Alejandra Prieto-Davó

Dr. Alejandra Prieto-Davó

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
21 January 2022 in Scientific Reports
Verified
Journal Article
Open access
PDF file
PSPablo Suárez-Moo
Pablo Suárez-Moo
CRClaudia A. Remes-Rodríguez
Claudia A. Remes-Rodríguez
NMNorma A. Márquez-Velázquez
Norma A. Márquez-Velázquez
LFLuisa I. Falcón
Luisa I. Falcón
JGJosé Q. García-Maldonado
José Q. García-Maldonado
APAlejandra Prieto-Davó
Alejandra Prieto-Davó
The karst underground river ecosystem of Yucatan peninsula is composed of cave systems and sinkholes. The microbial diversity of water from this underground river has been studied, but, structure of the microbial community in its cave sediments remained largely unknown. Here we describe how the microbial community structure of these sediments changes due to different environmental conditions found in sediment zones along the caves of a coastal and an inland sinkhole. We found that dominant microbial groups varied according to the type of sinkhole (Coastal: Chloroflexi and Crenarchaeota; inland: Methylomirabilota and Acidobacteriota) and that the community structures differed both among sinkhole types, and within the sediment zones that were studied. These microorganisms are associated with different types of metabolism, and differed from a microbial community dominated by sulfate reducers at the coastal sinkhole, to one dominated by methylotrophs at the inland sinkhole, suggesting there are biogeochemical processes in the coastal and inland sinkholes that lead to changes in the microbial composition of the underground river ecosystem’s sediments. Our results suggest sediments from unexplored sinkhole caves are unique environmental niches with distinct microbial assemblages that putatively play an important role in the biogeochemical cycles of these ecosystems.

11 March 2013 in FEMS Microbiology Ecology
Verified
Journal Article
Open access
PDF file
APAlejandra Prieto-Davó
Alejandra Prieto-Davó
Luis Jesús Villarreal-GómezLuis Jesús Villarreal-Gómez
Luis Jesús Villarreal-Gómez
SFStephanie Forschner-Dancause
Stephanie Forschner-Dancause
ABAlan T. Bull
Alan T. Bull
JSJames E.M. Stach
James E.M. Stach
PJPaul Jensen
Paul Jensen
Sediment samples collected off the coast of San Diego were analyzed for actinomycete diversity using culture-independent techniques. Eight new operat

10 December 2014 in Biological Research
Verified
Journal Article
Open access
PDF file
AOAileen O'Connor-Sánchez
Aileen O'Connor-Sánchez
ARAdán J Rivera-Domínguez
Adán J Rivera-Domínguez
CSCésar De los Santos-Briones
César De los Santos-Briones
LLLluvia K López-Aguiar
Lluvia K López-Aguiar
Yuri Jorge Peña-RamirezYuri Jorge Peña-Ramirez
Yuri Jorge Peña-Ramirez
APAlejandra Prieto-Davó
Alejandra Prieto-Davó
Marine invertebrate-associated microbial communities are interesting examples of complex symbiotic systems and are a potential source of biotechnological products.

23 December 2021 in Marine Drugs
Verified
Journal Article
Open access
PDF file
AAAntónio Pinto Almeida
António Pinto Almeida
ABAnelize Bauermeister
Anelize Bauermeister
LLLuca Luppino
Luca Luppino
IGInês Grilo
Inês Grilo
JOJuliana Oliveira
Juliana Oliveira
Susana P. GaudencioSusana P. Gaudencio
Susana P. Gaudencio
The Estremadura Spur pockmarks are a unique and unexplored ecosystem located in the North Atlantic, off the coast of Portugal. A total of 85 marine-derived actinomycetes were isolated and cultured from sediments collected from this ecosystem at a depth of 200 to 350 m. Nine genera, Streptomyces, Micromonospora, Saccharopolyspora, Actinomadura, Actinopolymorpha, Nocardiopsis, Saccharomonospora, Stackebrandtia, and Verrucosispora were identified by 16S rRNA gene sequencing analyses, from which the first two were the most predominant. Non-targeted LC-MS/MS, in combination with molecular networking, revealed high metabolite diversity, including several known metabolites, such as surugamide, antimycin, etamycin, physostigmine, desferrioxamine, ikarugamycin, piericidine, and rakicidin derivatives, as well as numerous unidentified metabolites. Taxonomy was the strongest parameter influencing the metabolite production, highlighting the different biosynthetic potentials of phylogenetically related actinomycetes; the majority of the chemical classes can be used as chemotaxonomic markers, as the metabolite distribution was mostly genera-specific. The EtOAc extracts of the actinomycete isolates demonstrated antimicrobial and antioxidant activity. Altogether, this study demonstrates that the Estremadura Spur is a source of actinomycetes with potential applications for biotechnology. It highlights the importance of investigating actinomycetes from unique ecosystems, such as pockmarks, as the metabolite production reflects their adaptation to this habitat.

2 December 2021 in Molecules
Verified
Journal Article
Open access
PDF file
MMMiguel David Marfil-Santana
Miguel David Marfil-Santana
AMANAHI MARTINEZ MARTINEZ-CARDENAS
ANAHI MARTINEZ MARTINEZ-CARDENAS
ARAnaluisa Ruíz-Hernández
Analuisa Ruíz-Hernández
MVMario Vidal-Torres
Mario Vidal-Torres
NMNorma Angélica Márquez-Velázquez
Norma Angélica Márquez-Velázquez
APAlejandra Prieto-Davó
Alejandra Prieto-Davó
Mangrove sediment ecosystems in the coastal areas of the Yucatan peninsula are unique environments, influenced by their karstic origin and connection with the world’s largest underground river. The microbial communities residing in these sediments are influenced by the presence of mangrove roots and the trading chemistry for communication between sediment bacteria and plant roots can be targeted for secondary metabolite research. To explore the secondary metabolite production potential of microbial community members in mangrove sediments at the “El Palmar” natural reserve in Sisal, Yucatan, a combined meta-omics approach was applied. The effects of a cultivation medium reported to select for actinomycetes within mangrove sediments’ microbial communities was also analyzed. The metabolome of the microbial communities was analyzed by high-resolution liquid chromatography-tandem mass spectrometry, and molecular networking analysis was used to investigate if known natural products and their variants were present. Metagenomic results suggest that the sediments from “El Palmar” harbor a stable bacterial community independently of their distance from mangrove tree roots. An unexpected decrease in the observed abundance of actinomycetes present in the communities occurred when an antibiotic-amended medium considered to be actinomycete-selective was applied for a 30-day period. However, the use of this antibiotic-amended medium also enhanced production of secondary metabolites within the microbial community present relative to the water control, suggesting the treatment selected for antibiotic-resistant bacteria capable of producing a higher number of secondary metabolites. Secondary metabolite mining of “El Palmar” microbial community metagenomes identified polyketide synthase and non-ribosomal peptide synthetases’ biosynthetic genes in all analyzed metagenomes. The presence of these genes correlated with the annotation of several secondary metabolites from the Global Natural Product Social Molecular Networking database. These results highlight the biotechnological potential of the microbial communities from “El Palmar”, and show the impact selective media had on the composition of communities of actinobacteria.

14 February 2019 in Microbial Ecology
Verified
Journal Article
Closed access
PDF file
YPYessica Parera-Valadez
Yessica Parera-Valadez
AYAlejandro Yam-Puc
Alejandro Yam-Puc
LLLluvia Korynthia López-Aguiar
Lluvia Korynthia López-Aguiar
RBRocío Borges-Argáez
Rocío Borges-Argáez
MFMario Figueroa
Mario Figueroa
APAlejandra Prieto-Davó
Alejandra Prieto-Davó