» Articles » PMID: 31666699

Human Gut Bacteria Contain Acquired Interbacterial Defence Systems

Overview
Journal Nature
Specialty Science
Date 2019 Nov 1
PMID 31666699
Citations 65
Authors
Affiliations
Soon will be listed here.
Abstract

The human gastrointestinal tract consists of a dense and diverse microbial community, the composition of which is intimately linked to health. Extrinsic factors such as diet and host immunity are insufficient to explain the constituents of this community, and direct interactions between co-resident microorganisms have been implicated as important drivers of microbiome composition. The genomes of bacteria derived from the gut microbiome contain several pathways that mediate contact-dependent interbacterial antagonism. Many members of the Gram-negative order Bacteroidales encode the type VI secretion system (T6SS), which facilitates the delivery of toxic effector proteins into adjacent cells. Here we report the occurrence of acquired interbacterial defence (AID) gene clusters in Bacteroidales species that reside within the human gut microbiome. These clusters encode arrays of immunity genes that protect against T6SS-mediated intra- and inter-species bacterial antagonism. Moreover, the clusters reside on mobile elements, and we show that their transfer is sufficient to confer resistance to toxins in vitro and in gnotobiotic mice. Finally, we identify and validate the protective capability of a recombinase-associated AID subtype (rAID-1) that is present broadly in Bacteroidales genomes. These rAID-1 gene clusters have a structure suggestive of active gene acquisition and include predicted immunity factors of toxins derived from diverse organisms. Our data suggest that neutralization of contact-dependent interbacterial antagonism by AID systems helps to shape human gut microbiome ecology.

Citing Articles

Interbacterial warfare in the human gut: insights from Bacteroidales' perspective.

Jiang K, Pang X, Li W, Xu X, Yang Y, Shang C Gut Microbes. 2025; 17(1):2473522.

PMID: 40038576 PMC: 11901371. DOI: 10.1080/19490976.2025.2473522.


Perioperative Multi-Kingdom Gut Microbiota Alters in Coronary Artery Bypass Grafting.

Fu Z, Jia Y, Zhao J, Guo Y, Xie B, An K Biomedicines. 2025; 13(2).

PMID: 40002888 PMC: 11853347. DOI: 10.3390/biomedicines13020475.


Phages carry orphan antitoxin-like enzymes to neutralize the DarTG1 toxin-antitoxin defense system.

Johannesman A, Awasthi L, Carlson N, LeRoux M Nat Commun. 2025; 16(1):1598.

PMID: 39948090 PMC: 11825919. DOI: 10.1038/s41467-025-56887-7.


Decoding resistance in the age of T6SS warfare.

Shikuma N Proc Natl Acad Sci U S A. 2025; 122(7):e2500342122.

PMID: 39928881 PMC: 11848427. DOI: 10.1073/pnas.2500342122.


Global biogeography and projection of antimicrobial toxin genes.

Liu Y, Geng Y, Jiang Y, Sun J, Li P, Li Y Microbiome. 2025; 13(1):40.

PMID: 39905479 PMC: 11796102. DOI: 10.1186/s40168-025-02038-5.


References
1.
Whitney J, Peterson S, Kim J, Pazos M, Verster A, Radey M . A broadly distributed toxin family mediates contact-dependent antagonism between gram-positive bacteria. Elife. 2017; 6. PMC: 5555719. DOI: 10.7554/eLife.26938. View

2.
Zhang D, de Souza R, Anantharaman V, Iyer L, Aravind L . Polymorphic toxin systems: Comprehensive characterization of trafficking modes, processing, mechanisms of action, immunity and ecology using comparative genomics. Biol Direct. 2012; 7:18. PMC: 3482391. DOI: 10.1186/1745-6150-7-18. View

3.
Coyne M, Roelofs K, Comstock L . Type VI secretion systems of human gut Bacteroidales segregate into three genetic architectures, two of which are contained on mobile genetic elements. BMC Genomics. 2016; 17:58. PMC: 4714493. DOI: 10.1186/s12864-016-2377-z. View

4.
Russell A, Wexler A, Harding B, Whitney J, Bohn A, Goo Y . A type VI secretion-related pathway in Bacteroidetes mediates interbacterial antagonism. Cell Host Microbe. 2014; 16(2):227-236. PMC: 4136423. DOI: 10.1016/j.chom.2014.07.007. View

5.
Hood R, Singh P, Hsu F, Guvener T, Carl M, Trinidad R . A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria. Cell Host Microbe. 2010; 7(1):25-37. PMC: 2831478. DOI: 10.1016/j.chom.2009.12.007. View