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.  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.
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.
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.
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.
Citation: Farrell JJ, Sampath R, Ecker DJ, Bonomo RA (2013) “Salvage Microbiology”: Detection of Bacteria Directly from Clinical Specimens following Initiation of Antimicrobial Treatment. PLoS ONE 8(6): e66349. doi:10.1371/journal.pone.0066349
Editor: Richard C. Willson, University of Houston, United States of America
Received: February 18, 2013; Accepted: May 8, 2013; Published: June 25, 2013
Copyright: © 2013 Farrell et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported in part by the Veterans Affairs Merit Review Program, the National Institutes of Health (Grant AI072219-05 and AI063517-07), and the Geriatric Research Education and Clinical Center VISN 10. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have the following interests: Dr. Farrell none. Dr. Bonomo none. Dr. Sampath is a salaried employee of Ibis Biosciences, an Abbott Company. PCR/ESI-MS testing was erformed at Ibis Biosciences. There are no patents, products in development, or marketed products to declare. This does not alter the authors‚ adherence to all the PLOS ONE policies on sharing data and materials as detailed online in the guide for authors.
Infections are a major cause of morbidity and mortality in hospitalized patients. Because identification of bacterial pathogens requires time for the organisms to grow, when infection is suspected empiric antimicrobial treatment is administered based upon an assessment of likely organisms –. Bacterial meningitis is a primary example of the importance of appropriate empiric therapy before culture results are known. Here, a delay in the initiation of antimicrobial therapy correlates with increased mortality in this disease –, and antibiotics are routinely administered before cerebrospinal fluid (CSF) is obtained (the site likely to yield the pathogen). Other clinical scenarios such as febrile neutropenia, transplant associated infections, and severe sepsis also mandate that antibiotics are administered in a timely fashion and should not be delayed.
The sensitivity and timeliness of culture results are influenced by many factors, but in hospitalized patients previously administered and/or concurrent antimicrobial treatment is a commonly encountered confounding factor. When pathogens are not recovered in culture, the entire treatment course is likely to be “broad spectrum” including therapy for staphylococci, streptococci, as well as Gram negative and anaerobic bacteria. As a result, antibiotics are often used unnecessarily. Regrettably, a delay or failure in identification of pathogens impacts patient outcomes, exposes patients to the deleterious effects of extended courses of overly broad empirical antibiotics, and exacerbates the widespread problems of multidrug resistant organisms and Clostridium difficile associated disease.
The analysis of multilocus polymerase chain reaction (PCR) amplicons by electrospray ionization mass spectrometry (ESI/MS) on a platform in which PCR is coupled to ESI-MS is a technique that has demonstrated the capacity to detect microbes from both environmental samples and clinical patient specimens –. Detection does not require correct anticipation of the organisms in advance; the technology is designed to detect unknown and unculturable organisms, and is particularly useful when multiple microbes may be present.
We performed a prospective comparison of results from conventional microbiologic testing vs. PCR/ESI-MS in cases of suspected new onset, or recurrence of infection in patients where samples were obtained after at least one dose of antibiotic treatment. Our purpose is to demonstrate that PCR/ESI-MS may have value in the clinical microbiology laboratory when cultures do not yield a pathogen. Offering clinicians relevant, timely and specific information can have significant impact on the choice of therapy, clinical decision making, and antimicrobial stewardship.
Approval was obtained from both the University of Illinois College of Medicine and St. Francis Medical Center Institutional Review Boards (IRBs) for PCR/ESI-MS testing of specimens that were submitted to the microbiology laboratory from inpatients at St. Francis Medical Center, Peoria, IL. To test if PCR/ESI-MS serves a potential role in the detection of microorganisms in specimens collected from patients following administration of antimicrobial treatment, we prospectively identified patients with suspected infection between February 10, 2011 and November 10, 2012. Patients whose specimens were collected after at least one dose of antibiotic were included in the study. Gram stains, conventional aerobic and anaerobic culture and PCR/ESI-MS were performed on all specimens. The PCR/ESI-MS test results were not available to the patients' treatment teams and did not influence treatment decisions.
In each case, specimens were collected as part of the routine care of the patient and submitted to clinical microbiology lab at St. Francis Medical Center (Peoria, IL) for testing. After the specimen was processed by laboratory personal and all the requested tests and cultures ordered by the treating physician had been prepared, the remaining specimen was placed in storage at 4°C for subsequent PCR/ESI-MS testing. Because specimens included in this study were collected in the course of the patients medical care for diagnostic purposes, and no specimens were collected explicitly for the purposes of this study, both IRBs waived the requirement for patient informed consent.
PCR/ESI-MS was performed on all specimens. Specimens were kept in refrigeration, not frozen, and shipped overnight in a cold pack to Ibis Biosciences (Carlsbad, CA). We followed the PCR/ESI-MS protocol previously described . This PCR/ESI-MS assay is designed for detection of bacterial and Candida species, and is not capable of identifying invasive molds, dimorphic fungi, or viral pathogens. Consequently, immunocompromised patients, patients on chemotherapy for treatment of malignancy, or patients with HIV infection were excluded from the study. Compared to clinical samples, the assay performs with 98.7% and 96.6% concordance at the genus and species levels, respectively .
For reporting results, the level of detection (LOD) was calculated as genome equivalents per PCR reaction well. Results were reported for all detections with a Q score ≥0.90 in which the LOD was above threshold, and the internal isolation control was detected. Kappa (κ) was calculated using SAS software, version 9.1 (SAS Institute) to assess the agreement between culture and PCR/ESI-MS.
Conventional microbiology testing was performed on 76 specimens collected from 47 patients. Specimens included swabs, BACTEC blood culture bottles, fluid, and tissue samples that were submitted for culture from patients after initiation of antimicrobial treatment (Table 1). The results obtained from aerobic and anaerobic cultures were compared to results of PCR/ESI-MS testing (Table 2). PCR/ESI-MS detected probable pathogens in 20 cases in which standard microbial cultures were non-diagnostic. Results were in agreement for 38 specimens (49%); but 37% of the agreement (14 specimens) was attributed to specimens that were culture negative with no detection by PCR/ESI-MS. For patients with multiple specimens, only the culture positive specimen, when applicable, was considered for calculation of the Kappa statistic. Compared to agreement between culture and Gram stain, (κ = 0.643), agreement between culture and PCR/ESI-MS was poor (κ = 0.299).
Conventional culture methods were non-diagnostic in 33 of 47 cases: in 17 cases cultures were completely negative. Nine of the patients from whom respiratory specimens were collected grew either normal respiratory flora (5), or Candida spp. (3), or coagulase negative staphylococci (1). There was only one specimen, an endotracheal tube aspirate, from which an organism was cultured (C. albicans), but PCR/ESI-MS testing was negative. PCR/ESI-MS results were negative for detection in six of the 17 culture negative cases.
Bacterial pathogens were detected by PCR/ESI-MS in 60% (33/55) of the specimens in which cultures were either negative or nondiagnostic: Streptococcus spp. (17), Staphylococcus aureus (5), Staphylococcus epidermidis (4), Staphylococcus lugdunensis (1), anaerobes (4), Salmonella enterica (2), and blaKPC-3+ Klebsiella pneumoniae (1). In each case, the organism(s) detected by PCR/ESI-MS were consistent with the clinical scenario that was observed in the patient by one of our investigators (JJF). A selection of these cases requires special comment.
Recurrent infections: (Patients 15 and 16)
Patients 15 and 16 both were on antimicrobial treatment for presumed relapses of previous S. aureus prosthetic knee infections. Although this suspicion was not confirmed by culture, in both cases the previously identified organism (MSSA and MRSA, respectively) was detected by PCR/ESI-MS.
Coagulase-negative staphylococci: (Patients 3 and 10)
Coagulase negative staphylococcal infections were suspected in patients 3 and 10. Patient 3 had a history of coronary artery bypass surgery and aortic valve (AV) replacement in 1983. He was well until 2011 when he presented to an outside hospital with fever. He was diagnosed with prosthetic valve infective endocarditis based on the presence of prosthetic aortic valve vegetations and growth of methicillin susceptible Staphylococcus epidermidis (MSSE) in two of two sets of blood cultures. He was treated with IV vancomycin and oral rifampin for 30 days, and then transferred to our institution prior for AV replacement surgery. During surgery, Gram positive cocci (GPC) were detected on Gram stain of the valve tissue, but cultures proved to be negative. Staphylococcus epidermidis was detected by PCR/ESI-MS in both valve and annular myocardial tissue specimens. Given the presence of prosthetic AV vegetations, CNS in blood cultures obtained before surgery, and GPC in the valve tissue, the detection of MSSE by PCR/ESI-MS is noteworthy and bears significance.
In contrast, the growth of methicillin resistant CNS in the synovial fluid cultures from right knee fluid in patient 10, obtained 10 days prior to initiation of antibiotics, and subsequent negative aerobic intra-operative cultures and growth of only one colony of CNS in one of three anaerobic cultures obtained from during extraction of the infected prosthesis was of uncertain significance. Consideration of PCR/ESI-MS results eliminates any doubt, as MRSE was identified in all three specimens.
Mixed aerobic and anaerobic infections: (Patients 18, 20, 27, 33, 39, 40 and 41)
PCR/ESI-MS detected anaerobic organisms that were missed by culture in eight cases. Porphyromonas gingivalis was not appreciated in the culture of neck abscess fluid from patient 20, which was culture negative. And Bifidobacterium dentium was detected in BAL fluid from patient 33 that was only notable for Candida albicans in culture. Rothia mucilaginosa as well as C. albicans were identified in the respiratory specimens from patient 40, whose cultures were non-diagnostic (i.e., normal flora). Culture and PCR/ESI-MS also disagreed on patient 27: VRE was cultured from the original wound culture, but PCR/ESI-MS detected Fusobacterium varium.
PCR/ESI-MS performed particularly well with polymicrobic infections that included both aerobic and anaerobic pathogens. S. intermedius and MSSA grew in both aerobic and anaerobic cultures, from patients 18 and 41, respectively, but no strictly anaerobic organisms were cultured. Fusobacterium necrophorum and Streptococcus spp. were detected in purulent liver abscess drainage from patient 18, and MSSA and F. necrophorum were identified in the infected metatarsal bone from patient 41. Patient 38 had MSSA and C. albicans detected by culture and PCR/ESI-MS in the pleural fluid sample, but Bilophila wadsworthia was only detected by PCR/ESI-MS, and not in the anaerobic culture. Likewise, Streptoccocus oralis was found in ankle abscess tissue by both aerobic culture and PCR/ESI-MS from patient 39, but only PCR/ESI-MS detected Finegoldia magna.
Streptococcal infections: (Patients 1, 2, 4, 5, 7, 8, 13, 14, 18, 30, 37, 39 and 46)
Of the 13 patients (17 samples) from whom Streptococcus spp. were detected by PCR/ESI-MS, the only specimens from which Streptococcus was recovered by culture were from patients with brief or no antibiotic treatment prior to specimen collection. Two specimens that grew Streptococcus mitis/oralis: 1) purulent brain abscess drainage from Patient 4 obtained after two days of antibiotic treatment, and 2) the ankle abscess tissue from patient 39– three days after antibiotics were discontinued. S. intermedius was cultured from purulent liver abscess fluid from patient 18 after one day of antibiotic treatment. In patients who had received more than two days of antibiotic treatment, streptococci were no longer cultured. And, in the case of patient 14, one day of treatment was sufficient to suppress growth of streptococci: Left knee synovial fluid cultures from patient 14 grew α-hemolytic streptococci prior to initiation of antibiotics, but after one day of antibiotics, when the knee was drained in the OR, all cultures were negative. PCR/ESI-MS detected viridans streptococci/S. pneumoniae/mitis group in three of three surgical specimens from patient 14.
PCR/ESI-MS appeared to offer a particular advantage in detection of pneumococci from both cerebrospinal fluid (CSF), and bronchoalveolar lavage (BAL) fluid. Lumbar puncture (LP) was delayed in two cases of pneumococcal bacteremia and sepsis with presumed meningitis (Patients 7 and 13). In both cases, CSF cultures were negative, but S. pneumoniae were detected by PCR/ESI-MS (thereby “salvaging” clinical decision making). Dexamethasone was not administered in either case. Interestingly, PCR/ESI-MS did not remain positive in the CSF indefinitely. CSF from a follow-up LP two weeks later on patient 13 was negative by both culture and PCR/ESI-MS (see table 2). In two cases of apparent pneumococcal pneumonia (Patients 5 and 8) and a third case of viridans streptococcus pneumonia (patient 46), culture was either unable to detect S. pneumoniae, or unable to distinguish pathogenic streptococci from normal respiratory flora.
Prosthetic arterial graft infections: (Patients 33 and 43)
Infection of prosthetic intravascular graft material is a difficult problem, as vascular grafts are not readily exchanged. Endovascular graft infection was suspected in Patients 33 and 43. Both patients were bacteremic, and both were on antimicrobial treatment prior to surgical extraction of the vascular grafts. Cultures of graft material and surrounding tissue were negative, but in both cases, the organism that had grown in the initial blood cultures was detected by PCR/ESI-MS from the extracted the graft material.
Carbapenem resistantEnterobacteriaceae (CRE): (Patients 27 and 31)
CRE infections were detected in one patient by culture and two patients by PCR/ESI-MS. In patient 27, K. pneumoniae that tested positive for KPC-3 by PCR for the blaKPC gene was recovered from an infected surgical wound. PCR/ESI-MS detected both the pathogen (K. pneumoniae), and the resistance gene (blaKPC-3). Patient 31 was known to be colonized with blaKPC-3+ Klebsiella pneumoniae, and although cultures of synovial fluid from her right knee were negative, PCR/ESI-MS detected K. pneumoniae (also positive for blaKPC-3).
Extended antibiotic treatment and serial specimens: (Patients 13 and 32)
Just as with culture, duration of antibiotic treatment does influence ability of PCR/ESI-MS to detect evidence of a pathogen. In the case of serial CSF samples from patient 13, a patient with S. pneumoniae bacteremia and sepsis, S. pneumoniae was only detected by PCR/ESI-MS in the first CSF sample. In the case of patient 32, both culture and PCR/ESI-MS of neck abscess tissue were negative after more than 34 days of empiric antibiotic treatment.
Acinetobacter junii: (Patients 6, 16, 41, 43)
In these four cases Acinetobacter junii was detected by PCR/ESI-MS in tissue and synovial fluid specimens collected during surgical resection and drainage of infected tissue. Acinetobacter junii is unlikely to represent a pathogen in these cases. This organism appears to have been detected as an artifact of the tissue extraction process.
PCR/ESI-MS is an emerging diagnostic technology that is capable of rapid detection of microorganisms directly from clinical specimens. As this PCR-based approach requires only the presence of small amounts of DNA for amplification, bacteria that have been “killed” by bactericidal antibiotics (e.g., β-lactams, aminoglycosides or quinolones) or are in stationary phase from the effect of bacteriostatic drugs (e.g., linezolid, macrolides) can be detected if sufficient DNA for amplification is present in the sample. Up to this time, data testing this assertion in the clinical arena have not yet been provided.
In our series, 72% (55/76) of cultures obtained following initiation of antimicrobial treatment were nondiagnostic. In contrast, PCR/ESR-MS detected organisms in 83% (39/47) of cases and 76% (58/76) of the specimens. Calculation of the Kappa coefficient confirmed poor agreement between conventional cultures and PCR/ESI-MS. The poor agreement is primarily attributable to detection of bacteria by PCR/ESI-MS in culture negative specimens. PCR/ESI-MS detected ≥ one bacterial pathogen(s) in 60% (27/45) of the culture negative specimens. In 67% of negative culture cases (18/27), an organism that was consistent with the clinical scenario was detected by PCR/ESI-MS.
Reliance on clinical judgment to distinguish colonizers and contaminants from true pathogens is required with any microbiology test result. As with culture-based identification of organisms from clinical samples, the correct interpretation of PCR/ESI-MS results requires an appreciation for the clinical context associated with the specimen tested. In several cases the organisms detected by PCR/ESI-MS were consistent with contaminants that would have been unlikely to alter patient management. For example, detection of Candida spp. in respiratory secretions by either culture or molecular methods does not merit treatment in our relatively immunocompetent patient population. But, as evidenced in the case of Patient 6, the role of other potential pathogens still needs to be defined. In this case, low level detection (17 genome copies/well) of Propionibacterium acnes, a pathogen with well described association with prosthetic shoulder joint infections, in culture negative right shoulder synovial fluid would pose a challenge for the clinician responsible for interpreting this additional data.
Selecting appropriate antimicrobial therapy for patients with evidence of infection, but negative cultures is a common dilemma in practice. The implications of our findings are profound: that antimicrobial treatment in “culture negative” cases can be directed against both pathogens and genetic markers of resistance (i.e., mecA in MRSA, mutations in qrdr, blaKPC, etc.) that are readily identified by PCR/ESI-MS. Particularly compelling supporting evidence for pathogen detection derives from our two cases of breakthrough recurrent prosthetic knee infections that occurred while the patients were taking chronic suppressive antibiotics (patients 15 and 16): the previous organism was not recovered in tissue cultures taken during extraction of the infected knee prostheses in either case, but was detected by PCR/ESI-MS. As well as our case of culture and Gram stain positive streptococcal septic arthritis (Patient 14), in which a single preoperative dose of cefazolin was sufficient to cause surgical cultures to be negative. The disappearance of PCR evidence of S. pneumoniae in a second CSF specimen from patient 13, who was recovering from pneumococcal bacteremia and sepsis, suggests that organism detection may be eradicated with effective antimicrobial treatment. This finding may help with decisions to tailor and/or stop therapy. These early findings could have impact on the current status of “duration of therapy” and antibiotic stewardship.
Limitations of this study include: i) the small sample size and lack of a control group; ii) relevance of “mixed cultures”; and iii) co-identification of streptococci (viridians streptococci, Streptococcus mitis and pneumococcus). This study was performed as an open investigation, and not a validation; and is not appropriate for, nor was it designed to calibrate sensitivity or specificity. Our PCR primers successfully captured organisms not detected by culture, but we maintain that microbiological culture results are still the “gold standard” for comparison. Based upon studies such as this, that “standard” cannot be applied as the evidence it offers is not present, but combining broad range PCR with mass spectrometry or 16S ribosomal gene sequencing has appeal for selected situations in the clinical microbiology lab. In addition, the role of fungal, viral or parasitic infections was also not evaluated in this small series. Truly, larger studies are needed.
The everyday practice of treating patients with empiric antibiotic regimes provides an enormous opportunity for novel approaches to target antimicrobial therapy and “salvage” both individual treatment regimens as well as institutional antimicrobial stewardship efforts. These results suggest that PCR/ESI-MS may have a role in detection of clinically relevant pathogens from specimens obtained following initiation of antimicrobial treatment when cultures are negative. Larger studies are planned to determine if PCR/ESI-MS can assist in the clinical evaluation and treatment of patients on empiric antimicrobial treatment for suspected infection with negative cultures.
The Kappa calculation of agreement was performed on SAS software with the assistance of Huagping Wang, Ph.D. Department of Medicine. University of Illinois College of Medicine.
PCR/ESI-MS testing was performed by Kristin S. Lowery, Ph.D at Ibis Biosciences, a Division of Abbott Molecular, Inc., in Carlsbad, CA, USA.
Conceived and designed the experiments: JJF DJE. Performed the experiments: RS. Analyzed the data: JJF RAB DJE. Contributed reagents/materials/analysis tools: RS DJE. Wrote the paper: JJF RAB.
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