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Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus
Among parasitic helminths, biological features of Echinococcus granulosus have been a focus of particular interest in biology and medicine. The determinants and underlying molecular mechanisms of Echinococcus development in different host settings is largely unknown. The phenomenal bi-directional de...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406006/ https://www.ncbi.nlm.nih.gov/pubmed/30846822 http://dx.doi.org/10.1038/s41598-019-40656-w |
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author | Mousavi, Seyed Mohammad Afgar, Ali Mohammadi, Mohammad Ali Mortezaei, Seifollah Sadeghi, Balal Harandi, Majid Fasihi |
author_facet | Mousavi, Seyed Mohammad Afgar, Ali Mohammadi, Mohammad Ali Mortezaei, Seifollah Sadeghi, Balal Harandi, Majid Fasihi |
author_sort | Mousavi, Seyed Mohammad |
collection | PubMed |
description | Among parasitic helminths, biological features of Echinococcus granulosus have been a focus of particular interest in biology and medicine. The determinants and underlying molecular mechanisms of Echinococcus development in different host settings is largely unknown. The phenomenal bi-directional development of E. granulosus protoscoleces into multi-proglottid and/or microcysts, is a fascinating feature of the parasite cultivation. Calmodulin (CaM) is the major intracellular Ca2+ binding protein in plant and animal organisms. Many Ca(2+)-related processes in the physiology of eukaryotic organisms are CaM-dependent, however little is known on the role of CaM in platyhelminths growth and development. Small interfering (si) RNA-induced manipulations of the genes involving in the parasite development is an opportunity to explore novel approaches for cystic echinococcosis (CE) prevention and management. Regarding the fundamental role of CaM in cellular function of the parasites, in this study, we investigated the molecular and morphological changes induced by siRNA on CaM in different in vitro stages of E. granulosus. Three developmental stages of the tapeworm, protoscoleces, microcysts and strobilated worms, were cultivated in vitro in mono- and di-phasic media and three delivery methods, i.e. electroporation, soaking and electro-soaking, were used for RNA interference. The level of mRNA suppression as well as the phenotypic changes of the parasites were measured. Following RNA interference, EgCaM mRNA suppressions of 65–99% were recorded in different stages of the tapeworm as compared to untreated/unrelated siRNA controls. Lower viability, growth retardation, morphological abnormalities as well as EgCaM expression suppression were documented in the parasite implying potential of siRNA technology for the prevention and management of CE. |
format | Online Article Text |
id | pubmed-6406006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64060062019-03-12 Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus Mousavi, Seyed Mohammad Afgar, Ali Mohammadi, Mohammad Ali Mortezaei, Seifollah Sadeghi, Balal Harandi, Majid Fasihi Sci Rep Article Among parasitic helminths, biological features of Echinococcus granulosus have been a focus of particular interest in biology and medicine. The determinants and underlying molecular mechanisms of Echinococcus development in different host settings is largely unknown. The phenomenal bi-directional development of E. granulosus protoscoleces into multi-proglottid and/or microcysts, is a fascinating feature of the parasite cultivation. Calmodulin (CaM) is the major intracellular Ca2+ binding protein in plant and animal organisms. Many Ca(2+)-related processes in the physiology of eukaryotic organisms are CaM-dependent, however little is known on the role of CaM in platyhelminths growth and development. Small interfering (si) RNA-induced manipulations of the genes involving in the parasite development is an opportunity to explore novel approaches for cystic echinococcosis (CE) prevention and management. Regarding the fundamental role of CaM in cellular function of the parasites, in this study, we investigated the molecular and morphological changes induced by siRNA on CaM in different in vitro stages of E. granulosus. Three developmental stages of the tapeworm, protoscoleces, microcysts and strobilated worms, were cultivated in vitro in mono- and di-phasic media and three delivery methods, i.e. electroporation, soaking and electro-soaking, were used for RNA interference. The level of mRNA suppression as well as the phenotypic changes of the parasites were measured. Following RNA interference, EgCaM mRNA suppressions of 65–99% were recorded in different stages of the tapeworm as compared to untreated/unrelated siRNA controls. Lower viability, growth retardation, morphological abnormalities as well as EgCaM expression suppression were documented in the parasite implying potential of siRNA technology for the prevention and management of CE. Nature Publishing Group UK 2019-03-07 /pmc/articles/PMC6406006/ /pubmed/30846822 http://dx.doi.org/10.1038/s41598-019-40656-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mousavi, Seyed Mohammad Afgar, Ali Mohammadi, Mohammad Ali Mortezaei, Seifollah Sadeghi, Balal Harandi, Majid Fasihi Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title | Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title_full | Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title_fullStr | Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title_full_unstemmed | Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title_short | Calmodulin-specific small interfering RNA induces consistent expression suppression and morphological changes in Echinococcus granulosus |
title_sort | calmodulin-specific small interfering rna induces consistent expression suppression and morphological changes in echinococcus granulosus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406006/ https://www.ncbi.nlm.nih.gov/pubmed/30846822 http://dx.doi.org/10.1038/s41598-019-40656-w |
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