Evidence map›Paper›PMID 17517860›Full record

ArticleInfection and immunity2007

Multiple consecutive lavage samplings reveal greater burden of disease and provide direct access to the nontypeable Haemophilus influenzae biofilm in experimental otitis media.

Magali Leroy, Howard Cabral, Marisol Figueira, Valérie Bouchet, Heather Huot, Sanjay Ram, Stephen I Pelton, Richard Goldstein

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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 3 institutions in 1 country.

Magali LeroySection of Molecular Genetics, Division of Pediatric Infectious Diseases, The Maxwell Finland Laboratory for Infectious Diseases, Boston University School of Medicine, Boston Medical Center, 774 Albany Street, Boston, MA 02118, USA.
Howard Cabral
Marisol Figueira
Valérie Bouchet
Heather Huot
Sanjay Ram
Stephen I Pelton
Richard Goldstein
Boston University · USBoston Medical Center · USUniversity of Massachusetts Amherst · US

Funding

Complement Activation on Neisseria meningitidisR01AI054544 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RAM, SANJAY · 2004 to 2014
$3.4M
NTHi LPS: virulence factor and vaccine candidateR01DC005855 · NIDCD · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GOLDSTEIN, RICHARD · 2003 to 2006
$1.5M
Role of sialylated LPS in H. influenzae otitis mediaR21DC005564 · NIDCD · BOSTON MEDICAL CENTER · PI GOLDSTEIN, RICHARD · 2002 to 2003
$161k
MICROBIAL POPULATION STRATEGY FOR VACCINE DEVELOPMENTR55DC004583 · NIDCD · BOSTON MEDICAL CENTER · PI GOLDSTEIN, RICHARD · 2001 to 2001
$100k
NIAID NIH HHS AI 054544NIAID NIH HHS R01 AI054544NIDCD NIH HHS DC 005855NIDCD NIH HHS DC 05483NIDCD NIH HHS DC 05564NIDCD NIH HHS R01 DC005855NIDCD NIH HHS R21 DC005564NIDCD NIH HHS R55 DC004583
6 · The paper itself

Abstract

The typically recovered quantity of nontypeable Haemophilus influenzae (NTHi) bacteria in an ex vivo middle ear (ME) aspirate from the chinchilla model of experimental otitis media is insufficient for direct analysis of gene expression by microarray or of lipopolysaccharide glycoforms by mass spectrometry. This prompted us to investigate a strategy of multiple consecutive lavage samplings to increase ex vivo bacterial recovery. As multiple consecutive lavage samples significantly increased the total number of bacterial CFU collected during nasopharyngeal colonization or ME infection, this led us to evaluate whether bacteria sequentially acquired from consecutive lavages were similar. Comparative observation of complete ex vivo sample series by microscopy initially revealed ME inflammatory fluid consisting solely of planktonic-phase NTHi. In contrast, subsequent lavage samplings of the same infected ear revealed the existence of bacteria in two additional growth states, filamentous and biofilm encased. Gene expression analysis of such ex vivo samples was in accord with different bacterial growth phases in sequential lavage specimens. The existence of morphologically distinct NTHi subpopulations with varying levels of gene expression indicates that the pooling of specimens requires caution until methods for their separation are developed. This study based on multiple consecutive lavages is consistent with prior reports that NTHi forms a biofilm in vivo, describes the means to directly acquire ex vivo biofilm samples without sacrificing the animal, and has broad applicability for a study of mucosal infections. Moreover, this approach revealed that the actual burden of bacteria in experimental otitis media is significantly greater than was previously reported. Such findings may have direct implications for antibiotic treatment and vaccine development against NTHi.

Indexed as

BiofilmsAnimalsBody FluidsChinchillaColony Count, MicrobialDisease Models, AnimalEar, MiddleGene Expression ProfilingHaemophilus InfectionsHaemophilus influenzaeMicroscopy, FluorescenceOtitis MediaTherapeutic Irrigation

Identifiers

PMID17517860
PMCPMC1952021
OpenAlexW2116381597

What OpenQuestion holds

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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.