Direct identification of clinical pathogens from liquid culture media by MALDI-TOF MS analysis. (June 2018)

• Record Type: Journal Article
• Authors: Oviaño, M.; Rodríguez-Sánchez, B.; Gómara, M.; Alcalá, L.; Zvezdanova, E.; Ruíz, A.; Velasco, D.; Gude, M.J.; Bouza, E.; Bou, G.
• Is Part Of: Clinical microbiology and infection. Volume 24:Number 6(2018)
• Page Start: 624
• Page End: 629
• Publication Date: 2018-06
• Subjects: Clinical microbiology -- Diagnostic method -- Identification -- Liquid cultures -- MALDI-TOF MS; Medical microbiology -- Periodicals; Diagnostic microbiology -- Periodicals; Communicable diseases -- Periodicals; Infection -- Periodicals; 616.01
• DOI: 10.1016/j.cmi.2017.09.010
• Languages: English
• ISSNs: 1198-743X

Abstract

Abstract: Objectives: We propose using MALDI-TOF MS as a tool for identifying microorganisms directly from liquid cultures after enrichment of the clinical sample in the media, to obtain a rapid microbiological diagnosis and an adequate administration of the antibiotic therapy in a clinical setting. Methods: To evaluate this approach, a series of quality control isolates were grown in thioglycollate (TG) broth and brain heart infusion (BHI) broth and extracted under four different protocols before finally being identified by MALDI-TOF MS. After establishing the best extraction protocol, we validated the method in a total of 300 liquid cultures (150 in TG broth and 150 in BHI broth) of different types of clinical samples obtained from two tertiary Spanish hospitals. Results: The initial evaluation showed that the extraction protocol including a 5 minute sonication step yielded 100% valid identifications, with an average score value of 2.305. In the clinical validation of the procedure, 98% of the microorganisms identified from the TG broth were correctly identified relative to 97% of those identified from the BHI broth. In 24% of the samples analysed, growth by direct sowing was only successful in the liquid medium, and no growth was observed in the direct solid agar cultures. Conclusions: Use of MALDI-TOF MS plus the sonication-based extraction method enabled direct and accurate identification of microorganisms in liquid culture media in 15 minutes, in contrast to the 24 hours of subculture required for conventional identification, allowing the administration of a targeted antimicrobial therapy.