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1.
Mol Pharmacol ; 54(5): 761-9, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9804611

ABSTRACT

An aspartate-to-alanine point mutation in the catalytic domain (D853A) of guanylyl cyclase-C (GC-C), the heat-stable enterotoxin (STa) receptor, rendered the enzyme catalytically inactive. Mn2+/Triton X-100-stimulated guanylyl cyclase activity was detected in membranes from COS7 cells overexpressing GC-C but not GC-CD853A. STa treatment of paired cells resulted in cGMP production in those transiently expressing GC-C but not GC-CD853A. GC-C and GC-CD853A showed similar Bmax and Kd values for [125I]STa binding in these cells, indicating that the lack of catalytic activity in the latter was not due to differing expression levels or reduced binding affinity. The involvement of the catalytic domain in aldosteronogenesis was studied in human adrenocortical H295R cells. COS7 and H295R cells infected with vaccinia virus-expressing GC-C and GC-CD853A (VVGC-CD853A) had [125I]STa-binding characteristics akin to those in transfected cells. Immunoblot confirmed that both GC-C and GC-CD853A formed similar higher order oligomers in infected cells. Virus-mediated expression of GC-C in H295R cells revealed concentration-dependent STa-stimulated cGMP formation that was undetectable in VVGC-CD853A-infected cells. STa decreased angiotensin II-stimulated human aldosterone generation in a concentration-dependent manner in vaccinia virus-expressing GC-C-infected cells but not in those infected with VVGC-CD853A. These results demonstrate that a catalytically active guanylyl cyclase is required for the inhibition of aldosteronogenesis.


Subject(s)
Aldosterone/biosynthesis , Guanylate Cyclase/physiology , Receptors, Peptide/physiology , Angiotensin II/pharmacology , Animals , Bacterial Toxins/metabolism , Bacterial Toxins/pharmacology , Binding Sites , COS Cells/metabolism , COS Cells/virology , Cells, Cultured , Cyclic GMP/biosynthesis , Enterotoxins/metabolism , Enterotoxins/pharmacology , Escherichia coli Proteins , Guanylate Cyclase/genetics , Guanylate Cyclase/metabolism , Humans , Immunoblotting , Iodine Radioisotopes , Kinetics , Point Mutation , Receptors, Enterotoxin , Receptors, Guanylate Cyclase-Coupled , Receptors, Peptide/genetics , Receptors, Peptide/metabolism , Sensitivity and Specificity , Stimulation, Chemical , Transfection , Vaccinia virus/genetics , Vaccinia virus/metabolism
2.
Virology ; 250(1): 135-9, 1998 Oct 10.
Article in English | MEDLINE | ID: mdl-9770427

ABSTRACT

During the screening of human lymphoblastoid cells as suitable hosts for retrovirus transmission studies, the Epstein-Barr virus (EBV)-negative, B-lymphoblastoid cell line DG-75 was found to be chronically infected with a heretofore unrecognized retrovirus. Two DG-75 sublines obtained from different sources (designated UW and KAR) were found to produce constitutively particles identified as retroviral by electron microscopy and reverse transcriptase activity. The ultrastructure, morphogenesis, and density in sucrose of the particles were typical of C-type retroviruses. Immunoblot analysis of the DG-75(UW) retrovirus proteins showed antigenic similarity to Moloney murine leukemia virus. A third DG-75 subline in early passage, designated HAD, was free of retrovirus. The DG-75(UW) retrovirus was infectious and produced progeny virions that could be passaged to uninfected cells. We have thus demonstrated that DG-75 cells, which have been used extensively in studies of the biological effects of EBV-encoded genes and their promoters, may be chronically infected with a murine retrovirus and that an early passage subline is retrovirus free and available for such studies.


Subject(s)
B-Lymphocytes/virology , Gammaretrovirus/isolation & purification , Animals , Antigens, Viral/analysis , Cell Line , Gammaretrovirus/physiology , Gammaretrovirus/ultrastructure , Humans , Mice , RNA-Directed DNA Polymerase/metabolism , Virion/ultrastructure
4.
Res Virol ; 148(3): 191-206, 1997.
Article in English | MEDLINE | ID: mdl-9201810

ABSTRACT

The human B-lymphoblastoid cell line, designated JHK-3, with pre-B-cell characteristics, chronically produces two viruses, Epstein-Barr virus (EBV) and JHK virus, an apparently novel retrovirus. The JHK-3 cells are much more productive of extracellular EBV than the high-producer marmoset line B95-8. The extracellular virus of the JHK-3 EBV strain is relatively fragile, more broadly dispersed in an ultracentrifuged sucrose gradient than the B95-8 EBV and more susceptible to disruption by combined treatment with urea and dithiothreitol. By restriction fragment length polymorphism analysis, the JHK-3 EBV strain resembles the EBV strain FF-41. The JHK-3 cells also produce an incompletely characterized, relatively fragile, enveloped, icosahedral RNA virus that contains Mn(++)-dependent reverse transcriptase. JHK virions measure 85 nm in ultrathin sections, much smaller than other Retroviridae. The JHK virus exhibits a distinctive morphogenesis, most nearly resembling C-type retroviruses. The JHK-3 cell line provides a human cell model for investigating virus/virus interactions and their pathogenetic affects on host cells which chronically and simultaneously produce DNA and RNA viruses.


Subject(s)
B-Lymphocytes/virology , Herpesvirus 4, Human/physiology , Retroviridae/physiology , Virus Replication , Animals , B-Lymphocytes/cytology , Callithrix , Cell Line , DNA, Viral , Herpesvirus 4, Human/genetics , Herpesvirus 4, Human/ultrastructure , Humans , RNA-Directed DNA Polymerase/metabolism , Retroviridae/enzymology , Retroviridae/ultrastructure , Retroviridae Proteins/metabolism , Tumor Cells, Cultured
5.
J Virol ; 70(11): 8160-4, 1996 Nov.
Article in English | MEDLINE | ID: mdl-8892946

ABSTRACT

The cytotoxic T-lymphocyte (CTL) response in reovirus-infected C3H mice was investigated by using reovirus-vaccinia virus recombinants. Results of cytotoxicity assays indicated that the nonstructural protein sigma1NS elicited a significant CTL response. Experiments with sigma1NS-specific CTL lines showed that both strain-specific and cross-reactive epitopes exist in the sigma1NS protein.


Subject(s)
Antigens, Viral/immunology , Mammalian orthoreovirus 3/immunology , T-Lymphocytes, Cytotoxic/immunology , Viral Nonstructural Proteins/immunology , Animals , Antigens, Viral/genetics , Base Sequence , Cells, Cultured , Cytotoxicity Tests, Immunologic , Genetic Vectors , L Cells , Mammalian orthoreovirus 3/genetics , Mice , Mice, Inbred C3H , Molecular Sequence Data , T-Lymphocytes, Cytotoxic/cytology , Vaccinia virus/genetics , Viral Nonstructural Proteins/genetics
6.
Res Virol ; 145(5): 277-85, 1994.
Article in English | MEDLINE | ID: mdl-7839005

ABSTRACT

The putative reovirus RNA polymerase, protein lambda 3, was characterized using antiserum prepared against a TrpE-lambda 3 fusion protein synthesized in Escherichia coli. Immunofluorescence microscopy showed that lambda 3 accumulated in perinuclear inclusion bodies in reovirus-infected cells. Analysis of lambda 3 accumulation in infected cells indicates that, once synthesized, lambda 3 is quite stable throughout the course of infection. Anti-lambda 3 serum did not immunoprecipitate virions, core particles or iodinated surface proteins of either virions or cores. These results indicate that lambda 3 is located in the inner part of the core. Experiments involving urea denaturation of purified reovirus cores indicate that lambda 3 cannot be selectively removed from the core without total denaturation of the core structure. When the dsRNA genome was eliminated from the core, lambda 3 remained associated with the other viral proteins in the core. Thus, lambda 3 appears to be a stable, structural component of the reovirus core, not bound to genomic dsRNA or free in soluble form inside the core.


Subject(s)
DNA-Directed RNA Polymerases/biosynthesis , Mammalian orthoreovirus 3/growth & development , RNA-Dependent RNA Polymerase/biosynthesis , Viral Proteins , Animals , Antibodies, Viral/immunology , Antibody Specificity , Antigens, Viral/immunology , Cells, Cultured , DNA-Directed RNA Polymerases/immunology , DNA-Directed RNA Polymerases/isolation & purification , Fibroblasts/virology , Fluorescent Antibody Technique , Immunoblotting , Isotope Labeling , Mammalian orthoreovirus 3/drug effects , Mammalian orthoreovirus 3/enzymology , Mice , Precipitin Tests , RNA-Dependent RNA Polymerase/immunology , RNA-Dependent RNA Polymerase/isolation & purification , Sulfur Radioisotopes , Time Factors , Urea/pharmacology , Virion/immunology , Virus Replication
7.
Virology ; 182(1): 336-45, 1991 May.
Article in English | MEDLINE | ID: mdl-2024469

ABSTRACT

The oligomerization domain of the reovirus cell attachment protein (sigma 1) was probed using the type 3 reovirus sigma 1 synthesized in vitro. Trypsin cleaved the sigma 1 protein (49K molecular weight) approximately in the middle and yielded a 26K N-terminal fragment and a 23K C-terminal fragment. Under conditions which allowed for the identification of intact sigma 1 in the oligomeric form (approximately 200K) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the N-terminal 26K fragment was found to exist as stable trimers (80K) and, to a less extent, as dimers (54K), whereas the C-terminal fragment remained in the monomeric form. A polypeptide (161 amino acids) containing the N-terminal heptad repeat region synthesized in vitro was capable of forming stable dimers and trimers. Using various criteria, we demonstrated that the stability of the intact sigma 1 oligomer is conferred mainly by the N-terminal heptad repeat region. Our results are summarized in a model in which individual heptad repeats are held together in a three-stranded alpha-helical coiled-coil structure via both hydrophobic and electrostatic interactions.


Subject(s)
Capsid Proteins , Reoviridae/analysis , Viral Proteins/chemistry , Amino Acid Sequence , Base Sequence , Cloning, Molecular , Dithiothreitol , Ions , Macromolecular Substances , Mercaptoethanol , Molecular Sequence Data , Molecular Weight , Oligonucleotides/chemistry , Protein Binding , Structure-Activity Relationship , Trypsin/pharmacology , Viral Proteins/genetics
8.
Viral Immunol ; 4(3): 167-75, 1991.
Article in English | MEDLINE | ID: mdl-1725700

ABSTRACT

Reovirus has previously been classified into three serotypes based on hemagglutination inhibition assays. In the present study, the specificity of cytotoxic T lymphocytes (CTL) generated in reovirus type 3-infected C3H/HeN mice was investigated at the population and clonal levels. Short-term CTL lines generated in response to reovirus type 3 preferentially lysed cells infected with reovirus type 1 or 3 and, in some instances, type 2-infected cells as well. Eleven CTL clones established from the lines demonstrated two unique patterns of recognition. A single clone was exquisitely specific for reovirus type 3-infected cells and did not cross-react on reovirus type 1- or 2-infected cells. Ten of the clones recognized reovirus type 1- and type 3-infected cells. These clones had low levels of cross-reactivity on reovirus type 2-infected cells that was revealed only at high effector:target cell ratios. Precursor frequency analysis further revealed that the majority of the CTL generated against reovirus type 3 could cross-react on both reovirus type 1- and type 2-infected cells. Some CTL could be detected that had a more restricted pattern of recognition and recognized reovirus type 3-infected cells exclusively or recognized reovirus type 3-infected cells and either reovirus type 1- or type 2-infected cells. These results indicate that a minimum of four epitopes are recognized by reovirus-specific CTL and that the response is dominated by CTL that recognize an epitope common to all three serotypes of reovirus.


Subject(s)
Antigens, Viral/immunology , Mammalian orthoreovirus 3/immunology , Reoviridae/immunology , T-Lymphocytes, Cytotoxic/immunology , Animals , Cell Line , Colony-Forming Units Assay , Cross Reactions , Cytotoxicity, Immunologic , Epitopes/immunology , Mice , Mice, Inbred C3H
9.
Virology ; 174(2): 399-409, 1990 Feb.
Article in English | MEDLINE | ID: mdl-2305549

ABSTRACT

Sequence analysis of reovirus serotype 1 (ST1) and 2 (ST2) S1 genome segment cDNAs identified several differences from previously reported versions of their sequences. The sequences reported here comprise 1463 and 1440 base pairs, respectively; for comparison, the ST3 S1 genome segment is 1416 nucleotides long. The serotype 1 and 2 sigma 1 proteins are predicted to contain 470 and 462 amino acids, respectively; the ST3 sigma 1 protein is 455 amino acids long. As previously observed, the ST1 and ST2 sigma 1 proteins are much more closely related to each other than to that of ST3 (about 48 and 25% similarity, respectively, using a computer program that finds about 14% similarity among unrelated proteins). The sequences of the three S1 genome segments have diverged very extensively in all three codon positions, in some cases almost to the extent of randomness. Despite this, not only function but also shape and configuration have been retained (since the three sigma 1 proteins can be incorporated efficiently into completely heterologous capsids). Seventy-nine amino acid residues are conserved among all three serotypes, many of them clustered into five regions in which one-third or more of the residues are triply conserved. These regions may represent functionally conserved domains involved in oligomerization, cell attachment, and hemagglutination.


Subject(s)
Capsid Proteins , Reoviridae/analysis , Viral Proteins/analysis , Amino Acid Sequence , Base Sequence , Codon , Genes, Viral , Molecular Sequence Data , Reoviridae/classification , Reoviridae/genetics , Serotyping , Viral Proteins/genetics
10.
Virology ; 170(1): 62-70, 1989 May.
Article in English | MEDLINE | ID: mdl-2470196

ABSTRACT

Purified native sigma 1 proteins from [35S]methionine-labeled reovirions [serotypes 1 (T1) and 3 (T3)] were subjected to limited trypsin and chymotrypsin digestion. It was found that T1 sigma 1 was resistant to both trypsin and chymotrypsin, whereas T3 sigma 1 (49K molecular weight) was cleaved by trypsin to yield a 24K and a 25K fragment, and by chymotrypsin to yield a 42K fragment. The 24K tryptic fragment, but not the 25K tryptic fragment, was shown to possess L-cell binding capacity, and represents the carboxy-terminal half of T3 sigma 1 since it contains the single cysteine residue (amino acid 351) as revealed by tryptic analysis of [35S]cysteine-labeled sigma 1. Neither tryptic fragment was able to bind to glycophorin, the reovirus receptor on human erythrocytes. Thus, the mechanism of reovirus host cell attachment is distinct from that of reovirus hemagglutination. The two tryptic fragments were recognized by different neutralizing monoclonal anti-sigma 1 antibodies, indicating that neutralizing and cell attachment sites are not necessarily equivalent. The 42K chymotryptic fragment of T3 sigma 1 was shown to be generated by a cleavage proximal to the carboxy-terminus. Like intact T3 sigma 1, the 42K protein retained its capacity to bind to both L cells and glycophorin, and was recognized by all the neutralizing monoclonal anti-sigma 1 antibodies tested. Thus, the host cell receptor binding site on T3 sigma 1 is located between the trypsin-sensitive and the chymotrypsin-sensitive sites.


Subject(s)
Antigens, Surface/analysis , Antigens, Viral/analysis , Chymotrypsin/pharmacology , Mammalian orthoreovirus 3/analysis , Reoviridae/analysis , Trypsin/pharmacology , Viral Proteins/analysis , Binding Sites , Cell Adhesion Molecules , Epitopes , Glycophorins/metabolism , In Vitro Techniques , L Cells , Molecular Weight , Neutralization Tests , Peptide Fragments/analysis , Precipitin Tests , Protein Binding , Receptors, Virus/metabolism
11.
Virology ; 168(1): 183-6, 1989 Jan.
Article in English | MEDLINE | ID: mdl-2642627

ABSTRACT

A bacterial expression vector, pATH 3, was used to produce high levels of a fusion protein composed of a portion of the trpE protein of Escherichia coli and the putative sigma 1S coding region from the S1 gene of reovirus serotype 2. The fusion protein was purified and injected into rabbits to prepare antisera. This antibody was able to detect sigma 1S being synthesized in L929 cells infected with reovirus serotype 2 by means of immunoprecipitation and immunoblotting techniques. The peak of sigma 1S accumulation in type 2-infected cells was shown to occur approximately 20 hr after infection. This report represents the first description of sigma 1S production in reovirus serotype 2-infected cells.


Subject(s)
Antibodies, Viral/immunology , Capsid Proteins , Recombinant Fusion Proteins/immunology , Recombinant Proteins/immunology , Reoviridae/metabolism , Viral Proteins/analysis , Cell Line , Electrophoresis, Polyacrylamide Gel , Escherichia coli/genetics , Genetic Vectors , Immune Sera/immunology , Immunoblotting , Precipitin Tests , Viral Proteins/biosynthesis
12.
Proc Natl Acad Sci U S A ; 82(1): 24-8, 1985 Jan.
Article in English | MEDLINE | ID: mdl-3855545

ABSTRACT

The S1 genes of the three serotypes of reovirus have been cloned and sequenced. The S1 genes encode protein sigma 1, the protein against which serotype-specific neutralizing antibodies are directed; it is also the reovirus hemagglutinin and cell-attachment protein and is a major determinant of host range/tissue specificity and of the nature of the interaction of reovirus with cells of the immune system. The S1 genes of serotypes 1, 2, and 3 are 1458, 1442, and 1416 nucleotides long, respectively. They possess untranslated regions 13, 13, and 12 nucleotides long at their 5' termini and 188, 229, and 36 nucleotides long at their 3' termini. They possess two open reading frames. The first starts with a "weak" initiation codon and extends for 418, 399, and 455 codons, respectively; this is the size expected for the sigma 1 proteins. The other reading frame starts at a "strong" initiation codon about 70 residues downstream from the 5' terminus but extends for only about 120 codons, being terminated by 3 in-phase termination codons in all three genes. The proteins encoded by these short open reading frames are quite basic. The serotype 1 and 2 S1 genes are much more closely related to each other (28% homology) than to the serotype 3 S1 gene (5% and 9% homology, respectively). These figures are based on direct homology calculations, adjusted for 25% random coincidence. Serologic evidence and hydrophobicity profiles agree that the sigma 1 proteins of serotypes 1 and 2 are much more closely related to each other (about 40% homology) than to that of serotype 3 (only about 20% homology). The fact that the serotype 1 and 2 S1 genes are much more closely related to each other than to the serotype 3 S1 gene is remarkable since for all other nine reovirus genes the serotype 1 and 3 genes are much more closely related to each other than to the serotype 2 gene. Mechanisms that may effect this remarkable evolutionary pattern are discussed.


Subject(s)
Capsid Proteins , Reoviridae/genetics , Viral Proteins/genetics , Amino Acid Sequence , Base Sequence , Genes, Viral , RNA, Viral/genetics , Serotyping , Solubility
13.
Virology ; 133(1): 191-6, 1984 Feb.
Article in English | MEDLINE | ID: mdl-6546631

ABSTRACT

All 10 genes of the Dearing strain of reovirus serotype 3 have been cloned in their entirety into pBR322. This has been proved by sequencing the terminal regions (50-100 residues long) of all 10 cloned genes; all such regions were found to be identical to the corresponding terminal regions of the double-stranded RNA genes that are present in reovirus particles. The lengths of the cloned reovirus genes were estimated by comparing their electrophoretic mobilities (and those of their PstI cleavage fragments) with those of accurately known marker DNA molecules. The genes range in size from about 3825 bp for the L genes to about 1200 bp for the S4 gene.


Subject(s)
Cloning, Molecular , Genes, Viral , Mammalian orthoreovirus 3/genetics , Reoviridae/genetics , Base Sequence , DNA/metabolism , Molecular Weight , Plasmids , RNA, Double-Stranded/genetics , RNA, Double-Stranded/isolation & purification , Transcription, Genetic
14.
J Gen Virol ; 64 ( Pt 12): 2585-95, 1983 Dec.
Article in English | MEDLINE | ID: mdl-6319550

ABSTRACT

The genes of a field isolate of human rotavirus were cloned into pBR322. The strategy used involved polyadenylation of denatured double-stranded (ds) genomic RNA, followed by cDNA synthesis using reverse transcriptase. Oligo(dC) tails were added to the 3' end of the single-stranded cDNA and then separated by alkaline agarose electrophoresis. Sized cDNA of both polarities were allowed to hybridize and inserted into the PstI site of pBR322. Transformations done with sized cDNA always resulted in the selection of hybrid plasmids carrying inserts with a size representative of the original cDNA. Four individual clones were selected for preliminary characterization. One clone has an insert of 1360 base pairs (bp) and corresponds to gene 6. The second clone has an insert of 1140 bp and corresponds to one of the genes in the triplet 7-8-9. The other two genes, with inserts of 780 and 660 bp, were identified as corresponding to dsRNA segments 10 and 11.


Subject(s)
Cloning, Molecular , Genes, Viral , Rotavirus/genetics , Base Sequence , DNA/biosynthesis , DNA Restriction Enzymes , Humans , Nucleic Acid Hybridization , Plasmids , RNA, Messenger/genetics , RNA, Viral/genetics , Transformation, Genetic
15.
Proc Natl Acad Sci U S A ; 79(24): 7644-8, 1982 Dec.
Article in English | MEDLINE | ID: mdl-6961439

ABSTRACT

The genes of the Dearing strain of reovirus serotype 3, which consist of double-stranded RNA, have been cloned into pBR322 by tailing both strands of each gene with poly(A), transcribing them with reverse transcriptase, self-hybridizing the cognate plus and minus cDNA strands, incubating them with Escherichia coli DNA polymerase I to ensure that they are complete, and cloning the double-stranded cDNA molecules by standard procedures. The sequence of the cloned S2 gene has been determined. The sequence at the termini are exactly the same as those at the ends of the native double-stranded RNA gene. The gene is 1,329 nucleotides long and possesses a single long open reading frame that starts at the first initiation codon (residue 19) and extends for 331 codons, sufficient to encode a protein of the same size as the known S2 gene product, protein sigma 2, a major reovirus core component (Mr, 38,000). A second open reading frame of 85 codons, in a different phase, starts close to where the first ends. The protein translated from this reading frame is unknown.


Subject(s)
Genes, Viral , RNA, Double-Stranded/genetics , Reoviridae/genetics , Amino Acid Sequence , Base Sequence , Cloning, Molecular , Viral Proteins/genetics
16.
J Virol ; 35(3): 895-901, 1980 Sep.
Article in English | MEDLINE | ID: mdl-6252345

ABSTRACT

Phenotypic transformation of the host cell affected the formation of polyoma pseuodovirions. Polyoma virus infection of various transformed derivatives of mouse 3T3 cells resulted in the formation of predominantly pseudovirions, whereas infection of mouse 3T3 cells produced mainly polyoma virus. The effect that transformation of the host cell had on polyoma pseudovirus formation was further demonstrated by using phenotypic revertants isolated from some of the transformed cell lines. The revertants were characterized by their morphology, saturation densities, and colony-forming ability in methylcellulose suspension. By these criteria they were distinct from their transformed parents and similar to 3T3 cells. After infection, the revertants produced predominantly polyoma virus and few pseudovirus. Thus, for the cell lines used in this study, phenotypic transformation enhanced the formationof polyoma pseudovirions.


Subject(s)
Cell Transformation, Viral , Polyomavirus/growth & development , Virion/growth & development , Animals , Cell Line , DNA/analysis , Mice , Polyomavirus/analysis , Virion/analysis
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