Evidence map›Paper›PMID 35216307›Full record

ArticleInternational journal of molecular sciences2022

Development of Bactericidal Peptides against Multidrug-Resistant

Prakash Kishore Hazam, Chin-Cheng Cheng, Chu-Yi Hsieh, Wen-Chun Lin, Po-Hsien Hsu, Te-Li Chen, Yi-Tzu Lee, Jyh-Yih Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  3. Threat and Control ofFoods (Basel, Switzerland) · 2025
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  5. The challenges of difficult-to-treatClinical microbiology reviews · 2024
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Antimicrobial Peptide Cec4 Eradicates Multidrug-ResistantDrug design, development and therapy · 2023
    Article
  12. Article
  13. Article
  14. Article
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 at 4 institutions in 1 country.

Prakash Kishore HazamMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road., Ilan 262, Taiwan.
Chin-Cheng ChengInstitute of Fisheries Science, National Taiwan University, 1 Roosevelt Road, Section 4, Taipei 112, Taiwan.
Chu-Yi HsiehMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road., Ilan 262, Taiwan.
Wen-Chun LinMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road., Ilan 262, Taiwan.
Po-Hsien HsuInstitute of Fisheries Science, National Taiwan University, 1 Roosevelt Road, Section 4, Taipei 112, Taiwan.
Te-Li ChenGraduate Institute of Life Sciences, National Defense Medical Center, Taipei 112, Taiwan.
Yi-Tzu LeeDepartment of Emergency Medicine, Taipei Veterans General Hospital, No. 201, Section 2, Shipai Road, Taipei 112, Taiwan.ORCID 0000-0002-6183-4987
Jyh-Yih ChenMarine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road., Ilan 262, Taiwan.ORCID 0000-0001-7858-8236
Institute of Cellular and Organismic Biology, Academia Sinica · TWNational Taiwan University · TWNational Yang Ming Chiao Tung University · TWNational Chung Hsing University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic superbugs are the root cause of untreatable complex infections with limited or no treatment options. These infections are becoming more common as clinical antibiotics have lost their effectiveness over time. Therefore, the development of novel antibacterial agents is urgently needed to counter these microbes. Antimicrobial peptides (AMPs) are a viable treatment option due to their bactericidal potency against multiple microbial classes. AMPs are naturally selected physiological microbicidal agents that are found in all forms of organisms. In the present study, we developed two tilapia piscidin 2 (TP2)-based AMPs for antimicrobial application. Unlike the parent peptide, the redesigned peptides showed significant antimicrobial activity against multidrug-resistant bacterial species. These peptides also showed minimal cytotoxicity. In addition, they were significantly active in the presence of physiological salts, 50% human serum and elevated temperature. The designed peptides also showed synergistic activity when combined with clinical antibiotics. The current approach demonstrates a fruitful strategy for developing potential AMPs for antimicrobial application. Such AMPs have potential for progression to further trials and drug development investigations.

Indexed as

Acinetobacter baumanniiAnti-Infective AgentsAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialHumansMicrobial Sensitivity TestsAnti-Bacterial AgentsAnti-Infective Agentsantimicrobial peptideantimicrobial resistanceMDR infectiontilapia piscidin

Identifiers

PMID35216307
PMCPMC8875074
OpenAlexW4213141484

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.