{
"id": "https://doi.org/10.6084/m9.figshare.12011136",
"doi": "10.6084/M9.FIGSHARE.12011136",
"url": "https://tandf.figshare.com/articles/dataset/L-lysine_potentiates_aminoglycosides_against_i_Acinetobacter_baumannii_i_via_regulation_of_proton_motive_force_and_antibiotics_uptake/12011136",
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"creators": [
{
"name": "Deng, Wanyan",
"givenName": "Wanyan",
"familyName": "Deng"
},
{
"name": "Fu, Tiwei",
"givenName": "Tiwei",
"familyName": "Fu"
},
{
"name": "Zhang, Zhen",
"givenName": "Zhen",
"familyName": "Zhang"
},
{
"name": "Jiang, Xiao",
"givenName": "Xiao",
"familyName": "Jiang"
},
{
"name": "Xie, Jianping",
"givenName": "Jianping",
"familyName": "Xie"
},
{
"name": "Sun, Hang",
"givenName": "Hang",
"familyName": "Sun"
},
{
"name": "Hu, Peng",
"givenName": "Peng",
"familyName": "Hu"
},
{
"name": "Ren, Hong",
"givenName": "Hong",
"familyName": "Ren"
},
{
"name": "Zhou, Peifu",
"givenName": "Peifu",
"familyName": "Zhou"
},
{
"name": "Liu, Qi",
"givenName": "Qi",
"familyName": "Liu"
},
{
"name": "Long, Quanxin",
"givenName": "Quanxin",
"familyName": "Long"
}
],
"titles": [
{
"title": "L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake"
}
],
"publisher": {
"name": "Taylor & Francis"
},
"container": {},
"subjects": [
{
"subject": "Biophysics"
},
{
"subject": "Space Science"
},
{
"subject": "Medicine"
},
{
"subject": "Microbiology"
},
{
"subject": "FOS: Biological sciences",
"schemeUri": "http://www.oecd.org/science/inno/38235147.pdf",
"subjectScheme": "Fields of Science and Technology (FOS)"
},
{
"subject": "Cell Biology"
},
{
"subject": "Environmental Sciences not elsewhere classified"
},
{
"subject": "Chemical Sciences not elsewhere classified"
},
{
"subject": "Immunology"
},
{
"subject": "FOS: Clinical medicine",
"schemeUri": "http://www.oecd.org/science/inno/38235147.pdf",
"subjectScheme": "Fields of Science and Technology (FOS)"
},
{
"subject": "Cancer"
},
{
"subject": "Infectious Diseases"
},
{
"subject": "FOS: Health sciences",
"schemeUri": "http://www.oecd.org/science/inno/38235147.pdf",
"subjectScheme": "Fields of Science and Technology (FOS)"
},
{
"subject": "Virology"
},
{
"subject": "Computational Biology"
}
],
"contributors": [],
"dates": [
{
"date": "2023-01-20",
"dateType": "Created"
},
{
"date": "2023-05-31",
"dateType": "Updated"
},
{
"date": "2023",
"dateType": "Issued"
}
],
"publicationYear": 2023,
"identifiers": [],
"sizes": [
"52016878 Bytes"
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{
"rights": "Creative Commons Attribution 4.0 International",
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"schemeUri": "https://spdx.org/licenses/",
"rightsIdentifier": "cc-by-4.0",
"rightsIdentifierScheme": "SPDX"
}
],
"descriptions": [
{
"description": "Acinetobacter baumannii, a Gram-negative opportunistic pathogen, is a leading cause of hospital- and community-acquired infections. Acinetobacter baumannii can rapidly acquire diverse resistance mechanisms and undergo genetic modifications that confer resistance and persistence to all currently used clinical antibiotics. In this study, we found exogenous L-lysine sensitizes Acinetobacter baumannii, other Gram-negative bacteria (Escherichia coli and Klebsiella pneumoniae) and a Gram-positive bacterium (Mycobacterium smegmatis) to aminoglycosides. Importantly, the combination of L-lysine with aminoglycosides killed clinically isolated multidrug-resistant Acinetobacter baumannii and persister cells. The exogenous L-lysine can increase proton motive force via transmembrane chemical gradient, resulting in aminoglycoside acumination that further accounts for reactive oxygen species production. The combination of L-lysine and antibiotics highlights a promising strategy against bacterial infection.",
"descriptionType": "Abstract"
}
],
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"relatedIdentifiers": [
{
"relationType": "IsSupplementTo",
"relatedIdentifier": "10.1080/22221751.2020.1740611",
"relatedIdentifierType": "DOI"
}
],
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