ABSTRACT
The objective of this study was to determine the presence of Strongyloides stercoralis in urban garbage collectors through the use of immunological and parasitological methods. A total of 92 individuals were evaluated from August, 1997, to June, 1998. For the parasitological diagnosis Baermann and Lutz' methods were applied. The immunological diagnosis involved the indirect fluorescence antibody test (IFAT) and the enzyme-linked immunosorbent assay (ELISA) to detect specific IgG antibodies. Of the 92 workers examined, six (6.5 percent) were infected with larvae of S. stercoralis. The IFAT detected 19 (16.3 percent) and the ELISA 17 (18.5 percent) positive serum samples. The differences between the results of parasitological and immunological methods were statistically significant (p<0.05). These results demonstrate that there is a need to improve the health conditions of this category of city employees.
Subject(s)
Humans , Animals , Male , Female , Adult , Middle Aged , Occupational Diseases/parasitology , Strongyloidiasis/diagnosis , Strongyloidiasis/epidemiology , Garbage , Strongyloides stercoralis/immunology , Age and Sex Distribution , Antibodies, Helminth/analysis , Brazil , Enzyme-Linked Immunosorbent Assay , Occupational Diseases/diagnosis , Strongyloidiasis/immunology , Strongyloidiasis/transmission , Fluorescent Antibody Technique, Indirect , Immunoglobulin G/analysis , Occupational Exposure , Intestinal Diseases, Parasitic/epidemiology , Strongyloides stercoralis/isolation & purification , Strongyloides stercoralis/growth & developmentABSTRACT
BRCA1 mutations are known to be responsible for the majority of hereditary breast and ovarian cancers in women with early onset and a family history of the disease. In this paper we present a mutational survey conducted in 47 Brazilian patients with breast/ovarian cancer, selected based on age at diagnosis, family history, tumor laterality, and presence of breast cancer in male patients. All 22 coding exons and intron-exon junctions were sequenced. Constitutional mutations were found in seven families, consisting of one insertion (insC5382) in exon 20 (four patients), one four base-pair deletion (3450-3453delCAAG) in exon 11 resulting in a premature stop codon (one patient), one transition (IVS17+2T> C) in intron 17 affecting a mRNA splicing site (one patient), and a C> T transition resulting in a stop-codon (Q1135X) in exon 11 (one patient). The identification of these mutations which are associated to hereditary breast and ovarian cancers will contribute to the characterization of the mutational spectrum of BRCA1 and to the improvement of genetic counseling for familial breast/ovarian cancer patients in Brazil.