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Talanta ; 203: 322-327, 2019 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-31202346

RESUMO

Fast detection of bacteria in samples presumed to be un-contaminated, such as blood, is of great importance. Indeed, rapid diagnosis allows the set-up of appropriate antibiotic treatment. Besides clinical issues, there are many other domains, such as food processing or drug manufacturing, where the strict absence of any bacteria has to be assessed. Because the bacterial load found in most contaminated samples is often below the limit of detection for currently validated assays, a preliminary enrichment step is required to allow bacterial multiplication before proceeding to the analysis step, whatever it might be - cultural, immunological or molecular methods. In this study, we describe the use of a biosensor for single-step bacteria detection. The whole analysis is performed in less than 20 h, during the growth phase of the micro-organisms, using an array of antimicrobial peptides (AMPs) coupled with a surface plasmon resonance imager (SPRI). A wide range of bacterial strains are assayed, showing differentiated affinity patterns with the immobilized peptides, which are confirmed by multivariate analysis. This work establishes the evidence that antimicrobial peptides, mostly used so far in the antibiotic drug industry, are suited for the wide-spectrum detection of unknown bacteria in samples, even at very low initial loads. Moreover, the small set of AMPs that were assayed provided a specific affinity profile for each pathogen, as confirmed by multivariate analyses. Furthermore, this work opens up the possibility of applying this method in more complex and relevant samples such as foodstuff, urine or blood.


Assuntos
Peptídeos Catiônicos Antimicrobianos/metabolismo , Bactérias/isolamento & purificação , Bacteriocinas/metabolismo , Sequência de Aminoácidos , Peptídeos Catiônicos Antimicrobianos/química , Bactérias/metabolismo , Bacteriocinas/química , Técnicas Biossensoriais/métodos , Limite de Detecção , Análise Multivariada , Análise de Componente Principal , Ligação Proteica , Ressonância de Plasmônio de Superfície/métodos
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