Study record

MOTS-c peptide increases survival and decreases bacterial load in mice infected with MRSA

Zhai D, Ye Z, Jiang Y et al. · Mol Immunol · 2017

AnimalMOTS-c administeredEvidence tier CAlso: Cell study (in vitro)

What this study reported

In MRSA-challenged mice, MOTS-c was associated with higher survival and lower bacterial load, lower pro-inflammatory cytokines (TNF-α, IL-6, IL-1β) and higher IL-10. In macrophages, MOTS-c was reported to enhance bactericidal capacity, inhibit MAPK phosphorylation and increase AhR and STAT3 expression.

Limitations

Single infection model with group sizes, sex and administration details not reported in the abstract; macrophage source not specified.

Study record

Annotated fields for this study
Study modelAnimal study (in vivo)
Substance studiedMOTS-c administeredSynthetic MOTS-c was given to cells, animals or people.
Speciesmouse
System studiedMice challenged with methicillin-resistant Staphylococcus aureus (MRSA); macrophages
PopulationNot reported
DesignControlled animal experiment with macrophage experiments
Sample size as reportedNot reported
Control groupMRSA-challenged mice not given MOTS-c (implied)
Route (data field only)Not reported
Endpoints measuredsurvival; bacterial load; serum cytokines (TNF-α, IL-6, IL-1β, IL-10); macrophage bactericidal capacity; MAPK phosphorylation; AhR and STAT3 expression
Pathways measuredInflammation · MAPK signalling
Research areasInflammation & immunity
Evidence tierC — Animal in vivo
Publication typesJournal Article, Research Support, Non-U.S. Gov't

Appraisal

Each dimension is recorded separately and never combined into a single score. A study can be well controlled and still tell you little about people.

Relevance to MOTS-c
Direct
Model applicability
Mammalian
Sample size
Not reported
Controls
Limited
Outcome validity
Surrogate
Support for its own conclusion
Moderate

Provenance

  • Bibliographic fields retrieved from PubMed E-utilities efetch (title, journal, date, authors, DOI) on 2026-11-11.
  • Annotated from the published abstract.
  • Editorial review: approved (2026-11-11).
  • Classification follows the site methodology; the record describes the study, not what MOTS-c does in people.