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1.
J Virol ; 74(13): 5836-44, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10846063

ABSTRACT

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.


Subject(s)
Gene Products, env/genetics , Retroviridae Proteins, Oncogenic/genetics , Simian Immunodeficiency Virus/genetics , Viral Fusion Proteins/genetics , Animals , Antibodies, Viral/immunology , COS Cells , Gene Products, env/immunology , Gene Products, nef/genetics , Gene Products, nef/physiology , Humans , Kinetics , Macaca mulatta , Protein Structure, Tertiary/genetics , Retroviridae Proteins, Oncogenic/immunology , Simian Acquired Immunodeficiency Syndrome/virology , Simian Immunodeficiency Virus/immunology , Simian Immunodeficiency Virus/physiology , Viral Fusion Proteins/immunology , Virus Replication
2.
Exp Parasitol ; 93(4): 198-206, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10600445

ABSTRACT

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.


Subject(s)
Antigens, Helminth/genetics , Genetic Heterogeneity , Genome , Onchocerca volvulus/genetics , Onchocerciasis, Ocular/parasitology , Africa , Americas , Animals , Antigens, Helminth/chemistry , Base Sequence , Cell Nucleus/chemistry , DNA, Complementary/chemistry , DNA, Helminth/chemistry , DNA, Mitochondrial/chemistry , Epitopes/chemistry , Epitopes/genetics , Genetic Variation , Helminth Proteins/chemistry , Helminth Proteins/genetics , Humans , Molecular Sequence Data , Onchocerca volvulus/immunology , Onchocerca volvulus/pathogenicity , Onchocerciasis, Ocular/immunology , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Sequence Alignment , Virulence
3.
Mol Biochem Parasitol ; 95(1): 111-27, 1998 Sep 01.
Article in English | MEDLINE | ID: mdl-9763293

ABSTRACT

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%.


Subject(s)
DNA, Mitochondrial/analysis , Genome , Mitochondria/genetics , Onchocerca volvulus/genetics , Phylogeny , Animals , Ascaris suum/genetics , Base Sequence , Caenorhabditis elegans/genetics , Chromosome Mapping , Codon , DNA, Helminth/analysis , DNA, Helminth/genetics , DNA, Mitochondrial/genetics , Genes, rRNA/genetics , Helminth Proteins/genetics , Molecular Sequence Data , Nucleic Acid Conformation , Protein Biosynthesis , RNA, Transfer/chemistry , RNA, Transfer/genetics , Sequence Analysis, DNA
4.
J Acquir Immune Defic Syndr (1988) ; 7(7): 747-53, 1994 Jul.
Article in English | MEDLINE | ID: mdl-8207658

ABSTRACT

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.


Subject(s)
Disinfection , HIV Infections/blood , HIV-1/drug effects , Sodium Hypochlorite/pharmacology , Substance Abuse, Intravenous/blood , 1-Propanol/pharmacology , Acetates/pharmacology , Acetic Acid , Alcoholic Beverages , Beverages , Cell Line , Detergents/pharmacology , Ethanol/pharmacology , HIV Infections/complications , HIV Infections/prevention & control , Humans , Needles , Substance Abuse, Intravenous/complications , Syringes
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