Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

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Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System. / Canovas de la Nuez, Jaime; Baldry, Mara; Bojer, Martin Saxtorph; Andersen, Paal Skytt; Grzeskowiak, Piotr K; Stegger, Marc; Damborg, Peter Panduro; Olsen, Christian Adam; Ingmer, Hanne.

In: Frontiers in Microbiology, Vol. 7, 1733, 2016.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Canovas de la Nuez, J, Baldry, M, Bojer, MS, Andersen, PS, Grzeskowiak, PK, Stegger, M, Damborg, PP, Olsen, CA & Ingmer, H 2016, 'Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System', Frontiers in Microbiology, vol. 7, 1733. https://doi.org/10.3389/fmicb.2016.01733

APA

Canovas de la Nuez, J., Baldry, M., Bojer, M. S., Andersen, P. S., Grzeskowiak, P. K., Stegger, M., Damborg, P. P., Olsen, C. A., & Ingmer, H. (2016). Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System. Frontiers in Microbiology, 7, [1733]. https://doi.org/10.3389/fmicb.2016.01733

Vancouver

Canovas de la Nuez J, Baldry M, Bojer MS, Andersen PS, Grzeskowiak PK, Stegger M et al. Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System. Frontiers in Microbiology. 2016;7. 1733. https://doi.org/10.3389/fmicb.2016.01733

Author

Canovas de la Nuez, Jaime ; Baldry, Mara ; Bojer, Martin Saxtorph ; Andersen, Paal Skytt ; Grzeskowiak, Piotr K ; Stegger, Marc ; Damborg, Peter Panduro ; Olsen, Christian Adam ; Ingmer, Hanne. / Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System. In: Frontiers in Microbiology. 2016 ; Vol. 7.

Bibtex

@article{9510ca399bc3440586fa76aa09ef6d2a,
title = "Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System",
abstract = "Staphylococci are associated with both humans and animals. While most are non-pathogenic colonizers, Staphylococcus aureus is an opportunistic pathogen capable of causing severe infections. S. aureus virulence is controlled by the agr quorum sensing system responding to secreted auto-inducing peptides (AIPs) sensed by AgrC, a two component histidine kinase. agr loci are found also in other staphylococcal species and for Staphylococcus epidermidis, the encoded AIP represses expression of agr regulated virulence genes in S. aureus. In this study we aimed to better understand the interaction between staphylococci and S. aureus, and show that this interaction may eventually lead to the identification of new anti-virulence candidates to target S. aureus infections. Here we show that culture supernatants of 37 out of 52 staphylococcal isolates representing 17 different species inhibit S. aureus agr. The dog pathogen, Staphylococcus schleiferi, expressed the most potent inhibitory activity and was active against all four agr classes found in S. aureus. By employing a S. aureus strain encoding a constitutively active AIP receptor we show that the activity is mediated via agr. Subsequent cloning and heterologous expression of the S. schleiferi AIP in S. aureus demonstrated that this molecule was likely responsible for the inhibitory activity, and further proof was provided when pure synthetic S. schleiferi AIP was able to completely abolish agr induction of an S. aureus reporter strain. To assess impact on S. aureus virulence, we co-inoculated S. aureus and S. schleiferi in vivo in the Galleria mellonella wax moth larva, and found that expression of key S. aureus virulence factors was abrogated. Our data show that the S. aureus agr locus is highly responsive to other staphylococcal species suggesting that agr is an inter-species communication system. Based on these results we speculate that interactions between S. aureus and other colonizing staphylococci will significantly influence the ability of S. aureus to cause infection, and we propose that other staphylococci are potential sources of compounds that can be applied as anti-virulence therapy for combating S. aureus infections.",
author = "{Canovas de la Nuez}, Jaime and Mara Baldry and Bojer, {Martin Saxtorph} and Andersen, {Paal Skytt} and Grzeskowiak, {Piotr K} and Marc Stegger and Damborg, {Peter Panduro} and Olsen, {Christian Adam} and Hanne Ingmer",
year = "2016",
doi = "10.3389/fmicb.2016.01733",
language = "English",
volume = "7",
journal = "Frontiers in Microbiology",
issn = "1664-302X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Cross-Talk between Staphylococcus aureus and Other Staphylococcal Species via the agr Quorum Sensing System

AU - Canovas de la Nuez, Jaime

AU - Baldry, Mara

AU - Bojer, Martin Saxtorph

AU - Andersen, Paal Skytt

AU - Grzeskowiak, Piotr K

AU - Stegger, Marc

AU - Damborg, Peter Panduro

AU - Olsen, Christian Adam

AU - Ingmer, Hanne

PY - 2016

Y1 - 2016

N2 - Staphylococci are associated with both humans and animals. While most are non-pathogenic colonizers, Staphylococcus aureus is an opportunistic pathogen capable of causing severe infections. S. aureus virulence is controlled by the agr quorum sensing system responding to secreted auto-inducing peptides (AIPs) sensed by AgrC, a two component histidine kinase. agr loci are found also in other staphylococcal species and for Staphylococcus epidermidis, the encoded AIP represses expression of agr regulated virulence genes in S. aureus. In this study we aimed to better understand the interaction between staphylococci and S. aureus, and show that this interaction may eventually lead to the identification of new anti-virulence candidates to target S. aureus infections. Here we show that culture supernatants of 37 out of 52 staphylococcal isolates representing 17 different species inhibit S. aureus agr. The dog pathogen, Staphylococcus schleiferi, expressed the most potent inhibitory activity and was active against all four agr classes found in S. aureus. By employing a S. aureus strain encoding a constitutively active AIP receptor we show that the activity is mediated via agr. Subsequent cloning and heterologous expression of the S. schleiferi AIP in S. aureus demonstrated that this molecule was likely responsible for the inhibitory activity, and further proof was provided when pure synthetic S. schleiferi AIP was able to completely abolish agr induction of an S. aureus reporter strain. To assess impact on S. aureus virulence, we co-inoculated S. aureus and S. schleiferi in vivo in the Galleria mellonella wax moth larva, and found that expression of key S. aureus virulence factors was abrogated. Our data show that the S. aureus agr locus is highly responsive to other staphylococcal species suggesting that agr is an inter-species communication system. Based on these results we speculate that interactions between S. aureus and other colonizing staphylococci will significantly influence the ability of S. aureus to cause infection, and we propose that other staphylococci are potential sources of compounds that can be applied as anti-virulence therapy for combating S. aureus infections.

AB - Staphylococci are associated with both humans and animals. While most are non-pathogenic colonizers, Staphylococcus aureus is an opportunistic pathogen capable of causing severe infections. S. aureus virulence is controlled by the agr quorum sensing system responding to secreted auto-inducing peptides (AIPs) sensed by AgrC, a two component histidine kinase. agr loci are found also in other staphylococcal species and for Staphylococcus epidermidis, the encoded AIP represses expression of agr regulated virulence genes in S. aureus. In this study we aimed to better understand the interaction between staphylococci and S. aureus, and show that this interaction may eventually lead to the identification of new anti-virulence candidates to target S. aureus infections. Here we show that culture supernatants of 37 out of 52 staphylococcal isolates representing 17 different species inhibit S. aureus agr. The dog pathogen, Staphylococcus schleiferi, expressed the most potent inhibitory activity and was active against all four agr classes found in S. aureus. By employing a S. aureus strain encoding a constitutively active AIP receptor we show that the activity is mediated via agr. Subsequent cloning and heterologous expression of the S. schleiferi AIP in S. aureus demonstrated that this molecule was likely responsible for the inhibitory activity, and further proof was provided when pure synthetic S. schleiferi AIP was able to completely abolish agr induction of an S. aureus reporter strain. To assess impact on S. aureus virulence, we co-inoculated S. aureus and S. schleiferi in vivo in the Galleria mellonella wax moth larva, and found that expression of key S. aureus virulence factors was abrogated. Our data show that the S. aureus agr locus is highly responsive to other staphylococcal species suggesting that agr is an inter-species communication system. Based on these results we speculate that interactions between S. aureus and other colonizing staphylococci will significantly influence the ability of S. aureus to cause infection, and we propose that other staphylococci are potential sources of compounds that can be applied as anti-virulence therapy for combating S. aureus infections.

UR - https://www.frontiersin.org/articles/10.3389/fmicb.2017.01075/full

UR - http://10.3389/fmicb.2017.01949

U2 - 10.3389/fmicb.2016.01733

DO - 10.3389/fmicb.2016.01733

M3 - Journal article

C2 - 27877157

VL - 7

JO - Frontiers in Microbiology

JF - Frontiers in Microbiology

SN - 1664-302X

M1 - 1733

ER -

ID: 169435927