Prabhala Bala K, Aduri Nanda G, Iqbal Mazhar, Rahman Moazur, Gajhede Michael, Hansen Paul R, Mirza Osman
Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering, Faisalabad, Pakistan.
Res Microbiol. 2017 Jun;168(5):443-449. doi: 10.1016/j.resmic.2017.01.005. Epub 2017 Feb 16.
Proton-dependent oligopeptide transporters (POTs) are secondary active transporters found in all kingdoms of life. POTs utilize the proton electrochemical gradient for the uptake of nutrient dipeptides and tripeptides. The human POT hPepT1 is known to transport a number of drugs. As part of ongoing studies on substrate specificities of POTs from Escherichia coli, our aim in this study was to investigate whether bacterial POTs could also transport these drugs. For this, we selected the common orally administered drugs sulpiride, bestatin, valacyclovir, ampicillin and oseltamivir, that are all transported by hPepT1. The transport of these drugs was evaluated using the prototypical POT YdgR from E. coli. The transport studies were pursued through combining cell-based assays with liquid chromatography-tandem mass spectrometric (LC-MS/MS) analysis. These investigations revealed that YdgR from E. coli is able to transport five (sulpiride, bestatin, valacyclovir, ampicillin and oseltamivir) drugs. Furthermore, cells not overexpressing YdgR were also able to transport these drugs in a POT-like manner. Orthologues of YdgR are found in several species in the gut microbiome; hence, our findings could have implications for further understanding about the interaction between gut microbes and orally administered drugs.
质子依赖性寡肽转运体(POTs)是在所有生命王国中都能找到的次级主动转运体。POTs利用质子电化学梯度来摄取营养二肽和三肽。已知人类POT hPepT1能转运多种药物。作为对大肠杆菌POTs底物特异性进行的持续研究的一部分,我们在本研究中的目的是调查细菌POTs是否也能转运这些药物。为此,我们选择了都能被hPepT1转运的常见口服药物舒必利、贝抑素、伐昔洛韦、氨苄青霉素和奥司他韦。使用大肠杆菌的典型POT YdgR评估这些药物的转运情况。通过将基于细胞的分析与液相色谱 - 串联质谱(LC-MS/MS)分析相结合来进行转运研究。这些研究表明,大肠杆菌的YdgR能够转运五种(舒必利、贝抑素、伐昔洛韦、氨苄青霉素和奥司他韦)药物。此外,未过表达YdgR的细胞也能够以类似POT的方式转运这些药物。在肠道微生物群的多个物种中发现了YdgR的直系同源物;因此,我们的发现可能对进一步理解肠道微生物与口服药物之间的相互作用具有启示意义。