Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression
Тип публикации: Journal Article
Дата публикации: 2011-11-30
SCImago Q1
WOS Q2
БС1
SJR: 1.258
CiteScore: 7.3
Impact factor: 3.6
ISSN: 03057453, 14602091
PubMed ID:
22129590
Pharmacology
Microbiology (medical)
Infectious Diseases
Pharmacology (medical)
Краткое описание
This study characterized the multiple biological activities of the natural compound tomatidine against Staphylococcus aureus. Notably, this work examined the antibacterial activity of tomatidine in combination with other antibiotics and the influence of this compound on the expression of virulence factors in S. aureus.The effect of tomatidine on the susceptibility of S. aureus to several antibiotic classes was determined by a broth microdilution procedure and a chequerboard protocol to measure fractional inhibitory concentration indices and to reveal drug interactions. Time-kill experiments for aminoglycoside/tomatidine combinations were also performed. The haemolytic ability of several strains in the presence of tomatidine was measured on blood agar plates and the expression of virulence-associated genes in strain ATCC 29213 treated with tomatidine was monitored by quantitative PCR.Tomatidine specifically potentiated the inhibitory effect of aminoglycosides but not of other classes of drugs. This potentiating effect was observed against strains of different clinical origins (human blood, cystic fibrosis airways, osteomyelitis, skin tissues and bovine mastitis), including aminoglycoside-resistant bacteria possessing the aac(6')-aph(2″), ant(4')-Ia and aph(3')-IIIa genes. The killing kinetics for the combination of aminoglycosides with tomatidine revealed strong bactericidal activity. Although tomatidine did not possess growth-inhibitory activity of its own against prototypical S. aureus, it inhibited the haemolytic activity of several strains and, more specifically, blocked the expression of several genes normally influenced by the agr system.These results show that tomatidine is an aminoglycoside potentiator that also acts as an anti-virulence agent targeting both antibiotic-susceptible and antibiotic-resistant S. aureus.
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MITCHELL G. et al. Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression // Journal of Antimicrobial Chemotherapy. 2011. Vol. 67. No. 3. pp. 559-568.
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MITCHELL G., Lafrance M., Boulanger S., Seguin D. L., Guay I., Gattuso M., Marsault É., Bouarab K., Malouin F. Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression // Journal of Antimicrobial Chemotherapy. 2011. Vol. 67. No. 3. pp. 559-568.
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RIS
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TY - JOUR
DO - 10.1093/jac/dkr510
UR - https://doi.org/10.1093/jac/dkr510
TI - Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression
T2 - Journal of Antimicrobial Chemotherapy
AU - MITCHELL, G
AU - Lafrance, M
AU - Boulanger, S.
AU - Seguin, D L
AU - Guay, I
AU - Gattuso, M.
AU - Marsault, Éric
AU - Bouarab, K
AU - Malouin, F.
PY - 2011
DA - 2011/11/30
PB - Oxford University Press
SP - 559-568
IS - 3
VL - 67
PMID - 22129590
SN - 0305-7453
SN - 1460-2091
ER -
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@article{2011_MITCHELL,
author = {G MITCHELL and M Lafrance and S. Boulanger and D L Seguin and I Guay and M. Gattuso and Éric Marsault and K Bouarab and F. Malouin},
title = {Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression},
journal = {Journal of Antimicrobial Chemotherapy},
year = {2011},
volume = {67},
publisher = {Oxford University Press},
month = {nov},
url = {https://doi.org/10.1093/jac/dkr510},
number = {3},
pages = {559--568},
doi = {10.1093/jac/dkr510}
}
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MLA
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MITCHELL, G., et al. “Tomatidine acts in synergy with aminoglycoside antibiotics against multiresistant Staphylococcus aureus and prevents virulence gene expression.” Journal of Antimicrobial Chemotherapy, vol. 67, no. 3, Nov. 2011, pp. 559-568. https://doi.org/10.1093/jac/dkr510.
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