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Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system
OBJECTIVES: Cell-culture studies reported that prokaryotic RNA molecules among the various microbe-associated molecular patterns (MAMPs) were uniquely present in live bacteria and were categorized as viability-associated MAMPs. They also reported that specific nucleotide modifications are instrument...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942260/ https://www.ncbi.nlm.nih.gov/pubmed/31900206 http://dx.doi.org/10.1186/s13104-019-4878-8 |
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author | Basu, Abhishikta Yoshihama, Maki Uechi, Tamayo Kenmochi, Naoya |
author_facet | Basu, Abhishikta Yoshihama, Maki Uechi, Tamayo Kenmochi, Naoya |
author_sort | Basu, Abhishikta |
collection | PubMed |
description | OBJECTIVES: Cell-culture studies reported that prokaryotic RNA molecules among the various microbe-associated molecular patterns (MAMPs) were uniquely present in live bacteria and were categorized as viability-associated MAMPs. They also reported that specific nucleotide modifications are instrumental in the discrimination between self and nonself RNAs. The aim of this study was to characterize the in vivo immune induction potential of prokaryotic and eukaryotic ribosomal RNAs (rRNAs) using zebrafish embryos as novel whole animal model system. Additionally, we aimed to test the possible role of rRNA modifications in immune recognition. RESULTS: We used three immune markers to evaluate the induction potential of prokaryotic rRNA derived from Escherichia coli and eukaryotic rRNAs from chicken (nonself) and zebrafish (self). Lipopolysaccharide (LPS) of Pseudomonas aeruginosa served as a positive control. E. coli rRNA had an induction potential equivalent to that of LPS. The zebrafish innate immune system could discriminate between self and nonself rRNAs. Between the nonself rRNAs, E. coli rRNA was more immunogenic than chicken rRNA. The in vitro transcript of zebrafish 18S rRNA gene without the nucleotide modifications was not recognized by its own immune system. Our data suggested that prokaryotic rRNA is immunostimulatory in vivo and could be useful as an adjuvant. |
format | Online Article Text |
id | pubmed-6942260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69422602020-01-07 Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system Basu, Abhishikta Yoshihama, Maki Uechi, Tamayo Kenmochi, Naoya BMC Res Notes Research Note OBJECTIVES: Cell-culture studies reported that prokaryotic RNA molecules among the various microbe-associated molecular patterns (MAMPs) were uniquely present in live bacteria and were categorized as viability-associated MAMPs. They also reported that specific nucleotide modifications are instrumental in the discrimination between self and nonself RNAs. The aim of this study was to characterize the in vivo immune induction potential of prokaryotic and eukaryotic ribosomal RNAs (rRNAs) using zebrafish embryos as novel whole animal model system. Additionally, we aimed to test the possible role of rRNA modifications in immune recognition. RESULTS: We used three immune markers to evaluate the induction potential of prokaryotic rRNA derived from Escherichia coli and eukaryotic rRNAs from chicken (nonself) and zebrafish (self). Lipopolysaccharide (LPS) of Pseudomonas aeruginosa served as a positive control. E. coli rRNA had an induction potential equivalent to that of LPS. The zebrafish innate immune system could discriminate between self and nonself rRNAs. Between the nonself rRNAs, E. coli rRNA was more immunogenic than chicken rRNA. The in vitro transcript of zebrafish 18S rRNA gene without the nucleotide modifications was not recognized by its own immune system. Our data suggested that prokaryotic rRNA is immunostimulatory in vivo and could be useful as an adjuvant. BioMed Central 2020-01-03 /pmc/articles/PMC6942260/ /pubmed/31900206 http://dx.doi.org/10.1186/s13104-019-4878-8 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Note Basu, Abhishikta Yoshihama, Maki Uechi, Tamayo Kenmochi, Naoya Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title | Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title_full | Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title_fullStr | Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title_full_unstemmed | Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title_short | Prokaryotic ribosomal RNA stimulates zebrafish embryonic innate immune system |
title_sort | prokaryotic ribosomal rna stimulates zebrafish embryonic innate immune system |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942260/ https://www.ncbi.nlm.nih.gov/pubmed/31900206 http://dx.doi.org/10.1186/s13104-019-4878-8 |
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