45 resultados para Abbott, Edwin Abbott, 1838-1926.
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Para cada doador de sangue soropositivo (ELISA, Abbott®) para HTLV-I/II, de dezembro de 1998 a março de 2001, também foram selecionados dois soronegativos. As amostras séricas foram re-testadas pelo ELISA (Murex®) e aquelas que permaneceram soropositivas foram testadas pelo Western Blot e pela PCR. Das 11.121 amostras séricas, 73 (0,66%) foram positivas (Abbott®), mas somente 12 (0,11%) permaneceram positivas (Murex®), enquanto que as 146 soronegativas foram confirmadas, apesar de ser sofrível o índice de concordância entre os dois ELISA. O Western Blot confirmou as 12 amostras como soropositivas: 8 (0,07%) HTLV-I; duas (0,02%) HTLV-II e duas (0,02%) indeterminadas - sendo pela PCR uma pelo HTLV-I e a outra pelo HTLV-II. Em conclusão, nessa população da Amazônia Ocidental foi muito baixa a soroprevalência de HTLV-I/II, apesar de ser esperada maior prevalência do HTLV-II devido a grande miscigenação racial indígena.
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A ligase chain reaction DNA amplification method for direct detection of Mycobacterium tuberculosis (Abbott LCx MTB) in respiratory specimens was evaluated. Results from LCx MTB Assay were compared with those from acid fast bacilli smear, culture, and final clinical diagnosis for each patient. A total of 297 respiratory specimens (sputum and bronchial lavage) from 193 patients were tested. The sensitivity, specificity, positive predictive value and negative predictive value of LCx vs culture were 92.7%, 93%, 67.8% and 98.7%, respectively. When compared to the clinical final diagnosis, the sensitivity, specificity, PPV and NPV for LCx were 88.9%, 96.8%, 86.5% and 97.4%, respectively. The sensitivity of LCx MTB assay was 75% for smear-negative, culture positive samples. The results indicate that LCx MTB assay is a rapid, simple and valuable technique as a complementary tool for the diagnosis of tuberculosis.
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Os autores analisaram em condições de laboratório, a taxa de sobrevida das ninfas, duração mínima e máxima de cada estádio, tempo de vida das formas adultas e postura das fêmeas. Foram acompanhados dois grupos de 100 ovos. Lote A, exemplares criados em um único cristalizador. Lote B os exemplares foram mantidos isolados um a um e ao atingir a fase alada formaram 20 casais, possibilitando o controle da postura das fêmeas e o tempo de vida de cada exemplar. O percentual de eclosão dos ovos foi de 96%; a taxa de vida no final da fase ninfal foi de 69,5% no Lote A e de 78,4% no Lote B. A maior freqüência observada no tempo decorrido entre postura e eclosão da ninfa do 1º estádio foi de 28 dias. O tempo de permanência na fase de ninfa foi de 4 a 8 meses e de 5 meses na fase adulta. A postura total (média) no Lote B foi de 181,6 ovos por fêmea.
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INTRODUCTION: Hepatitis B infection constitutes an important cause of morbidity and mortality worldwide. In Brazil, however, the current epidemiological situation is not clear. Considering the importance of establishing this prevalence, the aim of this study was to determine the prevalence of HBV markers in voluntary adolescents, junior high (secondary school) students, in the City of Itajaí, State of Santa Catarina, Brazil. METHODS: A seroepidemiological, transverse study was conducted with 353 randomly chosen adolescents from elementary school in 2008. Blood samples were analyzed for HBsAg, anti-HBc and anti-HBs. All analyses were conducted by automated microparticle enzyme immunosorbent assay (Abbott®, AxSYM system, Deerfield, IL, USA), according to the manufacturer's instructions. RESULTS: The prevalence of HBsAg was 0.6% (CI 95% 0.1 - 2.0), that of anti-HBc was 1.1% (CI 95% 0.3 - 2.9) and that of detectable anti-HBs was 83.6% (CI 95% 79.3 - 87.3). Hepatitis B vaccination coverage was 97.5% (CI 95% 95.2 - 98.8). CONCLUSIONS: These results demonstrate the success of the vaccination program against hepatitis B in the region studied and indicate that prevention strategies must be maintained and, if possible, expanded to contribute to the establishment of positive prevalence rates in all age groups.
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Introduction: Hepatitis C virus (HCV) infection is diagnosed by the presence of antibodies and is supplemented by confirmatory testing methods, such as recombinant immunoblot assay (RIBA) and HCV-RNA detection. This study aimed to evaluate the efficacy of RIBA testing to diagnose HCV infection in blood donors positive for anti-HCV antibodies. Methods: A total of 102 subjects positive for anti-HCV determined by enzyme-linked immunosorbent assay (ELISA) at the Hematology and Hemotherapy Foundation of Bahia (HEMOBA) were later assessed with new samples using the Abbott Architect anti-HCV test (Abbott Diagnostics, Wiesbaden, Germany), the RIBA III test (Chiron RIBA HCV 3.0 SIA, Chiron Corp., Emeryville, CA, USA), the polymerase chain reaction (PCR; COBAS® AMPLICOR HCV Roche Diagnostics Corp., Indianapolis, IN, USA) and line probe assay (LiPA - Siemens, Tarrytown, NY, USA) genotyping for HCV diagnosis. Results: Of these new samples, 38.2% (39/102) were positive, 57.8% (59/102) were negative and 3.9% (4/102) were indeterminate for anti-HCV; HCV-RNA was detected in 22.5% (23/102) of the samples. RIBA results were positive in 58.1% (25/43), negative in 9.3% (4/43) and indeterminate in 32.6% (14/43) of the samples. The prevailing genotypes were 1 (78.3%, 18/23), 3 (17.4%, 4/23) and 2 (4.3%, 1/23). All 14 samples with indeterminate RIBA results had undetectable viral loads (detection limit ≤50 IU/mL). Of these samples, 71.4% (10/14) were reevaluated six months later. Eighty percent (8/10) of these samples remained indeterminate by RIBA, and 20% (2/10) were negative. Conclusions: In this study, individuals with indeterminate RIBA results had no detectable HCV-RNA.
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Of eleven proteins analyzed in four Amazonian populations, the esterases showed the greatest variation, with five activity zones. EST1, EST2 and EST5 showed variation in each of the populations studied. EST1 and EST2 are each controlled by two, and EST5 by four, codomi-nant alleles. LAP presented six activity zones, with codominant variation in LAP5and LAP6.oc—GPDH was monomorphic with one activity band on starch gel and two on polyacrylamide gel. 1DH presented two activity zones, with variation in the IDHl region. PGM had a single activity zone, with variation in all populations. The Ariquemes populations showed five alleles and the other populations three, all of then codominant. Three activity zones with two codominant alleles were observed for ODH. Aldehyde Oxidase showed two activity zones, with variation in AOl only in the Ariquemes and Porto Velho/Samuel populations. 6-PGDH showed only one activity zone and variation only in the Ariquemes population. The remaing systems - XDH, G-6-PDH and GDH. was monomorphic.
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Devido à falta de informações sobre Urbanus acawoios (Williams, 1926) (Lepidoptera: Hesperiidae), e pelos danos severos por ele causados em árvores de Clitoria racemosa, o presente trabalho foi desenvolvido sob condições de laboratório para verificar a possibilidade de utilizar Bacillus thuringiensis var. kurstaki (H-3a:3b) como agente microbiano para o seu controle. O pH do intestino médio do hesperídeo mostrou ser bastante alcalino, variando de 8,4 a 9,2 (média de 8,7), indicando a possibilidade das larvas serem susceptíveis ao patógeno. Os ensaios confirmaram a alta susceptibilidade a dosagens equivalentes a 110 g / ha, resultando em tempos letais medianos (TL50) de 42,28, 37,18, 28,00 e 51,87 horas para larvas de 3o, 4°, início e final do 5º ínstares, respectivamente. Três outras dosagens (80, 150 e 280 g/h) foram aplicadas para larvas do 3º ínstar, resultando em TLs50 de 42,62, 30,77 e 30,06 horas, respectivamente. Descrições detalhadas sobre os sintomas externos nas larvas infectadas foram dadas. As alterações histológicas do intestino médio afetado pela d-endotoxina de B. thuringiensis foram descritas. Os resultados obtidos no presente trabalho revelam a grande possibilidade de controlar esta praga utilizando-se produtos e formulados à base desta bactéria.
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Devido aos danos dos ataques de Urbanus acawoios (Williams, 1926) (Lepidoptera: Hesperiidae) em palheteiras (Clitoria racemosa) (Leguminosae) em Manaus, AM e a total ausência de qualquer informação a respeito desta espécie, o presente trabalho foi desenvolvido visando a obtenção de conhecimentos que facilitem a identificação de métodos seguros e eficientes para o seu controle. Os estudos biológicos revelaram que este inseto é multivoltino, tendo duração média de 41,89 ± 0,98 dias por geração. As condições climáticas na cidade de Manaus, a disponibilidade de alimentos, e possivelmente a ausência de inimigos naturais eficientes, parecem ser os fatores principais responsáveis pela ocorrência de erupções populacionais desta espécie. Enquanto o estágio larval consiste de 5 fases (ínstares) e dura em média 18,46 ± 1,28 dias, o da pupa necessita 9,96 ± 1,05, e o adulto 13,47 ± 0,27 dias, sob condições de 30°C e 85% UR. Estudos morfológicos foram incluídos.
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The most severe drought in tropical South America during the 20th century occurred in 1926. This extreme El Nino year is further documented anecdotally, in an update of the river stage observations at Manaus, and in annual rainfall records. The annual rainfall anomaly is an east-west dipole over tropical South America, with drought to the west over the Amazon basin whose discharge is documented at Manaus, and with a surplus to the east and including the Nordeste region of Brazil. Speculations about a role for aerosol in aggravating the drought are discussed.
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A survey of the Streblidae batflies on the phyllostomid bats was conducted in the northeastern Rio Grande do Sul State, Brazil, during 1997. Hundred thirty three streblids were collected on 44 parasited hosts. Eleven species of batflies (Trichobius dugesii Townsend, 1891, T. tiptoni Wenzel, 1976, Trichobius sp., Paratrichobius longicrus (Miranda Ribeiro, 1907), Megistopoda aranea (Coquillett, 1899), M. proxima (Séguy, 1926), Exastinion clovisi (Pessoa & Guimarães, 1936), Paraeuctenodes longipes Pessoa & Guimarães, 1936, Anastrebla modestini Wenzel, 1966, A. caudiferae Wenzel, 1976 and Metelasmus pseudopterus Coquillett, 1907) were found on six species of phyllostomid bats (Artibeus lituratus (Olfers, 1818), A. fimbriatus Gray, 1838, Sturnira lilium (E. Geoffroy, 1810), Glossophaga soricina (Pallas, 1766), Anoura caudifera (E. Geoffroy, 1818) and A. geoffroyi Gray, 1838). All records are new for the Rio Grande do Sul and Anastrebla caudiferae is firstly recorded in Brazil. Differences in the batflies community composition in Artibeus fimbriatus and A. lituratus are discussed.
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The author divides the article in thee parts. In the first part he studies the literature on the genotype of Dipetalonema DIESING, 1861 - D. caudispina (MOLIN, 1858), and gives a new generic diagnosis of the Diesing's genus, based upon its type species. In the second one he studies the literature on the validity of Acanthocheilonema COBBOLD, 1870, and, comparing both generic defvinition and type-species description of Acanthocheilonema dracunculoides COBBOLD, 1870 and Dipetalonema caudispina (MOLIN, 1858), concludes that Cobbold's genus Acanthocheilonema must be, definitely, considered as a synonym of Dipetalonema DIESING, 1861. In the third part a comparative study, based on the literature, is made between generic definitions and type-species descriptions of Breinlia trichosuri (BREINL, 1913) and Dipetalonema caudipina (MOLIN, 1858), and the author concludes that Breinlia must be considered as a valid genus, distinguished from Dipetalonema, principally, by the morphology fo the longer spicule.
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Aedes albifasciatus is a flood water mosquito ocurring in the southern countries of South America. It is a competent vector of the Western Equine Encephalitis (WEE) and causes important losses on milk and beef production in central Argentina. Field work was carried out from December 1990 to March 1993, on a monthly basis during the dry season and biweekly during the rainy season. Larvae were collected using the 'dipping' technique and females with CDC traps baited with CO2. Field collected larvae were used to build laboratory cohorts, from which basic population parameters were estimated. Eggs survived up to six months on dry soil, although there was a linear decrease of viability with time. At 23ºC, larval development time was around nine days, and all adults emerged within one week. The estimation of larval development in the laboratory seems to be very near the development on the field, as larvae have been collected on average eight days after a rainfall. Egg to adult survival was 83%, with the highest mortality on fourth larval instar (6%). In the laboratory studies, sex proportion among the adults was 1:1, females lived longer than males (median 13 and five days, respectively), and adult survival pattern showed a constant number of individuals dying per unit time. Field collected females layed an average of 84 eggs per batch, and completing up to five gonotrophic cycles, suggesting an estimated survival of up to 35-50 days.