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. Issue 8 (4th March 2020)

• Record Type: Journal Article
• 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
• Is Part Of: American journal of epidemiology. Volume 189:Issue 8(2020)
• Page Start: 841
• Page End: 849
• Publication Date: 2020-03-04
• Subjects: drug resistance -- genomics -- infection -- nosocomial outbreaks -- polymerase chain reaction -- Pseudomonas aeruginosa; Epidemiology -- Periodicals; Public health -- Periodicals; 614.4
• DOI: 10.1093/aje/kwaa025
• Languages: English
• ISSNs: 0002-9262

Abstract

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.