIV-2 as a limited spreading virus
As in all zoonosis, the emergence of HIV-1 and HIV-2, as successful new human pathogens, involved not only a close contact with animal reservoirs but also the capability of the cross-species viruses to: encounter and efficiently infect human host cells, and to be able to be effectively transmitted within the human population.
Although HIV-1 and HIV-2 shared common transmission routes, they show a clear distinct epidemiology. While HIV-1, particularly group M, has spread literally worldwide, HIV-2 infection reveal a much more confined geographic distribution: West Africa and countries that maintained social-economic links to this region (e.g. Portugal, France and their former colonies). Since both viruses had begun to spread nearly at the same time, somewhere between 1950 and 1970, this limited expansion of HIV-2 indicates a less efficient human transmission. Heterosexual spread of HIV-2 is remarkably lower than in HIV-1: it seems that HIV-2 is five to nine times less efficiently transmitted than HIV-1 by sexual route . Likewise, mother-to-child transmission rate of HIV-2 is 0-4%, while in HIV-1 this transmission occurs in 15-40% of untreated pregnancies .
This poor capability to infect new hosts could lead HIV-2 to a dead end. Viral ecology imposes two ideal conditions: maintain the host alive as long as possible while being efficiently transmitted within host population. HIV-2 only fulfils the first condition leading to a decline in HIV-2 prevalence even in regions (i.e. West Africa) where, in the early stages of AIDS epidemic, a clear predominance of HIV-2 infections existed compared to HIV-1 .
4.1. Viral load and transmission
Many different factors account for a successful transmission of HIV by sexual route. One of the most critical is the amount of infectious viral particles present in the transmitting body fluid (e.g. blood, semen or cervicovaginal secretion). Higher concentrations are more likely associated with transmission events. Apparently, in HIV-1, the cutoff of 1500 copies of viral RNA per ml of plasma is required for efficient transmission .
Not surprisingly, plasma and semen viral loads are significantly lower in patients infected with HIV-2 compared to those infected with HIV-1 [26, 27], providing a likely explanation for the reduced transmission rate and spread within human population. This lower viral load is observed throughout the infection and persists until late in the course of the disease, but is remarkably important during asymptomatic stage. During this stage, which in HIV-2 could last for several decades, an undetectable viremia is a hallmark of almost every HIV-2 patients. However, a similar proviral burden is detected in both HIV-1 and HIV-2-infected individuals [28, 29]. This apparent paradox suggests that the lower plasma viral load observed in HIV-2 infection may be due to lower levels of infectious virus production, or a better host-driven suppression of viral replication, or both.
4.2. The mucosal barrier
Besides viral load, numerous barriers decrease the efficiency of mucosal transmission. The foundations of this important notion emanates from studies of couples discordant for HIV-1 infection, which demonstrated that heterosexual transmission is very inefficient requiring multiple exposures for a successful transmission [30, 31]. A detailed understanding of the events surrounding transmission should provide important clues how HIV establishes a new infection and what additional vulnerabilities HIV-2 has, at this stage, that can help explain its lower spread.
Although HIV-1 and HIV-2 (as well as SIV) are commonly referred as “lentivirus” based on the long incubation period and slow onset of disease, it is now clear from data using rhesus macaque model infected with SIV, that initial virus-host interactions, crucial to establishing systemic infection, take place in a rapid succession of related events, soon after mucosal transmission (recently reviewed in ). In sexual transmission, the most common form of HIV transmission, these events involve the interactions with cells present in cervical/vaginal mucosa epithelial surfaces. To establish infection, HIV present in semen must go through mucus that covers female genital epithelia and penetrate through the epithelial layer to access susceptible cells such as T lymphocytes, macrophages, Langerhans cells and dendritic cells. Mucus, particularly abundant in upper female genital tract, provides the first barrier to HIV infection. Mucus protective role of underlying epithelial cells is provided by the presence of soluble factors (e.g. chemokines produced by epithelial cells) that decrease viral infectivity and by mechanical trapping of virions in the dense protein mesh that constitutes the cervical mucus . By slowing viral diffusion, mucus reduces the probability of infectious virus reach the surface of underlying cells.
Virions that successfully crossed the mucus encounters the epithelial cells layer that line the different compartments of the female genital tract. These different compartments show remarkable differences in the structure of epithelial layer. The mucosa from the lower female genital tract (i.e. exocervix and vagina) consists of stratified squamous epithelium, several layers thick. In contrast, in the upper reproductive compartment (i.e. endocervix and endometrium) the mucosal lining is composed of a single layer of columnar epithelium over the basement membrane and is characterized by the presence of tight junctions between cells.
As expected by their different composition, the lower female genital epithelium is much more robust and provides a more effective physical barrier than the fragile single columnar layer of upper genital epithelium. Furthermore, the junction between the exocervix and the endocervix, where the structure of the epithelium abruptly changes from stratified to single layer (called the transitional or transformational zone), is characterized by an intense immunologic activity and thus enriched with abundant lymphocytes and antigen presenting cells (e.g. dendritic cells and macrophages), particularly during inflammatory processes . The physical vulnerability and the presence of abundant target cells in transitional zone, make this region highly susceptible to HIV entry and infection .
Even the thicker vaginal epithelial barrier could quickly expose susceptible cells in the submucosa to HIV. In fact, the stratified squamous epithelium changes markedly through the menstrual cycle, in response to progesterone , leading to a thinning of this physical barrier. Additionally, breaches could occur because of microulcerations and breaks in the epithelium due to sexual intercourse, inflammatory processes, sexually transmitted infections, and other genital infections, increasing the likelihood of establishing an HIV infection [37-39].
Additionally, the mere exposure of genital mucosa to semen induces local alterations that could potentiate the transmission of HIV-1 and (probably) HIV-2. These include the neutralization of the acidic pH of the cervicovaginal secretions, the regulation of inflammatory cytokines in genital tract epithelial cells, and the promotion of leukocyte infiltration and the attraction of Langerhans cells in cervical and vaginal mucosae [40, 41]. Semen could also directly promote HIV infection of epithelial target cells through the formation of amyloid fibrils that capture HIV particles and enhances virus-cell attachment and fusion . This amyloidogenic activity of human semen seems to be related with fragments of prostatic acidic phosphatase . Apparently this enhancement is semen donor-dependent but independent of HIV strain or cell type used .
In contrast to female genital tract, HIV transmission through male genital tract is poorly understood. Despite the presence of CD4+ T lymphocytes, Langerhans cells, dendritic cells and macrophages in the foreskin and glans of the penis [44, 45], the mechanisms underlying the transmission across these mucosae are not completed elucidated. Foreskin seems to play a crucial role in female-to-male transmission of HIV-1, since several randomized controlled clinical trials have shown that circumcision reduce this route of transmission by approximately 60% . One plausible mechanism for greater susceptibility to HIV-1 infection in uncircumcised men could be the increased risk for sexually transmitted infections and consequent inflammation of the foreskin (reviewed in ). This predisposition to local infection and inflammatory reactions will lead to the recruitment of activated target cells that facilitates the early events of HIV transmission and provides a local environment suitable for productive HIV systemic infection.
The vaginal flora could in some circumstances also favour female-to-male HIV transmission. The predominance of potential pathogenic bacteria instead of normal
4.3. Crossing the intact mucosal barrier
Although infection of mucosal epithelial cells could happen, HIV must gain access to permissive host cells present in underlying submucosa tissue (e.g. dendritic cells macrophages and CD4+ T-lymphocytes) to facilitate virus production and dissemination. The mechanisms for crossing intact stratified squamous epithelium of the vagina or the simple columnar epithelium of the cervix could be one (or more) of the following: (i) transcytosis by a vesicular pathway  – an apparently rare but possible event ; (ii) capture or infection of dendritic cells resident in the stratified squamous epithelium of the vaginal mucosa and in the underlying tissues of the vagina and cervix ; and (iii) direct infection of intraepithelial lymphocytes in the endocervical mucosa .
Regardless the pathway used by cell-free HIV virions to penetrate the epithelial cell barrier, they ultimately lead to viral exposure of dendritic cells, macrophages and CD4+ T-lymphocytes present in underlying submucosal tissues, allowing the initiation of infection. Dendritic cells can capture HIV virions through C-type lectin receptors (CLRs) present at cell membrane (e.g. DC-SIGN, DCIR), and internalize the captured virus without being infected. This internalized virus, as well as those bound to dendritic cell membrane, remains full infectious and able to be transmitted to surrounding CD4+ T-lymphocytes through a structure analogous to the immunological synapse, named “virological synapse”. This tight adhesive junction between an HIV-exposed dendritic cell and an uninfected CD4+ T-lymphocyte allows the virus to be efficiently transferred from one cell to the other, in a process named
Alternatively, HIV can directly infect the dendritic cell subset, present in submucosal tissues (
Interestingly, although HIV can infect dendritic cells, extensive viral replication only takes place after dendritic cells come into contact with CD4+ T lymphocytes in lymphoid tissue . The dendritic cell-T lymphocyte interaction provides activation signaling to the latter, allowing HIV to be presented to a population of highly activated and susceptible T-lymphocytes. This further indicates that the infection of dendritic cells by HIV-1 is a double-edged sword: dendritic cells must deliver appropriate signals to T lymphocytes in order to induce an HIV-specific immune response; however, this interaction imposes a close contact between dendritic cells and T lymphocytes (immunological synapse) leaving the latter susceptible to infection by the HIV-1 carried by dendritic cells.
In conclusion, dendritic cell-mediated virus transfer occurs in two distinct phases: in the first phase (
All the data reviewed until now was obtained almost exclusively using HIV-1 model (and in some instances SIV). As referred earlier in this chapter, HIV-2 is a lentivirus that shows a decreased capacity to spread between humans, and probably with additional vulnerabilities during transmission, compared with HIV-1. Besides the lower viral load both in plasma and semen referred previously, little is know about HIV-2 interaction with mucosal cells and how the described physical barriers counteract effective HIV-2 transmission to a new host. For example, very few data exists about HIV-2 interaction with DC-SIGN or the way HIV-2 uses
Early reports referred that dendritic cells derived from hematopoietic progenitor cells or from peripheral blood monocytes are less susceptible to productive infection by HIV-2 compared with HIV-1 [67, 68]. Paradoxically, recent data have disclosed a cellular protein (SAMHD1) that inhibits HIV-1 replication in immature monocytes-derived dendritic cells, in dendritic cells derived from PMA-differentiated THP-1 monocytic cell line  and in macrophages . This restriction factor affects the efficiency of reverse transcription leading to a reduced amount of viral cDNA . SAMHD1 is counteracted by the HIV-2/SIV Vpx protein and its inhibitory mechanism, in the absence of Vpx, helps to explain the different permissivity of these non-dividing cells to lentiviral infection . In this scenario, the non-permissiveness of dendritic cells to HIV-1 infection favours viral dissemination by
5. HIV-2 chronic infection in human host: a natural long-term non progressive infection
The long-term non-progressive infection that characterizes the HIV-2 infection in humans is determined by several host-virus interactions that, in contrast to HIV-1, enable the control and the confinement of HIV-2 pathogenic potential.
As referred above, the different pathogenic outcome observed in HIV-2 infection compared to HIV-1 seems to be dictated as early as the initial interactions with dendritic cells and macrophages present at mucosae surfaces. The expression of Vpx by HIV-2, allowing the bypass of SAMHD1 restriction and the consequent productive infection of dendritic cells and macrophages (
Noteworthy, and despite the described mechanisms that could lead to a hindrance in HIV-2 dissemination at early stages during acute infection, a similar proviral load is observed in HIV-2 and HIV-1 infected patients. These observations suggest that HIV-2, like HIV-1, is able to disseminate and an equal number of target cells are infected during acute and chronic phase or, alternatively, that in HIV-1 a greater number of infected CD4+ T-cells are destroyed in the course of the disease, leading to a similar number of cells containing integrated HIV-1 or HIV-2 genomes.
Typically, infection with HIV-1 is characterized by a gradual and irreversible depletion of CD4+ T-lymphocytes, leading to severe immune dysfunction and the development of AIDS within a median time of 10 years. However, in contrast to the aforementioned typical progression, virtually all HIV-2 and a small percentage  of HIV-1 infections (appropriately referred as “long-term nonprogressors” or “elite controllers”) remain healthy for several decades without any antiretroviral therapy, with undetectable plasma viral load and CD4+ cell counts above 500 cells/µL.
A longer asymptomatic phase and slower progression to AIDS are indeed hallmarks of the natural course of HIV-2 infection [1-3]. A clear demonstration of both features was provided by a prospective study conducted with untreated Senegalese sex workers, where 67% of HIV-1-infected women remain AIDS-free 5 years after seroconversion, in contrast with 100% for HIV-2-infected women . The rate of developing CD4+ lymphocyte counts bellow 400 cells/µl was also reduced in HIV-2 participants . Thus, as a rule, HIV-2-infection has no effect on survival in adults .
The mechanisms responsible for this less pathogenic course of HIV-2 infection are still poorly understood but surely result from a combination of distinct factors involving the virus, the infected cell and the equilibrium established between viral replication and host immunologic response. This equilibrium is clearly much well preserved in HIV-2 than in HIV-1 infection and it is paradoxical that the study of HIV-2 interaction with host cells remains poorly explored and sometimes neglected. Interestingly, a recent report indicates that a pre-existing infection by HIV-2 appears to inhibit the rate of HIV-1 disease progression , together with higher CD4+ T-cell counts and lower viral diversity of HIV-1. This apparent protective effect of HIV-2 may be explained by several viral and immunological mechanisms, namely the higher immunosupression of surface glycoprotein of HIV-2 compared to HIV-1 counterpart , or the ability of HIV-2 Nef protein to promote the downmodulation of TCR-CD3 from the surface of CD4+ T-cells  and thus the impairment of immunological synapse, established between these lymphocytes and antigen presenting cells (i.e. dendritic cells and macrophages). Both mechanisms have direct impact on immune activation and may help explain the better outcome of HIV-2 infection alone or after superinfection with HIV-1.
5.1. HIV-2 entry into target cells — Early events
HIV replication cycle begins by a specific interaction between viral envelope glycoproteins and cellular receptors allowing the binding of virion to target cell. Further sequential interactions eventually lead to viral envelope and cell membrane fusion. The cellular receptors involved in these early events are the CD4 molecule [79, 80] and a member of seven-transmembrane, G-protein-coupled, receptors' family (GPCRs), referred as coreceptor. According to the proposed model, the specific binding of SU envelope glycoprotein to CD4 induces structural changes in this glycoprotein that expose, create or stabilize the coreceptor-binding regions, enabling the SU to engage the coreceptor molecule. This second binding event causes further conformational changes in SU that allows the disclosure of an amino-terminal hydrophobic region (fusion peptide) of the TM envelope glycoprotein subunit. The insertion of the fusion peptide in the cell surface leads to the fusion of viral envelope with the cell membrane and the release of viral nucleocapside into the cell cytoplasm (reviewed in [81, 82]). This fusion process as long been assumed to occur at the cell surface through a direct fusion mechanism independent of the pH . However, more recent data describe HIV-1 entry and fusion occurs following endocytosis [84, 85].
After the initial identification of CXCR4 and CCR5 in 1996 [86, 87], several other GPCRs have been described as being able to act as coreceptors for HIV-1, HIV-2 and SIV: CCR1, CCR2b, CCR3, CCR4, CCR5, CCR8, CCR9, CCR10, CXCR2, CXCR4, CXCR5, CXCR6, CX3CR1, XCR1, FPRL1, GPR1, GPR15, APJ, ChemR23, CXCR7/ RDC1, D6, BLTR and US28 [88-92]. Despite this extensive array of potential HIV entry coreceptors, only CCR5 and CXCR4 have been considered important for HIV-1 infection
Genetic studies of HIV-1 variants present soon after sexual transmission have shown that only R5, and occasionally dual tropic R5X4, are transmitted regardless the diversity of viral population present in initial inoculum. During chronic infection HIV genetic diversity increases due to viral replication based on an error-prone reverse transcriptase. The resulting viral population (or
The analysis by single-genome amplification, together with full-length cloning of transmitted/founder variants, has provided remarkable data on HIV transmission and viral evolution during acute infection. Based on this data, the selection of transmitted/founder viruses encompasses three main signatures: usage of CCR5, high replication rate in CD4+ T-lymphocytes and lack of macrophage tropism (reviewed in ). The deficient replication in monocyte-derived macrophages observed in HIV-1 transmitted viruses, although requiring confirmation using tissue macrophages, is consistent with data obtained in nonhuman primates infected with SIV, indicating that CD4+ T-lymphocytes are the predominant cellular substrate for viral replication soon after transmission.
However, a recent and unprecedented observation, regarding HIV coreceptor usage and transmission, revealed that a transmitted/founder HIV-1 was unable to efficiently use either CCR5 or CXCR4 to infect CD4+ cell lines or peripheral blood mononuclear cells . Alternate GPCRs (GPR15, APJ, and FPRL-1) were efficiently used, further emphasizing the notion that “rare” coreceptors could be used
In HIV-2 no data exists regarding transmitted/founder viruses, or the characteristics or the viral evolution during primary infection. The mechanisms described for HIV-1 and SIV should also be present in HIV-2 infection. However, the identification of HIV-2 isolates unable to infect target cells using the CCR5 or CXCR4 coreceptors [96, 109] obtained from individuals at asymptomatic stage of infection and immunologically competent , raises the possibility that, at least in some patients, CCR5 usage is acquired
5.2. Molecular determinants of coreceptor usage
Identification of the biochemical processes required for HIV fusion and the engagement of chemokine receptors as critical step for HIV entry, has also unveiled several important aspects on envelope glycoproteins structure crucial to the fusion process. HIV-1 and HIV-2 SU glycoprotein contain five conserved regions (C1 to C5), separated by an equal number of variable regions (V1 to V5). The variable regions are limited by cysteine residues forming flexible loops on the outer domain of SU glycoprotein [110-112]. HIV coreceptor usage seems to be largely determined by variable regions of the SU subunit. In HIV-1, the most studied model, the third variable (V3) region has been referred as the major determinant of coreceptor engagement [113-117]. Higher positive net charge (above +5) in V3 region of HIV-1 has been associated with CXCR4 usage (or usage of both CXCR4 and CCR5) [118, 119]. Structural models of SU bound to CD4 and chemokine receptor have provided further information about the functional roles played by several regions of SU, revealing that the V1V2 region is also involved in coreceptor binding, by a direct cooperation with the V3 region [120-124].
In HIV-2, structural and functional studies of the envelope glycoproteins regions are much more scarce and in some aspects contradictory. The genetic characterization of HIV-2 SU has revealed a limited variability, probably as a result of the lower replication rate within the infected individual. Noteworthy, in contrast to HIV-1, the V3 region of HIV-2 SU glycoprotein appears to be highly conserved. Conversely, the V1V2 region is much more prone to genetic variation , suggesting that either this region is more exposed and under a stronger selective pressure, or that the lack of V3 loop variation is related to some functional constraints that impairs its evolution. Accordingly, the role of HIV-2 V3 region as a target for neutralizing antibodies has been controversial [126-132].
Similar to neutralization data, molecular determinants of coreceptor usage by HIV-2 is also controversial. Some studies had claimed an association between V3 loop sequence and CCR5 or CXCR4 usage [133-137], while others had found no genetic signature underlying coreceptors usage [138-140]. Particularly, the C-terminal region of the V3 loop, a global net charge above +6 and the presence of mutations in amino acids 18 and 19, appear to dictate the ability to use CXCR4 alone or in addition to CCR5 [134, 137]. However, those studies have some limitations due to the low number of X4 or R5X4 strains and because they restricted the coreceptors usage to the dichotomy R5 vs. X4, without considering the concomitant or alternative use of other coreceptors. We have shown in the molecular characterization of the
5.3. Evolution of coreceptor usage during HIV-2 chronic infection
Earlier studies addressing the correlation between HIV infection stages (i.e. acute/primary infection, asymptomatic stage and AIDS) and
Identification of the biochemical processes required for HIV fusion and the engagement of chemokine receptors, clarified the determinants of HIV tropism. Consistent with the proposed model, HIV cell tropism is largely determined by the expression patterns of the appropriate coreceptor molecule at the target-cell membrane. T-tropic viruses (in general with rapid/high and SI phenotype) required the presence of CXCR4 coreceptor (X4 strains) while M-tropic (associated generally with slow/low and NSI phenotype) use CCR5 as coreceptor (R5 strains). The evolution that was observed in viral phenotype has now an explanation based on the coreceptors used: isolates obtained during asymptomatic stage are R5 (formerly NSI, M-tropic and slow/low) while in later stages of infection, coincident with immunodeficiency and opportunistic infections, the predominant variants are X4 (formerly SI, T-tropic and rapid/high). This shift from predominance of R5 variants to X4, during disease progression, occurs in about 40% of the patients and could be seen as an additional consequence of an already deteriorated immune response, which contributes to an accelerated depletion of T-lymphocytes and disease progression.
In HIV-2, the usage of cell receptors seems to be much more complex and the correlation between disease stage and receptors usage is apparently less clear-cut than in HIV-1. The key notions about cell receptors engagement by HIV-2 are: (i) non-usage of CCR5 or CXCR4 as coreceptors; (ii) a broader coreceptor usage compared to HIV-1; and (iii) the CD4-independent infection of target cells.
5.3.1. Non-usage of CCR5 or CXCR4 as coreceptors
Although CCR5 or CXCR4 usage seems to be an absolute requirement for HIV to fuse its envelope with target-cell membrane, we and others have identified HIV-2 variants that
The main inference made from studies addressing coreceptors usage by HIV is that the acquisition of CCR5 usage is crucial for HIV pathogenesis. And why CCR5 usage is so important and provides a clear selective advantage
In addition, the persistence of R5 viruses throughout the asymptomatic stage and in some cases even in individuals with clinical symptoms, suggests that they may escape immune surveillance mechanisms (e.g. neutralization by specific antibodies) or that they could infect long-lived cell reservoirs, such as macrophages and dendritic cells, thus providing long-lasting R5 viruses production.
Interestingly, the described CCR5/CXCR4-independent HIV-2 variants were obtained during asymptomatic stage of infection [96, 109]. As referred, HIV-1 and HIV-2 infections are strikingly different during this period: a longer asymptomatic period with higher CD4+ T-cell counts and undetectable viremia is observed in HIV-2. The host and viral factors that contributes for this high level of control remain poorly understood, but we hypothesized that one of the viral factors that could be involved is the existence of a less fitted viral population, during a variable period of the asymptomatic stage. This population has lower replicative capacity and, at least in some cases, they do not efficiently use CCR5 and/or CXCR4 coreceptors.
5.3.2. Broad coreceptor usage
A hallmark of earlier studies addressing the coreceptors usage by HIV-2 primary isolates was that HIV-2 entry into target cells could be mediated by an array of different GPCRs
The ability to use a larger set of coreceptors should constitute an advantage for HIV-2, since it contributes to a potentially broader cell tropism, with the inherent ability to infect different cell types in different compartments [98, 135, 148]. Yet, as referred in R5-to-X4 evolution (see above) this could lead to the infection of non-activated cells, and thus to abortive cycles. Moreover, the engagement of alternative GPCRs, although being sufficient to mediate HIV-2 entry, could be inadequate to trigger appropriate intracellular signaling required for productive infection. Several studies have shown a direct correlation between the capacity of envelope glycoproteins to elicit appropriate signaling and the ability to perform a productive infection in several cell types (reviewed in ). Such signalling events affect multiple intracellular pathways (in a process mimicking chemokine signaling through binding to their receptors) and include: actin depolymerization, cytoskeleton rearrangement, migration of cells and activation of kinases and transcription factors associated with cell activation (Table 2). Although the relevance of coreceptor signaling in HIV pathogenesis has not been clearly defined, it seems that HIV takes advantage of the chemokine signaling network to create an intracellular environment suitable to accomplish a productive infection .
Another factor that may account for the apparent paradox of HIV-2 broad coreceptor usage and low virus production
Recently we have studied the contribution of CCR8 as an effective coreceptor for HIV-1 and HIV-2 primary isolates . A major and interesting finding arise from this report: a minor coreceptor such as CCR8 was used much more frequently by HIV-1 than by HIV-2 primary isolates, regardless the clinical stage, the plasma viral load or the CD4+ T-cell counts of patients. The rationale for revisiting CCR8 as coreceptor was based on our earlier findings, revealing the existence of HIV-2 unable to use CCR5 or CXCR4 as coreceptors to infect primary CD4+ lymphocytes or CD4-expressing cell lines [96, 125]. CCR8, formerly known as TER1, ChemR1 and CKR-L1, is the receptor for the chemokine CCL1/I-309 [156, 157]. It is expressed in a wide range of cells; some of them are primary targets for HIV infection
|Activation of phospholipase C-γ||Transcriptional activation.|
Cell migration (chemotaxis)
|Activation of phospholipase C-γ||Transcriptional activation.|
|Activation of lipid kinase PI3K||Transcriptional activation.|
|Activation of lipid kinase PI3K||Cell adhesion.|
|Activation of guanine nucleotide exchange factors specific for Rho family GTPases||Modulation of cytoskeleton: actin rearrangement; myosin light-chain phosphorilation and microtubule rearrangement||Activation of guanine nucleotide exchange factors specific for Rho family GTPases||Modulation of cytoskeleton: actin rearrangement|
It is widely recognized that during later stages of HIV-1 infection, a significant proportion of viral variants that constitute the
However, in HIV-2 the correlation between disease progression and coreceptor usage was not consistently observed and a clear pattern of R5-to-X4 evolution, along with disease progression, has been difficult to establish. Even so, R5 viruses are mainly observed in asymptomatic or early symptomatic patients, and strains showing a restricted CXCR4 usage are only observed in late symptomatic individuals [96, 166-168]. In a study comparing CCR5, CXCR4 and CCR8 usage by HIV-1 and HIV-2, an interesting observation was withdrawn pointing to a more frequent usage of CXCR4 by HIV-1 than by HIV-2 primary isolates . Conversely, CCR5 use was significantly more common in HIV-2 isolates than in HIV-1. According to the described enhancement of T-cell depletion by X4 variants, the predominance of a non-X4 viral population, mostly observed in HIV-2 cohort, may contribute to better preserve CD4+ lymphocyte repertoire and immune system functionality and help explain the slower disease progression, generally observed in HIV-2 infected patients compared with HIV-1.
5.3.3. CD4-independent infection
Despite the potential advantage of broader cell tropism associated with lower CD4 dependency, CD4-independent HIV-1 variants, although readily derived
The ability to entry cells through direct interaction with the coreceptor molecule, bypassing the requirement of prior CD4 engagement, may enable viruses to infect a broader range of cells CD4 negative/coreceptor positive, or cells where CD4 expression is lower and thus limiting. This notion is consistent with studies showing that neutopathogenic HIV-1 variants show reduced CD4 dependence and the ability to infect CD4-negative cells. Viruses with a CD4-independent phenotype could infect cells in different tissue compartments within an infected individual, besides haematopoietic CD4+ cells, such as the brain, testes, lymphoid tissue, kidneys or lungs, further suggesting that CD4-independence could constitute an advantage and might play an important role in some particular tissue settings [148, 173-175, 180, 181]. Interestingly, the CD4-independent phenotype not only appears to be a potential advantage but it can be easily acquired as a consequence of very few amino acids changes in viral envelope glycoproteins [169-172, 182, 183]. Therefore, a central question may arise: why CD4-independent HIV-1 variants are so rare, or why the occurrence of such variants in HIV-2 is not associated with an increased pathogenic outcome?
The infrequent detection of CD4-independent HIV-1 isolates should reflect the selective advantage of CD4 interaction prior to coreceptor engagement. One of the reasons could be the high affinity of CD4-SU envelope glycoprotein binding, stabilizing virion attachment to target cell. However, many other surface molecules have been described to interact with HIV-1 (reviewed in ) and thus capable of mediate a stabilizing interaction with virions. Another possible explanation for CD4 dependency could be the shielding of coreceptor binding sites from neutralizing antibodies [170, 182, 185-189]. Considering the proposed mechanism for HIV fusion, the CD4-independent infection imposes that the coreceptor-binding site is already formed or exposed allowing the virus to circumvent the need for prior CD4 interaction. The conformation of envelope glycoproteins allowing the direct interaction with coreceptor (as well as the interaction with different coreceptors) might elicit neutralizing antibodies targeting these critical regions, favoring the host immunological control in HIV-2 infection. Consistent with this notion, sera from HIV-2 infected individuals have higher and broader neutralizing capacity compared to those of HIV-1 [126, 190].
Studies conducted with HIV-2 CD4-independent strains clearly demonstrated a less fitted interaction and a reduced replication rate
6. Concluding remarks
Two lentiviruses infect humans with different outcomes. HIV-1 and HIV-2, both a result of cross-species transmission, have similar genomic and structural characteristics, and yet they distinctively affect human host. While HIV-1 infection leads to severe immune dysfunction and the development of AIDS within a median time of 10 years, HIV-2 usually takes decades to accomplish that.
Through this chapter, I have provided several data that help to explain this different pathogenic potential of HIV-1 and HIV-2 (see Table 3 for a brief summary). I have focused on those viral characteristics that determines different virus-host interactions and outcomes:
Lower viral load in body fluids directly involved in HIV-2 transmission.
Avoidance of SAMHD1 degradation of viral cDNA during infection of dendritic cells, leading to sensing and stronger innate immune response by HIV-2.
Inability to use CCR5 or CXCR4 that severely affects viral fitness during asymptomatic phase of infection.
A less common acquisition of CXCR4 usage during the course of infection and the consequent maintenance of a predominant less cytopathic R5 population, which may help to better preserve CD4+ lymphocyte repertoire and immune system functionality in HIV-2 infected individuals.
Usage of alternate coreceptors that ultimately could lead to inappropriate cell signalling and/or infection of cell populations unable to fully support the HIV-2 replication cycle.
CD4-independent infection of target cells, providing the potential to infect cells in different compartments but also exposing critical regions of coreceptor binding site to host neutralizing immune response.
A more relaxed envelope glycoproteins structure that could modulate HIV-2 interaction with cellular receptors, helping explaining the exotic coreceptor usage and CD4-independency but also a less fitted interaction with those receptors and thus to an inappropriate cell signalling.
Much more data is needed to fully comprehend the way human host is able to cope with HIV-2 but not with HIV-1 infection. Further studies addressing HIV-2-cell interactions are warranted as they could reveal undisclosed mechanisms and pathways that may help to clarify the underlying causes for the different pathogenic potential observed between HIV-2 and HIV-1, en route to assist in HIV vaccine development and new therapeutic strategies.
|Conflicting results. Susceptible to antiviral activity of cellular factor SAMHD1||Conflicting results. Resistant to antiviral activity of cellular factor SAMHD1 (by Vpx protein)|
|Less efficiently triggered due to several factors, namely to the restricted infection of dendritic cells||More robust than in HIV-1 namely because infection of dendritic cells could trigger IFN-I mediated response|
|Generally described has only being able to efficiently use CCR5 and CXCR4||Generally described has being able to efficiently use other coreceptors besides CCR5 and CXCR4|
|Rarely described||Several primary isolates reported|
|Mostly the V3 region of SU envelope glycoprotein||Conflicting data. Probably V1/V2 region and, to a lesser extend, V3 region|
|Reduced||Higher and broader|
The author wish to acknowledge bioMérieux Portugal for the financial support in the article processing charge of this chapter.