Are outer-membrane targets the solution for MDR Gram-negative bacteria?

被引:23
作者
Walker, Scott S. [1 ]
Black, Todd A. [1 ]
机构
[1] Merck & Co Inc, Infect Dis & Vaccines Basic Res, 770 Sumneytown Pike, West Point, PA 19486 USA
关键词
Antibacterial; Outer-membrane; Resistance; Discovery; AMR; ESCHERICHIA-COLI; BAD BUGS; LIPOPOLYSACCHARIDE; TRANSLOCATION; INHIBITION; COMPLEMENT; RESISTANCE; DRUGS;
D O I
10.1016/j.drudis.2021.03.027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The outer membrane (OM) of Gram-negative bacteria confers a significant barrier to many antibac-terial agents targeting periplasmic and cytosolic functions. 'Synergist' approaches to disrupt the OM have been hampered by poor specificity and accompanying toxicities. The OM contains proteins required for optimal growth and pathogenesis, including lipopolysaccharide (LPS) and capsular polysaccharide (CPS) transport, porins for uptake of macromolecules, and transporters for essential elements (such as iron). Does the external proximity of these proteins offer an enhanced potential to identify effective therapies? Here, we review recent experiences in exploiting Gram-negative OM proteins (OMPs) to address the calamity of exploding antimicrobial resistance. Teaser: Multidrug-resistant (MDR) Gram-negative bacteria are a growing crisis. Few new antimicro-bial chemotypes or targets have been identified after decades of screening. Are OMP targets a solution to MDR Gram-negative bacteria?
引用
收藏
页码:2152 / 2158
页数:7
相关论文
共 59 条
[11]   Small molecules with antimicrobial activity against E-coli and P-aeruginosa identified by high-throughput screening [J].
De La Fuente, R. ;
D Sonawane, N. ;
Arumainayagam, D. ;
Verkman, A. S. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (05) :551-559
[12]   Complement resistance mechanisms of Klebsiella pneumoniae [J].
Doorduijn, Dennis J. ;
Rooijakkers, Suzan H. M. ;
van Schaik, Willem ;
Bardoel, Bart W. .
IMMUNOBIOLOGY, 2016, 221 (10) :1102-1109
[13]   Multidrug efflux pumps: structure, function and regulation [J].
Du, Dijun ;
Wang-Kan, Xuan ;
Neuberger, Arthur ;
van Veen, Hendrik W. ;
Pos, Klaas M. ;
Piddock, Laura J. V. ;
Luisi, Ben F. .
NATURE REVIEWS MICROBIOLOGY, 2018, 16 (09) :523-539
[14]   Dynamics of an LPS translocon induced by substrate and an antimicrobial peptide [J].
Fiorentino, Francesco ;
Sauer, Joshua B. ;
Qiu, Xingyu ;
Corey, Robin A. ;
Cassidy, C. Keith ;
Mynors-Wallis, Benjamin ;
Mehmood, Shahid ;
Bolla, Jani R. ;
Stansfeld, Phillip J. ;
Robinson, Carol V. .
NATURE CHEMICAL BIOLOGY, 2021, 17 (02) :187-195
[15]   Lifting the Mask: Identification of New Small Molecule Inhibitors of Uropathogenic Escherichia coli Group 2 Capsule Biogenesis [J].
Goller, Carlos C. ;
Arshad, Mehreen ;
Noah, James W. ;
Ananthan, Subramaniam ;
Evans, Carrie W. ;
Nebane, N. Miranda ;
Rasmussen, Lynn ;
Sosa, Melinda ;
Tower, Nichole A. ;
White, E. Lucile ;
Neuenswander, Benjamin ;
Porubsky, Patrick ;
Maki, Brooks E. ;
Rogers, Steven A. ;
Schoenen, Frank ;
Seed, Patrick C. .
PLOS ONE, 2014, 9 (07)
[16]   High-Throughput Identification of Chemical Inhibitors of E. coli Group 2 Capsule Biogenesis as Anti-Virulence Agents [J].
Goller, Carlos C. ;
Seed, Patrick C. .
PLOS ONE, 2010, 5 (07)
[17]   Lipopolysaccharide is Inserted into the Outer Membrane through An Intramembrane Hole, A Lumen Gate, and the Lateral Opening of LptD [J].
Gu, Yinghong ;
Stansfeld, Phillip J. ;
Zeng, Yi ;
Dong, Haohao ;
Wang, Wenjian ;
Dong, Changjiang .
STRUCTURE, 2015, 23 (03) :496-504
[18]   High-Throughput Screening Assay for Inhibitors of TonB-Dependent Iron Transport [J].
Hanson, Mathew ;
Jordan, Lorne D. ;
Shipelskiy, Yan ;
Newton, Salete M. ;
Klebba, Phillip E. .
JOURNAL OF BIOMOLECULAR SCREENING, 2016, 21 (03) :316-322
[19]   Functions of the BamBCDE Lipoproteins Revealed by Bypass Mutations in BamA [J].
Hart, Elizabeth M. ;
Silhavy, Thomas J. .
JOURNAL OF BACTERIOLOGY, 2020, 202 (21)
[20]   The gain-of-function allele bamAE470K bypasses the essential requirement for BamD in β-barrel outer membrane protein assembly [J].
Hart, Elizabeth M. ;
Gupta, Meera ;
Wuehr, Martin ;
Silhavy, Thomas J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (31) :18737-18743