» Articles » PMID: 27393124

Post-invasion Events After Infection with Staphylococcus Aureus Are Strongly Dependent on Both the Host Cell Type and the Infecting S. aureus Strain

Overview
Publisher Elsevier
Date 2016 Jul 10
PMID 27393124
Citations 85
Authors
Affiliations
Soon will be listed here.
Abstract

Host cell invasion is a major feature of Staphylococcus aureus and contributes to infection development. The intracellular metabolically active bacteria can induce host cell activation and death but they can also persist for long time periods. In this study a comparative analysis was performed of different well-characterized S. aureus strains in their interaction with a variety of host cell types. Staphylococcus aureus (strains 6850, USA300, LS1, SH1000, Cowan1) invasion was compared in different human cell types (epithelial and endothelial cells, keratinocytes, fibroblasts, osteoblasts). The number of intracellular bacteria was determined, cell inflammation was investigated, as well as cell death and phagosomal escape of bacteria. To explain strain-dependent differences in the secretome, a proteomic approach was used. Barrier cells took up high amounts of bacteria and were killed by aggressive strains. These strains expressed high levels of toxins, and possessed the ability to escape from phagolysosomes. Osteoblasts and keratinocytes ingested less bacteria, and were not killed, even though the primary osteoblasts were strongly activated by S. aureus. In all cell types S. aureus was able to persist. Strong differences in uptake, cytotoxicity, and inflammatory response were observed between primary cells and their corresponding cell lines, demonstrating that cell lines reflect only partially the functions and physiology of primary cells. This study provides a contribution for a better understanding of the pathomechanisms of S. aureus infections. The proteomic data provide important basic knowledge on strains commonly used in the analysis of S. aureus-host cell interaction.

Citing Articles

Implant-Derived Isolates Drive Strain-Specific Invasion Dynamics and Bioenergetic Alterations in Osteoblasts.

Song L, Schwinn L, Barthel J, Ketter V, Lechler P, Linne U Antibiotics (Basel). 2025; 14(2).

PMID: 40001363 PMC: 11852183. DOI: 10.3390/antibiotics14020119.


Staphylococcal SplA and SplB serine proteases target ubiquitin(-like) specific proteases.

Glinka F, Schmoker O, Singh A, Steil L, Hentschker C, Volker U AMB Express. 2025; 15(1):32.

PMID: 39985644 PMC: 11846797. DOI: 10.1186/s13568-025-01841-5.


Harnessing light-activated gallium porphyrins to combat intracellular Staphylococcus aureus using an in vitro keratinocyte infection model.

Szymczak K, Rychlowski M, Zhang L, Nakonieczna J Sci Rep. 2025; 15(1):1295.

PMID: 39779728 PMC: 11711192. DOI: 10.1038/s41598-024-84312-4.


Intracellular bactericidal activity and action mechanism of MDP1 antimicrobial peptide against VRSA and MRSA in human endothelial cells.

Dashtbin S, Razavi S, Ganjali Koli M, Barneh F, Ekhtiari-Sadegh S, Akbari R Front Microbiol. 2024; 15:1416995.

PMID: 39252832 PMC: 11381295. DOI: 10.3389/fmicb.2024.1416995.


Osteomyelitis-relevant antibiotics at clinical concentrations show limited effectivity against acute and chronic intracellular infections in osteocytes.

Zelmer A, Yang D, Gunn N, Solomon L, Nelson R, Kidd S Antimicrob Agents Chemother. 2024; 68(10):e0080824.

PMID: 39194210 PMC: 11459924. DOI: 10.1128/aac.00808-24.