Development of CRISPR-Cas13a-based antimicrobials capable of sequence-specific killing of target bacteria

被引:129
作者
Kiga, Kotaro [1 ]
Tan, Xin-Ee [1 ]
Ibarra-Chavez, Rodrigo [2 ]
Watanabe, Shinya [1 ]
Aiba, Yoshifumi [1 ]
Sato'o, Yusuke [1 ]
Li, Feng-Yu [1 ]
Sasahara, Teppei [1 ]
Cui, Bintao [1 ]
Kawauchi, Moriyuki [1 ]
Boonsiri, Tanit [1 ]
Thitiananpakorn, Kanate [1 ]
Taki, Yusuke [1 ]
Azam, Aa Haeruman [1 ]
Suzuki, Masato [3 ]
Penades, Jose R. [2 ]
Cui, Longzhu [1 ]
机构
[1] Jichi Med Univ, Sch Med, Dept Infect & Immun, Div Bacteriol, Shimotsuke, Tochigi, Japan
[2] Univ Glasgow, Inst Infect Immun & Inflammat, Glasgow G12 8TA, Lanark, Scotland
[3] Natl Inst Infect Dis, Antimicrobial Resistance Res Ctr, Tokyo, Japan
关键词
STAPHYLOCOCCAL PHAGE; RESISTANCE; ENTEROBACTERIACEAE; INTEGRASE;
D O I
10.1038/s41467-020-16731-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The emergence of antimicrobial-resistant bacteria is an increasingly serious threat to global health, necessitating the development of innovative antimicrobials. Here we report the development of a series of CRISPR-Cas13a-based antibacterial nucleocapsids, termed CapsidCas13a(s), capable of sequence-specific killing of carbapenem-resistant Escherichia coli and methicillin-resistant Staphylococcus aureus by recognizing corresponding antimicrobial resistance genes. CapsidCas13a constructs are generated by packaging programmed CRISPR-Cas13a into a bacteriophage capsid to target antimicrobial resistance genes. Contrary to Cas9-based antimicrobials that lack bacterial killing capacity when the target genes are located on a plasmid, the CapsidCas13a(s) exhibit strong bacterial killing activities upon recognizing target genes regardless of their location. Moreover, we also demonstrate that the CapsidCas13a(s) can be applied to detect bacterial genes through gene-specific depletion of bacteria without employing nucleic acid manipulation and optical visualization devices. Our data underscore the potential of CapsidCas13a(s) as both therapeutic agents against antimicrobial-resistant bacteria and nonchemical agents for detection of bacterial genes.
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页数:11
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共 35 条
  • [1] C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector
    Abudayyeh, Omar O.
    Gootenberg, Jonathan S.
    Konermann, Silvana
    Joung, Julia
    Slaymaker, Ian M.
    Cox, David B. T.
    Shmakov, Sergey
    Makarova, Kira S.
    Semenova, Ekaterina
    Minakhin, Leonid
    Severinov, Konstantin
    Regev, Aviv
    Lander, Eric S.
    Koonin, Eugene V.
    Zhang, Feng
    [J]. SCIENCE, 2016, 353 (6299)
  • [2] The biological cost of mutational antibiotic resistance: any practical conclusions?
    Andersson, Dan I.
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2006, 9 (05) : 461 - 465
  • [3] Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection
    Baba, Tomoya
    Ara, Takeshi
    Hasegawa, Miki
    Takai, Yuki
    Okumura, Yoshiko
    Baba, Miki
    Datsenko, Kirill A.
    Tomita, Masaru
    Wanner, Barry L.
    Mori, Hirotada
    [J]. MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) : 2006.0008
  • [4] Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials
    Bikard, David
    Euler, Chad W.
    Jiang, Wenyan
    Nussenzweig, Philip M.
    Goldberg, Gregory W.
    Duportet, Xavier
    Fischetti, Vincent A.
    Marraffini, Luciano A.
    [J]. NATURE BIOTECHNOLOGY, 2014, 32 (11) : 1146 - 1150
  • [5] Clinically Relevant Plasmid-Host Interactions Indicate that Transcriptional and Not Genomic Modifications Ameliorate Fitness Costs of Klebsiella pneumoniae Carbapenemase-Carrying Plasmids
    Buckner, Michelle M. C.
    Saw, Howard T. H.
    Osagie, Rachael N.
    McNally, Alan
    Ricci, Vito
    Wand, Matthew E.
    Woodford, Neil
    Ivens, Alasdair
    Webber, Mark A.
    Piddock, Laura J. V.
    [J]. MBIO, 2018, 9 (02):
  • [6] Centers for Disease Control and Prevention, 2019, AR threats report
  • [7] Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases
    Citorik, Robert J.
    Mimee, Mark
    Lu, Timothy K.
    [J]. NATURE BIOTECHNOLOGY, 2014, 32 (11) : 1141 - 1145
  • [8] Carbapenemases in Enterobacteriaceae: Detection and Antimicrobial Therapy
    Cui, Xiaoyan
    Zhang, Haifang
    Du, Hong
    [J]. FRONTIERS IN MICROBIOLOGY, 2019, 10
  • [9] One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
    Datsenko, KA
    Wanner, BL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) : 6640 - 6645
  • [10] Next-generation precision antimicrobials: towards personalized treatment of infectious diseases
    de la Fuente-Nunez, Cesar
    Torres, Marcelo D. T.
    Mojica, Francisco J. M.
    Lu, Timothy K.
    [J]. CURRENT OPINION IN MICROBIOLOGY, 2017, 37 : 95 - 102