Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach

Cyclic di-adenosine monophosphate (c-di-AMP) is a second messenger involved in diverse metabolic processes such as cell wall homeostasis, biofilm formation, antibiotics and heat resistance, among others. In Lactococcus lactis and Enterococcus faecalis, Lactic Acid Bacteria used not only as research...

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Autor principal: Quintana, Ingrid M.
Otros Autores: Magni, Christian
Formato: doctoralThesis Tésis de Doctorado publishedVersion Material Didáctico
Lenguaje:Inglés
Publicado: 2019
Materias:
c-di-AMP
Lactococcus lactis
Metabolic processes
Acceso en línea:http://hdl.handle.net/2133/15229
http://hdl.handle.net/2133/15229
Aporte de:
Repositorio Hipermedial de la Universidad Nacional de Rosario (UNR) de Universidad Nacional de Rosario
id I15-R121-2133-15229
record_format dspace
institution Universidad Nacional de Rosario
institution_str I-15
repository_str R-121
collection Repositorio Hipermedial de la Universidad Nacional de Rosario (UNR)
language Inglés
orig_language_str_mv eng
topic c-di-AMP
Lactococcus lactis
Metabolic processes
spellingShingle c-di-AMP
Lactococcus lactis
Metabolic processes
Quintana, Ingrid M.
Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
topic_facet c-di-AMP
Lactococcus lactis
Metabolic processes
description Cyclic di-adenosine monophosphate (c-di-AMP) is a second messenger involved in diverse metabolic processes such as cell wall homeostasis, biofilm formation, antibiotics and heat resistance, among others. In Lactococcus lactis and Enterococcus faecalis, Lactic Acid Bacteria used not only as research models but also as a cell factory in biotechnological processes, the only reported interaction partner of c-di-AMP is the pyruvate carboxylase enzyme, PyrCarb. Nevertheless, in the last year investigations directed its main role towards potassium metabolism. In this thesis, KupA and KupB, two potassium transporters encoded in L. lactis IL1403 genome, are described for the first time. According to an in silico analysis, these proteins, which belong to the Kup/HAK/KT family, are highly conserved in this species, being therefore a strain independent potassium uptake system. In addition, evidence shows that both proteins are able to uptake this cation with high affinity, and we demonstrate that KupA as well as KupB bind to and are down-regulated by c-di-AMP. On the other hand, different strains derived from L. lactis IL1403 were developed aiming to modify intracellular pools of c-di-AMP in a stable system. One strategy for the reduction of c-di-AMP levels was the obtaining of ΔgdpP mutants via homologous recombination. Maintenance of this second messenger levels close to wild type ones, suggested the presence of another c-di-AMP degrading enzyme. A first description of a putative enzyme with this activity, encoded by yheB gene was done by BNPP assay. In addition, by use of a pH inducible vector, construction of strain L. lactis LL03 with concentrations of this second messenger above 15 times basal levels was possible. This system was therefore selected for further investigations on the development of a vaccine prototype against Chagas disease. On the other hand, L. lactis is a promising candidate for the development of mucosal vaccines with more than 20 years of experimental research. Moreover, c-di-AMP has been reported as a strong mucosal adjuvant promoting both humoral and cellular immune responses. Altogether, in this thesis the development of a recombinant L. lactis strain is reported, able to produce both an antigen as well as an adjuvant in order to develop a novel vaccine prototype against the Trypanosoma cruzi parasite, the causal agent of Chagas disease. This is a tropical disease originated in a specific area of South America but currently spreading in four continents. Finally, an initial approach was done on c-di-AMP metabolism in E. faecalis. The presence of a Kup transporter was also corroborated in this species, and some basic characteristics of the c-di-AMP degradative pathway were explored via a ΔgdpP mutant construction. Finally, the impact of GdpP on the virulence of E. faecalis was analyzed by use of the infection model Galleria mellonella.
author2 Magni, Christian
author_facet Magni, Christian
Quintana, Ingrid M.
format doctoralThesis
Tésis de Doctorado
publishedVersion
Material Didáctico
author Quintana, Ingrid M.
author_sort Quintana, Ingrid M.
title Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
title_short Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
title_full Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
title_fullStr Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
title_full_unstemmed Cyclic di-nucleotide monophosphate cyclase in Firmicutes: from basic to practical approach
title_sort cyclic di-nucleotide monophosphate cyclase in firmicutes: from basic to practical approach
publishDate 2019
url http://hdl.handle.net/2133/15229
http://hdl.handle.net/2133/15229
work_keys_str_mv AT quintanaingridm cyclicdinucleotidemonophosphatecyclaseinfirmicutesfrombasictopracticalapproach
bdutipo_str Repositorios
_version_ 1764820408660393984

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