Table 1 Efficiency of CRISPR-based editing of ADE2 in multiple isolates of C. parapsilosis.

From: Gene editing in clinical isolates of Candida parapsilosis using CRISPR/Cas9

Strain

sgRNA

% pink transformantsa

−RTc

+RTc

Exp 1

Exp 2

Exp 1

Exp 2

CLIB214d

sgADE2-B

0%

0%

80%

100%

CLIB214d

sgADE2-D

0%

0%

94%

100%

103d

sgADE2-B

0%

12%

50%

80%

02-203d

sgADE2-B

0%

0%

87%

94%

73/037

sgADE2-B

11%

0%

5%

17%

73/107d

sgADE2-B

4%

0%b

4%

16%

74/046

sgADE2-B

0%

0%b

30%

4%

81/040

sgADE2-B

0%

0%

0%

0%

81/042d

sgADE2-B

0%

0%b

8%

14%

81/253d

sgADE2-B

0%

1%

12%

35%

90–137

sgADE2-B

20%

10%

37%

67%

CDC165d

sgADE2-B

20%

1%

0%

87%

CDC167

sgADE2-B

0%

1%

15%

14%

CDC173

sgADE2-B

0%

3%

13%

10%

CDC177d

sgADE2-B

4%

0%b

3%

24%

CDC179

sgADE2-B

0%

11%

35%

25%

CDC317

sgADE2-B

0%

13%

16%

16%

J931058

sgADE2-B

0%

31%

100%

77%

J931845

sgADE2-B

0%

0%b

28%

13%

J950218

sgADE2-B

11%

1%

14%

7%

J951066

sgADE2-B

0%

14%

11%

85%

J960578d

sgADE2-B

0%

4%

25%

13%

J961250

sgADE2-B

0%

0%b

29%

19%

  1. aTransformation efficiencies from two experiments performed by two people. 81/040 and CLIB214 were transformed several times and the results from two experiments are shown.
  2. b<1% pink colonies.
  3. cRT = repair template.
  4. dIsolates sequenced to confirm mutation (Fig. S3).