RESUMEN
The melanin concentrating hormone (MCH) system is a new target to treat human disorders. Our aim was the preparation of the first PET-tracer for the MCHR1. [(11)C]SNAP-7941 is a carbon-11 labeled analog of the published MCHR1 antagonist SNAP-7941. The optimum reaction conditions were 2 min reaction time, ≤25°C reaction temperature, and 2 mg/mL precursor (SNAP-acid) in acetonitrile, using [(11)C]CH(3)OTf as methylation agent. [(11)C]SNAP-7941 was prepared in a reliable and feasible manner with high radiochemical yields (2.9±1.6 GBq; 11.5±6.4% EOB, n=15).
Asunto(s)
Radioisótopos de Carbono/química , Piperidinas/síntesis química , Tomografía de Emisión de Positrones , Pirimidinas/síntesis química , Receptores de Somatostatina/metabolismo , Humanos , Espectroscopía de Resonancia Magnética , Espectrometría de Masas , Control de CalidadRESUMEN
Herpesviridae comprises over 120 viruses infecting a wide range of vertebrates including humans and livestock. Herpesvirus infections typically produce dermal lesions or immune cell destruction, but can also lead to oncogenesis, especially with KSHV (Kaposi's sarcoma-associated herpesvirus). All herpesviruses are nuclear replicating viruses that subvert cellular processes such as nucleocytoplasmic transport for their advantage. For virus replication to take over the cell and produce lytic infection requires that virus gene expression outpace that of the host cell. KSHV ORF57 (open reading frame 57) appears to play a major role in this by (i) serving as a nuclear export receptor to carry intronless viral mRNAs out of the nucleus and (ii) inhibiting expression of intron-containing host mRNAs. As most of the virally encoded mRNAs are intronless compared with host cell mRNAs, these two mechanisms are critical to overcoming host gene expression.
Asunto(s)
Regulación Viral de la Expresión Génica , Herpesviridae/genética , Herpesviridae/aislamiento & purificación , Proteínas Represoras/genética , Sarcoma de Kaposi/virología , Transactivadores/genética , Proteínas Virales/genética , Núcleo Celular/fisiología , Núcleo Celular/virología , Citoplasma/fisiología , Citoplasma/virología , Humanos , Transporte de Proteínas , Virus ARN/genética , ARN Mensajero/genéticaRESUMEN
The nuclear lamina is a meshwork of intermediate-type filament proteins (lamins) that lines the inner nuclear membrane. The lamina is proposed to be an important determinant of nuclear structure, but there has been little direct testing of this idea. To investigate lamina functions, we have characterized a novel lamin B1 mutant lacking the middle approximately 4/5 of its alpha-helical rod domain. Though retaining only 10 heptads of the rod, this mutant assembles into intermediate filament-like structures in vitro. When expressed in cultured cells, it concentrates in patches at the nuclear envelope. Concurrently, endogenous lamins shift from a uniform to a patchy distribution and lose their complete colocalization, and nuclei become highly lobulated. In vitro binding studies suggest that the internal rod region is important for heterotypic associations of lamin B1, which in turn are required for proper organization of the lamina. Accompanying the changes in lamina structure induced by expression of the mutant, nuclear pore complexes and integral membrane proteins of the inner membrane cluster, principally at the patches of endogenous lamins. Considered together, these data indicate that lamins play a major role in organizing other proteins in the nuclear envelope and in determining nuclear shape.
Asunto(s)
Núcleo Celular/ultraestructura , Proteínas de Filamentos Intermediarios/metabolismo , Lamina Tipo B , Membrana Nuclear/ultraestructura , Proteínas Nucleares/metabolismo , Animales , Células COS , Núcleo Celular/metabolismo , Células HeLa , Humanos , Filamentos Intermedios/metabolismo , Laminas , Mutación , Membrana Nuclear/metabolismo , Poro Nuclear/metabolismo , Unión Proteica , Ingeniería de Proteínas , Estructura Terciaria de Proteína , Proteínas Recombinantes/metabolismo , Eliminación de SecuenciaRESUMEN
Point mutations in either of the two nucleotide-binding domains (NBD) of Hsp104 (NBD1 and NBD2) eliminate its thermotolerance function in vivo. In vitro, NBD1 mutations virtually eliminate ATP hydrolysis with little effect on hexamerization; analogous NBD2 mutations reduce ATPase activity and severely impair hexamerization. We report that high protein concentrations overcome the assembly defects of NBD2 mutants and increase ATP hydrolysis severalfold, changing V(max) with little effect on K(m). In a complementary fashion, the detergent 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate inhibits hexamerization of wild-type (WT) Hsp104, lowering V(max) with little effect on K(m). ATP hydrolysis exhibits a Hill coefficient between 1.5 and 2, indicating that it is influenced by cooperative subunit interactions. To further analyze the effects of subunit interactions on Hsp104, we assessed the effects of mutant Hsp104 proteins on WT Hsp104 activities. An NBD1 mutant that hexamerizes but does not hydrolyze ATP reduces the ATPase activity of WT Hsp104 in vitro. In vivo, this mutant is not toxic but specifically inhibits the thermotolerance function of WT Hsp104. Thus, interactions between subunits influence the ATPase activity of Hsp104, play a vital role in its biological functions, and provide a mechanism for conditionally inactivating Hsp104 function in vivo.
Asunto(s)
Adenosina Trifosfato/metabolismo , Proteínas de Choque Térmico/química , Proteínas de Choque Térmico/metabolismo , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/metabolismo , Adenosina Trifosfatasas/química , Adenosina Trifosfatasas/metabolismo , Sustitución de Aminoácidos , Sitios de Unión , Estradiol/farmacología , Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Cinética , Mutagénesis Sitio-Dirigida , Mutación Puntual , Subunidades de Proteína , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Saccharomyces cerevisiae/efectos de los fármacos , Saccharomyces cerevisiae/crecimiento & desarrolloRESUMEN
We present here a detailed analysis of a rat polypeptide termed Nup50 (formerly NPAP60) that was previously found to be associated with the nuclear pore complex (F. Fan et al., Genomics 40:444-453, 1997). We have found that Nup50 (and/or a related 70-kDa polypeptide) is present in numerous rat cells and tissues. By immunofluorescence microscopy, Nup50 was found to be highly concentrated at the nuclear envelope of rat liver nuclei, whereas in cultured NRK cells it also is abundant in intranuclear regions. On the basis of immunogold electron microscopy of both rat liver nuclear envelopes and NRK cells, we determined that Nup50 is specifically localized in the nucleoplasmic fibrils of the pore complex. Microinjection of anti-Nup50 antibodies into the nucleus of NRK cells resulted in strong inhibition of nuclear export of a protein containing a leucine-rich nuclear export sequence, whereas nuclear import of a protein containing a classical nuclear localization sequence was unaffected. Correspondingly, CRM1, the export receptor for leucine-rich export sequences, directly bound to a fragment of Nup50 in vitro, whereas several other import and export receptors did not significantly interact with this fragment. Taken together, our data indicate that Nup50 has a direct role in nuclear protein export and probably serves as a binding site on the nuclear side of the pore complex for export receptor-cargo complexes.
Asunto(s)
Núcleo Celular/metabolismo , Proteínas de Complejo Poro Nuclear , Proteínas Nucleares/metabolismo , Porinas/metabolismo , Receptores Citoplasmáticos y Nucleares , Animales , Transporte Biológico , Proteínas Portadoras/metabolismo , Células Cultivadas , Proteína de Susceptibilidad a Apoptosis Celular , Carioferinas , Hígado/citología , Hígado/metabolismo , Microscopía Fluorescente , Proteínas/metabolismo , Ratas , Proteína Exportina 1RESUMEN
Adenovirus, a respiratory virus with a double-stranded DNA genome, replicates in the nuclei of mammalian cells. We have developed a cytosol-dependent in vitro assay utilizing adenovirus nucleocapsids to examine the requirements for adenovirus docking to the nuclear pore complex and for DNA import into the nucleus. Our assay reveals that adenovirus DNA import is blocked by a competitive excess of classical protein nuclear localization sequences and other inhibitors of nuclear protein import and indicates that this process is dependent on hsc70. Previous work revealed that the hexon (coat) protein of adenovirus is the only major protein on the surface of the adenovirus nucleocapsid that docks at the nuclear pore complex. This, together with our finding that in vitro nuclear import of hexon is inhibited by an excess of classical nuclear localization sequences, suggests a role for the hexon protein in adenovirus DNA import. However, recombinant transport factors that are sufficient for hexon import in permeabilized cells do not support DNA import, indicating that there are other as yet unidentified factors required for this process.
Asunto(s)
Adenoviridae/metabolismo , Proteínas de la Cápside , Núcleo Celular/metabolismo , ADN Viral/metabolismo , Proteínas HSP70 de Choque Térmico/metabolismo , Anticuerpos/farmacología , Cápside/metabolismo , Técnica del Anticuerpo Fluorescente , Proteínas HSP70 de Choque Térmico/inmunología , Células HeLa , Humanos , Hibridación in Situ , Microscopía Electrónica , Membrana Nuclear/metabolismo , Membrana Nuclear/ultraestructura , Señales de Localización Nuclear , Proteínas Nucleares/metabolismo , Nucleocápside/metabolismo , Proteínas Recombinantes/metabolismoRESUMEN
Hsp104 is crucial for stress tolerance in Saccharomyces cerevisiae, and both of its nucleotide-binding domains (NBD1 and NBD2) are required. Here, we characterize the ATPase activity and oligomerization properties of wild-type (WT) Hsp104 and of NBD mutants. In physiological ionic strength buffers (pH 7.5, 37 degreesC) WT Hsp104 exhibits Michaelis-Menten kinetics between 0.5 and 25 mM ATP (Km approximately 5 mM, Vmax approximately 2 nmol min-1 microg-1). ATPase activity is strongly influenced by factors that vary with cell stress (e.g. temperature, pH, and ADP). Mutations in the P-loop of NBD1 (G217V or K218T) severely reduce ATP hydrolysis but have little effect on oligomerization. Analogous mutations in NBD2 (G619V or K620T) have smaller effects on ATPase activity but impair oligomerization. The opposite relationship was reported for another member of the HSP100 protein family, the Escherichia coli ClpA protein, in studies employing lower ionic strength buffers. In such buffers, the Km of WT Hsp104 for ATP hydrolysis decreased 10-fold and its stability under stress conditions increased, but the effects of the NBD mutations on ATPase activity and oligomerization remained opposite to those of ClpA. Either the functions of the two NBDs in ClpA and Hsp104 have been reversed or both contribute to ATP hydrolysis and oligomerization in a complex manner that can be idiosyncratically affected by such mutations.
Asunto(s)
Adenosina Trifosfatasas/metabolismo , Proteínas de Escherichia coli , Proteínas Fúngicas/metabolismo , Proteínas de Choque Térmico/metabolismo , Mutación Puntual , Proteínas de Saccharomyces cerevisiae , Adenosina Trifosfato/metabolismo , Endopeptidasa Clp , Proteínas Fúngicas/genética , Proteínas de Choque Térmico/genética , Hidrólisis , Cinética , Mutagénesis Sitio-Dirigida , Concentración Osmolar , Serina Endopeptidasas/genética , Serina Endopeptidasas/metabolismo , Relación Estructura-ActividadAsunto(s)
Proteínas de Choque Térmico/química , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/química , Adenosina Trifosfatasas/análisis , Clonación Molecular , Escherichia coli/química , Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Expresión Génica/genética , Proteínas de Choque Térmico/genética , Proteínas de Choque Térmico/aislamiento & purificación , Proteínas de Choque Térmico/metabolismo , Proteínas de Choque Térmico/toxicidad , Mutación/genética , Plásmidos/genética , Conformación ProteicaRESUMEN
The [PSI+] factor of S. cerevisiae represents a new form of inheritance: cytosolic transmission of an altered phenotype is apparently based upon inheritance of an altered protein structure rather than an altered nucleic acid. The molecular basis of its propagation is unknown. We report that purified Sup35 and subdomains that induce [PSI+] elements in vivo form highly ordered fibers in vitro. Fibers bind Congo red and are rich in beta sheet, characteristics of amyloids found in certain human diseases, including the prion diseases. Some fibers have distinct structures and these, once initiated, are self-perpetuating. Preformed fibers greatly accelerate fiber formation by unpolymerized protein. These data support a "protein-only" seeded polymerization model for the inheritance of [PSI+].
Asunto(s)
Proteínas Fúngicas/química , Priones/química , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae , Proteínas Fúngicas/ultraestructura , Humanos , Microscopía Electrónica , Factores de Terminación de Péptidos , Priones/ultraestructura , Conformación ProteicaRESUMEN
[PSI+] is a genetic element in yeast for which a heritable change in phenotype appears to be caused by a heritable change in the conformational state of the Sup35 protein. The inheritance of [PSI+] and the physical state of Sup35 in vivo depend on the protein chaperone Hsp104 (heat shock protein 104). Although these observations provide a strong genetic argument in support of the "protein-only" or "prion" hypothesis for [PSI+], there is, as yet, no direct evidence of an interaction between the two proteins. We report that when purified Sup35 and Hsp104 are mixed, the circular dichroism (CD) spectrum differs from that predicted by the addition of the proteins' individual spectra, and the ATPase activity of Hsp104 is inhibited. Similar results are obtained with two other amyloidogenic substrates, mammalian PrP and beta-amyloid 1-42 peptide, but not with several control proteins. With a group of peptides that span the PrP protein sequence, those that produced the largest changes in CD spectra also caused the strongest inhibition of ATPase activity in Hsp104. Our observations suggest that (i) previously described genetic interactions between Hsp104 and [PSI+] are caused by direct interaction between Hsp104 and Sup35; (ii) Sup35 and PrP, the determinants of the yeast and mammalian prions, respectively, share structural features that lead to a specific interaction with Hsp104; and (iii) these interactions couple a change in structure to the ATPase activity of Hsp104.
Asunto(s)
Proteínas Fúngicas/metabolismo , Proteínas de Choque Térmico/metabolismo , Priones/metabolismo , Proteínas de Saccharomyces cerevisiae , Adenosina Trifosfatasas/antagonistas & inhibidores , Adenosina Trifosfatasas/química , Adenosina Trifosfatasas/metabolismo , Amiloide/farmacología , Animales , Dicroismo Circular , Cricetinae , Proteínas Fúngicas/química , Proteínas Fúngicas/genética , Genes Fúngicos , Proteínas de Choque Térmico/química , Proteínas de Choque Térmico/genética , Técnicas In Vitro , Ratones , Fragmentos de Péptidos/química , Fragmentos de Péptidos/metabolismo , Factores de Terminación de Péptidos , Priones/química , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismoRESUMEN
Human herpesviruses 6 and 7 (HHV-6 and HHV-7) are prevalent lymphotropic viruses that infect more than 80% of children at infancy or during early childhood. Infection ranges from asymptomatic to severe disease. HHV-6B causes exanthem subitum. The virus can be recovered from peripheral blood mononuclear cells during the acute phase of exanthem subitum, but the host remains latently infected throughout life. In immunocompromised patients undergoing kidney, liver, or bone marrow transplantation latent HHV-6B is reactivated, at times causing severe or fatal disease. Here, we describe the establishment of an in vitro system for reactivation of HHV-6B and HHV-7 from latency. HHV-7 is reactivated from latently infected peripheral blood mononuclear cells by T-cell activation. HHV-6B could not be reactivated under similar conditions; however, the latent HHV-6B could be recovered after the cells were infected with HHV-7. Once reactivated, the HHV-6B genomes became prominent and the HHV-7 disappeared. We conclude that HHV-7 can provide a transacting function(s) mediating HHV-6 reactivating from latency. Understanding the activation process is critical for the development of treatments to control the activation of latent viruses so as to avoid these sometimes life threatening infections in transplant recipients.
Asunto(s)
Herpesvirus Humano 6/crecimiento & desarrollo , Herpesvirus Humano 7/crecimiento & desarrollo , Activación Viral , Electroforesis en Gel de Poliacrilamida , Humanos , Activación de Linfocitos , Prueba de Cultivo Mixto de Linfocitos , Latencia del VirusRESUMEN
The HSP100/Clp proteins are a newly discovered family with a great diversity of functions, such as increased tolerance to high temperatures, promotion of proteolysis of specific cellular substrates and regulation of transcription. HSP100/Clp proteins are also synthesized in a variety of specific patterns and, in eukaryotes, are localized to different subcellular compartments. Recent data suggest that a common ability to disassemble higher-order protein structures and aggregates unifies the molecular functions of this diverse family.
Asunto(s)
Proteínas de Choque Térmico/clasificación , Proteínas de Choque Térmico/fisiología , Proteínas de Saccharomyces cerevisiae , ATPasas Asociadas con Actividades Celulares Diversas , Adenosina Trifosfatasas/metabolismo , Adenosina Trifosfatasas/fisiología , Secuencia de Aminoácidos , Animales , Bacteriófago mu/fisiología , Endopeptidasa Clp , Proteínas de Escherichia coli , Proteínas de Choque Térmico/química , Humanos , Ratones , Modelos Biológicos , Chaperonas Moleculares , Datos de Secuencia Molecular , Conformación Proteica , Proteínas Protozoarias/fisiología , Serina Endopeptidasas/fisiología , Estrés FisiológicoRESUMEN
The heat shock protein Hsp104 of the yeast Saccharomyces cerevisiae plays a key role in promoting survival at extreme temperatures. We found that when diverse higher plant species are exposed to high temperatures they accumulate proteins that are antigenically related to Hsp104. We isolated a cDNA corresponding to one of these proteins from Arabidopsis. The protein, AtHSP101, is 43% identical to yeast Hsp104. DNA gel blot analysis indicated that AtHSP101 is encoded by a single- or low-copy number gene. AtHsp101 mRNA was undetectable in the absence of stress but accumulated to high levels during exposure to high temperatures. When AtHSP101 was expressed in yeast, it complemented the thermotolerance defect caused by a deletion of the HSP104 gene. The ability of AtHSP101 to protect yeast from severe heat stress strongly suggests that this HSP plays an important role in thermotolerance in higher plants.
Asunto(s)
Adaptación Fisiológica/genética , Arabidopsis/genética , Prueba de Complementación Genética , Proteínas de Choque Térmico/genética , Proteínas de Plantas/genética , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Secuencia de Aminoácidos , Cloroplastos/metabolismo , Clonación Molecular , Calor , Datos de Secuencia Molecular , Homología de Secuencia de AminoácidoRESUMEN
Cell-substratum adhesion plays a crucial part in the cascade of events that control growth or turn on and consummate a differentiation program. We are investigating the molecular basis of oligodendrocyte (OLG) cytodifferentiation, employing pure cultures of OLGs isolated from postmyelination brains. We have shown that such OLGs will regenerate in vitro and reenact the ontogenic development of myelin, but to do so they need a signal. Adherence to a polylysine surface in the presence of 20% horse serum generates such a signal. Among the events that are turned on upon OLG adhesion is the phosphorylation of myelin basic protein; no such phosphorylation takes place in the non-adhered cell. We postulated that horse serum provides an adhesion molecule. Laminin, fibronectin, collagen and native vitronectin failed to replace horse serum. Hence, we set out to fractionate horse serum by screening with an adhesion assay. We report here the identification, purification and partial characterization of a novel, heparin-binding horse serum glycoprotein that we have termed Glycine-Rich Adhesion Serum Protein--GRASP--to stress the fact that this protein has a high content of glycine and functions, in vitro, as an adhesion molecule for OLGs. There is 61% similarity at the N-terminus between GRASP and histidine-rich glycoprotein precursor (HRGP), an alpha 2-glycoprotein from human plasma. However, our data suggest that GRASP is not the horse serum homolog of HRGP. First, the two Gps are functionally distinct: HRGP does not promote the adhesion of OLGs. Second, the amino acid compositions differ significantly, e.g., GRASP is not histidine- but rather glycine-rich. Third, the region of sequence similarity between GRASP and HRGP is conserved throughout the cystatin superfamily. Fourth, anti-Gp55 polyclonal Abs recognize a similar set of polypeptides--save for slight differences in M(r)-in human serum as in horse serum, indicating that HRGP and GRASP are two distinct but related proteins and are both present in human and horse sera. GRASP is a dimer trimer of seemingly identical subunits of M(r) approximately 55,000 ; the native protein has an M(r) x 10(-3) approximately 120-140, of which 24-27% is contributed by carbohydrate. Using GRASP as a substratum allows the growth of OLGs in serum-free medium. GRASP is as good an effector of myelin basic protein phosphorylation as 20% horse serum. We conjecture that the mechanism of GRASP function features: 1) exposure of a cryptic sequence--after a change in conformation induced upon binding to polylysine--with affinity for an OLG signal-transducing receptor; and 2) interaction of its heparin-binding domain with OLG surface heparin sulfate proteoglycans and/or the aforementioned receptor.
Asunto(s)
Encéfalo/fisiología , Moléculas de Adhesión Celular Neuronal/sangre , Moléculas de Adhesión Celular/sangre , Adhesión Celular , Oligodendroglía/fisiología , Secuencia de Aminoácidos , Animales , Encéfalo/citología , Moléculas de Adhesión Celular Neuronal/aislamiento & purificación , Moléculas de Adhesión Celular Neuronal/farmacología , Supervivencia Celular , Células Cultivadas , Cromatografía de Afinidad , Colágeno/farmacología , Fibronectinas/farmacología , Glicoproteínas/sangre , Glicoproteínas/farmacología , Heparina , Caballos , Humanos , Laminina/farmacología , Sustancias Macromoleculares , Datos de Secuencia Molecular , Oligodendroglía/citología , Fosforilación , Polilisina , Homología de Secuencia de Aminoácido , Ovinos , VitronectinaRESUMEN
Human herpesvirus 6 (HHV-6) causes exanthem subitum (ES, roseola infantum), a childhood disease characterized by high fever and skin rash. We have analyzed restriction enzyme cleavage patterns of the DNAs of ES virus isolates from Japan and the United States. The patterns of all the ES viral DNAs were highly conserved, except for variable sequences within the terminal repeat sequences. They resembled closely the restriction enzyme patterns of the Z29 strain of HHV-6 but were distinct from those of the U1102 strain. That all ES isolates were closely related whereas the U1102 patterns were very different suggests that the U1102 strain represents a distinct virus. Moreover, the ES isolates all resembled the Z29 strain and not the U1102 strain with respect to reactivity with HHV-6 monoclonal antibodies. These findings provide evidence for the existence of two distinct classes of viruses previously classified as HHV-6. Whereas the Z29-like viruses are involved in ES infections, the association of the U1102-like viruses with human disease has yet to be determined.
Asunto(s)
Herpesvirus Humano 6/clasificación , Antígenos Virales/análisis , Southern Blotting , Sondas de ADN , ADN Viral/genética , Infecciones por Herpesviridae/inmunología , Infecciones por Herpesviridae/microbiología , Herpesvirus Humano 6/genética , Herpesvirus Humano 6/crecimiento & desarrollo , Herpesvirus Humano 6/inmunología , Japón , Secuencias Repetitivas de Ácidos Nucleicos , Mapeo Restrictivo , Estados UnidosRESUMEN
We have investigated whether T-cell activation is required for the replication of the T-lymphotropic human herpesvirus 6. The virus did not replicate in quiescent peripheral blood lymphocytes but replicated efficiently following exposure of the cells to the polyclonal mitogen phytohemagglutinin (PHA). When purified T cells were treated with PHA in the absence of accessory cells, no virus replication was observed unless exogenous interleukin-2 (IL-2) was added to the medium, promoting cell division. Incubation of peripheral blood lymphocytes in the absence of PHA but in the presence of IL-2 resulted in delayed cell blastogenesis and virus replication. Cell blastogenesis and virus replication did not occur in the purified T-cell cultures incubated with IL-2 alone. Taken together, the results show that human herpesvirus 6 replication requires full progression of the cell cycle. This finding might have implications for the pathogenicity of the virus in the human host.
Asunto(s)
Activación de Linfocitos , Simplexvirus/fisiología , Linfocitos T/inmunología , Replicación Viral , Recuento de Células , Células Cultivadas , Replicación del ADN , Humanos , Interleucina-2/farmacología , Fitohemaglutininas , Simplexvirus/genética , Linfocitos T/microbiologíaRESUMEN
Human herpesvirus 6 (HHV-6) is a newly identified lymphotropic herpesvirus. We have analyzed viral and host DNA replication in peripheral blood lymphocytes infected in the absence of drugs or infected in the presence of phosphonoacetic acid (PAA) or acyclovir (ACV). The results revealed the following: (i) Infection with HHV-6 resulted in the shutoff of host DNA replication. (ii) PAA at concentrations of 100 and 300 micrograms/ml significantly reduced virus replication. The drug inhibited viral DNA replication, whereas host cell DNA replication was not affected. This strongly suggests that HHV-6 encodes a PAA sensitive viral DNA polymerase. (iii) ACV at 20 microM did not interfere with virus production and virus spread. ACV at 100 microM only partly interfered with virus replication, whereas at 400 microM the block was more complete. Viral DNA replication was not affected by ACV at 20 microM. However, approximately 60 and 85% inhibition in viral DNA replication was observed in the presence of 100 and 400 microM of ACV. (iv) Assays for viral thymidine kinase (TK) revealed no significant increase in TK activity, whereas increased TK activity was noted following infection of the same peripheral blood lymphocytes with herpes simplex virus. Thus, either HHV-6 does not encode a tk enzyme which can phosphorylate ACV or the inefficient block may reflect lower sensitivity of the HHV-6 DNA polymerase to the drug.
Asunto(s)
Transformación Celular Viral , Replicación del ADN , ADN Viral/genética , ADN/genética , Simplexvirus/genética , Aciclovir/farmacología , Células Cultivadas , ADN/análisis , Replicación del ADN/efectos de los fármacos , ADN Viral/análisis , Técnica del Anticuerpo Fluorescente , Humanos , Linfocitos/metabolismo , Linfocitos/microbiología , Linfocitos/ultraestructura , Microscopía Electrónica , Ácido Fosfonoacético/farmacología , Simplexvirus/efectos de los fármacos , Simplexvirus/ultraestructura , Timidina Quinasa/análisisRESUMEN
A new human herpesvirus has been isolated from CD4+ T cells purified from peripheral blood mononuclear cells of a healthy individual (RK), following incubation of the cells under conditions promoting T-cell activation. The virus could not be recovered from nonactivated cells. Cultures of lymphocytes infected with the RK virus exhibited a cytopathic effect, and electron microscopic analyses revealed a characteristic herpesvirus structure. RK virus DNA did not hybridize with large probes derived from herpes simplex virus, Epstein-Barr virus, varicella-zoster virus, and human cytomegalovirus. The genetic relatedness of the RK virus to the recently identified T-lymphotropic human herpesvirus 6 (HHV-6) was investigated by restriction enzyme analyses using 21 different enzymes and by blot hybridization analyses using 11 probes derived from two strains of HHV-6 (Z29 and U1102). Whereas the two HHV-6 strains exhibited only limited restriction enzyme polymorphism, cleavage of the RK virus DNA yielded distinct patterns. Of the 11 HHV-6 DNA probes tested, only 6 cross-hybridized with DNA fragments derived from the RK virus. Taken together, the maximal homology amounted to 31 kilobases of the 75 kilobases tested. We conclude that the RK virus is distinct from previously characterized human herpesviruses. We propose to designate it as the prototype of a new herpesvirus, the seventh human herpesvirus identified to date.