O surto de peste suína africana ocorrido em 1978 no município de Paracambi, Rio de Janeiro / The outbreak of African swine fever which ocurred in 1978 in the county of Paracambi, Rio de Janeiro, Brazil

Em função das dúvidas que ainda perduram 25 anos após a ocorrência do surto de peste suína africana (PSA), em Paracambi, Estado do Rio de Janeiro, Brasil, em 1978, são apresentados os resultados, relativos a este foco, obtidos pelos estudos epidemiológico, clínico-patológico, virológico, bacteriológico e ultra-estrutural dos casos naturais, bem como os relativos à reprodução experimental da doença no Brasil e sua confirmação por isolamento e determinação de patogenicidade realizada no Plum Island Animal Disease Center, New York, EUA. Os animais se infectaram pela ingestão de restos de comida de aviões procedentes de Portugal e da Espanha, países nos quais a doença existia. De acordo com publicação do Ministério da Agricultura, após o diagnóstico do surto de PSA descrito neste trabalho, 223 novos focos foram relatados, entre 1978 e 1979, em todas Regiões do país (Norte, Nordeste, Centro-Oeste, Sudeste e Sul) e focos adicionais em 1981, sem informações exatas referentes ao seu número. O último caso foi relatado em 15 de novembro de 1981, e em 5 de dezembro 1984 o Brasil foi declarado livre da PSA. Para o diagnóstico da PSA foram processadas 54.002 amostras no Departamento de Virologia do Instituto de Microbiologia da Universidade Federal do Rio de Janeiro, no período de 1978 a 1981. No processamento das amostras foram usadas as técnicas de hemadsorção em cultura de leucócitos (HAd), imunoflorescência em cortes de tecido (FATS), imunoflorescência em cultivo celular (FATCC), imuno-eletrosmoforese (IEOP) e imunoflorescência...

O surto de peste suína africana ocorrido em 1978 no município de Paracambi, Rio de Janeiro / The outbreak of African swine fever which ocurred in 1978 in the county of Paracambi, Rio de Janeiro, Brazil

Em função das dúvidas que ainda perduram 25 anos após a ocorrência do surto de peste suína africana (PSA), em Paracambi, Estado do Rio de Janeiro, Brasil, em 1978, são apresentados os resultados, relativos a este foco, obtidos pelos estudos epidemiológico, clínico-patológico, virológico, bacteriológico e ultra-estrutural dos casos naturais, bem como os relativos à reprodução experimental da doença no Brasil e sua confirmação por isolamento e determinação de patogenicidade realizada no Plum Island Animal Disease Center, New York, EUA. Os animais se infectaram pela ingestão de restos de comida de aviões procedentes de Portugal e da Espanha, países nos quais a doença existia. De acordo com publicação do Ministério da Agricultura, após o diagnóstico do surto de PSA descrito neste trabalho, 223 novos focos foram relatados, entre 1978 e 1979, em todas Regiões do país (Norte, Nordeste, Centro-Oeste, Sudeste e Sul) e focos adicionais em 1981, sem informações exatas referentes ao seu número. O último caso foi relatado em 15 de novembro de 1981, e em 5 de dezembro 1984 o Brasil foi declarado livre da PSA. Para o diagnóstico da PSA foram processadas 54.002 amostras no Departamento de Virologia do Instituto de Microbiologia da Universidade Federal do Rio de Janeiro, no período de 1978 a 1981. No processamento das amostras foram usadas as técnicas de hemadsorção em cultura de leucócitos (HAd), imunoflorescência em cortes de tecido (FATS), imunoflorescência em cultivo celular (FATCC), imuno-eletrosmoforese (IEOP) e imunoflorescência...(AU)

Due to doubts which still persist 25 years after the outbreak of African swine fever (ASF) which ocurred in the county of Paracambi, Rio de Janeiro, Brazil, in 1978, the results obtained through the studies to establish and confirm the diagnosis are presented. These include data on the epidemiology, clinic-pathological aspects, bacteriological, virological and ultramicroscopic examinations, the experimental reproduction of the disease and cross immunity tests with classical swine fever virus performed in Brazil, and on the confirmation with isolation of the virus and determination of its identity at the Plum Island Animal Disease Center, New York, USA. The pigs of the affected herd had been fed untreated remains of meals from airplanes of international lines flying to Brazil from Portugal and Spain where ASF was occurring at the time. According to publication by the Ministry of Agriculture, after the diagnosis of the outbreak of ASF described in this paper, 223 additional outbreaks were reported in Brazil between 1978 and 1979, in all the Brazilian regions (North, Northeast, Central-West, Southeast and South). Further outbreaks were reported in 1981, but their number is not known. The last case was reported to have occurred on November 15, 1981, and on December 5, 1984, Brazil was declared free of ASF. For the diagnosis of ASF 54,002 samples were examined by the Department of Virology of the Institute of Microbiology, Federal University of Rio de Janeiro, from 1978 to 1981, by the techniques of haemadsorption in leucocyte cultures (HAd), direct immunoflorescence in tissue sections (FATS), direct immunoflorescence in cell cultures (FATCC), immuno-electro-osmophoresis (IEOP) and indirect immunoflorescence assay (IIF). Only 4 samples were positive with the FATCC procedure. This is the only technique which includes virus isolation; the origin of these positive samples was not reported, but probably they were from the Paracambi outbreak... (AU)

Syphilis serology among transvestite prostitutes attending an HIV unit in Rome, Italy.

Sixty-seven transvestite prostitutes from Latin America (49 from Brazil and 18 from Colombia) who attended an HIV unit located in the inner city of Rome between January 1991 and June 1992 were studied for syphilis markers by means of both the Treponema pallidum haemoagglutination test (TPHA) and a solid phase haemadsorption test for detection of specific IgM (SPHA-IgM) which are typically present in recent infections. All participants reported more than 500 sexual partners in the past year, and 67.1% of them more than 1500 partners (between 5 and 10 partners per working day). The overall prevalence of anti-HIV antibodies in this population was 65.7%. The prevalence of positive TPHA tests in the population studied was 73.1%, while that of positive SPHA-IgM tests was 10.4%. The prevalence of positive TPHA and SPHA-IgM tests was higher among Columbians than among Brazilians (83.3% vs 69.4% and 22.2% vs 6.1%, respectively) and also showed a positive correlation with the duration of their permanence in Italy. The TPHA and SPHA-IgM positivities were significantly higher among subjects older than 29 years. Positive TPHA was also significantly higher in subjects who reported a history of heroin and/or cocaine abuse while positive SPHA-IgM was higher in subjects who did not use condoms or reported irregular use of them than in subjects who regularly used condoms. No overall correlation was evident between TPHA positivity and anti-HIV positivity, while SPHA-IgM positivity was found to be higher among anti-HIV-negative subjects.(ABSTRACT TRUNCATED AT 250 WORDS)

Partial characterization of hemagglutinin activity of the marine sponge Anthosigmella varians.

The marine sponge Anthosigmella varians contains proteins that agglutinate human erythrocytes irrespective of their ABO group antigens. The hemagglutination reaction depends on divalent cations and is not inhibited by L-arabinose, D-xylose, L-rhamnose, D-galactose, D-glucose, L and D-fucose, N-acetyl-D-galac-tosamine, N-acetyl-D-glucosamine, methyl-alpha-D-mannopiranoside, D-cellobiose, lactose, maltose, melibiose nor raffinose (33 mM each). A partial purification of the hemagglutinins with 31-fold increase in SA and 80% recovery of activity was obtained after gel filtration and ion-exchange gradient elution chromatography. Hemadsorption experiments carried out with the semipurified fraction using glutaraldehyde-fixed human erythrocytes suggest that proteins with molecular weight of 90 and 34 kDa participate in this reaction.

Partial characterization of hemagglutinin activity of the marine sponge Anthosigmella varians

The marine sponge Anthosigmella varians contains proteins that agglutinate human erythrocytes irrespective of their ABO group antigens. The hemagglutination reaction depends on divalent cations andf is not inhibited by L-arabinose, D-xylose, L-rhamnose, D-galactose, D-glucose, L and D-fucose, N-acetyl-D-galactosamine, N-acetyl-D-glucosamine, methyl-alpha-Dmannopiranoside, D-cellobiose, lactose, maltose, melibiose nor raffinose (33 mM each). A partial purification of the hemagglutinins with 31-fold ioncrease in SA and 80% recovery of activity was obtained after gel filtration and ion-exchange gradient elution chromatography. Hemadsorption experiments carried our with out with the semipurified fraction using glutaraldehyde-fixed human erythrocytes suggest that protein with molecular weight of 90 and 34 kDa participate in this rection

The virology of variola minor. Correlation of laboratory tests with the geographic distribution and human virulence of variola isolates.

Several groups of variola isolates were compared in DNA structure, and by four independent biologic markers. Isolates of variola minor from Europe and South America (alastrim virus) could be distinguished from African isolates of variola minor by DNA structure and by two of the four biologic markers. Taken as a group, the properties of African isolates, in general, differed from those of variola major, but this difference was confined to properties which depended (in the laboratory) on the recent history of the virus concerned. The suggestion made previously that there was an "intermediate" or "African" variety of variola virus is discounted. Laboratory tests did not distinguish any individual African isolate from variola major virus. It is concluded that a virus which may be called "alastrim" represents a "fixed" variant of variola virus, whose distribution is consistent with the dramatic spread of variola minor through the Americas and Europe in the early part of this century, and that variola minor in Africa in recent years was due to variola virus which was not alastrim and which laboratory evidence fails to identify as an entity distinguishable from variola major virus.

Characterization of a paramyxovirus isolated from the brain of a piglet in Mexico.

A virus morphologically resembling members of the family Paramyxoviridae has been isolated from the brain of a piglet with a central nervous disorder accompanied by pneumonia and corneal opacity. The virus, designated LPM, grows in a large variety of cultured cell types and elicits a cytopathic effect including formation of syncytia and cytoplasmic inclusion bodies. The virus has hemagglutinating, neuraminidase and hemolytic activities. Studies on experimental transmission showed that young pigs are susceptible to infection which induced a disease similar to that in natural cases. The virus killed mice and chicken embryos. The structural proteins of LPM virus, as resolved by polyacrylamide gel electrophoresis are similar to those described for other paramyxoviruses. Serologically the virus proved to be distinct from the paramyxoviruses tested so far.

Virulence in African swine fever: its measurement and implications.

A method of measuring and expressing the virulence of African swine fever virus in numerical terms was developed. Seventeen viruses (13 hemadsorbing and 4 nonhemadsorbing) were tested and classified into 3 groups: highly infectious and highly virulent, highly infectious and moderately virulent, and slightly infectious and slightly virulent. This classification was based on the number of 50% hemadsorption unit (HA50) or TCID50 required to produce 1 LD50 for swine, the number of HA50 or TCID50 required to produce one 50% pig infectious dose (PID50), and the number of PID50 required for each LD50. The virulent virus (group 1) required less than or equal to 10 virus units (HA50 or TCID50) for 1 PID50 and LD50 (highly infectious and highly lethal), respectively, and had a ratio of 1.0 for PID50/LD50, ie, all infected pigs died from acute African swine fever. Tengani, L'60, and DR-I isolants and nonhemadsorbing viruses of Haiti-1 isolant belong to this group. The moderately virulent virus (group 2) required less than 10 virus units for 1 PID50 and 20 to 562 virus units for 1 LD50 (highly infectious and moderately lethal), respectively, and recoveries from the clinical disease and immunologic deaths were frequent. Madrid '75, Haiti-1, DR-II, and BR-I isolants belong to this group. The slightly virulent virus (group 3) required 56 to 10,000 virus units for 1 PID50 and 56,200 to 3,120,000 virus units for 1 LD50 (slightly infectious and less lethal).(ABSTRACT TRUNCATED AT 250 WORDS)