Evidence map›Paper›PMID 22384012›Full record

ArticlePloS one2012

Visualization of murine intranasal dosing efficiency using luminescent Francisella tularensis: effect of instillation volume and form of anesthesia.

Mark A Miller, Jennifer M Stabenow, Jyothi Parvathareddy, Andrew J Wodowski, Thomas P Fabrizio, Xiaowen R Bina, Lillian Zalduondo, James E Bina

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

60 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
  2. Article
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  5. Article
  6. CRISPRi-mediated validation of candidatebioRxiv : the preprint server for biology · 2025
    Article
  7. Nrf2/cyclooxygenase 2 signaling in Cr(VI)-induced carcinogenesis.Ecotoxicology and environmental safety · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Optimizing anesthesia and delivery approaches for dosing into lungs of mice.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  16. Article
  17. Article
  18. Review
  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

8 authors at 1 institution in 1 country.

Mark A MillerThe University of Tennessee Health Science Center, Memphis, Tennessee, United States of America. mamiller@uthsc.edu
Jennifer M Stabenow
Jyothi Parvathareddy
Andrew J Wodowski
Thomas P Fabrizio
Xiaowen R Bina
Lillian Zalduondo
James E Bina
University of Tennessee Health Science Center · US

Funding

Yessinia autotransporters (Yaps): Structure, function, and host responseU54AI057157 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CROWE, JAMES E · 2003 to 2013
$91.4M
VSV as a vector for cytokine-assisted tularemia vaccinesU01AI061260 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI MILLER, MARK A · 2005 to 2009
$2.9M
Identification of Francisella tularensis extracellular proteins expressed in vivoR21AI079482 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI BINA, JAMES EDWARD · 2009 to 2010
$407k
Amino acid prototrophy as a positive selective marker in FrancisellaR21AI074582 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI BINA, JAMES EDWARD · 2007 to 2008
$397k
NIAID NIH HHS AI074582NIAID NIH HHS R21 AI074582NIAID NIH HHS R21 AI079482NIAID NIH HHS U01 AI061260NIAID NIH HHS #U54 AI057157NIAID NIH HHS U54 AI057157
6 · The paper itself

Abstract

Intranasal instillation is a widely used procedure for pneumonic delivery of drugs, vaccine candidates, or infectious agents into the respiratory tract of research mice. However, there is a paucity of published literature describing the efficiency of this delivery technique. In this report we have used the murine model of tularemia, with Francisella tularensis live vaccine strain (FTLVS) infection, to evaluate the efficiency of pneumonic delivery via intranasal dosing performed either with differing instillation volumes or different types of anesthesia. FTLVS was rendered luminescent via transformation with a reporter plasmid that constitutively expressed the Photorhabdus luminescens lux operon from a Francisella promoter. We then used an IVIS Spectrum whole animal imaging system to visualize FT dissemination at various time points following intranasal instillation. We found that instillation of FT in a dose volume of 10 µl routinely resulted in infection of the upper airways but failed to initiate infection of the pulmonary compartment. Efficient delivery of FT into the lungs via intranasal instillation required a dose volume of 50 µl or more. These studies also demonstrated that intranasal instillation was significantly more efficient for pneumonic delivery of FTLVS in mice that had been anesthetized with inhaled (isoflurane) vs. parenteral (ketamine/xylazine) anesthesia. The collective results underscore the need for researchers to consider both the dose volume and the anesthesia type when either performing pneumonic delivery via intranasal instillation, or when comparing studies that employed this technique.

Indexed as

Administration, IntranasalAnesthesiaAnimalsFemaleFrancisella tularensisIsofluraneKetamineKineticsLuminescent ProteinsMiceMice, Inbred BALB CModels, GeneticPhotorhabdusPromoter Regions, GeneticTularemiaXylazineIsofluraneKetamineLuminescent ProteinsXylazine

Identifiers

PMID22384012
PMCPMC3286442
OpenAlexW2029649995

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.