Evidence map›Paper›PMID 17570853›Full record

ArticleBMC microbiology2007

Virulence phenotypes of low-passage clinical isolates of nontypeable Haemophilus influenzae assessed using the chinchilla laniger model of otitis media.

Farrel J Buchinsky, Michael L Forbes, Jay D Hayes, Kai Shen, Suzanne Ezzo, James Compliment, Justin Hogg, N Luisa Hiller, Fen Ze Hu, J Christopher Post and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. ThemBio · 2026
    Article
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  4. Panel 3: Genomics, precision medicine and targeted therapies.International journal of pediatric otorhinolaryngology · 2020
    Review
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  19. What makes pathogens pathogenic.Genome biology · 2008
    Review
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

11 authors at 3 institutions in 1 country.

Farrel J BuchinskyCenter for Genomic Sciences, Allegheny-Singer Research Institute/Allegheny General Hospital, Pittsburgh, Pennsylvania 15212, USA. fjbuch@gmail.com <fjbuch@gmail.com>
Michael L Forbes
Jay D Hayes
Kai Shen
Suzanne Ezzo
James Compliment
Justin Hogg
N Luisa Hiller
Fen Ze Hu
J Christopher Post
Garth D Ehrlich
Allegheny General Hospital · USAllegheny-Singer Research Institute · USDrexel University · US

Funding

THE ROLE OF BIOFILMS IN THE PATHOGENESIS OF OTORRHEAR01DC004173 · NIDCD · ALLEGHENY-SINGER RESEARCH INSTITUTE · PI EHRLICH, GARTH D. · 2000 to 2008
$7.0M
MOLECULAR ANALYSIS OF PATHOGENS IN OTITIS MEDIA BY PCRR01DC002148 · NIDCD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI EHRLICH, GARTH D. · 1994 to 2017
$6.5M
Pneumococcal Biofilms in Otitis MediaR01DC005659 · NIDCD · ALLEGHENY-SINGER RESEARCH INSTITUTE · PI POST, JAMES CHRISTOPHER · 2003 to 2007
$3.1M
NIDCD NIH HHS DC02148NIDCD NIH HHS DC04173NIDCD NIH HHS DC05659NIDCD NIH HHS R01 DC002148NIDCD NIH HHS R01 DC004173NIDCD NIH HHS R01 DC005659PHS HHS C76HF03009
6 · The paper itself

Abstract

backgroundThe nontypeable Haemophilus influenzae (NTHi) are associated with a spectrum of respiratory mucosal infections including: acute otitis media (AOM); chronic otitis media with effusion (COME); otorrhea; locally invasive diseases such as mastoiditis; as well as a range of systemic disease states, suggesting a wide range of virulence phenotypes. Genomic studies have demonstrated that each clinical strain contains a unique genic distribution from a population-based supragenome, the distributed genome hypothesis. These diverse clinical and genotypic findings suggest that each NTHi strain possesses a unique set of virulence factors that contributes to the course of the disease.

resultsThe local and systemic virulence patterns of ten genomically characterized low-passage clinical NTHi strains (PittAA - PittJJ) obtained from children with COME or otorrhea were stratified using the chinchilla model of otitis media (OM). Each isolate was used to bilaterally inoculate six animals and thereafter clinical assessments were carried out daily for 8 days by blinded observers. There was no statistical difference in the time it took for any of the 10 NTHi strains to induce otologic (local) disease with respect to any or all of the other strains, however the differences in time to maximal local disease and the severity of local disease were both significant between the strains. Parameters of systemic disease indicated that the strains were not all equivalent: time to development of the systemic disease, maximal systemic scores and mortality were all statistically different among the strains. PittGG induced 100% mortality while PittBB, PittCC, and PittEE produced no mortality. Overall Pitt GG, PittII, and Pitt FF produced the most rapid and most severe local and systemic disease. A post hoc determination of the clinical origins of the 10 NTHi strains revealed that these three strains were of otorrheic origin, whereas the other 7 were from patients with COME.

conclusionCollectively these data suggest that the chinchilla OM model is useful for discriminating between otorrheic and COME NTHi strains as to their disease-producing potential in humans, and combined with whole genome analyses, point the way towards identifying classes of virulence genes.

Indexed as

ChinchillaDisease Models, AnimalAnimalsBacterial Typing TechniquesChildCluster AnalysisGenome, BacterialHaemophilus InfectionsHaemophilus influenzaeHumansOtitis MediaPolymerase Chain ReactionSurvival AnalysisTime FactorsVirulence

Identifiers

PMID17570853
PMCPMC1914350
OpenAlexW1986352201

What OpenQuestion holds

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LicenceCC BY
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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.