Evidence map›Paper›PMID 36765333›Full record

ArticleBMC veterinary research2023

Host defence peptide LEAP2 contributes to antimicrobial activity in a mustache toad (Leptobrachium liui).

Jie Chen, Chi-Ying Zhang, Jing-Yi Chen, Rachel Wan Xin Seah, Le Zhang, Li Ma, Guo-Hua Ding

Abstract read
In one paragraph

Article in BMC veterinary research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
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  5. Review
  6. LEAP2 in Physiology-A Narrative Review.International journal of molecular sciences · 2025
    Review
  7. Article
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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

7 authors.

Jie Chen *Laboratory of Amphibian Diversity Investigation, College of Ecology, Lishui University, Lishui, 323000, China.
Chi-Ying Zhang *Laboratory of Amphibian Diversity Investigation, College of Ecology, Lishui University, Lishui, 323000, China.
Jing-Yi ChenLaboratory of Amphibian Diversity Investigation, College of Ecology, Lishui University, Lishui, 323000, China.
Rachel Wan Xin SeahDepartment of Biological Science, National University of Singapore, Singapore, 117558, Singapore.
Le ZhangSchool of Medicine, Lishui University, Lishui, 323000, China.
Li MaLaboratory of Amphibian Diversity Investigation, College of Ecology, Lishui University, Lishui, 323000, China.
Guo-Hua DingLaboratory of Amphibian Diversity Investigation, College of Ecology, Lishui University, Lishui, 323000, China. guwoding@lsu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe liver-expressed antimicrobial peptide 2 (LEAP2) is essential in host immunity against harmful pathogens and is only known to act as an extracellular modulator to regulate embryonic development in amphibians. However, there is a dearth of information on the antimicrobial function of amphibian LEAP2. Hence, a LEAP2 homologue from Leptobrachium liui was identified, characterized, and chemically synthesized, and its antibacterial activities and mechanisms were determined.

resultsIn this study, LEAP2 gene (Ll-LEAP2) cDNA was cloned and sequenced from the Chong'an Moustache Toad (Leptobrachium liui). The predicted amino acid sequence of Ll-LEAP2 comprises a signal peptide, a mature peptide, and a prodomain. From sequence analysis, it was revealed that Ll-LEAP2 belongs to the cluster of amphibian LEAP2 and displays high similarity to the Tropical Clawed Frog (Xenopus tropicalis)'s LEAP2. Our study revealed that LEAP2 protein was found in different tissues, with the highest concentration in the kidney and liver of L. liui; and Ll-LEAP2 mRNA transcripts were expressed in various tissues with the kidney having the highest mRNA expression level. As a result of Aeromonas hydrophila infection, Ll-LEAP2 underwent a noticeable up-regulation in the skin while it was down-regulated in the intestines. The chemically synthesized Ll-LEAP2 mature peptide was selective in its antimicrobial activity against several in vitro bacteria including both gram-positive and negative bacteria. Additionally, Ll-LEAP2 can kill specific bacteria by disrupting bacterial membrane and hydrolyzing bacterial gDNA.

conclusionsThis study is the first report on the antibacterial activity and mechanism of amphibian LEAP2. With more to uncover, the immunomodulatory functions and wound-healing activities of Ll-LEAP2 holds great potential for future research.

Indexed as

Anti-Bacterial AgentsAntimicrobial Cationic PeptidesAmino Acid SequenceAnimalsBase SequenceRNA, MessengerAnti-Bacterial AgentsAntimicrobial Cationic PeptidesRNA, MessengerAantibacterial activityAantibacterial mechanismAmphibianGgene expressionLliver-expressed antimicrobial peptide 2

Identifiers

PMID36765333
PMCPMC9921027

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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.