"Salvage Microbiology": Detection of Bacteria Directly from Clinical Specimens following Initiation of Antimicrobial Treatment

被引:24
作者
Farrell, John J. [1 ]
Sampath, Rangarajan [2 ]
Ecker, David J. [2 ]
Bonomo, Robert A. [3 ,4 ,5 ,6 ]
机构
[1] Univ Illinois, Sch Med, Dept Med, Peoria, IL USA
[2] Ibis Biosci, Carlsbad, CA USA
[3] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Dept Mol Microbiol, Cleveland, OH 44106 USA
[6] Louis Stokes Cleveland Dept Vet Affairs Med Ctr, Cleveland, OH USA
基金
美国国家卫生研究院;
关键词
IONIZATION MASS-SPECTROMETRY; RAPID IDENTIFICATION; PCR; MENINGITIS; PATHOGENS; DIAGNOSIS;
D O I
10.1371/journal.pone.0066349
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: PCR coupled with electrospray ionization mass spectrometry (ESI-MS) is a diagnostic approach that has demonstrated the capacity to detect pathogenic organisms from culture negative clinical samples after antibiotic treatment has been initiated. [1] We describe the application of PCR/ESI-MS for detection of bacteria in original patient specimens that were obtained after administration of antibiotic treatment in an open investigation analysis. Methods: We prospectively identified cases of suspected bacterial infection in which cultures were not obtained until after the initiation of antimicrobial treatment. PCR/ESI-MS was performed on 76 clinical specimens that were submitted for conventional microbiology testing from 47 patients receiving antimicrobial treatment. Findings: In our series, 72% (55/76) of cultures obtained following initiation of antimicrobial treatment were non-diagnostic (45 negative cultures; and 10 respiratory specimens with normal flora (5), yeast (4), or coagulase-negative staphylococcus (1)). PCR/ESR-MS detected organisms in 83% (39/47) of cases and 76% (58/76) of the specimens. Bacterial pathogens were detected by PCR/ESI-MS in 60% (27/45) of the specimens in which cultures were negative. Notably, in two cases of relapse of prosthetic knee infections in patients on chronic suppressive antibiotics, the previous organism was not recovered in tissue cultures taken during extraction of the infected knee prostheses, but was detected by PCR/ESI-MS. Conclusion: Molecular methods that rely on nucleic acid amplification may offer a unique advantage in the detection of pathogens collected after initiation of antimicrobial treatment and may provide an opportunity to target antimicrobial therapy and "salvage" both individual treatment regimens as well as, in select cases, institutional antimicrobial stewardship efforts.
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