CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes

Bibliographic Details
Main Author: Sáez Moreno, David
Publication Date: 2025
Other Authors: Cunha, Joana, Melo, Luís Daniel Rodrigues, Tanaka, Kenya, Bamba, Takahiro, Hasunuma, Tomosiha, Azeredo, Joana, Domingues, Lucília
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://hdl.handle.net/1822/95445
Summary: Listeriosis is an infection caused by the consumption of food contaminated with Listeria monocytogenes. It leads to febrile gastroenteritis, central nervous system infections, and even death in risk populations. Bacteriophage endolysins selectively kill bacteria hydrolyzing their cell walls and have emerged as a potential tool for listeriosis control. Ply511 is an anti-Listeria endolysin that has activity against all serovars of L. monocytogenes. The yeast Saccharomyces cerevisiae has been used to produce endolysins for biocontrol, but prior efforts relied on plasmids, which can lead to gene loss and include selection markers unsuitable for therapeutic use. Integration of endolysins in its genome has also been previously demonstrated, relying however, on selection markers for selection and maintenance of the modifications. This study explores S. cerevisiae as a generally regarded as safe (GRAS) platform for producing and displaying Ply511 through CRISPR-Cas9 integration, offering a marker-free and stable solution for Listeria biocontrol. Our results demonstrate that the surface display of Ply511 does not lead to bacterial reduction. In contrast, we show that yeast secreting endolysin significantly reduces L. monocytogenes in cells, supernatants, and cell extracts. The strongest effect was observed with concentrated spent supernatant and cell extract, which reduced L. monocytogenes below the lower limit of quantification. Additionally, the spent supernatant exhibited active anti-Listeria activity in milk. This study highlights yeast-secreted endolysins as a promising platform for listeriosis control and demonstrates the yeast secretion of endolysins can be used for the biocontrol of pathogenic bacteria.
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spelling CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenesListeria monocytogenesEndolysinCRISPR-Cas9BiocontrolEngineered Saccharomyces cerevisiaeProbioticsListeriosis is an infection caused by the consumption of food contaminated with Listeria monocytogenes. It leads to febrile gastroenteritis, central nervous system infections, and even death in risk populations. Bacteriophage endolysins selectively kill bacteria hydrolyzing their cell walls and have emerged as a potential tool for listeriosis control. Ply511 is an anti-Listeria endolysin that has activity against all serovars of L. monocytogenes. The yeast Saccharomyces cerevisiae has been used to produce endolysins for biocontrol, but prior efforts relied on plasmids, which can lead to gene loss and include selection markers unsuitable for therapeutic use. Integration of endolysins in its genome has also been previously demonstrated, relying however, on selection markers for selection and maintenance of the modifications. This study explores S. cerevisiae as a generally regarded as safe (GRAS) platform for producing and displaying Ply511 through CRISPR-Cas9 integration, offering a marker-free and stable solution for Listeria biocontrol. Our results demonstrate that the surface display of Ply511 does not lead to bacterial reduction. In contrast, we show that yeast secreting endolysin significantly reduces L. monocytogenes in cells, supernatants, and cell extracts. The strongest effect was observed with concentrated spent supernatant and cell extract, which reduced L. monocytogenes below the lower limit of quantification. Additionally, the spent supernatant exhibited active anti-Listeria activity in milk. This study highlights yeast-secreted endolysins as a promising platform for listeriosis control and demonstrates the yeast secretion of endolysins can be used for the biocontrol of pathogenic bacteria.Open access funding provided by FCT|FCCN (b-on). This study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UIDB/04469/2020 and UIDP/04469/2020 unit and a Ph.D. grant UI/ BD/151411/2021 to D.S.M. This work was also supported by Kobe University Strategic International Collaborative Research Grant (Type B Fostering Joint Research).info:eu-repo/semantics/publishedVersionSpringer NatureUniversidade do MinhoSáez Moreno, DavidCunha, JoanaMelo, Luís Daniel RodriguesTanaka, KenyaBamba, TakahiroHasunuma, TomosihaAzeredo, JoanaDomingues, Lucília2025-04-022025-04-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/95445engSáez, David; Cunha, Joana T.; Melo, Luís Daniel Rodrigues; Tanaka, Kenya; Bamba, Takahiro; Hasunuma, Tomosiha; Azeredo, Joana; Domingues, Lucília, CRISPR-Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes. Applied Microbiology and Biotechnology, 109(81), 20250175-75981432-061410.1007/s00253-025-13464-8http://www.springer.com/chemistry/biotechnology/journal/253info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-05-03T01:19:53Zoai:repositorium.sdum.uminho.pt:1822/95445Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T06:57:35.987660Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
title CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
spellingShingle CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
Sáez Moreno, David
Listeria monocytogenes
Endolysin
CRISPR-Cas9
Biocontrol
Engineered Saccharomyces cerevisiae
Probiotics
title_short CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
title_full CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
title_fullStr CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
title_full_unstemmed CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
title_sort CRISPR‑Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes
author Sáez Moreno, David
author_facet Sáez Moreno, David
Cunha, Joana
Melo, Luís Daniel Rodrigues
Tanaka, Kenya
Bamba, Takahiro
Hasunuma, Tomosiha
Azeredo, Joana
Domingues, Lucília
author_role author
author2 Cunha, Joana
Melo, Luís Daniel Rodrigues
Tanaka, Kenya
Bamba, Takahiro
Hasunuma, Tomosiha
Azeredo, Joana
Domingues, Lucília
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Sáez Moreno, David
Cunha, Joana
Melo, Luís Daniel Rodrigues
Tanaka, Kenya
Bamba, Takahiro
Hasunuma, Tomosiha
Azeredo, Joana
Domingues, Lucília
dc.subject.por.fl_str_mv Listeria monocytogenes
Endolysin
CRISPR-Cas9
Biocontrol
Engineered Saccharomyces cerevisiae
Probiotics
topic Listeria monocytogenes
Endolysin
CRISPR-Cas9
Biocontrol
Engineered Saccharomyces cerevisiae
Probiotics
description Listeriosis is an infection caused by the consumption of food contaminated with Listeria monocytogenes. It leads to febrile gastroenteritis, central nervous system infections, and even death in risk populations. Bacteriophage endolysins selectively kill bacteria hydrolyzing their cell walls and have emerged as a potential tool for listeriosis control. Ply511 is an anti-Listeria endolysin that has activity against all serovars of L. monocytogenes. The yeast Saccharomyces cerevisiae has been used to produce endolysins for biocontrol, but prior efforts relied on plasmids, which can lead to gene loss and include selection markers unsuitable for therapeutic use. Integration of endolysins in its genome has also been previously demonstrated, relying however, on selection markers for selection and maintenance of the modifications. This study explores S. cerevisiae as a generally regarded as safe (GRAS) platform for producing and displaying Ply511 through CRISPR-Cas9 integration, offering a marker-free and stable solution for Listeria biocontrol. Our results demonstrate that the surface display of Ply511 does not lead to bacterial reduction. In contrast, we show that yeast secreting endolysin significantly reduces L. monocytogenes in cells, supernatants, and cell extracts. The strongest effect was observed with concentrated spent supernatant and cell extract, which reduced L. monocytogenes below the lower limit of quantification. Additionally, the spent supernatant exhibited active anti-Listeria activity in milk. This study highlights yeast-secreted endolysins as a promising platform for listeriosis control and demonstrates the yeast secretion of endolysins can be used for the biocontrol of pathogenic bacteria.
publishDate 2025
dc.date.none.fl_str_mv 2025-04-02
2025-04-02T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/95445
url https://hdl.handle.net/1822/95445
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Sáez, David; Cunha, Joana T.; Melo, Luís Daniel Rodrigues; Tanaka, Kenya; Bamba, Takahiro; Hasunuma, Tomosiha; Azeredo, Joana; Domingues, Lucília, CRISPR-Cas9 engineered Saccharomyces cerevisiae for endolysin delivery to combat Listeria monocytogenes. Applied Microbiology and Biotechnology, 109(81), 2025
0175-7598
1432-0614
10.1007/s00253-025-13464-8
http://www.springer.com/chemistry/biotechnology/journal/253
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Springer Nature
publisher.none.fl_str_mv Springer Nature
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