Rapid Identification of Protein Biomarkers of Escherichia coli O157:H7 by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight-Time-of-Flight Mass Spectrometry and Top-Down Proteomics

被引:108
作者
Fagerquist, Clifton K. [1 ]
Garbus, Brandon R. [1 ]
Miller, William G. [1 ]
Williams, Katherine E. [2 ]
Yee, Emma [1 ]
Bates, Anna H. [1 ]
Boyle, Siobhan [1 ]
Harden, Leslie A. [1 ]
Cooley, Michael B. [1 ]
Mandrell, Robert E. [1 ]
机构
[1] USDA ARS, Western Reg Res Ctr, Albany, CA 94710 USA
[2] Univ Calif San Francisco, Sch Med, Dept Gynecol & Reprod Sci, San Francisco, CA 94143 USA
关键词
MICROORGANISM IDENTIFICATION; CAMPYLOBACTER-UPSALIENSIS; INTACT MICROORGANISMS; C-HELVETICUS; COLI O157H7; DESORPTION/IONIZATION; BACTERIA; SEQUENCE; SPECIATION; STRAINS;
D O I
10.1021/ac902455d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Six protein biomarkers from two strains of Escherichia coli O157:H7 and one non-O157:H7, nonpathogenic strain of E. coli have been identified by matrix-assisted laser desorption ionization time-of-flight time-of-flight tandem mass spectrometry (MALDI-TOF TOF-MS/MS) and top-down proteomics. Proteins were extracted from bacterial cell lysates, ionized by MALDI, and analyzed by MS/MS. Protein biomarker ions were identified from their sequence-specific fragment ions by comparison to a database of in silico fragment ions derived from bacterial protein sequences. Web-based software, developed in-house, was used to rapidly compare the mass-to-charge (m/z) of MS/MS fragment ions to the m/z of in silico fragment ions derived from hundreds of bacterial protein sequences. A peak matching algorithm and a p-value algorithm were used to independently score and rank identifications on the basis of the number of MS/MS-in silico matches. The six proteins identified were the acid stress chaperone-like proteins, HdeA and HdeB; the cold shock protein, CspC; the YbgS (or homeobox protein); the putative stress-response protein YjbJ (or CsbD family protein); and a protein of unknown function, YahO. HdeA, HdeB, YbgS, and YahO proteins were found to be modified post-translationally with removal of an N-terminal signal peptide. Gene sequencing of hdeA, hdeB, cspC, ybgS, yahO, and yjbJ for 11 strains of E. coli O157:H7 and 7 strains of the "near-neighbor" serotype O55:H7 revealed a high degree sequence homology between these two serotypes. Although it was not possible to distinguish O157:H7 from O55:H7 from these six biomarkers, it was possible to distinguish E. coli O157:H7 from a nonpathogenic E. coli by top-down proteomics of the YahO and YbgS. In the case of the YahO protein, a single amino acid residue substitution in its sequence (resulting in a molecular weight difference of only 1 Da) was sufficient to distinguish E. coli O157:H7 from a non-O157:H7, non-pathogenic E. coli by MALDI-TOF TOF-MS/MS, whereas this would be difficult to distinguish by MALDI-TOF-MS. Finally, a protein biomarker ion at m/z similar to 9060 observed in the MS spectra of non-O157:H7 E. coli strains but absent from MS spectra of E. coli O157:H7 strains was identified by top-down analysis to be the HdeB acid stress chaperone-like protein consistent with previous identifications by gene sequencing and bottom-up proteomics.
引用
收藏
页码:2717 / 2725
页数:9
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