Evidence map›Paper›PMID 16723577›Full record

ArticleAntimicrobial agents and chemotherapy2006

Antimicrosporidial activities of fumagillin, TNP-470, ovalicin, and ovalicin derivatives in vitro and in vivo.

Peter J Didier, Jennifer N Phillips, Dorothy J Kuebler, Mohamed Nasr, Paul J Brindley, Mary E Stovall, Lisa C Bowers, E S Didier

Open access · greenAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 81 citations in OpenAlex.

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  16. Successful Treatment of DisseminatedOpen forum infectious diseases · 2016
    Article
  17. Review
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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

8 authors at 2 institutions in 1 country.

Peter J DidierDivision of Comparative Pathology, Tulane National Primate Research Center, Tulane University, Covington, LA 70433, USA.
Jennifer N Phillips
Dorothy J Kuebler
Mohamed Nasr
Paul J Brindley
Mary E Stovall
Lisa C Bowers
E S Didier
Tulane University · USNational Institute of Allergy and Infectious Diseases · US

Funding

ZCM:A NOVEL BROAD-SPECTRUM MICROBICIDE FOR SEXUALLY TRANSMITTED INFECTIONSP51RR000164 · NCRR · TULANE UNIVERSITY OF LOUISIANA · PI VEAZEY, RONALD S. · 1985 to 2011
$100.1M
PRECLINICAL EVAL. OF THERAPIES FOR MICROSPORIDIAL INFECTN01AI075327 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI DIDIER, ELIZABETH SCHMIDT · 1997 to 2000
$398k
NCRR NIH HHS P51 RR000164NCRR NIH HHS RR00164NIAID NIH HHS N01-AI75327
6 · The paper itself

Abstract

Therapies for microsporidiosis in humans are limited, and fumagillin, which appears to be the most broadly effective antimicrosporidial drug, is considered to be moderately toxic. The purpose of this study was to apply an in vitro drug screening assay for Encephalitozoon intestinalis and Vittaforma corneae and an in vivo athymic mouse model of V. corneae infection to assess the efficacy of TNP-470 (a semisynthetic analogue of fumagillin), ovalicin, and eight ovalicin derivatives. TNP-470, ovalicin, and three of the ovalicin derivatives inhibited both E. intestinalis and V. corneae replication by more than 70% in vitro. Another three of the ovalicin derivatives inhibited one of the two microsporidian species by more than 70%. None of the treated athymic mice survived the V. corneae infection, but they did survive statistically significantly longer than the untreated controls after daily treatment with fumagillin administered at 5, 10, and 20 mg/kg of body weight subcutaneously (s.c.), TNP-470 administered at 20 mg/kg intraperitoneally (i.p.), or ovalicin administered at 5 mg/kg s.c. Of two ovalicin derivatives that were assessed in vivo, NSC 9665 given at 10 mg/kg i.p. daily also statistically significantly prolonged survival of the mice. No lesions associated with drug toxicity were observed in the kidneys or livers of uninfected mice treated with these drugs at the highest dose of 20 mg/kg daily. These results thus support continued studies to identify more effective fumagillin-related drugs for treating microsporidiosis.

Indexed as

AnimalsCyclohexanesDrug Evaluation, PreclinicalEncephalitozoonFatty Acids, UnsaturatedIn Vitro TechniquesMaleMiceMice, NudeMicrosporidiaMicrosporidiosisO-(Chloroacetylcarbamoyl)fumagillolSesquiterpenesTime FactorsVittaformaCyclohexanesFatty Acids, UnsaturatedfumagillinO-(Chloroacetylcarbamoyl)fumagillolovalicinSesquiterpenes

Identifiers

PMID16723577
PMCPMC1479127
OpenAlexW2122305262

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.