Early and specific targeted mass spectrometry-based identification of bacteria in endotracheal aspirates of patients suspected with ventilator-associated pneumonia
Rapid and reliable pathogen identification is compulsory to confirm ventilator-associated pneumonia (VAP) in order to initiate appropriate antibiotic treatment. In the present proof of concept, the effectiveness of rapid microorganism identification with a targeted bottom-up proteomics approach was...
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Veröffentlicht in: | European journal of clinical microbiology & infectious diseases 2021-06, Vol.40 (6), p.1291-1301 |
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Sprache: | eng |
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Zusammenfassung: | Rapid and reliable pathogen identification is compulsory to confirm ventilator-associated pneumonia (VAP) in order to initiate appropriate antibiotic treatment. In the present proof of concept, the effectiveness of rapid microorganism identification with a targeted bottom-up proteomics approach was investigated in endotracheal aspirate (ETA) samples of VAP patients. To do so, a prototype selected-reaction monitoring (SRM)-based assay was developed on a triple quadrupole mass spectrometer tracking proteotypic peptide surrogates of bacterial proteomes. Through the concurrent monitoring of 97 species-specific peptides, this preliminary assay was dimensioned to characterize the occurrence of six most frequent bacterial species responsible for over more than 65% of VAP. Assay performance was subsequently evaluated by analyzing early and regular 37 ETA samples collected from 15 patients. Twenty-five samples were above the significant threshold of 10
5
CFU/mL and five samples showed mixed infections (both pathogens ≥ 10
5
CFU/mL). The targeted proteomics assay showed 100% specificity for
Acinetobacter baumannii
,
Escherichia coli
,
Haemophilus influenzae
,
Pseudomonas aeruginosa
,
Staphylococcus aureus
, and
Streptococcus pneumoniae
. No false bacterial identification was reported and no interference was detected arising from the commensal flora. The overall species identification sensitivity was 19/25 (76%) and was higher at the patient level (84.6%). This successful proof of concept provides a rational to broaden the panel of bacteria for further clinical evaluation. |
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ISSN: | 0934-9723 1435-4373 1435-4373 |
DOI: | 10.1007/s10096-020-04132-y |