The future of CRISPR in Mycobacterium tuberculosis infection
- Autores
- Zein Eddine, Rima; Refrégier, Guislaine; Cervantes, Jorge; Yokobori, Noemí
- Año de publicación
- 2023
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Clustered Regularly Interspaced Short Palindromic repeats (CRISPR)-Cas systems rapidly raised from a bacterial genetic curiosity to the most popular tool for genetic modifications which revolutionized the study of microbial physiology. Due to the highly conserved nature of the CRISPR locus in Mycobacterium tuberculosis, the etiological agent of one of the deadliest infectious diseases globally, initially, little attention was paid to its CRISPR locus, other than as a phylogenetic marker. Recent research shows that M. tuberculosis has a partially functional Type III CRISPR, which provides a defense mechanism against foreign genetic elements mediated by the ancillary RNAse Csm6. With the advent of CRISPR-Cas based gene edition technologies, our possibilities to explore the biology of M. tuberculosis and its interaction with the host immune system are boosted. CRISPR-based diagnostic methods can lower the detection threshold to femtomolar levels, which could contribute to the diagnosis of the still elusive paucibacillary and extrapulmonary tuberculosis cases. In addition, one-pot and point-of-care tests are under development, and future challenges are discussed. We present in this literature review the potential and actual impact of CRISPR-Cas research on human tuberculosis understanding and management. Altogether, the CRISPR-revolution will revitalize the fight against tuberculosis with more research and technological developments.
Fil: Zein Eddine, Rima. Laboratoire D'optique Et Biosciences Ecole Polytechnique; Francia
Fil: Refrégier, Guislaine. Universite Paris-saclay (universite Paris-saclay);
Fil: Cervantes, Jorge. University of Texas; Estados Unidos
Fil: Yokobori, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Institutos de Investigación. Administración Nacional de Laboratorios e Institutos de Salud. Instituto Nacional de Enfermedades Infecciosas; Argentina - Materia
-
CRISPR-CAS
CRISPRI
DIAGNOSTIC METHODS
FUNCTIONAL GENOMICS
MTBC
MYCOBACTERIUM TUBERCULOSIS
SPOLIGOTYPING - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/219483
Ver los metadatos del registro completo
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The future of CRISPR in Mycobacterium tuberculosis infectionZein Eddine, RimaRefrégier, GuislaineCervantes, JorgeYokobori, NoemíCRISPR-CASCRISPRIDIAGNOSTIC METHODSFUNCTIONAL GENOMICSMTBCMYCOBACTERIUM TUBERCULOSISSPOLIGOTYPINGhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Clustered Regularly Interspaced Short Palindromic repeats (CRISPR)-Cas systems rapidly raised from a bacterial genetic curiosity to the most popular tool for genetic modifications which revolutionized the study of microbial physiology. Due to the highly conserved nature of the CRISPR locus in Mycobacterium tuberculosis, the etiological agent of one of the deadliest infectious diseases globally, initially, little attention was paid to its CRISPR locus, other than as a phylogenetic marker. Recent research shows that M. tuberculosis has a partially functional Type III CRISPR, which provides a defense mechanism against foreign genetic elements mediated by the ancillary RNAse Csm6. With the advent of CRISPR-Cas based gene edition technologies, our possibilities to explore the biology of M. tuberculosis and its interaction with the host immune system are boosted. CRISPR-based diagnostic methods can lower the detection threshold to femtomolar levels, which could contribute to the diagnosis of the still elusive paucibacillary and extrapulmonary tuberculosis cases. In addition, one-pot and point-of-care tests are under development, and future challenges are discussed. We present in this literature review the potential and actual impact of CRISPR-Cas research on human tuberculosis understanding and management. Altogether, the CRISPR-revolution will revitalize the fight against tuberculosis with more research and technological developments.Fil: Zein Eddine, Rima. Laboratoire D'optique Et Biosciences Ecole Polytechnique; FranciaFil: Refrégier, Guislaine. Universite Paris-saclay (universite Paris-saclay);Fil: Cervantes, Jorge. University of Texas; Estados UnidosFil: Yokobori, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Institutos de Investigación. Administración Nacional de Laboratorios e Institutos de Salud. Instituto Nacional de Enfermedades Infecciosas; ArgentinaBioMed Central2023-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/219483Zein Eddine, Rima; Refrégier, Guislaine; Cervantes, Jorge; Yokobori, Noemí; The future of CRISPR in Mycobacterium tuberculosis infection; BioMed Central; Journal Of Biomedical Science; 30; 1; 5-2023; 1-121021-7770CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1186/s12929-023-00932-4info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:55:10Zoai:ri.conicet.gov.ar:11336/219483instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:55:10.491CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
The future of CRISPR in Mycobacterium tuberculosis infection |
title |
The future of CRISPR in Mycobacterium tuberculosis infection |
spellingShingle |
The future of CRISPR in Mycobacterium tuberculosis infection Zein Eddine, Rima CRISPR-CAS CRISPRI DIAGNOSTIC METHODS FUNCTIONAL GENOMICS MTBC MYCOBACTERIUM TUBERCULOSIS SPOLIGOTYPING |
title_short |
The future of CRISPR in Mycobacterium tuberculosis infection |
title_full |
The future of CRISPR in Mycobacterium tuberculosis infection |
title_fullStr |
The future of CRISPR in Mycobacterium tuberculosis infection |
title_full_unstemmed |
The future of CRISPR in Mycobacterium tuberculosis infection |
title_sort |
The future of CRISPR in Mycobacterium tuberculosis infection |
dc.creator.none.fl_str_mv |
Zein Eddine, Rima Refrégier, Guislaine Cervantes, Jorge Yokobori, Noemí |
author |
Zein Eddine, Rima |
author_facet |
Zein Eddine, Rima Refrégier, Guislaine Cervantes, Jorge Yokobori, Noemí |
author_role |
author |
author2 |
Refrégier, Guislaine Cervantes, Jorge Yokobori, Noemí |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
CRISPR-CAS CRISPRI DIAGNOSTIC METHODS FUNCTIONAL GENOMICS MTBC MYCOBACTERIUM TUBERCULOSIS SPOLIGOTYPING |
topic |
CRISPR-CAS CRISPRI DIAGNOSTIC METHODS FUNCTIONAL GENOMICS MTBC MYCOBACTERIUM TUBERCULOSIS SPOLIGOTYPING |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.3 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Clustered Regularly Interspaced Short Palindromic repeats (CRISPR)-Cas systems rapidly raised from a bacterial genetic curiosity to the most popular tool for genetic modifications which revolutionized the study of microbial physiology. Due to the highly conserved nature of the CRISPR locus in Mycobacterium tuberculosis, the etiological agent of one of the deadliest infectious diseases globally, initially, little attention was paid to its CRISPR locus, other than as a phylogenetic marker. Recent research shows that M. tuberculosis has a partially functional Type III CRISPR, which provides a defense mechanism against foreign genetic elements mediated by the ancillary RNAse Csm6. With the advent of CRISPR-Cas based gene edition technologies, our possibilities to explore the biology of M. tuberculosis and its interaction with the host immune system are boosted. CRISPR-based diagnostic methods can lower the detection threshold to femtomolar levels, which could contribute to the diagnosis of the still elusive paucibacillary and extrapulmonary tuberculosis cases. In addition, one-pot and point-of-care tests are under development, and future challenges are discussed. We present in this literature review the potential and actual impact of CRISPR-Cas research on human tuberculosis understanding and management. Altogether, the CRISPR-revolution will revitalize the fight against tuberculosis with more research and technological developments. Fil: Zein Eddine, Rima. Laboratoire D'optique Et Biosciences Ecole Polytechnique; Francia Fil: Refrégier, Guislaine. Universite Paris-saclay (universite Paris-saclay); Fil: Cervantes, Jorge. University of Texas; Estados Unidos Fil: Yokobori, Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Dirección Nacional de Institutos de Investigación. Administración Nacional de Laboratorios e Institutos de Salud. Instituto Nacional de Enfermedades Infecciosas; Argentina |
description |
Clustered Regularly Interspaced Short Palindromic repeats (CRISPR)-Cas systems rapidly raised from a bacterial genetic curiosity to the most popular tool for genetic modifications which revolutionized the study of microbial physiology. Due to the highly conserved nature of the CRISPR locus in Mycobacterium tuberculosis, the etiological agent of one of the deadliest infectious diseases globally, initially, little attention was paid to its CRISPR locus, other than as a phylogenetic marker. Recent research shows that M. tuberculosis has a partially functional Type III CRISPR, which provides a defense mechanism against foreign genetic elements mediated by the ancillary RNAse Csm6. With the advent of CRISPR-Cas based gene edition technologies, our possibilities to explore the biology of M. tuberculosis and its interaction with the host immune system are boosted. CRISPR-based diagnostic methods can lower the detection threshold to femtomolar levels, which could contribute to the diagnosis of the still elusive paucibacillary and extrapulmonary tuberculosis cases. In addition, one-pot and point-of-care tests are under development, and future challenges are discussed. We present in this literature review the potential and actual impact of CRISPR-Cas research on human tuberculosis understanding and management. Altogether, the CRISPR-revolution will revitalize the fight against tuberculosis with more research and technological developments. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/219483 Zein Eddine, Rima; Refrégier, Guislaine; Cervantes, Jorge; Yokobori, Noemí; The future of CRISPR in Mycobacterium tuberculosis infection; BioMed Central; Journal Of Biomedical Science; 30; 1; 5-2023; 1-12 1021-7770 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/219483 |
identifier_str_mv |
Zein Eddine, Rima; Refrégier, Guislaine; Cervantes, Jorge; Yokobori, Noemí; The future of CRISPR in Mycobacterium tuberculosis infection; BioMed Central; Journal Of Biomedical Science; 30; 1; 5-2023; 1-12 1021-7770 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12929-023-00932-4 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
BioMed Central |
publisher.none.fl_str_mv |
BioMed Central |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.070432 |