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Published on: January 26, 2024
Acquisition, transmission and strain diversity of human gut-colonizing crAss-like phages
Benjamin A Siranosian1, Fiona B Tamburini1, Gavin Sherlock1
1Department of Genetics, Stanford University, Stanford, CA, USA.
Abstract:
CrAss-like phages are double-stranded DNA viruses that are prevalent in human gut microbiomes. Here, we analyze gut metagenomic data from mother-infant pairs and patients undergoing fecal microbiota transplantation to evaluate the patterns of acquisition, transmission and strain diversity of crAss-like phages. We find that crAss-like phages are rarely detected at birth but are increasingly prevalent in the infant microbiome after one month of life. We observe nearly identical genomes in 50% of cases where the same crAss-like clade is detected in both the mother and the infant, suggesting vertical transmission. In cases of putative transmission of prototypical crAssphage (p-crAssphage), we find that a subset of strains present in the mother are detected in the infant, and that strain diversity in infants increases with time. Putative tail fiber proteins are enriched for nonsynonymous strain variation compared to other genes, suggesting a potential evolutionary benefit to maintaining strain diversity in specific genes. Finally, we show that p-crAssphage can be acquired through fecal microbiota transplantation.
Insights
CrAss-like phages are common in human guts. Infants acquire these viruses after birth, often from mothers, and their diversity increases over time, with potential transmission via fecal transplants.
Area of Science:
- Microbiology
- Virology
- Human Microbiome
Background:
- CrAss-like phages are prevalent double-stranded DNA viruses in the human gut microbiome.
- Understanding their acquisition and transmission is crucial for microbiome research.
Purpose of the Study:
- To investigate crAss-like phage acquisition, transmission, and strain diversity in mother-infant pairs.
- To evaluate crAss-like phage transmission through fecal microbiota transplantation (FMT).
Main Methods:
- Analysis of gut metagenomic data from mother-infant pairs.
- Tracking crAss-like phage clades and specific strains.
- Assessment of phage genomes and protein variations.
- Evaluation of FMT samples for phage acquisition.
Main Results:
- CrAss-like phages are rare at birth but prevalent by one month in infants.
- Vertical transmission from mother to infant is suggested by near-identical genomes.
- Infant crAss-like phage strain diversity increases over time.
- Putative tail fiber proteins show high strain variation, suggesting evolutionary importance.
- Prototypical crAssphage (p-crAssphage) can be acquired via FMT.
Conclusions:
- CrAss-like phages colonize the infant gut postnatally, with mothers as a likely source.
- Strain diversity, particularly in tail fiber proteins, is a key feature of crAss-like phages.
- Fecal microbiota transplantation is a viable route for crAss-like phage acquisition.
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