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Production, characterization, and application of antibodies against heat-labile type-I toxin for detection of enterotoxigenic Escherichia coli
Menezes, Caroline A; Imamura, Sergio Y; Trabulsi, Luiz R; Fernandes-Filho, Antônio; Martinez, Marina B; Guth, Beatriz E. C; Girao, Dennys M; Piazza, Roxane M. F.
  • Menezes, Caroline A; Instituto Butantan. Laboratório de Bacteriologia. Sao Paulo. BR
  • Imamura, Sergio Y; Instituto Butantan. Laboratório de Bacteriologia. Sao Paulo. BR
  • Trabulsi, Luiz R; s.af
  • Fernandes-Filho, Antônio; Universidade de Sao Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Análises Clínicas e Toxicológicas. Sao Paulo. BR
  • Martinez, Marina B; Universidade de Sao Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Análises Clínicas e Toxicológicas. Sao Paulo. BR
  • Guth, Beatriz E. C; Universidade Federal de Sao Paulo. Departamento de Microbiologia, Imunologia e Parasitologia. Sao Paulo. BR
  • Girao, Dennys M; Universidade Federal do Rio de Janeiro. Instituto Prof.Paulo de Góes. Departamento de Microbiologia Médica. Rio de Janeiro. BR
  • Piazza, Roxane M. F; Instituto Butantan. Laboratório de Bacteriologia. Sao Paulo. BR
Mem. Inst. Oswaldo Cruz ; 101(8): 875-880, Dec. 2006. ilus, graf
Article in English | LILACS | ID: lil-440575
ABSTRACT
Strains of enterotoxigenic Escherichia coli (ETEC) are responsible for significant rates of morbidity and mortality among children, particularly in developing countries. The majority of clinical and public health laboratories are capable of isolating and identifying Salmonella, Shigella, Campylobacter, and Escherichia coli O157H7 from stool samples, but ETEC cannot be identified by routine methods. The method most often used to identify ETEC is polymerase chain reaction for heat-stable and heat-labile enterotoxin genes, and subsequent serotyping, but most clinical and public health laboratories do not have the capacity or resources to perform these tests. In this study, polyclonal rabbit and monoclonal mouse IgG2b antibodies against ETEC heat-labile toxin-I (LT) were characterized and the potential applicability of a capture assay was analyzed. IgG-enriched fractions from rabbit polyclonal and the IgG2b monoclonal antibodies recognized LT in a conformational shape and they were excellent tools for detection of LT-producing strains. These findings indicate that the capture immunoassay could be used as a diagnostic assay of ETEC LT-producing strains in routine diagnosis and in epidemiological studies of diarrhea in developing countries as enzyme linked immunosorbent assay techniques remain as effective and economical choice for the detection of specific pathogen antigens in cultures.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Bacterial Toxins / Immunoglobulin G / Enterotoxins / Escherichia coli / Antibodies, Monoclonal Type of study: Diagnostic study / Prognostic study Limits: Animals / Humans Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2006 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Instituto Butantan/BR / Universidade Federal de Sao Paulo/BR / Universidade Federal do Rio de Janeiro/BR / Universidade de Sao Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Bacterial Toxins / Immunoglobulin G / Enterotoxins / Escherichia coli / Antibodies, Monoclonal Type of study: Diagnostic study / Prognostic study Limits: Animals / Humans Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2006 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Instituto Butantan/BR / Universidade Federal de Sao Paulo/BR / Universidade Federal do Rio de Janeiro/BR / Universidade de Sao Paulo/BR