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In vitro susceptibility to pentavalent antimony in Leishmania infantum strains is not modified during in vitro or in vivo passages but is modified after host treatment with meglumine antimoniate.

作者信息

Carrió Jaume, Portús Montserrat

机构信息

Laboratory of Parasitology, Departament de Microbiologia i Parasitologia Sanitàries, Facultat de Farmàcia, Universitat de Barcelona, 08028 Barcelona, Spain.

出版信息

BMC Pharmacol. 2002 May 2;2:11. doi: 10.1186/1471-2210-2-11.


DOI:10.1186/1471-2210-2-11
PMID:12019027
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC113748/
Abstract

BACKGROUND: Leishmaniasis is a common parasitic disease in Southern Europe, caused by Leishmania infantum. The failures of current treatment with pentavalent antimonials are partially attributable to the emergence of antimony-resistant Leishmania strains. This study analyses the in vitro susceptibility to pentavalent antimony of intracellular amastigotes from a range of L. infantum strains, derived from the same infected animal, during in vitro and in vivo passages and after host treatment with meglumine antimoniate. RESULTS: SbV-IC50 values for strains from two distinct isolates from the same host and one stock after two years of culture in NNN medium and posterior passage to hamster were similar (5.0 +/- 0.2; 4.9 +/- 0.2 and 4.4 +/- 0.1 mgSbV/L, respectively). In contrast, a significant difference (P < 0.01, t test) was observed between the mean SbV-IC50 values in the stocks obtained before and after treatment of hosts with meglumine antimoniate (4.7 +/- 0.4 mgSbV/L vs. 7.7 +/- 1.5 mgSbV/L). Drug-resistance after drug pressure in experimentally infected dogs increased over repeated drug administration (6.4 +/- 0.5 mgSbV/L after first treatment vs. 8.6 +/- 1.4 mgSbV/L after the second) (P < 0.01, t test). CONCLUSIONS: These results confirm previous observations on strains from Leishmania/HIV co-infected patients and indicate the effect of the increasing use of antimony derivatives for treatment of canine leishmaniasis in endemic areas on the emergence of Leishmania antimony-resistant strains.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa8/113748/0844c5fe17ec/1471-2210-2-11-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa8/113748/0844c5fe17ec/1471-2210-2-11-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa8/113748/0844c5fe17ec/1471-2210-2-11-1.jpg

相似文献

[1]
In vitro susceptibility to pentavalent antimony in Leishmania infantum strains is not modified during in vitro or in vivo passages but is modified after host treatment with meglumine antimoniate.

BMC Pharmacol. 2002-5-2

[2]
Decreased sensitivity to meglumine antimoniate (Glucantime) of Leishmania infantum isolated from dogs after several courses of drug treatment.

Ann Trop Med Parasitol. 1992-12

[3]
Decreased antimony uptake and overexpression of genes of thiol metabolism are associated with drug resistance in a canine isolate of Leishmania infantum.

Int J Parasitol Drugs Drug Resist. 2016-8

[4]
Canine visceral leishmaniasis: comparison of in vitro leishmanicidal activity of marbofloxacin, meglumine antimoniate and sodium stibogluconate.

Vet Parasitol. 2006-1-30

[5]
In vitro and in vivo resistance of Leishmania infantum to meglumine antimoniate: a study of 37 strains collected from patients with visceral leishmaniasis.

Antimicrob Agents Chemother. 1997-4

[6]
Leishmania infantum: stage-specific activity of pentavalent antimony related with the assay conditions.

Exp Parasitol. 2000-7

[7]
In vitro activity of pentavalent antimony derivatives on promastigotes and intracellular amastigotes of Leishmania infantum strains from humans and dogs in Spain.

Acta Trop. 2001-5-25

[8]
Meglumine Antimoniate (Glucantime) Causes Oxidative Stress-Derived DNA Damage in BALB/c Mice Infected by Leishmania (Leishmania) infantum.

Antimicrob Agents Chemother. 2017-5-24

[9]
Stage-specific activity of pentavalent antimony against Leishmania donovani axenic amastigotes.

Antimicrob Agents Chemother. 1999-2

[10]
In vitro drug susceptibility of Leishmania infantum isolated from humans and dogs.

Exp Parasitol. 2013-6-6

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[8]
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[9]
Decreased antimony uptake and overexpression of genes of thiol metabolism are associated with drug resistance in a canine isolate of Leishmania infantum.

Int J Parasitol Drugs Drug Resist. 2016-8

[10]
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本文引用的文献

[1]
Virulence of Leishmania infantum is expressed as a clonal and dominant phenotype in experimental infections.

Infect Immun. 2001-12

[2]
The increase in risk factors for leishmaniasis worldwide.

Trans R Soc Trop Med Hyg. 2001

[3]
A randomised, blinded, placebo-controlled clinical trial with allopurinol in canine leishmaniosis.

Vet Parasitol. 2001-7-27

[4]
In vitro activity of pentavalent antimony derivatives on promastigotes and intracellular amastigotes of Leishmania infantum strains from humans and dogs in Spain.

Acta Trop. 2001-5-25

[5]
Long term improvement in the treatment of canine leishmaniosis using an antimony liposomal formulation.

Vet Parasitol. 2001-5-9

[6]
In vitro susceptibility of Leishmania infantum to meglumine antimoniate in isolates from repeated leishmaniasis episodes in HIV-coinfected patients.

J Antimicrob Chemother. 2001-1

[7]
Leishmania infantum: stage-specific activity of pentavalent antimony related with the assay conditions.

Exp Parasitol. 2000-7

[8]
Serological and parasitological follow-up in dogs experimentally infected with Leishmania infantum and treated with meglumine antimoniate.

Vet Parasitol. 1999-7

[9]
Evidence that the high incidence of treatment failures in Indian kala-azar is due to the emergence of antimony-resistant strains of Leishmania donovani.

J Infect Dis. 1999-8

[10]
Epidemiology of canine leishmaniosis in Catalonia (Spain) the example of the Priorat focus.

Vet Parasitol. 1999-6-15

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