Evidence map›Paper›PMID 18648543›Full record

ArticlePloS one2008

Specific and sensitive detection of H. pylori in biological specimens by real-time RT-PCR and in situ hybridization.

Hui Liu, Arifur Rahman, Cristina Semino-Mora, Sonia Q Doi, Andre Dubois

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. MixedHealthcare (Basel, Switzerland) · 2019
    Article
  4. Article
  5. Laboratory animal research · 2018
    Article
  6. Review
  7. Article
  8. Dyspepsia: When and How to Test for Helicobacter pylori Infection.Gastroenterology research and practice · 2016
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mechanism of H. pylori intracellular entry: an in vitro study.Frontiers in cellular and infection microbiology · 2012
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Hui LiuDepartment of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Arifur Rahman
Cristina Semino-Mora
Sonia Q Doi
Andre Dubois
Uniformed Services University of the Health Sciences · US

Funding

BACTERIAL &CHEMICAL CARCINOGENS IN GASTRIC ONCOGENESISR01CA082312 · NCI · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MERRELL, D. SCOTT · 2000 to 2012
$4.0M
NCI NIH HHS R01 CA082312NCI NIH HHS R01-CA082312
6 · The paper itself

Abstract

PCR detection of H. pylori in biological specimens is rendered difficult by the extensive polymorphism of H. pylori genes and the suppressed expression of some genes in many strains. The goal of the present study was to (1) define a domain of the 16S rRNA sequence that is both highly conserved among H. pylori strains and also specific to the species, and (2) to develop and validate specific and sensitive molecular methods for the detection of H. pylori. We used a combination of in silico and molecular approaches to achieve sensitive and specific detection of H. pylori in biologic media. We sequenced two isolates from patients living in different continents and demonstrated that a 546-bp domain of the H. pylori 16S rRNA sequence was conserved in those strains and in published sequences. Within this conserved sequence, we defined a 229-bp domain that is 100% homologous in most H. pylori strains available in GenBank and also is specific for H. pylori. This sub-domain was then used to design (1) a set of high quality RT-PCR primers and probe that encompassed a 76-bp sequence and included at least two mismatches with other Helicobacter sp. 16S rRNA; and (2) in situ hybridization antisense probes. The sensitivity and specificity of the approaches were then demonstrated by using gastric biopsy specimens from patients and rhesus monkeys. This H. pylori-specific region of the 16S rRNA sequence is highly conserved among most H. pylori strains and allows specific detection, identification, and quantification of this bacterium in biological specimens.

Indexed as

AnimalsBase SequenceBiopsyCloning, MolecularConserved SequenceDNA PrimersGastritisHelicobacter InfectionsHelicobacter pyloriIn Situ HybridizationMacaca mulattaMolecular Sequence DataRNA, Ribosomal, 16SSequence Analysis, DNAStomachDNA PrimersRNA, Ribosomal, 16S

Identifiers

PMID18648543
PMCPMC2481290
OpenAlexW2160431243

What OpenQuestion holds

Textmetadata
LicenceCC0
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.