4.3 Article

Transcriptional effects of electroporation on Echinococcus multilocularis primary cell culture

期刊

PARASITOLOGY RESEARCH
卷 121, 期 4, 页码 1155-1168

出版社

SPRINGER
DOI: 10.1007/s00436-022-07427-5

关键词

Echinococcus multilocularis; Transcriptomic analysis; Electroporation; Primary cell culture

资金

  1. ERANET LAC Project [ELAC2015/T080544]
  2. Wellcome Trust [107475/Z/15/Z, WT 098051]
  3. Agencia Nacional de Promocion Cientifica y Tecnologica (ANPCyT), Argentina [PICT 2017-2966]
  4. Agencia Nacional de Promocion Cientifica y Tecnologica, Argentina [2121, 3367]
  5. Consultant Laboratory for Echinococcosis of the Robert Koch Institute
  6. Consejo Nacional de Investigaciones Cientificas y Tecnologicas (CONICET), Project: PIP 2015

向作者/读者索取更多资源

This study compared the genome-wide expression profiles between primary cells of E. multilocularis and primary cells under electroporated conditions after 48 hours of culture using transcriptome data and bioinformatic analyses. They found that about 15% of genes showed significant variation in expression level in electroporated cells, including highly upregulated genes involved in detoxification and membrane remodeling. Genes related to carbohydrate metabolism, proteolysis, calcium ion binding, and microtubule processing were also significantly altered.
Echinococcus multilocularis is the etiological agent of alveolar echinococcosis (AE), a serious parasitic disease in the Northern Hemisphere. The E. multilocularis primary cell cultivation system, together with E. multilocularis genome data and a range of pioneering molecular-based tools have advanced the research on this and other cestodes. RNA interference (RNAi) and microRNA knock-down have recently contributed to the study of the cellular and molecular basis of tapeworm development and host-parasite interaction. These, as well as other techniques, normally involve an electroporation step for the delivery of RNA, DNA, peptides, and small molecules into cells. Using transcriptome data and bioinformatic analyses, we herein report a genome-wide comparison between primary cells of E. multilocularis and primary cells under electroporated conditions after 48 h of culture. We observed that similar to 15% of genes showed a significant variation in expression level, including highly upregulated genes in electroporated cells, putatively involved in detoxification and membrane remodeling. Furthermore, we found genes related to carbohydrate metabolism, proteolysis, calcium ion binding and microtubule processing significantly altered, which could explain the cellular dispersion and the reduced formation of cellular aggregates observed during the first 48 h after electroporation.

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