Diversity-generating retroelements (DGRs) accelerate evolution by rapidly diversifying variable proteins. The human gastrointestinal microbiota harbors the greatest density of DGRs known in nature, suggesting they play adaptive roles in this environment. We identified >1,100 unique DGRs among human-associated species and discovered a subset that diversify adhesive components of Type V pili and related proteins. We show that DGRs are horizontally transferred across species, that some are highly active while others are tightly controlled, and that they preferentially alter the functional characteristics of ligand-binding residues on adhesive organelles. Specific variable protein sequences are enriched when strains compete with other commensal bacteria in gnotobiotic mice. Analysis of >2,700 DGRs from diverse phyla in mother-infant pairs shows that DGRs are preferentially transferred to vaginally delivered infants where they actively diversify. Our observations provide a foundation for understanding the roles of stochastic, targeted genome plasticity in shaping host-associated microbial communities.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11601372PMC
http://dx.doi.org/10.1101/2024.11.15.621889DOI Listing

Publication Analysis

Top Keywords

diversity-generating retroelements
8
dgrs
6
targeted protein
4
protein evolution
4
evolution gut
4
gut microbiome
4
microbiome diversity-generating
4
retroelements diversity-generating
4
retroelements dgrs
4
dgrs accelerate
4

Similar Publications

Diversity-generating retroelements (DGRs) create massive protein sequence variation (up to 10) in ecologically diverse microorganisms. A recent survey identified around 31,000 DGRs from more than 1,500 bacterial and archaeal genera, constituting more than 90 environment types. DGRs are especially enriched in the human gut microbiome and nano-sized microorganisms that seem to comprise most microbial life and maintain DGRs despite reduced genomes.

View Article and Find Full Text PDF
Article Synopsis
  • Metagenomics has uncovered a vast diversity of phages in the human gut, but detailed studies on these phages are limited.
  • A new bioinformatics method was developed to identify prophages in cultured gut bacteria, leading to the discovery of 15 candidate prophages, with five validated as active.
  • The study also found that some active phages had unique genetic features and varied host ranges, while noting a difference in prevalence among inflammatory bowel disease patients compared to healthy individuals, emphasizing the potential of studying prophage dynamics in understanding microbial ecology.
View Article and Find Full Text PDF

Background: The diversity-generating retroelements (DGRs) are a family of genetic elements that can produce mutations in target genes often related to ligand-binding functions, which possess a C-type lectin (CLec) domain that tolerates massive variations. They were first identified in viruses, then in bacteria and archaea from human-associated and environmental genomes. This DGR mechanism represents a fast adaptation of organisms to ever- changing environments.

View Article and Find Full Text PDF

Diversity-generating retroelements (DGRs) accelerate evolution by rapidly diversifying variable proteins. The human gastrointestinal microbiota harbors the greatest density of DGRs known in nature, suggesting they play adaptive roles in this environment. We identified >1,100 unique DGRs among human-associated species and discovered a subset that diversify adhesive components of Type V pili and related proteins.

View Article and Find Full Text PDF

CrAss-like phages play an important role in maintaining ecological balance in the human intestinal microbiome. However, their genetic diversity and lifestyle are still insufficiently studied. In this study, a novel CrAssE-Sib phage genome belonging to the epsilon crAss-like phage genomes was found.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!