Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus

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Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus. / Liu, Liping; Ingmer, Hanne; Vestergaard, Martin.

I: Antibiotics, Bind 10, Nr. 1, 82, 2021, s. 1-9.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Liu, L, Ingmer, H & Vestergaard, M 2021, 'Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus', Antibiotics, bind 10, nr. 1, 82, s. 1-9. https://doi.org/10.3390/antibiotics10010082

APA

Liu, L., Ingmer, H., & Vestergaard, M. (2021). Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus. Antibiotics, 10(1), 1-9. [82]. https://doi.org/10.3390/antibiotics10010082

Vancouver

Liu L, Ingmer H, Vestergaard M. Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus. Antibiotics. 2021;10(1):1-9. 82. https://doi.org/10.3390/antibiotics10010082

Author

Liu, Liping ; Ingmer, Hanne ; Vestergaard, Martin. / Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus. I: Antibiotics. 2021 ; Bind 10, Nr. 1. s. 1-9.

Bibtex

@article{6fc108745d7a4fb194b46171c7633b3d,
title = "Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus",
abstract = "Resveratrol has been extensively studied due to its potential health benefits in multiple diseases, for example, cancer, obesity and cardiovascular diseases. Besides these properties, resveratrol displays inhibitory activity against a wide range of bacterial species; however, the cellular effects of resveratrol in bacteria remain incompletely understood, especially in the human pathogen, Staphylococcus aureus. In this study, we aimed to identify intrinsic resistance genes that aid S. aureus in tolerating the activity of resveratrol. We screened the Nebraska Transposon Mutant Library, consisting of 1920 mutants with inactivation of non-essential genes in S. aureus JE2, for increased susceptibly to resveratrol. On agar plates containing 0.5× the minimum inhibitory concentration (MIC), 17 transposon mutants failed to grow. Of these, four mutants showed a two-fold reduction in MIC, being the clpP protease mutant and three mutants with deficiencies in the electron transport chain (menD, hemB, aroC). The remaining 13 mutants did not show a reduction in MIC, but were confirmed by spot-assays to have increased susceptibility to resveratrol. Several genes were associated with DNA damage repair (recJ, xerC and xseA). Treatment of S. aureus JE2 with sub-inhibitory concentrations of resveratrol did not affect the expression of recJ, xerC and xseA, but increased expression of the SOS-stress response genes lexA and recA, suggesting that resveratrol interferes with DNA integrity in S. aureus. Expression of error-prone DNA polymerases are part of the SOS-stress response and we could show that sub-inhibitory concentrations of resveratrol increased overall mutation frequency as measured by formation of rifampicin resistant mutants. Our data show that DNA repair systems are important determinants aiding S. aureus to overcome the inhibitory activity of resveratrol. Activation of the SOS response by resveratrol could potentially facilitate the development of resistance towards conventional antibiotics in S. aureus.",
keywords = "DNA damage, Intrinsic resistance, Resveratrol, SOS response, Staphylococcus aureus",
author = "Liping Liu and Hanne Ingmer and Martin Vestergaard",
year = "2021",
doi = "10.3390/antibiotics10010082",
language = "English",
volume = "10",
pages = "1--9",
journal = "Antibiotics",
issn = "2079-6382",
publisher = "M D P I AG",
number = "1",

}

RIS

TY - JOUR

T1 - Genome-wide identification of resveratrol intrinsic resistance determinants in staphylococcus aureus

AU - Liu, Liping

AU - Ingmer, Hanne

AU - Vestergaard, Martin

PY - 2021

Y1 - 2021

N2 - Resveratrol has been extensively studied due to its potential health benefits in multiple diseases, for example, cancer, obesity and cardiovascular diseases. Besides these properties, resveratrol displays inhibitory activity against a wide range of bacterial species; however, the cellular effects of resveratrol in bacteria remain incompletely understood, especially in the human pathogen, Staphylococcus aureus. In this study, we aimed to identify intrinsic resistance genes that aid S. aureus in tolerating the activity of resveratrol. We screened the Nebraska Transposon Mutant Library, consisting of 1920 mutants with inactivation of non-essential genes in S. aureus JE2, for increased susceptibly to resveratrol. On agar plates containing 0.5× the minimum inhibitory concentration (MIC), 17 transposon mutants failed to grow. Of these, four mutants showed a two-fold reduction in MIC, being the clpP protease mutant and three mutants with deficiencies in the electron transport chain (menD, hemB, aroC). The remaining 13 mutants did not show a reduction in MIC, but were confirmed by spot-assays to have increased susceptibility to resveratrol. Several genes were associated with DNA damage repair (recJ, xerC and xseA). Treatment of S. aureus JE2 with sub-inhibitory concentrations of resveratrol did not affect the expression of recJ, xerC and xseA, but increased expression of the SOS-stress response genes lexA and recA, suggesting that resveratrol interferes with DNA integrity in S. aureus. Expression of error-prone DNA polymerases are part of the SOS-stress response and we could show that sub-inhibitory concentrations of resveratrol increased overall mutation frequency as measured by formation of rifampicin resistant mutants. Our data show that DNA repair systems are important determinants aiding S. aureus to overcome the inhibitory activity of resveratrol. Activation of the SOS response by resveratrol could potentially facilitate the development of resistance towards conventional antibiotics in S. aureus.

AB - Resveratrol has been extensively studied due to its potential health benefits in multiple diseases, for example, cancer, obesity and cardiovascular diseases. Besides these properties, resveratrol displays inhibitory activity against a wide range of bacterial species; however, the cellular effects of resveratrol in bacteria remain incompletely understood, especially in the human pathogen, Staphylococcus aureus. In this study, we aimed to identify intrinsic resistance genes that aid S. aureus in tolerating the activity of resveratrol. We screened the Nebraska Transposon Mutant Library, consisting of 1920 mutants with inactivation of non-essential genes in S. aureus JE2, for increased susceptibly to resveratrol. On agar plates containing 0.5× the minimum inhibitory concentration (MIC), 17 transposon mutants failed to grow. Of these, four mutants showed a two-fold reduction in MIC, being the clpP protease mutant and three mutants with deficiencies in the electron transport chain (menD, hemB, aroC). The remaining 13 mutants did not show a reduction in MIC, but were confirmed by spot-assays to have increased susceptibility to resveratrol. Several genes were associated with DNA damage repair (recJ, xerC and xseA). Treatment of S. aureus JE2 with sub-inhibitory concentrations of resveratrol did not affect the expression of recJ, xerC and xseA, but increased expression of the SOS-stress response genes lexA and recA, suggesting that resveratrol interferes with DNA integrity in S. aureus. Expression of error-prone DNA polymerases are part of the SOS-stress response and we could show that sub-inhibitory concentrations of resveratrol increased overall mutation frequency as measured by formation of rifampicin resistant mutants. Our data show that DNA repair systems are important determinants aiding S. aureus to overcome the inhibitory activity of resveratrol. Activation of the SOS response by resveratrol could potentially facilitate the development of resistance towards conventional antibiotics in S. aureus.

KW - DNA damage

KW - Intrinsic resistance

KW - Resveratrol

KW - SOS response

KW - Staphylococcus aureus

U2 - 10.3390/antibiotics10010082

DO - 10.3390/antibiotics10010082

M3 - Journal article

C2 - 33467002

AN - SCOPUS:85099984647

VL - 10

SP - 1

EP - 9

JO - Antibiotics

JF - Antibiotics

SN - 2079-6382

IS - 1

M1 - 82

ER -

ID: 256513424