Evidence map›Paper›PMID 33913058›Full record

ArticleAMB Express2021

Engineered endolysin-based "artilysins" for controlling the gram-negative pathogen Helicobacter pylori.

Dengyuan Xu, Shanshan Zhao, Jun Dou, Xiaofeng Xu, Yanyan Zhi, Liangzhu Wen

Open access · goldAbstract read
In one paragraph

Article in AMB Express, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  7. Article
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  9. Review
  10. Opportunities forMicroorganisms · 2024
    Review
  11. Genetically Engineered Microorganisms and Their Impact on Human Health.International journal of clinical practice · 2024
    Review
  12. Article
  13. Review
  14. Characterization of the LysP2110-HolP2110 Lysis System inInternational journal of molecular sciences · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Review
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

6 authors at 2 institutions in 1 country.

Dengyuan XuChina Pharmaceutical University, Nanjing, 211100, China.
Shanshan ZhaoWanbang Pharmatech Co., Ltd, Xuzhou, 221004, China.
Jun DouChina Pharmaceutical University, Nanjing, 211100, China.
Xiaofeng XuWanbang Pharmatech Co., Ltd, Xuzhou, 221004, China.
Yanyan ZhiWanbang Pharmatech Co., Ltd, Xuzhou, 221004, China.
Liangzhu WenWanbang Pharmatech Co., Ltd, Xuzhou, 221004, China. wlz@wbpharma.com.ORCID http://orcid.org/0000-0002-5539-0144
China Pharmaceutical University · CNShanghai Techwell Biopharmaceutical (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Helicobacter pylori infection can cause a variety of gastrointestinal diseases. In severe cases, there is a risk of gastric cancer. Antibiotics are often used for clinical treatment of H. pylori infections. However, because of antibiotic overuse in recent years and the emergence of multidrug-resistant bacteria, there is an urgent need to develop new treatment methods and drugs to achieve complete eradication of H. pylori. Endolysins and holins encoded by bacterial viruses (i.e., phages) represent a promising avenue of investigation. These lyase-based antibacterial drugs act on the bacterial cell wall to destroy the bacteria. Currently, a type of endolysin that has been studied more frequently acts on the amide bond between peptidoglycans, and holin is a transmembrane protein that can punch holes in the cell membrane. However, as a Gram-negative bacterium, H. pylori possesses a layer of impermeable lipopolysaccharides on the cell wall, which prevents endolysin interaction with the cell wall. Therefore, we designed a genetic linkage between an endolysin enzyme and a holin enzyme with a section of polypeptides (e.g., polycations and hydrophobic peptides) that enable penetration of the outer membrane. These complexes were designated "artilysins" and were efficiently expressed in Escherichia coli. In vitro bacteriostasis experiments showed that the purified artilysins had strong bacteriostatic effects on H. pylori. In addition, the surface of H. pylori was perforated and destroyed, as confirmed by electron microscopy, which was proved that artilysins had bacteriolytic effect on H. pylori.

Indexed as

Escherichia coli expression systemHelicobacter pyloriHolin and endolysin phageIn vitro antibacterial assays

Identifiers

PMID33913058
PMCPMC8081812
OpenAlexW3155332721

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.