sábado, 11 de mayo de 2019

Ahead of Print - Phenotypic and Genomic Analyses of Burkholderia stabilis Clinical Contamination, Switzerland - Volume 25, Number 6—June 2019 - Emerging Infectious Diseases journal - CDC

Ahead of Print - Phenotypic and Genomic Analyses of Burkholderia stabilis Clinical Contamination, Switzerland - Volume 25, Number 6—June 2019 - Emerging Infectious Diseases journal - CDC



Volume 25, Number 6—June 2019
Research

Phenotypic and Genomic Analyses of Burkholderia stabilis Clinical Contamination, Switzerland

Helena M.B. Seth-SmithComments to Author , Carlo Casanova, Rami Sommerstein, Dominik M. Meinel1, Mohamed M.H. Abdelbary2, Dominique S. Blanc, Sara Droz, Urs Führer, Reto Lienhard, Claudia Lang, Olivier Dubuis, Matthias Schlegel, Andreas Widmer, Peter M. Keller, Jonas Marschall, and Adrian EgliComments to Author 
Author affiliations: University Hospital Basel, Basel, Switzerland (H.M.B. Seth-Smith, D.M. Meinel, A. Widmer, A. Egli)University of Basel, Basel (H.M.B. Seth-Smith, D.M. Meinel, A. Egli)University of Bern, Bern, Switzerland (C. Casanova, S. Droz)Bern University Hospital, Bern (R. Sommerstein, J. Marschall)Lausanne University Hospital, Lausanne, Switzerland (M.M.H. Abdelbary, D.S. Blanc)Biel Hospital, Biel, Switzerland (U. Führer)ADMED, La Chaux-de-Fonds, Switzerland (R. Lienhard)Viollier AG, Allschwil, Switzerland (C. Lang, O. Dubuis)Cantonal Hospital St. Gallen, St. Gallen, Switzerland (M. Schlegel)Swissnoso, National Center for Infection Prevention, Bern (M. Schlegel, A. Widmer, J. Marschall)University of Zurich, Zurich, Switzerland (P.M. Keller)

Abstract

A recent hospital outbreak related to premoistened gloves used to wash patients exposed the difficulties of defining Burkholderia species in clinical settings. The outbreak strain displayed key B. stabilis phenotypes, including the inability to grow at 42°C; we used whole-genome sequencing to confirm the pathogen was B. stabilis. The outbreak strain genome comprises 3 chromosomes and a plasmid, sharing an average nucleotide identity of 98.4% with B. stabilis ATCC27515 BAA-67, but with 13% novel coding sequences. The genome lacks identifiable virulence factors and has no apparent increase in encoded antimicrobial drug resistance, few insertion sequences, and few pseudogenes, suggesting this outbreak was an opportunistic infection by an environmental strain not adapted to human pathogenicity. The diversity among outbreak isolates (22 from patients and 16 from washing gloves) is only 6 single-nucleotide polymorphisms, although the genome remains plastic, with large elements stochastically lost from outbreak isolates.
Burkholderia is a diverse genus of gram negative bacteria, with isolates identified from a variety of environments, and ever more species being identified and classified. Whereas some Burkholderia species are associated with bioremediation potential and antimicrobial and antifungal production, others are animal and human pathogens that generally fall within the B. cepacia complex (Bcc) (1). Burkholderiabacteria have large, flexible, multi-replicon genomes, a large metabolic repertoire, various virulence factors, and inherent resistance to many antimicrobial drugs (2,3).
An outbreak of B. stabilis was identified among hospitalized patients across several cantons in Switzerland during 2015–2016 (4). The bacterium caused bloodstream infections, noninvasive infections, and wound contaminations. The source of the infection was traced to contaminated commercially available, premoistened washing gloves used for bedridden patients. After hospitals discontinued use of these gloves, the outbreak resolved.
Many instances of Bcc strain contamination of medical devices and solutions have been described (4), including an outbreak in Korea associated with a 0.5% chlorhexidine solution (5). B. stabilis also has been identified in nosocomial infections (68).
We conducted in-depth characterization of the B. stabilis strain from the Switzerland outbreak by using clinical methods and whole-genome sequencing (WGS). We generated a complete draft genome by combining short- and long-read genomic data and compared it to other outbreak isolates to provide a complete genomic assessment of this strain. We provide a thorough comparative genomic analysis of this outbreak strain.

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