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Natural and hemi-synthetic pentacyclic triterpenes as antimicrobials and resistance modifying agents against Staphylococcus aureus: a review

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Abstract

Staphylococcus aureus infections are considered as seriously problematic for human health and necessitate the development of new medicines and innovative antimicrobial strategies. Plant secondary metabolites have already demonstrated their potential as antibacterials when used alone but also in combination with other antimicrobial agents to potentiate their activity. Triterpenoids are widely distributed in the plant kingdom and known to have many beneficial effects, including anti-inflammatory, immunomodulatory, anti-proliferative, antimycotic, or antimicrobial activity. The aim of this paper is to review the activity of pentacyclic triterpenoids belonging to the ursane, oleanane, or lupane groups against Staphylococcus aureus. We summarize their activity as anti-staphylococcal compounds but also as resistance modifying agents when combined with common antibiotics.

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Abbreviations

ATCC:

American type culture collection

BA:

betulinic acid

CA:

ceanothic acid

FICI:

fractional inhibitory concentration index

MA:

maslinic acid

MIC:

minimum inhibitory concentration

MSSA:

methicillin-sensitive Staphylococcus aureus

MRSA:

methicillin-resistant Staphylococcus aureus

MTCC:

microbial type culture collection

NBRC:

NITE (National Institute of Technology and Evaluation) Biological Resource Center

OA:

oleanolic acid

PBP:

penicillin binding protein

SAR:

structure activity-relationship

UA:

ursolic acid

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Correspondence to Lucy Catteau.

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Catteau, L., Zhu, L., Van Bambeke, F. et al. Natural and hemi-synthetic pentacyclic triterpenes as antimicrobials and resistance modifying agents against Staphylococcus aureus: a review. Phytochem Rev 17, 1129–1163 (2018). https://doi.org/10.1007/s11101-018-9564-2

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  • DOI: https://doi.org/10.1007/s11101-018-9564-2

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