Improved ultrastructure of marine invertebrates using non-toxic buffers

Many marine biology studies depend on field work on ships or remote sampling locations where sophisticated sample preservation techniques (e.g., high-pressure freezing) are often limited or unavailable. Our aim was to optimize the ultrastructural preservation of marine invertebrates, especially when...

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Main Authors: Jacqueline Montanaro, Daniela Gruber, Nikolaus Leisch
Format: Article
Language:English
Published: PeerJ Inc. 2016-03-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/1860.pdf
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spelling doaj-b3d9ee76d08c49e69b66d204e49169632020-11-24T23:51:08ZengPeerJ Inc.PeerJ2167-83592016-03-014e186010.7717/peerj.1860Improved ultrastructure of marine invertebrates using non-toxic buffersJacqueline Montanaro0Daniela Gruber1Nikolaus Leisch2OCUVAC—Center of Ocular Inflammation and Infection, Laura Bassi Centers of Expertise, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, AustriaCore Facility Cell Imaging and Ultrastructure Research, University of Vienna, Vienna, AustriaMax Planck Institute for Marine Microbiology, Bremen, GermanyMany marine biology studies depend on field work on ships or remote sampling locations where sophisticated sample preservation techniques (e.g., high-pressure freezing) are often limited or unavailable. Our aim was to optimize the ultrastructural preservation of marine invertebrates, especially when working in the field. To achieve chemically-fixed material of the highest quality, we compared the resulting ultrastructure of gill tissue of the mussel Mytilus edulis when fixed with differently buffered EM fixatives for marine specimens (seawater, cacodylate and phosphate buffer) and a new fixative formulation with the non-toxic PHEM buffer (PIPES, HEPES, EGTA and MgCl2). All buffers were adapted for immersion fixation to form an isotonic fixative in combination with 2.5% glutaraldehyde. We showed that PHEM buffer based fixatives resulted in equal or better ultrastructure preservation when directly compared to routine standard fixatives. These results were also reproducible when extending the PHEM buffered fixative to the fixation of additional different marine invertebrate species, which also displayed excellent ultrastructural detail. We highly recommend the usage of PHEM-buffered fixation for the fixation of marine invertebrates.https://peerj.com/articles/1860.pdfElectron microscopyImmersion fixationPHEM buffer
collection DOAJ
language English
format Article
sources DOAJ
author Jacqueline Montanaro
Daniela Gruber
Nikolaus Leisch
spellingShingle Jacqueline Montanaro
Daniela Gruber
Nikolaus Leisch
Improved ultrastructure of marine invertebrates using non-toxic buffers
PeerJ
Electron microscopy
Immersion fixation
PHEM buffer
author_facet Jacqueline Montanaro
Daniela Gruber
Nikolaus Leisch
author_sort Jacqueline Montanaro
title Improved ultrastructure of marine invertebrates using non-toxic buffers
title_short Improved ultrastructure of marine invertebrates using non-toxic buffers
title_full Improved ultrastructure of marine invertebrates using non-toxic buffers
title_fullStr Improved ultrastructure of marine invertebrates using non-toxic buffers
title_full_unstemmed Improved ultrastructure of marine invertebrates using non-toxic buffers
title_sort improved ultrastructure of marine invertebrates using non-toxic buffers
publisher PeerJ Inc.
series PeerJ
issn 2167-8359
publishDate 2016-03-01
description Many marine biology studies depend on field work on ships or remote sampling locations where sophisticated sample preservation techniques (e.g., high-pressure freezing) are often limited or unavailable. Our aim was to optimize the ultrastructural preservation of marine invertebrates, especially when working in the field. To achieve chemically-fixed material of the highest quality, we compared the resulting ultrastructure of gill tissue of the mussel Mytilus edulis when fixed with differently buffered EM fixatives for marine specimens (seawater, cacodylate and phosphate buffer) and a new fixative formulation with the non-toxic PHEM buffer (PIPES, HEPES, EGTA and MgCl2). All buffers were adapted for immersion fixation to form an isotonic fixative in combination with 2.5% glutaraldehyde. We showed that PHEM buffer based fixatives resulted in equal or better ultrastructure preservation when directly compared to routine standard fixatives. These results were also reproducible when extending the PHEM buffered fixative to the fixation of additional different marine invertebrate species, which also displayed excellent ultrastructural detail. We highly recommend the usage of PHEM-buffered fixation for the fixation of marine invertebrates.
topic Electron microscopy
Immersion fixation
PHEM buffer
url https://peerj.com/articles/1860.pdf
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