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1.
J Phys Condens Matter ; 33(47)2021 Sep 13.
Artículo en Inglés | MEDLINE | ID: mdl-34438373

RESUMEN

The dynamic structure factorS(Q,E), whereQandEare momentum and energy transfer, respectively, has been measured for liquid Sb, using inelastic x-ray scattering. A modified damped harmonic oscillator model function was applied to analyseS(Q,E) of liquid Sb and also to that of liquid Bi by Inuiet al(2015Phys. Rev.B92, 054206). The obtained excitation energy was in fairly good agreement with that predicted byab initiomolecular dynamics simulations on these liquid semi-metals. The excitation energy of the longitudinal acoustic mode in liquid Sb and liquid Bi exhibits flat-toppedQdependence whereas the lower excitation energy below the longitudinal acoustic excitation showsQ-gap behaviour. From the viscosity estimated from theQ-gap experimentally obtained, it is inferred that the lower energy excitation arises from the transverse acoustic excitation in the liquids.

2.
Arch Virol ; 149(5): 929-41, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15098108

RESUMEN

To elucidate the mode of transmission of Puumala-related hantavirus in a population of gray red-backed voles, Clethrionomys rufocanus bedfordiae, in Hokkaido, Japan, we analyzed the kin structure and dispersal patterns of individual voles using microsatellite and mitochondrial DNA markers. Siblings or dam/offsprings was identified within the population based on the relatedness calculation with the microsatellite data. The pairwise relatedness values obtained could reveal kinship among all vole individuals within the population. Based on the assessment of kinship, we did not find a positive relationship between hantavirus transmission and close kinship. Males infected with the hantavirus carried a relatively uncommon mitochondrial haplotype. However, these infected males shared low relatedness values and were not considered closely related, i.e., they were not siblings or parent/offspring. These observations imply that hantavirus transmission in the vole population may not be related to close kinship but by random horizontal infection.


Asunto(s)
Arvicolinae/virología , ADN Mitocondrial/análisis , Transmisión de Enfermedad Infecciosa/veterinaria , Fiebre Hemorrágica con Síndrome Renal/veterinaria , Virus Puumala , Animales , Arvicolinae/genética , ADN Mitocondrial/genética , Femenino , Frecuencia de los Genes , Marcadores Genéticos , Fiebre Hemorrágica con Síndrome Renal/transmisión , Japón , Masculino , Repeticiones de Microsatélite , Factores Sexuales
3.
Arch Virol ; 148(9): 1671-85, 2003 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-14505081

RESUMEN

Seoul virus is a hantavirus that causes hemorrhagic fever with renal syndrome (HFRS). The virion has a tripartite (S, M, and L) negative-stranded RNA genome, which is characteristic of the family Bunyaviridae. However, the molecular basis of virus replication is not well known. We established a Northern blot hybridization (NB) procedure using digoxygenin-labeled RNA probes, to quantitate the hantaviral plus- and minus-strand RNAs separately. Virus RNA replication was analyzed in infected Vero E6 cells. When the Vero E6 cells were infected with Seoul virus strain KI-83-262 (KI) at m.o.i. = 0.25, the plus-strand RNA was detected within 1 h post-infection (hpi), and the minus-strand RNA was detected subsequently. Using laser confocal microscopy, the nucleocapsid protein (NP) was detected within 2 hpi, and accumulated as scattered granules in the cytoplasm until 24 hpi. In contrast, the G2 protein first appeared at 8 hpi, was immediately transported to the Golgi, and accumulated in the Golgi until 24 hpi. Infectious virus particles were released into the medium at 24 h hpi. These findings indicate that hantavirus RNA replication starts with the appearance of NP at 2 hpi, glycoproteins then accumulate gradually in the Golgi, and virion formation is initiated once the viral RNAs and proteins have accumulated.


Asunto(s)
ARN Viral/biosíntesis , Virus Seoul/fisiología , Proteínas Virales/biosíntesis , Animales , Chlorocebus aethiops , Glicoproteínas/biosíntesis , Proteínas de la Nucleocápside , Nucleoproteínas/biosíntesis , Sondas ARN , Células Vero , Proteínas del Núcleo Viral/biosíntesis , Replicación Viral
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