Evidence map›Paper›PMID 25673672›Full record

ArticlePathogens and disease2015

Genomic variant representation in a Chlamydia population is dynamic and adaptive with dependence on in vitro and in vivo passage.

Deana K Jasper, Ira M Sigar, Justin H Schripsema, Carlyn K Sainvil, Christopher L Smith, Laxmi Yeruva, Roger G Rank, Ashlesh K Murthy, Jared R Widder, Kyle H Ramsey

Abstract read
In one paragraph

Article in Pathogens and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

10 authors.

Deana K JasperDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Ira M SigarDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Justin H SchripsemaDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Carlyn K SainvilDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Christopher L SmithDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Laxmi YeruvaDepartment of Pediatrics and Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72202, USA.
Roger G RankDepartment of Pediatrics and Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72202, USA.
Ashlesh K MurthyDepartment of Pathology, Midwestern University, Downers Grove, IL 60515, USA.
Jared R WidderDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Kyle H RamseyDepartment of Microbiology and Immunology, Chicago College Of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA kramse@midwestern.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have previously shown that Chlamydia muridarum has multiple genomic variants that concomitantly vary in their in vitro and in vivo phenotype. Herein, we used real-time polymerase chain reaction-based genotyping assays to query plaque-cloned isolates of C. muridarum for the frequency of eight selected polymorphisms. These strains had no history of passage in vivo since their original isolation from laboratory mice. There was significant variance in the frequency of two of the eight polymorphisms assessed with the remaining exhibiting a low rate of variance. To determine if any of these polymorphisms were more favorable for in vivo conditions, we blindly passaged non-clonal C. muridarum three times at 7-day intervals through the urogenital tract of mice. Seven of the eight polymorphisms varied in frequency following in vivo passage and four of these varied between C. muridarum strains. Selected isolates displayed variable growth rates and cytopathic effect in vitro. We conclude that multiple genotypic variants are present within the existing known C. muridarum strains and that the frequency of these variants changes upon introduction into the mouse host. These findings lend support to the concept that genotypic proportional representation in a chlamydial population is dynamic and adaptive.

Indexed as

Polymorphism, GeneticAnimalsChlamydia InfectionsChlamydia muridarumFemaleFemale Urogenital DiseasesGenotypeGenotyping TechniquesMice, Inbred BALB CMice, Inbred C3HReal-Time Polymerase Chain ReactionalleleChlamydiagenomegenotypehostpolymorphism

Identifiers

PMID25673672
PMCPMC4399565

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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.