使用CRISPR-Cas9对烈性噬菌体进行靶向基因组编辑

Marie-Laurence  Lemay; Ariane C.  Renaud; Geneviève M.  Rousseau; Sylvain   Moineau

doi:10.21769/BioProtoc.2674

Improve Research Reproducibility A Bio-protocol resource

提交稿件
订阅
登录
/
注册
- 个人主页
- 编辑个人信息
- 修改密码
- 退出
CN
- EN - English
- CN - 中文

Peer-reviewed

Targeted Genome Editing of Virulent Phages Using CRISPR-Cas9

使用CRISPR-Cas9对烈性噬菌体进行靶向基因组编辑

Marie-Laurence Lemay

Ariane C. Renaud

Geneviève M. Rousseau

Sylvain Moineau email

发布: 2018年01月05日第8卷第1期 DOI: 10.21769/BioProtoc.2674 浏览次数: 17055

评审: Modesto Redrejo-RodriguezRajesh ThippeshappaAnonymous reviewer(s)

PDF

Q&A

引用

Cited by

参见作者原研究论文

The authors used this protocol in:

Cover of ACS Synthetic Biology, featuring study using the protocol.

Mar 2017

Special Issue on Protocols for Organoid Research

实验方案合集

Cell Imaging - A Special Collection for Cell Bio 2023

相关实验方案

使用PER-PCR进行基因步移挖掘未知侧翼DNA的实验方案

Zhou Yu [...] Haixing Li

2025年02月20日 1664 阅读

利用RATE-PCR全面定位EZ-Tn5转座子在阿根廷假单胞菌SA190中的插入位点

Büsra Elkatmis [...] Maged M. Saad

2025年07月20日 1998 阅读

利用等位基因交换方法编辑变形斑沙雷氏菌基因组

Ksenia Chukhontseva [...] Ilya Demidyuk

2025年09月20日 1582 阅读

Abstract

This protocol describes a straightforward method to generate specific mutations in the genome of strictly lytic phages. Briefly, a targeting CRISPR-Cas9 system and a repair template suited for homologous recombination are provided inside a bacterial host, here the Gram-positive model Lactococcus lactis MG1363. The CRISPR-Cas9 system is programmed to cleave a specific region present on the genome of the invading phage, but absent from the recombination template. The system either triggers the recombination event or exerts the selective pressure required to isolate recombinant phages. With this methodology, we generated multiple gene knockouts, a point mutation and an insertion in the genome of the virulent lactococcal phage p2. Considering the broad host range of the plasmids used in this protocol, the latter can be extrapolated to other phage-host pairs.

Keywords: Phage (噬菌体)

Lactococcus lactis (乳酸乳球菌)

Genome editing (基因组编辑)

CRISPR-Cas9 (CRISPR-Cas9)

Homologous recombination (同源重组)

Background

Phages are bacterial viruses found in abundance in every ecosystem (Suttle, 2005; Breitbart and Rohwer, 2005) and unsurprisingly, they are natural inhabitants of milk. Phage p2 is a model for the most prevalent group (Sk1virus) of virulent lactococcal phages found in the dairy industry (Deveau et al., 2006; Mahony et al., 2012) and it infects the Gram-positive bacterium Lactococcus lactis MG1363, also a model strain for basic research. Despite the status of p2 as a reference phage, almost half of its genes encode uncharacterized proteins. Likewise, a clear majority of phage genes identified by metagenomics have no functional assignment and no homolog in public databases (Hurwitz et al., 2016; Paez-Espino et al., 2016).

One of the ways to study genes is through their modification and subsequent observation of the resulting phenotypes. Phage genomes can only be modified inside a host, in their biologically active form. Virulent phages are strictly lytic; thus, their genome never integrates into the bacterial chromosome. This adds a time constraint for the in vivo modification of their DNA, which can be manipulated only during their short infection cycle. The emergence of CRISPR-Cas research in the last decade lead to the adaptation of this natural prokaryotic defense mechanism into a powerful tool to edit the genome of a plethora of organisms and viruses, including virulent phages (Kiro et al., 2014; Martel and Moineau, 2014; Box et al., 2015; Pires et al., 2016; Bari et al., 2017; Lemay et al., 2017; Manor and Qimron, 2017; Tao et al., 2017).

Here, we detail a simple and reproducible protocol to edit the genome of phage p2 using the well-known Streptococcus pyogenes Cas9 (SpCas9) cloned into the lactic acid bacterium L. lactis MG1363 (Lemay et al., 2017). Within our laboratory, this protocol has also been successfully applied to edit the genome of a virulent phage infecting the Gram-negative E. coli (unpublished), illustrating its broad applicability.

Materials and Reagents

Materials
1. Disposable Pasteur pipettes (VWR, catalog number: 14672-200 )
2. 3 mm glass beads (VWR, catalog number: 26396-508 )
  Manufacturer: Walter Stern, catalog number: 100C .
3. 100 mm glass tubes with caps (Fisher Scientific, catalog numbers: 14-961-27 and 05-888-1A )
  Manufacturer: Bal Supply, catalog number: 13144UL .
4. 150 mm glass tubes with caps (Fisher Scientific, catalog numbers: 14-961-32 and 05-888C )
  Manufacturer: Bal Supply, catalog number: 18144CL .
5. 0.5 ml micro-tubes (SARSTEDT, catalog number: 72.699 )
6. 1.5 ml micro-tubes (SARSTEDT, catalog number: 72.690 )
7. Sterile 100 x 15 mm plastic Petri dishes (‘plates’) (VWR, catalog number: 25384-302 )
8. 10 ml sterile BD Luer-Lok^TM Tip syringe (BD, catalog number: 309604 )
9. 0.2 µm sterile PES syringe filter (SARSTEDT, catalog number: 83.1826.001 )
10. 0.45 µm sterile PES syringe filter (SARSTEDT, catalog number: 83.1826 )
Phage and bacterial strain
1. Lactococcus lactis MG1363 (Félix d’Hérelle Reference Center for Bacterial Viruses, catalog number: HER1439 )
  Note: L. lactis is generally recognized as a safe bacterium and all the experiments can be performed in a biosafety level 1 laboratory.
2. Phage p2 (Félix d’Hérelle Reference Center for Bacterial Viruses, catalog number: HER457 )
Plasmids
1. pL2Cas9 (Lemay et al., 2017) (Addgene, catalog number: 98841 )
2. pNZ123 (de Vos, 1987) (L. lactis MG1363 (pNZ123)) (Félix d’Hérelle Reference Center for Bacterial Viruses, catalog number: HER1532 )
Enzymes
1. Antarctic phosphatase (5,000 U per ml) (New England Biolabs, catalog number: M0289S )
2. BsaI (10,000 U per ml) (New England Biolabs, catalog number: R0535S )
3. Lysozyme (20,000 U per mg dry weight) (Thermo Fisher Scientific, catalog number: 89833 )
4. Q5 DNA polymerase (2,000 U per ml) (New England Biolabs, catalog number: M0491S )
5. T4 DNA ligase (1,000 U per ml) (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 15224017 )
6. T4 polynucleotide kinase (10,000 U per ml) (Thermo Fisher Scientific, Thermo Scientific^TM, catalog number: EK0031 )
7. Taq DNA polymerase (5,000 U per ml) (NBS Biologicals, catalog number: 9K-001-0034 )
8. XbaI (20,000 U per ml) (New England Biolabs, catalog number: R0145S )
Reagents
1. AccuGENE^TM molecular biology water (Lonza, catalog number: 51200 )
2. Agarose LE (Roche Diagnostics, catalog number: 11685678001 )
3. BD^TM Bacto^TM Brain Heart Infusion (BHI) (Fisher Scientific, catalog number: DF0037-17-8 )
  Manufacturer: BD, catalog number: 237500 .
4. Calcium chloride dihydrate (CaCl₂·2H₂O) (Sigma-Aldrich, catalog number: C5080 )
5. Chloramphenicol (Sigma-Aldrich, catalog number: C0378 )
6. EDTA-Na₂ (Sigma-Aldrich, catalog number: E5134 )
7. Erythromycin (Fisher Scientific, catalog number: 10583315 )
8. 95% ethanol (Commercial Alcohols, catalog number: P016EA95 )
9. 100% ethanol (Commercial Alcohols, catalog number: P016EAAN )
10. EZ-Vision^® Three (VWR, catalog number: 97063-166 )
11. Glacial acetic acid (Caledon Laboratories, catalog number: 1000-1-29 )
12. Glucose monohydrate (Sigma-Aldrich, catalog number: 49159 )
13. Glycerol (Merck, catalog number: GX0185-2 )
14. Glycine (Merck, catalog number: 4810-OP )
15. Granulated agar (Fisher Scientific, catalog number: BP1423-500 )
16. Hydrochloric acid ( HCl) (Fisher Scientific, catalog number: 351285-212 )
17. High DNA Mass Ladder (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 10496016 )
18. 1 Kb Plus DNA Ladder (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 10787018 )
19. Low DNA Mass Ladder (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 10068013 )
20. Oxoid^TM M17 broth (Thermo Fisher Scientific, Thermo Scientific^TM, catalog number: CM0817 )
21. Magnesium sulfate heptahydrate ( MgSO₄·7H₂O) (Caledon Laboratories, catalog number: 4860-1-70 )
22. Magnesium chloride hexahydrate (MgCl₂·6H₂O) (VWR, catalog number: BDH9244 )
23. Sodium chloride (NaCl) (Anachemia, catalog number: 81708-380 )
24. Primers (Table 1) (customized by Thermo Fisher Scientific, www.thermofisher.com)
  
  Table 1. Primers used in this protocol
  
  ^aRestriction sites for ligation and overhangs for Gibson Assembly are underlined. ‘N’ stands for any nucleotides and ‘x’ for any number of nucleotides required for the amplification of a fragment of interest.
25. Sodium acetate (NaAc) (Sigma-Aldrich, catalog number: S2889 )
26. Sucrose (Sigma-Aldrich, catalog number: S0389 )
27. Tris (Base), Ultrapure (Avantor Performance Materials, catalog number: 4109-6 )
28. 0.8% and 2% agarose gel (see Recipes)
29. BHI agar medium supplemented with erythromycin (see Recipes)
30. BHI medium supplemented with erythromycin (see Recipes)
31. 2 M CaCl₂ (see Recipes)
32. 10 mg/ml chloramphenicol stock solution (see Recipes)
33. 10 mg/ml and 75 mg/ml erythromycin stock solution (see Recipes)
34. 70% ethanol (see Recipes)
35. GM17 agar medium supplemented with CaCl₂ or antibiotics (see Recipes)
36. GM17 medium (see Recipes)
37. GM17 soft agar medium supplemented with CaCl₂(see Recipes)
38. Glycine shock solution (see Recipes)
39. 1 M MgCl₂ (see Recipes)
40. 10x Phage buffer (see Recipes)
41. Recovery solution (see Recipes)
42. 50x TAE buffer (see Recipes)
43. Wash solution (see Recipes)
Kits
1. Gibson Assembly^® Master Mix (New England Biolabs, catalog number: E2611S )
2. QIAGEN Plasmid Maxi Kit (QIAGEN, catalog number: 12162 )
3. QIAquick PCR Purification Kit (QIAGEN, catalog number: 28104 )

Equipment

Autoclave
Benchtop microcentrifuge (Eppendorf, model: 5415 D )
Bunsen burner
Centrifuge bottles (SS-34)
Centrifuge Sorvall RC5C and rotor SS-34 (Thermo Fisher Scientific, catalog number: 28020 )
Dry bath with heating block (VWR, catalog numbers: 13259-034 and 13259-130 )
Electroporation cuvettes, 0.2 cm electrode gap (Bio-Rad Laboratories, catalog number: 1652086 )
Gene Pulser II electroporator (Bio-Rad Laboratories, catalog number: 165-2109 )
Incubator-shaker set to 37 °C
Note: Incubator that can be set to 30 °C (shaking not necessary) and 37 °C.
Micropipettes (Nichiryo, catalog numbers: 00-NPX2-10 , 00-NPX2-100 , 00-NPX2-1000 )
Note: Sterile filtered pipette tips to reduce contamination of the micropipettes by bioaerosols.
Microwave
MultiDoc-It^TM Imaging System (UVP, catalog number: 97-0200-01 )
PCR Thermal Cycler (MJ Research, model: PTC-200 )
Power supply (Bio-Rad Laboratories, model: PowerPac 300 )
Spectra/Por^® 1 dialysis membranes, MWCO 6-8000 (VWR, catalog number: 28170-138 )
Manufacturer: Spectrum, catalog number: S632650 .
Spectrophotometer Spectronic 20D
Tweezers
VWR^® Midi Plus 15 Horizontal Electrophoresis Systems (VWR, catalog number: 89032-296 )

Procedure

English

中文翻译

文章信息

版权信息

如何引用

Lemay, M., Renaud, A., Rousseau, G. M. and Moineau, S. (2018). Targeted Genome Editing of Virulent Phages Using CRISPR-Cas9. Bio-protocol 8(1): e2674. DOI: 10.21769/BioProtoc.2674.