Trypanosoma cruzi STIB980: A TcI Strain for Drug Discovery and Reverse Genetics

被引:2
|
作者
Fesser, Anna [1 ,2 ]
Beilstein, Sabina [1 ,2 ]
Kaiser, Marcel [1 ,2 ]
Schmidt, Remo S. [1 ,2 ]
Maeser, Pascal [1 ,2 ]
Menna-Barreto, Rubem F. S.
机构
[1] Swiss Trop & Publ Hlth Inst, Dept Med Parasitol & Infect Biol, CH-4123 Allschwil, Switzerland
[2] Univ Basel, CH-4001 Basel, Switzerland
来源
PATHOGENS | 2023年 / 12卷 / 10期
基金
瑞士国家科学基金会;
关键词
Trypanosoma cruzi; genome sequencing; reverse genetics; drug efficacy testing; IDENTIFICATION; BENZNIDAZOLE; POSACONAZOLE; INFECTIONS; ALIGNMENT; PARASITES; DISEASE;
D O I
10.3390/pathogens12101217
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Since the first published genome sequence of Trypanosoma cruzi in 2005, there have been tremendous technological advances in genomics, reverse genetics, and assay development for this elusive pathogen. However, there is still an unmet need for new and better drugs to treat Chagas disease. Here, we introduce a T. cruzi assay strain that is useful for drug research and basic studies of host-pathogen interactions. T. cruzi STIB980 is a strain of discrete typing unit TcI that grows well in culture as axenic epimastigotes or intracellular amastigotes. We evaluated the optimal parameters for genetic transfection and constructed derivatives of T. cruzi STIB980 that express reporter genes for fluorescence- or bioluminescence-based drug efficacy testing, as well as a Cas9-expressing line for CRISPR/Cas9-mediated gene editing. The genome of T. cruzi STIB980 was sequenced by combining short-read Illumina with long-read Oxford Nanopore technologies. The latter served as the primary assembly and the former to correct mistakes. This resulted in a high-quality nuclear haplotype assembly of 28 Mb in 400 contigs, containing 10,043 open-reading frames with a median length of 1077 bp. We believe that T. cruzi STIB980 is a useful addition to the antichagasic toolbox and propose that it can serve as a DTU TcI reference strain for drug efficacy testing.
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页数:12
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