Peptide Biomarker Discovery for Identification of Methicillin-Resistant and Vancomycin-Intermediate Staphylococcus aureus Strains by MALDI-TOF

被引:58
|
作者
Lu, Jang-Jih [4 ,5 ]
Tsai, Fuu-Jen [2 ,6 ]
Ho, Cheng-Mao [3 ,5 ]
Liu, Yu-Ching [1 ]
Chen, Chao-Jung [1 ,7 ]
机构
[1] China Med Univ Hosp, Prote Core Lab, Dept Med Res, Taichung 40402, Taiwan
[2] China Med Univ Hosp, Dept Med Genet Pediat & Med Res, Taichung 40402, Taiwan
[3] China Med Univ Hosp, Dept Lab Med, Taichung 40402, Taiwan
[4] Chang Gung Mem Hosp, Dept Lab Med, Tao Yuan 33305, Taiwan
[5] China Med Univ, Grad Inst Clin Med Sci, Taichung 40402, Taiwan
[6] China Med Univ, Coll Chinese Med, Taichung 40402, Taiwan
[7] China Med Univ, Grad Inst Integrated Med, Taichung 40402, Taiwan
关键词
FLIGHT MASS-SPECTROMETRY; ASSISTED-LASER-DESORPTION/IONIZATION; RAPID IDENTIFICATION; SUSCEPTIBILITY; PROTEOMICS; BACTERIA; TIME; MICROORGANISMS; INFECTIONS; MRSA;
D O I
10.1021/ac300855z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Rapid identification of community-associated (CA) methicillin-resistant Staphylococcus aureus (MASA), hospital-associated (HA) MRSA, and vancomycin-intermediate S. aureus (VISA) is essential for proper therapy and timely intervention of outbreaks. In this study, peptide biomarkers for rapid identification of methicillin-resistant and vancomycin-intermediate S. aureus strains were discovered by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The results showed that the 1774.1 and 1792.1 m/z peaks corresponding to the phenol-soluble modulin alpha 1 and phenol-soluble modulin alpha 2 peptides, respectively, were present in the majority (95%, 121 of 127) of SCCmec types IV and V isolates, but only in 8% (15 of 185) of SCCmec types I-III isolates. Since SCCmec types isolates are recognized as HA-MRSA and most CA-MRSA isolates belong to SCCmec types IV and V, these two peptides may serve as markers for discrimination between HA-MRSA and CA-MRSA isolates. The 1835.0 and 1863.0 m/z peaks were present in 50% (4 of 8) of heterogeneous VISA and 88% (14 of 16) of VISA isolates. The peptides of these two peaks were identified as proteolytic products of the acyl carrier protein. The results of this study provide the possibility to develop methods for identification of CA-MRSA, HA-MRSA, and vancomycin-resistant S. aureus isolates based on the presence of these peptides.
引用
收藏
页码:5685 / 5692
页数:8
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