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Relating the gut metagenome and metatranscriptome to immunotherapy responses in melanoma patients

Authors
  • Peters, Brandilyn A.1
  • Wilson, Melissa2, 3, 4
  • Moran, Una3, 5
  • Pavlick, Anna2, 3
  • Izsak, Allison5
  • Wechter, Todd5
  • Weber, Jeffrey S.2, 3
  • Osman, Iman2, 3, 5
  • Ahn, Jiyoung1, 3
  • 1 NYU School of Medicine, Department of Population Health, New York, NY, 10016, USA , New York (United States)
  • 2 NYU School of Medicine, Department of Medicine, New York, NY, USA , New York (United States)
  • 3 NYU Perlmutter Cancer Center, New York, NY, USA , New York (United States)
  • 4 Thomas Jefferson University, Present Address: Sidney Kimmel Cancer Center, Philadelphia, PA, USA , Philadelphia (United States)
  • 5 NYU School of Medicine, The Ronald O. Perelman Department of Dermatology, New York, NY, USA , New York (United States)
Type
Published Article
Journal
Genome Medicine
Publisher
Springer (Biomed Central Ltd.)
Publication Date
Oct 09, 2019
Volume
11
Issue
1
Identifiers
DOI: 10.1186/s13073-019-0672-4
Source
Springer Nature
Keywords
License
Green

Abstract

BackgroundRecent evidence suggests that immunotherapy efficacy in melanoma is modulated by gut microbiota. Few studies have examined this phenomenon in humans, and none have incorporated metatranscriptomics, important for determining expression of metagenomic functions in the microbial community.MethodsIn melanoma patients undergoing immunotherapy, gut microbiome was characterized in pre-treatment stool using 16S rRNA gene and shotgun metagenome sequencing (n = 27). Transcriptional expression of metagenomic pathways was confirmed with metatranscriptome sequencing in a subset of 17. We examined associations of taxa and metagenomic pathways with progression-free survival (PFS) using 500 × 10-fold cross-validated elastic-net penalized Cox regression.ResultsHigher microbial community richness was associated with longer PFS in 16S and shotgun data (p < 0.05). Clustering based on overall microbiome composition divided patients into three groups with differing PFS; the low-risk group had 99% lower risk of progression than the high-risk group at any time during follow-up (p = 0.002). Among the species selected in regression, abundance of Bacteroides ovatus, Bacteroides dorei, Bacteroides massiliensis, Ruminococcus gnavus, and Blautia producta were related to shorter PFS, and Faecalibacterium prausnitzii, Coprococcus eutactus, Prevotella stercorea, Streptococcus sanguinis, Streptococcus anginosus, and Lachnospiraceae bacterium 3 1 46FAA to longer PFS. Metagenomic functions related to PFS that had correlated metatranscriptomic expression included risk-associated pathways of l-rhamnose degradation, guanosine nucleotide biosynthesis, and B vitamin biosynthesis.ConclusionsThis work adds to the growing evidence that gut microbiota are related to immunotherapy outcomes, and identifies, for the first time, transcriptionally expressed metagenomic pathways related to PFS. Further research is warranted on microbial therapeutic targets to improve immunotherapy outcomes.

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