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1.
J Virol Methods ; 174(1-2): 60-4, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21458496

ABSTRACT

A polyclonal antibody-based, group-specific, competitive ELISA (C-ELISA) for the detection of antibodies to equine encephalosis virus (EEV) was developed. The assay measures the competition between a specific guinea pig antiserum and a test serum, for a pre-titrated EEV antigen. The C-ELISA detected antibodies to the seven known EEV serotypes. Reference antisera raised against other arboviruses did not cross react with EEV antigen. Negative sera from horses in the United Kingdom were used to establish the baseline for a negative population. Negative and positive populations of South African horses, selected on the basis of virus neutralisation were assayed subsequently. Optimal test parameters, where sensitivity≅specificity≅100%, were calculated by two-graph receiver operator characteristic (TG-ROC) analysis to be at a cut-off value of 29.5% inhibition. Results show the EEV C-ELISA described to be sensitive, specific and reliable. Used in conjunction with ELISAs available for African horse sickness virus (AHSV), differential serological diagnosis between EEV and AHSV can be achieved.


Subject(s)
Antibodies, Viral/blood , Clinical Laboratory Techniques/methods , Horse Diseases/diagnosis , Orbivirus/isolation & purification , Reoviridae Infections/veterinary , Virology/methods , Animals , Enzyme-Linked Immunosorbent Assay/methods , Horse Diseases/virology , Horses , Orbivirus/immunology , Reoviridae Infections/diagnosis , Reoviridae Infections/virology , Sensitivity and Specificity , South Africa , United Kingdom
2.
J Virol Methods ; 112(1-2): 129-35, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12951221

ABSTRACT

A polyclonal antibody-based, group-specific, indirect, sandwich ELISA (S-ELISA) for the detection of equine encephalosis virus (EEV) antigen was developed. Purified EEV particles were titrated in the S-ELISA and the limit of detection was determined to be approximately 9.0 ng of antigen/ml (0.45 ng/well). Positive S-ELISA reactions were recorded with seven serologically distinct EEV serotypes. No cross-reactions were recorded with other arboviruses including African horse sickness virus (AHSV) serotypes 1-9, bluetongue serotypes 1-24, epizootic haemorrhagic disease serotypes 1-8 and isolate 318, and selected isolates of Palyam, Eubenangee, Corriparta, Warrego, Akabane and bovine ephemeral fever viruses. The assay proved to be sensitive and specific for the rapid detection of EEV in cell cultures and in homogenated suckling mouse brain (MB). The data generated in this study suggest that the ELISA will be valuable for epidemiological studies of EE and will assist in making a reliable differential diagnosis between EEV and AHSV infections.


Subject(s)
Antigens, Viral/analysis , Enzyme-Linked Immunosorbent Assay/methods , Horse Diseases/diagnosis , Reoviridae Infections/veterinary , Reoviridae/immunology , Animals , Guinea Pigs , Horse Diseases/blood , Horse Diseases/immunology , Horse Diseases/virology , Horses , Mice , Rabbits , Reoviridae/isolation & purification , Reoviridae Infections/blood , Reoviridae Infections/diagnosis , Reproducibility of Results , Sensitivity and Specificity
3.
J Gen Virol ; 84(Pt 1): 227-235, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12533719

ABSTRACT

Bluetongue virus (BTV) and several other Orbivirus species are transmitted between mammalian hosts via bites from adults of certain species of Culicoides midges. However, BTV can survive for 9-12 months (typically during the winter), in the absence of adult vectors, with no detectable cases of viraemia, disease or seroconversion in the host. The survival of the virus from one 'vector season' to the next is called 'overwintering' but the mechanism involved is not fully understood. It is demonstrated that BTV can persistently infect ovine gammadelta T-cells in vitro, a process that may also occur during infection and viraemia in mammalian hosts, thus providing a mechanism for virus persistence. Interaction of persistently BTV-infected gammadelta T-cells with antibody to the gammadelta T-cell-specific surface molecule WC-1 resulted in conversion to a lytic infection and increased virus release. Skin fibroblasts induce a similar conversion, indicating that they express a counter ligand for WC-1. Feeding of Culicoides midges induces skin inflammation, which is accompanied by recruitment of large numbers of activated gammadelta T-cells. The interaction of persistently infected gammadelta T-cells with skin fibroblasts would result in increased virus production at 'biting sites', favouring transmission to the insect vector. This suggested mechanism might also involve up-regulation of the WC-1 ligand at inflamed sites. It has been shown previously that cleavage of virus surface proteins by protease enzymes (which may also be associated with inflammation) generates infectious subvirus particles that have enhanced infectivity (100 times) for the insect vector.


Subject(s)
Bluetongue virus/physiology , Bluetongue/transmission , Bluetongue/virology , Ceratopogonidae/physiology , Insect Vectors/physiology , Seasons , Animals , Cattle , Cell Line , Ceratopogonidae/virology , Coculture Techniques , Fibroblasts/virology , Insect Vectors/virology , Receptors, Antigen, T-Cell, gamma-delta/metabolism , Sheep , Skin/cytology , Skin/virology , T-Lymphocytes/virology
4.
J Virol ; 76(18): 9533-6, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12186935

ABSTRACT

Double-stranded RNA (dsRNA) viruses conceal their genome from the host to avoid triggering unfavorable cellular responses. The crystal structure of the core of one such virus, bluetongue virus, reveals an outer surface festooned with dsRNA. This may represent a deliberate strategy to sequester dsRNA released from damaged particles to prevent host cell shutoff.


Subject(s)
Bluetongue virus/metabolism , RNA, Double-Stranded/metabolism , RNA, Viral/metabolism , Viral Core Proteins/metabolism , Binding Sites , Crystallography, X-Ray , Humans , Models, Molecular , Protein Conformation , RNA, Double-Stranded/chemistry , RNA, Viral/chemistry , Viral Core Proteins/chemistry , X-Ray Diffraction
5.
EMBO J ; 20(24): 7229-39, 2001 Dec 17.
Article in English | MEDLINE | ID: mdl-11742999

ABSTRACT

The bluetongue virus core is a molecular machine that simultaneously and repeatedly transcribes mRNA from 10 segments of viral double-stranded RNA, packaged in a liquid crystalline array. To determine how the logistical problems of transcription within a sealed shell are solved, core crystals were soaked with various ligands and analysed by X-ray crystallography. Mg(2+) ions produce a slight expansion of the capsid around the 5-fold axes. Oligonucleotide soaks demonstrate that the 5-fold pore, opened up by this expansion, is the exit site for mRNA, whilst nucleotide soaks pinpoint a separate binding site that appears to be a selective channel for the entry and exit of substrates and by-products. Finally, nucleotides also bind to the outer core layer, providing a substrate sink.


Subject(s)
Bluetongue virus/physiology , Transcription, Genetic , Base Sequence , Binding Sites , Bluetongue virus/genetics , Calcium/metabolism , Crystallography, X-Ray , Magnesium/metabolism , Phosphates/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sulfates/metabolism
6.
Cell ; 97(4): 481-90, 1999 May 14.
Article in English | MEDLINE | ID: mdl-10338212

ABSTRACT

The concentration of double-stranded RNA within the bluetongue virus core renders the genome segments liquid crystalline. Powder diffraction rings confirm this local ordering with a 30 A separation between strands. Determination of the structure of the bluetongue virus core serotype 10 and comparison with that of serotype 1 reveals most of the genomic double-stranded RNA, packaged as well-ordered layers surrounding putative transcription complexes at the apices of the particle. The outer layer of RNA is sufficiently well ordered by interaction with the capsid that a model can be built and extended to the less-ordered inner layers, providing a structural framework for understanding the mechanism of this complex transcriptional machine. We show that the genome segments maintain local order during transcription.


Subject(s)
Bluetongue virus/genetics , Nucleic Acid Conformation , RNA, Double-Stranded/chemistry , RNA, Viral/chemistry , Animals , Bluetongue virus/physiology , Crystallography, X-Ray , Genome, Viral , Ions , RNA, Double-Stranded/metabolism , RNA, Viral/metabolism , Transcription, Genetic , Viral Core Proteins/chemistry , Viral Core Proteins/metabolism , Virus Assembly , X-Ray Diffraction
7.
Arch Virol Suppl ; 14: 235-50, 1998.
Article in English | MEDLINE | ID: mdl-9785510

ABSTRACT

We are using crystallographic methods to investigate the structure of AHSV and BTV. Our initial approach was to investigate the structure of the major protein component of the viral core, VP7(T13). This trimeric protein has been studied in several crystal forms from both orbiviruses and reveals a structure made up of conserved domains, capable of conformational changes and possessing a cleavage site. Further crystallographic analyses of native particles have provided a picture of the VP7(T13) and VP3(T2) layers of the BTV core. The VP7(T13) layer consists of 260 trimers arranged rather symmetrically and possessing very similar structures, thereby following the rules of quasi equivalence. The VP3(T2) layer is thin and contains 120 copies of 100 kDa protein arranged as 60 approximate dimers. This type of icosahedral construction has not been observed before and appears to contain a genome which is highly ordered. We anticipate that all of these features will be common to AHSV.


Subject(s)
African Horse Sickness Virus/chemistry , Bluetongue virus/chemistry , Viral Structural Proteins/chemistry , Virion/chemistry , Animals , Antigens, Viral/chemistry , Crystallography , Protein Conformation , Viral Core Proteins/chemistry
8.
Arch Virol Suppl ; 14: 211-9, 1998.
Article in English | MEDLINE | ID: mdl-9785508

ABSTRACT

An established mouse model system was used to evaluate the effectiveness of the major outer core protein VP7 of African horse sickness virus (AHSV) serotype 9 as a subunit vaccine. Balb C mice were immunised with VP7 crystals purified from AHSV infected BHK cells. In groups of mice, each of which was immunised with > or = 1.5 micrograms of the protein in Freund's adjuvant, > or = 80% of mice survived challenge with a virulent strain of a heterologous AHSV serotype (AHSV 7), that killed > or = 80% of the mice in the uninoculated control groups. This level of protection was significantly greater than that observed in mice inoculated with equivalent amounts of either denatured VP7 (50% survival), or GST/VP7 fusion protein (50-70% survival), or which were vaccinated with AHSV 9 (40-50% survival). The VP7 protein folding, or its assembly into crystals, are thought to play some role in the effectiveness of the protective response observed. Titres of circulating antibodies against AHSV VP7 were determined by competitive ELISA but did not appear to correlate with the levels of protection observed. Passive transfer of these antibodies to syngeneic recipients also failed to protect Balb C mice from the AHSV 7 challenge. The observed protection is therefore unlikely to be due to an antibody mediated immune response.


Subject(s)
African Horse Sickness/prevention & control , Antigens, Viral/immunology , Viral Core Proteins/immunology , Viral Vaccines , Animals , Antibodies, Viral/blood , Disease Models, Animal , Female , Horses , Immunization, Passive , Mice , Mice, Inbred BALB C
9.
Arch Virol Suppl ; 14: 259-79, 1998.
Article in English | MEDLINE | ID: mdl-9785512

ABSTRACT

Attenuated (att) and wild type (wt) strains of the nine AHSV serotypes were evaluated for virulence in adult Balb C mice. Although most were avirulent in this system, isolates of AHSV 1att, 3wt, 3att, 4wt, 5att, 7att and 8att caused some mortality when administered via an intranasal route. After plaque cloning, only the attenuated vaccine strain of AHSV 7att caused any mortality via an intravenous route. AHSV 3att and AHSV 8wt were virulent (V) and avirulent (AV) (respectively) in the mouse model and were selected as parental strains for production of genome segment reassortants. These progeny virus strains were plaque cloned, then characterised to identify the genome segments that influence virulence of AHSV in the mouse model. Three virulence phenotypes were observed: fully virulent (V); fully avirulent (A); and a novel intermediate virulence (N) not expressed by either parental strain. Genome segment 2 (encoding outer capsid protein VP2) from the avirulent parent appeared to have a controlling influence in production of the A phenotype. Reassortants with the V phenotype all contained segment 2 from the virulent parent, however in each case they also contained genome segments 5 and 10, also from AHSV 3 (V). Genome segments 5 and 10 encode the smaller outer capsid protein VP5 and the non structural proteins NS3/NS3a, respectively. A combination of genome segments 2, 5 and 6 from the avirulent parent and segment 10 from the virulent parent were found in each of the virus strains with the N phenotype. However, comparison of two reassortants (A79 and A790), which differ only in a single segment, showed that replacement of genome segment 10 from the avirulent parent with that from the virulent parent, conferred the N phenotype on A790.


Subject(s)
African Horse Sickness Virus/genetics , African Horse Sickness/virology , African Horse Sickness/mortality , African Horse Sickness Virus/classification , African Horse Sickness Virus/pathogenicity , Animals , Cell Line , Cricetinae , Disease Models, Animal , Electrophoresis, Polyacrylamide Gel , Genome, Viral , Horses , Mice , Mice, Inbred BALB C , RNA, Double-Stranded/analysis , RNA, Double-Stranded/genetics , RNA, Viral/analysis , RNA, Viral/genetics , Rabbits , Serial Passage , Serotyping , Vaccines, Attenuated , Viral Proteins/genetics , Viral Vaccines , Virulence/genetics
10.
Nature ; 395(6701): 470-8, 1998 Oct 01.
Article in English | MEDLINE | ID: mdl-9774103

ABSTRACT

The structure of the core particle of bluetongue virus has been determined by X-ray crystallography at a resolution approaching 3.5 A. This transcriptionally active compartment, 700 A in diameter, represents the largest molecular structure determined in such detail. The atomic structure indicates how approximately 1,000 protein components self-assemble, using both the classical mechanism of quasi-equivalent contacts, which are achieved through triangulation, and a different method, which we term geometrical quasi-equivalence.


Subject(s)
Bluetongue virus/chemistry , Viral Core Proteins/chemistry , Amino Acid Sequence , Crystallography, X-Ray , Models, Molecular , Molecular Sequence Data , Protein Binding , Protein Conformation , RNA, Viral/chemistry , Viral Core Proteins/metabolism
11.
J Gen Virol ; 78 ( Pt 7): 1611-6, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9225037

ABSTRACT

An established mouse model was used to evaluate the effectiveness of the major outer core protein of African horsesickness virus (AHSV), VP7, as a subunit vaccine. Adult female BALB/c mice were immunized with VP7 crystals purified from BHK cells infected with AHSV serotype 9 (AHSV-9), using three inoculations in Freund's adjuvant. Eighty to one hundred per cent of the immunized mice were protected against a heterologous challenge with a known lethal dose of AHSV-7. The protected immunized mice did not develop any clinical signs characteristic of virulent AHSV infection in this model during the study. In contrast, 80-100% mortality was observed in the non-immunized mice that received the same challenge virus. Subsequent studies indicated that a single inoculation of 1.5 micrograms purified AHSV VP7 in Freund's complete adjuvant was sufficient to protect at least 90% of mice from AHSV-7 challenge. If the antigen was presented in the absence of Freund's complete adjuvant, 70% of the mice were still protected by one inoculation of VP7 crystals. Titres of circulating antibody against AHSV VP7, determined by competitive ELISA, did not appear to correlate with protection and passive antibody transfer from immunized BALB/c mice failed to protect syngeneic recipients from AHSV-7 challenge. Therefore, the observed protection is unlikely to be due to an antibody-mediated immune response. The number of viraemic mice and the duration of viraemia post-challenge was significantly reduced in vaccinated mice compared to non-vaccinated controls. However, the levels of viraemia were similar.


Subject(s)
African Horse Sickness Virus/immunology , African Horse Sickness/prevention & control , Antigens, Viral/immunology , Vaccines, Synthetic/immunology , Viral Core Proteins/immunology , Viral Vaccines/immunology , African Horse Sickness/immunology , African Horse Sickness Virus/isolation & purification , African Horse Sickness Virus/pathogenicity , Animals , Antibodies, Viral/blood , Antigens, Viral/genetics , Cell Line , Cricetinae , Female , Immunization, Passive , Mice , Mice, Inbred BALB C , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/immunology , Serotyping , Tissue Distribution , Viral Core Proteins/genetics , Viremia
12.
J Virol Methods ; 57(2): 117-26, 1996 Apr 05.
Article in English | MEDLINE | ID: mdl-8801224

ABSTRACT

A monoclonal antibody based competitive enzyme-linked immunosorbent assay (MC-ELISA) for the detection of antibodies against epizootic haemorrhagic disease of deer viruses (EHDV) is described. Test sera were competed with a monoclonal antibody against the VP7 protein of EHDV serotype 1. The assay was capable of detecting antibodies to all serotypes of EHDV but unlike the agar gel immunodiffusion (AGID) test, gave no cross-reactions with antibodies against bluetongue, Palyam or Tilligery viruses. The MC-ELISA was more sensitive than a polyclonal based ELISA reported previously (Thevasagayam et al., 1995b) and would be ideal for epidemiological surveys since it is suitable for the examination of antisera from all animal species without the need for individual anti-species enzyme conjugates.


Subject(s)
Antibodies, Monoclonal/immunology , Antibodies, Viral/analysis , Antigens, Viral , Capsid Proteins , Capsid/immunology , Enzyme-Linked Immunosorbent Assay/methods , Hemorrhagic Disease Virus, Epizootic/isolation & purification , Animals , Antibodies, Viral/immunology , Antibody Specificity , Cattle , Cell Line , Cricetinae , Deer/virology , Hemorrhagic Disease Virus, Epizootic/immunology , Mice , Mice, Inbred BALB C , Sheep
13.
Virology ; 217(2): 582-93, 1996 Mar 15.
Article in English | MEDLINE | ID: mdl-8610450

ABSTRACT

Previous studies (Mertens et al., Virology 157, 375-386, 1987) have shown that removal of the outer capsid layer from bluetongue virus (BTV) significantly reduces (approximately x 10(-4)) the infectivity of the resultant core particle for mammalian cells (BHK 21 cells). In contrast, the studies reported here, using a cell line (KC cells) derived from a species of Culicoides that can act as a vector for BTV (Culicoides variipennis), demonstrated a much higher infectivity of core particles than that in mammalian cells (approximately x 10(3)). This increase resulted in a specific infectivity for cores that was only 20-fold less than that of purified disaggregated virus particles (stored in the presence of 0.1% sodium-N-lauroylsarcosine (NLS)). Removal of this detergent caused intact virus particle aggregation and (as previously reported) resulted in an approximately 1 log10 drop in the specific infectivity of those virus particles which remained in suspension. In consequence the specific infectivity of core particles for the KC cells was directly comparable to that of the intact but aggregated virus. These data are compared with the results from oral infectivity studies using two vector species (C. variipennis and Culicoides nubeculosus), which showed similar infection rates at comparable concentrations of purified cores, or of the intact but aggregated virus particles (NLS was toxic to adult flies). The role of the outer core proteins (VP7) in cell attachment and penetration, as an alternative route of initiation of infection, is discussed. Previous studies (Mertens et al., Virology 157, 375-386, 1987) also showed that the outer capsid layer of BTV can be modified by proteases (including trypsin or chymotrypsin), thereby generating infectious subviral particles (ISVP). The specific infectivity of ISVP for mammalian cells (BHK21 cells) was shown to be similar to that of disaggregated virus particles. In contrast, we report a significantly higher specific infectivity of ISVP but not of the intact virus (approximately x 100) for two insect cell lines (KC cells and C6/36 mosquito cells (derived from Aedes albopictus)). In oral infection studies with adults of the two vector species, ISVP produced the same infection rate at approximately 100-fold lower concentrations than either core particles or the intact but aggregated virus particles. The importance of mammalian host serum proteases, or insect gut proteases, in modification of the intact virus particle to form ISVP and their role in initiation of infection and the vector status of the insect is discussed.


Subject(s)
Bluetongue virus/pathogenicity , Diptera/microbiology , Insect Vectors/microbiology , Animals , Bluetongue virus/growth & development , Bluetongue virus/ultrastructure , Cell Line , Cricetinae , Female , Molecular Weight , Protease Inhibitors/pharmacology , Viral Proteins/analysis
14.
J Virol Methods ; 56(1): 49-57, 1996 Jan.
Article in English | MEDLINE | ID: mdl-8690767

ABSTRACT

A serogroup specific sandwich ELISA was developed for the detection of epizootic haemorrhagic disease of deer viruses (EHDV) in infected insects and tissue culture preparations. Polyclonal rabbit antiserum against purified EHDV core particles was used to capture viral antigen and specific binding detected using guinea pig antisera against EHDV core particles followed by anti-guinea pig immunoglobulin enzyme-labelled conjugate. The assay is EHDV specific and detects all 8 serotypes. No cross-reactions were found with related viruses such as bluetongue (BTV), Palyam, Tilligery or African horse sickness virus (AHSV). A similar serogroup specific sandwich ELISA was also developed for BTV. The assays showed a similar sensitivity in detecting the respective EHDV or BTV antigens in a pool of 500 midges where only 2 were infected. These assays allow a simple and rapid means of detecting and differentiating members of these closely related serogroups. The sensitivity of the tests will allow more extensive studies on vector competence and virus/vector distribution.


Subject(s)
Bluetongue virus/isolation & purification , Ceratopogonidae/virology , Enzyme-Linked Immunosorbent Assay , Hemorrhagic Disease Virus, Epizootic/isolation & purification , Animals , Cell Line , Chick Embryo , Cricetinae , Deer , Guinea Pigs , Rabbits , Sensitivity and Specificity
15.
J Virol Methods ; 55(3): 417-25, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8609206

ABSTRACT

A competitive enzyme-linked immunosorbent assay is described for the detection of antibodies against epizootic haemorrhagic disease of deer viruses (EHDV). Test antisera were tested against a guinea-pig antiserum raised against EHDV core particles. The assay detected antibodies to all serotypes of EHDV, but unlike the agar gel immunodiffusion (AGID) test, gave no cross-reactions with antibodies against bluetongue, Palyam and Tilligery viruses. The C-ELISA would be ideal for use in epidemiological surveys since it is suitable for the examination of antisera from all susceptible species without the need for individual species-specific enzyme conjugates.


Subject(s)
Antibodies, Viral/blood , Enzyme-Linked Immunosorbent Assay/methods , Hemorrhagic Disease Virus, Epizootic/isolation & purification , Viral Core Proteins/immunology , Animals , Antibodies, Viral/immunology , Cattle , Cell Line , Cricetinae , Cross Reactions , Deer , Guinea Pigs , Hemorrhagic Disease Virus, Epizootic/immunology , Horses , Reoviridae Infections/diagnosis , Reoviridae Infections/veterinary , Sensitivity and Specificity , Sheep , Time Factors
16.
J Gen Virol ; 76 ( Pt 10): 2607-11, 1995 Oct.
Article in English | MEDLINE | ID: mdl-7595366

ABSTRACT

Purified African horse sickness virus (AHSV) was fed, as part of a blood meal, to adult females from a susceptible colony of Culicoides variipennis, established in the insectories at the Institute for Animal Health, Pirbright Laboratory, UK. The meal consisted of heparinized blood obtained from ovine, bovine, equine (horse and donkey) or canine sources spiked with AHSV serotype 9 (AHSV9). The infectivity levels observed for C. variipennis varied significantly, according to the source of the blood sample. Comparison of the protein profiles obtained from AHSV9 incubated with the individual serum of plasma samples indicated that some species-specific serum proteases were able to cleave the outer capsid protein, VP2. The blood samples containing serum proteases that were able to cleave VP2 also showed an increase in infectivity for the insect vector when spiked with purified AHSV.


Subject(s)
African Horse Sickness Virus/pathogenicity , Capsid/metabolism , Ceratopogonidae/virology , Endopeptidases/blood , Animals , Blood , Capsid Proteins , Cattle , Dogs , Endopeptidases/metabolism , Equidae , Female , Horses , Insect Vectors/virology , Sheep , Species Specificity
17.
Virology ; 210(1): 217-20, 1995 Jun 20.
Article in English | MEDLINE | ID: mdl-7793074

ABSTRACT

Core particles of bluetongue virus serotype 1 (South Africa) have been crystallized. The crystals, which grow up to 0.8 mm in diameter, belong to a primitive orthorhombic space group and have point group symmetry 222. The unit cell dimensions are 754 x 796 x 823 A3 and the crystallographic asymmetric unit contains one-half of a core particle. The best crystals diffract strongly to 4.8 A Bragg spacings, which is the maximum resolution to which we can measure data with the detectors available, suggesting that useful diffraction extends well beyond this. Core particles of serotype 10 have also been crystallized but the crystals have yet to be analyzed by X-ray diffraction.


Subject(s)
Bluetongue virus/chemistry , Viral Core Proteins/chemistry , Viral Core Proteins/ultrastructure , Animals , Bluetongue virus/classification , Bluetongue virus/ultrastructure , Cattle , Crystallization , Crystallography, X-Ray/methods , Goats , Ruminants , Sheep , South Africa , X-Ray Diffraction/methods
18.
Semin Oncol ; 21(5 Suppl 12): 7-19, 1994 Oct.
Article in English | MEDLINE | ID: mdl-7992070

ABSTRACT

Data from women with advanced ovarian cancer (International Federation of Gynecology and Obstetrics stage III or IV) were analyzed to evaluate the pharmacokinetic/pharmacodynamic relationships of carboplatin-based combination chemotherapy. With the equation area under the plasma concentration versus time curve (AUC) = dose/(creatinine clearance + 25), carboplatin AUC was calculated in each of up to six treatment cycles in 224 women with advanced ovarian cancer who had been randomized to receive carboplatin 300 mg/m2 plus cyclophosphamide 600 mg/m2. In addition, for each patient, the predicted nadir count (obtained by rearranging the University of Maryland single-agent carboplatin dosing formula) was compared with the actual observed nadir count, received and relative received dose intensities were calculated, and carboplatin exposure intensity was defined. Relationships were sought between these treatment indices and the clinical outcomes of time to progression and survival. When combined with cyclophosphamide 600 mg/m2, any carboplatin AUC was found to be associated with greater myelotoxicity and a higher likelihood of both leukopenia and thrombocytopenia occurring than had been determined for single-agent carboplatin. Furthermore, the platelet nadir in 83% of patients was equal to or below that predicted to result from the same dose of single-agent carboplatin. There was a relatively narrow range of received dose intensities within this patient population, but carboplatin exposure intensity was calculated as being distributed over a two-fold range within the population. Therefore, received carboplatin dose intensity underestimates the range of plasma drug exposure associated with a fixed dosing regimen of carboplatin. However, there were no consistent relationships between received dose intensity, relative received dose intensity, or carboplatin exposure intensity and the clinical outcomes of time to progression or survival. The relationships between carboplatin exposure and the pharmacodynamic measures of toxicity and response are likely to require definition in each regimen that includes carboplatin and for each tumor type treated.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Models, Biological , Ovarian Neoplasms/drug therapy , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Antineoplastic Combined Chemotherapy Protocols/pharmacokinetics , Carboplatin/administration & dosage , Cyclophosphamide/administration & dosage , Dose-Response Relationship, Drug , Female , Humans , Leukopenia/chemically induced , Thrombocytopenia/chemically induced
19.
J Gen Virol ; 75 ( Pt 8): 1849-57, 1994 Aug.
Article in English | MEDLINE | ID: mdl-8046387

ABSTRACT

Methods were developed for the purification, at high yield, of four different particle types of African horsesickness virus serotype 9 (AHSV-9). These products included virus particles purified on CsCl gradients which contain proteins apparently directly comparable to those of bluetongue virus (VP1 to VP7); virus particles purified on sucrose gradients which also contain, as a variable component, protein NS2; infectious subviral particles (ISVPs), containing chymotrypsin cleavage products of VP2; and cores, obtained by treating purified ISVPs with 1 M-MgCl2 to remove the components of the outer capsid layer (VP5 and VP2 cleavage products). Additional protein bands migrating with apparent M(r)s lower than that of VP5 were detected during SDS-PAGE analysis of virus particles. These appear to be conformational variants of VP5 and are identified as VP5' and VP5". BHK-21 cells infected with this strain of AHSV-9 produce large quantities of flat, usually hexagonal crystals of VP7, a major group antigen and core protein; these were also purified. Either 20 mg of virus particles, 20 mg of ISVPs or 10 mg of cores as well as 20 mg of VP7 crystals could be purified from approximately 8 x 10(9) infected cells. None of the preparations of particles or crystals showed any detectable contamination with BHK-21 cell proteins or antigens, as determined by SDS-PAGE or indirect ELISA. Virus particle and ISVP preparations had similar specific infectivities for BHK-21 cells (approximately 1 x 10(9) TCID50/A260 unit) but the infectivity of cores was approximately 10(5)-fold lower.


Subject(s)
African Horse Sickness Virus/isolation & purification , Antigens, Viral/isolation & purification , Viral Core Proteins/isolation & purification , African Horse Sickness Virus/classification , African Horse Sickness Virus/pathogenicity , African Horse Sickness Virus/ultrastructure , Animals , Antigens, Viral/ultrastructure , Cells, Cultured , Cricetinae , Crystallization , Microscopy, Electron , Viral Core Proteins/ultrastructure , Virulence
20.
J Clin Oncol ; 11(6): 1156-64, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8501502

ABSTRACT

PURPOSE: To determine (1) the impact of cyclophosphamide 600 mg/m2 on previously defined relationships between carboplatin area under the plasma concentration versus time curve (AUC) and indices of toxicity and response in women with advanced ovarian cancer; and (2) the relationships between indices of cumulative drug exposure and clinical outcomes. METHODS: Carboplatin AUC = dose/(creatinine clearance [CCr] + 25) and was calculated in 224 women who received carboplatin 300 mg/m2 and cyclophosphamide 600 mg/m2. The likelihood of grade 3 or greater myelotoxicity at any carboplatin AUC was compared with the likelihood of myelotoxicity at the same single-agent carboplatin AUC. The nadir count predicted using the University of Maryland single-agent carboplatin dosing formula was compared with the nadir count observed. Received and relative-received dose-intensity were calculated. Carboplatin exposure-intensity was defined by substituting cumulative carboplatin exposure for total dose. Relationships were sought between these indices and therapeutic outcomes. RESULTS: The incidence of leukopenia and thrombocytopenia at any carboplatin AUC was greater for the two-drug combination than for single-agent carboplatin. The platelet nadir in 83% of patients was less than or equal to the nadir predicted for the same single-agent carboplatin AUC. Despite a narrow range of received dose-intensities, carboplatin exposure-intensity was distributed over a twofold range. There were no relationships between received and relative-received dose-intensity or carboplatin exposure-intensity and time to progression or survival. CONCLUSION: Any carboplatin AUC when administered with cyclophosphamide 600 mg/m2 produces greater myelotoxicity than the same AUC of single-agent carboplatin. Received carboplatin dose-intensity underestimates the range of plasma drug exposure resulting from a fixed carboplatin dosing regimen. Whether higher carboplatin exposures can improve outcome requires prospective validation.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Carboplatin/adverse effects , Ovarian Neoplasms/drug therapy , Adult , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Carboplatin/administration & dosage , Carboplatin/pharmacokinetics , Cyclophosphamide/administration & dosage , Cyclophosphamide/pharmacokinetics , Dose-Response Relationship, Drug , Female , Humans , Leukopenia/chemically induced , Middle Aged , Ovarian Neoplasms/pathology , Thrombocytopenia/chemically induced
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