HIV Databases HIV Databases home HIV Databases home
HIV sequence database



HIV-1 Coreceptor Use: A Molecular Window into Viral Tropism

Robert W. Doms 1and John P. Moore2

1Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104
2The Aaron Diamond AIDS Research Center, The Rockefeller University, 455 First Avenue, New York, NY 10016

The identification of the chemokine receptors CCR5 and CXCR4 as the major coreceptors for HIV-1 has provided a new framework for understanding viral tropism and pathogenesis at the molecular level. It is now possible to assign molecular designations to virus isolates, based on their coreceptor use, that largely explain viral phenotype (reviewed in Berger97a, 3Border97,8Doms9 7,15Moore9731). The need to accurately describe viral phenotype arises because HIV-1 strains can exhibit distinct cellular tropisms that have important implications for viral pathogenesis and disease progression. Generally, virus strains that are transmitted between individuals are able to infect both macrophages and primary CD4+ T-cells, but are unable to replicate in transformed T-cell lines (Connor93,11Roos92,37Schuitemaker92,41Zhu9352). As a result, they fail to form syncytia when grown in MT-2 cells or in certain other commonly used cell lines. Viruses with these properties have been referred to both as macrophage tropic (M-tropic) due to their ability to infect macrophages, non-syncytium inducing (NSI) due to their inability to form syncytia on T-cell lines, or slow-low (SL) in reference to their replication kinetics in culture (Fenyo88,22Schuitemaker9241) . With time, typically about 4-5 years after infection, virus strains evolve in some individuals (about 50) which can infect T-cell lines in addition to primary T-cells (Tersmette88,43Tersmette8944). While this shift in tropism can sometimes be accompanied by a loss of ability to infect macrophages, more often primary isolates retain this property and so are referred to as dual-tropic (Collman9210). Viruses able to infect T-cell lines have been variously referred to as T-tropic, syncytium-inducing (SI), or rapid-high (RH) according to the nomenclature schemes mentioned above. The emergence of these virus types is correlated with accelerated disease progression (Connor9311). Finally, viruses that are well-adapted to grow on transformed cell lines by continual passage are referred to as T-cell line adapted (TCLA). TCLA viruses exhibit greater sensitivity to neutralization by both antibodies and soluble CD4.

The above three systems for classifying viral strains are problematic for several reasons. The M-tropic designation, for example, can be taken incorrectly to mean that a virus is unable to replicate in primary T-cells. Likewise, T-tropic viruses have been described that retain the ability to infect macrophages. The NSI designation is also misleading, as it suggests that there is something inherently wrong with the env protein from these virus strains. It also implies that SI viruses are more fusogenic and cytopathic, which is not necessarily so when they are grown in primary CD4+ T-cells. It is now known that the SI/NSI designation is an artifact resulting from the fact that T-cell lines express CXCR4 but not CCR5; the env proteins from NSI viruses are perfectly capable of forming syncytia provided that target cells expressing CCR5 are used. Finally, an additional complication arising from the current classification schemes is that the terms M-tropic, NSI, and SL are often used synonymously, as are T-tropic, SI, and RH. While this is sometimes appropriate, there are many instances in which these terms are not synonymous.

Chemokine Receptors and Viral Tropism

The major determinant of viral tropism is at the level of entry, more specifically at the level of membrane fusion with CD4+ cells. This occurs efficiently only if the appropriate coreceptor is present. Thus, M-tropic, NSI viruses use CCR5 in conjunction with CD4 for fusion. Direct interactions between the env glycoprotein and CCR5 have been detected (Trkola96,46Wu9648), and it is likely that this interaction triggers the final conformational changes in env that promote fusion between the viral and cellular membranes. The importance of CCR5 for HIV-1 infection in vivo was shown by the discovery that approximately 1 of Caucasians lack CCR5, and that these individuals are highly resistant but not entirely immune to virus infection (Dean96, 12Liu96,28Michael97,30Samson9640). Thus, CCR5 is the major coreceptor for HIV-1 transmission in vivo. However, while CD4-positive cells obtained from CCR5-negative individuals are resistant to infection by viruses that require this coreceptor, they are readily infectable by viruses which use CXCR4 (Liu96,28Rana97,35Samson96,40Zhang9750). It is not clear why CCR5-negative individuals are only rarely infected by viruses that can use CXCR4 for cellular entry (for some examples see (Balotta97,2Theodorou97,45OBrien97,32Biti975). It appears that viruses which use CXCR4 are inefficient at establishing an infection in a naive host, for unknown reasons.

While M-tropic NSI viruses use CCR5 for cellular entry, CXCR4 is the coreceptor most commonly used by T-tropic, SI virus strains (Feng9621). Viruses that use CCR5 for entry can evolve to use CXCR4 through mutations in the env glycoprotein, usually but not always in the V3-loop. Despite less than 20 amino acid identity between CCR5 and CXCR4 in their extracellular domains, several viruses are known to efficiently use both coreceptors for cellular entry. Use of CXCR4 is largely dependent upon the first and second extracellular loops of this receptor, which are considerably more anionic than the corresponding domains in CCR5 (Brelot97,7Lu9729). It may be relevant that the V3-loops of T-tropic HIV-1 env proteins tend to be more basic than those found in viruses which use CCR5 as a coreceptor (De Jong92,25Fouchier9223), suggesting a charge-charge interaction may be involved in the gp120-CXCR4 interaction.

In addition to CCR5 and CXCR4, at least nine other chemokine or orphan receptors have been shown to support the cellular entry of one or more virus strains. These include CCR2b, CCR3, CCR8, GPR1, GPR15, STRL33, US28, V28, and ChemR23 (Choe96,9Deng97,13Doranz96,16Farzan97,20Liao97,27Pleskoff97a,33Reeves97,36Rucker97,38Samson9739). Though the in vivo significance of these alternative coreceptors is not clear, it is possible that the use of receptors other than CCR5 and CXCR4 may be important for certain aspects of viral pathogenesis. For example, CCR3 is expressed in microglia, and use of this receptor may be correlated with neurotropism (He9724). A major challenge in this rapidly developing field will be to determine if use of these additional receptors has implications for viral pathogenesis.

A Classification System Based on Coreceptor Use

The importance of viral phenotype for pathogenesis and disease progression coupled with the imprecise nature of the current systems for classifying virus strains calls for the development of a more accurate classification scheme. Recently, a new system based on coreceptor use has been proposed (Berger97b4). In this scheme, virus strains that use CCR5 as a coreceptor are designated R5, while those that use CXCR4 are designated X4. Viruses that use both coreceptors are designated R5X4. Thus, under this system the HIV-1 strains most commonly transmitted would be called R5 viruses. However, this designation makes no assumptions about the cells in which HIV-1 replication must occur (unlike the M-tropic/T-tropic designation), or the rate of virus replication (unlike the SL/RH system). Viruses that evolve the capacity to use CXCR4 in infected individuals with or without concurrent use of CCR5 would now be called R5X4 or X4 viruses, respectively. The primary advantage of this classification system is that it offers a precise molecular description of the major coreceptors used by any given virus strain without assuming that this necessarily results in the ability to efficiently replicate in a particular target cell. Furthermore, this system can be readily modified, taking into account other coreceptors (such as CCR3 by using an R3 designation) if their use proves to be a major determinant of tropism. We have compiled a table listing the coreceptors used by more than 100 HIV-1 strains, and discuss some of the nuances of co-receptor use below.

Issues Pertaining to Coreceptor Use

As shown in the Table, the major coreceptors used by greater than 100 HIV-1 strains have been determined in little more than a year. All strains listed in the Table have been examined for the ability to use CCR5 or CXCR4, though not necessarily for other coreceptors such as CCR3. From the studies published to date, it is clear that CCR5 and CXCR4 are the major HIV-1 coreceptors since all HIV-1 strains examined thus far use one or both of these receptors. In addition, coreceptor use is phenotype but not genotype dependent. All NSI viruses (irrespective of genetic subtype) studied to date use CCR5 while all SI viruses use CXCR4 (though many also use CCR5). Further, our review of the literature has shown that determining which of these receptors is used by a given virus strain is straightforward and independent of technique or assay. We have found no discrepancies between various virus infection, virus-cell fusion, and cell-cell fusion assays that have been used to determine if virus strains use CCR5 or CXCR4. The only differences concern the relative efficiencies with which R5X4 viruses use CCR5 and CXCR4, but these are relatively insignificant in terms of magnitude. For the purposes of the Table, we have arbitrarily chosen 10 efficiency as the cut-off for relevant coreceptor use. Thus, a virus that uses CCR5 as its most efficient coreceptor is listed as a R5X4 virus if it uses CXCR4 to levels 10 of that observed for CCR5. The efficiency with which different co-receptors are used by some strains is likely to vary between assay systems, and low-level entry via several co-receptors may not be uncommon. Whether this low level of relative efficiency can support virus infection in vivo is not known. As a result, the threshold efficiency for assigning relevance to coreceptor use may have to be raised or lowered in the future.

While many virus strains have been examined for the ability to use CCR5 and CXC R4, only a small number have been tested for use of most of the other viral coreceptors (see Table). Thus, we have not listed coreceptors that are NOT used by a given virus strain. Unlike studies in which use of CCR5 and CXCR4 was examined, we occasionally found discrepancies between different studies with regards to the use of additional coreceptors by some virus strains. The reasons for this are not clear, but may well be due to the fact that use of coreceptors other than CCR5 and CXCR4 tends to be inefficient, thus magnifying assay dependent differences. Perhaps the most significant variable in determining whether a given chemokine or orphan receptor can function as a coreceptor is the level of its expression. Very high levels of CCR3 expression support env-mediated membrane fusion by the majority of HIV-1 strains tested, while at lower levels only a few virus strains could use CCR3 (Rucker9738). Thus, expression levels can strongly influence coreceptor use. Another important variable is the expression level of the coreceptor relative to CD4 (Kozak9726). When CD4 is present on the cell surface at high levels, surprisingly low levels of CCR5 or CXCR4 are needed to support virus entry. However, if CD4 is expressed at low levels, higher expression levels of the coreceptors are needed (Kozak9726). Whether this will hold true for other coreceptors is not known, but clearly both CD4 and coreceptor cell surface expression levels can influence the efficiency of viral entry. As antibodies to additional chemokine and orphan receptors are identified, it will be possible to determine expression levels on relevant target cells. This will make it possible to assess the significance of coreceptor use determined from in vitro assays using cell lines or transient expression systems.

Determining the levels at which various receptors are expressed is but one step in determining their significance in vivo, since it is also important to determine if they are expressed in relevant target cells. In general, this is likely to be limited to CD4-positive cells. However, HIV-1 has been detected in a variety of CD4-negative cells, and several HIV-2 and many SIV strains have been identified that can utilize either CXCR4 or CCR5 for cellular entry in the absence of CD4 (Edinger97,18Endres96,19Reeves9736). In the case of SIV, a number of neurotropic SIV isolates have been shown to infect brain capillary endothelial cells, the principal component of the blood-brain barrier, in a CD4-independent, CCR5-dependent manner (Edinger9718). Thus, expression of an HIV-1 coreceptor in some CD4 negative cells may still have implications for viral pathogenesis. In fact, for many receptors, expression in cells other than T-cells and macrophages may be the only place that they support virus infection, at least during the early stages of disease - it is becoming increasingly clear that the R5 viruses which predominate during the asymptomatic period of the disease fail to infect stimulated PBMCs from individuals who lack CCR5, indicating that receptors such as CCR2b and CCR3 do not play a significant role in supporting virus entry into the primary targets of HIV-1 in vivo (Zhang9750). However, this may not be the case for viruses which emerge later in the course of disease.

Another important consideration in determining the in vivo relevance of an alternative coreceptor is the number and type of virus strains than can use the coreceptor, and if there is any correlation between viral phenotype and its use. Also, studies of sequential virus isolates may reveal correlations between the acquisition of the ability to use a given coreceptor and clinical aspects of HIV-1 disease, such as the development of neurological symptoms. Ultimately, identification of the ligands for orphan receptors and the development of specific antibodies should make it possible to identify the coreceptors that can be used by HIV-1 to enter various cell types.

The expression of a given coreceptor in conjunction with CD4 is not necessarily sufficient for virus infection. For example, CXCR4 is expressed on the surface of macrophages, which are resistant to infection by virus strains which use this receptor. Interestingly, infection of macrophages obtained from CCR5-negative individuals by a dual-tropic virus isolate, 89.6, is inhibited by the CXCR4 ligand SDF-1, suggesting that CXCR4 can be used as a coreceptor on the surface of macrophages, albeit rarely Yi98 . There are a variety of reasons why CXCR4 may not generally support entry of HIV-1 into macrophages, including differential posttranslational processing, surface expression levels relative to CD4 (as discussed above), and the way in which CXCR4 is presented in relation to CD4. At present, very little is known about the architecture of the fusion site - the number of molecules of env, CD4, and coreceptor that are required for a productive membrane fusion reaction, and their spatial relationships relative to one another.

Summary

The discovery of the HIV-1 coreceptors has important implications for understanding viral tropism and pathogenesis. Identifying which coreceptors are used by particular virus strains, and then determining whether their use correlates with particular aspects of viral pathogenesis, will be of general interest. Thus, a list of coreceptors used by virus strains will be maintained and updated yearly in this database. In addition, this will provide a forum where recent advances in the field can be discussed, particularly with regards as to how coreceptor usage patterns can be determined and our understanding of the significance of receptors other than CCR5 and CXCR4. If other receptors are found to be important for viral pathogenesis, then the classification scheme that we have proposed can be modified to take these new findings into account.

Acknowledgements

The authors thank Satish Pillai and Brian Foley for carefully reviewing.

Strain	   Proposed 	Primary 	Other 		Designationc	Receptord	Receptorse	References
      	   Accessiona    Clade		Tropismb
      
DJ258 	   L22939          A 		   NSI 		   R5 		  CCR5				Trkola97  
92RW026	   NA		   A	           NSI		   R5 		  CCR5				Trkola97  
93KE101    NA		   A 	           NSI 		   R5 		  CCR5				Zhang96  
93IN103    NA		   A               NSI 		   R5 		  CCR5				Zhang96  
92UG037-8 U51190 	   A               NSI 		   R5 		  CCR5 		CCR8*           Bjorndal97,Rucker97  
92RW020-5 U08794	   A               NSI 		   R5 		  CCR5				Rucker97  
92UG31    L34667           A               NSI 		   R5 		  CCR5				Dittmar97  
92RW20    U08794           A               NSI 		   R5 		  CCR5				Dittmar97  
92UG029    NA              A                SI 		   X4 		  CXCR4				Trkola97  
92RW009   U88823           A                SI 		   R5X4           CXCR4, CCR5    		Zhang96  
JR-FL     U63632           B               NSI             R5             CCR5          CCR3            Deng97,Farzan97,Rucker97 
JR-CSF    M38429           B               NSI             R5             CCR5                          Simmons96,Trkola97,Zhang96  
SF162     M65024           B               NSI             R5             CCR5          STRL33*         Liao97,Rucker97  
YU2       M93258           B               NSI             R5             CCR5          CCR3, GPR15     Choe96,Farzan97  
ADA       AF004394         B               NSI             R5             CCR5          CCR3, GPR15,    Choe96,Farzan97,Rucker97
                                                                                        STRL33*, CCR8
Ba-L      M68893           B               NSI             R5             CCR5          CCR3, STRL33*   Deng97,Dragic96,Liao97,Rucker97  
92US657   U04908           B               NSI             R5             CCR5                          Trkola97  
92US715.6 U08451           B               NSI             R5             CCR5                          Bjorndal97  
92Br20-4  U08797           B               NSI             R5             CCR5                          Choe96,Rucker97  
91US005.11U27434           B               NSI             R5             CCR5                          Bjorndal97,Rucker97  
SL-2      NA               B               NSI             R5             CCR5                          Simmons96  
92TH014.12U08801           B               NSI             R5             CCR5                          Bjorndal97  
CM243     NA               B               NSI             R5             CCR5          GPR15, STRL33   Rucker97  
M23       NA               B               NSI             R5             CCR5                          Dittmar97  
E80       NA               B               NSI             R5             CCR5                          Dittmar97  
BR92      NA               B               NSI             R5             CCR5                          Dittmar97  
BR49      NA               B               NSI             R5             CCR5                          Dittmar97  
BR53      NA               B               NSI             R5             CCR5                          Dittmar97  
BR90      NA               B               NSI             R5             CCR5                          Dittmar97  
92HA593g  U08444           B 		   SI 		   R5X4 	  CXCR4, CCR5    		Zhang96  
92HT593.1gU08444 	   B               NSI             R5X4           CXCR4, CCR5   		Bjorndal97  
 
2028      NA               B                SI             R5X4           CXCR4, CCR5   CCR3            Dittmar97,Simmons96  
2076      NA               B                SI             R5X4           CXCR4, CCR5                   Dittmar97,Simmons96,Trkola97  
89.6      U39362           B                SI             R5X4           CXCR4, CCR5   CCR3, CCR2b,    Farzan97,Rucker97 
                                                                                        CCR8, V28
DH123     NA               B                SI             R5X4           CXCR4, CCR5                   Trkola97  
Isolate   NA               B                SI             R5X4           CXCR4, CCR5                   Trkola97  
C 7/86 
92HA594   U08445           B                SI             R5X4           CXCR4, CCR5                   Zhang96  
92HA596   U08446           B                SI             R5X4           CXCR4, CCR5                   Zhang96  
M13       NA               B                SI             R5X4           CXCR4, CCR5                   Simmons96  
2006      NA               B                SI             R5X4           CXCR4, CCR5                   Simmons96  
2044      NA               B                SI             R5X4           CXCR4, CCR5                   Simmons96  
2036      NA               B                SI             R5X4           CXCR4, CCR5                   Simmons96  
2005      NA               B                SI             R5X4           CXCR4, CCR5                   Simmons96  
92HT599.24U08447           B                SI             X4             CXCR4                         Bjorndal97  
BK132     L03697           B                SI             X4             CXCR4         CCR3*, CCR8*    Rucker97  
BR65      NA               B                SI             X4             CXCR4                         Dittmar97  
HC4       NA               B                SI             X4             CXCR4                         Trkola97  
SF2       K02007           B                SI/TCLA        R5X4           CXCR4, CCR5                   Trkola97  
RF        M17451           B                SI/TCLA        R5X4           CXCR4, CCR5                   Alkhatib96,Deng97,Rucker97  
NL 4-3    M19921           B                SI/TCLA        X4             CXCR4                         Trkola97,Zhang96  
LAI       X01762           B                SI/TCLA        X4             CXCR4                         Trkola97  
HXBc2     K03455           B                SI/TCLA        X4             CXCR4                         Choe96  
GUN-1     D34590           B                SI/TCLA        R5X4           CXCR4, CCR5                   Simmons96  
BH8       K02011           B                SI/TCLA        X4             CXCR4         CCR3*, STRL33*  Rucker97  
92ZW101   NA               C                NSI            R5             CCR5                          Zhang96  
92BR025.9 U52953           C                NSI            R5             CCR5                          Bjorndal97,Dittmar97  
BR28      NA	           C                NSI            R5             CCR5                          Dittmar97  
93MW965.26U08455           C                NSI            R5             CCR5                          Bjorndal97  
BR70      NA               C                NSI            R5             CCR5                          Dittmar97  
JW1       NA               C                NSI            R5             CCR5                          Dittmar97  
JW4       NA               C                NSI            R5             CCR5                          Dittmar97  
92ZW102   NA               C                NSI            R5             CCR5                          Zhang96  
 
DJ259     L22940           C                NSI            R5             CCR5                          Trkola97  
94ZW103   NA               C                NSI            R5             CCR5                          Trkola97  
94ZW109   NA               C                NSI            R5             CCR5                          Trkola97  
92ZW106   NA               C                 SI            X4             CXCR4                         Zhang96  
ZAM20     L22956           C                 SI            X4             CXCR4                         Trkola97  
94ZW106   NA               C                 SI            X4             CXCR4                         Trkola97  
94KE102   NA               D                NSI            R5             CCR5                          Trkola97,Zhang96  
94KE103   NA               D                NSI            R5             CCR5                          Trkola97,Zhang96  
92UG046   U08737           D                 SI            X4             CXCR4                         Trkola97  
UG270     NA               D                 SI            X4             CXCR4                         Trkola97  
92UG024.2 U08726           D                 SI            X4             CXCR4         CCR8*, V28*,    Bjorndal97,Rucker97,Trkola97
                                                                                        CCR3f
92UG021.16U27399           D                 SI            X4             CXCR4                         Bjorndal97  
JW5       NA               D                 SI            X4             CXCR4                         Dittmar97  
NDK       M27323           D                 SI            X4             CXCR4         GPR15           Deng97,Pleskoff97b  
93ZR001.3 U27419           D                 NA            X4             CXCR4         V28*            Rucker97  
CM235     NA               E                NSI            R5             CCR5                          Trkola97  
92TH001   NA               E                NSI            R5             CCR5                          Trkola97  
M53       NA               E                NSI            R5             CCR5                          Dittmar97  
92TH22    U09131           E                NSI            R5             CCR5                          Dittmar97  
92TH23    NA               E                NSI            R5             CCR5                          Dittmar97  
C2        NA               E                NSI            R5             CCR5                          Dittmar97  
93TH305   NA               E                NSI            R5             CCR5                          Zhang96  
93TH307   NA               E                NSI            R5             CCR5                          Zhang96  
93TH966.8 U08456           E                NSI            R5             CCR5                          Bjorndal97  
93TH976.17U08458           E                 NA            R5             CCR5                          Bjorndal97  
93TH304   NA               E                 SI            R5X4           CXCR4, CCR5                   Zhang96  
SL6       NA               E                 SI            X4             CXCR4                         Dittmar97  
SL7       NA               E                 SI            X4             CXCR4                         Dittmar97  
SL8       NA               E                 SI            X4             CXCR4                         Dittmar97  
94TH304   NA               E                 SI            X4             CXCR4                         Trkola97  
BR58      NA               F                 SI            R5X4           CXCR4, CCR5   CCR3            Dittmar97  
BZ162     L22084           F                NSI            R5             CCR5                          Trkola97  
R1        NA               F                NSI            R5             CCR5                          Trkola97  
93BR029.2 U27413           F                 NA            R5             CCR5                          Rucker97  
92UG975.10U27426           G                NSI            R5             CCR5                          Bjorndal97  
CA9       NA               O                NSI            R5             CCR5                          Zhang96  
MVP5180   L20571           O                 SI            R5X4           CXCR4, CCR5                   Zhang96  

Footnotes:
a Accession numbers refer to sequences from the described isolate that contain the longest available sequence including Env (full length genome when available, down to a minimum of the V3 region), but may not pertain directly to the sample used to determine the isolate's phenotype. Accession numbers have been deemed "NA" if there are no related locus names in the HIV Database, or if there is insufficient information to conclude that a similarly named locus in the database is referring to the same isolate.
b The tropism for each virus strain is indicated. SI = syncytium inducing; NSI = non syncytium inducing; SI/TCLA = syncytium inducing T-cell line adapted; NA = not available.
c As described in the text, we have proposed that viruses which use CCR5 be termed R5 viruses, viruses that use CXCR4 be termed X4 viruses, and viruses that use both be termed R5X4 viruses. For a virus to be termed an R5X4 virus, CXCR4 must be used at > 10% of the efficiency of CCR5 for viruses that use CCR5 as their primary receptor, or CCR5 must be used at > 10% of the efficiency of CXCR4 for viruses that use CXCR4 as their primary receptor.
d All virus strains in the Table have been tested for the ability to use CCR5 and CXCR4. The receptors used by each strain are indicated. For both receptors to be listed, the least efficiently used receptor must support virus entry by >10% of the levels supported by the most efficiently used receptor. For viruses that use both receptors, CXCR4 is listed first; this does not mean that CXCR4 is used more efficiently than CCR5.
e Receptors other than CCR5 or CXCR4 that are used by the indicated strains are listed. Since most viruses have not yet been tested for the ability to use receptors other than CCR5 and CXCR4, the absence of other receptors used in the Table should not be taken to mean that a virus uses only CCR5 or CXCR4. For example, if CCR3 is not listed as being used by a given virus strain, it may be because it has not yet been tested. Receptors that have been shown by experiments not to be used by a given virus strain are not indicated. Occasionally there are discrepancies in the literature concerning the use of one or more receptors. In these cases, we opted for `majority rules'. If two papers report a positive result and one a negative result, the receptor is shown as being used.
f The virus isolate used CCR3 whereas the cloned env from this isolate did not [Bjorndal97].
*Indicates that coreceptor use was determined only by fusion assays rather than by virus infection.
g 92HT593.1 (cloned env gene) and 92HA593 (whole virus) come from the same isolate and gave slightly different results in references [Dittmar97] and [Zhang96].

References.

1. [Alkhatib etal.(1996)] G.Alkhatib, C.Combadiere, C.C. Broder, Y.Feng, P.E. Kennedy, P.M. Murphy, E.A. Berger. CC CKR5: a RANTES, MIP-1alpha, MIP-1beta receptor as a fusion cofactor for macrophage-tropic HIV-1. Science 272: 1955-8, 1996.

2. [Balotta etal.(1997)] C.Balotta, P.Bagnarelli, M.Violin, A.L. Ridolfo, D.Zhou, A.Berlusconi, S.Corvasce, M.Corbellino, M.Clementi, M.Clerici, M.Moroni, M.Galli. Homozygous delta 32 deletion of the CCR-5 chemokine receptor gene in an HIV-1-infected patient. AIDS 11: F67-71, 1997.

3. [Berger(1997)] E.A.Berger. HIV-1 entry and tropism: the chemokine receptor connection. AIDS 11 (supplement A): S3-S16, 1997.

4. [Berger etal.(1997)]: E.A. Berger, R.W. Doms, E.-M. Fenyo, B.T.M. Korber, D.R. Littman, J.P. Moore, Q.J. Sattentau, H.Schuitmaker, J.Sodroski, R.A. Weiss HIV-1: phenotypes classified by coreceptor usage. Nature: In press: , 1997.

5. [Biti etal.(1997)]: Biti97: R.Biti, R.Ffrench, J.Young, B.Bennetts, G.Stewart, T.Liang HIV-1: infection in an individual homozygous for the CCR5 deletion allele (letter; comment). Nat Med: 3: 252-3, 1997.

6. [Bjorndal etal.(1997)]: Bjorndal97: A.Bjorndal, H.Deng, M.Jansson, J.R. Fiore, C.Colognesi, A.Karlsson, J.Albert, G.Scarlatti, D.R. Littman, E.M. Fenyo. Coreceptor usage of primary human immunodeficiency virus type 1 isolates varies according to biological phenotype. J Virol: 71: 7478-87, 1997.

7. [Brelot etal.(1997)]: Brelot97: A.Brelot, N.Heveker, O.Pleskoff, N.Sol, M.Alizon. Role of the first and third extracellular domains of CXCR-4 in human immunodeficiency virus coreceptor activity. J Virol: 71: 4744-51, 1997.

8. [Broder Collman(1997)]: Broder97: C.C. Broder R.G. Collman. Chemokine receptors and : HIV.: J Leukoc Biol: 62: 20-9, 1997.

9. [Choe etal.(1996)]: Choe96: H.Choe, M.Farzan, Y.Sun, N.Sullivan, B.Rollins, P.D. Ponath, L.Wu, C.R. Mackay, G LaRosa, W.Newman, N.Gerard, C.Gerard, J.Sodroski. The beta-chemokine receptors CCR3 and CCR5 facilitate infection by primary HIV-1 isolates. Cell: 85: 1135-48, 1996.

10. [Collman etal.(1992)] Collman92 R.Collman, J.W. Balliet, S.A. Gregory, H.Friedman, D.L. Kolson, N.Nathanson, A.Srinivasan. An infectious molecular clone of an unusual macrophage-tropic and highly cytopathic strain of human immunodeficiency virus type 1. J Virol: 66: 7517-21, 1992.

11. [Connor etal.(1993)] Connor93 R.I. Connor, H.Mohri, Y.Cao, D.D. Ho. Increased viral burden and cytopathicity correlate temporally with CD4+ T-lymphocyte decline and clinical progression in human immunodeficiency virus type 1-infected individuals. J Virol: 67: 1772-7, 1993.

12. [Dean etal.(1996)]: Dean96: M.Dean, M.Carrington, C.Winkler, G.A. Huttley, M.W. Smith, R.Allikmets, J.J. Goedert, S.P. Buchbinder, E.Vittinghoff, E.Gomperts, S.Donfield, D.Vlahov, R.Kaslow, A.Saah, C.Rinaldo, R.Detels, S.J. O'Brien, Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Hemophilia Growth and Development Study, Multicenter AIDS Cohort Study, Multicenter Hemophilia Cohort Study, San Francisco City Cohort, ALIVE Study (see comments) (published erratum appears in Science 1996 Nov 15;274(5290):1069). Science: 273: 1856-62, 1996.

13. [Deng etal.(1997)]: Deng97: H.K. Deng, D.Unutmaz, V.N. KewalRamani , D.R. Littman. Expression cloning of new receptors used by simian and human immunodeficiency viruses (see comments). Nature: 388: 296-300, 1997.

14. [Dittmar etal.(1997)]: Dittmar97 M.T. Dittmar, G.Simmons, S.Hibbitts, M. O'Hare , S.Louisirirotchanakul, S.Beddows, J.Weber, P.R. Clapham, R.A. Weiss. Langerhans cell tropism of human immunodeficiency virus type 1 subtype A through F isolates derived from different transmission groups. J Virol: 71: 8008-13, 1997.

15. [Doms Peiper(1997)]: Doms97: R.W. Doms S.C. Peiper. Unwelcomed guests with master keys how HIV uses chemokine receptors for cellular entry. Virology: 235: 179-90, 1997.

16. [Doranz etal.(1996)]: Doranz96: B.J. Doranz, J.Rucker, Y.Yi, R.J. Smyth, M.Samson, S.C. Peiper, M.Parmentier, R.G. Collman, R.W. Doms. A dual-tropic primary HIV-1 isolate that uses fusin and the beta- chemokine receptors CKR-5,: : CKR-3, and CKR-2b: as fusion cofactors. Cell: 85: 1149-58, 1996.

17. [Dragic etal.(1996)]: Dragic96 T.Dragic, V.Litwin, G.P. Allaway, S.R. Martin, Y.Huang, K.A. Nagashima, C.Cayanan, P.J. Maddon, R.A. Koup, J.P. Moore, W.A. Paxton. HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC- CKR-5 (see comments). Nature: 381: 667-73, 1996.

18. [Edinger etal.(1997)] Edinger97 A.L. Edinger, J.L. Mankowski, B.J. Doranz, B.J. Margulies, B.Lee, J.Rucker, M.Sharron, T.L. Hoffman, J.F. Berson, M.C. Zink, V.M. Hirsch, J.E. Clements, R.W. Doms. CD4-independent , CCR5-dependent infection of brain capillary endothelial cells by neurovirulent SIV . Proc. Natl. Acad. Sci. USA: In press: 1997.

19. [Endres etal.(1996)]: Endres96: M.J. Endres, P.R. Clapham, M.Marsh, M.Ahuja, J.D. Turner, A. McKnight: , J.F. Thomas, B. Stoebenau-Haggarty: , S.Choe, P.J. Vance, T.N. Wells, C.A. Power, S.S. Sutterwala, R.W. Doms, N.R. Landau, J.A. Hoxie. CD4-independent infection by HIV-2: is mediated by fusin/CXCR4. Cell: 87 745-56, 1996.

20. [Farzan etal.(1997)]: Farzan97: M.Farzan, H.Choe, K.Martin, L.Marcon, W.Hofmann, G.Karlsson, Y.Sun, P.Barrett, N.Marchand, N.Sullivan, N.Gerard, C.Gerard, J.Sodroski. Two orphan seven-transmembrane segment receptors which are expressed in : CD4-positive: cells support simian immunodeficiency virus infection. J Exp Med. 186 405-11, 1997.

21. [Feng etal.(1996)] Feng96 Y.Feng, C.C. Broder, P.E. Kennedy, E.A. Berger. HIV-1 entry cofactor functional cDNA: cloning of a seven-transmembrane, G protein-coupled receptor (see comments). Science: 272: 872-7, 1996.

22. [Fenyo etal.(1988)] Fenyo88 E.M. Fenyo, L. Morfeldt-Manson , F.Chiodi, B.Lind, G.von A., J.Albert, E.Olausson, B.Asjo. Distinct replicative and cytopathic characteristics of human immunodeficiency virus isolates. J Virol: 62: 4414-9, 1988.

23. [Fouchier etal.(1992)] Fouchier92 R.A. Fouchier, M.Groenink, N.A. Kootstra, M.Tersmette, H.G. Huisman, F.Miedema, H.Schuitemaker. Phenotype-associated sequence variation in the third variable domain of the human immunodeficiency virus type 1 gp120 molecule. J Virol: 66: 3183-7, 1992.

24. [He etal.(1997)] He97: J.He, Y.Chen, M.Farzan, H.Choe, A.Ohagen, S.Gartner, J.Busciglio, X.Yang, W.Hofmann, W.Newman, C.R. Mackay, J.Sodroski, D.Gabuzda. CCR3 and CCR5 are co-receptors for : HIV-1: infection of microglia. Nature: 385: 645-9, 1997.

25. [J. etal.(1992)] DeJong92 d.J. J., J.Goudsmit, W.Keulen, B.Klaver, W.Krone, M.Tersmette, d.A. Human immunodeficiency virus type 1 clones chimeric for the envelope V3 domain differ in syncytium formation and replication capacity. J Virol: 66: 757-65, 1992.

26. [Kozak etal.(1997)] Kozak97 S.L. Kozak, E.J. Platt, N.Madani, F.E.F. Jr, K.Peden, D.Kabat. CD4, CXCR-4, and CCR-5 dependencies for infections by primary patient and laboratory-adapted isolates of human immunodeficiency virus type 1. J Virol: 71: 873-82, 1997.

27. [Liao etal.(1997)] Liao97 F.Liao, G.Alkhatib, K.W. Peden, G.Sharma, E.A. Berger, J.M. Farber. STRL33, A novel chemokine receptor-like protein, functions as a fusion cofactor for both macrophage-tropic and T cell line-tropic HIV-1. J Exp Med: 185: 2015-23, 1997.

28. [Liu etal.(1996)] Liu96 R.Liu, W.A. Paxton, S.Choe, D.Ceradini, S.R. Martin, R.Horuk, M.E. MacDonald , H.Stuhlmann, R.A. Koup, N.R. Landau. Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection. Cell: 86: 367-77, 1996.

29. [Lu etal.(1997)] Lu97 Z.Lu, J.F. Berson, Y.Chen, J.D. Turner, T.Zhang, M.Sharron, M.H. Jenks, Z.Wang, J.Kim, J.Rucker, J.A. Hoxie, S.C. Peiper, R.W. Doms. Evolution of HIV-1: coreceptor usage through interactions with distinct CCR5 and CXCR4 domains. Proc Natl Acad Sci U S A: 94: 6426-31, 1997.

30. [Michael etal.(1997)] Michael97 N.L. Michael, G.Chang, L.G. Louie, J.R. Mascola, D.Dondero, D.L. Birx, H.W. Sheppard. The role of viral phenotype and : CCR-5: gene defects in HIV-1 transmission and disease progression. Nat Med: 3: 338-40, 1997.

31. [Moore(1997)] Moore97 J.P. Moore. Coreceptors implications for HIV pathogenesis and therapy. Science: 276: 51-2, 1997.

32. [: O'Brien: etal.(1997)] OBrien97 T.R. O'Brien , C.Winkler, M.Dean, J.A. Nelson, M.Carrington, N.L. Michael, G.C.W. 2nd. HIV-1 infection in a man homozygous for : CCR5: delta 32 (letter). Lancet: 349: 1219, 1997.

33. [Pleskoff etal.(1997a)] Pleskoff97b O.Pleskoff, N.Sol, B.Labrosse, M.Alizon. Human immunodeficiency virus strains differ in their ability to infect CD4+ cells expressing the rat homolog of CXCR-4 (fusin). J Virol: 71: 3259-62, 1997a.

34. [Pleskoff etal.(1997b)] Pleskoff97a O.Pleskoff, C.Treboute, A.Brelot, N.Heveker, M.Seman, M.Alizon. Identification of a chemokine receptor encoded by human cytomegalovirus as a cofactor for : HIV-1: entry (see comments). Science: 276: 1874-8, 1997b.

35. [Rana etal.(1997)] Rana97 S.Rana, G.Besson, D.G. Cook, J.Rucker, R.J. Smyth, Y.Yi, J.D. Turner, H.H. Guo, J.G. Du, S.C. Peiper, E.Lavi, M.Samson, F.Libert, C.Liesnard, G.Vassart, R.W. Doms, M.Parmentier, R.G. Collman. Role of CCR5 in infection of primary macrophages and lymphocytes by macrophage-tropic strains of human immunodeficiency virus: resistance to patient-derived and prototype isolates resulting from the delta ccr5 mutation. J Virol: 71: 3219-27, 1997.

36. [Reeves etal.(1997)] Reeves97 J.D. Reeves, A.: McKnight , S.Potempa, G.Simmons, P.W. Gray, C.A. Power, T.Wells, R.A. Weiss, S.J. Talbot. CD4-independent infection by : HIV-2: (ROD/B) use of the 7-transmembrane receptors CXCR-4, CCR-3, and V28 for entry. Virology: 231: 130-4, 1997.

37. [Roos etal.(1992)] Roos92 M.T. Roos, J.M. Lange, d.R. E., R.A. Coutinho, P.T. Schellekens, F.Miedema, M.Tersmette. Viral phenotype and immune response in primary human immunodeficiency virus type 1 infection. J Infect Dis: 165: 427-32, 1992.

38. [Rucker etal.(1997)] Rucker97 J.Rucker, A.L. Edinger, M.Sharron, M.Samson, B.Lee, J.F. Berson, Y.Yi, B.Margulies, R.G. Collman, B.J. Doranz, M.Parmentier, R.W. Doms. Utilization of chemokine receptors, orphan receptors, and herpesvirus encoded receptors by diverse human and simian immunodeficiency viruses. J Virol: 71: 8999-9007, 1997.

39. [Samson etal.(1997)] Samson97 M.Samson, A.L. Edinger, S.P., J.Rucker, V.Verhasselt, M.Sharron, C.Govaerts, C.Mollereau, G.Vassart, R.W. Doms, M.Parmentier. ChemR23: , a putative chemoattractant receptor, is expressed in dendritic cells and is a coreceptor for SIV and some primary HIV-1 strains. Submitted: 1997.

40. [Samson etal.(1996)] Samson96 M.Samson, F.Libert, B.J. Doranz, J.Rucker, C.Liesnard, C.M. Farber, S.Saragosti, C.Lapoumeroulie, J.Cognaux, C.Forceille, G.Muyldermans, C.Verhofstede, G.Burtonboy, M.Georges, T.Imai, S.Rana, Y.Yi, R.J. Smyth, R.G. Collman, R.W. Doms, G.Vassart, M.Parmentier. Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene (see comments). Nature: 382: 722-5, 1996.

41. [Schuitemaker etal.(1992)] Schuitemaker92 H.Schuitemaker, M.Koot, N.A. Kootstra, M.W. Dercksen, d.R. E., S.van R.P., J.M. Lange, J.K. Schattenkerk, F.Miedema, M.Tersmette. Biological phenotype of human immunodeficiency virus type 1 clones at different stages of infection: progression of disease is associated with a shift from monocytotropic to : T-cell-tropic: virus population. J Virol: 66: 1354-60, 1992.

42. [Simmons etal.(1996)] Simmons96 G.Simmons, D.Wilkinson, J.D. Reeves, M.T. Dittmar, S.Beddows, J.Weber, G.Carnegie, U.Desselberger, P.W. Gray, R.A. Weiss, P.R. Clapham. Primary, syncytium-inducing human immunodeficiency virus type 1 isolates are dual-tropic and most can use either Lestr or CCR5 as coreceptors for virus entry. J Virol: 70: 8355-60, 1996.

43. [Tersmette etal.(1988)] Tersmette88 M.Tersmette, d.R. E., B.J. Al, I.N. Winkel, R.A. Gruters, H.T. Cuypers, H.G. Huisman, F.Miedema. Differential syncytium-inducing capacity of human immunodeficiency virus isolates frequent detection of syncytium-inducing isolates in patients with acquired immunodeficiency syndrome (AIDS) and AIDS- related complex. J Virol: 62: 2026-32, 1988.

44. [Tersmette etal.(1989)] Tersmette89 M.Tersmette, J.M. Lange, d.R. E., W.F., J.K. Eeftink-Schattenkerk , P.T. Schellekens, R.A. Coutinho, J.G. Huisman, J.Goudsmit, F.Miedema. Association between biological properties of human immunodeficiency virus variants and risk for AIDS and AIDS mortality. Lancet: 1: 983-5, 1989.

45. [Theodorou etal.(1997)] Theodorou97 I.Theodorou, L.Meyer, M.Magierowska, C.Katlama, C.Rouzioux. HIV-1 infection in an individual homozygous for CCR5 delta 32. Seroco Study Group (letter). Lancet: 349: 1219-20, 1997.

46. [Trkola etal.(1996)] Trkola96 A.Trkola, T.Dragic, J.Arthos, J.M. Binley, W.C. Olson, G.P. Allaway, C. Cheng-Mayer , J.Robinson, P.J. Maddon, J.P. Moore. CD4-dependent, antibody-sensitive interactions between HIV-1 and its co- receptor CCR-5 (see comments). Nature: 384: 184-7, 1996.

47. [Trkola etal.(1997)] Trkola97 A.Trkola, W.A. Paxton, S.P. Monard, J.A. Hoxie, M.A. Siani, D.A. Thompson, L.Wu, C.R. Mackay, R.Horuk, , J.P. Moore. Genetic subtype-independent inhibition of human immunodeficiency virus type 1 replication by CC and CXC-chemokines . Submitted: 1997.

48. [Wu etal.(1996)] Wu96 L.Wu, N.P. Gerard, R.Wyatt, H.Choe, C.Parolin, N.Ruffing, A.Borsetti, A.A. Cardoso, E.Desjardin, W.Newman, C.Gerard, J.Sodroski. CD4-induced interaction of primary HIV-1 gp120 glycoproteins with the chemokine receptor CCR-5 (see comments). Nature: 384: 179-83, 1996.

49. [Yi etal.(1998)] Yi98 Y.Yi, J.D. Turner, N.Gaddis, R.G. Collman. Cxcr4 is expressed by primary macrophages and supports ccr5-independent infection by dual-tropic but not t-tropic isolates of HIV-1. J Virol: Submitted: 1998.

51. [Zhang etal.(1996)] Zhang96 L.Zhang, Y.Huang, T.He, Y.Cao, D.D. Ho. HIV-1 subtype and second-receptor use (letter). Nature: 383: 768, 1996.

52. [Zhu etal.(1993)] Zhu93 T.Zhu, H.Mo, N.Wang, D.S. Nam, Y.Cao, R.A. Koup, D.D. Ho. Genotypic and phenotypic characterization of HIV-1 patients with primary infection. Science: 261: 1179-81, 1993.

last modified: Wed Mar 17 15:23 2010


Questions or comments? Contact us at seq-info@lanl.gov.

 
Operated by Los Alamos National Security, LLC, for the U.S. Department of Energy's National Nuclear Security Administration
Copyright © 2005-2012 LANS LLC All rights reserved | Disclaimer/Privacy

Dept of Health & Human Services Los Alamos National Institutes of Health