Evidence map›Paper›PMID 15731073›Full record

ArticleInfection and immunity2005

Age alterations in extent and severity of experimental intranasal infection with Chlamydophila pneumoniae in BALB/c mice.

C Scott Little, Andrew Bowe, Richard Lin, Jason Litsky, Robert M Fogel, Brian J Balin, Kerin L Fresa-Dillon

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Infections withFrontiers in aging neuroscience · 2025
    Review
  4. Frontiers in neuroscience · 2024
    Review
  5. Review
  6. The Adult Neurogenesis Theory of Alzheimer's Disease.Journal of Alzheimer's disease : JAD · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Frontiers in cellular and infection microbiology · 2020
    Article
  11. Frontiers in aging neuroscience · 2018
    Review
  12. Review
  13. Microbes and Alzheimer's Disease.Journal of Alzheimer's disease : JAD · 2016
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  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

7 authors at 1 institution in 1 country.

C Scott LittleDepartment of Pathology, Microbiology, and Immunology, the Philadelphia College of Osteopathic Medicine, 4170 City Ave., Philadelphia, PA 19131, USA.
Andrew Bowe
Richard Lin
Jason Litsky
Robert M Fogel
Brian J Balin
Kerin L Fresa-Dillon
Philadelphia College of Osteopathic Medicine · US

Funding

Immunosenescence and Chlamydia PneumoniaeR15AG018320 · NIA · PHILADELPHIA COLLEGE OF OSTEOPATHIC MED · PI FRESA-DILLON, KERIN L · 2001 to 2001
$131k
NIA NIH HHS AG-18320NIA NIH HHS R15 AG018320
6 · The paper itself

Abstract

The intracellular bacterium Chlamydophila ("Chlamydia") pneumoniae is a pathogen for several respiratory diseases and may be a factor in the pathogenesis of chronic diseases of aging including atherosclerosis and Alzheimer's disease. We assessed whether aging is coupled with increased burden of infection in BALB/c mice after intranasal infection by C. pneumoniae. Six- and twenty-month-old BALB/c mice were infected intranasally with 5 x 10(4) inclusion forming units (IFU) or 5 x 10(5) IFU of C. pneumoniae. Lung, brain, and heart tissue were analyzed for infectious C. pneumoniae and for Chlamydophila antigen by immunohistochemistry. At both doses, aging was associated with a decreased proportion of animals that cleared infection from the lung and greater burden of infectious organism within the lung. We observed dose-dependent spread to the heart/ascending aorta in animals infected with C. pneumoniae. In mice given 5 x 10(4) IFU, spread to the heart by day 14 was only observed in old mice. By day 28, all animals inoculated with 5 x 10(4) IFU showed evidence of spread to the heart, although higher C. pneumoniae titers were observed in the hearts from old mice. In mice inoculated with 5 x 10(5) IFU, spread of C. pneumoniae to the heart was evident by day 14, with no discernible age effect. C. pneumoniae was also recovered from the central nervous system (brain and olfactory bulb) of all mice by day 28 postinfection, with higher C. pneumoniae titers in old animals than in young animals. Our results suggest that infection with C. pneumoniae may be more severe in old animals.

Indexed as

Administration, IntranasalAgingAnimalsBrainChlamydophila InfectionsChlamydophila pneumoniaeFemaleHeartLungMiceMice, Inbred BALB CMyocardiumSeverity of Illness Index

Identifiers

PMID15731073
PMCPMC1064908
OpenAlexW2140796553

What OpenQuestion holds

Textmetadata
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.