RCMI-CCRHD Research Grants Program 2022–2027 “The Microbiome as a risk factor for hr-HPV persistence and Cervical Cancer, Center for Collaborative Research in Health Disparities”

Research Areas

  • Human and animal microbiome ecology
  • Metagenomics and multi-omics integration
  • Microbiome – Host symbioses in cancer biology and HPV persistence
  • Host–microbiome–environment interactions
  • Microbial biodiversity, conservation and restoration

Scientific Achievements

  • Discoveries: First works in the region linking microbial gut physiology in vertebrate and invertebrate animals and revealed the first bacterial and fungal biomarkers of HPV infections in cancer progression; co-discovery of a bacterial phylum Rokubacteria; interindividual microbiome variation in animals
  • Capacity Building: Founded Puerto Rico’s first microbiome laboratory, training 100+ students, postdocs, and faculty
  • International Leadership: Global Ambassador for the Americas Applied Microbiology International; ISME Ambassador for Puerto Rico and the Caribbean

Funding

RCMI Funding:

  • NIH/NIMHD U54MD007600

Other funding obtained with RCMI support:

  • R21DE027226, NIH/NIDCR, “Cross-sectional associations of oral microbiota with oral HPV infection among high-risk Hispanic adults”
  • R21ES034191, NIH/NIEHS, “Effects of environmental contaminants on anxiety-like and fear behaviors, and gut-microbiota in rodents”
  • 1P20GM156713, NIH/NIGMS: “COBRE Phase 1: Puerto Rico Center for Microbiome Sciences”

Scientific Advance

Oncolytic Virotherapies and Adjuvant Gut Microbiome Therapeutics to Enhance Efficacy Against Malignant Gliomas
Published in Viruses, Volume 16, 2024, PMCID: PMC11599061
This review explores combining oncolytic virotherapy (viruses engineered to infect and kill cancer cells) with interventions targeting the gut microbiome to treat malignant gliomas (a type of aggressive brain tumor). The authors summarize how certain viruses are able to enter, replicate in, and destroy glioma cells, and how the gut microbiome might influence patient outcomes — for example by modulating immune responses, inflammation, or how well the virus can reach tumors. They also discuss how probiotics, prebiotics, or other microbiome-modifying strategies may enhance the effectiveness of oncolytic viruses, potentially making treatments more potent and less toxic. The review offers insights into recent clinical trials, preclinical data, possible mechanisms, and suggests how further research might optimize therapy by considering both virus and microbiome together.
U54 MD007600/NIMHD NIH HHS/United States, U54 CA096297/NCI NIH HHS/United States, 2U54CA096297/ NCI NIH HHS/United States, R01 CA256006/NCI NIH HHS/United States, R01CA256006/NCI NIH HHS/United States, R25 GM061838/NIGMS NIH HHS/United States
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