RESUMEN
In 2013, the national surveillance case definition for West Nile virus (WNV) disease was revised to remove fever as a criterion for neuroinvasive disease and require at most subjective fever for non-neuroinvasive disease. The aims of this project were to determine how often afebrile WNV disease occurs and assess differences among patients with and without fever. We included cases with laboratory evidence of WNV disease reported from four states in 2014. We compared demographics, clinical symptoms and laboratory evidence for patients with and without fever and stratified the analysis by neuroinvasive and non-neuroinvasive presentations. Among 956 included patients, 39 (4%) had no fever; this proportion was similar among patients with and without neuroinvasive disease symptoms. For neuroinvasive and non-neuroinvasive patients, there were no differences in age, sex, or laboratory evidence between febrile and afebrile patients, but hospitalisations were more common among patients with fever (P < 0.01). The only significant difference in symptoms was for ataxia, which was more common in neuroinvasive patients without fever (P = 0.04). Only 5% of non-neuroinvasive patients did not meet the WNV case definition due to lack of fever. The evidence presented here supports the changes made to the national case definition in 2013.
Asunto(s)
Enfermedades Asintomáticas/epidemiología , Fiebre/epidemiología , Fiebre del Nilo Occidental/diagnóstico , Fiebre del Nilo Occidental/epidemiología , Virus del Nilo Occidental/aislamiento & purificación , California/epidemiología , Técnicas de Laboratorio Clínico/métodos , Femenino , Fiebre/diagnóstico , Humanos , Incidencia , Louisiana/epidemiología , Masculino , Massachusetts/epidemiología , Minnesota/epidemiología , Vigilancia de la Población , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la EnfermedadRESUMEN
Accurate data on the incidence of West Nile virus (WNV) disease are important for directing public health education and control activities. The objective of this project was to assess the underdiagnosis of WNV neuroinvasive disease through laboratory testing of patients with suspected viral meningitis or encephalitis at selected hospitals serving WNV-endemic regions in three states. Of the 279 patients with cerebrospinal fluid (CSF) specimens tested for WNV immunoglobulin M (IgM) antibodies, 258 (92%) were negative, 19 (7%) were positive, and two (1%) had equivocal results. Overall, 63% (12/19) of patients with WNV IgM-positive CSF had WNV IgM testing ordered by their attending physician. Seven (37%) cases would not have been identified as probable WNV infections without the further testing conducted through this project. These findings indicate that over a third of WNV infections in patients with clinically compatible neurological illness might be undiagnosed due to either lack of testing or inappropriate testing, leading to substantial underestimates of WNV neuroinvasive disease burden. Efforts should be made to educate healthcare providers and laboratorians about the local epidemiology of arboviral diseases and the optimal tests to be used in different clinical situations.
Asunto(s)
Encefalitis Viral/epidemiología , Meningitis Viral/epidemiología , Fiebre del Nilo Occidental/epidemiología , Virus del Nilo Occidental/aislamiento & purificación , Adolescente , Adulto , Anciano , Anticuerpos Antivirales/líquido cefalorraquídeo , Arizona/epidemiología , California/epidemiología , Niño , Encefalitis Viral/líquido cefalorraquídeo , Encefalitis Viral/virología , Femenino , Hospitales , Humanos , Incidencia , Masculino , Meningitis Viral/líquido cefalorraquídeo , Meningitis Viral/virología , Persona de Mediana Edad , Minnesota/epidemiología , Vigilancia de la Población , Fiebre del Nilo Occidental/líquido cefalorraquídeo , Fiebre del Nilo Occidental/complicaciones , Adulto JovenRESUMEN
UNLABELLED: This case report describes an interproximal cervical lesion caused by the incorrect use of dental floss. A 58-year-old man who was asymptomatic, presented with unusual notch-like cervical lesions. After clinical and radiographical examinations, it was concluded that the aetiology of these lesions was an incorrect flossing technique. The treatment plan included extraction of maxillary 3rd molars and re-education of the patient in oral hygiene technique. CONCLUSION: These lesions are irreversible and often go undiagnosed; therefore, it is important for the clinician to be familiar with the clinical presentation and aetiology.
Asunto(s)
Dispositivos para el Autocuidado Bucal/efectos adversos , Higiene Bucal/efectos adversos , Educación del Paciente como Asunto , Abrasión de los Dientes/etiología , Cuello del Diente/lesiones , Humanos , Masculino , Persona de Mediana Edad , Autocuidado/efectos adversos , Abrasión de los Dientes/prevención & control , Resultado del TratamientoRESUMEN
This report examines the role of African swine fever virus (ASFV) structural protein pE120R in virus replication. Immunoelectron microscopy revealed that protein pE120R localizes at the surface of the intracellular virions. Consistent with this, coimmunoprecipitation assays showed that protein pE120R binds to the major capsid protein p72. Moreover, it was found that, in cells infected with an ASFV recombinant that inducibly expresses protein p72, the incorporation of pE120R into the virus particle is dependent on p72 expression. Protein pE120R was also studied using an ASFV recombinant in which E120R gene expression is regulated by the Escherichia coli lac repressor-operator system. In the absence of inducer, pE120R expression was reduced about 100-fold compared to that obtained with the parental virus or the recombinant virus grown under permissive conditions. One-step virus growth curves showed that, under conditions that repress pE120R expression, the titer of intracellular progeny was similar to the total virus yield obtained under permissive conditions, whereas the extracellular virus yield was about 100-fold lower than in control infections. Immunofluorescence and electron microscopy demonstrated that, under restrictive conditions, intracellular mature virions are properly assembled but remain confined to the replication areas. Altogether, these results indicate that pE120R is necessary for virus dissemination but not for virus infectivity. The data also suggest that protein pE120R might be involved in the microtubule-mediated transport of ASFV particles from the viral factories to the plasma membrane.
Asunto(s)
Virus de la Fiebre Porcina Africana/metabolismo , Proteínas de la Cápside , Proteínas de Unión al ADN/metabolismo , Proteínas Estructurales Virales/metabolismo , Ensamble de Virus , Virus de la Fiebre Porcina Africana/fisiología , Virus de la Fiebre Porcina Africana/ultraestructura , Animales , Transporte Biológico , Cápside/biosíntesis , Cápside/metabolismo , Membrana Celular/metabolismo , Chlorocebus aethiops , Proteínas de Unión al ADN/genética , Porcinos , Células Vero , Proteínas Estructurales Virales/genética , Virión/metabolismo , Ensamble de Virus/fisiologíaRESUMEN
This qualitative study explores the intimate relationship between parents as conceived by ten and 11 years old children. In a semi-structured interview and a semi-projective test, twelve children (6B/6G) were as to "imagine" the motivations that make parents want to be alone together. The content analysis of the children's stories showed at an affective level some indications of a: 1) capacity to recognize the exclusivity of the parental intimacy; 2) reluctance to recognize the sexual dimension of the parental intimacy. At a cognitive level, the content analysis indicates that 10 and 11 year old boys and girls have the capacity for decentralization, that is, to take the point of view of their parents. These results were discussed in light of the literature data. Educational implications were considered.
Asunto(s)
Padres , Percepción , Sexualidad , Niño , Cognición , Femenino , Humanos , Período de Latencia Psicosexual , Masculino , Psicología InfantilRESUMEN
African swine fever virus (ASFV) A224L is a member of the inhibitor of apoptosis protein (IAP) family. We have investigated the antiapoptotic function of the viral IAP both in stably transfected cells and in ASFV-infected cells. A224L was able to substantially inhibit caspase activity and cell death induced by treatment with tumor necrosis factor alpha and cycloheximide or staurosporine when overexpressed in Vero cells by gene transfection. We have also observed that ASFV infection induces caspase activation and apoptosis in Vero cells. Furthermore, using a deletion mutant of ASFV lacking the A224L gene, we have shown that the viral IAP modulates the proteolytic processing of the effector cell death protease caspase-3 and the apoptosis which are induced in the infected cells. Our findings indicate that A224L interacts with the proteolytic fragment of caspase-3 and inhibits the activity of this protease during ASFV infection. These observations could indicate a conserved mechanism of action for ASFV IAP and other IAP family members to suppress apoptosis.
Asunto(s)
Virus de la Fiebre Porcina Africana/fisiología , Apoptosis , Proteínas Bacterianas/fisiología , Caspasas/metabolismo , Proteínas de Insectos , Proteínas , Proteínas Estructurales Virales/fisiología , Virus de la Fiebre Porcina Africana/genética , Animales , Proteínas Bacterianas/genética , Western Blotting , Caspasa 3 , Supervivencia Celular , Chlorocebus aethiops , Activación Enzimática , Citometría de Flujo , Eliminación de Gen , Proteínas Inhibidoras de la Apoptosis , Transfección , Células Vero , Proteínas Estructurales Virales/genéticaRESUMEN
African swine fever virus (ASFV) is a complex DNA virus that employs polyprotein processing at Gly-Gly-Xaa sites as a strategy to produce several major core components of the viral particle. The virus gene S273R encodes a 31-kDa protein that contains a "core domain" with the conserved catalytic residues characteristic of SUMO-1-specific proteases and the adenovirus protease. Using a COS cell expression system, it was found that protein pS273R is capable of cleaving the viral polyproteins pp62 and pp220 in a specific way giving rise to the same intermediates and mature products as those produced in ASFV-infected cells. Furthermore, protein pS273R, like adenovirus protease and SUMO-1-specific enzymes, is a cysteine protease, because its activity is abolished by mutation of the predicted catalytic histidine and cysteine residues and is inhibited by sulfhydryl-blocking reagents. Protein pS273R is expressed late after infection and is localized in the cytoplasmic viral factories, where it is found associated with virus precursors and mature virions. In the virions, the protein is present in the core shell, a domain where the products of the viral polyproteins are also located. The identification of the ASFV protease will allow a better understanding of the role of polyprotein processing in virus assembly and may contribute to our knowledge of the emerging family of SUMO-1-specific proteases.
Asunto(s)
Virus de la Fiebre Porcina Africana/enzimología , Cisteína Endopeptidasas/metabolismo , Exopeptidasas/metabolismo , Proteínas Virales/metabolismo , Secuencia de Aminoácidos , Animales , Sitios de Unión , Células COS , Chlorocebus aethiops , Cisteína Endopeptidasas/química , Cisteína Endopeptidasas/genética , Técnica del Anticuerpo Fluorescente , Regulación Enzimológica de la Expresión Génica , Regulación Viral de la Expresión Génica , Histidina/genética , Histidina/metabolismo , Microscopía Inmunoelectrónica , Datos de Secuencia Molecular , Peso Molecular , Mutagénesis , Poliproteínas/química , Poliproteínas/metabolismo , Procesamiento Proteico-Postraduccional , Alineación de Secuencia , Especificidad por Sustrato , Transfección , Células VeroRESUMEN
High-resolution two-dimensional electrophoresis followed by computer analysis has been used to study quantitatively the patterns of protein synthesis produced in porcine alveolar macrophages and in Vero cells infected with African swine fever virus (ASFV). Initially, a protein database for each cell type was constructed. The porcine alveolar macrophage database includes 995 polypeptides (818 acidic, isoelectric focusing (IEF) and 177 basic, nonequilibrium pH gradient electrophoresis (NEPHGE)) whereas the Vero database contains 1,398 polypeptides (1,127 acidic, IEF and 271 basic, NEPHGE). Taking these databases as reference, ASFV highly virulent strain E70 induces 57 acid and 43 basic polypeptides in porcine alveolar macrophages, which account for most of the information content of the virus DNA. The kinetics of synthesis of the virus-induced polypeptides showed the existence of three classes of proteins: one whose synthesis starts early after infection, continues for a period and then switches off; another whose synthesis also starts early but continues for prolonged periods; and a third which requires DNA replication. The attenuated, cell adapted, strain BA71V induces 92 acidic and 37 basic proteins in Vero cells. Significant differences were observed when comparing the patterns of polypeptides induced by the two viral strains. In both cell systems studied, ASFV infection produces a general shutoff of protein synthesis that affects up to 65% of the cellular proteins. Interestingly, 28 proteins of porcine alveolar macrophages and 48 proteins of Vero cells are stimulated at least two times by ASFV infection.
Asunto(s)
Virus de la Fiebre Porcina Africana/metabolismo , Electroforesis en Gel Bidimensional/métodos , Macrófagos Alveolares/metabolismo , Péptidos/química , Animales , Línea Celular , Chlorocebus aethiops , Biosíntesis de Proteínas , Proteínas/química , Programas Informáticos , Porcinos , Factores de Tiempo , Células VeroRESUMEN
The African swine fever virus (ASFV) gene E165R, which is homologous to dUTPases, has been characterized. A multiple alignment of dUTPases showed the conservation in ASFV dUTPase of the motifs that define this protein family. A biochemical analysis of the purified recombinant enzyme showed that the virus dUTPase is a trimeric, highly specific enzyme that requires a divalent cation for activity. The enzyme is most probably complexed with Mg(2+), the preferred cation, and has an apparent K(m) for dUTP of 1 microM. Northern and Western blotting, as well as immunofluorescence analyses, indicated that the enzyme is expressed at early and late times of infection and is localized in the cytoplasm of the infected cells. On the other hand, an ASFV dUTPase-deletion mutant (vDeltaE165R) has been obtained. Growth kinetics showed that vDeltaE165R replicates as efficiently as parental virus in Vero cells but only to 10% or less of parental virus in swine macrophages. Our results suggest that the dUTPase activity is dispensable for virus replication in dividing cells but is required for productive infection in nondividing swine macrophages, the natural host cell for the virus. The viral dUTPase may play a role in lowering the dUTP concentration in natural infections to minimize misincorporation of deoxyuridine into the viral DNA and ensure the fidelity of genome replication.
Asunto(s)
Virus de la Fiebre Porcina Africana/fisiología , Genes Virales , Macrófagos/virología , Pirofosfatasas/metabolismo , Replicación Viral , Fiebre Porcina Africana/virología , Virus de la Fiebre Porcina Africana/enzimología , Virus de la Fiebre Porcina Africana/genética , Secuencia de Aminoácidos , Animales , Northern Blotting , Western Blotting , Chlorocebus aethiops , Inducción Enzimática , Técnica del Anticuerpo Fluorescente , Eliminación de Gen , Magnesio/metabolismo , Datos de Secuencia Molecular , Filogenia , Pirofosfatasas/química , Pirofosfatasas/genética , Proteínas Recombinantes/aislamiento & purificación , Proteínas Recombinantes/metabolismo , Porcinos , Transcripción Genética , Células VeroRESUMEN
In a previous study, it was shown that the protein encoded by the gene B318L of African swine fever virus (ASFV) is a trans-prenyltransferase that catalyzes in vitro the condensation of farnesyl diphosphate and isopentenyl diphosphate to synthesize geranylgeranyl diphosphate and longer chain prenyl diphosphates (Alejo, A., Yáñez, R. J., Rodríguez, J. M., Viñuela, E., and Salas, M. L. (1997) J. Biol. Chem. 272, 9417-9423). To investigate the in vivo function of the viral enzyme, we have determined, in this work, its subcellular localization and activity in cell extracts. Two systems were used in these studies: cells infected with ASFV and cells infected with a recombinant pseudo-Sindbis virus carrying the complete B318L gene. In this latter system, the trans-prenyltransferase was found to colocalize with the endoplasmic reticulum marker protein-disulfide isomerase, whereas in cells infected with ASFV, the viral enzyme was present in cytoplasmic viral assembly sites, associated with precursor viral membranes derived from the endoplasmic reticulum. In addition, after subcellular fractionation, the viral enzyme partitioned into the membrane fraction. Extraction of membrane proteins with alkaline carbonate and Triton X-114 indicated that the ASFV enzyme behaved as an integral membrane protein. The membrane enzyme synthesized predominantly all-trans-geranylgeranyl diphosphate from farnesyl diphosphate and isopentenyl diphosphate. These results indicate that the viral B318L protein is a trans-geranylgeranyl-diphosphate synthase, being the only enzyme of this type that is known to have a membrane localization.
Asunto(s)
Virus de la Fiebre Porcina Africana/enzimología , Transferasas Alquil y Aril/metabolismo , Dimetilaliltranstransferasa/metabolismo , Virus de la Fiebre Porcina Africana/genética , Animales , Chlorocebus aethiops , Dimetilaliltranstransferasa/genética , Diterpenos/análisis , Farnesiltransferasa , Microscopía Fluorescente , Microscopía Inmunoelectrónica , Virus Sindbis/enzimología , Virus Sindbis/genética , Células Vero , Proteínas Virales/metabolismoRESUMEN
We have examined the ultrastructural localization of African swine fever virus DNA in thin-sections of infected cells by in situ hybridization and autoradiography. Virus-specific DNA sequences were found in the nucleus of infected Vero cells at early times in the synthesis of the viral DNA, forming dense foci localized in proximity to the nuclear membrane. At later times, the viral DNA was found exclusively in the cytoplasm. Electron microscopic autoradiography of African swine fever virus-infected macrophages showed that the nucleus is also a site of viral DNA replication at early times. These results provide further evidence of the existence of nuclear and cytoplasmic stages in the synthesis of African swine fever virus DNA. On the other hand, alkaline sucrose sedimentation analysis of the replicative intermediates synthesized in the nucleus and cytoplasm of infected macrophages showed that small DNA fragments ( approximately 6-12S) were synthesized in the nucleus at an early time, whereas at later times, larger fragments of approximately 37-49S were labeled in the cytoplasm. Pulse-chase experiments demonstrated that these fragments are precursors of the mature cross-linked viral DNA. The formation of dimeric concatemers, which are predominantly head-to-head linked, was observed by pulsed-field electrophoresis and restriction enzyme analysis at intermediate and late times in the replication of African swine fever virus DNA. Our findings suggest that the replication of African swine fever virus DNA proceeds by a de novo start mechanism with the synthesis of small DNA fragments, which are then converted into larger size molecules. Ligation or further elongation of these molecules would originate a two-unit concatemer with dimeric ends that could be resolved to generate the genomic DNA by site-specific nicking, rearrangement, and ligation as has been proposed in the de novo start model of Baroudy et al. (B. M. Baroudy, S. Venkatesam, and B. Moss, 1982, Cold Spring Harbor Symp. Quant. Biol. 47, 723-729) for the replication of vaccinia virus DNA.
Asunto(s)
Virus de la Fiebre Porcina Africana/genética , Replicación del ADN , ADN Viral/biosíntesis , Replicación Viral , Virus de la Fiebre Porcina Africana/fisiología , Álcalis , Animales , Autorradiografía , Fraccionamiento Celular , Núcleo Celular/ultraestructura , Núcleo Celular/virología , Centrifugación por Gradiente de Densidad , Chlorocebus aethiops , Citoplasma/ultraestructura , Citoplasma/virología , Desoxirribonucleasa HindIII , Hibridación in Situ , Macrófagos/ultraestructura , Microscopía Electrónica , Hibridación de Ácido Nucleico , Sacarosa , Porcinos , Células VeroRESUMEN
An examination by electron microscopy of the viral assembly sites in Vero cells infected with African swine fever virus showed the presence of large clusters of mitochondria located in their proximity. These clusters surround viral factories that contain assembling particles but not factories where only precursor membranes are seen. Immunofluorescence microscopy revealed that these accumulations of mitochondria are originated by a massive migration of the organelle to the virus assembly sites. Virus infection also promoted the induction of the mitochondrial stress-responsive proteins p74 and cpn 60 together with a dramatic shift in the ultrastructural morphology of the mitochondria toward that characteristic of actively respiring organelles. The clustering of mitochondria around the viral factory was blocked in the presence of the microtubule-disassembling drug nocodazole, indicating that these filaments are implicated in the transport of the mitochondria to the virus assembly sites. The results presented are consistent with a role for the mitochondria in supplying the energy that the virus morphogenetic processes may require and make of the African swine fever virus-infected cell a paradigm to investigate the mechanisms involved in the sorting of mitochondria within the cell.
Asunto(s)
Virus de la Fiebre Porcina Africana/fisiología , Mitocondrias/fisiología , Ensamble de Virus , Animales , Chlorocebus aethiops , Microtúbulos/fisiología , ATPasas de Translocación de Protón/metabolismo , Células VeroRESUMEN
Certain viruses have evolved mechanisms to counteract innate immunity, a host response in which nuclear factor kappaB (NF-kappaB) transcription factors play a central role. African swine fever virus encodes a protein of 28.2 kDa containing ankyrin repeats similar to those of cellular IkappaB proteins, which are inhibitors of NF-kappaB. Transfection of the African swine fever virus IkappaB gene inhibited tumor necrosis factor- or phorbol ester-induced activation of kappaB- but not AP-1-driven reporter genes. Moreover, African swine fever virus IkappaB co-immunoprecipitated with p65 NF-kappaB, and the purified recombinant protein prevented the binding of p65-p50 NF-kappaB proteins to their target sequences in the DNA. NF-kappaB activation induced by tumor necrosis factor, as detected by mobility shift assays or by transfection of kappaB-driven reporter genes, is impaired in African swine fever virus-infected cells. These results indicate that the African swine fever virus IkappaB gene homologue interferes with NF-kappaB activation, likely representing a new mechanism to evade the immune response during viral infection.
Asunto(s)
Virus de la Fiebre Porcina Africana/genética , Proteínas de Unión al ADN/genética , Genes Virales , Proteínas I-kappa B , FN-kappa B/antagonistas & inhibidores , Proteínas Virales/genética , Virus de la Fiebre Porcina Africana/crecimiento & desarrollo , Secuencia de Aminoácidos , Animales , Chlorocebus aethiops , Proteínas de Unión al ADN/metabolismo , Proteínas de Unión al ADN/farmacología , Regulación de la Expresión Génica , Genes Reporteros , Datos de Secuencia Molecular , Inhibidor NF-kappaB alfa , FN-kappa B/metabolismo , Unión Proteica , Proteínas Recombinantes/metabolismo , Proteínas Recombinantes/farmacología , Homología de Secuencia de Aminoácido , Células Vero/virología , Proteínas Virales/metabolismo , Proteínas Virales/farmacologíaRESUMEN
The present study describes the characterization of an African swine fever virus gene homologous to prenyltransferases. The gene, designated B318L, is located within the EcoRI B fragment in the central region of the virus genome, and encodes a polypeptide with a predicted molecular weight of 35,904. The protein is characterized by the presence of a putative hydrophobic transmembrane domain at the amino end. The gene is expressed at the late stage of virus infection, and transcription is initiated at positions -118, -119, -120, and -122 relative to the first nucleotide of the translation start codon. Protein B318L presents a colinear arrangement of the four highly conserved regions and the two aspartate-rich motifs characteristic of geranylgeranyl diphosphate synthases, farnesyl diphosphate synthases, and other prenyltransferases. Throughout these regions, the percentages of identity between protein B318L and various prenyltransferases range from 28.6 to 48.7%. The gene was cloned in vector pTrxFus without the amino-terminal hydrophobic region and expressed in Escherichia coli. The recombinant protein, purified essentially to homogeneity by affinity chromatography, catalyzes the sequential condensation of isopentenyl diphosphate with different allylic diphosphates, farnesyl diphosphate being the best allylic substrate of the reaction. All-trans-polyprenyl diphosphates containing 3-13 isoprene units are synthesized, which identifies the B318L protein as a trans-prenyltransferase.
Asunto(s)
Virus de la Fiebre Porcina Africana/enzimología , Dimetilaliltranstransferasa/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Chlorocebus aethiops , Desoxirribonucleasa EcoRI/metabolismo , Dimetilaliltranstransferasa/química , Genes Virales , Isomerismo , Magnesio/metabolismo , Manganeso/metabolismo , Datos de Secuencia Molecular , Peso Molecular , Sistemas de Lectura Abierta , Fosfatos de Poliisoprenilo/metabolismo , Alineación de Secuencia , Células VeroRESUMEN
The function of the African swine fever virus (ASFV) bcl-2 homologue, gene A179L, in the regulation of apoptosis was investigated using as a model system the human myeloid leukemia cell line K562 induced to die by apoptosis with inhibitors of macromolecular synthesis, a process that is prevented by overexpression of human bcl-2. It is shown that transfection of K562 cells with the ASFV A179L gene protects these cells from apoptotic cell death induced by a combination of cycloheximide and actinomycin D or by treatment with cytosine arabinoside. To test the functional role of the highly conserved BH1 domain present in the A179L protein, the Gly residue at position 85 was mutated to Ala, since it has been shown that substitution of the corresponding Gly in human Bcl-2 abrogates its death-repressor activity. It was found that the Gly-to-Ala mutation in the BH1 domain of the viral protein abolished its capacity to protect the K562 cells from apoptosis, indicating that this Gly is essential for A179L action. This finding stresses the functional similarity of the BH1 domains of the viral protein and cellular Bcl-2.
Asunto(s)
Virus de la Fiebre Porcina Africana/fisiología , Apoptosis , Proteínas Proto-Oncogénicas c-bcl-2/genética , Proteínas Virales/fisiología , Virus de la Fiebre Porcina Africana/genética , Alanina , Secuencia de Aminoácidos , Animales , Sitios de Unión , Cicloheximida/farmacología , Citarabina/farmacología , Dactinomicina/farmacología , Glicina , Humanos , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida , Proteínas Proto-Oncogénicas c-bcl-2/fisiología , Conejos , Células Tumorales Cultivadas , Proteínas Virales/genéticaRESUMEN
One of the major constraints for studies on the sporogonic cycle of the parasites causing human malaria, and on the protective efficacy of pre-erythrocytic vaccines, is the scarcity of laboratory-reared Anopheles mosquitoes as a source of infective sporozoites. The aim of the present study was to reproduce the life-cycles of Plasmodium falciparum and P. vivax in the laboratory and so develop the ability to produce infective sporozoites of these two species regularly under laboratory conditions. Colonized Anopheles albimanus, of Buenaventura and Tecojate strains, were infected by feeding either on Plasmodium-infected blood, from human patients or experimentally inoculated Aotus monkeys, or on gametocytes of the P. falciparum NF-54 isolate grown in vitro. The monkeys were infected with the blood stages of a Colombian P. vivax isolate and then, after recovery, with the Santa Lucia strain of P. falciparum from El Salvador. Although both of the mosquito strains used were successfully infected with both parasite species, the Buenaventura strain of mosquito was generally more susceptible to infection than the Tecojate strain, and particularly to infection with the parasites from the patients, who lived where this strain of mosquitoes was originally isolated. Monkeys injected intravenously with the P. vivax sporozoites produced in the mosquitoes developed patent sexual and asexual parasitaemias; the gametocytes that developed could then be used to infect mosquitoes, allowing the development of more sporozoites. However, experimental infections failed to establish after the P. falciparum sporozoites were used to inoculate monkeys. The ability to reproduce the complete life cycle of P. vivax in the laboratory, from human to mosquito and then to monkey, should greatly facilitate many studies on vivax malaria and on the efficacy of candidate malaria vaccines. The availability of the sporogonic cycles of P. falciparum from three different sources should also permit a variety of biological studies.
Asunto(s)
Anopheles/parasitología , Plasmodium falciparum/crecimiento & desarrollo , Plasmodium vivax/crecimiento & desarrollo , Animales , Aotidae/parasitología , Humanos , Malaria/parasitología , ParasitemiaRESUMEN
African swine fever virus (ASFV) encodes a novel DNA polymerase, constituted of only 174 amino acids, belonging to the polymerase (pol) X family of DNA polymerases. Biochemical analyses of the purified enzyme indicate that ASFV pol X is a monomeric DNA-directed DNA polymerase, highly distributive, lacking a proofreading 3'-5'-exonuclease, and with a poor discrimination against dideoxynucleotides. A multiple alignment of family X DNA polymerases, together with the extrapolation to the crystal structure of mammalian DNA polymerase beta (pol beta), showed the conservation in ASFV pol X of the most critical residues involved in DNA binding, nucleotide binding, and catalysis of the polymerization reaction. Therefore, the 20-kDa ASFV pol X most likely represents the minimal functional version of an evolutionarily conserved pol beta-type DNA polymerase core, constituted by only the "palm" and "thumb" subdomains. It is worth noting that such an "unfingered" DNA polymerase is able to handle templated DNA polymerization with a considerable high fidelity at the base discrimination level. Base excision repair is considered to be a cellular defense mechanism repairing modified bases in DNA. Interestingly, the fact that ASFV pol X is able to conduct filling of a single nucleotide gap points to a putative role in base excision repair during the ASFV life cycle.
Asunto(s)
Virus de la Fiebre Porcina Africana/enzimología , Reparación del ADN , ADN Viral/fisiología , ADN Polimerasa Dirigida por ADN/química , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cristalografía por Rayos X , ADN Polimerasa Dirigida por ADN/metabolismo , Humanos , Modelos Moleculares , Datos de Secuencia Molecular , Peso Molecular , Conformación Proteica , Alineación de SecuenciaRESUMEN
A transcriptional analysis of the African swine fever virus (ASFV) I226R and I243L genes is presented. Steady-state kinetics and transfection experiments showed the existence of a new temporal class of ASFV mRNAs transcribed from these genes, with the characteristics of the poxvirus intermediate transcripts. Transcription of the I226R gene gave rise to intermediate and late mRNAs that started from different sites, while the I243L gene produced early, intermediate, and late mRNAs, also starting from different sites. The presence of intermediate genes suggests a cascade model for the regulation of ASFV gene expression.
Asunto(s)
Virus de la Fiebre Porcina Africana/genética , ARN Mensajero , ARN Viral , Animales , Chlorocebus aethiops , Secuencia Conservada , Expresión Génica , Cinética , Iniciación de la Cadena Peptídica Traduccional , Células VeroRESUMEN
Sequencing of restriction fragment EcoRI A-SalI C of African swine fever virus has revealed the existence of a multigene family, designated family 505 because of the average number of amino acids in the proteins, composed of seven homologous and tandemly arranged genes. All the genes of family 505 are expressed during infection. Primer extension analysis showed that transcription is initiated a short distance (3 to 62 nucleotides) from the start codon of the corresponding open reading frame. The proteins of family 505 showed similarity to those of family 360 from African swine fever virus. In particular, a striking conservation of three regions at the amino terminus of the polypeptides was observed.
Asunto(s)
Virus de la Fiebre Porcina Africana/genética , Familia de Multigenes/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , ADN Viral/genética , Datos de Secuencia Molecular , ARN Mensajero/genética , Secuencias Repetitivas de Ácidos Nucleicos , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Células VeroRESUMEN
The sporogonic cycle of Plasmodium vivax was established and maintained under laboratory conditions in two different strains of Anopheles albimanus mosquitoes using as a parasite source blood from human patients or from Aotus monkeys infected with the VCC-2 P.vivax colombian isolate. Both the Tecojate strain isolate from Guatemala and the Cartagena strain from the colombian Pacific coast were susceptible to infections with P.vivax. A higher percentage of Cartagena mosquitoes was infected per trial, however the Tecojate strain developed higher sporozoite loads. Intravenous inoculation of Aotus monkeys with sporozoites obtained from both anopheline strains resulted in successful blood infections. Animals infected with sporozoites from the Tecojate strain presented a patent period of 21-32 days whereas parasitemia appeared between days 19-53 in monkeys infected with sporozites from Cartagena strain.