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Cell lines from the soft tick Ornithodoros moubata

Primary cell cultures (n = 16) were initiated from tissues of embryonic and neonatal larval Ornithodoros moubata following methods developed for hard ticks. After maintenance for 20–25 months in vitro, cell multiplication commenced in surviving cultures, leading to the establishment of six cell line...

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Detalles Bibliográficos
Autores principales: Bell-Sakyi, Lesley, Růžek, Daniel, Gould, Ernest A.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755799/
https://www.ncbi.nlm.nih.gov/pubmed/19252822
http://dx.doi.org/10.1007/s10493-009-9258-y
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author Bell-Sakyi, Lesley
Růžek, Daniel
Gould, Ernest A.
author_facet Bell-Sakyi, Lesley
Růžek, Daniel
Gould, Ernest A.
author_sort Bell-Sakyi, Lesley
collection PubMed
description Primary cell cultures (n = 16) were initiated from tissues of embryonic and neonatal larval Ornithodoros moubata following methods developed for hard ticks. After maintenance for 20–25 months in vitro, cell multiplication commenced in surviving cultures, leading to the establishment of six cell lines designated OME/CTVM21, 22, 24, 25, 26 and 27. All lines are maintained at 28°C, with subculture at 2–8 week intervals. The cultures comprise heterogeneous populations of large cells of 15–100 μm in diameter, often with finger-like protrusions and/or intracellular crystals, rarely attached, predominantly floating and forming clumps or hollow multicellular vesicles up to 1 mm in diameter. Attempts to cryopreserve the cells are described. Tick-borne encephalitis virus has been serially passaged ten times in OME/CTVM21 cells without significant decrease in virus production and with no change in its biological properties as shown by the size and morphology of plaques produced in porcine kidney cells.
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spelling pubmed-27557992009-10-07 Cell lines from the soft tick Ornithodoros moubata Bell-Sakyi, Lesley Růžek, Daniel Gould, Ernest A. Exp Appl Acarol Article Primary cell cultures (n = 16) were initiated from tissues of embryonic and neonatal larval Ornithodoros moubata following methods developed for hard ticks. After maintenance for 20–25 months in vitro, cell multiplication commenced in surviving cultures, leading to the establishment of six cell lines designated OME/CTVM21, 22, 24, 25, 26 and 27. All lines are maintained at 28°C, with subculture at 2–8 week intervals. The cultures comprise heterogeneous populations of large cells of 15–100 μm in diameter, often with finger-like protrusions and/or intracellular crystals, rarely attached, predominantly floating and forming clumps or hollow multicellular vesicles up to 1 mm in diameter. Attempts to cryopreserve the cells are described. Tick-borne encephalitis virus has been serially passaged ten times in OME/CTVM21 cells without significant decrease in virus production and with no change in its biological properties as shown by the size and morphology of plaques produced in porcine kidney cells. Springer Netherlands 2009-03-01 2009-11 /pmc/articles/PMC2755799/ /pubmed/19252822 http://dx.doi.org/10.1007/s10493-009-9258-y Text en © Springer Science+Business Media B.V. 2009
spellingShingle Article
Bell-Sakyi, Lesley
Růžek, Daniel
Gould, Ernest A.
Cell lines from the soft tick Ornithodoros moubata
title Cell lines from the soft tick Ornithodoros moubata
title_full Cell lines from the soft tick Ornithodoros moubata
title_fullStr Cell lines from the soft tick Ornithodoros moubata
title_full_unstemmed Cell lines from the soft tick Ornithodoros moubata
title_short Cell lines from the soft tick Ornithodoros moubata
title_sort cell lines from the soft tick ornithodoros moubata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2755799/
https://www.ncbi.nlm.nih.gov/pubmed/19252822
http://dx.doi.org/10.1007/s10493-009-9258-y
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