Ultrasensitive multiplex optical quantification of bacteria in large samples of biofluids

Efficient treatments in bacterial infections require the fast and accurate recognition of pathogens, with concentrations as low as one per milliliter in the case of septicemia. Detecting and quantifying bacteria in such low concentrations is challenging and typically demands cultures of large sample...

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Detalles Bibliográficos
Autores: Pazos Pérez, Nicolas, Pazos, Elena, Catala, Carme, Mir Simon, Bernat, Gómez de Pedro, Sara, Sagales, Juan, Villanueva, Carlos, Vila Estapé, Jordi, Soriano Viladomiu, Alex, García de Abajo, F. Javier, Álvarez Puebla, Ramón A.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/101576
Acceso en línea:https://hdl.handle.net/2445/101576
Access Level:acceso abierto
Palabra clave:Malalties bacterianes
Nanopartícules
Bacterial diseases
Nanoparticles
Descripción
Sumario:Efficient treatments in bacterial infections require the fast and accurate recognition of pathogens, with concentrations as low as one per milliliter in the case of septicemia. Detecting and quantifying bacteria in such low concentrations is challenging and typically demands cultures of large samples of blood (~1 milliliter) extending over 24-72 hours. This delay seriously compromises the health of patients. Here we demonstrate a fast microorganism optical detection system for the exhaustive identification and quantification of pathogens in volumes of biofluids with clinical relevance (~1 milliliter) in minutes. We drive each type of bacteria to accumulate antibody functionalized SERS-labelled silver nanoparticles. Particle aggregation on the bacteria membranes renders dense arrays of inter-particle gaps in which the Raman signal is exponentially amplified by several orders of magnitude relative to the dispersed particles. This enables a multiplex identification of the microorganisms through the molecule-specific spectral fingerprints.