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Rapid time-resolved luminescence based screening of bacteria in urine with luminescence modulating biosensing phages.
Kulpakko, Janne; Rantakokko-Jalava, Kaisu; Eerola, Erkki; Hänninen, Pekka E.
Afiliação
  • Kulpakko J; Medicity Research Laboratories and Laboratory of Biophysics, Institute of Biomedicine, Faculty of Medicine, University of Turku, Finland. Electronic address: jkkulp@utu.fi.
  • Rantakokko-Jalava K; Clinical Microbiology Laboratory, Turku University Hospital and University of Turku, Finland.
  • Eerola E; Clinical Microbiology Laboratory, Turku University Hospital and University of Turku, Finland.
  • Hänninen PE; Medicity Research Laboratories and Laboratory of Biophysics, Institute of Biomedicine, Faculty of Medicine, University of Turku, Finland.
Anal Biochem ; 570: 21-26, 2019 04 01.
Article em En | MEDLINE | ID: mdl-30735666
Urinary tract infections (UTIs) are a common problem worldwide. The most prevalent causative pathogen of UTI is Escherichia coli, focus of this study. The current golden standard for detecting UTI is bacterial culture, creating a major workload for hospital laboratories - cost-effective and rapid mass screening of patient samples is needed. Here we present an alternative approach to screen patient samples with a single-step assay utilising time-resolved luminescence and luminescence modulating biosensing phages. Filamentous phage M13 was biopanned for binding luminescence quenching metal (copper) and further E. coli. The screening assay luminescence modulation was further enhanced by selecting right chemical environment for the functioning phage clones. Semi-specific interaction between phage, target bacteria and metal was detected by modulation in the signal of a weakly chelating, easily quenchable lanthanide complex. In the presence of the target pathogen, the phages collected quenching metal from solution to the bacterial surface changing the quenching effect on the lanthanide label and thus modulating the signal. Our method was compared with the bacterial culture data obtained from 70 patient samples. The developed proof-of-principle screening assay showed sensitivity and a specificity at the 90% mark when compared to culture method although some samples had high turbidity and even blood. The detection limit of E. coli was in the range of 1000-10 000 colony forming units/mL. Untreated urine sample was screened and time-resolved luminescence signal result was achieved within 10 min in a single incubation step.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urina / Técnicas Biossensoriais / Bacteriófago M13 / Escherichia coli Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Urina / Técnicas Biossensoriais / Bacteriófago M13 / Escherichia coli Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article