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细粒棘球蚴基因型 III 对免疫缺陷和免疫功能正常的小鼠均表现出对阿苯达唑治疗的耐药性。

Encephalitozoon cuniculi Genotype III Evinces a Resistance to Albendazole Treatment in both Immunodeficient and Immunocompetent Mice.

机构信息

Institute of Parasitology, Biology Centre, Czech Academy of Science, České Budějovice, Czech Republic

Faculty of Science, University of South Bohemia in České Budějovice, České Budějovice, Czech Republic.

出版信息

Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.00058-20.

Abstract

Of four genotypes of , genotype II is considered to represent a parasite that occurs in many host species in a latent asymptomatic form, whereas genotype III seems to be more aggressive, and infections caused by this strain can lead to the death of even immunocompetent hosts. Although albendazole has been considered suitable for treatment of species, its failure in control of genotype III infection has been reported. This study determined the effect of a 100× recommended daily dose of albendazole on an genotype III course of infection in immunocompetent and immunodeficient mice and compared the results with those from experiments performed with a lower dose of albendazole and genotype II. The administration of the regular dose of abendazole during the acute phase of infection reduced the number of affected organs in all strains of mice and absolute counts of spores in screened organs. However, the effect on genotype III was minor. Surprisingly, no substantial effect was recorded after the use of a 100× dose of albendazole, with larger reductions seen only in the number of affected organs and absolute counts of spores in all strains of mice, implying variations in albendazole resistance between these genotypes. These results imply that differences in the course of infection and the response to treatment depend not only on the immunological status of the host but also on the genotype causing the infection. Understanding how microsporidia survive in hosts despite targeted antimicrosporidial treatment could significantly contribute to research related to human health.

摘要

在 4 种 基因型中,基因型 II 被认为是以潜伏无症状形式存在于许多宿主物种中的寄生虫,而基因型 III 似乎更具侵略性,由这种菌株引起的感染甚至可能导致免疫功能正常的宿主死亡。尽管阿苯达唑被认为是治疗 物种的合适药物,但已有报道称其在控制基因型 III 感染方面失败。本研究旨在确定 100 倍推荐日剂量的阿苯达唑对免疫功能正常和免疫功能低下的小鼠感染基因型 III 的影响,并将结果与用较低剂量的阿苯达唑和基因型 II 进行的实验结果进行比较。在感染急性期给予常规剂量的阿苯达唑可减少所有小鼠菌株受影响器官的数量和筛查器官中孢子的绝对计数。然而,对基因型 III 的影响较小。令人惊讶的是,使用 100 倍剂量的阿苯达唑后并未记录到明显的效果,仅在所有小鼠菌株的受影响器官数量和孢子的绝对计数方面观察到较大的减少,这表明这些基因型之间存在阿苯达唑耐药性的差异。这些结果表明,感染过程和对治疗的反应不仅取决于宿主的免疫状态,还取决于引起感染的基因型。了解微孢子虫如何在宿主中存活,尽管进行了靶向抗微孢子虫治疗,这可能会对与人类健康相关的研究产生重大影响。

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本文引用的文献

1
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Microbes Infect. 2020 Oct;22(9):467-473. doi: 10.1016/j.micinf.2020.06.004. Epub 2020 Jun 21.
3
Limited effect of adaptive immune response to control encephalitozoonosis.
Parasite Immunol. 2017 Dec;39(12). doi: 10.1111/pim.12496. Epub 2017 Nov 1.
4
The course of infection caused by Encephalitozoon cuniculi genotype III in immunocompetent and immunodeficient mice.
Exp Parasitol. 2017 Nov;182:16-21. doi: 10.1016/j.exppara.2017.09.022. Epub 2017 Sep 21.
5
Effects of selected Indonesian plant extracts on E. cuniculi infection in vivo.
Exp Parasitol. 2017 Oct;181:94-101. doi: 10.1016/j.exppara.2017.07.014. Epub 2017 Aug 2.
6
Isothermal Diagnostic Assays for Monitoring Single Nucleotide Polymorphisms in Necator americanus Associated with Benzimidazole Drug Resistance.
PLoS Negl Trop Dis. 2016 Dec 8;10(12):e0005113. doi: 10.1371/journal.pntd.0005113. eCollection 2016 Dec.
7
Prevalence and molecular characteristics of urinary and intestinal microsporidia infections in renal transplant recipients.
Clin Microbiol Infect. 2016 May;22(5):462.e5-9. doi: 10.1016/j.cmi.2016.01.014. Epub 2016 Jan 28.
9
Postnatal Hematopoiesis and Gut Microbiota in NOD Mice Deviate from C57BL/6 Mice.
J Diabetes Res. 2016;2016:6321980. doi: 10.1155/2016/6321980. Epub 2015 Dec 10.

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