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Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review

Staphylococci sp. are the most commonly associated pathogens in infective endocarditis, especially within high-income nations. This along with the increasing burden of healthcare, aging populations, and the protracted infection courses, contribute to a significant challenge for healthcare systems. A...

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Autores principales: Nappi, Francesco, Avtaar Singh, Sanjeet Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341754/
https://www.ncbi.nlm.nih.gov/pubmed/37446247
http://dx.doi.org/10.3390/ijms241311068
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author Nappi, Francesco
Avtaar Singh, Sanjeet Singh
author_facet Nappi, Francesco
Avtaar Singh, Sanjeet Singh
author_sort Nappi, Francesco
collection PubMed
description Staphylococci sp. are the most commonly associated pathogens in infective endocarditis, especially within high-income nations. This along with the increasing burden of healthcare, aging populations, and the protracted infection courses, contribute to a significant challenge for healthcare systems. A systematic review was conducted using relevant search criteria from PubMed, Ovid’s version of MEDLINE, and EMBASE, and data were tabulated from randomized controlled trials (RCT), observational cohort studies, meta-analysis, and basic research articles. The review was registered with the OSF register of systematic reviews and followed the PRISMA reporting guidelines. Thirty-five studies met the inclusion criteria and were included in the final systematic review. The role of Staphylococcus aureus and its interaction with the protective shield and host protection functions was identified and highlighted in several studies. The interaction between infective endocarditis pathogens, vascular endothelium, and blood constituents was also explored, giving rise to the potential use of antiplatelets as preventative and/or curative agents. Several factors allow Staphylococcus aureus infections to proliferate within the host with numerous promoting and perpetuating agents. The complex interaction with the hosts’ innate immunity also potentiates its virulence. The goal of this study is to attain a better understanding on the molecular pathways involved in infective endocarditis supported by S. aureus and whether therapeutic avenues for the prevention and treatment of IE can be obtained. The use of antibiotic-treated allogeneic tissues have marked antibacterial action, thereby becoming the ideal substitute in native and prosthetic valvular infections. However, the development of effective vaccines against S. aureus still requires in-depth studies.
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spelling pubmed-103417542023-07-14 Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review Nappi, Francesco Avtaar Singh, Sanjeet Singh Int J Mol Sci Review Staphylococci sp. are the most commonly associated pathogens in infective endocarditis, especially within high-income nations. This along with the increasing burden of healthcare, aging populations, and the protracted infection courses, contribute to a significant challenge for healthcare systems. A systematic review was conducted using relevant search criteria from PubMed, Ovid’s version of MEDLINE, and EMBASE, and data were tabulated from randomized controlled trials (RCT), observational cohort studies, meta-analysis, and basic research articles. The review was registered with the OSF register of systematic reviews and followed the PRISMA reporting guidelines. Thirty-five studies met the inclusion criteria and were included in the final systematic review. The role of Staphylococcus aureus and its interaction with the protective shield and host protection functions was identified and highlighted in several studies. The interaction between infective endocarditis pathogens, vascular endothelium, and blood constituents was also explored, giving rise to the potential use of antiplatelets as preventative and/or curative agents. Several factors allow Staphylococcus aureus infections to proliferate within the host with numerous promoting and perpetuating agents. The complex interaction with the hosts’ innate immunity also potentiates its virulence. The goal of this study is to attain a better understanding on the molecular pathways involved in infective endocarditis supported by S. aureus and whether therapeutic avenues for the prevention and treatment of IE can be obtained. The use of antibiotic-treated allogeneic tissues have marked antibacterial action, thereby becoming the ideal substitute in native and prosthetic valvular infections. However, the development of effective vaccines against S. aureus still requires in-depth studies. MDPI 2023-07-04 /pmc/articles/PMC10341754/ /pubmed/37446247 http://dx.doi.org/10.3390/ijms241311068 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nappi, Francesco
Avtaar Singh, Sanjeet Singh
Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title_full Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title_fullStr Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title_full_unstemmed Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title_short Host–Bacterium Interaction Mechanisms in Staphylococcus aureus Endocarditis: A Systematic Review
title_sort host–bacterium interaction mechanisms in staphylococcus aureus endocarditis: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341754/
https://www.ncbi.nlm.nih.gov/pubmed/37446247
http://dx.doi.org/10.3390/ijms241311068
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