In-Depth Study of a Nosocomial Outbreak Caused by Extensively Drug-Resistant Pseudomonas aeruginosa Using Whole Genome Sequencing Coupled With a Polymerase Chain Reaction Targeting Strain-Specific Single Nucleotide Polymorphisms

• Published in: American journal of epidemiology 2020-08, Vol.189 (8), p.841-849
• Main Authors: Acosta, Fermín, Fernández-Cruz, Ana, Maus, Sandra R, Sola-Campoy, Pedro J, Marín, Mercedes, Cercenado, Emilia, Sierra, Olalla, Muñoz, Patricia, García de Viedma, Darío, Pérez-Lago, Laura
• Format: Article
• Language: English
• Subjects: Drug resistance; Electrophoresis; Gel electrophoresis; Gene sequencing; Genetic diversity; Genomes; Hospitals; Nosocomial infection; Nucleotides; Outbreaks; Polymerase chain reaction; Pseudomonas aeruginosa; Pulsed-field gel electrophoresis; Single-nucleotide polymorphism; Whole genome sequencing
• ISSN: 0002-9262; 1476-6256
• DOI: 10.1093/aje/kwaa025

Abstract In 2013–2014, an outbreak involving 14 patients infected by an extensively drug-resistant strain of Pseudomonas aeruginosa was detected in a hospital in Madrid, Spain. Our objective was to evaluate an alternative strategy for investigating the outbreak in depth by means of molecular and genomic approaches. Pulsed-field gel electrophoresis (PFGE) was applied as a first-line approach, followed by a more refined whole genome sequencing analysis. Single nucleotide polymorphisms identified by whole genome sequencing were used to design a specific polymerase chain reaction (PCR) for screening unsuspected cases infected by the outbreak strain. Whole genome sequencing alerted us to the existence of greater genetic diversity than was initially assumed, splitting the PFGE-associated outbreak isolates into 4 groups, 2 of which represented coincidental transmission unrelated to the outbreak. A multiplex allele-specific PCR targeting outbreak-specific single nucleotide polymorphisms was applied to 290 isolates, which allowed us to identify 25 additional cases related to the outbreak during 2011–2017. Whole genome sequencing coupled with an outbreak-strain-specific PCR enabled us to markedly redefine the initial picture of the outbreak by 1) ruling out initially suspected cases, 2) defining likely independent coincidental transmission events, 3) predating the starting point of the outbreak, 4) capturing new unsuspected cases, and 5) revealing that the outbreak was still active.