CRISPR基因组编辑技术在传染病致病机理研究和防诊治中的应用
收稿日期: 2023-07-31
修回日期: 2023-10-06
网络出版日期: 2023-10-24
基金资助
广州实验室应急攻关项目(EKPG21-19);Supported by the Emergency Key Program of Guangzhou Laboratory No(EKPG21-19)
The application of CRISPR genome editing technologies in the pathogenesis studies, diagnosis, prevention and treatment of infectious diseases
Received date: 2023-07-31
Revised date: 2023-10-06
Online published: 2023-10-24
CRISPR基因组编辑技术在基因操作和传染病研究等方面展现出巨大的应用前景,对于有效控制和治愈传染病具有重要价值。通过其构建的细胞、类器官和动物疾病模型,为探索传染病相关分子机制提供了极大便利。CRISPR筛选技术使得高通量鉴定传染病相关风险因子成为可能。基于CRISPR的新型分子诊断工具为病原体的检测提供了更灵敏和快速的方法。利用CRISPR工具敲入抗性基因或破坏风险基因和病毒基因组,有望实现预防或治疗传染病。本综述讨论了CRISPR基因组编辑技术在疾病模型制备、传染病风险因子筛选、病原体诊断和传染病防治中的应用,以期为后续传染病的研究和防诊治提供参考。
杨臻嵘, 周钢桥 . CRISPR基因组编辑技术在传染病致病机理研究和防诊治中的应用[J]. 遗传, 2023 , 45(11) : 950 -962 . DOI: 10.16288/j.yczz.23-206
The CRISPR genome editing technology shows great application prospects in gene manipulation and infectious disease research, and is of great value for effective control and cure of infectious diseases. It has been utilized to generate specific disease models in cells, organoids and animals, which provide great convenience for research into the molecular mechanisms associated with infectious diseases. CRISPR screening technology enables high-throughput identification of risk factors. New molecular diagnostic tools based on CRISPR offer a more sensitive and faster method for detecting pathogens. The use of CRISPR tools to introduce resistance genes or to specifically destroy risk genes and virus genomes is intended to help prevent or treat infectious diseases. This review discusses the application of CRISPR genome editing technologies in the construction of disease models, screening of risk factors, pathogen diagnosis, and prevention and treatment of infectious diseases, thereby providing a reference for follow-up research in pathogenesis, diagnosis, prevention and treatment of infectious diseases.
Key words: infectious diseases; CRISPR; pathogenesis; diagnosis
| [1] | Barrangou R, Fremaux C, Deveau H, Richards M, Boyaval P, Moineau S, Romero DA, Horvath P. CRISPR provides acquired resistance against viruses in prokaryotes. Science, 2007, 315(5819): 1709-1712. |
| [2] | Stoddard BL. Homing endonuclease structure and function. Q Rev Biophys, 2005, 38(1): 49-95. |
| [3] | Bos JL, Heyting C, Borst P, Arnberg AC, Van Bruggen EF. An insert in the single gene for the large ribosomal RNA in yeast mitochondrial DNA. Nature, 1978, 275(5678): 336-338. |
| [4] | Stoddard BL. Homing endonucleases from mobile group I introns: discovery to genome engineering. Mob DNA, 2014, 5(1): 7. |
| [5] | Sargent RG, Brenneman MA, Wilson JH. Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination. Mol Cell Biol, 1997, 17(1): 267-277. |
| [6] | Cohen-Tannoudji M, Robine S, Choulika A, Pinto D, El Marjou F, Babinet C, Louvard D, Jaisser F. I-SceI-induced gene replacement at a natural locus in embryonic stem cells. Mol Cell Biol, 1998, 18(3): 1444-1448. |
| [7] | Cabaniols JP, Paques F. Robust cell line development using meganucleases. Methods Mol Biol, 2008, 435: 31-45. |
| [8] | Cabaniols JP, Ouvry C, Lamamy V, Fery I, Craplet ML, Moulharat N, Guenin SP, Bedut S, Nosjean O, Ferry G, Devavry S, Jacqmarcq C, Lebuhotel C, Mathis L, Delenda C, Boutin JA, Duchateau P, Cogé F, Paques F. Meganuclease-driven targeted integration in CHO-K1 cells for the fast generation of HTS-compatible cell-based assays. J Biomol Screen, 2010, 15(8): 956-967. |
| [9] | Redondo P, Prieto J, Mu?oz IG, Alibés A, Stricher F, Serrano L, Cabaniols JP, Daboussi F, Arnould S, Perez C, Duchateau P, Paques F, Blanco FJ, Montoya G. Molecular basis of xeroderma pigmentosum group C DNA recognition by engineered meganucleases. Nature, 2008, 456(7218): 107-111. |
| [10] | Seligman LM, Stephens KM, Savage JH, Monnat RJ. Genetic analysis of the Chlamydomonas reinhardtii I-CreI mobile intron homing system in Escherichia coli. Genetics, 1997, 147(4): 1653-1664. |
| [11] | Pósfai G, Kolisnychenko V, Bereczki Z, Blattner FR. Markerless gene replacement in Escherichia coli stimulated by a double-strand break in the chromosome. Nucleic Acids Res, 1999, 27(22): 4409-4415. |
| [12] | Puchta H, Dujon B, Hohn B. Two different but related mechanisms are used in plants for the repair of genomic double-strand breaks by homologous recombination. Proc Natl Acad Sci USA, 1996, 93(10): 5055-5060. |
| [13] | Antunes MS, Smith JJ, Jantz D, Medford JI. Targeted DNA excision in Arabidopsis by a re-engineered homing endonuclease. BMC Biotechnol, 2012, 12: 86. |
| [14] | Djukanovic V, Smith J, Lowe K, Yang MZ, Gao HR, Jones S, Nicholson MG, West A, Lape J, Bidney D, Carl Falco S, Jantz D, Alexander Lyznik L. Male-sterile maize plants produced by targeted mutagenesis of the cytochrome P450-like gene (MS26) using a re-designed I-CreI homing endonuclease. Plant J, 2013, 76(5): 888-899. |
| [15] | Rouet P, Smih F, Jasin M. Introduction of double- strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease. Mol Cell Biol, 1994, 14(12): 8096-8106. |
| [16] | Gouble A, Smith J, Bruneau S, Perez C, Guyot V, Cabaniols JP, Leduc S, Fiette L, Avé P, Micheau B, Duchateau P, Paques F. Efficient in toto targeted recombination in mouse liver by meganuclease-induced double-strand break. J Gene Med, 2006, 8(5): 616-622. |
| [17] | Kim YG, Cha J, Chandrasegaran S. Hybrid restriction enzymes: zinc finger fusions to Fok I cleavage domain. Proc Natl Acad Sci USA, 1996, 93(3): 1156-1160. |
| [18] | Cathomen T, Keith Joung J,. Zinc-finger nucleases: the next generation emerges. Mol Ther, 2008, 16(7): 1200-1207. |
| [19] | Pavletich NP, Pabo CO. Zinc finger-DNA recognition: crystal structure of a Zif268-DNA complex at 2.1 ?. Science, 1991, 252(5007): 809-817. |
| [20] | Bitinaite J, Wah DA, Aggarwal AK, Schildkraut I. FokI dimerization is required for DNA cleavage. Proc Natl Acad Sci USA, 1998, 95(18): 10570-10575. |
| [21] | Bibikova M, Golic M, Golic KG, Carroll D. Targeted chromosomal cleavage and mutagenesis in Drosophila using zinc-finger nucleases. Genetics, 2002, 161(3): 1169-1175. |
| [22] | Bibikova M, Beumer K, Trautman JK, Carroll D. Enhancing gene targeting with designed zinc finger nucleases. Science, 2003, 300(5620): 764. |
| [23] | Morton J, Davis MW, Jorgensen EM, Carroll D. Induction and repair of zinc-finger nuclease-targeted double-strand breaks in Caenorhabditis elegans somatic cells. Proc Natl Acad Sci USA, 2006, 103(44): 16370-16375. |
| [24] | Meng XD, Noyes MB, Zhu LJ, Lawson ND, Wolfe SA. Targeted gene inactivation in zebrafish using engineered zinc-finger nucleases. Nat Biotechnol, 2008, 26(6): 695-701. |
| [25] | Doyon Y, McCammon JM, Miller JC, Faraji F, Ngo C, Katibah GE, Amora R, Hocking TD, Zhang L, Rebar EJ, Gregory PD, Urnov FD, Amacher SL. Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases. Nat Biotechnol, 2008, 26(6): 702-708. |
| [26] | Connelly JP, Barker JC, Pruett-Miller S, Porteus MH. Gene correction by homologous recombination with zinc finger nucleases in primary cells from a mouse model of a generic recessive genetic disease. Mol Ther, 2010, 18(6): 1103-1110. |
| [27] | Meyer M, de Angelis MH, Wurst W, Kühn R. Gene targeting by homologous recombination in mouse zygotes mediated by zinc-finger nucleases. Proc Natl Acad Sci USA, 2010, 107(34): 15022-15026. |
| [28] | Carbery ID, Ji D, Harrington A, Brown V, Weinstein EJ, Liaw L, Cui XX. Targeted genome modification in mice using zinc-finger nucleases. Genetics, 2010, 186(2): 451-459. |
| [29] | Cui XX, Ji D, Fisher DA, Wu YM, Briner DM, Weinstein EJ. Targeted integration in rat and mouse embryos with zinc-finger nucleases. Nat Biotechnol, 2011, 29(1): 64-67. |
| [30] | Tebas P, Stein D, Tang WW, Frank I, Wang SQ, Lee G, Spratt SK, Surosky RT, Giedlin MA, Nichol G, Holmes MC, Gregory PD, Ando DG, Kalos M, Collman RG, Binder-Scholl G, Plesa G, Hwang WT, Levine BL, June CH. Gene editing of CCR5 in autologous CD4 T cells of persons infected with HIV. N Engl J Med, 2014, 370(10): 901-910. |
| [31] | Christian M, Cermak T, Doyle EL, Schmidt C, Zhang F, Hummel A, Bogdanove AJ, Voytas DF. Targeting DNA double-strand breaks with TAL effector nucleases. Genetics, 2010, 186(2): 757-761. |
| [32] | Bak RO, Gomez-Ospina N, Porteus MH. Gene editing on center stage. Trends Genet, 2018, 34(8): 600-611. |
| [33] | Joung JK, Sander JD. TALENs: a widely applicable technology for targeted genome editing. Nat Rev Mol Cell Biol, 2013, 14(1): 49-55. |
| [34] | Qasim W, Zhan H, Samarasinghe S, Adams S, Amrolia P, Stafford S, Butler K, Rivat C, Wright G, Somana K, Ghorashian S, Pinner D, Ahsan G, Gilmour K, Lucchini G, Inglott S, Mifsud W, Chiesa R, Peggs KS, Chan L, Farzeneh F, Thrasher AJ, Vora A, Pule M, Veys P. Molecular remission of infant B-ALL after infusion of universal TALEN gene-edited CAR T cells. Sci Transl Med, 2017, 9(374): eaaj2013. |
| [35] | Ishino Y, Shinagawa H, Makino K, Amemura M, Nakata A. Nucleotide sequence of the iap gene, responsible for alkaline phosphatase isozyme conversion in Escherichia coli, and identification of the gene product. J Bacteriol, 1987, 169(12): 5429-5433. |
| [36] | Mojica FJ, Díez-Villase?or C, Soria E, Juez G. Biological significance of a family of regularly spaced repeats in the genomes of Archaea, Bacteria and mitochondria. Mol Microbiol, 2000, 36(1): 244-246. |
| [37] | Jansen R, Gaastra W, Schouls LM. Identification of genes that are associated with DNA repeats in prokaryotes. Mol Microbiol, 2002, 43(6): 1565-1575. |
| [38] | Wang JY, Doudna JA. CRISPR technology: a decade of genome editing is only the beginning. Science, 2023, 379(6629): eadd8643. |
| [39] | Mojica FJM, Díez-Villase?or C, García-Martínez J, Soria E. Intervening sequences of regularly spaced prokaryotic repeats derive from foreign genetic elements. J Mol Evol, 2005, 60(2): 174-182. |
| [40] | Pourcel C, Salvignol G, Vergnaud G. CRISPR elements in Yersinia pestis acquire new repeats by preferential uptake of bacteriophage DNA, and provide additional tools for evolutionary studies. Microbiology (Reading), 2005, 151(Pt 3): 653-663. |
| [41] | Bolotin A, Quinquis B, Sorokin A, Ehrlich SD. Clustered regularly interspaced short palindrome repeats (CRISPRs) have spacers of extrachromosomal origin. Microbiology (Reading), 2005, 151(Pt 8): 2551-2561. |
| [42] | Makarova KS, Grishin NV, Shabalina SA, Wolf YI, Koonin EV. A putative RNA-interference-based immune system in prokaryotes: computational analysis of the predicted enzymatic machinery, functional analogies with eukaryotic RNAi, and hypothetical mechanisms of action. Biol Direct, 2006, 1: 7. |
| [43] | Makarova KS, Wolf YI, Iranzo J, Shmakov SA, Alkhnbashi OS, Brouns SJJ, Charpentier E, Cheng D, Haft DH, Horvath P, Moineau S, Mojica FJM, Scott D, Shah SA, Siksnys V, Terns MP, Venclovas ?, White MF, Yakunin AF, Yan W, Zhang F, Garrett RA, Backofen R, van der Oost J, Barrangou R, Koonin EV. Evolutionary classification of CRISPR-Cas systems: a burst of class 2 and derived variants. Nat Rev Microbiol, 2020, 18(2): 67-83. |
| [44] | Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna JA, Charpentier E. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science, 2012, 337(6096): 816-821. |
| [45] | Doudna JA, Charpentier E.The new frontier of genome engineering with CRISPR-Cas9. Science, 2014, 346(6213): 1258096. |
| [46] | Zetsche B, Gootenberg JS, Abudayyeh OO, Slaymaker IM, Makarova KS, Essletzbichler P, Volz SE, Joung J, van der Oost J, Regev A, Koonin EV, Zhang F.Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system. Cell, 2015, 163(3): 759-771. |
| [47] | Abudayyeh OO, Gootenberg JS, Konermann S, Joung J, Slaymaker IM, Cox DBT, Shmakov S, Makarova KS, Semenova E, Minakhin L, Severinov K, Regev A, Lander ES, Koonin EV, Zhang F. C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector. Science, 2016, 353(6299): aaf5573. |
| [48] | Chen JS, Ma EB, Harrington LB, Da Costa M, Tian XR, Palefsky JM, Doudna JA. CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity. Science, 2018, 360(6387): 436-439. |
| [49] | Broughton JP, Deng XD, Yu GX, Fasching CL, Servellita V, Singh J, Miao X, Streithorst JA, Granados A, Sotomayor-Gonzalez A, Zorn K, Gopez A, Hsu E, Gu W, Miller S, Pan CY, Guevara H, Wadford DA, Chen JS, Chiu CY.CRISPR-Cas12-based detection of SARS-CoV-2. Nat Biotechnol, 2020, 38(7): 870-874. |
| [50] | Nguyen LT, Smith BM, Jain PK. Enhancement of trans-cleavage activity of Cas12a with engineered crRNA enables amplified nucleic acid detection. Nat Commun, 2020, 11(1): 4906. |
| [51] | Gootenberg JS, Abudayyeh OO, Lee JW, Essletzbichler P, Dy AJ, Joung J, Verdine V, Donghia N, Daringer NM, Freije CA, Myhrvold C, Bhattacharyya RP, Livny J, Regev A, Koonin EV, Hung DT, Sabeti PC, Collins JJ, Zhang F.Nucleic acid detection with CRISPR-Cas13a/C2c2. Science, 2017, 356(6336): 438-442. |
| [52] | Gootenberg JS, Abudayyeh OO, Kellner MJ, Joung J, Collins JJ, Zhang F.Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6. Science, 2018, 360(6387): 439-444. |
| [53] | Iwasaki RS, Batey RT. SPRINT: a Cas13a-based platform for detection of small molecules. Nucleic Acids Res, 2020, 48(17): e101. |
| [54] | Gasiunas G, Barrangou R, Horvath P, Siksnys V. Cas9-crRNA ribonucleoprotein complex mediates specific DNA cleavage for adaptive immunity in bacteria. Proc Natl Acad Sci USA, 2012, 109(39): E2579-E2586. |
| [55] | Rees HA, Liu DR. Base editing: precision chemistry on the genome and transcriptome of living cells. Nat Rev Genet, 2018, 19(12): 770-788. |
| [56] | Konermann S, Brigham MD, Trevino AE, Joung J, Abudayyeh OO, Barcena C, Hsu PD, Habib N, Gootenberg JS, Nishimasu H, Nureki O, Zhang F. Genome-scale transcriptional activation by an engineered CRISPR- Cas9 complex. Nature, 2015, 517(7536): 583-588. |
| [57] | Gilbert LA, Larson MH, Morsut L, Liu ZR, Brar GA, Torres SE, Stern-Ginossar N, Brandman O, Whitehead EH, Doudna JA, Lim WA, Weissman JS, Qi LS. CRISPR- mediated modular RNA-guided regulation of transcription in eukaryotes. Cell, 2013, 154(2): 442-451. |
| [58] | Hilton IB, D'Ippolito AM, Vockley CM, Thakore PI, Crawford GE, Reddy TE, Gersbach CA. Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers. Nat Biotechnol, 2015, 33(5): 510-517. |
| [59] | Zhang HX, Zhang Y, Yin H. Genome editing with mRNA encoding ZFN, TALEN, and Cas9. Mol Ther, 2019, 27(4): 735-746. |
| [60] | Ren YX, Xiao RD, Lou XM, Fang XD. Research advance and application in the gene therapy of gene editing technologies. Hereditas(Beijing), 2019, 41(1): 18-27. |
| [60] | 任云晓, 肖茹丹, 娄晓敏, 方向东. 基因编辑技术及其在基因治疗中的应用. 遗传, 2019, 41(1): 18-27. |
| [61] | McCarty NS, Graham AE, Studena L, Ledesma-Amaro R. Multiplexed CRISPR technologies for gene editing and transcriptional regulation. Nat Commun, 2020, 11(1): 1281. |
| [62] | Ye L, Wang JM, Beyer AI, Teque F, Cradick TJ, Qi ZX, Chang JC, Bao G, Muench MO, Yu JW, Levy JA, Kan YW. Seamless modification of wild-type induced pluripotent stem cells to the natural CCR5Δ32 mutation confers resistance to HIV infection. Proc Natl Acad Sci USA, 2014, 111(26): 9591-9596. |
| [63] | Yusa K, Zhou LQ, Li MA, Bradley A, Craig NL. A hyperactive piggyBac transposase for mammalian applications. Proc Natl Acad Sci USA, 2011, 108(4): 1531-1536. |
| [64] | Zhou J, Li C, Liu XJ, Chiu MC, Zhao XY, Wang D, Wei YX, Lee A, Zhang AJ, Chu H, Cai JP, Yip CCY, Chan IHY, Wong KKY, Tsang OTY, Chan KH, Chan JFW, To KKW, Chen HL, Yuen KY.Infection of bat and human intestinal organoids by SARS-CoV-2. Nat Med, 2020, 26(7): 1077-1083. |
| [65] | Lamers MM, Haagmans BL. SARS-CoV-2 pathogenesis. Nat Rev Microbiol, 2022, 20(5): 270-284. |
| [66] | Sun SH, Chen Q, Gu HJ, Yang G, Wang YX, Huang XY, Liu SS, Zhang NN, Li XF, Xiong R, Guo Y, Deng YQ, Huang WJ, Liu Q, Liu QM, Shen YL, Zhou Y, Yang X, Zhao TY, Fan CF, Zhou YS, Qin CF, Wang YC. A mouse model of SARS-CoV-2 infection and pathogenesis. Cell Host Microbe, 2020, 28(1): 124-133.e4. |
| [67] | Li B, Clohisey SM, Chia BS, Wang B, Cui A, Eisenhaure T, Schweitzer LD, Hoover P, Parkinson NJ, Nachshon A, Smith N, Regan T, Farr D, Gutmann MU, Bukhari SI, Law A, Sangesland M, Gat-Viks I, Digard P, Vasudevan S, Lingwood D, Dockrell DH, Doench JG, Baillie JK, Hacohen N. Genome-wide CRISPR screen identifies host dependency factors for influenza A virus infection. Nat Commun, 2020, 11(1): 164. |
| [68] | Hyrina A, Jones C, Chen D, Clarkson S, Cochran N, Feucht P, Hoffman G, Lindeman A, Russ C, Sigoillot F, Tsang T, Uehara K, Xie LL, Ganem D, Holdorf M. A genome-wide CRISPR screen identifies ZCCHC14 as a host factor required for hepatitis B surface antigen production. Cell Rep, 2019, 29(10): 2970-2978.e6. |
| [69] | Mei H, Zha Z, Wang W, Xie YS, Huang YG, Li WP, Wei D, Zhang XX, Qu JM, Liu J. Surfaceome CRISPR screen identifies OLFML3 as a rhinovirus-inducible IFN antagonist. Genome Biol, 2021, 22(1): 297. |
| [70] | Wei J, Alfajaro MM, DeWeirdt PC, Hanna RE, Lu-Culligan WJ, Cai WL, Strine MS, Zhang SM, Graziano VR, Schmitz CO, Chen JS, Mankowski MC, Filler RB, Ravindra NG, Gasque V, de Miguel FJ, Patil A, Chen HC, Oguntuyo KY, Abriola L, Surovtseva YV, Orchard RC, Lee B, Lindenbach BD, Politi K, van Dijk D, Kadoch C, Simon MD, Yan Q, Doench JG, Wilen CB. Genome-wide CRISPR screens reveal host factors critical for SARS-CoV-2 infection. Cell, 2021, 184(1): 76-91.e13. |
| [71] | Baggen J, Persoons L, Vanstreels E, Jansen S, Van Looveren D, Boeckx B, Geudens V, De Man J, Jochmans D, Wauters J, Wauters E, Vanaudenaerde BM, Lambrechts D, Neyts J, Dallmeier K, Thibaut HJ, Jacquemyn M, Maes P, Daelemans D.Genome-wide CRISPR screening identifies TMEM106B as a proviral host factor for SARS-CoV-2. Nat Genet, 2021, 53(4): 435-444. |
| [72] | Biering SB, Sarnik SA, Wang E, Zengel JR, Leist SR, Sch?fer A, Sathyan V, Hawkins P, Okuda K, Tau C, Jangid AR, Duffy CV, Wei J, Gilmore RC, Alfajaro MM, Strine MS, Nguyenla X, Van Dis E, Catamura C, Yamashiro LH, Belk JA, Begeman A, Stark JC, Shon DJ, Fox DM, Ezzatpour S, Huang E, Olegario N, Rustagi A, Volmer AS, Livraghi-Butrico A, Wehri E, Behringer RR, Cheon DJ, Schaletzky J, Aguilar HC, Puschnik AS, Button B, Pinsky BA, Blish CA, Baric RS, O’Neal WK, Bertozzi CR, Wilen CB, Boucher RC, Carette JE, Stanley SA, Harris E, Konermann S, Hsu PD. Genome-wide bidirectional CRISPR screens identify mucins as host factors modulating SARS-CoV-2 infection. Nat Genet, 2022, 54(8): 1078-1089. |
| [73] | Zhu SY, Liu Y, Zhou Z, Zhang ZY, Xiao X, Liu ZH, Chen A, Dong XJ, Tian F, Chen SH, Xu YY, Wang CH, Li QH, Niu XR, Pan Q, Du S, Xiao JY, Wang JW, Wei WS. Genome-wide CRISPR activation screen identifies candidate receptors for SARS-CoV-2 entry. Sci China Life Sci, 2022, 65(4): 701-717. |
| [74] | Lai Y, Cui L, Babunovic GH, Fortune SM, Doench JG, Lu TK. High-throughput CRISPR screens to dissect macrophage-Shigella interactions. mBio, 2021, 12(6): e0215821. |
| [75] | Bosch B, DeJesus MA, Poulton NC, Zhang WZ, Engelhart CA, Zaveri A, Lavalette S, Ruecker N, Trujillo C, Wallach JB, Li SQ, Ehrt S, Chait BT, Schnappinger D, Rock JM. Genome-wide gene expression tuning reveals diverse vulnerabilities of M. tuberculosis. Cell, 2021, 184(17): 4579-4592.e24. |
| [76] | Rousset F, Bikard D. CRISPR screens in the era of microbiomes. Curr Opin Microbiol, 2020, 57: 70-77. |
| [77] | Yan MY, Zheng DD, Li SS, Ding XY, Wang CL, Guo XP, Zhan LJ, Jin Q, Yang J, Sun YC. Application of combined CRISPR screening for genetic and chemical-genetic interaction profiling in Mycobacterium tuberculosis. Sci Adv, 2022, 8(47): eadd5907. |
| [78] | Yan MY, Li SS, Ding XY, Guo XP, Jin Q, Sun YC. A CRISPR-assisted nonhomologous end-joining strategy for efficient genome editing in Mycobacterium tuberculosis. mBio, 2020, 11(1): e02364-19. |
| [79] | Myhrvold C, Freije CA, Gootenberg JS, Abudayyeh OO, Metsky HC, Durbin AF, Kellner MJ, Tan AL, Paul LM, Parham LA, Garcia KF, Barnes KG, Chak B, Mondini A, Nogueira ML, Isern S, Michael SF, Lorenzana I, Yozwiak NL, MacInnis BL, Bosch I, Gehrke L, Zhang F, Sabeti PC.Field-deployable viral diagnostics using CRISPR-Cas13. Science, 2018, 360(6387): 444-448. |
| [80] | An JH, Liao XJ, Xiao TY, Qian S, Yuan J, Ye HC, Qi FR, Shen CG, Wang LF, Liu Y, Cheng XY, Li N, Cai QX, Wang F, Chen J, Li GJ, Cai QE, Liu YX, Wang YF, Zhang F, Fu Y, He Q, Tan XH, Liu L, Zhang Z. Clinical characteristics of recovered COVID-19 patients with re-detectable positive RNA test. Ann Transl Med, 2020, 8(17): 1084. |
| [81] | Joung J, Ladha A, Saito M, Segel M, Bruneau R, Huang MLW, Kim NG, Yu X, Li J, Walker BD, Greninger AL, Jerome KR, Gootenberg JS, Abudayyeh OO, Zhang F. Point-of-care testing for COVID-19 using SHERLOCK diagnostics. medRxiv, 2020, doi: 10.1101/2020.05.04.20091231. |
| [82] | Joung J, Ladha A, Saito M, Kim NG, Woolley AE, Segel M, Barretto RPJ, Ranu A, Macrae RK, Faure G, Ioannidi EI, Krajeski RN, Bruneau R, Huang MLW, Yu XG, Li JZ, Walker BD, Hung DT, Greninger AL, Jerome KR, Gootenberg JS, Abudayyeh OO, Zhang F. Detection of SARS-CoV-2 with SHERLOCK one-pot testing. N Engl J Med, 2020, 383(15): 1492-1494. |
| [83] | Ranson H, Lissenden N. Insecticide resistance in African Anopheles mosquitoes: a worsening situation that needs urgent action to maintain malaria control. Trends Parasitol, 2016, 32(3): 187-196. |
| [84] | Moyes CL, Vontas J, Martins AJ, Ng LC, Koou SY, Dusfour I, Raghavendra K, Pinto J, Corbel V, David JP, Weetman D. Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans. PLoS Negl Trop Dis, 2017, 11(7): e0005625. |
| [85] | Gantz VM, Jasinskiene N, Tatarenkova O, Fazekas A, Macias VM, Bier E, James AA.Highly efficient Cas9-mediated gene drive for population modification of the malaria vector mosquito Anopheles stephensi. Proc Natl Acad Sci USA, 2015, 112(49): E6736-E6743. |
| [86] | Kyrou K, Hammond AM, Galizi R, Kranjc N, Burt A, Beaghton AK, Nolan T, Crisanti A. A CRISPR-Cas 9 gene drive targeting doublesex causes complete population suppression in caged Anopheles gambiae mosquitoes. Nat Biotechnol, 2018, 36(11): 1062-1066. |
| [87] | Chen JY, Luo JJ, Wang YJ, Gurav AS, Li M, Akbari OS, Montell C. Suppression of female fertility in Aedes aegypti with a CRISPR-targeted male-sterile mutation. Proc Natl Acad Sci USA, 2021, 118(22): e2105075118. |
| [88] | Xu L, Wang J, Liu YL, Xie LF, Su B, Mou DL, Wang LT, Liu TT, Wang XB, Zhang B, Zhao L, Hu LD, Ning HM, Zhang YF, Deng K, Liu LF, Lu XF, Zhang T, Xu J, Li C, Wu H, Deng HK, Chen H. CRISPR-edited stem cells in a patient with HIV and acute lymphocytic leukemia. N Engl J Med, 2019, 381(13): 1240-1247. |
| [89] | Dash PK, Chen C, Kaminski R, Su H, Mancuso P, Sillman B, Zhang C, Liao SR, Sravanam S, Liu H, Waight E, Guo LL, Mathews S, Sariyer R, Mosley RL, Poluektova LY, Caocci M, Amini S, Gorantla S, Burdo TH, Edagwa B, Gendelman HE, Khalili K. CRISPR editing of CCR5 and HIV-1 facilitates viral elimination in antiretroviral drug-suppressed virus-infected humanized mice. Proc Natl Acad Sci USA, 2023, 120(19): e2217887120. |
| [90] | Kennedy EM, Bassit LC, Mueller H, Kornepati AVR, Bogerd HP, Nie T, Chatterjee P, Javanbakht H, Schinazi RF, Cullen BR. Suppression of hepatitis B virus DNA accumulation in chronically infected cells using a bacterial CRISPR/Cas RNA-guided DNA endonuclease. Virology, 2015, 476: 196-205. |
| [91] | Ramanan V, Shlomai A, Cox DBT, Schwartz RE, Michailidis E, Bhatta A, Scott DA, Zhang F, Rice CM, Bhatia SN. CRISPR/Cas9 cleavage of viral DNA efficiently suppresses hepatitis B virus. Sci Rep, 2015, 5: 10833. |
| [92] | Li H, Sheng CY, Wang S, Yang L, Liang Y, Huang Y, Liu HB, Li P, Yang CJ, Yang XX, Jia LL, Xie J, Wang LG, Hao RZ, Du XY, Xu DP, Zhou JJ, Li MZ, Sun YS, Tong YG, Li Q, Qiu SF, Song HB.Removal of integrated hepatitis B virus DNA using CRISPR-Cas9. Front Cell Infect Microbiol, 2017, 7: 91. |
| [93] | Russell TA, Stefanovic T, Tscharke DC. Engineering herpes simplex viruses by infection-transfection methods including recombination site targeting by CRISPR/Cas9 nucleases. J Virol Methods, 2015, 213: 18-25. |
| [94] | Lin CL, Li HH, Hao MR, Xiong D, Luo Y, Huang CH, Yuan Q, Zhang J, Xia NS. Increasing the efficiency of CRISPR/Cas9-mediated precise genome editing of HSV-1 virus in human cells. Sci Rep, 2016, 6: 34531. |
| [95] | Freije CA, Myhrvold C, Boehm CK, Lin AE, Welch NL, Carter A, Metsky HC, Luo CY, Abudayyeh OO, Gootenberg JS, Yozwiak NL, Zhang F, Sabeti PC.Programmable inhibition and detection of RNA viruses using Cas13. Mol Cell, 2019, 76(5): 826-837.e11. |
| [96] | Wilbie D, Walther J, Mastrobattista E. Delivery aspects of CRISPR/Cas for in vivo genome editing. Acc Chem Res, 2019, 52(6): 1555-1564. |
| [97] | Niu XR, Yin SM, Chen X, Shao TT, Li DL. Gene editing technology and its recent progress in disease therapy. Hereditas(Beijing), 2019, 41(7): 582-598. |
| [97] | 牛煦然, 尹树明, 陈曦, 邵婷婷, 李大力. 基因编辑技术及其在疾病治疗中的研究进展. 遗传, 2019, 41(7): 582-598. |
/
| 〈 |
|
〉 |