Evidence map›Paper›PMID 31138863›Full record

ArticleScientific reports2019

Internalization, distribution, and activity of peptide H2 against the intracellular multidrug-resistant bovine mastitis-causing bacterium Staphylococcus aureus.

Xiao Wang, Da Teng, Xiumin Wang, Ya Hao, Huixian Chen, Ruoyu Mao, Jianhua Wang

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Effect of Two Different Drug-ResistantFrontiers in veterinary science · 2022
    Article
  10. Effect of NZ2114 againstFrontiers in microbiology · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

7 authors.

Xiao WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Da TengKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Xiumin WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Ya HaoKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Huixian ChenKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China.
Ruoyu MaoKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China. maoruoyu@caas.cn.
Jianhua WangKey Laboratory of Feed Biotechnology, Ministry of Agriculture, Beijing, 100081, People's Republic of China. 2681298635@qq.com.ORCID http://orcid.org/0000-0002-4048-6055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bovine mastitis is mainly caused by Staphylococcus aureus, which is difficult to eliminate, prone to escape from antibacterial agents, and may cause recurring infections due to the intracellular nature of its infection and multidrug resistance. In this study, the intracellular activities of the NZ2114 derivative peptide H18R (H2) against methicillin-resistant S. aureus (MRSA) and multidrug-resistant bovine S. aureus strains were investigated in bovine mammary epithelial MAC-T cells and mouse mammary glands. The minimum inhibitory concentrations of H2 against S. aureus were 0.5‒1 μg/ml; H2 displayed a lower cytotoxicity than its parental peptide NZ2114 (survival rates of MAC-T cells: 100% [H2 treatment] vs 60.7% [NZ2114 (256 μg/ml) treatment]). H2 was internalized into MAC-T cells mainly via clathrin-mediated endocytosis, and distributed in the cytoplasm. The intracellular inhibition rates against MRSA ATCC43300, the mastitis isolates S. aureus CVCC 3051 and E48 were above 99%, 99%, and 94%, respectively; these were higher than those in case of vancomycin (23-47%). In the mouse model of S. aureus E48-induced mastitis, after treatment with 100 μg of H2 and vancomycin, bacterial numbers in each mammary gland were reduced by 3.96- and 1.59-log CFU, respectively. Additionally, similar to NZ2114 and vancomycin, H2 alleviated the histopathological damage of the mammary tissue and polymorphonuclear neutrophil infiltration in the alveoli. These results suggest that H2 can be used as a safe and effective candidate for treating S. aureus-induced mastitis.

Indexed as

AnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCattleCell LineDrug Resistance, Multiple, BacterialEndocytosisEpithelial CellsFemaleMammary Glands, AnimalMastitis, BovineMethicillin-Resistant Staphylococcus aureusMiceMicrobial Sensitivity TestsNeutrophil InfiltrationStaphylococcal InfectionsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesVancomycin

Identifiers

PMID31138863
PMCPMC6538662

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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.