Genomic Surveillance Reveals Diversity of Multidrug-Resistant Organism Colonization and Infection: A Prospective Cohort Study in Liver Transplant Recipients. (28th April 2018)

• Record Type: Journal Article
• Authors: Macesic, Nenad; Gomez-Simmonds, Angela; Sullivan, Sean B; Giddins, Marla J; Ferguson, Samantha A; Korakavi, Gautam; Leeds, David; Park, Sarah; Shim, Kevin; Sowash, Madeleine G; Hofbauer, Melanie; Finkel, Ryan; Hu, Yue; West, Jared; Toussaint, Nora C; Greendyke, William G; Miko, Benjamin A; Pereira, Marcus R; Whittier, Susan; Verna, Elizabeth C; Uhlemann, Anne-Catrin
• Is Part Of: Clinical infectious diseases. Volume 67:Number 6(2018)
• Page Start: 905
• Page End: 912
• Publication Date: 2018-04-28
• Subjects: multidrug-resistant organism colonization -- multidrug-resistant organism infection -- carbapenem-resistant Enterobacteriaceae -- whole-genome sequencing -- liver transplantation; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciy199
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract : In a prospective genomic surveillance study of liver transplant patients, we found that temporal dynamics differed between multidrug-resistant organisms with respect to onset of intestinal colonization, clearance, and infections. Whole-genome sequencing revealed an unexpected diversity of carbapenem-resistant Enterobacteriaceae. Abstract: Background: Multidrug-resistant organisms (MDROs) are an important cause of morbidity and mortality after solid organ transplantation. We aimed to characterize MDRO colonization dynamics and infection in liver transplant (LT) recipients through innovative use of active surveillance and whole-genome sequencing (WGS). Methods: We prospectively enrolled consecutive adult patients undergoing LT from March 2014 to March 2016. Fecal samples were collected at multiple timepoints from time of enrollment to 12 months posttransplant. Samples were screened for carbapenem-resistant Enterobacteriaceae (CRE), Enterobacteriaceae resistant to third-generation cephalosporins (Ceph-RE), and vancomycin-resistant enterococci. We performed WGS of CRE and selected Ceph-RE isolates. We also collected clinical data including demographics, transplant characteristics, and infection data. Results: We collected 998 stool samples and 119 rectal swabs from 128 patients. MDRO colonization was detected in 86 (67%) patients at least once and was significantly associated with subsequent MDRO infection (0 vs 19.8%, P = .002). Child-Turcotte-Pugh score at LT and duration of post-LT hospitalization were independent predictors of both MDRO colonization and infection. Temporal dynamics differed between MDROs with respect to onset of colonization, clearance, and infections. We detected an unexpected diversity of CRE colonizing isolates and previously unrecognized transmission that spanned Ceph-RE and CRE phenotypes, as well as a cluster of mcr-1– producing isolates. Conclusions: Active surveillance and WGS showed that MDRO colonization is a highly dynamic and complex process after LT. Understanding that complexity is crucial for informing decisions regarding MDRO infection control, use of therapeutic decolonization, and empiric treatment regimens.