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Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments
Alteration of organic remains during the transition from the bio- to lithosphere is affected strongly by biotic processes of microbes influencing the potential of dead matter to become fossilized or vanish ultimately. If fossilized, bones, cartilage, and tooth dentine often display traces of bioeros...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708646/ https://www.ncbi.nlm.nih.gov/pubmed/33262401 http://dx.doi.org/10.1038/s41598-020-77964-5 |
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author | Feichtinger, Iris Lukeneder, Alexander Topa, Dan Kriwet, Jürgen Libowitzky, Eugen Westall, Frances |
author_facet | Feichtinger, Iris Lukeneder, Alexander Topa, Dan Kriwet, Jürgen Libowitzky, Eugen Westall, Frances |
author_sort | Feichtinger, Iris |
collection | PubMed |
description | Alteration of organic remains during the transition from the bio- to lithosphere is affected strongly by biotic processes of microbes influencing the potential of dead matter to become fossilized or vanish ultimately. If fossilized, bones, cartilage, and tooth dentine often display traces of bioerosion caused by destructive microbes. The causal agents, however, usually remain ambiguous. Here we present a new type of tissue alteration in fossil deep-sea shark teeth with in situ preservation of the responsible organisms embedded in a delicate filmy substance identified as extrapolymeric matter. The invading microorganisms are arranged in nest- or chain-like patterns between fluorapatite bundles of the superficial enameloid. Chemical analysis of the bacteriomorph structures indicates replacement by a phyllosilicate, which enabled in situ preservation. Our results imply that bacteria invaded the hypermineralized tissue for harvesting intra-crystalline bound organic matter, which provided nutrient supply in a nutrient depleted deep-marine environment they inhabited. We document here for the first time in situ bacteria preservation in tooth enameloid, one of the hardest mineralized tissues developed by animals. This unambiguously verifies that microbes also colonize highly mineralized dental capping tissues with only minor organic content when nutrients are scarce as in deep-marine environments. |
format | Online Article Text |
id | pubmed-7708646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77086462020-12-03 Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments Feichtinger, Iris Lukeneder, Alexander Topa, Dan Kriwet, Jürgen Libowitzky, Eugen Westall, Frances Sci Rep Article Alteration of organic remains during the transition from the bio- to lithosphere is affected strongly by biotic processes of microbes influencing the potential of dead matter to become fossilized or vanish ultimately. If fossilized, bones, cartilage, and tooth dentine often display traces of bioerosion caused by destructive microbes. The causal agents, however, usually remain ambiguous. Here we present a new type of tissue alteration in fossil deep-sea shark teeth with in situ preservation of the responsible organisms embedded in a delicate filmy substance identified as extrapolymeric matter. The invading microorganisms are arranged in nest- or chain-like patterns between fluorapatite bundles of the superficial enameloid. Chemical analysis of the bacteriomorph structures indicates replacement by a phyllosilicate, which enabled in situ preservation. Our results imply that bacteria invaded the hypermineralized tissue for harvesting intra-crystalline bound organic matter, which provided nutrient supply in a nutrient depleted deep-marine environment they inhabited. We document here for the first time in situ bacteria preservation in tooth enameloid, one of the hardest mineralized tissues developed by animals. This unambiguously verifies that microbes also colonize highly mineralized dental capping tissues with only minor organic content when nutrients are scarce as in deep-marine environments. Nature Publishing Group UK 2020-12-01 /pmc/articles/PMC7708646/ /pubmed/33262401 http://dx.doi.org/10.1038/s41598-020-77964-5 Text en © The Author(s) 2020 Open Access This 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/. |
spellingShingle | Article Feichtinger, Iris Lukeneder, Alexander Topa, Dan Kriwet, Jürgen Libowitzky, Eugen Westall, Frances Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title | Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title_full | Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title_fullStr | Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title_full_unstemmed | Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title_short | Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
title_sort | fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708646/ https://www.ncbi.nlm.nih.gov/pubmed/33262401 http://dx.doi.org/10.1038/s41598-020-77964-5 |
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