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1.
J Med Virol ; 82(1): 175-85, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19950229

ABSTRACT

Nucleotide sequences of two regions of the genomes of 11 yellow fever virus (YFV) samples isolated from monkeys or humans with symptomatic yellow fever (YF) in Brazil in 2000, 2004, and 2008 were determined with the objective of establishing the genotypes and studying the genetic variation. Results of the Bayesian phylogenetic analysis showed that sequences generated from strains from 2004 and 2008 formed a new subclade within the clade 1 of the South American genotype I. The new subgroup is here designated as 1E. Sequences of YFV strains recovered in 2000 belong to the subclade 1D, which comprises previously characterized YFV strains from Brazil. Molecular dating analyses suggested that the new subclade 1E started diversifying from 1D about 1975 and that the most recent 2004-2008 isolates arose about 1985.


Subject(s)
Genetic Variation , Monkey Diseases/epidemiology , Phylogeny , Yellow Fever/epidemiology , Yellow fever virus , 3' Untranslated Regions/genetics , Animals , Bayes Theorem , Brazil/epidemiology , Evolution, Molecular , Genotype , Humans , Molecular Sequence Data , Monkey Diseases/virology , Sequence Analysis, DNA , South America , Viral Envelope Proteins , Yellow Fever/veterinary , Yellow Fever/virology , Yellow fever virus/classification , Yellow fever virus/genetics , Yellow fever virus/isolation & purification
2.
Rev Inst Med Trop Sao Paulo ; 47(5): 281-5, 2005.
Article in English | MEDLINE | ID: mdl-16302112

ABSTRACT

This paper reports the isolation of St. Louis encephalitis virus (SLEV) from a febrile human case suspected to be dengue, in São Pedro, São Paulo State. A MAC-ELISA done on the patient's acute and convalescent sera was inconclusive and hemagglutination inhibition test detected IgG antibody for flaviviruses. An indirect immunofluorescent assay done on the C6/36 cell culture inoculated with the acute serum was positive for flaviviruses but negative when tested with dengue monoclonal antibodies. RNA extracted from the infected cell culture supernatant was amplified by RT-PCR in the presence of NS5 universal flavivirus primers and directly sequenced. Results of BLAST search indicated that this sequence shares 93% nucleotide similarity with the sequence of SLEV (strain-MSI.7), confirmed by RT-PCR performed with SLEV specific primers. Since SLEV was identified as the cause of human disease, it is necessary to improve surveillance in order to achieve early detection of this agent in the state of São Paulo and in Brazil. This finding is also an alert to health professionals about the need for more complete clinical and epidemiological investigations of febrile illnesses as in the reported case. SLEV infections can be unrecognized or confused with other ones caused by an arbovirus, such as dengue.


Subject(s)
Antibodies, Viral/blood , Encephalitis Virus, St. Louis/isolation & purification , Encephalitis, St. Louis/diagnosis , Brazil , Encephalitis Virus, St. Louis/genetics , Encephalitis Virus, St. Louis/immunology , Enzyme-Linked Immunosorbent Assay/methods , Female , Humans , Immunoglobulin G/blood , Middle Aged , RNA, Viral/analysis , Reverse Transcriptase Polymerase Chain Reaction
3.
Rev. Inst. Med. Trop. Säo Paulo ; 47(5): 281-285, Sept.-Oct. 2005.
Article in English | LILACS | ID: lil-417087

ABSTRACT

O presente estudo relata o isolamento do vírus da encefalite São Luis (SLEV) de um caso febril humano suspeito de dengue, em São Pedro, Estado de São Paulo. MAC-ELISA realizado com soros das fases aguda e convalescente foi inconclusivo e anticorpos IgG foram detectados por inibição da hemaglutinação para flavivirus. Imunofluorescência indireta com cultura de células C6/36 inoculadas com soro da fase aguda foi positivo para flavivirus mas negativo quando testado com anticorpos monoclonais para dengue. O RNA extraído de cultura de células infectadas foi amplificado na presença de primers universais para o gênero Flavivirus, deduzidos de uma região da proteína não estrutural 5 e diretamente sequenciado. Os resultados da pesquisa no BLAST indicaram que a seqüência apresenta 93% de similaridade de nucleotídeos com a seqüência de SLEV (cepa MS1.7), confirmado por RT-PCR, realizado com primers específicos para SLEV. O fato de SLEV ter sido identificado como a causa de doença humana indica a necessidade de aprimorar a vigilância a fim de detectar precocemente esse agente no Estado de São Paulo e no Brasil. Esse caso é também um alerta para os profissionais de saúde sobre a necessidade de investigações clínicas e epidemiológicas mais completas sobre doenças febris como no caso relatado. Infecções por SLEV podem não ser reconhecidas ou confundidas com outras causadas por arbovírus como a dengue.


Subject(s)
Female , Humans , Middle Aged , Antibodies, Viral/blood , Encephalitis Virus, St. Louis/isolation & purification , Encephalitis, St. Louis/diagnosis , Brazil , Encephalitis Virus, St. Louis/genetics , Encephalitis Virus, St. Louis/immunology , Enzyme-Linked Immunosorbent Assay/methods , Immunoglobulin G/blood , Reverse Transcriptase Polymerase Chain Reaction , RNA, Viral/analysis
4.
Antiviral Res ; 60(3): 201-8, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14638396

ABSTRACT

Two galactomannans, one extracted from seeds of Mimosa scabrella, having a mannose to galactose ratio of 1.1, and another with a 1.4 ratio from seeds of Leucaena leucocephala, were sulfated. The products from M. scabrella (BRS) and L. leucocephala (LLS) had a degree of sulfation of 0.62 and 0.50, and an average molecular weight of 620x10(3) and 574x10(3) gmol(-1), respectively. Their activities against yellow fever virus (YFV; BeH111 strain) and dengue 1 virus (DEN-1; Hawaii strain) were evaluated. This was carried out in young mice following intraperitoneal infection with YFV. At a dose of 49 mgkg(-1), BRS and LLS gave protection against death in 87.7 and 96.5% of the mice, respectively. When challenged with 37.5 LD50 of YFV, mice previously inoculated with BRS+virus or LLS+virus, showed 93.3 and 100% resistance, respectively, with neutralization titers similar to mice injected with 25 LD50 of formaldehyde-inactivated YFV. In vitro experiments with YFV and DEN-1 in C6/36 cell culture assays in 24-well microplates showed that concentrations that produced a 100-fold decrease in virus titer of YFV were 586 and 385 mgl(-1) for BRS and LLS, respectively. For DEN-1 they were 347 and 37 mgl(-1), respectively. Sulfated galactomannans, thus demonstrate in vitro and in vivo activity against flaviviruses.


Subject(s)
Antiviral Agents/pharmacology , Dengue Virus/drug effects , Mannans/pharmacology , Yellow Fever/drug therapy , Yellow fever virus/drug effects , Animals , Antibodies, Viral/blood , Antiviral Agents/chemistry , Antiviral Agents/therapeutic use , Carbohydrates/analysis , Cell Line , Dengue Virus/growth & development , Fabaceae , Female , Galactose/analogs & derivatives , Mannans/chemistry , Mannans/therapeutic use , Mice , Mimosa , Molecular Weight , Neutralization Tests , Phytotherapy , Proteins/analysis , Seeds/chemistry , Sulfates/analysis , Yellow Fever/immunology , Yellow fever virus/growth & development , Yellow fever virus/immunology
5.
Rev. Inst. Med. Trop. Säo Paulo ; 37(4): 337-41, jul.-ago. 1995. ilus, tab
Article in English | LILACS | ID: lil-159107

ABSTRACT

Os autores estudaram um caso humano de febre amarela silvestre, sob os aspectos clinico, laboratorial e epidemiologico. O paciente apresentava febre (39ºC), calafrios, sudorese, cefaleia, dor lombar, mialgia, dor abdominal em epigastrico, nauseas, vomitos, diarreia e prostracao. Realatava permanencia em areas onde foram constatados casos de febre amarela silvestre e nao havia historico de vacinacao anterior...


Subject(s)
Humans , Male , Adult , Aedes/isolation & purification , Yellow Fever/diagnosis , Enzyme-Linked Immunosorbent Assay , Fever/etiology , Yellow Fever/blood , Yellow Fever/epidemiology
6.
Ciênc. cult. (Säo Paulo) ; 44(2/3): 164-6, Mar.-Jun. 1992. tab
Article in English | LILACS | ID: lil-188342

ABSTRACT

In 1975-1976 an extensive epidemic of Rocio encephalitis occurred in the South region of the Sao Paulo State, Brazil. Since June 1976 no serological confirmation of this diagnosis has been made. Sera from 90 patients clinically suspected of having contracted Rocio encephalitis between July 1976 and December 1982, were tested with an immunoglobulin M (IgM) antibody capture enzyme immunoassay (MAC ELISA). Only one serum sample was available for each of these patients. Four presumptive cases of Rocio encephalitis were identified. Three of these sera had been collected in August and September of 1976. The fourth one, from a boy one year of age who died from the disease, was collected in April 1980. These results indicate that Rocio virus was circulating in the human population causing severe disease, at least until 1980. MAC ELISA is useful for surveillance of Rocio encephalitis in an area where the collection of paired sera samples is very difficult.


Subject(s)
Humans , Encephalitis, Viral/virology , Immunoglobulin M , Encephalitis, Viral/diagnosis , Enzyme-Linked Immunosorbent Assay
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