Tina Keller-Costa

Dr. Tina Keller-Costa

Institute for Bioengineering and Biosciences (iBB), Instituto Superior Técnico (IST), Universidade de Lisboa, 1049-001 Lisbon, Portugal
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Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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21 July 2022 in Nature Microbiology
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Journal Article
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RPRaquel Peixoto
Raquel Peixoto
CVChristian Voolstra
Christian Voolstra
MSMichael Sweet
Michael Sweet
CDCarlos M Duarte
Carlos M Duarte
SCSusana Carvalho
Susana Carvalho
GBGabriele Berg
Gabriele Berg

29 June 2021 in mSystems
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Journal Article
Open access
MSMichael Sweet
Michael Sweet
HVHelena Villela
Helena Villela
Tina Keller-CostaTina Keller-Costa
Tina Keller-Costa
RCRodrigo Costa
Rodrigo Costa
SRStefano Romano
Stefano Romano
RPRaquel Peixoto
Raquel Peixoto
Our paper is the first study to synthesize currently available but decentralized data of cultured microbes associated with corals. We were able to collate 3,055 isolates across a number of published studies and unpublished collections from various laboratories and researchers around the world.

4 December 2018 in Marine Drugs
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Journal Article
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IRInês Raimundo
Inês Raimundo
Sandra Godinho SilvaSandra Godinho Silva
Sandra Godinho Silva
RCRodrigo Costa
Rodrigo Costa
Tina Keller-CostaTina Keller-Costa
Tina Keller-Costa
Octocorals (Cnidaria, Anthozoa Octocorallia) are magnificent repositories of natural products with fascinating and unusual chemical structures and bioactivities of interest to medicine and biotechnology. However, mechanistic understanding of the contribution of microbial symbionts to the chemical diversity of octocorals is yet to be achieved. This review inventories the natural products so-far described for octocoral-derived bacteria and fungi, uncovering a true chemical arsenal of terpenes, steroids, alkaloids, and polyketides with antibacterial, antifungal, antiviral, antifouling, anticancer, anti-inflammatory, and antimalarial activities of enormous potential for blue growth. Genome mining of 15 bacterial associates (spanning 12 genera) cultivated from Eunicella spp. resulted in the identification of 440 putative and classifiable secondary metabolite biosynthetic gene clusters (BGCs), encompassing varied terpene-, polyketide-, bacteriocin-, and nonribosomal peptide-synthase BGCs. This points towards a widespread yet uncharted capacity of octocoral-associated bacteria to synthetize a broad range of natural products. However, to extend our knowledge and foster the near-future laboratory production of bioactive compounds from (cultivatable and currently uncultivatable) octocoral symbionts, optimal blending between targeted metagenomics, DNA recombinant technologies, improved symbiont cultivation, functional genomics, and analytical chemistry are required. Such a multidisciplinary undertaking is key to achieving a sustainable response to the urgent industrial demand for novel drugs and enzyme varieties.

1 September 2015 in General and Comparative Endocrinology
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Journal Article
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Tina Keller-CostaTina Keller-Costa
Tina Keller-Costa
Adelino V. M. CanarioAdelino V. M. Canario
Adelino V. M. Canario
PHPeter Hubbard
Peter Hubbard

13 February 2019 in Scientific Reports
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EKElham Karimi
Elham Karimi
Tina Keller-CostaTina Keller-Costa
Tina Keller-Costa
BSBeate Slaby
Beate Slaby
CCCymon J. Cox
Cymon J. Cox
URUlisses Nunes da Rocha
Ulisses Nunes da Rocha
RCRodrigo Costa
Rodrigo Costa
Marine sponges are early-branching, filter-feeding metazoans that usually host complex microbiomes comprised of several, currently uncultivatable symbiotic lineages. Here, we use a low-carbon based strategy to cultivate low-abundance bacteria from Spongia officinalis. This approach favoured the growth of Alphaproteobacteria strains in the genera Anderseniella, Erythrobacter, Labrenzia, Loktanella, Ruegeria, Sphingorhabdus, Tateyamaria and Pseudovibrio, besides two likely new genera in the Rhodobacteraceae family. Mapping of complete genomes against the metagenomes of S. officinalis, seawater, and sediments confirmed the rare status of all the above-mentioned lineages in the marine realm. Remarkably, this community of low-abundance Alphaproteobacteria possesses several genomic attributes common to dominant, presently uncultivatable sponge symbionts, potentially contributing to host fitness through detoxification mechanisms (e.g. heavy metal and metabolic waste removal, degradation of aromatic compounds), provision of essential vitamins (e.g. B6 and B12 biosynthesis), nutritional exchange (especially regarding the processing of organic sulphur and nitrogen) and chemical defence (e.g. polyketide and terpenoid biosynthesis). None of the studied taxa displayed signs of genome reduction, indicative of obligate mutualism. Instead, versatile nutrient metabolisms along with motility, chemotaxis, and tight-adherence capacities - also known to confer environmental hardiness – were inferred, underlying dual host-associated and free-living life strategies adopted by these diverse sponge-associated Alphaproteobacteria.

14 February 2021 in Microbiome
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Journal Article
Open access
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IRI. Raimundo
I. Raimundo
RSR. Silva
R. Silva
LML. Meunier
L. Meunier
SVS. M. Valente
S. M. Valente
ALA. Lago-Lestón
A. Lago-Lestón
RCRodrigo Costa
Rodrigo Costa
Background: Chitin ranks as the most abundant polysaccharide in the oceans yet knowledge of shifts in structure and diversity of chitin-degrading communities across marine niches is scarce. Here, we integrate cultivation-dependent and -independent approaches to shed light on the chitin processing potential within the microbiomes of marine sponges, octocorals, sediments, and seawater.Results: We found that cultivatable host-associated bacteria in the generaAquimarina,Enterovibrio,Microbulbifer,Pseudoalteromonas,Shewanella, andVibriowere able to degrade colloidal chitin in vitro. Congruent with enzymatic activity bioassays, genome-wide inspection of cultivated symbionts revealed thatVibrioandAquimarinaspecies, particularly, possess several endo- and exo-chitinase-encoding genes underlying their ability to cleave the large chitin polymer into oligomers and dimers. Conversely,Alphaproteobacteriaspecies were found to specialize in the utilization of the chitin monomer N-acetylglucosamine more often. Phylogenetic assessments uncovered a high degree of within-genome diversification of multiple, full-length endo-chitinase genes forAquimarinaandVibriostrains, suggestive of a versatile chitin catabolism aptitude. We then analyzed the abundance distributions of chitin metabolism-related genes across 30 Illumina-sequenced microbial metagenomes and found that the endosymbiotic consortium ofSpongia officinalisis enriched in polysaccharide deacetylases, suggesting the ability of the marine sponge microbiome to convert chitin into its deacetylated—and biotechnologically versatile—form chitosan. Instead, the abundance of endo-chitinase and chitin-binding protein-encoding genes in healthy octocorals leveled up with those from the surrounding environment but was found to be depleted in necrotic octocoral tissue. Using cultivation-independent, taxonomic assignments of endo-chitinase encoding genes, we unveiled previously unsuspected richness and divergent structures of chitinolytic communities across host-associated and free-living biotopes, revealing putative roles for uncultivatedGammaproteobacteriaandChloroflexisymbionts in chitin processing within sessile marine invertebrates.Conclusions: Our findings suggest that differential chitin degradation pathways, utilization, and turnover dictate the processing of chitin across marine micro-niches and support the hypothesis that inter-species cross-feeding could facilitate the co-existence of chitin utilizers within marine invertebrate microbiomes. We further identified chitin metabolism functions which may serve as indicators of microbiome integrity/dysbiosis in corals and reveal putative novel chitinolytic enzymes in the genusAquimarinathat may find applications in the blue biotechnology sector.