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1.
Artigo em Inglês | MEDLINE | ID: mdl-11127321

RESUMO

Several antigens from the microfilarial stage of Wuchereria bancrofti have been identified using immunoblots of microfilarial antigens and screening with immune sera and tropical pulmonary eosinophilia (TPE) sera. This analysis revealed an array of antigens with apparent molecular weights of 14kDa, 35kDa, 42kDa, 63kDa, 88kDa, 97kDa and 200kDa. Among these only the 14kDa and 42kDa antigens were consistently recognized by most of the immune sera. A 132kDa antigen was recognized only by TPE sera. Analysis of rabbit immune sera revealed that the 42kDa antigen was shared by two developmental stages of W. bancrofti, namely L3 and mF. This antigen could become a potential vaccine candidate. The 14kDa antigen seems specific for the microfilarial stage and therefore could be a diagnostic marker for active infection. The 132kDa antigen could aid in the diagnosis of TPE.


Assuntos
Antígenos de Helmintos , Filariose/diagnóstico , Wuchereria bancrofti/imunologia , Animais , Anticorpos Anti-Helmínticos/sangue , Anticorpos Anti-Helmínticos/imunologia , Antígenos de Helmintos/imunologia , Reações Cruzadas , Filariose/imunologia , Imunofluorescência , Humanos , Soros Imunes , Imunização , Immunoblotting , Microfilárias/imunologia , Peso Molecular , Eosinofilia Pulmonar/imunologia , Coelhos , Vacinas/imunologia , Wuchereria bancrofti/crescimento & desenvolvimento
2.
Int J Parasitol ; 30(2): 119-24, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10704593

RESUMO

Wuchereria bancrofti is the major cause of lymphatic filariasis in humans. Although it is responsible for this immensely morbid and debilitating disease, very little is known of the basic molecular biology of this parasite, and there is a vast lack of knowledge on its gene organisation. In this study, the actin gene of W. bancrofti has been characterised by sequencing a clone isolated from a genomic DNA library of this parasite. The 5' flanking region had a potential TATA box and a putative mRNA initiation site. The gene had five exons encoding 376 amino acids, and four introns ranging in size from 109 to 190bp. The 3' flanking region had a potential polyadenylation signal with the sequence ATTAAA which is a common natural variant of the conventional sequence AATAAA. The gene was AT-rich, with a GC content of 37.2%. Southern blot analysis of W. bancrofti genomic DNA indicated that the gene is possibly found as a single copy. The actin amino acid sequence of W. bancrofti showed a high degree of homology to the actin of many organisms of different taxonomic groups, but the highest homology was observed with the free-living nematode Plectus acuminatus. This suggests that P. acuminatus may bear a close evolutionary relationship to W. bancrofti.


Assuntos
Actinas/genética , Wuchereria bancrofti/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Sequência Consenso , Filariose Linfática/genética , Filariose Linfática/parasitologia , Biblioteca Gênica , Humanos , Dados de Sequência Molecular , Mapeamento por Restrição , Alinhamento de Sequência , TATA Box
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