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Utilization of proliferable extracellular amastigotes for transient gene expression, drug sensitivity assay, and CRISPR/Cas9-mediated gene knockout in Trypanosoma cruzi.
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- المؤلفون: Takagi Y;Takagi Y; Akutsu Y; Akutsu Y; Doi M; Doi M; Furukawa K; Furukawa K
- المصدر:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2019 Jan 14; Vol. 13 (1), pp. e0007088. Date of Electronic Publication: 2019 Jan 14 (Print Publication: 2019).
- نوع النشر :
Journal Article; Research Support, Non-U.S. Gov't
- اللغة:
English
- معلومة اضافية
- المصدر:
Publisher: Public Library of Science Country of Publication: United States NLM ID: 101291488 Publication Model: eCollection Cited Medium: Internet ISSN: 1935-2735 (Electronic) Linking ISSN: 19352727 NLM ISO Abbreviation: PLoS Negl Trop Dis Subsets: MEDLINE
- بيانات النشر:
Original Publication: San Francisco, CA : Public Library of Science
- الموضوع:
- نبذة مختصرة :
Trypanosoma cruzi has three distinct life cycle stages; epimastigote, trypomastigote, and amastigote. Amastigote is the replication stage in host mammalian cells, hence this stage of parasite has clinical significance in drug development research. Presence of extracellular amastigotes (EA) and their infection capability have been known for some decades. Here, we demonstrate that EA can be utilized as an axenic culture to aid in stage-specific study of T. cruzi. Amastigote-like property of axenic amastigote can be sustained in LIT medium at 37°C at least for 1 week, judging from their morphology, amastigote-specific UTR-regulated GFP expression, and stage-specific expression of selected endogenous genes. Inhibitory effect of benznidazole and nifurtimox on axenic amastigotes was comparable to that on intracellular amastigotes. Exogenous nucleic acids can be transfected into EA via conventional electroporation, and selective marker could be utilized for enrichment of transfectants. We also demonstrate that CRISPR/Cas9-mediated gene knockout can be performed in EA. Essentiality of the target gene can be evaluated by the growth capability of the knockout EA, either by continuation of axenic culturing or by host infection and following replication as intracellular amastigotes. By taking advantage of the accessibility and sturdiness of EA, we can potentially expand our experimental freedom in studying amastigote stage of T. cruzi.
Competing Interests: The authors have declared that no competing interests exist.
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- الرقم المعرف:
0 (Antiprotozoal Agents)
0 (Nitroimidazoles)
EC 3.1.- (CRISPR-Associated Protein 9)
M84I3K7C2O (Nifurtimox)
YC42NRJ1ZD (benzonidazole)
- الموضوع:
Date Created: 20190115 Date Completed: 20190211 Latest Revision: 20200309
- الموضوع:
20240628
- الرقم المعرف:
PMC6347291
- الرقم المعرف:
10.1371/journal.pntd.0007088
- الرقم المعرف:
30640901
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