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Jimenez, P. C.

Publications and source records attributed to Jimenez, P. C..

3 recordsLinked to original sources

Isolation and Genomic Characterization of Myxococcus faecalis Strains from Mangroves in Southeastern Brazil

Myxococcus faecalis was recently described from human fecal isolates, although subsequent evidence indicates an environmental distribution for this lineage. Here, we report the isolation and genomic characterization of two M. faecalis strains (BRX-014 and BRX-032) recovered from mangrove ecosystems along the southeastern coast of Brazil, representing the first record of the species in a marine-coastal biome. Phylogenomic reconstruction based on 120 conserved bacterial marker genes, together with Average Nucleotide Identity (ANI >97.6%) and digital DNA-DNA hybridization (dDDH 77.7-90.4%) analyses, confirmed their assignment to M. faecalis and demonstrated high genomic relatedness to strains previously recovered from soil and human feces samples. Pangenome analysis of five available genomes revealed a total repertoire of 9,827 genes, with a large core genome comprising 7,499 genes (76.3%), consistent with a highly conserved and nearly closed pangenome structure. Functional classification based on COG categories showed uniform distributions across all isolates. Comparative analysis of the degradome further revealed strong conservation of proteolytic and carbohydrate-active enzyme repertoires, dominated by serine and metallopeptidases and diverse glycoside hydrolases. The extensive genomic and functional similarity among isolates from geographically distant and ecologically distinct environments supports a broad ecological distribution of M. faecalis and suggests that its large and conserved genomic repertoire underpins its persistence across contrasting habitats. These findings expand the known ecological range of the species and provide a comparative genomic framework for future investigations into its distribution and functional potential across different habitats.

bioinformatics↗

Anticancer potential of piericidin A1 and derivatives isolated from Streptomyces sp. associated with Palythoa variabilis from Brazilian Reefs

Marine holobionts are prolific sources of bioactive natural products. Previously, our group investigated cytotoxic compounds in zoantharians of the genus Palythoa and, herein, we further explored the anticancer potential of marine bacteria associated with P. variabilis. After isolating 10 culturable bacterial strains, we screened for cytotoxic activity on metastatic prostate tumor cells (PC-3/M) using the MTT assay. The crude extract of one of the strains (BRA-035), identified as Streptomyces sp., was selected due to its bioactivity profile and submitted to cytotoxicity-guided fractionation. This approach allowed us to isolate piericidin A1 and identify other 2 piericidin derivatives. Piericidin A1 displayed a wide range of potency, with IC50 varying from pM to low nM for several tumor cells (OVCAR, PC-3, PC-3/M, HCT-116) or non active (IC50 >12uM) for leukemia cell line (HL-60) and murine melanoma (B16-F10). Overall, our findings demonstrate that P. variabilis hosts bacteria with biotechnological potential, confirming piericidin A1 as a promising candidate for anticancer applications.

pharmacology and toxicology↗

A Taxonomically-informed Mass Spectrometry Search Tool for Microbial Metabolomics Data

MicrobeMASST, a taxonomically-informed mass spectrometry (MS) search tool, tackles limited microbial metabolite annotation in untargeted metabolomics experiments. Leveraging a curated database of >60,000 microbial monocultures, users can search known and unknown MS/MS spectra and link them to their respective microbial producers via MS/MS fragmentation patterns. Identification of microbial-derived metabolites and relative producers, without a priori knowledge, will vastly enhance the understanding of microorganisms role in ecology and human health.

microbiology↗