4.7 Article

Genomic Epidemiology of MRSA During Incarceration at a Large Inner-City Jail

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 11, 页码 E3708-E3717

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1937

关键词

MRSA; Whole genome sequencing; jail

资金

  1. National Institute of Allergy and Infectious Diseases [R01AI114688]
  2. Molecular Mechanisms of Microbial Pathogenesis training grant (NIH) [T32 AI007528]

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This study examined MRSA transmission in jails and found a high burden of MRSA upon intake. Genomic analysis indicated potential spread of incoming strains and networks of spread during incarceration, with transmission often occurring among detainees housed in similar locations. Sharing personal items during incarceration was associated with MRSA acquisition and could be a target for intervention.
Background. Congregate settings, such as jails, may be a location where colonized detainees transmit methicillin-resistant Staphylococcus aureus (MRSA). We examined MRSA acquisition during incarceration and characterized the genomic epidemiology of MRSA entering the jail and isolated during incarceration. Methods. Males incarcerated at the Cook County Jail were enrolled within 72 h of intake and MRSA surveillance cultures collected. Detainees in jail at Day 30 were re-cultured to determine MRSA acquisition. A survey was administered to identify acquisition predictors. Genomic sequencing of surveillance and clinical isolates was integrated with epidemiologic and jail location data to track MRSA transmission pathways. Results. 800 males were enrolled; 19% MRSA colonized at intake. Of 184 who reached Day 30 visit, 12 acquired MRSA. Heroin use before entering (OR 3.67, P = .05) and sharing personal items during incarceration (OR = 4.92, P = .01) were predictors of acquisition. Sequenced clinical USA300 isolates (n = 112) were more genetically similar than diverse intake USA300 strains (P < .001), suggesting jail transmission. Four acquired colonization isolates were within 20 single-nucleotide variant (SNVs) of other isolates; 4 were within 20 SNVs of an intake isolate, 2 for an acquisition isolate, and 1 for a clinical isolate. Individuals with genetically similar isolates were more likely to have had overlapping stays in the same buildings. Conclusion. There was a high MRSA burden entering jail. Genomic analysis of acquisition and clinical isolates suggests potential spread of incoming strains and networks of spread during incarceration, with spread often occurring among detainees housed in similar locations. Sharing personal items during incarceration is associated with MRSA acquisition and could be a focus for intervention.

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