Evidence map›Paper›PMID 27363525›Full record

ArticleBMC evolutionary biology2016

Deciphering the recent phylogenetic expansion of the originally deeply rooted Mycobacterium tuberculosis lineage 7.

Solomon A Yimer, Amine Namouchi, Ephrem Debebe Zegeye, Carol Holm-Hansen, Gunnstein Norheim, Markos Abebe, Abraham Aseffa, Tone Tønjum

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Infection and drug resistance · 2023
    Article
  5. Comparative whole-genome sequence analysis ofFrontiers in microbiology · 2023
    Article
  6. Article
  7. Article
  8. Lineage-Specific Proteomic Signatures in theFrontiers in microbiology · 2020
    Article
  9. Line-probe assay and molecular typing reveal a potential drug resistant clone ofTropical diseases, travel medicine and vaccines · 2018
    Article
  10. Comparative Proteomic Analysis ofFrontiers in microbiology · 2017
    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 2 countries.

Solomon A YimerDepartment of Microbiology, Oslo University Hospital, PO Box 4950, NO-0424, Oslo, Nydalen, Norway. s.a.yimer@medisin.uio.no.
Amine NamouchiDepartment of Microbiology, Oslo University Hospital, PO Box 4950, NO-0424, Oslo, Nydalen, Norway.
Ephrem Debebe ZegeyeUni Research Environment, Centre for Applied Biotechnology, PO Box 7803, N-5020, Bergen, Norway.
Carol Holm-HansenInfection Control and Environmental Health, Norwegian Institute of Public Health, PO Box 4404, 0403, Oslo, Nydalen, Norway.
Gunnstein NorheimInfection Control and Environmental Health, Norwegian Institute of Public Health, PO Box 4404, 0403, Oslo, Nydalen, Norway.
Markos AbebeArmauer Hansen Research Institute, Jimma Road, PO Box 1005, Addis Ababa, Ethiopia.
Abraham AseffaArmauer Hansen Research Institute, Jimma Road, PO Box 1005, Addis Ababa, Ethiopia.
Tone TønjumDepartment of Microbiology, Oslo University Hospital, PO Box 4950, NO-0424, Oslo, Nydalen, Norway.
Oslo University Hospital · NOArmauer Hansen Research Institute · ETNorwegian Institute of Public Health · NOUni Research (Norway) · NO

Funding

Ethiopia-Emory TB Research Training ProgramD43TW009127 · FIC · EMORY UNIVERSITY · PI HENRY M BLUMBERG, Kidist Bobosha · 2013 to 2026
$3.4M
FIC NIH HHS D43 TW009127
6 · The paper itself

Abstract

backgroundA deeply rooted phylogenetic lineage of Mycobacterium tuberculosis (M. tuberculosis) termed lineage 7 was discovered in Ethiopia. Whole genome sequencing of 30 lineage 7 strains from patients in Ethiopia was performed. Intra-lineage genome variation was defined and unique characteristics identified with a focus on genes involved in DNA repair, recombination and replication (3R genes).

resultsMore than 800 mutations specific to M. tuberculosis lineage 7 strains were identified. The proportion of non-synonymous single nucleotide polymorphisms (nsSNPs) in 3R genes was higher after the recent expansion of M. tuberculosis lineage 7 strain started. The proportion of nsSNPs in genes involved in inorganic ion transport and metabolism was significantly higher before the expansion began. A total of 22346 bp deletions were observed. Lineage 7 strains also exhibited a high number of mutations in genes involved in carbohydrate transport and metabolism, transcription, energy production and conversion.

conclusionsWe have identified unique genomic signatures of the lineage 7 strains. The high frequency of nsSNP in 3R genes after the phylogenetic expansion may have contributed to recent variability and adaptation. The abundance of mutations in genes involved in inorganic ion transport and metabolism before the expansion period may indicate an adaptive response of lineage 7 strains to enable survival, potentially under environmental stress exposure. As lineage 7 strains originally were phylogenetically deeply rooted, this may indicate fundamental adaptive genomic pathways affecting the fitness of M. tuberculosis as a species.

Indexed as

Biological EvolutionEthiopiaGenome, BacterialHumansMycobacterium tuberculosisPhylogenyPolymorphism, Single NucleotideSequence DeletionTuberculosis3R genesAmhara RegionEthiopiaLineage 7MutationsMycobacterium tuberculosisSingle nucleotide polymorphismWhole genome sequencing

Identifiers

PMID27363525
PMCPMC4929747
OpenAlexW2469636134

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.