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使用一项初步研究确定体内甲氧苄啶的从头最小选择浓度

Determination of the De Novo Minimum Selection Concentration of Trimethoprim In Vivo for Using A Pilot Study.

作者信息

Macleod Jaime Knox, Gestels Zina, Abdellati Said, Vanbaelen Thibaut, Kenyon Chris, Manoharan-Basil Sheeba Santhini

机构信息

STI Unit, Department of Clinical Sciences, Institute of Tropical Medicine, 2000 Antwerp, Belgium.

Division of Infectious Diseases and HIV Medicine, University of Cape Town, Cape Town 7700, South Africa.

出版信息

Microorganisms. 2024 Dec 24;13(1):3. doi: 10.3390/microorganisms13010003.

Abstract

We investigated whether the maximum residual levels of trimethoprim permitted in food (Acceptable Daily Intake-ADI) could select for de novo trimethoprim resistance in in vivo. We designed chronic infection models of in and exposed them to sub-ADI doses of trimethoprim through a single-dosing regimen. The emergence of trimethoprim resistance was determined by isolating the target bacteria on selective agar plates, followed by species confirmation using MALDI-TOF mass spectrometry. The minimum inhibitory concentration (MIC) was assessed via the E-test to determine susceptibility to trimethoprim. Notably, exposure to as low as one-tenth of the ADI dose through a single-dosing regimen resulted in the selection of trimethoprim-resistant . Our findings indicate that trimethoprim doses ten-fold lower than the established ADI threshold could induce resistance to trimethoprim in . These results highlight the importance of considering antimicrobial resistance induction as a key factor when determining ADI levels in food.

摘要

我们研究了食品中允许的甲氧苄啶最大残留量(每日允许摄入量 - ADI)是否会在体内选择出新的甲氧苄啶抗性。我们设计了体内慢性感染模型,并通过单次给药方案将它们暴露于低于ADI剂量的甲氧苄啶。通过在选择性琼脂平板上分离目标细菌,然后使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行菌种确认来确定甲氧苄啶抗性的出现。通过E-test评估最低抑菌浓度(MIC)以确定对甲氧苄啶的敏感性。值得注意的是,通过单次给药方案暴露于低至ADI剂量十分之一的剂量会导致甲氧苄啶抗性菌的选择。我们的研究结果表明,比既定ADI阈值低十倍的甲氧苄啶剂量可诱导体内对甲氧苄啶产生抗性。这些结果凸显了在确定食品中的ADI水平时将抗菌药物抗性诱导作为关键因素加以考虑的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00aa/11767374/40352efcac2d/microorganisms-13-00003-g001.jpg

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