Evidence map›Paper›PMID 38531781›Full record

ArticleThe ISME journal2024

Role of Type VI secretion system in pathogenic remodeling of host gut microbiota during Aeromonas veronii infection.

Xiaoli Jiang, Hanzeng Li, Jiayue Ma, Hong Li, Xiang Ma, Yanqiong Tang, Juanjuan Li, Xue Chi, Yong Deng, Sheng Zeng and 1 more

Open access · goldAbstract read
In one paragraph

Article in The ISME journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Xiaoli JiangSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Hanzeng LiSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Jiayue MaSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Hong LiSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Xiang MaSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Yanqiong TangSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Juanjuan LiSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Xue ChiSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Yong DengWuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074, China.
Sheng ZengSusheng Biotech (Hainan) Co., Ltd, Haikou 570228, China.
Zhu LiuSchool of Life and Health Sciences, Hainan University, Haikou 570228, China.
Hainan University · CNWuhan National Laboratory for Optoelectronics · CN

Funding

National Natural Science Foundation of China 32160038Open Project Program of Wuhan National Laboratory for Optoelectronics 2020WNLOKF019
6 · The paper itself

Abstract

Intestinal microbial disturbance is a direct cause of host disease. The bacterial Type VI secretion system (T6SS) often plays a crucial role in the fitness of pathogenic bacteria by delivering toxic effectors into target cells. However, its impact on the gut microbiota and host pathogenesis is poorly understood. To address this question, we characterized a new T6SS in the pathogenic Aeromonas veronii C4. First, we validated the secretion function of the core machinery of A. veronii C4 T6SS. Second, we found that the pathogenesis and colonization of A. veronii C4 is largely dependent on its T6SS. The effector secretion activity of A. veronii C4 T6SS not only provides an advantage in competition among bacteria in vitro, but also contributes to occupation of an ecological niche in the nutritionally deficient and anaerobic environment of the host intestine. Metagenomic analysis showed that the T6SS directly inhibits or eliminates symbiotic strains from the intestine, resulting in dysregulated gut microbiome homeostasis. In addition, we identified three unknown effectors, Tse1, Tse2, and Tse3, in the T6SS, which contribute to T6SS-mediated bacterial competition and pathogenesis by impairing targeted cell integrity. Our findings highlight that T6SS can remodel the host gut microbiota by intricate interplay between T6SS-mediated bacterial competition and altered host immune responses, which synergistically promote pathogenesis of A. veronii C4. Therefore, this newly characterized T6SS could represent a general interaction mechanism between the host and pathogen, and may offer a potential therapeutic target for controlling bacterial pathogens.

Indexed as

Gastrointestinal MicrobiomeType VI Secretion SystemsAeromonas veroniiBacterial ProteinsEcosystemSymbiosisBacterial ProteinsType VI Secretion Systemsbacteria competitioneffector-immunity protein pairsgut microbiomehost–pathogen interactionmetagenomicsT6SS

Identifiers

PMID38531781
PMCPMC11014884
OpenAlexW4394761720

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.