Perfil do produtor de leite da região de Joanópolis/SP: como ele lida com o controle do carrapato Rhipicephalus microplus e de outras doenças de importância veterinária / Profile of dairy farmers of the Joanópolis/SP region, Brazil: how they deal with Rhipicephalus microplus control and other diseases of veterinary interest

Este estudo verificou o perfil do produtor de leite do município de Joanópolis, SP, situado a 115 km de São Paulo, e como esse produtor lida com o controle do carrapato e outras doenças importantes na pecuária leiteira. Quarenta produtores de leite foram entrevistados. Verificou-se que grande parte deles se enquadra em agricultura familiar: pequenas propriedades com mão-de-obra familiar. Verificou-se que 72,5% possuem outra fonte de renda além do leite; 75% produzem menos que 100 litros de leite por dia, e a maioria não é tecnificada (ordenha manual: 72,5 %; não faz escrituração zootécnica: 55%; não aduba pastos: 80%; não utiliza inseminação artificial: 87,5%). O controle do carrapato é feito sem critérios técnicos; a aplicação do carrapaticida é feita no mesmo local da ordenha; 90% não usam equipamentos de proteção individual para aplicar o carrapaticida. O gado prevalente é o mestiço Girolando (87,5%), que, por ser mais resistente ao carrapato, deve contribuir para que 57,5% dos entrevistados estejam satisfeitos com o controle do carrapato. Verificou-se que poucos produtores (apenas 12,5%) possuem assistência técnica constante. Isso pode ser a explicação para o baixo uso de tecnologias e nas falhas observadas no diagnóstico das doenças e no controle do carrapato.(AU)

This study made a detailed description of the milk producer of the municipality of Joanópolis/SP, situated 115 km from the largest city of Brazil, São Paulo, and how they deal with tick control and other important diseases for dairy farming. Forty milk producers were interviewed. It was found that most of them fit into family farms: small farms with family labor; 72.5% have another source of income in addition to the milk; 75% produce less than 100 liters of milk per day; and most of them are not technified (72.5% do manual milking; 55% do not keep zootechnical records; 80% do not fertilize the pastures; 87.5 % do not use artificial insemination). Tick control is made without technical criteria. A hundred percent of the interviewed applied the acaricide in the same place of milking; 90% do not use protective equipment to apply the acaricide. The prevalent cattle breed is the crossbred Girolando (87.5%), a more tick resistant breed. This may contribute to 57.5% that are satisfied with tick control. It was found that few producers (only 12.5%) have constant technical assistance. This may be the explanation for the low use of technologies and the failures observed in the diagnosis of diseases and the use of tick control.(AU)

Frequência de genes codificadores de toxinas em Staphylococcus aureus isolados de leite de tanques expansão comunitários / Frequency of toxin-encoding genes in Staphylococcus aureus isolated from community milk tanks

A capacidade de produção de toxinas pelo Staphylococcus aureus no leite e produtos derivados está relacionado com surtos de intoxicação alimentar. Objetivou-se nesta pesquisa, estudar a ocorrência de genes que codificam para enterotoxinas estafilocócicas (sea, seb, sed, seg, seh e sei) e toxinas α e ß hemolítica (hla e hlb) em S. aureus isolados de 53 amostras de leite de tanques expansão comunitários no Estado de Alagoas, Brasil. Foram identificados 27 isolados (50,94%) como S. aureus pela amplificação do gene nuc. 13/27 isolados (48,1%) foram positivos para pelo menos um gene das enterotoxinas estudadas, sendo as frequências dos genes sea 33,3%, seh 18,5%, sei 11,1% e sed 7,4%; não entanto não foram identificados os genes seb e seg nestas bactérias. Para as toxinas hemolíticas, 51,9% dos isolados portavam ambos genes (hla e hlb), sendo a frequência para o gene hla de 81,5% e para o gene hlb de 51,9%. A frequência de genes das toxinas avaliadas é alta o que constitui um risco potencial para a saúde pública em especial, as enterotoxinas por serem termoestáveis e estarem asssociados com surtos de intoxicação alimentar.(AU)

The capacity of toxin production by Staphylococcus aureus in milk and dairy products is associated with food poisoning outbreaks. The objective of this research was to study the frequency of genes encoding staphylococcal enterotoxin (sea, seb, sed, seg, seh and sei) and α and ß hemolytic toxins (hla and hlb) in S. aureus isolates from 53 milk samples from community tanks in the State of Alagoas, Brazil. Twenty-seven isolates (50.94%) were identified as S. aureus by nuc gene amplification; 13/27 isolates (48.1%) were positive for at least one gene of the studied enterotoxins and the frequency of genes sea was 33.3%, seh 18.5%, sei 11.1% and sed 7.4%; the seb and sec genes have not been identified in the bacteria. For the hemolytic toxins, 51.9% of isolates harbored both genes (hla and hlb), the frequency of hla gene was 81.5% and 51.9% for the hlb gene. The evaluated toxin-encoding gene frequency is high and constitutes a potential risk for public health, especially staphylococcal enterotoxin genes; because they are heat-stable enterotoxins and have been associated with food poisoning.(AU)

High genetic diversity and connectivity in Colossoma macropomum in the Amazon basin revealed by microsatellite markers

Abstract Colossoma macropomum is the second largest scaled fish of the Amazon. It is economically important for commercial fisheries and for aquaculture, but few studies have examined the diversity and genetic structure of natural populations of this species. The aim of this study was to investigate the levels of genetic variability and connectivity that exist between three natural populations of C. macropomum from the Amazon basin. In total, 247 samples were collected from the municipalities of Tefé, Manaus, and Santarém. The populations were genotyped using a panel of 12 multiplex microsatellite markers. The genetic diversity found in these populations was high and similar to other populations described in the literature. These populations showed a pattern of high gene flow associated with the lack of a genetic structure pattern, indicating that the number of migrants per generation and recent migration rates are high. The values of the FST, RST, and exact test of differentiation were not significant for pairwise comparisons between populations. The Bayesian population clustering analysis indicated a single population. Thus, the data provide evidence for high genetic diversity and high gene flow among C. macropomum populations in the investigated region of the Amazon basin. This information is important for programs aiming at the conservation of natural populations.

Estudo de mutações no gene GJB2 e deleção delGJB6-D13S1830 em indivíduos com surdez não sindrômica da região Amazônica / A study of GJB2 and delGJB6-D13S1830 mutations in Brazilian non-syndromic deaf children from the Amazon region

A deficiência auditiva afeta cerca de 1 em cada 1000 recém-nascidos. Mutações no gene da conexina 26 (GJB2) são as causas mais frequentes de surdez não sindrômica em diferentes populações e é sabido que a mutação delGJB6-D13S1830 em DFNB30 é causadora de surdez neurossensorial. Muitos estudos descrevem o envolvimento de mutações no gene GJB2 com a deficiência auditiva em diferentes populações. Entretanto, existe pouca informação sobre a surdez genética no Brasil, especialmente na região Amazônica. OBJETIVO: Determinar a prevalência de mutações no gene GJB2 e da mutação delGJB6-D13S1830 em 77 casos esporádicos de surdez não sindrômicas. MÉTODO: A região codificante do gene GJB2 foi sequenciada e a PCR foi realizada para detectar a mutação delGJB6-D13S1830. RESULTADOS: O alelo 35delG foi encontrado em 9% dos pacientes (7/77). As mutações M34T e V95M foram detectadas em dois distintos pacientes heterozigotos. A mutação não patogênica V27I foi detectada em 28,6% (22/77). Não foi detectada a mutação delGJB6-D13S1830 em nenhum paciente estudado. CONCLUSÃO: Alelos mutantes no gene GJB2 foram observados em 40% (31/77) da amostra. Variantes patogênicas foram detectadas em apenas 12% (9/77). Mais estudos são necessários para elucidar causas genéticas de deficiência auditiva em populações miscigenadas.

Hearing impairment affects about 1 in 1000 newborns. Mutations in the connexin 26 (GJB2) gene rank among the most frequent causes of non-syndromic deafness in different populations, while delGJB6-D13S1830 mutation located in the DFNB30 locus is known to cause sensorineural hearing loss. Despite the many studies on the involvement of GJB2 mutations in hearing impairment in different populations, there is little information on genetic deafness in Brazil, especially in the Amazon region. OBJECTIVE: To determine the prevalence of GJB2 mutations and delGJB6-D13S1830 in 77 sporadic non-syndromic deaf patients. METHOD: The coding region of the GJB2 gene was sequenced and polymerase chain reaction was performed to detect the delGJB6-D13S1830 mutation. RESULTS: Mutant allele 35delG was found in 9% of the patients (7/77). Mutations M34T and V95M were detected in two distinct heterozygous patients. Non-pathogenic mutation V27I was detected in 28.6% of the patients (22/77). None of the deaf patients carried the delGJB6-D13S1830 mutation. CONCLUSION: Mutant alleles on gene GJB2 were observed in 40% (31/77) of the subjects in the sample. Pathogenic variants were detected in only 12% (9/77) of the individuals. More studies are required to elucidate the genetic causes of hearing loss in miscegenated populations.

Haplotype diversity of 17 Y-str loci in an admixed population from the Brazilian Amazon

The allelic and haplotype frequencies of 17 Y-STR loci most commonly used in forensic testing were estimated in a sample of 138 unrelated healthy males from Macapá, in the northern Amazon region of Brazil. The average gene diversity was 0.6554 ± 0.3315. 134 haplotypes of the 17 loci were observed, 130 of them unique and four present in two individuals each. The haplotype diversity index was 0.9996 + 0.0009, with the most frequent haplogroups being R1b (52.2 percent), E1b1b (11.6 percent), J2 (10.1 percent) and Q (7.2 percent). Most haplogroups of this population belonged to European male lineages (89.2 percent), followed by Amerindian (7.2 percent) and African (3.6 percent) lineages.

A vivência do ser enfermeiro e preceptor em um hospital escola: olhar fenomenológico / The experience of being a nurse and preceptor in a school hospital: phenomenological view

Este estudo teve como objetivo compreender a experiência do fenômeno vivenciado pelos enfermeiros preceptores de graduandos do último ano em Enfermagem. O referencial metodológico utilizado foi a fenomenologia e os sujeitos, quinze enfermeiros preceptores do Hospital Universitário Professor Alberto Antunes, em Maceió, Alagoas. As entrevistas foram realizadas nos meses de agosto e setembro de 2010, com a seguinte questão norteadora: Como é para você vivenciar o papel de enfermeiro preceptor de graduandos em Enfermagem no Hospital Universitário Professor Alberto Antunes? Foram reveladas cinco categorias: Satisfação em receber graduandos; Estímulo à atualização; Sobrecarga de Trabalho; Apoio da academia aos enfermeiros e Características do graduando x Sucesso do estágio. Com o desvelar do fenômeno, foi possível obter subsídios para colaborar com as academias formadoras com um suporte teórico para possível reestruturação do planejamento do estágio curricular obrigatório na área hospitalar.

Allelic frequencies and statistical data obtained from 12 codis STR loci in an admixed population of the Brazilian Amazon

The allelic frequencies of 12 short tandem repeat loci were obtained from a sample of 307 unrelated individuals living in Macapá, a city in the northern Amazon region, Brazil. These loci are the most commonly used in forensics and paternity testing. Based on the allele frequency obtained for the population of Macapá, we estimated an interethnic admixture for the three parental groups (European, Native American and African) of, respectively, 46 percent, 35 percent and 19 percent. Comparing these allele frequencies with those of other Brazilian populations and of the Iberian Peninsula population, no significant distances were observed. The interpopulation genetic distances (F ST coefficients) to the present database ranged from F ST = 0.0016 between Macapá and Belém to F ST = 0.0036 between Macapá and the Iberian Peninsula.

Human aging and somatic point mutations in mtDNA: a comparative study of generational differences (grandparents and grandchildren)

The accumulation of somatic mutations in mtDNA is correlated with aging. In this work, we sought to identify somatic mutations in the HVS-1 region (D-loop) of mtDNA that might be associated with aging. For this, we compared 31 grandmothers (mean age: 63 ± 2.3 years) and their 62 grandchildren (mean age: 15 ± 4.1 years), the offspring of their daughters. Direct DNA sequencing showed that mutations absent in the grandchildren were detected in a presumably homoplasmic state in three grandmothers and in a heteroplasmic state in an additional 13 grandmothers; no mutations were detected in the remaining 15 grandmothers. However, cloning followed by DNA sequencing in 12 grandmothers confirmed homoplasia in only one of the three mutations previously considered to be homoplasmic and did not confirm heteroplasmy in three out of nine grandmothers found to be heteroplasmic by direct sequencing. Thus, of 12 grandmothers in whom mtDNA was analyzed by cloning, eight were heteroplasmic for mutations not detected in their grandchildren. In this study, the use of genetically related subjects allowed us to demonstrate the occurrence of age-related (> 60 years old) mutations (homoplasia and heteroplasmy). It is possible that both of these situations (homoplasia and heteroplasmy) were a long-term consequence of mitochondrial oxidative phosphorylation that can lead to the accumulation of mtDNA mutations throughout life.

Fator de Necrose Tumoral Alfa eGravidade Clínica em Primoinfectadospelo Plasmodium Vivax / Tumor Necrosis Factor Alpha and Clinical Severity in Non-Immune Plasmodium Vivax

Avaliar a relação entre o FNT-α, a gravidade daapresentaçمo clيnica e a trombocitopenia, além da freqüênciado FNT2 e sua influência sobre os nيveis da citocina. Materiale Métodos: Foram avaliados pacientes primoinfectados peloP. vivax, ³ 15 anos, provenientes de Belém, Parل, com sintomashل £ 21 dias, atendidos e acompanhados clinicamente noInstituto Evandro Chagas (IEC) ou hospitalizados. A parasitemiafoi quantificada todos os dias até a negativaçمo. Adotou-se acloroquina e a primaquina por via oral, durante sete dias,como tratamento. Amostras sanguيneas foram coletadas emD0 e D7 para anلlises hematolَgicas e bioquيmicas, tيtulos doFNT-α e a freqüência do FNT2. Os programas Biostat 2.0 eExcel-Windows foram utilizados para as anلlises estatيsticasdas diferenças e das correlaçُes entre os parâmetros obtidos.Resultados: Oitenta e três pacientes foram atendidos eacompanhados clinicamente no D0, D1, D2, D3 e D7, defevereiro/2002 a março/2003. O FNT-α se correlacionoupositivamente e significativamente com a parasitemia (rs =0,33; p < 0,01) e com os escores clيnicos (rs = 0,48; p = 0,0001),porém negativamente com as plaquetas (rs = -0,48; p < 0,001)em D0. Os nيveis elevados de FNT-a foram responsلveis pelaintensidade das manifestaçُes clيnicas e pela trombocitopenianestes pacientes, porém o FNT2 nمo produziu tيtulos altos dacitocina. Conseqüentemente, tيtulos elevados de FNT-a forambenéficos na maioria dos casos, a plaquetopenia é um sinalde gravidade e outros fatores genéticos foram responsلveispelos nيveis elevados dessa citocina nesta amostra...

Evaluate the relationship between the TNF-a, theseverity of clinical presentation, the thrombocytopenia, thefrequency of TNF2 and its influence over cytokine levels.Material e Methods: We evaluated patients with first episodeof vivax malaria, ³ 15 years, with disease duration £ 21 days,coming from the city of Belém, Parل, attended at the InstitutoEvandro Chagas (IEC) or hospitalized. The parasitemia wasquantified every day till the negativation. The adoptedtreatment was cloroquine and primaquine PO, during sevendays. Blood samples were collected at D0 and D7 to realizequantification of hematological and biochemical parameters,TNF-a titles and TNF2 frequency. The programs Biostat 2.0and Excel for Windows were applied to analyze the differencesand correlations between the parameters. Results: Eighty threepatients were attended and accompanied clinically at D0, D1,D2, D3 and D7, from february/2002 till march/2003. TheTNF-a level correlated positively and significantly withparasitemia (rs = 0.33, p < 0.01) and clinical scores (rs = 0.48,p = 0.0001), but negatively with the platelets (rs = -0.48, p <0.0001) at D0. Consequently, high titles of TNF-a levels werebeneficial to the majority of the cases; the thrombocytopeniais a signal of severity, and others genetic factors were responsiblefor the high levels of this cytokine and phenotypicmanifestations on this sample...

Mitochondrial DNA mapping of social-biological interactions in Brazilian Amazonian African-descendant populations

The formation of the Brazilian Amazonian population has historically involved three main ethnic groups, Amerindian, African and European. This has resulted in genetic investigations having been carried out using classical polymorphisms and molecular markers. To better understand the genetic variability and the micro-evolutionary processes acting in human groups in the Brazilian Amazon region we used mitochondrial DNA to investigate 159 maternally unrelated individuals from five Amazonian African-descendant communities. The mitochondrial lineage distribution indicated a contribution of 50.2 percent from Africans (L0, L1, L2, and L3), 46.6 percent from Amerindians (haplogroups A, B, C and D) and a small European contribution of 1.3 percent. These results indicated high genetic diversity in the Amerindian and African lineage groups, suggesting that the Brazilian Amazonian African-descendant populations reflect a possible population amalgamation of Amerindian women from different Amazonian indigenous tribes and African women from different geographic regions of Africa who had been brought to Brazil as slaves. The present study partially mapped the historical biological and social interactions that had occurred during the formation and expansion of Amazonian African-descendant communities.

Article Molecular analysis of three FUT3 gene single nucleotide polymorphisms and their relationship with the lewis erythrocytary phenotype in a human population of japanese-ancestry living in Tomé Açu, a town in the Brazilian Amazon

The Lewis blood group system involves two major antigens, Leª and Le b. Their antigenic determinants are not primary gene products but are synthesized by the transfer of sugar subunits to a precursory chain by a specific enzyme which is the product of the FUT3 gene (Lewis gene). The presence of three FUT3 gene single nucleotide polymorphisms (SNPs) (59T > G; 508G > A and 1067T > A) was related to the Lewis phenotype of erythrocytes from 185 individuals of Japanese ancestry living in the town of Tomé-Açu in the Brazilian Amazon region. This relationship was detected using a serological hemagglutination test and the Dot-ELISA assay along with the molecular technique PCR-RFLP. We found that the three SNPs investigated in this study only accounted for a proportion of the Lewis-negative phenotype of the erythrocytes.

Efeito da metoclopramida sobre a produção leiteira de porcas no puerpério e o ganho de peso dos leitões / Effect of metoclopramide on sow's milk production and the performance of piglets

A metoclopramida vem sendo utilizada em mulheres como terapia para incremento lactogênico não havendo na literatura informações sobre a utilização desta droga em suínos. O estudo objetivou, avaliar os efeitos da metoclopramida na produção de leite e desempenho da leitegada. Foram utilizadas 12 fêmeas suínas, as quais foram homogeneizadas de acordo com a ordem de parto. A padronização das leitegadas foi estabelecida em 10 leitões por fêmea, totalizando 120 leitões. O delineamento experimental foi inteiramente casualizado caracterizado por medidas repetidas no tempo, sendo definidos dois tratamentos com seis respectivos cada. No tratamento controle (T1) foi feita a aplicação intra-muscular de soro fisiológico nos três primeiros dias pós-parto e no tratamento 2 (T2) foi aplicado metoclopramida. A metoclopramida influenciou significativamente (p < 0,05) na produção de leite, nos três primeiros dias, havendo maior produção em relação ao controle. Não houve diferenças significativas quanto ao ganho de peso dos leitões nas faixas etárias avaliadas, havendo diferença significativa (p < 0,05) no peso dos leitões no 7° dia de vida. Destacou-se no estudo maior homogeneidade e menor dispersão da leitegada proveniente das fêmeas tratadas com metoclopramida, evidenciados pelos valores máximos e mínimos observados aos 21 dias de idade (p < 0,06). Concluiu-se que a metoclopramida provocou aumento do aporte lactacional em fêmeas suínas, nos três primeiros dias de lactação, cujo efeito traduziu-se na melhor homogeneidade da leitegada.

Metoclopramide has been used in humans as a therapy to increase milk production. There is no information available about this drug in swine for the same purpose. The objective of the study was to evaluate the effects of metoclopramide on lactation of swine females and litter development. For this reason 12 females were used in this study. They were assigned in two graups (T1 and T2) and were drug-induced farrowing. T1 females received saline solution during three days after farrowing and T2 group received metoclopramide. The experimental period lasted 42 days starting fram the administration of the drug. Metoclopramide significantly (p <0,05) affected milk praduction at the first three days compared to the control females. Inthe study we found greater homogeneity and smaller dispersion of litter weight fram females treated with metoclopramida, based upon piglet weight at 21 days of age. In conclusion metoclopramide induced higher milk praduction in swine on the first tree days oflactation and affected litter homogeneity.

Clinical and pathological importance of vacA allele heterogeneity and cagA status in peptic ulcer disease in patients from north Brazil

We have examined the prevalence of gene cagA and vacA alleles in 129 patients, 69 with gastritis and 60 with peptic ulcer diseases from North Brazil and their relation with histopathological data. vacA and cagA genotype were determined by polymerase chain reaction. Hematoxylin-eosin staining was used for histological diagnosis. 96.6 percent of the patients were colonized by Helicobacter pylori strains harboring single vacA genotype (nont-mixed infection). Among them, 11.8 percent had subtype s1a, 67.8 percent had subtype s1b, and 17 percent subtype s2. In regard to the middle region analysis, m1 alleles were found in 75.4 percent and m2 in 21.2 percent of patients. The cagA gene was detected in 78 percent patients infected with H. pylori and was associated with the s1-m1 vacA genotype. The H. pylori strains, vacA s1b m1/cagA-positive, were associated with increased risk of peptic ulcer disease and higher amounts of lymphocytic and neutrophilic infiltrates and the presence of intestinal metaplasia. These findings show that cagA and vacA genotyping may have clinical relevance in Brazil.

Genetic characterization of the population of São Luís, MA, Brazil

Five loci (vWA1, F13A1, D12S67, Apo-B and D1S80) were investigated by polyacrylamide gel electrophoresis followed by silver staining in a sample of 177 individuals from the population of São Luís, State of Maranhão, Brazil. A total of 70 different alleles were identified. A statistically significant deviation from the Hardy-Weinberg equilibrium was observed in a single locus (F13A1, p = 0.0075). The average heterozygosity (H) was estimated at 77.7 percent, the mean number of alleles per locus as 14. The PD (capacity of genotype differentiation at each locus) ranged from 88.9 percent (vWA1) to 96.7 percent (F13A1). The combined PE (power of exclusion) of these five loci was 99.8 percent. In terms of racial admixture (42 percent European, 39 percent Indian, and 19 percent African Black ancestry), São Luís presented an estimate similar to Belém, another trihybrid Amazonian population.

Frequency of the Q192R and L55M polymorphisms of the human serum paraoxonase gene (PON1) in ten Amazonian Amerindian tribes

Human serum paraoxonase (PON1) is an esterase associated with high density lipoproteins (HDLs) in the plasma and may confer protection against coronary artery disease. Serum PON1 levels and activity vary widely among individuals and populations of different ethnic groups, such variations appearing to be related to two coding region polymorphisms (L55M and Q192R). Several independent studies have indicated that the polymorphism at codon 192 (the R form) is a significant risk factor for cardiovascular disease in some populations, although this association has not been confirmed in other populations. Given the possible associations of these mutations with heart diseases and the fact that little or nothing is known of their prevalence in Amerindian populations, we investigated the variability of both polymorphisms in ten Amazonian Indian tribes and compared the variation found with that of other Asian populations in which both polymorphisms have been investigated. The results show that the LR haplotype is the most frequent and the MR haplotype is absent in all Amerindians and Asian populations. We also found that South America Amerindians present the highest frequency of the PON1192*R allele (considered a significant risk factor for heart diseases in some populations) of all the Amerindian and Asian populations so far studied.

Avaliaçäo da resistência ao cisalhamento da uniäo resina composta/porcelana em funçäo de diferentes tipos de adesivos dentinários / Shear bond strength between composite and porcelain while using different kinds of adhesive systems

A presente pesquisa teve a finalidade de determinar a resistência adesiva, através de ensaios de cisalhamento da uniäo resina composta porcelana, em funçäo de diferentes adesivos dentinários. Foram confeccionados cilindros de porcelana e divididos em dois grupos. No grupo I, a superfície da porcelana recebeu tratamento com ácido fluorídrico a 9,5 por cento por um minuto, sendo lavada com água e seca com jatos de ar; foi aplicado ácido fosfórico a 37 por cento, por um minuto, sendo novamente lavada e seca com jatos de ar; em seguida, recebeu a aplicaçäo do primer sinalizador, adesivo dentinário do tipo One-Step© e resina composta até completar os espécimes, com as dimensöes de 14 mm de comprimento, por 5 mm de diâmetro, sendo estes, 7 mm em porcelana, e 7 mm em resina composta. No grupo II, a superfície da porcelana foi condicionada e tratada da mesma maneira dos espécimes do grupo I, mudando-se apenas o tipo de adesivo, onde neste grupo foi utilizado Single Bond©. Após esta seqüência de procedimentos e prontos, os corpos de prova foram submetidos ao teste de cisalhamento na máquina de ensaio Kratos, a uma velocidade de 5 mm/min, aplicada através de uma haste metálica. Os resultados permitiram a seguinte conclusäo: näo houve diferença entre os grupos I e II, demonstrando que a composiçäo química dos adesivos empregados näo interfere na adesäo porcelana/resina composta

Heterogeneous ethnic distribution of the factor V leiden mutation

Inherited resistance to activated protein C caused by the factor V Leiden (FVL) mutation is the most common genetic cause of venous thrombosis yet described, being found in 20-60 per cent of patients with venous thrombophilia. A relationship between the FVL mutation and an increased predisposition to arterial thrombosis in young women was recently reported. We assessed the prevalence of the FVL mutation in 440 individuals (880 chromosomes) belonging to four different ethnic groups: Caucasians, African Blacks, Asians and Amerindians. PCR amplification followed by MnlI digestion was employed to define the genotype. The FVL mutation was found in a heterozygous state in four out of 152 Whites (2.6 per cent), one out of 151 Amerindians (0.6 per cent), and was absent among 97 African Blacks and 40 Asians. Our results confirm that FVL has a heterogeneous distribution in different human populations, a fact that may contribute to geographic and ethnic differences in the prevalence of thrombotic diseases. In addition, these data may be helpful in decisions regarding the usefulness of screening for the FVL mutation in subjects at risk for thrombosis.

Genetical-demographic data from two amazonian populations composed of descendants of african slaves: Pacoval and Curiau

The Amazon region of Brazil includes communities founded by escaped slaves, some of which still remain relatively isolated. We studied two such Afro-Brazilian communities (Pacoval and Curiau), in the rural area of Alenquer, Pará, and in the metropolitan region of Macapá, Amapá, respectively. Among 12 blood loci, alleles considered as markers of African ancestry, such as HBB*S, HBB*C, TF*D1, HP*2M, ABO*B, RH*D-, and CA2*2 were found at frequencies that are expected for populations with a predominantly African origin. Estimates of interethnic admixture indicated that the degree of the African component in Curiau (74 per cent) is higher than that of Pacoval (44 per cent); an Amerindian contribution was not detected in Curiau. Estimated values of African ancestry fit well with the degree of isolation and mobility of the communities. Pacoval exhibited a high proportion of immigrants among the parents and grandparents of the individuals studied, whereas persons living in Curiau exhibited a low level of mobility, despite its location in the metropolitan area of Macapá city, suggesting a relatively strong barrier against the interethnic admixture in this population. In addition, analysis of genetic data in a sub-sample consisting of individuals whose parents and grandparents were born in the study site, and that probably represents the populations two generations ago, indicated that gene flow from non-black people is not a recent event in both populations.

Absence of the E2 allele of apolipoprotein in Amerindians

A determinaçäo da distribuiçäo do alelo ApoE em cinco tribos de índios sulamericanos revelou ausência do alelo ApoE2, acompanhada por freqüência alta do alelo ApoE3 e baixa do alelo ApoE4 na maioria das tribos, uma distribuiçäo previamente relatada apenas para os esquimós Inuit da Groenlândia.

Migration and ethnic change in an admixed population from the Amazon region (Santarém, Pará)

Dados genéticos e demográficos da populaçäo de Santarém, PA, foram analisados. Oitenta e dois por cento dos indivíduos estudados nasceram no Estado do Pará e 11,7 por cento dos imigrantes nasceram na regiäo Nordeste do Brasil. A análise da migraçäo individual média, distância marital média, distância genitor-prole e índice de exogamia identificou uma elevada mobilidade populacional. Alelos característicos dos três principais grupos étnicos foram encontrados, como BCHE*A (caucasóides) ALB*Maku (indígenas) e HBB*S e HBB*C (negros). As proporçöes de ancestralidade negra, índia e branca foram estimadas em 28 por cento, 35 por cento e 37 por cento, respectivamente. Condiderando-se o local de nascimento dos avós, a presença de uma subpopulaçäo pôde ser observada (nativos de Santarém). As proporçöes de ancestralidade negra e índia foram de 11 por cento e 52 por cento respectivamente, significantemente diferentes da amostra total. A estratégia usada, portanto, mostrou-se eficiente para a caracterizaçäo dos fatores responsáveis pela estrutura genético-demográfica desta populaçäo.