Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783416967987724288 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6507137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chamberlainnicholasb infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT mehariyohannest infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT hayesbjason infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT rodencolleenm infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT kidanedestaalemt infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT swehlaandrewj infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT lorenzanadewittmarioa infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT faroneanthonyl infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT gundersonjohnh infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT berksharong infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae AT faronemaryb infectionandnuclearinteractioninmammaliancellsbycandidatusberkiellacookevillensisanovelbacteriumisolatedfromamoebae |