Evidence map›Paper›PMID 40382556›Full record

ArticleBMC microbiology2025

The natural symbiotic bacterium Enterococcus faecalis LX10 drives Bombyx mori refractoriness to Nosema bombycis infection via the secretion of enterococcin.

Xiancui Zhang, Liang Yang, Tong Cai, Haoran Liao, Peiwen Cai, Xinkuang Zhao, Nengjie Gu, Zihan Yue, Yanzhou Gu, Fan Zhang and 2 more

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Xiancui ZhangSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Liang YangInstitute of Sericulture, Huzhou Academy of Agricultural Sciences, Huzhou, 313002, China.
Tong CaiShandong Center for Disease Control and Prevention, Jinan, 250014, China.
Haoran LiaoSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Peiwen CaiSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Xinkuang ZhaoSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Nengjie GuSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Zihan YueSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Yanzhou GuSchool of Life Science, Huzhou University, Huzhou, 313000, China.
Fan ZhangCollege of Life Science, Shandong Normal University, Jinan, 250358, China.
Choufei WuSchool of Life Science, Huzhou University, Huzhou, 313000, China. 02407@zjhu.edu.cn.
Xingmeng LuLaboratory of Invertebrate Pathology, College of Animal Sciences, Zhejiang University, Hangzhou, 310058, China. xmlu@zju.edu.cn.

Funding

A Project Supported by Scientific Research Fund of Zhejiang Provincial Education Department Y20235377The General Plan Project of Huzhou Science and Technology Bureau 2024YZ07
6 · The paper itself

Abstract

backgroundThe microsporidian Nosema bombycis is an obligate intracellular fungal-related parasites of the Bombyx mori, causing the epidemic disease Pebrine and extensive economic losses in the agricultural and sericulture industry. Enterococcus has emerged as one of the predominant gut microorganisms of the major model organism, Bombyx mori. However, the potential interactions mechanism between B. mori, N. bombycis and Enterococcus have not been well demonstrated.

methodsTo address this gap, we used an insect model, silkworm to examine the potential mechanism of the natural symbiotic bacterium Enterococcus faecalis LX10 drives B. mori refractoriness to N. bombycis infection. E. faecalis LX10 was isolated from the gut of healthy silkworms, and its inhibitory activity against N. bombycis was evaluated at both the cellular and individual levels using posttranslational modifications, gene and protein expression analysis, transfected cells, and in vitro immunofluorescence.

resultsWe demonstrated that enterococcin (EntLX), the first antimicrobial protein family in gut commensal bacterium Enterococcus faecalis LX10 of B. mori, contributes to defending against N. bombycis infection resistance depends on the enzyme gelatinase (GelE), disulfide bond and disulfide bond formation proteinA (DsbA). The EntLX protein, abundantly expressed in transgenic BmN cells and gut organs(gut epithelium, peritrophic membrane and contents), can reduce the infection rate of cells and alleviate intestinal damage caused by N. bombycis infection. After simultaneous vaccination with E. faecalis LX10 and N. bombycis, the differentially key metabolites, physiological characteristics(larval mass), or economic traits(cocoon length, cocoon width, whole-cocoon weight, cocoon shell weight, pupation rate and adult emergence rate) showed a certain degrees of recovery and correction compared with those of single N. bombycis inoculation at the individual level.

conclusionsThis study advances the understanding of the anti-microsporidia activity of enterococci and paves the way for the expression of these molecules as antifungal agents via the genetic transformation of Enterococcus symbionts from disease-transmitting insects. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Bacterial ProteinsBombyxEnterococcus faecalisNosemaSymbiosisAnimalsBacterial ProteinsBombyx moriEnterococcinEnterococcus faecalisNosema bombycisSymbionts

Identifiers

PMID40382556
PMCPMC12084927

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.