A rapid procedure for bacterial identification and antimicrobial susceptibility testing directly from positive blood cultures

There is an urgent need to develop a rapid procedure that can rapidly identify and obtain antimicrobial susceptibility testing (AST) results directly from positive blood cultures. Here, we report a semi-automatic bacterial diagnosis procedure, which includes (1) a bacterial concentration process to...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analyst (London) 2021-12, Vol.147 (1), p.147-154
Hauptverfasser: Sun, Bo, Kang, Xixiong, Yue, Shuhua, Lan, Lu, Li, Rui, Chen, Chen, Zhang, Weifeng, He, Shipei, Zhang, Chenxi, Fan, Yubo, Wang, Pu, Zheng, Guanghui, Hong, Weili
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:There is an urgent need to develop a rapid procedure that can rapidly identify and obtain antimicrobial susceptibility testing (AST) results directly from positive blood cultures. Here, we report a semi-automatic bacterial diagnosis procedure, which includes (1) a bacterial concentration process to isolate bacteria from a positive blood culture bottle (PBCB), (2) an identification process using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS), and (3) a rapid AST process based on stimulated Raman scattering imaging of deuterium oxide (D 2 O) incorporation in bacteria. A total of 105 samples were tested for bacterial identification, and a bacterial identification accuracy of 92.3% was achieved. AST takes about 2.5 h after identification. This semi-automatic procedure only takes 3.5 h, which is demonstrated to be the fastest process to obtain identification and AST results starting from PBCBs. This semi-automatic procedure only takes 3.5 h to obtain bacterial identification and antimicrobial susceptibility testing results starting from positive blood cultures.
ISSN:0003-2654
1364-5528
DOI:10.1039/d1an01210j