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1.
J Virol ; 74(13): 5836-44, 2000 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10846063

RESUMEN

The human and simian immunodeficiency virus (HIV-1 and SIVmac) transmembrane proteins contain unusually long intracytoplasmic domains (ICD-TM). These domains are suggested to play a role in envelope fusogenicity, interaction with the viral matrix protein during assembly, viral infectivity, binding of intracellular calmodulin, disruption of membranes, and induction of apoptosis. Here we describe a novel mutant virus, SIVmac-M4, containing multiple mutations in the coding region for the ICD-TM of pathogenic molecular clone SIVmac239. Parental SIVmac239-Nef+ produces high-level persistent viremia and simian AIDS in both juvenile and newborn rhesus macaques. The ICD-TM region of SIVmac-M4 contains three stop codons, a +1 frameshift, and mutation of three highly conserved, charged residues in the conserved C-terminal alpha-helix referred to as lentivirus lytic peptide 1 (LLP-1). Overlapping reading frames for tat, rev, and nef are not affected by these changes. In this study, four juvenile macaques received SIVmac-M4 by intravenous injection. Plasma viremia, as measured by branched-DNA (bDNA) assay, reached a peak at 2 weeks postinoculation but dropped to below detectable levels by 12 weeks. At over 1.5 years postinoculation, all four juvenile macaques remain healthy and asymptomatic. In a subsequent experiment, four neonatal rhesus macaques were given SIVmac-M4 intravenously. These animals exhibited high levels of viremia in the acute phase (2 weeks postinoculation) but are showing a relatively low viral load in the chronic phase of infection, with no clinical signs of disease for 1 year. These findings demonstrated that the intracytoplasmic domain of the transmembrane Env (Env-TM) is a locus for attenuation in rhesus macaques.


Asunto(s)
Productos del Gen env/genética , Proteínas Oncogénicas de Retroviridae/genética , Virus de la Inmunodeficiencia de los Simios/genética , Proteínas Virales de Fusión/genética , Animales , Anticuerpos Antivirales/inmunología , Células COS , Productos del Gen env/inmunología , Productos del Gen nef/genética , Productos del Gen nef/fisiología , Humanos , Cinética , Macaca mulatta , Estructura Terciaria de Proteína/genética , Proteínas Oncogénicas de Retroviridae/inmunología , Síndrome de Inmunodeficiencia Adquirida del Simio/virología , Virus de la Inmunodeficiencia de los Simios/inmunología , Virus de la Inmunodeficiencia de los Simios/fisiología , Proteínas Virales de Fusión/inmunología , Replicación Viral
2.
Exp Parasitol ; 93(4): 198-206, 1999 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-10600445

RESUMEN

West African populations of Onchocerca volvulus endemic to the rain forest and savanna bioclimes of West Africa differ in their ability to induce ocular disease in infected individuals. In recent years, both clinical- and animal-model-based studies have implicated particular parasite antigens in the development of ocular onchocerciasis. To test the hypothesis that the difference in pathogenic potential of blinding and nonblinding parasites might be reflected in qualitative differences in antigens that have been implicated in the development of ocular onchocerciasis, we compared the sequences of two parasite antigens implicated in the development of ocular disease in blinding- and nonblinding-strain parasites. The results demonstrated a high level of homogeneity between the parasite strains in these genes. The study was extended to include additional nuclear genes encoding antigens that are commonly recognized by individuals infected with O. volvulus and to the mitochondrial genome of the parasite. The results demonstrate a high degree of homogeneity in both the nuclear and the mitochondrial genomes among O. volvulus isolates collected from several different sites in Africa and in the Americas. This high degree of genetic homogeneity may reflect the passage of the parasite through a recent genetic bottleneck.


Asunto(s)
Antígenos Helmínticos/genética , Heterogeneidad Genética , Genoma , Onchocerca volvulus/genética , Oncocercosis Ocular/parasitología , África , Américas , Animales , Antígenos Helmínticos/química , Secuencia de Bases , Núcleo Celular/química , ADN Complementario/química , ADN de Helmintos/química , ADN Mitocondrial/química , Epítopos/química , Epítopos/genética , Variación Genética , Proteínas del Helminto/química , Proteínas del Helminto/genética , Humanos , Datos de Secuencia Molecular , Onchocerca volvulus/inmunología , Onchocerca volvulus/patogenicidad , Oncocercosis Ocular/inmunología , Reacción en Cadena de la Polimerasa , Polimorfismo de Longitud del Fragmento de Restricción , Alineación de Secuencia , Virulencia
3.
Mol Biochem Parasitol ; 95(1): 111-27, 1998 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-9763293

RESUMEN

The complete DNA sequence of the mitochondrial genome of Onchocerca volvulus is described. The O. volvulus mitochondrial genome is 13747 bp, slightly smaller than the mitochondrial genomes of the nematodes Ascaris suum and Caenorhabditis elegans, and the smallest metazoan mitochondrial DNA molecule reported to date. The O. volvulus mitochondrial genome contains genes for two ribosomal RNAs, 22 transfer RNAs and 12 proteins. Consistent with the small size of the genome, four gene pairs overlap and eight contain no intergenic regions. Only 17 intergenic regions are found, ranging in size from 1 to 46 bp. As in C. elegans and A. suum, the O. volvulus mitochondrial genome lacks an open reading frame encoding ATPase subunit 8, and all genes are apparently transcribed in the same direction. However, the mitochondrial gene order of O. volvulus differs from that of A. suum, C. elegans and other metazoan mitochondrial genomes. A total of 20 of the 22 transfer RNAs encoded in the O. volvulus mitochondrial genome have the potential to fold into secondary structures lacking the TpsiC arm, as has been reported in other nematodes. The genome exhibits a striking codon bias, with 15/20 amino acids having a single codon preference of > 70%.


Asunto(s)
ADN Mitocondrial/análisis , Genoma , Mitocondrias/genética , Onchocerca volvulus/genética , Filogenia , Animales , Ascaris suum/genética , Secuencia de Bases , Caenorhabditis elegans/genética , Mapeo Cromosómico , Codón , ADN de Helmintos/análisis , ADN de Helmintos/genética , ADN Mitocondrial/genética , Genes de ARNr/genética , Proteínas del Helminto/genética , Datos de Secuencia Molecular , Conformación de Ácido Nucleico , Biosíntesis de Proteínas , ARN de Transferencia/química , ARN de Transferencia/genética , Análisis de Secuencia de ADN
4.
J Acquir Immune Defic Syndr (1988) ; 7(7): 747-53, 1994 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-8207658

RESUMEN

This report describes experiments assessing the effectiveness against HIV of potential disinfecting agents that are commonly available to IDU when they are sharing syringes. We exposed cell-free HIV, HIV-infected cells, and HIV-infected blood containing known quantities of HIV to household cleaning agents, alcohols, peroxide, and highly acidic materials for 1 min, in order to examine the effects of these materials on the infectivity of the HIV. Undiluted liquid laundry bleach and dilute liquid dish detergent reduced the number of culturable HIV to an undetectable level under the experimental conditions used. Diluted bleach was not completely effective. Other potential disinfecting agents, including ethanol, isopropyl alcohol, and hydrogen peroxide, were unable to disinfect high numbers of HIV-infected cells or infected blood. Liquid dish detergent warrants further study as a possible acceptable alternative to bleach. Our data provide support for recommendations to IDU that they disinfect shared syringes every time between users with full-strength liquid laundry bleach to reduce their risk of acquiring or transmitting HIV. When bleach is not available, liquid dish detergent or other available disinfecting agents such as rubbing alcohol, hydrogen peroxide, or high alcohol content beverages are more effective than water at disinfecting HIV, recognizing that these materials are less effective than bleach. Although these materials are effective, they should not be viewed as a substitute for decreased sharing of injection equipment by IDU, or increased availability of sterile needles and syringes.


Asunto(s)
Desinfección , Infecciones por VIH/sangre , VIH-1/efectos de los fármacos , Hipoclorito de Sodio/farmacología , Abuso de Sustancias por Vía Intravenosa/sangre , 1-Propanol/farmacología , Acetatos/farmacología , Ácido Acético , Bebidas Alcohólicas , Bebidas , Línea Celular , Detergentes/farmacología , Etanol/farmacología , Infecciones por VIH/complicaciones , Infecciones por VIH/prevención & control , Humanos , Agujas , Abuso de Sustancias por Vía Intravenosa/complicaciones , Jeringas
5.
Virology ; 194(2): 858-64, 1993 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-8503191

RESUMEN

Previous studies of HIV-1 replication in chimpanzee lymphocytes have been limited to a small number of virus isolates which generally replicated poorly and without cytopathic effect. Here, we describe an HIV-1 provirus (SG3), cloned as a single proviral unit, which replicates more efficiently in chimpanzee than in human lymphocytes, resulting in syncytium formation and cell death. This provirus also replicates efficiently and with extraordinary cytopathic effect in immortalized human T-cell lines. The SG3 genome was completely sequenced and found to contain all genes typical of HIV-1 with the exception of vpu. Phylogenetically, SG3 is representative of North American/European strains of HIV-1 and shows no greater similarity to SIVCPZ in its envelope sequence than do other HIV-1 strains. Pilot studies indicate that SG3 can infect and replicate in chimpanzees and SCID-hu mice in vivo following intravenous or intrathymic inoculation. The SG3 proviral clone, because of its replication efficiency in human and chimpanzee cells and its complete molecular description, represents a new virologic reagent for the coordinated molecular analysis of HIV-1 replication and pathogenesis in relevant animal model systems.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida/microbiología , VIH-1/crecimiento & desarrollo , Linfocitos/microbiología , Provirus/crecimiento & desarrollo , Síndrome de Inmunodeficiencia Adquirida/genética , Animales , Secuencia de Bases , Muerte Celular , Fusión Celular , Clonación Molecular , Efecto Citopatogénico Viral , Genoma Viral , VIH-1/genética , Humanos , Datos de Secuencia Molecular , Pan troglodytes , Filogenia , Provirus/genética , Especificidad de la Especie , Replicación Viral
6.
AIDS Res Hum Retroviruses ; 6(11): 1239-46, 1990 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-2078406

RESUMEN

Rhesus macaques (Macaca mulatta) immunized with an inactivated whole SIVmac vaccine and muramyl dipeptide (MDP), incomplete Freund's adjuvant (IFA), or aqueous suspension were challenged intravenously with 0.1 TCID50 of cell-free SIVmac. Whereas virus was readily recovered from the peripheral blood lymphocytes of 10 of 10 nonvaccinated controls following this challenge dose, virus was not recovered from the three animals that received the vaccine with MDP nor from one of two animals that received the vaccine with IFA and one of three animals that received the aqueous vaccine. The animals that were protected against challenge were those that had detectable SIV antibody response to the envelop, both the outer glycoprotein (gp120) and the truncated transmembrane glycoprotein (gp31). Protected monkeys tended to have higher titers of syncytial inhibition antibody prior to challenge. An anamnestic response after challenge was observed only in the vaccinated monkeys that became infected. Vaccinated animals that became challenge-infected tended to live longer than infected controls. These results confirm those at two other primate centers and indicate that killed whole SIV vaccines can protect against low challenge doses of SIV and prevent early death in those monkeys that do become infected. The mechanism of this protection remains undetermined. This finding adds optimism to the possibility of an eventual AIDS vaccine.


Asunto(s)
Síndrome de Inmunodeficiencia Adquirida del Simio/prevención & control , Virus de la Inmunodeficiencia de los Simios/inmunología , Vacunas Virales/inmunología , Acetilmuramil-Alanil-Isoglutamina/inmunología , Animales , Anticuerpos Antivirales/biosíntesis , Antígenos Virales/inmunología , Secuencia de Bases , Línea Celular , Adyuvante de Freund/inmunología , Células Gigantes/citología , Humanos , Immunoblotting , Técnicas para Inmunoenzimas , Memoria Inmunológica , Macaca mulatta , Datos de Secuencia Molecular , Vacunación , Vacunas de Productos Inactivados/inmunología , Proteínas del Envoltorio Viral/inmunología
7.
Br Med J (Clin Res Ed) ; 288(6418): 701-3, 1984 Mar 03.
Artículo en Inglés | MEDLINE | ID: mdl-6230134

RESUMEN

The increasing number of people aged over 75 in Britain makes heavy demands on health and social services. To obtain accurate information for rational allocation of resources to domiciliary and residential services a group of 98 housebound women over 75 were compared with a group of 99 women of the same age in residential care. They had a similar range of physical disorders with the exception that deafness was more common among women in residential care. A much higher proportion in residential care were demented. Though in many respects women in residential care had less physical incapacity, a higher proportion needed help at times of crisis. Important social factors were that women at home were more likely to be living with others, and that the principal helper was more likely to be a husband or relative than a neighbour. Both groups received the same amount of support from home helps and community nurses. Any reduction in the number of residential care places for elderly women whose relatives are not available or are unable to cope would require the establishment of an effective community psychogeriatric service and a system for providing appropriate subjects with 24 hour care and supervision.


Asunto(s)
Hogares para Ancianos , Admisión del Paciente , Anciano , Personas con Discapacidad , Familia , Femenino , Recursos en Salud/provisión & distribución , Necesidades y Demandas de Servicios de Salud , Servicios de Atención de Salud a Domicilio , Humanos , Trastornos Mentales/complicaciones , Escocia , Autocuidado , Condiciones Sociales
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