Evidence map›Paper›PMID 35192238›Full record

ArticlePest management science2022

The gut commensal bacterium Enterococcus faecalis LX10 contributes to defending against Nosema bombycis infection in Bombyx mori.

Xiancui Zhang, Huihui Feng, Jintao He, Xili Liang, Nan Zhang, Yongqi Shao, Fan Zhang, Xingmeng Lu

Abstract read
In one paragraph

Article in Pest management science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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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

8 authors.

Xiancui ZhangInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0002-8412-964X
Huihui FengInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Jintao HeInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Xili LiangInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Nan ZhangInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Yongqi ShaoInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Fan ZhangKey Laboratory of Animal Resistance Biology of Shandong Province, College of Life Science, Shandong Normal University, Jinan, China.ORCID https://orcid.org/0000-0002-3281-6325
Xingmeng LuInstitute of Sericulture and Apiculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.

Funding

China Agriculture Research System of MOF and MARANational Natural Science Foundation of China (81572027)
6 · The paper itself

Abstract

backgroundMicrosporidia, a group of obligate intracellular fungal-related parasites, have been used as efficient biocontrol agents for agriculture and forestry pests due to their host specificity and transovarial transmission. They mainly infect insect pests through the intestinal tract, but the interactions between microsporidia and the gut microbiota of the host have not been well demonstrated.

resultsBased on the microsporidia-Bombyx mori model, we report that the susceptibility of silkworms to exposure to the microsporidium Nosema bombycis was both dose and time dependent. Comparative analyses of the silkworm gut microbiome revealed substantially increased abundance of Enterococcus belonging to Firmicutes after N. bombycis infection. Furthermore, a bacterial strain (LX10) was obtained from the gut of B. mori and identified as Enterococcus faecalis based on 16S rRNA sequence analysis. E. faecalis LX10 reduced the N. bombycis spore germination rate and the infection efficiency in vitro and in vivo, as confirmed by bioassay tests and histopathological analyses. In addition, after simultaneous oral feeding with E. faecalis LX10 and N. bombycis, gene (Akirin, Cecropin A, Mesh, Ssk, DUOX and NOS) expression, hydrogen peroxide and nitric oxide levels, and glutathione S-transferase (GST) activity showed different degrees of recovery and correction compared with those under N. bombycis infection alone. Finally, the enterococcin LX protein was identified from sterile LX10 fermentation liquid based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis.

conclusionAltogether, the results revealed that E. faecalis LX10 with anti-N. bombycis activity might play an important role in protecting silkworms from microsporidia. Removal of these specific commensal bacteria with antibiotics and utilization of transgenic symbiotic systems may effectively improve the biocontrol value of microsporidia. © 2022 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Indexed as

BombyxNosemaAnimalsChromatography, LiquidEnterococcus faecalisRNA, Ribosomal, 16STandem Mass SpectrometryRNA, Ribosomal, 16Santi-Nosema bombycis activityBombyx moriEnterococcus faecalismicrosporidiaprotein

Identifiers

PMID35192238
PMCPMC9314687

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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.