DOI: 10.1128/spectrum.03672-25 ISSN: 2165-0497
Extensive library of
Ruminococcus gnavus
phages revealing genomic and phenotypic diversity with novel clusters
Arata Sakiyama, Ayaka Washizaki, Keiko Inaba-Hasegawa, Most Hushna Ara Naznin, Keigo Ide, Masayuki Takase, Yoriko Ibuki, Yuichi Sawaguchi, Shoichi Mitsunaka, Yutaro Ono, Islam Mohammad Shyful, Hiroki Ando ABSTRACT
Ruminococcus gnavus
is a prevalent member of human gut microbiota and is associated with inflammatory bowel disease. Phage-based microbiota engineering represents a promising approach for alleviating dysbiosis; however, knowledge regarding
R. gnavus
phages remains limited. We report the isolation and characterization of 29 novel
R. gnavus
phages from sewage samples. All isolates exhibited siphovirus morphology, with genome sizes ranging from 32.3 to 46.0 kbp, and represented 18 putative new genera and 24 new species. Whole-proteome clustering tools indicated that
R. gnavus
phages form a distinct new cluster and are divided into three clusters that could correspond to new subfamilies. Representative phages from each cluster were phenotypically characterized in detail, based on adsorption kinetics, one-step growth, and stress tolerance assays, which revealed diverse infection dynamics and structural features, such as unique globular appendages at distal tail fibers. Collectively, this study established the largest and most diverse
R. gnavus
phage library to date, providing fundamental insights into phage–host interactions and a valuable resource for the future development of phage-based strategies to modulate
R. gnavus
in the human gut.
IMPORTANCE
Ruminococcus gnavus
is a common gut commensal consistently associated with inflammatory bowel disease (IBD). Phage-based microbiota engineering has emerged as a promising strategy for alleviating dysbiosis. However, progress has been hampered by the limited availability of
R. gnavus
phages. In this study, we established and characterized a library of 29 novel
R. gnavus
phages. Whole-genome/proteome and phenotypic analyses revealed that these phages may represent a new taxonomic lineage and display variation in their infection strategies. This work substantially expands the known repertoire of
R. gnavus
phages and provides a critical resource for dissecting phage–host interactions in the human gut. Importantly, our findings lay the foundation for the future development of phage-based approaches to selectively modulate
R. gnavus
populations and inform therapeutic strategies for IBD.