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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Bifunctional Enzyme SpoT Is Involved in Biofilm Formation of Helicobacter pylori with Multidrug Resistance by Upregulating Efflux Pump Hp1174 (gluP)
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Bifunctional Enzyme SpoT Is Involved in Biofilm Formation of Helicobacter pylori with Multidrug Resistance by Upregulating Efflux Pump Hp1174 (gluP)

机译:双官能酶斑点参与生物膜形成幽门螺杆菌,通过上调电源泵HP1174(Glup)

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摘要

The drug resistance of Helicobacter pylori is gradually becoming a serious problem. Biofilm formation is an important factor that leads to multidrug resistance (MDR) in bacteria. The ability of H. pylori to form biofilms on the gastric mucosa is known. However, there are few studies on the regulatory mechanisms of H. pylori biofilm formation and multidrug resistance. Guanosine 3'-diphosphate 5'-triphosphate and guanosine 3',5'-bispyrophosphate [(p)ppGpp] are global regulatory factors and are synthesized in H. pylori by the bifunctional enzyme SpoT. It has been reported that (p)ppGpp is involved in the biofilm formation and multidrug resistance of various bacteria. In this study, we found that SpoT also plays an important role in H. pylori biofilm formation and multidrug resistance. Therefore, it was necessary to carry out some further studies regarding its regulatory mechanism. Considering that efflux pumps are of great importance in the biofilm formation and multi-drug resistance of bacteria, we tried to determine whether efflux pumps controlled by SpoT participate in these activities. We found that Hp1174 (glucose/galactose transporter (glue]), an efflux pump of the major facilitator superfamily (MFS), is highly expressed in biofilm-forming and multi-drug-resistant (MDR) H. pylori strains and is upregulated by SpoT. Through further research, we determined that gluP is involved in H. pylori biofilm formation and multidrug resistance. Furthermore, the average expression level of gluP in the clinical MDR strains (C-MDR) was considerably higher than that in the clinical drug-sensitive strains (C-DSS). Taken together, our results revealed a novel molecular mechanism of H. pylori resistance to multidrug exposure.
机译:幽门螺杆菌的耐药性逐渐成为一个严重的问题。生物膜形成是导致细菌中多药抗性(MDR)的重要因素。 H. Pylori在胃粘膜上形成生物膜的能力是已知的。然而,关于幽门螺杆菌生物膜形成和多药耐药性的调节机制少。鸟苷3'-二磷酸5'-三磷酸和鸟苷3',5'-双杂磷酸盐[(P)PPGPP]是全球性调节因子,并通过双官能酶斑点以H. Pylori合成。据报道,(P)PPGPP参与了各种细菌的生物膜形成和多药抗性。在这项研究中,我们发现该点也在H. Pylori Biofilm形成和多药耐药中起重要作用。因此,有必要对其监管机制进行一些进一步的研究。考虑到流出泵在生物膜形成和细菌的多药物抵抗力方面具有重要意义,我们试图确定通过点控制的Efflux泵是否参与这些活动。我们发现HP1174(葡萄糖/半乳糖转运蛋白(胶水)是主要促进剂超家族(MFS)的流出泵,在生物膜形成和多药物抗性(MDR)H.幽门螺杆菌菌株中高度表达并通过现货。通过进一步的研究,我们确定了GLUP涉及H. Pylori Biofilm的形成和多药抗性。此外,临床MDR菌株(C-MDR)中的GLUP的平均表达水平显着高于临床药物 - 敏感菌株(C-DSS)。我们的结果揭示了一种新的幽门螺杆菌抗性对多药暴露的分子机制。

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  • 作者单位

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Guiyang Med Univ Dept Microbiol Guiyang Guizhou Peoples R China;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Shandong Univ Sch Control Sci &

    Engn Jinan Shandong Peoples R China;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

    Shandong Univ Dept Microbiol Shandong Prov Key Lab Infect &

    Immunol Key Lab Expt Teratol Minist;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

    Helicobacter pylori; SpoT; efflux pump; biofilm; antibiotic resistance; GluP;

    机译:幽门螺杆菌;斑点;流出泵;生物膜;抗生素抗性;GLOUP;

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