Production, characterization, and application of antibodies against heat-labile type-I toxin for detection of enterotoxigenic Escherichia coli

Autor(es)

Caroline A Menezes ^[1] ; Sergio Y Imamura ^[2] ; Luiz R Trabulsi ; Antônio Fernandes-Filho ^[4] ; Marina B Martinez ^[5] ; Beatriz EC Guth ^[6] ; Dennys M Girão ^[7] ; Roxane MF Piazza ^[8]

Afiliação do(s) autor(es)

^[1] Instituto Butantan. Laboratório de Bacteriologia - Brasil

^[2] Instituto Butantan. Laboratório de Bacteriologia - Brasil

^[4] Universidade de São Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Análises Clínicas e Toxicológicas - Brasil

^[5] Universidade de São Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Análises Clínicas e Toxicológicas - Brasil

^[6] Universidade Federal de São Paulo. Departamento de Microbiologia, Imunologia e Parasitologia - Brasil

^[7] Universidade Federal do Rio de Janeiro. Instituto Prof. Paulo de Góes. Departamento de Microbiologia Médica - Brasil

^[8] Instituto Butantan. Laboratório de Bacteriologia - Brasil

• Tipo de documento: Artigo Científico
• Fonte: Memórias do Instituto Oswaldo Cruz; v. 101, n. 8, p. 875-880, 2006-12-00.

Resumo

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 O157:H7 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. (AU)

• Processo FAPESP: 99/09458-0 - Desenvolvimento de testes imunosorológicos para detecção das toxinas ST e LT produzidas por Escherichia coli enterotoxigênica e das toxinas STX produzidas por Escherichia coli enterohemorrágica
• Beneficiário: Roxane Maria Fontes Piazza
• Modalidade de apoio: Auxílio à Pesquisa - Regular