Whole genome sequencing as a tool to investigate a cluster of seven cases of listeriosis in Austria and Germany, 2011–2013. (28th April 2014)

• Record Type: Journal Article
• Authors: Schmid, D.; Allerberger, F.; Huhulescu, S.; Pietzka, A.; Amar, C.; Kleta, S.; Prager, R.; Preußel, K.; Aichinger, E.; Mellmann, A.; Raoult, D.
• Is Part Of: Clinical microbiology and infection. Volume 20:Number 5(2014:May)
• Page Start: 431
• Page End: 436
• Publication Date: 2014-04-28
• Subjects: Medical microbiology -- Periodicals; Diagnostic microbiology -- Periodicals; Communicable diseases -- Periodicals; Infection -- Periodicals; 616.01
• DOI: 10.1111/1469-0691.12638
• Languages: English
• ISSNs: 1198-743X

Abstract

<abstract abstract-type="main" id="clm12638-abs-0001"> <title>Abstract</title> <p>A cluster of seven human cases of listeriosis occurred in Austria and in Germany between April 2011 and July 2013. The <italic>Listeria monocytogenes</italic> serovar (SV) 1/2b isolates shared pulsed‐field gel electrophoresis (PFGE) and fluorescent amplified fragment length polymorphism (fAFLP) patterns indistinguishable from those from five food producers. The seven human isolates, a control strain with a different PFGE/fAFLP profile and ten food isolates were subjected to whole genome sequencing (WGS) in a blinded fashion. A gene‐by‐gene comparison (multilocus sequence typing (MLST)+) was performed, and the resulting whole genome allelic profiles were compared using SeqSphere<sup>+</sup> software version 1.0. On analysis of 2298 genes, the four human outbreak isolates from 2012 to 2013 had different alleles at ≤6 genes, i.e. differed by ≤6 genes from each other; the dendrogram placed these isolates in between five Austrian unaged soft cheese isolates from producer A (≤19‐gene difference from the human cluster) and two Austrian ready‐to‐eat meat isolates from producer B (≤8‐gene difference from the human cluster). Both food products appeared on grocery bills prospectively collected by these outbreak cases after hospital discharge. Epidemiological results on food consumption and MLST+ clearly separated the three cases in 2011 from the four 2012–2013 outbreak cases (≥48 different genes). We showed that WGS is capable of discriminating <italic>L. monocytogenes </italic>SV1/2b clones not distinguishable by PFGE and fAFLP. The listeriosis outbreak described clearly underlines the potential of sequence‐based typing methods to offer enhanced resolution and comparability of typing systems for public health applications.</p> </abstract>