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Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line

BACKGROUND: The aquatic pulmonate snail Biomphalaria glabrata is a significant vector and laboratory host for the parasitic flatworm Schistosoma mansoni, an etiological agent for the neglected tropical disease schistosomiasis. Much is known regarding the host-parasite interactions of these two organ...

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Autores principales: Wheeler, Nicolas J., Dinguirard, Nathalie, Marquez, Joshua, Gonzalez, Adrian, Zamanian, Mostafa, Yoshino, Timothy P., Castillo, Maria G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122571/
https://www.ncbi.nlm.nih.gov/pubmed/30180879
http://dx.doi.org/10.1186/s13071-018-3059-2
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author Wheeler, Nicolas J.
Dinguirard, Nathalie
Marquez, Joshua
Gonzalez, Adrian
Zamanian, Mostafa
Yoshino, Timothy P.
Castillo, Maria G.
author_facet Wheeler, Nicolas J.
Dinguirard, Nathalie
Marquez, Joshua
Gonzalez, Adrian
Zamanian, Mostafa
Yoshino, Timothy P.
Castillo, Maria G.
author_sort Wheeler, Nicolas J.
collection PubMed
description BACKGROUND: The aquatic pulmonate snail Biomphalaria glabrata is a significant vector and laboratory host for the parasitic flatworm Schistosoma mansoni, an etiological agent for the neglected tropical disease schistosomiasis. Much is known regarding the host-parasite interactions of these two organisms, and the B. glabrata embryonic (Bge) cell line has been an invaluable resource in these studies. The B. glabrata BB02 genome sequence was recently released, but nothing is known of the sequence variation between this reference and the Bge cell genome, which has likely accumulated substantial genetic variation in the ~50 years since its isolation. RESULTS: Here, we report the genome sequence of our laboratory subculture of the Bge cell line (designated Bge3), which we mapped to the B. glabrata BB02 reference genome. Single nucleotide variants (SNVs) were predicted and focus was given to those SNVs that are most likely to affect the structure or expression of protein-coding genes. Furthermore, we have highlighted and validated high-impact SNVs in genes that have often been studied using Bge cells as an in vitro model, and other genes that may have contributed to the immortalization of this cell line. We also resolved representative karyotypes for the Bge3 subculture, which revealed a mixed population exhibiting substantial aneuploidy, in line with previous reports from other Bge subcultures. CONCLUSIONS: The Bge3 genome differs from the B. glabrata BB02 reference genome in both sequence and structure, and these are likely to have significant biological effects. The availability of the Bge3 genome sequence, and an awareness of genomic differences with B. glabrata, will inform the design of experiments to understand gene function in this unique in vitro snail cell model. Additionally, this resource will aid in the development of new technologies and molecular approaches that promise to reveal more about this schistosomiasis-transmitting snail vector. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3059-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-61225712018-09-05 Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line Wheeler, Nicolas J. Dinguirard, Nathalie Marquez, Joshua Gonzalez, Adrian Zamanian, Mostafa Yoshino, Timothy P. Castillo, Maria G. Parasit Vectors Research BACKGROUND: The aquatic pulmonate snail Biomphalaria glabrata is a significant vector and laboratory host for the parasitic flatworm Schistosoma mansoni, an etiological agent for the neglected tropical disease schistosomiasis. Much is known regarding the host-parasite interactions of these two organisms, and the B. glabrata embryonic (Bge) cell line has been an invaluable resource in these studies. The B. glabrata BB02 genome sequence was recently released, but nothing is known of the sequence variation between this reference and the Bge cell genome, which has likely accumulated substantial genetic variation in the ~50 years since its isolation. RESULTS: Here, we report the genome sequence of our laboratory subculture of the Bge cell line (designated Bge3), which we mapped to the B. glabrata BB02 reference genome. Single nucleotide variants (SNVs) were predicted and focus was given to those SNVs that are most likely to affect the structure or expression of protein-coding genes. Furthermore, we have highlighted and validated high-impact SNVs in genes that have often been studied using Bge cells as an in vitro model, and other genes that may have contributed to the immortalization of this cell line. We also resolved representative karyotypes for the Bge3 subculture, which revealed a mixed population exhibiting substantial aneuploidy, in line with previous reports from other Bge subcultures. CONCLUSIONS: The Bge3 genome differs from the B. glabrata BB02 reference genome in both sequence and structure, and these are likely to have significant biological effects. The availability of the Bge3 genome sequence, and an awareness of genomic differences with B. glabrata, will inform the design of experiments to understand gene function in this unique in vitro snail cell model. Additionally, this resource will aid in the development of new technologies and molecular approaches that promise to reveal more about this schistosomiasis-transmitting snail vector. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-018-3059-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-04 /pmc/articles/PMC6122571/ /pubmed/30180879 http://dx.doi.org/10.1186/s13071-018-3059-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wheeler, Nicolas J.
Dinguirard, Nathalie
Marquez, Joshua
Gonzalez, Adrian
Zamanian, Mostafa
Yoshino, Timothy P.
Castillo, Maria G.
Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title_full Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title_fullStr Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title_full_unstemmed Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title_short Sequence and structural variation in the genome of the Biomphalaria glabrata embryonic (Bge) cell line
title_sort sequence and structural variation in the genome of the biomphalaria glabrata embryonic (bge) cell line
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122571/
https://www.ncbi.nlm.nih.gov/pubmed/30180879
http://dx.doi.org/10.1186/s13071-018-3059-2
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