Evidence map›Paper›PMID 36550444›Full record

ReviewBMC infectious diseases2022

Bacteriophages of Mycobacterium tuberculosis, their diversity, and potential therapeutic uses: a review.

Fatemeh Zeynali Kelishomi, Susan Khanjani, Fatemeh Fardsanei, Hediyeh Saghi Sarabi, Farhad Nikkhahi, Behzad Dehghani

Open access · goldAbstract readReview
In one paragraph

Review in BMC infectious diseases, 2022. 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
5.6field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Phage Therapy forInfectious disease reports · 2025
    Article
  5. Article
  6. Antibiotic Resistance ofPharmaceuticals (Basel, Switzerland) · 2025
    Review
  7. Human Gut Bacteriophageome: Insights Into Drug Resistance Mechanisms in Tuberculosis.Interdisciplinary perspectives on infectious diseases · 2025
    Review
  8. Review
  9. Article
  10. The Biological Characteristics ofInternational journal of molecular sciences · 2024
    Article
  11. Can We Exploit Inflammasomes for Host-Directed Therapy in the Fight againstInternational journal of molecular sciences · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  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

6 authors at 2 institutions in 1 country.

Fatemeh Zeynali KelishomiMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Susan KhanjaniMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Fatemeh FardsaneiMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Hediyeh Saghi SarabiMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Farhad NikkhahiMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran. farhadnikkhahi@gmail.com.
Behzad DehghaniDepartment of Bacteriology-Virology, Shiraz University of Medical Sciences, Shiraz, Iran.
Qazvin University of Medical Sciences · IRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) caused by Mycobacterium tuberculosis (M. tuberculosis) is a highly infectious disease and worldwide health problem. Based on the WHO TB report, 9 million active TB cases are emerging, leading to 2 million deaths each year. The recent emergence of multidrug-resistant tuberculosis (MDR-TB) and extensively drug-resistant tuberculosis (XDR-TB) strains emphasizes the necessity to improve novel therapeutic plans. Among the various developing antibacterial approaches, phage therapy is thought to be a precise hopeful resolution. Mycobacteriophages are viruses that infect bacteria such as Mycobacterium spp., containing the M. tuberculosis complex. Phages and phage-derived proteins can act as promising antimicrobial agents. Also, phage cocktails can broaden the spectrum of lysis activity against bacteria. Recent researches have also shown the effective combination of antibiotics and phages to defeat the infective bacteria. There are limitations and concerns about phage therapy. For example, human immune response to phage therapy, transferring antibiotic resistance genes, emerging resistance to phages, and safety issues. So, in the present study, we introduced mycobacteriophages, their use as therapeutic agents, and their advantages and limitations as therapeutic applications.

Indexed as

BacteriophagesExtensively Drug-Resistant TuberculosisMycobacterium tuberculosisTuberculosis, Multidrug-ResistantAntitubercular AgentsHumansAntitubercular AgentsDrug resistanceMycobacteriophagesMycobacterium tuberculosisPhage therapy

Identifiers

PMID36550444
PMCPMC9773572
OpenAlexW4312190689

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.