Publication:
Multiple roads lead to Rome: unique morphology and chemistry of endospores, exospores, myxospores, cysts and akinetes in bacteria.

cris.virtual.author-orcid0000-0001-7725-5579
cris.virtualsource.author-orciddc1d45e4-60c3-4161-9de5-d61fb548a88d
cris.virtualsource.author-orcid51932a34-54e3-4782-9f56-69b9e7bb7fb4
cris.virtualsource.author-orcide050e437-7048-4ed7-8f07-6eaad53734c2
datacite.rightsopen.access
dc.contributor.authorCorona Ramírez, Andrea
dc.contributor.authorLee, Kang Soo
dc.contributor.authorOdriozola Quesada, Adolfo
dc.contributor.authorKaminek, Marek
dc.contributor.authorStocker, Roman
dc.contributor.authorZuber, Benoît
dc.contributor.authorJunier, Pilar
dc.date.accessioned2024-10-25T15:39:46Z
dc.date.available2024-10-25T15:39:46Z
dc.date.issued2023-02
dc.description.abstractThe production of specialized resting cells is a remarkable survival strategy developed by many organisms to withstand unfavourable environmental factors such as nutrient depletion or other changes in abiotic and/or biotic conditions. Five bacterial taxa are recognized to form specialized resting cells: Firmicutes, forming endospores; Actinobacteria, forming exospores; Cyanobacteria, forming akinetes; the δ-Proteobacterial order Myxococcales, forming myxospores; and Azotobacteraceae, forming cysts. All these specialized resting cells are characterized by low-to-absent metabolic activity and higher resistance to environmental stress (desiccation, heat, starvation, etc.) when compared to vegetative cells. Given their similarity in function, we tested the potential existence of a universal morpho-chemical marker for identifying these specialized resting cells. After the production of endospores, exospores, akinetes and cysts in model organisms, we performed the first cross-species morphological and chemical comparison of bacterial sporulation. Cryo-electron microscopy of vitreous sections (CEMOVIS) was used to describe near-native morphology of the resting cells in comparison to the morphology of their respective vegetative cells. Resting cells shared a thicker cell envelope as their only common morphological feature. The chemical composition of the different specialized resting cells at the single-cell level was investigated using confocal Raman microspectroscopy. Our results show that the different specialized cells do not share a common chemical signature, but rather each group has a unique signature with a variable conservation of the signature of the vegetative cells. Additionally, we present the validation of Raman signatures associated with calcium dipicolinic acid (CaDPA) and their variation across individual cells to develop specific sorting thresholds for the isolation of endospores. This provides a proof of concept of the feasibility of isolating bacterial spores using a Raman-activated cell-sorting platform. This cross-species comparison and the current knowledge of genetic pathways inducing the formation of the resting cells highlights the complexity of this convergent evolutionary strategy promoting bacterial survival.
dc.description.numberOfPages16
dc.description.sponsorshipInstitut für Anatomie
dc.identifier.doi10.48350/179067
dc.identifier.pmid36804869
dc.identifier.publisherDOI10.1099/mic.0.001299
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/164355
dc.language.isoen
dc.publisherMicrobiology Society
dc.relation.ispartofMicrobiology
dc.relation.issn1465-2080
dc.relation.organization5EBDFFD4994748B4B44FD17D5E463CFB
dc.relation.organizationDCD5A442BCD7E17DE0405C82790C4DE2
dc.subjectCEMOVIS Raman microspectroscopy akinete calcium dipicolinic acid (CaDPA) cyst endospore exospore myxospore
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleMultiple roads lead to Rome: unique morphology and chemistry of endospores, exospores, myxospores, cysts and akinetes in bacteria.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue2
oaire.citation.volume169
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
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unibe.date.licenseChanged2023-02-23 12:59:59
unibe.description.ispublishedpub
unibe.eprints.legacyId179067
unibe.refereedtrue
unibe.subtype.articlejournal

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