Evidence map›Paper›PMID 18660809›Full record

ArticleNature genetics2008

High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi.

Kathryn E Holt, Julian Parkhill, Camila J Mazzoni, Philippe Roumagnac, François-Xavier Weill, Ian Goodhead, Richard Rance, Stephen Baker, Duncan J Maskell, John Wain and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 303 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
303citing papers in PubMed, 2 pooled it
75.8field-weighted citation impact, top 1% 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

303 citing papers in PubMed, 2 syntheses or guidelines pooled it, 518 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
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  16. Frontiers in cellular and infection microbiology · 2025
    Article
  17. Article
  18. Article
  19. Genetic heterogeneity in theMicrobial genomics · 2024
    Article
  20. Article

243 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 7 institutions in 5 countries.

Kathryn E HoltThe Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK. kh2@sanger.ac.uk
Julian Parkhill
Camila J Mazzoni
Philippe Roumagnac
François-Xavier Weill
Ian Goodhead
Richard Rance
Stephen Baker
Duncan J Maskell
John Wain
Christiane Dolecek
Mark Achtman
Gordon Dougan
Wellcome Sanger Institute · GBCharité - Universitätsmedizin Berlin · DEHospital for Tropical Diseases · VNInstitut Pasteur · FRMax Planck Institute for Infection Biology · DEOxford University Clinical Research Unit · VNUniversity of Cambridge · GB

Funding

Wellcome Trust 067321
6 · The paper itself

Abstract

Isolates of Salmonella enterica serovar Typhi (Typhi), a human-restricted bacterial pathogen that causes typhoid, show limited genetic variation. We generated whole-genome sequences for 19 Typhi isolates using 454 (Roche) and Solexa (Illumina) technologies. Isolates, including the previously sequenced CT18 and Ty2 isolates, were selected to represent major nodes in the phylogenetic tree. Comparative analysis showed little evidence of purifying selection, antigenic variation or recombination between isolates. Rather, evolution in the Typhi population seems to be characterized by ongoing loss of gene function, consistent with a small effective population size. The lack of evidence for antigenic variation driven by immune selection is in contrast to strong adaptive selection for mutations conferring antibiotic resistance in Typhi. The observed patterns of genetic isolation and drift are consistent with the proposed key role of asymptomatic carriers of Typhi as the main reservoir of this pathogen, highlighting the need for identification and treatment of carriers.

Indexed as

Evolution, MolecularGenome, BacterialBacteriophagesGenomic IslandsHumansMolecular Sequence DataPhylogenyPlasmidsPolymorphism, Single NucleotideRecombination, GeneticSalmonella typhiSequence Analysis, DNATyphoid Fever

Identifiers

PMID18660809
PMCPMC2652037
OpenAlexW2110397906

What OpenQuestion holds

Textmetadata
LicenceTDM
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.