Traditional microbiological work up is slow and sometimes inaccurate, relying on phenotypic culture identification followed by antimicrobial susceptibility testing. Newer technologies, such as matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) and real-time molecular detection (antimicrobial resistance genes microarrays) have advanced the diagnostic capabilities of clinical microbiology laboratories and have created an exciting field for research and development. Given the in-depth and highly accurate (sometimes complex) results that are produced by such platforms, careful detailed analyses are required to better understand the clinical significance of the organisms identified and the resistance mechanisms detected. During this fiscal year, we performed a large retrospective analysis on the clinical performance of HardyCHROM CRE media for the detection of carbapenemase-producing organisms from surveillance cultures. Data showed a positive predictive value ranging 8-56% depending on the definition carbapenem resistant organisms applied which varies between states and national guidelines. This has a tremendous effect on applied infection control practices and antimicrobial choices in response to a potential clinical infection. We also performed a comparative evaluation of three phenotypic assays for the detection of carbapenemases, as well as a retrospective analysis on the performance and accuracy of MALDI-TOF MS and susceptibility testing directly from positive blood cultures. The latter has provided informative results for clinical microbiology reporting while awaiting standardized testing results. Quality improvement projects have included a prospective comparative evaluation of blood culture volume monitoring methods (weight vs virtual system), comparative analysis of a multiplex gastrointestinal pathogen panel with traditional methods, and a large comparative assessment of product sterility testing systems for novel therapies (traditional USP<71> manual method vs automated Bactec FX system and BacTAlert Dual-T system).

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIACL060092-04
Application #
9552569
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
Zip Code
Luethy, Paul M; Murphy, Sean C; Seilie, Annette M et al. (2018) Diagnostic challenges of prolonged post-treatment clearance of Plasmodium nucleic acids in a pre-transplant autosplenectomized patient with sickle cell disease. Malar J 17:23
Weingarten, Rebecca A; Johnson, Ryan C; Conlan, Sean et al. (2018) Genomic Analysis of Hospital Plumbing Reveals Diverse Reservoir of Bacterial Plasmids Conferring Carbapenem Resistance. MBio 9:
Decker, B K; Lau, A F; Dekker, J P et al. (2018) Healthcare personnel intestinal colonization with multidrug-resistant organisms. Clin Microbiol Infect 24:82.e1-82.e4
Chen, Mark; Conlan, Sean; Lau, Anna F et al. (2017) Whole-Genome Sequencing Overrules a Suspected Case of Carbapenem-Resistant Enterobacter cloacae Transmission. J Clin Microbiol 55:2868-2870
Hughes, Heather Y; Conlan, Sean P; Lau, Anna F et al. (2016) Detection and Whole-Genome Sequencing of Carbapenemase-Producing Aeromonas hydrophila Isolates from Routine Perirectal Surveillance Culture. J Clin Microbiol 54:1167-70
Sleiman, Sue; Halliday, Catriona L; Chapman, Belinda et al. (2016) Performance of Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry for Identification of Aspergillus, Scedosporium, and Fusarium spp. in the Australian Clinical Setting. J Clin Microbiol 54:2182-6
Dekker, John P; Lau, Anna F (2016) An Update on the Streptococcus bovis Group: Classification, Identification, and Disease Associations. J Clin Microbiol 54:1694-9
Conlan, Sean; Lau, Anna F; NISC Comparative Sequencing Program et al. (2016) Complete Genome Sequence of a Klebsiella pneumoniae Strain Carrying blaNDM-1 on a Multidrug Resistance Plasmid. Genome Announc 4:
Conlan, Sean; Park, Morgan; Deming, Clayton et al. (2016) Plasmid Dynamics in KPC-Positive Klebsiella pneumoniae during Long-Term Patient Colonization. MBio 7:
Playford, E Geoffrey; Lipman, Jeffrey; Jones, Michael et al. (2016) Problematic dichotomisation of risk for ICU-acquired invasive candidiasis: results using a risk predictive model to categorise three levels of risk from a multicentre prospective cohort of Australian ICU patients. Clin Infect Dis :

Showing the most recent 10 out of 17 publications