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Identifying HIV-1 dual infections
Retrovirologyvolume 4, Article number: 67 (2007)
Transmission of human immunodeficiency virus (HIV) is no exception to the phenomenon that a second, productive infection with another strain of the same virus is feasible. Experiments with RNA viruses have suggested that both coinfections (simultaneous infection with two strains of a virus) and superinfections (second infection after a specific immune response to the first infecting strain has developed) can result in increased fitness of the viral population. Concerns about dual infections with HIV are increasing. First, the frequent detection of superinfections seems to indicate that it will be difficult to develop a prophylactic vaccine. Second, HIV-1 superinfections have been associated with accelerated disease progression, although this is not true for all persons. In fact, superinfections have even been detected in persons controlling their HIV infections without antiretroviral therapy. Third, dual infections can give rise to recombinant viruses, which are increasingly found in the HIV-1 epidemic. Recombinants could have increased fitness over the parental strains, as in vitro models suggest, and could exhibit increased pathogenicity. Multiple drug resistant (MDR) strains could recombine to produce a pan-resistant, transmittable virus.
We will describe in this review what is presently known about super- and re-infection among ambient viral infections, as well as the first cases of HIV-1 superinfection, including HIV-1 triple infections. The clinical implications, the impact of the immune system, and the effect of anti-retroviral therapy will be covered, as will as the timing of HIV superinfection. The methods used to detect HIV-1 dual infections will be discussed in detail. To increase the likelihood of detecting a dual HIV-1 infection, pre-selection of patients can be done by serotyping, heteroduplex mobility assays (HMA), counting the degenerate base codes in the HIV-1 genotyping sequence, or surveying unexpected increases in the viral load during follow-up. The actual demonstration of dual infections involves a great deal of additional research to completely characterize the patient's viral quasispecies. The identification of a source partner would of course confirm the authenticity of the second infection.
Some confusion surrounds the earliest nomenclature of viral dual, co-, super- and re-infections, especially with regard to HIV-1. By now, it has been more or less agreed upon that viral co-infection is a double infection occurring before antibodies are detectable in the blood (before seroconversion), and that a double infection is called superinfection when the second infection takes place after seroconversion. Double infections of unknown timing are referred to as dual infections, while the term reinfection is reserved for a new infection once an initial infection has been cleared. Due to the persistence of HIV-1 infection, reinfections as defined above do not occur as the first virus is never cleared. This review will focus on double HIV-1 infections with special emphasis on superinfections, as they have attracted the most attention from an immunologic and clinical point of view.
Super- and reinfection among different virus families
Contrary to popular belief that primary infection of an organism with a virus prevents the entry of a closely related virus, this is often not the case. In fact, the entry by the virus into the host is not prevented, but viral growth and the severity of clinical symptoms is reduced. The adaptive immune response is now primed for the incoming pathogen, commonly averting its spread and limiting subsequent damage. Thus, the strength of the response determines the precise outcome of the second infection. This principle applies both to viruses that are cleared and those that persist in the body such as retroviruses and herpesviruses. Superinfections with herpesviruses have been documented for herpes simplex virus type 1 , herpes simplex virus type 2 , Epstein-Barr virus , varicella-zoster virus (reviewed in ), cytomegalovirus [5–7] and human herpesvirus 8 . Superinfections with hepatitis B virus (HBV) have also been reported, e.g. in 0.8% of chronic HBV carriers and in 1.9% of patients with acute exacerbations in Taiwan . For hepatitis C virus, a virus that can be cleared, both co-, super- and reinfections have been documented (reviewed in ). Coinfection with retroviruses HTLV-I (human T-cell lymphotropic virus type I) and HTLV-II (human T-cell lymphotropic virus type II) has been reported in a Brazilian AIDS patient , but very little has been published about co- or superinfection with a same HTLV type. Dual infection with both HIV-1 and HIV-2 has already been described early in the HIV epidemic [12–14], and this finding is common in West Africa with a prevalence of 24% in HIV-infected female sex workers from Ivory Coast  to 40.4% in seropositive individuals from Senegal . Dual infections with different strains of HIV-2 have not been described so far. In contrast, dual infections with distinct HIV-1 strains are prevalent, and form the focus of this review.
Even for viruses that persist, many uninfected cells in the host are available for infection by a second viral strain. At the cellular level, superinfection of a single cell can be prevented by a phenomenon called "superinfection resistance" (SIR). Hence, the first infecting virus actively prevents re-infection of the same cell after a short time window, usually in the range of 4–24 hrs (reviewed in ). The molecular mechanism of SIR has been revealed in some cases. Expression of env and gag genes in a cell interferes with subsequent viral entry of the cell and with reverse transcription of simple retroviruses such as murine leukaemia virus. The env protein is most likely involved in blocking subsequent access to receptors. More intricate systems involving accessory proteins are implicated in SIR in complex retroviruses such as feline leukaemia virus and HIV. Many retroviruses down-regulate the viral receptor on the cell surface, but this is probably not the main mechanism of SIR for HIV.
HIV-1 superinfection: the first cases
The possibility of HIV-1 superinfection was not taken seriously for a long time, probably because the chances of acquiring a single HIV-1 infection were estimated to be low, not only for the general population but for most risk groups as well. Furthermore, it was assumed that an initial HIV-1 infection could protect against a secondary infection, as an idealized vaccine might do. Subsequently, the wealth of recombinant viruses that were detected worldwide provided the first indications that HIV-1 dual infections occur frequently, since recombinant viruses can only arise in doubly infected individuals. These dual infections were suspected to represent HIV-1 coinfections (i.e. both events occurring before HIV-1 adaptive immunity is established). However, as early as 1987, it was shown that superinfection of chimpanzees with HIV-1 by intravenous injection of a distinct strain could be achieved 6–15 months after the initial infection. Nonetheless, it was not until 2002 that the first reports of HIV-1 superinfection in humans appeared [18–20].
In three separate cases, patients were superinfected with distinct subtypes of HIV-1. In a report by Ramos et al., two intravenous drug users were superinfected with CRF01_AE (CRF = Circulating Recombinant Form) and subtype B after initial infection with subtype B and CRF01_AE, respectively . In the report by Jost et al. a male having sex with men was superinfected with subtype B after a first infection with CRF01_AE . In the paper by Altfeld et al., both the first and second virus were subtype B strains . Thus up to 2005, 17 case reports of HIV-1 superinfection have been published (reviewed in [21, 22]), and a few more cases have appeared in print since 2005 [23–29]. HIV-1 superinfection cases have also been identified in larger population studies [30–35].
HIV-1 triple infections
To date, four patients have been described who were infected with three HIV-1 strains. Two patients were African women: a Cameroonian woman infected with a group O virus, a subtype D virus, and a subtype A/G recombinant virus [36, 37]; and a patient from Tanzania infected with two subtype A strains and a subtype C virus or recombinants thereof . In these women, however, it could not be established whether the triple infections were the result of coinfections or superinfections, or both. An intravenous drug user from Spain ultimately was found to carry three HIV-1 subtype B strains following a dual superinfection twelve years after primo infection . Repeated superinfection was also documented for a homosexual man from the Netherlands, who was infected by a subtype B strain approximately one year after initial infection with another subtype B strain, and then with CRF01_AE one year after the second infection [24, 39].
From this small number of reports, it can be concluded that infection with more than two HIV-1 strains and especially serial superinfection are rare events, which are not impossible in high risk patients. Recombinant HIV-1 strains were detected in all the above four patients, but in only one patient were viral genomes detected that mix fragments from all three strains . Nevertheless, these case reports suggest that multiply infected patients could contribute to the HIV-1 viral diversity through the generation of complex recombinant viruses.
HIV-1 superinfections and anti-retroviral therapy
Antiretroviral therapy is now commonly used in developed countries and increasingly used in the developing world. It is generally assumed, but not well established, that the incidence of HIV-1 superinfection in individuals under therapy is low, and case reports in those settings are indeed rare . A productive infection will be difficult to establish as the incoming virus will immediately experience the pressure of antiretroviral drugs. No superinfections were detected during follow-up of 14 HIV-infected couples who practised high-risk behaviour, while being treated with antiretroviral drugs . Despite therapy, the plasma viral load was always measurable in these patients. To facilitate detection of superinfection in this study, couples were chosen in which partners carried different HIV strains.
Some superinfections have been reported to occur during treatment interruptions [19, 20] This is explained possibly because antiviral immune responses decrease during therapy. Eight superinfections have been reported which involve drug-resistant HIV-1 strains, either as the first [23, 30, 41] or the second [26, 30] infecting virus. In some cases both viruses were found to carry (multiple) drug-resistance mutations [27, 42]. One of the patients twice received a multidrug resistant (MDR) strain while not on therapy. When assessed, the replicative capacity of the drug-resistant variants was often [26, 41, 42], but not always  reduced compared to that of wild type, parental HIV-1 strains. Thus, superinfections can sometimes result in the introduction and outgrowth of a virus strain with greater fitness.
Infection with a drug-resistant virus strain severely hinders antiviral treatment options, and this is ultimately the outcome in patients infected with two MDR strains. In these cases, recombination could lead to a pan-resistant virus that cannot be treated with existing antiretroviral drugs. That such a scenario is feasible is illustrated by a case from the United States, in which a patient harbouring two MDR strains transmitted a highly drug-resistant recombinant virus .
Viral sex: are HIV-1 recombinants taking over?
Recombination between HIV-1 genomes is an important viral evolutionary strategy (for reviews, see [43, 44]), as it substantially enlarges the diversity of viral quasispecies within a patient [39, 45]. The two copies of the RNA genome incorporated in the virus particle make HIV-1 a "diploid" virus, whereby recombinant offspring's can be produced during replication, in a manner resembling sexual reproduction. Recombinant viruses found in an epidemic can either be intra-patient , intra-subtype , or inter-subtype. In the latter two settings, infection of an initial patient with two different virus strains is a prerequisite for the formation of offspring recombinants. Inter-subtype HIV-1 recombinants, which are the most easy to identify, have been detected since the early days of the epidemic (see e.g. ), suggesting that multiply infected patients were present early on. For some of the strains initially classified as recombinant viruses, there has been doubt raised about their recombinant status , but it is obvious that many recombinant strains are circulating worldwide.
More than 20% of the current HIV-1 infections in Africa are estimated to represent recombinant strains . Mathematical models indicate that a limited superinfection incidence can nevertheless lead to a high prevalence of recombinant viruses if there is a small core group of highly sexually active people and a large group of low-risk individuals [49, 50]. Indeed, a higher frequency of both dual infections and recombinant strains was found in a high-risk group of bar workers in Tanzania compared to a normal-risk population of antenatal care attendees and blood donors . As transmissions from these high-risk populations are likely to be frequent, it can be anticipated that HIV-1 recombinant strains will continue to expand in the HIV-1 epidemic.
This primitive sexual reproduction system might be an effective strategy for retroviruses to adapt to evolutionary constraints posed by the invasion into novel host species in the face of an error-prone viral reverse transcriptase enzyme. For vesicular stomatitis virus (VSV), an RNA virus, superinfection promotes faster adaptation than single infections [52, 53]. A higher fitness of VSV populations was reached after coinfection than after superinfection, but both conditions created viruses with a higher relative fitness than those arising from single infections . The authors explain this phenomenon through maximized competition for host resources between diverse populations by coinfection, whereby the fastest growing genotype from the whole genetic pool emerges, and through density-dependent selection by superinfection. Ignoring immune pressure, virus dynamics are affected in this latter model by at least three factors: the rate of exponential growth of the initial virus population, the initial decline of the population size for the secondary virus, and the finite duration of the infection passages. However, the strength of these factors reduces as the time interval between infections decreases, and adaptation is thus maximal if the time interval is zero, which equals a coinfection. Thus, in the superinfection model, the second virus swarm might contain a better competitor than any genotype present in the resident population, but the success rate of the second infecting virus is strongly context-dependent.
Superinfection and the immune system
It is not clear whether specific host factors play a role in a productive superinfection. It has been assumed that an HIV-1 coinfection, that is a second infection before anti-HIV antibodies are detectable, can always occur, unlike a superinfection. It is likely that the adaptive immune response plays a major role in preventing a superinfection from becoming productive. It has been speculated that the lack of heterologous neutralizing antibodies predisposes the host for superinfection, as three superinfected patients showed less cross-protective and neutralizing antibody response to both autologous and heterologous HIV-1 than non-superinfected controls . The authors speculated that two of their control patients with low neutralizing antibody titers should be equally susceptible to superinfection, but were less exposed. Lack of cross-neutralizing antibodies was also observed in two superinfection cases in injecting drug users from Thailand .
By contrast, CD8+ T-cells seem to play a less important role in protection against superinfection. A patient with strong and broadly reactive CD8+ T-cell responses that inhibit HIV-1 replication was found to be superinfected with another subtype B strain several years after the initial infection . In this patient, neutralizing antibody responses to the autologous virus were weak before superinfection, as observed in other studies [18, 54]; and they were not cross-reactive against the second virus. Yet, neutralizing antibody responses were measured during a period of antiretroviral treatment interruption when antiviral immunity can be expected to be low; although the CD8+ T-cell responses were powerful during that same period . A later study also described a patient with an initially effective CD8+ T-cell response that successfully controlled HIV-1 replication without antiviral treatment before he became superinfected with a second subtype B strain . In horses infected with equine infectious anaemia virus (EIAV, a lentivirus infecting equines), the situation seems to be the reverse. EIAV carrier horses can resist challenge with a heterologous strain in the absence of detectable cross-neutralizing antibody response to the heterologous virus . Some horses immunized with an inactivated virus vaccine also resisted homologous strain challenge without detectable levels of neutralizing antibodies, but they did show virus-specific cell-mediated immune responses .
Thus, from the limited studies on adaptive immunity, it can be cautiously concluded that neutralizing antibody responses play a more significant role in preventing HIV-1 superinfection than CTL-responses.
Clinical implications of HIV-1 dual infections
The first reports on HIV dual infections suggested an association of such findings with accelerated disease progression, particularly with clinical parameters such as a rise in the plasma viral load and a decline of the CD4+ T-cell numbers [19, 57, 58]. Alternatively, dual infections with fast disease progression may simply have been spotted earlier. In a doubly superinfected patient, the first superinfection was not associated with disease progression (as implied by stable CD4+ T cell counts above 500 cells/ml), while the second superinfection resulted in a permanent increase in the plasma viral load and a significant reduction in CD4+ T cells . In another longitudinal study, HIV-1 superinfection was associated with rapid CD4+ T cell decline and an increased plasma viral load, necessitating the start of HAART four months later; however, in a second patient there was no decline of CD4+ T cells nor persistently increased viral load after HIV-1 superinfection ( and unpublished data). That some individuals are more susceptible to superinfection because they somehow lack factors to contain HIV-1 infection was hypothesized in a patient with rapid progression to AIDS . This patient was superinfected with a dual-tropic (both CCR5 and CXCR4-using) HIV-1 strain 0.8–1.3 years after seroconversion that rapidly became the predominant virus strain . Retrospectively, it was shown that the rapid CD4+ cell decline experienced by this patient preceded his superinfection. This suggests that fast disease progression was not completely due to a second infection with a more virulent virus, and that the already failing immune system facilitated a new HIV-1 infection. A schematic representation of HIV-1 superinfection relative to the different stages of the infection and the plasma viral load is shown in Fig. 1.
In a cohort study of African women infected with subtype C strains, dual infection was associated with an elevated viral setpoint . Remarkably, two studies on HIV-1 controllers (also known as long-term non-progressors) indicated that HIV-1 dual infections are present in this patient group, but without obvious disease progression [35, 61]. In one of these patients, a superinfection without any clinical deterioration occurred nine years after primo-infection, which had shown excellent immune control of the first virus .
Taken together, these studies suggest that HIV-1 dual infections are frequently, but not always, associated with accelerated disease progression. Due to the lack of long-term systematic investigations in a cohort setting, it is currently unclear whether HIV-1 co- and superinfections have different effects on disease development.
Detection of dual infections
The detection and verification of HIV dual infections require extensive laboratory analyses, and it is vital that the appropriate blood samples are available. Dual infections can easily be missed, because the second infection can be transient with a very low level of virus replication . There can be severe fluctuations in the relative amounts of the two viruses in subsequent plasma samples , which is a problem if only a single sample is analysed. Recombination can happen and the recombinant virus can outgrow parental strains, which would thus be missed [62, 63]. PCR primers can be too selective, such that they do not recognize a second HIV-1 strain. It is, therefore, highly desirable that serial patient samples are available, especially from early moments, to increase the likelihood of detecting a dual infection. Very early in coinfections, we sometimes see the fast outgrowth of a single strain, with the second virus then being absent from all subsequent samples (unpublished results). One difficulty with analysis is that the second virus should not be too closely related to the first; otherwise the former will not appear as a distinct strain in a phylogenetic analysis, making it impossible to distinguish between virus evolution and superinfection. This phenomenon severely restricts the identification of novel transmissions from the same donor.
An assumed dual infection should be verified by sequencing the patient's viral quasi-species. Thus, detecting dual infections involves numerous analyses, and selecting the right group of higher-risk patients might be essential when planning large studies. Some options are available to identify patients with potential dual infections (Table 1). Serotyping based upon enzyme-linked immunosorbent assay (ELISA) which discern between HIV-1 group M (subtype B or non-B), HIV-1 group O, HIV-1 group N, and HIV-2 infections have been used to identify dual group M and O infections [36, 62, 64–67] and an HIV-1/HIV-2 dual infection . Nonetheless, serotyping is not a means to detect HIV intra-subtype dual infections, as this method lacks discriminatory power. Caution is also warranted when using inter-subtype serotyping assays. Although specificity is generally high, discordant results have been observed , and not all dually reactive specimens are due to dual infection . Heteroduplex mobility assay (HMA) analysis is a relatively fast and sensitive method to screen PCR amplification products for the presence of divergent sequences [34, 60, 71, 72]. It is again important that early control samples are available. After initial selection by serotyping or HMA, PCR amplification, cloning and sequencing are necessary to confirm dual HIV infection.
We recently described an easy method to detect dual infections that is based on the routine HIV-1 genotyping method, a population sequencing method . Protease/reverse transcriptase (prot/RT) sequencing is routinely performed in the Western world to assess drug resistance mutations. If the sequences are derived from a heterogeneous population of viral DNA fragments, heterogeneous positions will show up in the sequencing electropherogram as a double or triple peak, and will be assigned a degenerate base code. Degenerate base codes are codes for incompletely specified bases in nucleic acid sequences as recommended by the Union of Pure and Applied Chemistry and the International Union of Biochemistry and Molecular Biology (IUPAC-IUBMB) that signify double (R = A or G; Y = C or T; K = G or T; M = A or C; S = G or C; W = A or T), triple (e.g. B = C, G, or T; D = A, C, or T; H = A, C, or T; V = A, C, or G) or quadruple (N = A, C, T, or G) bases in a DNA sequence . From the polymerase gene sequences that yielded a high score of degenerate base codes, we measured a high percentage of dual infections. If the number of degenerate base codes in the reverse transcriptase (RT) fragment of the polymerase sequence is 34 or more, 43% of patients were confirmed to be dually infected . This percentage rose to 73% when degenerate base codes in RT increased to 45 or more. In the other patients, heterogeneity could be ascribed to massive viral evolution. Figure 2 shows the variation of degenerate base counts in RT over time in a patient twice superinfected with HIV-1. From this example it is apparent that a superinfection can easily be missed when testing only a single sample, as during the acute phase of the second superinfection when most of the viral RNA originated from the incoming virus, and thus no heterogeneity was detected in the RT sequence.
To detect HIV-1 superinfections, one should also be aware of sudden, unexpected rises in the viral load of at least 10-fold [31, 59]. HIV-1 superinfection is frequently accompanied by a steep rise in the plasma viral load. The first HIV-1 superinfections in patients were identified mainly because of such unexplained viral load increases [19, 20, 22, 24]. In 5 chronically infected intravenous drug users with an unexpected rise in the viraemia, 2 experienced a superinfection with a different HIV-1 subtype . A study of untreated patients experiencing a sudden rise in the plasma viral load indicated a superinfection in 2 out of 14 patients .
The only method currently available to detect some dual infections without further sequence analysis is the Multi-region Hybridization Assay (MHA), which is based on real-time PCR amplification of multiple genomic fragments, using and subtype-specific probes for detection. These MHA's can only be used in areas were multiple subtypes prevail, such as in Africa  or Asia , and will obviously miss intrasubtype dual infections. The success rate of the different pre-selection methods as calculated from published studies is variable (Table 1). Overall, the number of degenerate bases in RT is the best predictor of an HIV-1 dual infection, followed by HMA analysis. Dual reactivity in serological assays (serotyping) is highly predictable of intergroup dual HIV-1 infections, but intragroup predictability is limited . Using no pre-selection method results in very low success rates, as dual infections are relatively uncommon in all cohorts examined.
No matter what method was used to pre-select a suspected HIV dual infection, actual confirmation requires a phylogenetic analysis of viral sequences. To construct such a phylogenetic tree, several methods are available (see e.g. ). The neighbour-joining (NJ) method and, more recently, Bayesian inference of phylogeny, an approach similar to maximum-likelihood, are often used in HIV evolution studies . Whatever the method used to construct the tree, it is important that some statistical significance is given to the branching of sequences. With the NJ method, this is commonly done by applying a bootstrapping algorithm to the tree. For Bayesian trees, posterior probabilities can be calculated. Bootstrap numbers of 80 or over and posterior probabilities of 0.8–1.0 are generally taken as positive evidence for the accuracy of a cluster of sequences.
We outlined earlier  a number of criteria for the positive identification of HIV-1 dual infection based upon sequence analysis that should be true with two distinct phylogenetic methods: 1. Sequences of a single patient should cluster independently, or 2. Sequences of a patient cluster together, but the bootstrap/posterior probability value connecting the branches should be low (values under 80/0.8 are normally considered insignificant). Divergent sequence groups from a patient that cluster together with high confidence levels should always be attributed to viral evolution and not to dual infection. For definite proof of HIV superinfection, some scientists consider it essential to couple the sequences from a suspected superinfection case to those of an identified source partner. This can also be done by phylogenetic analysis of viral sequences. However, in many cases, especially with anonymous sexual contacts, the source will not be easy to identify. Sometimes, an indication of transmission may be retrieved from sequence databases [27, 79–82].
Timing of HIV superinfection
Superinfections have been described after long-term chronic infection , but the most optimal period for a second infection seems restricted to a window period of less than 3 years after the initial infection (see also ). The first few months after primary infection appear therefore to be the most favourable for superinfection. Such a window was described for macaques infected with simian immunodeficiency virus or HIV-2, although in monkeys the time of susceptibility to a second infection appears to be even shorter; no more than a few weeks after the first infection [83–88]. This uneven distribution of susceptibility to HIV superinfection suggests that the immune system is an important player in the defence against superinfection. As the adaptive immune response is usually in place within a few weeks to months after initial infection, it can be reasoned that in some patients either an effective immune response takes longer to mature, or that the immune system is quickly deteriorating, allowing a superinfection, or that other factors play a decisive role. Cellular and viral kinetics are also important for the susceptibility to and the timing of HIV-1 superinfection.
From studies of macaques infected with SIV it became clear that a main target site of SIV infection is the gut-associated lymphoid tissue . At the acute stage, a massive infection and subsequent destruction of 60–80% of memory CD4+ T cells takes place in the mucosa and lymph nodes, with initially little effect upon the peripheral blood CD4+ T cell numbers, mainly because local memory CD4+ T cell numbers are low [89–91]. Subsequently, CD4+ T cells from other compartments travel to the mucosa to replenish the lost T cells, and peripheral blood CD4+ T cells slowly start to decline. These findings were confirmed in HIV-1 infected humans . Initiation of HAART early in HIV infection resulted in a near-complete restoration of intestinal CD4+ T cells, but this was not the case if HAART is started during chronic infection. So how can HIV-1 superinfection occur when its main target cells are largely gone, and unlikely to return? Several factors could play a role. In macaques, the relative virulence of the infecting strain was associated with the rapidity and degree of T cell depletion in the intestine . Infecting monkeys with the SIVmac239Δnef straindid not result in a significant depletion of intestinal CD4+ T cells . In humans, long-term nonprogressors were found to maintain normal CD4+ T cell numbers not only in peripheral blood, but also in the intestinal mucosa . This suggests that both viral and host factors determine the extent of initial memory CD4+ T cell depletion in the host, and thus the susceptibility to HIV-1 superinfection. Sufficient memory CD4+ T cells to support a second HIV-1 infection should thus remain in patients infected with a less virulent virus, in patients efficiently controlling their HIV-1 infection (long-term nonprogressors), and in individuals who have started HAART very early in infection. Besides, it is possible that the 20–40% of memory CD4+ T cells that are left uninfected in the mucosal tissues of the average patient is enough to support a second HIV-1 infection, especially if new CD4+ T cells are recruited to these tissues.
Are HIV-1 superinfections increasing?
A major risk factor to acquire a second HIV infection is risk exposure, which itself consists of two aspects: risky behaviour and HIV-1 prevalence. Decreasing risky behaviour and the absence of HIV infected individuals surrounding the patient will diminish the frequency of HIV superinfections. If the HIV infection rate is relatively high, such as in areas where the epidemic is well established, then HIV dual infection rate will be higher than in regions where HIV was introduced more recently. This is reflected in studies in sub-Saharan Africa where HIV is highly prevalent in most populations, with many people demonstrating high risk behaviour. A study published in 2004 on HIV-1 dual infection in a cohort of commercial sex workers in Burkina Faso found that 2 out of 147 women were dually infected . A similar study in South Africa, published in 2004, showed that within 3 months of infection, 19% (6 out of 31) of female sex workers were dually infected with distinct subtype C viruses . Among female bar workers in Kenya, who are less exposed than sex workers, three cases of HIV-1 superinfection were detected in 20 persons examined (15%), suggesting that HIV-1 superinfection occurs as commonly as primary infections . In a similar risk group of bar workers in Tanzania, 19% of dual HIV-1 infections were seen, compared with 9% in the normal risk population of antenatal care attendees and blood donors . These figures correlate well with the HIV-1 prevalence data from the countries involved . HIV prevalence is the lowest in Burkina Faso (4.2% among the adult population in 2004, of which 88% HIV-1 and 12% HIV-2), intermediate in Kenya (7.4% among adults in 2004) and Tanzania (6.4–11.9% in 2003), and highest in South Africa with an estimated prevalence of 17.8–24.3% among the adult population in 2003.
Apart from heterosexual contacts, HIV-1 can be transmitted in several other ways. Among intravenous drug users (IDUs), the virus can be injected directly into the blood stream by means of used needles, providing an easy opportunity for infection as no mucosal barriers need to be taken. One would expect that the likelihood of productive superinfection is high in this risk group. In one cohort study of IDUs in Switzerland, 3 coinfections were found among 58 seroconverters . At a later time point, 1 of 40 (2.5%) of these seroconverters superinfected. In a similar study in Thailand, no dual infection was seen among 126 seroconverting IDUs . During follow-up a year later, 2 of 80 (2.5%) IDUs had acquired an HIV-1 superinfection, a number that is very similar to that of the Swiss cohort. In contrast, none of 37 IDUs with high-risk behaviour was superinfected during the 1987–2000 period in the San Francisco Bay area . Similarly, no HIV-1 superinfections were detected in 9 Brazilian IDUs with continuing high-risk practices . These numbers indicate a similar rate of HIV-1 dual infections in IDU cohorts when compared to African heterosexual cohorts. The absence of superinfections in the latter two groups may be due to a low incidence or the availability of effective therapy measures, although use of HAART was infrequent in the Brazilian study. A mathematical analysis suggested that 9% of new infections among IDU in Thailand represent superinfections .
No systematic studies on the prevalence of HIV-1 dual infections in exclusively homosexual cohorts have been performed. It could be imagined that the frequency of dual infections will be different, as the transmission route for men having sex with men is dissimilar from heterosexual or IDUs, as is perhaps also the risk behaviour. Two large studies were performed on HIV-1 infected patients in Western Europe and the USA, with the majority being men having sex with men. A few larger studies have also been published to date. In 2003, the analysis of prot/RT sequences of 718 patients in San Francisco with at least two sampling moments and persistent viraemia during therapy showed that in none of these patients therapy failure was due to a HIV-1 superinfection . In this study, degenerate base codes in the prot/RT sequence, representing viral mixtures, were artificially assigned a distance value to calculate nucleotide distances between serial samples. A large nucleotide distance between samples was taken as evidence for an HIV-1 superinfection. In addition, phylogenetic trees were constructed whereby monophyletic clustering of sequences from a single patient supposedly indicated evolution from a common ancestor, whereas paraphyletic clustering should imply HIV-1 superinfection. The HIV-1 prot/RT sequences routinely determined both at baseline and following therapy failure were used in a study in the Netherlands . Patients were selected for further analysis based on the number of degenerate base codes in the RT fragment of this sequence. Additional sequence analysis confirmed that 16 of 37 (42%) patients had a dual HIV-1 infection, equalling 1% of the total 1661 records available. Another extensive survey of 660 HIV-1 seroconverters in France with samples collected from 1988–2004 did not discover any HIV coinfections or early superinfections in these patients using HMA as initial screening method . In the studies from San Francisco, the Netherlands, and France, the risk group and the risk behaviour of the persons were not taken into account.
From the above studies, it cannot be concluded that the incidence of HIV-1 co- and superinfections is increasing. To reliably assess the incidence of HIV dual infections, additional cohort studies spanning an extended time of the epidemic are essential; these should encompass discrete risk groups of heterosexual, homosexual and shared needle transmission. However, it is clear that dual infections are more common in Africa than in the rest of the world, probably because of the significantly higher HIV-1 prevalence. A second HIV-1 infection occurs apparently as frequently as the first HIV-1 infection in African cohorts of heterosexual high risk individuals . Frequent dual infection is reflected by the large number of recombinant viruses discovered in Africa, albeit such findings are not only restricted there .
From the studies reviewed above, it can be concluded that the main risk of HIV superinfection is high risk exposure, which consists of two components: HIV prevalence and risk behaviour. Another important factor is time since the initial infection, and the optimal time for a second infection is close to the initial infection. Viral determinants (fitness), host factors (immune response) and the mode of transmission seem to play less important roles.
A rise in the number of new HIV infections and other sexually transmitted diseases in men having sex with men has been reported since the introduction of HAART in the Western world, suggesting that an increase in HIV superinfections can also be expected in this risk group . Men uninformed of their HIV status and seronegative men will likely also engage in more risky behaviour due to the availability of HAART treatment options. An acute infection can quickly be followed by HIV superinfection when most patients are still unaware of their HIV status. If superinfections usually take place close to the acute HIV infection, public counselling among HIV-infected individuals with known status is not likely to be effective in terms of prevention. Instead, overall public awareness campaigns of sexually transmitted disease prevention should be used to halt HIV superinfections with an emphasis on persons already infected with HIV to continue safe sex practices. Men having sex with men from San Francisco, who believed HIV superinfection can occur and that it damages their health, reported safer sex practices than men who did not believe in superinfection or did not believe that it could be harmful . Serosorting (i.e. having unprotected sex only with persons of similar HIV serostatus) has been used as a HIV prevention strategy. However, serosorting may actually increase the chance of HIV transmission when partners are not aware of, or not sincere about, their HIV-1 status . Unprotected sex with positive partners, which is becoming more and more frequent among HIV infected men having sex with men [102, 103] is likely to boost the incidence of HIV superinfections, and should thus be discouraged.
HIV-1 co-infection and superinfection are existing phenomena that contribute to viral diversity by the generation of recombinant viruses. The incidence of HIV superinfections is mainly controlled by risk exposure, which consists of two aspects: risk behaviour and HIV prevalence. Control by the immune system, in particular neutralizing antibodies, probably limits the time window of an HIV superinfection to the first two years after primary infection. In most, but not all superinfected patients, the second infection leads to faster disease progression. At present, it is unclear whether HIV-1 dual infections are increasing worldwide, but preliminary data from different cohorts suggest that dual infections increase when HIV-1 prevalence goes up, which is consistent with theoretical models.
Roest RW, Carman WF, Maertzdorf J, Scoular A, Harvey J, Kant M, Van Der Meijden WI, Verjans GM, Osterhaus AD: Genotypic analysis of sequential genital herpes simplex virus type 1 (HSV-1) isolates of patients with recurrent HSV-1 associated genital herpes. J Med Virol. 2004, 73: 601-604. 10.1002/jmv.20132.
Roest RW, Maertzdorf J, Kant M, Van Der Meijden WI, Osterhaus AD, Verjans GM: High incidence of genotypic variance between sequential herpes simplex virus type 2 isolates from HIV-1-seropositive patients with recurrent genital herpes. J Infect Dis. 2006, 194: 1115-1118. 10.1086/507683.
Van Baarle D, Hovenkamp E, Kersten MJ, Klein MR, Miedema F, Van Oers MH: Direct Epstein-Barr virus (EBV) typing on peripheral blood mononuclear cells: no association between EBV type 2 infection or superinfection and the development of acquired immunodeficiency syndrome-related non-Hodgkin's lymphoma. Blood. 1999, 93: 3949-3955.
Quinlivan M, Breuer J: Molecular studies of Varicella zoster virus. Rev Med Virol. 2006, 16: 225-250. 10.1002/rmv.502.
Drew WL, Sweet ES, Miner RC, Mocarski ES: Multiple infections by cytomegalovirus in patients with acquired immunodeficiency syndrome: documentation by Southern blot hybridization. J Infect Dis. 1984, 150: 952-953.
Spector SA, Hirata KK, Newman TR: Identification of multiple cytomegalovirus strains in homosexual men with acquired immunodeficiency syndrome. J Infect Dis. 1984, 150: 953-956.
Bale JF, Petheram SJ, Souza IE, Murph JR: Cytomegalovirus reinfection in young children. J Pediatr. 1996, 128: 347-352. 10.1016/S0022-3476(96)70279-2.
Beyari MM, Hodgson TA, Cook RD, Kondowe W, Molyneux EM, Scully CM, Teo CG, Porter SR: Multiple human herpesvirus-8 infection. J Infect Dis. 2003, 188: 678-689. 10.1086/377504.
Kao JH, Chen PJ, Lai MY, Chen DS: Acute exacerbations of chronic hepatitis B are rarely associated with superinfection of hepatitis B virus. Hepatology. 2001, 34: 817-823. 10.1053/jhep.2001.28188.
Blackard JT, Sherman KE: Hepatitis C virus coinfection and superinfection. J Infect Dis. 2007, 195: 519-524. 10.1086/510858.
Caterino-de-Araujo A, Favero A, los Santos-Fortuna E, Suleiman J, Chieco-Bianchi L, Calabro ML: HTLV-I/HTLV-II coinfection in an AIDS patient from Sao Paulo, Brazil. AIDS Res Hum Retroviruses. 2000, 16: 715-719. 10.1089/088922200308710.
Cot MC, Poulain M, Delagneau JF, Peeters M, Brun-Vezinet F: Dual HIV-1 and HIV-2 infection in West Africa supported by synthetic peptide analysis. AIDS Res Hum Retroviruses. 1988, 4: 239-241.
Evans LA, Moreau J, Odehouri K, Seto D, Thomson-Honnebier G, Legg H, Barboza A, Cheng-Mayer C, Levy JA: Simultaneous isolation of HIV-1 and HIV-2 from an AIDS patient. Lancet. 1988, 2: 1389-1391. 10.1016/S0140-6736(88)90586-7.
George JR, Ou CY, Parekh B, Brattegaard K, Brown V, Boateng E, De Cock KM: Prevalence of HIV-1 and HIV-2 mixed infections in Cote d'Ivoire. Lancet. 1992, 340: 337-339. 10.1016/0140-6736(92)91406-X.
Nkengasong JN, Kestens L, Ghys PD, Koblavi-Deme S, Otten RA, Bile C, Maurice C, Kalou M, Laga M, Wiktor SZ, Greenberg AE: Dual infection with human immunodeficiency virus type 1 and type 2: impact on HIV type 1 viral load and immune activation markers in HIV-seropositive female sex workers in Abidjan, Ivory Coast. AIDS Res Hum Retroviruses. 2000, 16: 1371-1378. 10.1089/08892220050140919.
Gottlieb GS, Sow PS, Hawes SE, Ndoye I, Coll-Seck AM, Curlin ME, Critchlow CW, Kiviat NB, Mullins JI: Molecular epidemiology of dual HIV-1/HIV-2 seropositive adults from Senegal, West Africa. AIDS Res Hum Retroviruses. 2003, 19: 575-584. 10.1089/088922203322230941.
Nethe M, Berkhout B, van der Kuyl AC: Retroviral superinfection resistance. Retrovirology. 2005, 2: 52-10.1186/1742-4690-2-52.
Ramos A, Hu DJ, Nguyen L, Phan KO, Vanichseni S, Promadej N, Choopanya K, Callahan M, Young NL, McNicholl J, Mastro TD, Folks TM, Subbarao S: Intersubtype human immunodeficiency virus type 1 superinfection following seroconversion to primary infection in two injection drug users. J Virol. 2002, 76: 7444-7452. 10.1128/JVI.76.15.7444-7452.2002.
Jost S, Bernard MC, Kaiser L, Yerly S, Hirschel B, Samri A, Autran B, Goh LE, Perrin L: A patient with HIV-1 superinfection. N Engl J Med. 2002, 347: 731-736. 10.1056/NEJMoa020263.
Altfeld M, Allen TM, Yu XG, Johnston MN, Agrawal D, Korber BT, Montefiori DC, O'Connor DH, Davis BT, Lee PK, Maier EL, Harlow J, Goulder PJ, Brander C, Rosenberg ES, Walker BD: HIV-1 superinfection despite broad CD8+ T-cell responses containing replication of the primary virus. Nature. 2002, 420: 434-439. 10.1038/nature01200.
Smith DM, Richman DD, Little SJ: HIV Superinfection. J Infect Dis. 2005, 192: 438-444. 10.1086/431682.
Plantier JC, Lemee V, Dorval I, Gueudin M, Braun J, Hutin P, Ruffault A, Simon F: HIV-1 group M superinfection in an HIV-1 group O-infected patient. AIDS. 2004, 18: 2444-2446.
Yang OO, Daar ES, Jamieson BD, Balamurugan A, Smith DM, Pitt JA, Petropoulos CJ, Richman DD, Little SJ, Brown AJ: Human immunodeficiency virus type 1 clade B superinfection: evidence for differential immune containment of distinct clade B strains. J Virol. 2005, 79: 860-868. 10.1128/JVI.79.2.860-868.2005.
van der Kuyl AC, Kozaczynska K, Van den Burg R, Zorgdrager F, Back N, Jurriaans S, Berkhout B, Reiss P, Cornelissen M: Triple HIV-1 infection. New England Journal of Medicine. 2005, 352: 2557-2559. 10.1056/NEJM200506163522420.
Pernas M, Casado C, Fuentes R, Perez-Elias MJ, Lopez-Galindez C: A dual superinfection and recombination within HIV-1 subtype B 12 years after primoinfection. J Acquir Immune Defic Syndr. 2006, 42: 12-18. 10.1097/01.qai.0000214810.65292.73.
Smith DM, Wong JK, Hightower GK, Ignacio CC, Koelsch KK, Petropoulos CJ, Richman DD, Little SJ: HIV drug resistance acquired through superinfection. AIDS. 2005, 19: 1251-1256.
Blick G, Kagan RM, Coakley E, Petropoulos C, Maroldo L, Greiger-Zanlungo P, Gretz S, Garton T: The Probable Source of Both the Primary Multidrug-Resistant (MDR) HIV-1 Strain Found in a Patient with Rapid Progression to AIDS and a Second Recombinant MDR Strain Found in a Chronically HIV-1-Infected Patient. J Infect Dis. 2007, 195: 1250-1259. 10.1086/512240.
McCutchan FE, Hoelscher M, Tovanabutra S, Piyasirisilp S, Sanders-Buell E, Ramos G, Jagodzinski L, Polonis V, Maboko L, Mmbando D, Hoffmann O, Riedner G, von Sonnenburg F, Robb M, Birx DL: In-depth analysis of a heterosexually acquired human immunodeficiency virus type 1 superinfection: evolution, temporal fluctuation, and intercompartment dynamics from the seronegative window period through 30 months postinfection. J Virol. 2005, 79: 11693-11704. 10.1128/JVI.79.18.11693-11704.2005.
Gottlieb GS, Nickle DC, Jensen MA, Wong KG, Kaslow RA, Shepherd JC, Margolick JB, Mullins JI: HIV type 1 superinfection with a dual-tropic virus and rapid progression to AIDS: a case report. Clin Infect Dis. 2007, 45: 501-509. 10.1086/520024.
Smith DM, Wong JK, Hightower GK, Ignacio CC, Koelsch KK, Daar ES, Richman DD, Little SJ: Incidence of HIV superinfection following primary infection. JAMA. 2004, 292: 1177-1178. 10.1001/jama.292.10.1177.
Yerly S, Jost S, Monnat M, Telenti A, Cavassini M, Chave JP, Kaiser L, Burgisser P, Perrin L: HIV-1 co/super-infection in intravenous drug users. AIDS. 2004, 18: 1413-1421. 10.1097/01.aids.0000131330.28762.0c.
Hu DJ, Subbarao S, Vanichseni S, Mock PA, Ramos A, Nguyen L, Chaowanachan T, Griensven F, Choopanya K, Mastro TD, Tappero JW: Frequency of HIV-1 dual subtype infections, including intersubtype superinfections, among injection drug users in Bangkok, Thailand. AIDS. 2005, 19: 303-308.
Chohan B, Lavreys L, Rainwater SM, Overbaugh J: Evidence for frequent reinfection with human immunodeficiency virus type 1 of a different subtype. J Virol. 2005, 79: 10701-10708. 10.1128/JVI.79.16.10701-10708.2005.
Manigart O, Courgnaud V, Sanou O, Valea D, Nagot N, Meda N, Delaporte E, Peeters M, Van de PP: HIV-1 superinfections in a cohort of commercial sex workers in Burkina Faso as assessed by an autologous heteroduplex mobility procedure. AIDS. 2004, 18: 1645-1651. 10.1097/01.aids.0000131333.30548.db.
Lamine A, Caumont-Sarcos A, Chaix ML, Saez-Cirion A, Rouzioux C, Delfraissy JF, Pancino G, Lambotte O: Replication-competent HIV strains infect HIV controllers despite undetectable viremia (ANRS EP36 study). AIDS. 2007, 21: 1043-1045. 10.1097/QAD.0b013e3280d5a7ac.
Takehisa J, Zekeng L, Miura T, Ido E, Yamashita M, Mboudjeka I, Gurtler LG, Hayami M, Kaptue L: Triple HIV-1 infection with group O and Group M of different clades in a single Cameroonian AIDS patient. J Acquir Immune Defic Syndr Hum Retrovirol. 1997, 14: 81-82.
Takehisa J, Zekeng L, Ido E, Yamaguchi-Kabata Y, Mboudjeka I, Harada Y, Miura T, Kaptu L, Hayami M: Human immunodeficiency virus type 1 intergroup (M/O) recombination in cameroon. J Virol. 1999, 73: 6810-6820.
Gerhardt M, Mloka D, Tovanabutra S, Sanders-Buell E, Hoffmann O, Maboko L, Mmbando D, Birx DL, McCutchan FE, Hoelscher M: In-depth, longitudinal analysis of viral quasispecies from an individual triply infected with late-stage human immunodeficiency virus type 1, using a multiple PCR primer approach. Journal of Virology. 2005, 79: 8249-8261. 10.1128/JVI.79.13.8249-8261.2005.
Kozaczynska K, Cornelissen M, Reiss P, Zorgdrager F, van der Kuyl AC: HIV-1 sequence evolution in vivo after superinfection with three viral strains. Retrovirology. 2007, 4: 59-10.1186/1742-4690-4-59.
Chakraborty B, Valer L, De Mendoza C, Soriano V, Quinones-Mateu ME: Failure to detect human immunodeficiency virus type 1 superinfection in 28 HIV-seroconcordant individuals with high risk of reexposure to the virus. AIDS Res Hum Retroviruses. 2004, 20: 1026-1031. 10.1089/aid.2004.20.1026.
Koelsch KK, Smith DM, Little SJ, Ignacio CC, Macaranas TR, Brown AJ, Petropoulos CJ, Richman DD, Wong JK: Clade B HIV-1 superinfection with wild-type virus after primary infection with drug-resistant clade B virus. AIDS. 2003, 17: F11-F16. 10.1097/00002030-200305020-00001.
Brenner B, Routy JP, Quan Y, Moisi D, Oliveira M, Turner D, Wainberg MA: Persistence of multidrug-resistant HIV-1 in primary infection leading to superinfection. AIDS. 2004, 18: 1653-1660. 10.1097/01.aids.0000131377.28694.04.
Burke DS: Recombination in HIV: an important viral evolutionary strategy. Emerg Infect Dis. 1997, 3: 253-259.
Najera R, Delgado E, Perez-Alvarez L, Thomson MM: Genetic recombination and its role in the development of the HIV-1 pandemic. AIDS. 2002, 16 Suppl 4: S3-16.
Charpentier C, Nora T, Tenaillon O, Clavel F, Hance AJ: Extensive recombination among human immunodeficiency virus type 1 quasispecies makes an important contribution to viral diversity in individual patients. J Virol. 2006, 80: 2472-2482. 10.1128/JVI.80.5.2472-2482.2006.
Rousseau CM, Learn GH, Bhattacharya T, Nickle DC, Heckerman D, Chetty S, Brander C, Goulder PJ, Walker BD, Kiepiela P, Korber BT, Mullins JI: Extensive intrasubtype recombination in South african human immunodeficiency virus type 1 subtype C infections. J Virol. 2007, 81: 4492-4500. 10.1128/JVI.02050-06.
Kalish ML, Robbins KE, Pieniazek D, Schaefer A, Nzilambi N, Quinn TC, St Louis ME, Youngpairoj AS, Phillips J, Jaffe HW, Folks TM: Recombinant viruses and early global HIV-1 epidemic. Emerg Infect Dis. 2004, 10: 1227-1234.
Anderson JP, Rodrigo AG, Learn GH, Madan A, Delahunty C, Coon M, Girard M, Osmanov S, Hood L, Mullins JI: Testing the hypothesis of a recombinant origin of human immunodeficiency virus type 1 subtype E. J Virol. 2000, 74: 10752-10765. 10.1128/JVI.74.22.10752-10765.2000.
Gross KL, Porco TC, Grant RM: HIV-1 superinfection and viral diversity. AIDS. 2004, 18: 1513-1520. 10.1097/01.aids.0000131361.75328.47.
Taylor JE, Korber BT: HIV-1 intra-subtype superinfection rates: estimates using a structured coalescent with recombination. Infect Genet Evol. 2005, 5: 85-95. 10.1016/j.meegid.2004.07.001.
Herbinger KH, Gerhardt M, Piyasirisilp S, Mloka D, Arroyo MA, Hoffmann O, Maboko L, Birx DL, Mmbando D, McCutchan FE, Hoelscher M: Frequency of HIV type 1 dual infection and HIV diversity: analysis of low- and high-risk populations in Mbeya Region, Tanzania. AIDS Res Hum Retroviruses. 2006, 22: 599-606. 10.1089/aid.2006.22.599.
Saldana J, Elena SF, Sole RV: Coinfection and superinfection in RNA virus populations: a selection-mutation model. Math Biosci. 2003, 183: 135-160. 10.1016/S0025-5564(03)00038-5.
Carrillo FY, Sanjuan R, Moya A, Cuevas JM: The effect of co- and superinfection on the adaptive dynamics of vesicular stomatitis virus. Infect Genet Evol. 2007, 7: 69-73. 10.1016/j.meegid.2006.04.004.
Smith DM, Strain MC, Frost SD, Pillai SK, Wong JK, Wrin T, Liu Y, Petropolous CJ, Daar ES, Little SJ, Richman DD: Lack of neutralizing antibody response to HIV-1 predisposes to superinfection. Virology. 2006, 355: 1-5. 10.1016/j.virol.2006.08.009.
Kono Y, Fukunaga Y, Kobayashi K: Resistance of horses infected chronically with equine infectious anemia virus against reinfection. Natl Inst Anim Health Q (Tokyo). 1973, 13: 173-181.
Issel CJ, Horohov DW, Lea DF, Adams WV, Hagius SD, McManus JM, Allison AC, Montelaro RC: Efficacy of inactivated whole-virus and subunit vaccines in preventing infection and disease caused by equine infectious anemia virus. J Virol. 1992, 66: 3398-3408.
Liu SL, Schacker T, Musey L, Shriner D, McElrath MJ, Corey L, Mullins JI: Divergent patterns of progression to AIDS after infection from the same source: human immunodeficiency virus type 1 evolution and antiviral responses. J Virol. 1997, 71: 4284-4295.
Gottlieb GS, Nickle DC, Jensen MA, Wong KG, Grobler J, Li F, Liu SL, Rademeyer C, Learn GH, Karim SS, Williamson C, Corey L, Margolick JB, Mullins JI: Dual HIV-1 infection associated with rapid disease progression. Lancet. 2004, 363: 619-622. 10.1016/S0140-6736(04)15596-7.
Jurriaans S, Kozaczynska K, Zorgdrager F, Steingrover R, Prins JM, van der Kuyl AC, Cornelissen M: A sudden rise in viral load is infrequently associated with HIV-1 superinfection. JAIDS. 2007, in press:
Grobler J, Gray CM, Rademeyer C, Seoighe C, Ramjee G, Karim SA, Morris L, Williamson C: Incidence of HIV-1 dual infection and its association with increased viral load set point in a cohort of HIV-1 subtype C-infected female sex workers. J Infect Dis. 2004, 190: 1355-1359. 10.1086/423940.
Casado C, Pernas M, Alvaro T, Sandonis V, Garcia S, Rodriguez C, Romero JD, Grau E, Ruiz L, Lopez-Galindez C: Coinfection and Superinfection in Patients with Long-Term, Nonprogressive HIV-1 Disease. J Infect Dis. 2007, 196: 895-899. 10.1086/520885.
Peeters M, Liegeois F, Torimiro N, Bourgeois A, Mpoudi E, Vergne L, Saman E, Delaporte E, Saragosti S: Characterization of a highly replicative intergroup M/O human immunodeficiency virus type 1 recombinant isolated from a Cameroonian patient. J Virol. 1999, 73: 7368-7375.
Songok EM, Lwembe RM, Kibaya R, Kobayashi K, Ndembi N, Kita K, Vulule J, Oishi I, Okoth F, Kageyama S, Ichimura H: Active generation and selection for HIV intersubtype A/D recombinant forms in a coinfected patient in Kenya. AIDS Res Hum Retroviruses. 2004, 20: 255-258. 10.1089/088922204773004996.
Brand D, Beby-Defaux A, Mace M, Brunet S, Moreau A, Godet C, Jais X, Cazein F, Semaille C, Barin F: First identification of HIV-1 groups M and O dual infections in Europe. AIDS. 2004, 18: 2425-2428.
Vergne L, Bourgeois A, Mpoudi-Ngole E, Mougnutou R, Mbuagbaw J, Liegeois F, Laurent C, Butel C, Zekeng L, Delaporte E, Peeters M: Biological and genetic characteristics of HIV infections in Cameroon reveals dual group M and O infections and a correlation between SI-inducing phenotype of the predominant CRF02_AG variant and disease stage. Virology. 2003, 310: 254-266.
Yamaguchi J, Bodelle P, Vallari AS, Coffey R, McArthur CP, Schochetman G, Devare SG, Brennan CA: HIV infections in northwestern Cameroon: identification of HIV type 1 group O and dual HIV type 1 group M and group O infections. AIDS Res Hum Retroviruses. 2004, 20: 944-957. 10.1089/aid.2004.20.944.
Barin F, Plantier JC, Brand D, Brunet S, Moreau A, Liandier B, Thierry D, Cazein F, Lot F, Semaille C, Desenclos JC: Human immunodeficiency virus serotyping on dried serum spots as a screening tool for the surveillance of the AIDS epidemic. J Med Virol. 2006, 78 Suppl 1: S13-S18. 10.1002/jmv.20600.
Rodes B, Toro C, Jimenez V, Soriano V: Viral response to antiretroviral therapy in a patient coinfected with HIV type 1 and type 2. Clin Infect Dis. 2005, 41: e19-e21. 10.1086/431204.
Murphy G, Belda FJ, Pau CP, Clewley JP, Parry JV: Discrimination of subtype B and non-subtype B strains of human immunodeficiency virus type 1 by serotyping: correlation with genotyping. J Clin Microbiol. 1999, 37: 1356-1360.
Gaywee J, Artenstein AW, VanCott TC, Trichavaroj R, Sukchamnong A, Amlee P, De Souza M, McCutchan FE, Carr JK, Markowitz LE, Michael R, Nittayaphan S: Correlation of genetic and serologic approaches to HIV-1 subtyping in Thailand. J Acquir Immune Defic Syndr Hum Retrovirol. 1996, 13: 392-396.
Barlow KL, Green J, Clewley JP: Viral genome characterisation by the heteroduplex mobility and heteroduplex tracking assays. Rev Med Virol. 2000, 10: 321-335. 10.1002/1099-1654(200009/10)10:5<321::AID-RMV288>3.0.CO;2-X.
Courgnaud V, Seng R, Becquart P, Boulahtouf A, Rouzioux C, Boufassa F, Deveau C, Van de PP, Meyer L, Foulongne V: HIV-1 co-infection prevalence in two cohorts of early HIV-1 seroconverters in France. AIDS. 2007, 21: 1055-1056. 10.1097/QAD.0b013e32810c8be1.
Cornelissen M, Jurriaans S, Kozaczynska K, Prins JM, Hamidjaja RA, Zorgdrager F, Bakker M, Back N, van der Kuyl AC: Routine HIV-1 genotyping as a tool to identify dual infections. AIDS. 2007, 21: 807-811. 10.1097/QAD.0b013e3280f3c08a.
International Union of Biochemistry and Molecular Biology. 2007, [http://www.iubmb.unibe.ch/]
Hoelscher M, Dowling WE, Sanders-Buell E, Carr JK, Harris ME, Thomschke A, Robb ML, Birx DL, McCutchan FE: Detection of HIV-1 subtypes, recombinants, and dual infections in east Africa by a multi-region hybridization assay. AIDS. 2002, 16: 2055-2064. 10.1097/00002030-200210180-00011.
Kijak GH, Tovanabutra S, Sanders-Buell E, Watanaveeradej V, de Souza MS, Nelson KE, Ketsararat V, Gulgolgarn V, Wera-arpachai M, Sriplienchan S, Khamboonrueng C, Birx DL, Robb ML, McCutchan FE: Distinguishing molecular forms of HIV-1 in Asia with a high-throughput, fluorescent genotyping assay, MHAbce v.2. Virology. 2007, 358: 178-191. 10.1016/j.virol.2006.07.055.
Holder M, Lewis PO: Phylogeny estimation: traditional and Bayesian approaches. Nat Rev Genet. 2003, 4: 275-284. 10.1038/nrg1044.
McCormack GP, Clewley JP: The application of molecular phylogenetics to the analysis of viral genome diversity and evolution. Rev Med Virol. 2002, 12: 221-238. 10.1002/rmv.355.
Hue S, Clewley JP, Cane PA, Pillay D: HIV-1 pol gene variation is sufficient for reconstruction of transmissions in the era of antiretroviral therapy. AIDS. 2004, 18: 719-728. 10.1097/00002030-200403260-00002.
Sturmer M, Preiser W, Gute P, Nisius G, Doerr HW: Phylogenetic analysis of HIV-1 transmission: pol gene sequences are insufficient to clarify true relationships between patient isolates. AIDS. 2004, 18: 2109-2113. 10.1097/00002030-200411050-00002.
Resik S, Lemey P, Ping LH, Kouri V, Joanes J, Perez J, Vandamme AM, Swanstrom R: Limitations to contact tracing and phylogenetic analysis in establishing HIV type 1 transmission networks in Cuba. AIDS Res Hum Retroviruses. 2007, 23: 347-356. 10.1089/aid.2006.0158.
Hecht FM, Wolf LE, Lo B: Lessons from an HIV transmission pair. J Infect Dis. 2007, 195: 1239-1241. 10.1086/512247.
Titti F, Sernicola L, Geraci A, Panzini G, Di Fabio S, Belli R, Monardo F, Borsetti A, Maggiorella MT, Koanga-Mogtomo M, Corrias F, Zamarchi R, Amadori A, Chieco-Bianchi L, Verani P: Live attenuated simian immunodeficiency virus prevents super-infection by cloned SIVmac251 in cynomolgus monkeys. J Gen Virol. 1997, 78 ( Pt 10): 2529-2539.
Cranage MP, Sharpe SA, Whatmore AM, Polyanskaya N, Norley S, Cook N, Leech S, Dennis MJ, Hall GA: In vivo resistance to simian immunodeficiency virus superinfection depends on attenuated virus dose. J Gen Virol. 1998, 79 ( Pt 8): 1935-1944.
Otten RA, Ellenberger DL, Adams DR, Fridlund CA, Jackson E, Pieniazek D, Rayfield MA: Identification of a window period for susceptibility to dual infection with two distinct human immunodeficiency virus type 2 isolates in a Macaca nemestrina (pig-tailed macaque) model. J Infect Dis. 1999, 180: 673-684. 10.1086/314968.
Sernicola L, Corrias F, Koanga-Mogtomo ML, Baroncelli S, Di Fabio S, Maggiorella MT, Belli R, Michelini Z, Macchia I, Cesolini A, Cioe L, Verani P, Titti F: Long-lasting protection by live attenuated simian immunodeficiency virus in cynomolgus monkeys: no detection of reactivation after stimulation with a recall antigen. Virology. 1999, 256: 291-302. 10.1006/viro.1999.9652.
Stebbings R, Berry N, Stott J, Hull R, Walker B, Lines J, Elsley W, Brown S, Wade-Evans A, Davis G, Cowie J, Sethi M, Almond N: Vaccination with live attenuated simian immunodeficiency virus for 21 days protects against superinfection. Virology. 2004, 330: 249-260. 10.1016/j.virol.2004.09.026.
Sharpe SA, Cope A, Dowall S, Berry N, Ham C, Heeney JL, Hopkins D, Easterbrook L, Dennis M, Almond N, Cranage M: Macaques infected long-term with attenuated simian immunodeficiency virus (SIVmac) remain resistant to wild-type challenge, despite declining cytotoxic T lymphocyte responses to an immunodominant epitope. J Gen Virol. 2004, 85: 2591-2602. 10.1099/vir.0.80050-0.
Veazey RS, DeMaria M, Chalifoux LV, Shvetz DE, Pauley DR, Knight HL, Rosenzweig M, Johnson RP, Desrosiers RC, Lackner AA: Gastrointestinal tract as a major site of CD4+ T cell depletion and viral replication in SIV infection. Science. 1998, 280: 427-431. 10.1126/science.280.5362.427.
Mattapallil JJ, Douek DC, Hill B, Nishimura Y, Martin M, Roederer M: Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection. Nature. 2005, 434: 1093-1097. 10.1038/nature03501.
Li Q, Duan L, Estes JD, Ma ZM, Rourke T, Wang Y, Reilly C, Carlis J, Miller CJ, Haase AT: Peak SIV replication in resting memory CD4+ T cells depletes gut lamina propria CD4+ T cells. Nature. 2005, 434: 1148-1152.
Brenchley JM, Schacker TW, Ruff LE, Price DA, Taylor JH, Beilman GJ, Nguyen PL, Khoruts A, Larson M, Haase AT, Douek DC: CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract. J Exp Med. 2004, 200: 749-759. 10.1084/jem.20040874.
Guadalupe M, Reay E, Sankaran S, Prindiville T, Flamm J, McNeil A, Dandekar S: Severe CD4+ T-cell depletion in gut lymphoid tissue during primary human immunodeficiency virus type 1 infection and substantial delay in restoration following highly active antiretroviral therapy. J Virol. 2003, 77: 11708-11717. 10.1128/JVI.77.21.11708-11717.2003.
World Health Organization. 2007, [http://www.who.int]
Tsui R, Herring BL, Barbour JD, Grant RM, Bacchetti P, Kral A, Edlin BR, Delwart EL: Human immunodeficiency virus type 1 superinfection was not detected following 215 years of injection drug user exposure. J Virol. 2004, 78: 94-103. 10.1128/JVI.78.1.94-103.2004.
Diaz RS, Pardini R, Catroxo M, Operskalski EA, Mosley JW, Busch MP: HIV-1 superinfection is not a common event. J Clin Virol. 2005, 33: 328-330. 10.1016/j.jcv.2004.11.021.
Xiridou M, van Griensven F, Tappero JW, Martin M, Gurwith M, Vanichseni S, Kittikraisak W, Coutinho R, Choopanya K: The Spread of HIV-1 Subtypes B and CRF01_AE Among Injecting Drug Users in Bangkok, Thailand. J Acquir Immune Defic Syndr. 2007
Gonzales MJ, Delwart E, Rhee SY, Tsui R, Zolopa AR, Taylor J, Shafer RW: Lack of detectable human immunodeficiency virus type 1 superinfection during 1072 person-years of observation. J Infect Dis. 2003, 188: 397-405. 10.1086/376534.
McCutchan FE: Global epidemiology of HIV. J Med Virol. 2006, 78 Suppl 1: S7-S12. 10.1002/jmv.20599.
Blackard JT, Mayer KH: HIV superinfection in the era of increased sexual risk-taking. Sex Transm Dis. 2004, 31: 201-204. 10.1097/01.OLQ.0000118082.45312.1F.
Colfax GN, Guzman R, Wheeler S, Mansergh G, Marks G, Rader M, Buchbinder SP: Beliefs about HIV reinfection (superinfection) and sexual behavior among a diverse sample of HIV-positive men who have sex with men. J Acquir Immune Defic Syndr. 2004, 36: 990-992. 10.1097/00126334-200408010-00017.
Butler DM, Smith DM: Serosorting can potentially increase HIV transmissions. AIDS. 2007, 21: 1218-1220. 10.1097/QAD.0b013e32814db7bf.
Elford J, Bolding G, Sherr L, Hart G: No evidence of an increase in serosorting with casual partners among HIV-negative gay men in London, 1998-2005. AIDS. 2007, 21: 243-245.
The authors thank Ben Berkhout and Kuan-Teh Jeang for critically reading the manuscript.
The author(s) declare that they have no competing interests.
ACvdK and MC designed the review; ACvdK drafted the manuscript.
About this article
- Human Immunodeficiency Virus
- Human Immunodeficiency Virus Infection
- Recombinant Virus
- Human Immunodeficiency Virus Prevalence
- Plasma Viral Load