Cryo-electron Microscopy Structure of the Acinetobacter baumannii 70S Ribosome and Implications for New Antibiotic Development

被引:21
作者
Morgan, Christopher E. [1 ]
Huang, Wei [1 ]
Rudin, Susan D. [5 ]
Taylor, Derek J. [1 ]
Kirby, James E. [2 ,3 ]
Bonomo, Robert A. [1 ,4 ,5 ,6 ,7 ,8 ,9 ]
Yu, Edward W. [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
[3] Harvard Med Sch, Boston, MA 02215 USA
[4] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[5] Louis Stokes Cleveland Vet Affairs Med Ctr, Cleveland, OH USA
[6] Case Western Reserve Univ, Sch Med, Dept Mol Biol & Microbiol, Cleveland, OH 44106 USA
[7] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
[8] Case Western Reserve Univ, Sch Med, Case Ctr Prote & Bioinformat, Cleveland, OH USA
[9] CWRU Cleveland VAMC Ctr Antimicrobial Resistance, Cleveland, OH USA
关键词
70S ribosome; Acinetobacter baumannii; cryo-EM; antibiotic resistance; structural biology; TIGECYCLINE RESISTANCE; BACTERIAL RIBOSOME; MECHANISMS;
D O I
10.1128/mBio.03117-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antimicrobial resistance is a major health threat as it limits treatment options for infection. At the forefront of this serious issue is Acinetobacter baumannii, a Gram-negative opportunistic pathogen that exhibits the remarkable ability to resist antibiotics through multiple mechanisms. As bacterial ribosomes represent a target for multiple distinct classes of existing antimicrobial agents, we here use single-particle cryo-electron microscopy (cryo-EM) to elucidate five different structural states of the A. baumannii ribosome, including the 70S, 50S, and 30S forms. We also determined inter-particle motions of the 70S ribosome in different tRNA bound states using three-dimensional (3D) variability analysis. Together, our structural data further our understanding of the ribosome from A. baumannii and other Gram-negative pathogens and will enable structure-based drug discovery to combat antibiotic-resistant bacterial infections. IMPORTANCE Acinetobacter baumannii is a severe nosocomial threat largely due to its intrinsic antibiotic resistance and remarkable ability to acquire new resistance determinants. The bacterial ribosome serves as a major target for modern antibiotics and the design of new therapeutics. Here, we present cryo-EM structures of the A. baumannii 70S ribosome, revealing several unique species-specific structural features that may facilitate future drug development to combat this recalcitrant bacterial pathogen.
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页数:12
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