Evidence map›Paper›PMID 20065052›Full record

ArticleAntimicrobial agents and chemotherapy2010

Impact of azithromycin resistance mutations on the virulence and fitness of Chlamydia caviae in guinea pigs.

Rachel Binet, Anne K Bowlin, Anthony T Maurelli, Roger G Rank

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-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

24 citing papers in PubMed, 33 citations in OpenAlex.

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  6. Dynamic energy dependency ofThe Journal of biological chemistry · 2018
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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

4 authors at 3 institutions in 1 country.

Rachel BinetDepartment of Microbiology and Immunology, F. Edward Hébert School of Medicine Uniformed Services University of Health Sciences, Bethesda, Maryland 20814-4799, USA. rachel.binet@fda.hhs.gov
Anne K Bowlin
Anthony T Maurelli
Roger G Rank
Uniformed Services University of the Health Sciences · USArkansas Children's Hospital · USUniversity of Arkansas for Medical Sciences · US

Funding

MOLECULAR GENETIC ANALYSIS OF CHLAMYDIA PATHOGENICITYR01AI044033 · NIAID · UNIVERSITY OF FLORIDA · PI MAURELLI, ANTHONY T · 1999 to 2016
$3.9M
Host response to Chlamydia genital infection in the maleR01AI059650 · NIAID · UNIV OF ARKANSAS FOR MED SCIS · PI RANK, ROGER G · 2005 to 2008
$1.4M
Molecular Genetic Analysis of Chlamydia PathogenicityR56AI044033 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MAURELLI, ANTHONY T · 2012 to 2012
$363k
Molecular Genetic Analysis of Chlamydia PathogenicityR21AI044033 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MAURELLI, ANTHONY T · 2004 to 2004
$301k
NIAID NIH HHS AI44033NIAID NIH HHS AI59650NIAID NIH HHS R01 AI044033NIAID NIH HHS R01 AI059650NIAID NIH HHS R21 AI044033NIAID NIH HHS R56 AI044033
6 · The paper itself

Abstract

Azithromycin (AZM) is a major drug used in the treatment and prophylaxis of infections caused by Chlamydia, yet no significant clinical resistance has been reported for these obligate intracellular bacteria. Nevertheless, spontaneous AZM resistance (Azm(r)) arose in vitro at frequencies ranging from 3 x 10(-8) to 8 x 10(-10) for clonal isolates of Chlamydia caviae, which is a natural pathogen of guinea pigs. Sequencing of the unique 23S rRNA gene copy in 44 independent Azm(r) isolates identified single mutations at position A(2058) or A(2059) (Escherichia coli numbering system). While SP(6)AZ(1) (A(2058)C) and SP(6)AZ(2) (A(2059)C) Azm(r) mutants showed growth defects in cell culture and were less pathogenic in the guinea pig ocular infection model than in the parent SP(6), the three isogenic C. caviae isolates grew equally well in the animal. On the other hand, coinoculation of the C. caviae parent strain with one of the Azm(r) strains was detrimental for the mutant strain. This apparent lack of association between pathology and bacterial load in vivo showed that virulence of the two Azm(r) mutants of C. caviae was attenuated. While chlamydial growth in vitro reflects the ability of the bacteria to multiply in permissive cells, survival in the host is a balance between cellular multiplication and clearance by the host immune system. The obligate intracellular nature of Chlamydia may therefore limit emergence of resistance in vivo due to the strength of the immune response induced by the wild-type antibiotic-sensitive bacteria at the time of antibiotic treatment.

Indexed as

MutationAnimalsAnti-Bacterial AgentsAzithromycinCells, CulturedChlamydiaChlamydia InfectionsConjunctivitis, InclusionCulture MediaDrug Resistance, BacterialFibroblastsGuinea PigsMiceMicrobial Sensitivity TestsVirulenceAnti-Bacterial AgentsAzithromycinCulture Media

Identifiers

PMID20065052
PMCPMC2826001
OpenAlexW2170447710

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.