Evidence map›Paper›PMID 10049283›Full record

ArticleAntimicrobial agents and chemotherapy1999

Esterases in serum-containing growth media counteract chloramphenicol acetyltransferase activity in vitro.

C D Sohaskey, A G Barbour

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. The In Vitro Antimicrobial Susceptibility ofPathogens (Basel, Switzerland) · 2023
    Review
  3. Article
  4. Genetic Transformation and Complementation.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Development of an extrachromosomal cloning vector system for use in Borrelia burgdorferi.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  11. Article
  12. Genetic Manipulation of Borrelia Spp.Current topics in microbiology and immunology
    Review
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

2 authors at 1 institution in 1 country.

C D SohaskeyDepartment of Microbiology & Molecular Genetics, University of California, Irvine 92697-4025, USA.
A G Barbour
University of California, Irvine · US

Funding

MOLECULAR BASIS OF BORRELIA PATHOGENESISR37AI024424 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI BARBOUR, ALAN G. · 2001 to 2010
$3.5M
MOLECULAR BASIS OF BORRELIA PATHOGENESISR01AI024424 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI BARBOUR, ALAN G. · 1987 to 2000
$339k
NIAID NIH HHS AI24424NIAID NIH HHS R01 AI024424NIAID NIH HHS R37 AI024424
6 · The paper itself

Abstract

The spirochete Borrelia burgdorferi was unexpectedly found to be as susceptible to diacetyl chloramphenicol, the product of the enzyme chloramphenicol acetyltransferase, as it was to chloramphenicol itself. The susceptibilities of Escherichia coli and Bacillus subtilis, as well as that of B. burgdorferi, to diacetyl chloramphenicol were then assayed in different media. All three species were susceptible to diacetyl chloramphenicol when growth media were supplemented with rabbit serum or, to a lesser extent, human serum. Susceptibility of E. coli and B. subtilis to diacetyl chloramphenicol was not observed in the absence of serum, when horse serum was used, or when the rabbit or human serum was heated first. In the presence of 10% rabbit serum, a strain of E. coli bearing the chloramphenicol acetyltransferase (cat) gene had a fourfold-lower resistance to chloramphenicol than in the absence of serum. A plate bioassay for chloramphenicol activity showed the conversion by rabbit, mouse, and human sera but not bacterial cell extracts or heated serum of diacetyl chloramphenicol to an inhibitory compound. Deacetylation of acetyl chloramphenicol by serum components was demonstrated by using fluorescent substrates and thin-layer chromatography. These studies indicate that esterases of serum can convert diacetyl chloramphenicol back to an active antibiotic, and thus, in vitro findings may not accurately reflect the level of chloramphenicol resistance by cat-bearing bacteria in vivo.

Indexed as

Culture MediaAnimalsAnti-Bacterial AgentsBacillus subtilisBorrelia burgdorferi GroupChloramphenicolChloramphenicol O-AcetyltransferaseChromatography, Thin LayerDrug Resistance, MicrobialEnzyme InhibitorsEscherichia coliEsterasesFemaleHorsesHumansMice1,3-diacetylchloramphenicolAnti-Bacterial AgentsChloramphenicolChloramphenicol O-AcetyltransferaseCulture MediaEnzyme InhibitorsEsterases

Identifiers

PMID10049283
PMCPMC89176
OpenAlexW2121558415

What OpenQuestion holds

Texttitle and abstract
measurements read1
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.