Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Vector Borne Zoonotic Dis ; 15(11): 694-700, 2015.
Article in English | LILACS, SES-SP, SESSP-IALPROD, SES-SP, SESSP-IALACERVO | ID: biblio-1022067

ABSTRACT

Arenavirus Sabiá was originally isolated from a fatal human infection in Brazil, and after the occurrence of the second fatal human case in São Paulo state, epidemiologic and virologic studies were performed in the area where the patient lived, aiming at the identification of the Sabiá natural rodent reservoir. A broadly cross-reactive enzyme-linked immunosorbent assay (ELISA) was used to screen for antibody-positive samples. Antibodies to arenavirus were detected in two of the 55 samples of Calomys tener, and from these results, samples of rodents were analyzed by a broad RT-PCR assay. RT-PCR amplification detected arenavirus sequences in five of the 55 C. tener samples, and sequencing showed that this virus is a distinct form of Sabiá virus. Thus, we describe here the evidence for the circulation of a new arenavirus in Brazil (proposed name Pinhal virus) and its genetic characterization compared to other arenaviruses. This study also suggests C. tener as a probable rodent reservoir for this virus and associates this new virus with the lineage C of New World arenaviruses. Although we have defined some characteristics of this virus, so far, there is no evidence of its involvement in human disease.


Subject(s)
Phylogeny , Brazil/epidemiology , Disease Reservoirs/veterinary , Enzyme-Linked Immunosorbent Assay , Sigmodontinae/virology , Arenaviruses, New World/isolation & purification , Arenaviruses, New World/classification , Arenaviruses, New World/genetics , Arenaviridae Infections/veterinary , Arenaviridae Infections/virology , Animals , Antibodies, Viral/blood
2.
Microsc. electron. biol. celular ; 15(1): 41-55, Jun. 1991. ilus
Article in English | LILACS | ID: lil-121634

ABSTRACT

Los genes clonados de las proteínas de nucleocápside, N, de los arenavirus Junín y LCM (choriomeningitis linfocitaria) se insertaron en el vector de expresión pKG4 regulado por el promotor tardío del virus SV40. Cuando estas construcciones se utilizaron para transfectar las líneas celulares BHK-21 (fibroblastos de hamster lactante) y CV-1 (fibroblastos de riñón de mono verde africano) se observó la expresión transiente de un polipéptido de tamaño e inmunoreactividad indistinguible de la proteína N sintetizada durante una infección viral. El análisis por inmunofluorescencia reveló un patrón de distribución intracelular semejante al observado en células infectadas. Este patrón presentó variaciones desde una tinción citoplásmica difusa hasta gránulos citoplásmicos dispersos o concentrados en la zona perinuclear. La asociación de la proteína N con gránulos basófilos es semejante a la descripta en el efecto citópático causado por los arenavirus en las células infectadas, y podría relacionarse con las características fisicoquímicas de la proteina N, que contiene numerosas secuencias de aminoácidos básicos capaces de interactuar con ácidos ribonucleicos celulares


Subject(s)
Animals , Cricetinae , Arenaviruses, New World/genetics , Capsid/biosynthesis , Lymphocytic Choriomeningitis/genetics , Recombinant Fusion Proteins/biosynthesis , Transfection , Viral Core Proteins/biosynthesis , Cells, Cultured , Chlorocebus aethiops , Cytopathogenic Effect, Viral , Fibroblasts/metabolism , Fibroblasts/ultrastructure , Gene Expression Regulation, Viral , Genetic Vectors , Cytoplasmic Granules/metabolism , Cytoplasmic Granules/ultrastructure , Mesocricetus , Simian virus 40
SELECTION OF CITATIONS
SEARCH DETAIL