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Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes
The Gram-positive spore-forming anaerobe Clostridium sporogenes is a significant cause of food spoilage, and it is also used as a surrogate for C. botulinum spores for testing the efficacy of commercial sterilization. C. sporogenes spores have also been proposed as a vector to deliver drugs to tumor...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661016/ https://www.ncbi.nlm.nih.gov/pubmed/29118741 http://dx.doi.org/10.3389/fmicb.2017.02047 |
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author | Wang, Shiwei Brunt, Jason Peck, Michael W. Setlow, Peter Li, Yong-Qing |
author_facet | Wang, Shiwei Brunt, Jason Peck, Michael W. Setlow, Peter Li, Yong-Qing |
author_sort | Wang, Shiwei |
collection | PubMed |
description | The Gram-positive spore-forming anaerobe Clostridium sporogenes is a significant cause of food spoilage, and it is also used as a surrogate for C. botulinum spores for testing the efficacy of commercial sterilization. C. sporogenes spores have also been proposed as a vector to deliver drugs to tumor cells for cancer treatments. Such an application of C. sporogenes spores requires their germination and return to life. In this study, Raman spectroscopy and differential interference contrast (DIC) microscopy were used to analyze the germination kinetics of multiple individual C. sporogenes wild-type and germination mutant spores. Most individual C. sporogenes spores germinated with L-alanine began slow leakage of ∼5% of their large Ca-dipicolinic acid (CaDPA) depot at T(1), all transitioned to rapid CaDPA release at T(lag1), completed CaDPA release at T(release), and finished peptidoglycan cortex hydrolysis at T(lys). T(1), T(lag1), T(release), and T(lys) times for individual spores were heterogeneous, but ΔT(release) (T(release) – T(lag1)) periods were relatively constant. However, variability in T(1) (or T(lag1)) times appeared to be the major reason for the heterogeneity between individual spores in their germination times. After T(release), some spores also displayed another lag in rate of change in DIC image intensity before the start of a second obvious DIC image intensity decline of 25–30% at T(lag2) prior to T(lys). This has not been seen with spores of other species. Almost all C. sporogenes spores lacking the cortex-lytic enzyme (CLE) CwlJ spores exhibited a T(lag2) in L-alanine germination. Sublethal heat treatment potentiated C. sporogenes spore germination with L-alanine, primarily by shortening T(1) times. Spores without the CLEs SleB or CwlJ exhibited greatly slowed germination with L-alanine, but spores lacking all germinant receptor proteins did not germinate with L-alanine. The absence of these various germination proteins also decreased but did not abolish germination with the non-GR-dependent germinants dodecylamine and CaDPA, but spores without CwlJ exhibited no germination with CaDPA. Finally, C. sporogenes spores displayed commitment in germination, but memory in GR-dependent germination was small, and less than the memory in Bacillus spore germination. |
format | Online Article Text |
id | pubmed-5661016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56610162017-11-08 Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes Wang, Shiwei Brunt, Jason Peck, Michael W. Setlow, Peter Li, Yong-Qing Front Microbiol Microbiology The Gram-positive spore-forming anaerobe Clostridium sporogenes is a significant cause of food spoilage, and it is also used as a surrogate for C. botulinum spores for testing the efficacy of commercial sterilization. C. sporogenes spores have also been proposed as a vector to deliver drugs to tumor cells for cancer treatments. Such an application of C. sporogenes spores requires their germination and return to life. In this study, Raman spectroscopy and differential interference contrast (DIC) microscopy were used to analyze the germination kinetics of multiple individual C. sporogenes wild-type and germination mutant spores. Most individual C. sporogenes spores germinated with L-alanine began slow leakage of ∼5% of their large Ca-dipicolinic acid (CaDPA) depot at T(1), all transitioned to rapid CaDPA release at T(lag1), completed CaDPA release at T(release), and finished peptidoglycan cortex hydrolysis at T(lys). T(1), T(lag1), T(release), and T(lys) times for individual spores were heterogeneous, but ΔT(release) (T(release) – T(lag1)) periods were relatively constant. However, variability in T(1) (or T(lag1)) times appeared to be the major reason for the heterogeneity between individual spores in their germination times. After T(release), some spores also displayed another lag in rate of change in DIC image intensity before the start of a second obvious DIC image intensity decline of 25–30% at T(lag2) prior to T(lys). This has not been seen with spores of other species. Almost all C. sporogenes spores lacking the cortex-lytic enzyme (CLE) CwlJ spores exhibited a T(lag2) in L-alanine germination. Sublethal heat treatment potentiated C. sporogenes spore germination with L-alanine, primarily by shortening T(1) times. Spores without the CLEs SleB or CwlJ exhibited greatly slowed germination with L-alanine, but spores lacking all germinant receptor proteins did not germinate with L-alanine. The absence of these various germination proteins also decreased but did not abolish germination with the non-GR-dependent germinants dodecylamine and CaDPA, but spores without CwlJ exhibited no germination with CaDPA. Finally, C. sporogenes spores displayed commitment in germination, but memory in GR-dependent germination was small, and less than the memory in Bacillus spore germination. Frontiers Media S.A. 2017-10-25 /pmc/articles/PMC5661016/ /pubmed/29118741 http://dx.doi.org/10.3389/fmicb.2017.02047 Text en Copyright © 2017 Wang, Brunt, Peck, Setlow and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Wang, Shiwei Brunt, Jason Peck, Michael W. Setlow, Peter Li, Yong-Qing Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title | Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title_full | Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title_fullStr | Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title_full_unstemmed | Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title_short | Analysis of the Germination of Individual Clostridium sporogenes Spores with and without Germinant Receptors and Cortex-Lytic Enzymes |
title_sort | analysis of the germination of individual clostridium sporogenes spores with and without germinant receptors and cortex-lytic enzymes |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661016/ https://www.ncbi.nlm.nih.gov/pubmed/29118741 http://dx.doi.org/10.3389/fmicb.2017.02047 |
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