2015
DOI: 10.1016/j.ijmm.2015.04.004
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MALDI-TOF mass spectrometry following short incubation on a solid medium is a valuable tool for rapid pathogen identification from positive blood cultures

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Cited by 72 publications
(47 citation statements)
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“…Preliminary identification of the isolates by mass spectrometry with the MALDI-TOF system (Bruker Daltonics, Bremen, Germany) was performed simultaneously from the same material. 10 When the Gram stain revealed the presence of gram-negative diplococci and the preliminary identification by mass spectrometry corresponded to Acinetobacter spp, we adapted the modification of the Carba NP test proposed by Dortet et al 11 for the detection of OXA-carbapenemases to the RBCT. Briefly, the inoculum was re-suspended in two tubes, one containing 100 μl of the test solution (bromothymol blue/ZnSO 4 ) plus 100 μl 5 M NaCl and the other containing the same solutions plus imipenem.…”
Section: Methodsmentioning
confidence: 99%
“…Preliminary identification of the isolates by mass spectrometry with the MALDI-TOF system (Bruker Daltonics, Bremen, Germany) was performed simultaneously from the same material. 10 When the Gram stain revealed the presence of gram-negative diplococci and the preliminary identification by mass spectrometry corresponded to Acinetobacter spp, we adapted the modification of the Carba NP test proposed by Dortet et al 11 for the detection of OXA-carbapenemases to the RBCT. Briefly, the inoculum was re-suspended in two tubes, one containing 100 μl of the test solution (bromothymol blue/ZnSO 4 ) plus 100 μl 5 M NaCl and the other containing the same solutions plus imipenem.…”
Section: Methodsmentioning
confidence: 99%
“…Direct testing of positive blood culture bottles by MALDI-TOF MS yields accurate identification; however, this approach requires the processing of the blood culture bottle contents, is not U.S. Food and Drug Administration (FDA) approved/cleared, and has a lower success rate than testing of colony isolates (4,6). As an alternative, the use of MALDI-TOF MS for the identification of bacterial isolates from positive blood cultures after short-term incubation (i.e., 2 to 6 h) of high-inoculum subcultures on solid media has been adopted by many laboratories, including our own (7)(8)(9). For example, we use this approach to test positive blood culture bottles showing Gram-negative bacilli upon Gram staining; in our hands, this method has excellent performance, enabling the identification of organisms in 92% (45/49) of blood culture bottles positive for Gramnegative bacilli following a 4-h incubation (our unpublished data).…”
Section: Rapid Testing Of Positive Blood Culture Bottlesmentioning
confidence: 99%
“…For the diagnosis of bacterial pathogens responsible for bloodstream infections the mean incubation time to identify Gram-positive bacteria was 5.9 h, which dropped to 3.1 h if a crude acidic extract was prepared [52]. In other studies, 97 to 69.5% of bacteria were correctly identified after a short incubation of positive blood cultures on solid media of only 3 to 5 h [53][54][55][56], which enabled identification on the same day as the positive blood sample was detected. By increasing the sample concentration (by reducing the sample spot size), creating reference spectra for different cell densities, and immunoaffinity enrichment of bacteria, it was possible to detect as few as 10 to 100 bacterial cells after a blood culture time of only 4 h [20].…”
Section: Shortening the Cultivation Time For Faster Maldi-tof Ms Idenmentioning
confidence: 96%