4.7 Article

Insights into the Variation in Bioactivities of Closely Related Streptomyces Strains from Marine Sediments of the Visayan Sea against ESKAPE and Ovarian Cancer

Journal

MARINE DRUGS
Volume 19, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/md19080441

Keywords

marine Streptomyces strains; antibiotics; marine sediments; chemodiversity; polyketide synthase; nonribosomal peptide synthetase; metabolomics; ESKAPE pathogens

Funding

  1. Tuklas Lunas Development Center Program of the Department of Science and Technology-Philippine Council for Health Research and Development (DOST-PCHRD)

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This study explored the biodiversity, bioactivities, and metabolite variation of culturable actinomycetes isolated from marine sediments in the Visayan Sea, Philippines. The research revealed that the chemical diversity among these strains influences the variation observed in their biological activities, with taxonomically identical strains producing core and strain-specific metabolites. The study highlights the potential of marine-derived Streptomyces as a source of small molecules against ESKAPE pathogens and cancer, and the unique strain-specific secondary metabolites produced by Streptomyces species strains offer new chemical space for natural product discovery.
Marine sediments host diverse actinomycetes that serve as a source of new natural products to combat infectious diseases and cancer. Here, we report the biodiversity, bioactivities against ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.) and ovarian cancer, and metabolites variation among culturable actinomycetes isolated from the marine sediments of Visayan Sea, Philippines. We identified 15 Streptomyces species based on a 16S rRNA gene sequence analysis. The crude extracts of 10 Streptomyces species have inhibited the growth of ESKAPE pathogens with minimum inhibitory concentration (MIC) values ranging from 0.312 mg/mL to 20 mg/mL depending on the strain and pathogens targeted. Additionally, ten crude extracts have antiproliferative activity against A2780 human ovarian carcinoma at 2 mg/mL. To highlight, we observed that four phylogenetically identical Streptomyces albogriseolus strains demonstrated variation in antibiotic and anticancer activities. These strains harbored type I and II polyketide synthase (PKS) and non-ribosomal synthetase (NRPS) genes in their genomes, implying that their bioactivity is independent of the polymerase chain reaction (PCR)-detected bio-synthetic gene clusters (BGCs) in this study. Metabolite profiling revealed that the taxonomically identical strains produced core and strain-specific metabolites. Thus, the chemical diversity among these strains influences the variation observed in their biological activities. This study expanded our knowledge on the potential of marine-derived Streptomyces residing from the unexplored regions of the Visayan Sea as a source of small molecules against ESKAPE pathogens and cancer. It also highlights that Streptomyces species strains produce unique strain-specific secondary metabolites; thus, offering new chemical space for natural product discovery.

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