Routine Whole-Genome Sequencing for Outbreak Investigations of Staphylococcus aureus in a National Reference Center

The French National Reference Center for Staphylococci currently uses DNA arrays and typing for the initial epidemiological characterization of strains. We here describe the use of whole-genome sequencing (WGS) to investigate retrospectively four distinct and virulent lineages [clonal complexes (CCs...

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Veröffentlicht in:Frontiers in microbiology 2018-03, Vol.9, p.511-511
Hauptverfasser: Durand, Geraldine, Javerliat, Fabien, Bes, Michèle, Veyrieras, Jean-Baptiste, Guigon, Ghislaine, Mugnier, Nathalie, Schicklin, Stéphane, Kaneko, Gaël, Santiago-Allexant, Emmanuelle, Bouchiat, Coralie, Martins-Simões, Patrícia, Laurent, Frederic, Van Belkum, Alex, Vandenesch, François, Tristan, Anne
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Sprache:eng
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Zusammenfassung:The French National Reference Center for Staphylococci currently uses DNA arrays and typing for the initial epidemiological characterization of strains. We here describe the use of whole-genome sequencing (WGS) to investigate retrospectively four distinct and virulent lineages [clonal complexes (CCs): CC1, CC5, CC8, CC30] involved in hospital and community outbreaks or sporadic infections in France. We used a WGS bioinformatics pipeline based on assembly (reference-free approach), single nucleotide polymorphism analysis, and on the inclusion of epidemiological markers. We examined the phylogeographic diversity of the French dominant hospital-acquired CC8-MRSA (methicillin-resistant ) Lyon clone through WGS analysis which did not demonstrate evidence of large-scale geographic clustering. We analyzed sporadic cases along with two outbreaks of a CC1-MSSA (methicillin-susceptible ) clone containing the Panton-Valentine leukocidin (PVL) and results showed that two sporadic cases were closely related. We investigated an outbreak of PVL-positive CC30-MSSA in a school environment and were able to reconstruct the transmission history between eight families. We explored different outbreaks among newborns due to the CC5-MRSA Geraldine clone and we found evidence of an unsuspected link between two otherwise distinct outbreaks. Here, WGS provides the resolving power to disprove transmission events indicated by conventional methods (same sequence type, type, toxin profile, and antibiotic resistance profile) and, most importantly, WGS can reveal unsuspected transmission events. Therefore, WGS allows to better describe and understand outbreaks and (inter-)national dissemination of lineages. Our findings underscore the importance of adding WGS for (inter-)national surveillance of infections caused by virulent clones of but also substantiate the fact that technological optimization at the bioinformatics level is still urgently needed for routine use. However, the greatest limitation of WGS analysis is the completeness and the correctness of the reference database being used and the conversion of floods of data into actionable results. The WGS bioinformatics pipeline (EpiSeq ) we used here can easily generate a uniform database and associated metadata for epidemiological applications.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2018.00511