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1.
Braz. j. med. biol. res ; 47(12): 1016-1020, 12/2014. tab
Article in English | LILACS | ID: lil-727662

ABSTRACT

The diagnostic usefulness of Ziehl-Neelsen (ZN)-stained sputum smears combined with conventional polymerase chain reaction (ZN/PCR) to amplify IS6110 region DNA extracted from ZN slides was evaluated. The objective was to verify if this association could improve tuberculosis (TB) diagnosis in patients at remote sites. The study was carried out in 89 patients with culture-confirmed pulmonary TB as defined by the Brazilian Manual for TB Treatment. The participants were recruited in a reference unit for TB treatment in Rondônia, a state in the Amazonian area in northern Brazil. ZN, PCR, and culture performed in the sputum samples from these patients were analyzed in different combinations (i.e., ZN plus PCR and ZN plus culture). The prevalence rates of pulmonary TB in these patients were 32.6 and 28.1% considering culture and ZN/PCR, respectively. The sensitivity and specificity of ZN/PCR were 86 and 93%, respectively. ZN/PCR was able to detect more TB cases than ZN alone. This method could offer a new approach for accurate tuberculosis diagnosis, especially in remote regions of the world where culture is not available.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult , DNA, Bacterial/isolation & purification , Mycobacterium tuberculosis/genetics , Polymerase Chain Reaction/methods , Rainforest , Sputum/microbiology , Tuberculosis, Pulmonary/diagnosis , Brazil/epidemiology , Cross-Sectional Studies , Molecular Diagnostic Techniques , Mycobacterium tuberculosis/growth & development , Prevalence , Sensitivity and Specificity , Staining and Labeling/methods , Tuberculosis, Pulmonary/epidemiology
2.
Braz. j. med. biol. res ; 42(6): 487-493, June 2009. ilus, tab
Article in English | LILACS | ID: lil-512759

ABSTRACT

We investigated the effect of the -278A>C polymorphism in the CYP7A1 gene on the response of plasma lipids to a reduced-fat diet for 6 to 8 weeks in a group of 82 dyslipidemic males with a mean age of 46.0 ± 11.7 years. Individuals who presented at least one high alteration in total cholesterol, low-density lipoprotein cholesterol or triglyceride values were considered to be dyslipidemic. Exclusion criteria were secondary dyslipidemia due to diabetes mellitus, renal, liver, or thyroid disease. None of the subjects were using lipid-lowering medication. Baseline and follow-up lipid concentrations were measured. The genotypes were determined by the digestion of PCR products with the BsaI restriction endonuclease. There were statistically significant reductions in plasma total cholesterol, low-density lipoprotein cholesterol and triglyceride concentrations after dietary intervention. The minor allele C has a frequency of 43 percent. Carriers of the C allele had significantly lower triglyceride concentrations (P = 0.02) than AA homozygotes. After adjustment of covariates, subjects with the AC and CC genotypes showed a greater reduction in triglyceride concentrations compared to subjects with the AA genotype. Multiple linear regression analyses showed that the AC and CC CYP7A1 genotypes accounted for 5.2 and 6.2 percent of triglyceride concentration during follow-up and adjusted percent of change of triglyceride concentration, respectively. The present study provides evidence that -278A>C polymorphism in the CYP7A1 gene can modify triglyceride concentrations in response to a reduced fat diet in a dyslipidemic male population. This gene represents a potential locus for a nutrigenetic directed approach.


Subject(s)
Adult , Humans , Male , Middle Aged , /genetics , Diet, Fat-Restricted , Dyslipidemias/enzymology , Polymorphism, Genetic/genetics , Triglycerides/blood , Body Mass Index , Dyslipidemias/blood , Dyslipidemias/diet therapy , Gene Frequency , Genotype , Lipids/blood , Promoter Regions, Genetic , Prospective Studies
3.
Braz. j. med. biol. res ; 26(6): 591-603, Jun. 1993. ilus
Article in English | LILACS | ID: lil-148711

ABSTRACT

1. cDNA recombinants containing the VP3 and VP1 sequences of foot-and-mouth disease virus were isolated and the VP3-VP1 sequence was reconstructed. 2. The reconstructed VP3-VP1 sequence was subcloned into expression vector pEX31b and a fusion protein of about 62,000 Da was expressed. 3. When injected into mice, the fusion protein was able to elicit the production of antibodies that recognized viral VP1 and VP3. 4. Antibodies present in sera from mice immunized with VP3-VP1 protein did not neutralize the foot-and-mouth disease virus in vitro


Subject(s)
Animals , Mice , Antibodies, Viral/biosynthesis , Aphthovirus/genetics , Escherichia coli/genetics , Viral Fusion Proteins/isolation & purification , Aphthovirus/immunology , Blotting, Western , Capsid/genetics , Capsid/immunology , Capsid/isolation & purification , Enzyme-Linked Immunosorbent Assay , Epitopes/immunology , Neutralization Tests , Viral Fusion Proteins/genetics , Viral Fusion Proteins/immunology
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