Evidence map›Paper›PMID 27400721›Full record

ArticleInfection and immunity2016

Infant Mouse Model for the Study of Shedding and Transmission during Streptococcus pneumoniae Monoinfection.

M Ammar Zafar, Masamitsu Kono, Yang Wang, Tonia Zangari, Jeffrey N Weiser

Abstract read
In one paragraph

Article in Infection and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
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

59 citing papers in PubMed.

  1. Lactate Oxidase (LctO) Acts as a Metabolic Checkpoint RestrainingbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
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  4. Influenza A Virus Coinfection AltersbioRxiv : the preprint server for biology · 2026
    Article
  5. Bacterial and host factors affecting acquisition ofbioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Mechanisms of bacterial host-to-host transmission.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  9. Review
  10. Article
  11. Mucosal colonization ofMicrobiology spectrum · 2025
    Article
  12. Colonization dynamics ofInfection and immunity · 2025
    Article
  13. Intra-serotype variation ofMicrobiology spectrum · 2025
    Article
  14. Article
  15. 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.

M Ammar ZafarDepartment of Microbiology, New York University, New York, New York, USA.
Masamitsu KonoDepartment of Microbiology, New York University, New York, New York, USA Department of Otolaryngology-Head and Neck Surgery, Wakayama Medical University, Wakayama, Japan.
Yang WangDepartment of Microbiology, New York University, New York, New York, USA School of Medicine, Tsing Hua University, Beijing, China.
Tonia ZangariDepartment of Microbiology, New York University, New York, New York, USA.
Jeffrey N WeiserDepartment of Microbiology, New York University, New York, New York, USA Jeffrey.Weiser@nyumc.org.

Funding

ROLE OF OPACITY VARIATION IN PNEUMOCOCCAL PATHOGENESISR01AI038446 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WEISER, JEFFREY NEAL · 1996 to 2019
$7.4M
Mechanisms of Pneumococcal Persistence During CarriageR37AI038446 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jeffrey Neal Weiser · 2020 to 2026
$3.8M
Early Events in Pneumococcal ColonizationR01AI105168 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WEISER, JEFFREY NEAL · 2014 to 2018
$2.1M
NIAID NIH HHS R01 AI105168NIAID NIH HHS R37 AI038446
6 · The paper itself

Abstract

One of the least understood aspects of the bacterium Streptococcus pneumoniae (pneumococcus) is its transmission from host to host, the critical first step in both the carrier state and the disease state. To date, transmission models have depended on influenza A virus coinfection, which greatly enhances pneumococcal shedding to levels that allow acquisition by a new host. Here, we describe an infant mouse model that can be utilized to study pneumococcal colonization, shedding, and transmission during bacterial monoinfection. Using this model, we demonstrated that the level of bacterial shedding is highest in pups infected intranasally at age 4 days and peaks over the first 4 days postchallenge. Shedding results differed among isolates of five different pneumococcal types. Colonization density was found to be a major factor in the level of pneumococcal shedding and required expression of capsule. Transmission within a litter occurred when there was a high ratio of colonized "index" pups to uncolonized "contact" pups. Transmission was observed for each of the well-colonizing pneumococcal isolates, with the rate of transmission proportional to the level of shedding. This model can be used to examine bacterial and host factors that contribute to pneumococcal transmission without the effects of viral coinfection.

Indexed as

AnimalsAnimals, NewbornBacterial SheddingCarrier StateDisease Models, AnimalMiceMice, Inbred C57BLPneumococcal InfectionsStreptococcus pneumoniae

Identifiers

PMID27400721
PMCPMC4995895

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.