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Staphylococcus aureus populations from the gut and the blood are not distinguished by virulence traits—a critical role of host barrier integrity

  • Elisa J.M. Raineri
  • , Sandra Maaß
  • , Min Wang
  • , Siobhan Brushett
  • , Laura M. Palma Medina
  • , Neus Sampol Escandell
  • , Dania Altulea
  • , Erwin Raangs
  • , Anne de Jong
  • , Elias Vera Murguia
  • , Edward J. Feil
  • , Alex W. Friedrich
  • , Girbe Buist
  • , Dörte Becher
  • , Silvia García-Cobos
  • , Natacha Couto
  • , Jan Maarten van Dijl
  • Rijksuniversiteit Groningen
  • Ernst-Moritz-Arndt Universität
  • Department of Medical Microbiology
  • The Karolinska Institute
  • Biotechnology Institute
  • Instituto de Salud Carlos III, Universidad Carlos III de Madrid

Research output: Contribution to journalArticlepeer-review

25   Link opens in a new tab Citations (SciVal)

Abstract

Background: The opportunistic pathogen Staphylococcus aureus is an asymptomatically carried member of the microbiome of about one third of the human population at any given point in time. Body sites known to harbor S. aureus are the skin, nasopharynx, and gut. In particular, the mechanisms allowing S. aureus to pass the gut epithelial barrier and to invade the bloodstream were so far poorly understood. Therefore, the objective of our present study was to investigate the extent to which genetic differences between enteric S. aureus isolates and isolates that caused serious bloodstream infections contribute to the likelihood of invasive disease. Results: Here, we present genome-wide association studies (GWAS) that compare the genome sequences of 69 S. aureus isolates from enteric carriage by healthy volunteers and 95 isolates from bloodstream infections. We complement our GWAS results with a detailed characterization of the cellular and extracellular proteomes of the representative gut and bloodstream isolates, and by assaying the virulence of these isolates with infection models based on human gut epithelial cells, human blood cells, and a small animal infection model. Intriguingly, our results show that enteric and bloodstream isolates with the same sequence type (ST1 or ST5) are very similar to each other at the genomic and proteomic levels. Nonetheless, bloodstream isolates are not necessarily associated with an invasive profile. Furthermore, we show that the main decisive factor preventing infection of gut epithelial cells in vitro is the presence of a tight barrier. Conclusions: Our data show that virulence is a highly variable trait, even within a single clone. Importantly, however, there is no evidence that blood stream isolates possess a higher virulence potential than those from the enteric carriage. In fact, some gut isolates from healthy carriers were more virulent than bloodstream isolates. Based on our present observations, we propose that the integrity of the gut epithelial layer, rather than the pathogenic potential of the investigated enteric S. aureus isolates, determines whether staphylococci from the gut microbiome will become invasive pathogens. [MediaObject not available: see fulltext.].

Original languageEnglish
Article number239
Number of pages23
JournalMicrobiome
Volume10
Issue number1
Early online date26 Dec 2022
DOIs
Publication statusPublished - 26 Dec 2022

Data Availability Statement

All genome sequences have been submitted to GenBank (submission ID SUB11497709) and are available under the accession number BioProject: PRJNA83958. All MS data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository (Vizcaíno, et al. 2016) with the dataset identifier PXD030971.

Acknowledgements

We thank Klaas Nico Faber, Raphael Fagundes Rosa, and Tjasso Blokzijl for stimulating discussions and for help in establishing the Caco2 cell infection experiments. We thank Wayel Abdulahad and Peter Heeringa for stimulating discussions and for the help in establishing the leukocyte infection experiments. We thank Xin Zhao for stimulating discussions and for the help in the MS data analysis.

Funding

E.J.M.R. received funding from the CEC MSCI-ITN grant 713482 (ALERT). M.W. was supported by the China Scholarship Council (grant 201708110184). Part of this work was performed at the UMCG Imaging and Microscopy Center (UMIC), which is sponsored by grants from The Netherlands Organization for Scientific Research (175.010.2009–023, Zeiss LSM7/780 confocal and ZonMW 91111.006, Zeiss Supra55 ATLAS). This work was partially supported by the INTERREG VA (202085) funded project EurHealth-1Health, part of a DutchGerman cross-border network supported by the European Commission, the Dutch Ministry of Health, Welfare and Sports (VWS), the Ministry of Economy, Innovation, Digitalisation and Energy of the German Federal State of North Rhine-Westphalia and the German Federal State of Lower Saxony.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Bacteremia
  • Barrier
  • Enteric carriage
  • S. aureus, Gut
  • Virulence

ASJC Scopus subject areas

  • Microbiology
  • Microbiology (medical)

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