Evidence map›Paper›PMID 30157763›Full record

ArticleBMC genomics2018

In vivo evolution of drug-resistant Mycobacterium tuberculosis in patients during long-term treatment.

Yuhui Xu, Fei Liu, Suting Chen, Jiannan Wu, Yongfei Hu, Baoli Zhu, Zhaogang Sun

Abstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
–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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. ClinicalFrontiers in microbiology · 2025
    Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Transcriptional regulation and drug resistance inFrontiers in cellular and infection microbiology · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Improving tuberculosis surveillance by detecting international transmission using publicly available whole genome sequencing data.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2021
    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

7 authors.

Yuhui XuInstitute of Chinese Materia medica, China Academy of Chinese Medical Science, Beijing, 100700, China.
Fei LiuCAS key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Science, Beijing, 100101, China.
Suting ChenNational Tuberculosis Clinical Laboratory, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China.
Jiannan WuNational Tuberculosis Clinical Laboratory, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China.
Yongfei HuCAS key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Science, Beijing, 100101, China.
Baoli ZhuCAS key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Science, Beijing, 100101, China. zhubaoli@im.ac.cn.
Zhaogang SunNational Tuberculosis Clinical Laboratory, Beijing Chest Hospital, Capital Medical University, Beijing, 101149, China. sunzg75@hotmail.com.

Funding

National Natural Science Foundation of China (CN) 31601081the Key Project Specialized for Infectious Diseases of the Chinese Ministry of Health 2013ZX10003009Tongzhou District Science and Technology Committee KJ2017CX053
6 · The paper itself

Abstract

backgroundIn the current scenario, the drug-resistant tuberculosis is a significant challenge in the control of tuberculosis worldwide. In order to investigate the in vivo evolution of drug-resistant M. tuberculosis, the present study envisaged sequencing of the draft genomes of 18 serial isolates from four pre-extensively drug-resistant (pre-XDR) tuberculosis patients for continuous genetic alterations.

resultsAll of the isolates harbored single nucleotide polymorphisms (SNPs) ranging from 1303 to 1309 with M. tuberculosis H37Rv as the reference. SNPs ranged from 0 to 12 within patients. The evolution rates were higher than the reported SNPs of 0.5 in the four patients. All the isolates exhibited mutations at sites of known drug targets, while some contained mutations in uncertain drug targets including folC, proZ, and pyrG. The compensatory substitutions for rescuing these deleterious mutations during evolution were only found in RpoC I491T in one patient. Many loci with microheterogeneity showed transient mutations in different isolates. Ninety three SNPs exhibited significant association with refractory pre-XDR TB isolates.

conclusionsOur results showed evolutionary changes in the serial genetic characteristics of the pre-XDR TB patients due to accumulation of the fixed drug-resistant related mutations, and the transient mutations under continuous antibiotics pressure over several years.

Indexed as

Evolution, MolecularAntitubercular AgentsGenotypeHumansMicrobial Sensitivity TestsMutationMycobacterium tuberculosisPolymorphism, Single NucleotideTime FactorsTuberculosis, Multidrug-ResistantAntitubercular AgentsDrug-resistant tuberculosisGenetic changesSNPTreatment

Identifiers

PMID30157763
PMCPMC6116439

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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.