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Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae

BACKGROUND: ‘Candidatus Berkiella cookevillensis’ and ‘Ca. Berkiella aquae’ have previously been described as intranuclear bacteria of amoebae. Both bacteria were isolated from amoebae and were described as appearing within the nuclei of Acanthamoeba polyphaga and ultimately lysing their host cells...

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Autores principales: Chamberlain, Nicholas B., Mehari, Yohannes T., Hayes, B. Jason, Roden, Colleen M., Kidane, Destaalem T., Swehla, Andrew J., Lorenzana-DeWitt, Mario A., Farone, Anthony L., Gunderson, John H., Berk, Sharon G., Farone, Mary B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507137/
https://www.ncbi.nlm.nih.gov/pubmed/31072343
http://dx.doi.org/10.1186/s12866-019-1457-z
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author Chamberlain, Nicholas B.
Mehari, Yohannes T.
Hayes, B. Jason
Roden, Colleen M.
Kidane, Destaalem T.
Swehla, Andrew J.
Lorenzana-DeWitt, Mario A.
Farone, Anthony L.
Gunderson, John H.
Berk, Sharon G.
Farone, Mary B.
author_facet Chamberlain, Nicholas B.
Mehari, Yohannes T.
Hayes, B. Jason
Roden, Colleen M.
Kidane, Destaalem T.
Swehla, Andrew J.
Lorenzana-DeWitt, Mario A.
Farone, Anthony L.
Gunderson, John H.
Berk, Sharon G.
Farone, Mary B.
author_sort Chamberlain, Nicholas B.
collection PubMed
description BACKGROUND: ‘Candidatus Berkiella cookevillensis’ and ‘Ca. Berkiella aquae’ have previously been described as intranuclear bacteria of amoebae. Both bacteria were isolated from amoebae and were described as appearing within the nuclei of Acanthamoeba polyphaga and ultimately lysing their host cells within 4 days. Both bacteria are Gammaproteobacteria in the order Legionellales with the greatest similarity to Coxiella burnetii. Neither bacterium grows axenically in artificial culture media. In this study, we further characterized ‘Ca. B. cookevillensis’ by demonstrating association with nuclei of human phagocytic and nonphagocytic cell lines. RESULTS: Transmission electron microscopy (TEM) and confocal microscopy were used to confirm nuclear co-localization of ‘Ca. B. cookevillensis’ in the amoeba host A. polyphaga with 100% of cells having bacteria co-localized with host nuclei by 48 h. TEM and confocal microscopy demonstrated that the bacterium was also observed to be closely associated with nuclei of human U937 and THP-1 differentiated macrophage cell lines and nonphagocytic HeLa human epithelial-like cells. Immunofluorescent staining revealed that the bacteria-containing vacuole invaginates the nuclear membranes and appears to cross from the cytoplasm into the nucleus as an intact vacuole. CONCLUSION: Results of this study indicate that a novel coccoid bacterium isolated from amoebae can infect human cell lines by associating with the host cell nuclei, either by crossing the nuclear membranes or by deeply invaginating the nuclear membranes. When associated with the nuclei, the bacteria appear to be bound within a vacuole and replicate to high numbers by 48 h. We believe this is the first report of such a process involving bacteria and human cell lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-019-1457-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-65071372019-05-13 Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae Chamberlain, Nicholas B. Mehari, Yohannes T. Hayes, B. Jason Roden, Colleen M. Kidane, Destaalem T. Swehla, Andrew J. Lorenzana-DeWitt, Mario A. Farone, Anthony L. Gunderson, John H. Berk, Sharon G. Farone, Mary B. BMC Microbiol Research Article BACKGROUND: ‘Candidatus Berkiella cookevillensis’ and ‘Ca. Berkiella aquae’ have previously been described as intranuclear bacteria of amoebae. Both bacteria were isolated from amoebae and were described as appearing within the nuclei of Acanthamoeba polyphaga and ultimately lysing their host cells within 4 days. Both bacteria are Gammaproteobacteria in the order Legionellales with the greatest similarity to Coxiella burnetii. Neither bacterium grows axenically in artificial culture media. In this study, we further characterized ‘Ca. B. cookevillensis’ by demonstrating association with nuclei of human phagocytic and nonphagocytic cell lines. RESULTS: Transmission electron microscopy (TEM) and confocal microscopy were used to confirm nuclear co-localization of ‘Ca. B. cookevillensis’ in the amoeba host A. polyphaga with 100% of cells having bacteria co-localized with host nuclei by 48 h. TEM and confocal microscopy demonstrated that the bacterium was also observed to be closely associated with nuclei of human U937 and THP-1 differentiated macrophage cell lines and nonphagocytic HeLa human epithelial-like cells. Immunofluorescent staining revealed that the bacteria-containing vacuole invaginates the nuclear membranes and appears to cross from the cytoplasm into the nucleus as an intact vacuole. CONCLUSION: Results of this study indicate that a novel coccoid bacterium isolated from amoebae can infect human cell lines by associating with the host cell nuclei, either by crossing the nuclear membranes or by deeply invaginating the nuclear membranes. When associated with the nuclei, the bacteria appear to be bound within a vacuole and replicate to high numbers by 48 h. We believe this is the first report of such a process involving bacteria and human cell lines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-019-1457-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-09 /pmc/articles/PMC6507137/ /pubmed/31072343 http://dx.doi.org/10.1186/s12866-019-1457-z Text en © The Author(s). 2019 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 Article
Chamberlain, Nicholas B.
Mehari, Yohannes T.
Hayes, B. Jason
Roden, Colleen M.
Kidane, Destaalem T.
Swehla, Andrew J.
Lorenzana-DeWitt, Mario A.
Farone, Anthony L.
Gunderson, John H.
Berk, Sharon G.
Farone, Mary B.
Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title_full Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title_fullStr Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title_full_unstemmed Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title_short Infection and nuclear interaction in mammalian cells by ‘Candidatus Berkiella cookevillensis’, a novel bacterium isolated from amoebae
title_sort infection and nuclear interaction in mammalian cells by ‘candidatus berkiella cookevillensis’, a novel bacterium isolated from amoebae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507137/
https://www.ncbi.nlm.nih.gov/pubmed/31072343
http://dx.doi.org/10.1186/s12866-019-1457-z
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