Literature DB >> 22872927

Comparison of bacterial identification by MALDI-TOF mass spectrometry and conventional diagnostic microbiology methods: agreement, speed and cost implications.

K El-Bouri1, S Johnston, E Rees, I Thomas, N Bome-Mannathoko, C Jones, M Reid, B Ben-Ismaeil, A R Davies, L G Harris, D Mack.   

Abstract

Identification of microbial pathogens still relies primarily on culture and phenotypic methods, which is labour-intensive and time-consuming. In this study, identification of bacteria with valid standard identification using BD Phoenix, API panels and other recommended procedures is compared to identification with matrix-assisted laser desorption/ionisation-time of flight (MALDI-TOF) mass spectrometry using the MALDI Biotyper (Bruker Daltonics) in the setting of a routine NHS diagnostic microbiology laboratory. In total, 928 bacterial isolates obtained from blood (n=463), wounds and pus (n=208), respiratory tract (n=100), faeces (n=86) and urines (n=71) were analysed. There were 721 (77.7%) isolates with a MALDI Biotyper score > or =2.0, indicating secure genus and probable species identification; and 149 (16.1%) isolates with a score > or =1.7 and <2.0 indicating probable genus identification. The isolates with scores of > or =2.0 and > or =1.7 comprised 31 and 33 genera and 65 and 67 species, respectively. Overall, 99.4% and 99.1% of organism identifications were in agreement between the MALDI Biotyper and conventional identification at the genus level, and 89.3% and 87.8% at species level when analysing organisms with MALDI Biotyper scores > or =2.0 and > or =1.7, respectively. With many but not all organisms, identification at the genus level is sufficient; however, MALDI Biotyper separation of 208 staphylococci into Staphylococcus aureus and coagulase-negative staphylococci was always correct when scores were > or =1.7. First results were obtained after 5-10 min and analysis of a full 96-well target plate was completed in approximately 90 min. Substantial savings of between pounds 1.79 and pounds 2.56 per isolate, depending on the cost model of acquisition of the MALDI Biotyper system and number of isolates tested, would be realised when all 928 isolates were identified using the MALDI Biotyper and disk-susceptibility testing when compared to the cost for 618 Phoenix ID panels and 158 API panels and disk-susceptibility tests only (i.e., not taking into account costs incurred for identification of the remaining 152 mixed isolates). Microbial identification by MALDI Biotyper offers a rare opportunity for significant cost-neutral or even cost-saving quality improvements in medical diagnostics.

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Year:  2012        PMID: 22872927

Source DB:  PubMed          Journal:  Br J Biomed Sci        ISSN: 0967-4845            Impact factor:   3.829


  13 in total

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Journal:  Eur J Clin Microbiol Infect Dis       Date:  2013-09-10       Impact factor: 3.267

2.  Multicenter evaluation of the Vitek MS matrix-assisted laser desorption ionization-time of flight mass spectrometry system for identification of Gram-positive aerobic bacteria.

Authors:  Jenna Rychert; Carey-Ann D Burnham; Maureen Bythrow; Omai B Garner; Christine C Ginocchio; Rebecca Jennemann; Michael A Lewinski; Ryhana Manji; A Brian Mochon; Gary W Procop; Sandra S Richter; Linda Sercia; Lars F Westblade; Mary Jane Ferraro; John A Branda
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5.  Accuracy of conventional identification methods used for Enterobacteriaceae isolates in three Nigerian hospitals.

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7.  Identification of clinical isolates of α-hemolytic streptococci by 16S rRNA gene sequencing, matrix-assisted laser desorption ionization-time of flight mass spectrometry using MALDI Biotyper, and conventional phenotypic methods: a comparison.

Authors:  Angharad Puw Davies; Michelle Reid; Stephen J Hadfield; Stuart Johnston; Jane Mikhail; Llinos G Harris; Howard F Jenkinson; Nidhika Berry; Ann M Lewis; Khalid El-Bouri; Dietrich Mack
Journal:  J Clin Microbiol       Date:  2012-09-19       Impact factor: 5.948

8.  Performance of lipid fingerprint-based MALDI-ToF for the diagnosis of mycobacterial infections.

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Authors:  Percy Schröttner; Jurek Schultz; Wolfram Rudolph; Florian Gunzer; Alexander Thürmer; Guido Fitze; Enno Jacobs
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10.  Screening cultures for detection of methicillin-resistant Staphylococcus aureus in a population at high risk for MRSA colonisation: identification of optimal combinations of anatomical sites.

Authors:  Khalid El-Bouri; Wahbi El-Bouri
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